Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 400746 |
| ensemblid | ENSG00000184454.7 |
| hgncid | 29332 |
| symbol | NCMAP |
| name | non-compact myelin associated protein |
| refseq_nuc | NM_001010980.5 |
| refseq_prot | NP_001010980.1 |
| ensembl_nuc | ENST00000374392.3 |
| ensembl_prot | ENSP00000363513.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 24556087 |
| end | 24609328 |
| strand | + |
| ver | v1.2 |
| region | chr1:24556087-24609328 |
| region5000 | chr1:24551087-24614328 |
| regionname0 | NCMAP_chr1_24556087_24609328 |
| regionname5000 | NCMAP_chr1_24551087_24614328 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 102 | 378 | 72 | 72 | 170 | 18 | 44 | 128 | NCMAP_chr1_24551087_24614328 | NCMAP | MTTAT others(97): Show |
chr1 | 24551087 | 24614328 |
| a0002 | 0/0 | 102 | 23 | 21 | 2 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | MTTAT others(97): Show |
chr1 | 24551087 | 24614328 |
| a0003 | 0/0 | 102 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | MTTAT others(97): Show |
chr1 | 24551087 | 24614328 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 306 | 378 | 72 | 72 | 170 | 18 | 44 | NCMAP_chr1_24551087_24614328 | NCMAP | ATGAC others(301): Show |
chr1 | 24551087 | 24614328 | ||
| a0002c0002 | 0/0 | 306 | 23 | 21 | 2 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | ATGAC others(301): Show |
chr1 | 24551087 | 24614328 | ||
| a0003c0003 | 0/0 | 306 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | ATGAC others(301): Show |
chr1 | 24551087 | 24614328 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3980 | 150 | 25 | 33 | 67 | 8 | 16 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0002 | 0/1 | 3981 | 86 | 0 | 17 | 50 | 4 | 14 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3976): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0003 | 0/0 | 3980 | 75 | 18 | 14 | 29 | 4 | 10 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0005 | 0/0 | 3981 | 18 | 0 | 3 | 15 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3976): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0006 | 0/0 | 3980 | 15 | 5 | 3 | 4 | 2 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0007 | 0/0 | 3980 | 10 | 10 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0008 | 0/0 | 3981 | 3 | 3 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3976): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0009 | 0/0 | 3980 | 3 | 3 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0010 | 0/0 | 3980 | 3 | 3 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0011 | 0/0 | 3980 | 3 | 1 | 2 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0013 | 0/0 | 3980 | 2 | 2 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0014 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0015 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0016 | 0/0 | 3981 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3976): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0017 | 0/0 | 4013 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(4008): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0018 | 0/0 | 3981 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3976): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0019 | 0/0 | 3981 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3976): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0021 | 0/0 | 3980 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0022 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0023 | 0/0 | 3980 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0001c0001t0025 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| a0002c0002t0004 | 0/0 | 3958 | 19 | 17 | 2 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3953): Show |
chr1 | 24551087 | 24614328 |
| a0002c0002t0012 | 0/0 | 3959 | 3 | 3 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3954): Show |
chr1 | 24551087 | 24614328 |
| a0002c0002t0024 | 0/0 | 3958 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3953): Show |
chr1 | 24551087 | 24614328 |
| a0003c0003t0020 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | GTGGC others(3975): Show |
chr1 | 24551087 | 24614328 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0008g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0008g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0008g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0010g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0010g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0010g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0011g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0011g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0013g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0014g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0015g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0016g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0017g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0018g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0019g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0021g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0022g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0023g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0025g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0012g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0024g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0003c0003t0020g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0345 | EUR | GBR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | GBR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0114 | EUR | GBR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0243 | EUR | GBR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0304 | EUR | FIN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0361 | EUR | FIN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0320 | EUR | FIN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0363 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00558 | hp1 | a0001 | c0001 | t0006 | g0283 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0171 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0374 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0381 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0357 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0240 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0377 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01069 | hp2 | a0001 | c0001 | t0011 | g0216 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01071 | hp2 | a0001 | c0001 | t0011 | g0203 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0347 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01099 | hp2 | a0002 | c0002 | t0004 | g0388 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0319 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0154 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0318 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0153 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01243 | hp1 | a0002 | c0002 | t0004 | g0018 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0278 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0330 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0177 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0370 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0143 | EUR | IBS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0346 | EUR | IBS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0142 | EUR | IBS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0293 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01884 | hp2 | a0002 | c0002 | t0004 | g0030 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0379 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01891 | hp2 | a0002 | c0002 | t0004 | g0394 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0172 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0178 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0338 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0339 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0166 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0397 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0033 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0373 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0353 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0176 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0023 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0352 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | CDX | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0350 | EAS | CDX | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CDX | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | CDX | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0272 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0396 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0276 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0068 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0384 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02572 | hp1 | a0002 | c0002 | t0004 | g0024 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0151 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0399 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0010 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02647 | hp2 | a0002 | c0002 | t0004 | g0031 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0368 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0066 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0334 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02723 | hp2 | a0002 | c0002 | t0012 | g0147 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02809 | hp1 | a0002 | c0002 | t0004 | g0389 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02818 | hp1 | a0002 | c0002 | t0004 | g0273 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0325 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0365 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02896 | hp2 | a0002 | c0002 | t0004 | g0390 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02897 | hp2 | a0002 | c0002 | t0004 | g0391 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0001 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0376 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02970 | hp1 | a0002 | c0002 | t0004 | g0017 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02976 | hp2 | a0002 | c0002 | t0004 | g0032 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0362 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03041 | hp2 | a0003 | c0003 | t0020 | g0275 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0294 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0392 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03139 | hp2 | a0002 | c0002 | t0004 | g0058 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0385 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0014 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03209 | hp2 | a0002 | c0002 | t0012 | g0002 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0009 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0359 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0378 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0274 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0386 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03486 | hp2 | a0002 | c0002 | t0012 | g0002 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03490 | hp1 | a0001 | c0001 | t0019 | g0101 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0355 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0354 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0380 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03540 | hp1 | a0002 | c0002 | t0004 | g0149 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0152 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0242 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | BEB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | BEB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0075 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0356 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0070 | SAS | BEB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04199 | hp1 | a0001 | c0001 | t0023 | g0004 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04204 | hp1 | a0001 | c0001 | t0021 | g0160 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0358 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0371 | AFR | YRI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18522 | hp2 | a0002 | c0002 | t0024 | g0025 | AFR | YRI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | CHB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0344 | EAS | CHB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | CHB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18906 | hp1 | a0001 | c0001 | t0025 | g0316 | AFR | YRI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0364 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18948 | hp1 | a0001 | c0001 | t0016 | g0174 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0369 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0343 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18961 | hp2 | a0001 | c0001 | t0015 | g0267 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0372 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0164 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0185 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18972 | hp2 | a0001 | c0001 | t0022 | g0360 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0367 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18992 | hp2 | a0001 | c0001 | t0018 | g0073 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0173 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18997 | hp1 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0337 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0281 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0351 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0197 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19004 | hp1 | a0001 | c0001 | t0017 | g0089 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0383 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0387 | AFR | LWK | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | LWK | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0382 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19066 | hp2 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19088 | hp1 | a0001 | c0001 | t0006 | g0315 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19240 | hp1 | a0002 | c0002 | t0004 | g0202 | AFR | YRI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0091 | EUR | TSI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0317 | EUR | TSI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0331 | EUR | TSI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | TSI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0333 | SAS | GIH | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | GIH | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0155 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0375 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0398 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0395 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02559 | hp1 | a0002 | c0002 | t0004 | g0034 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0326 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0393 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03471 | hp2 | a0002 | c0002 | t0004 | g0026 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG06807 | hp1 | a0002 | c0002 | t0004 | g0005 | AFR | USA | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | USA | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | USA | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20300 | hp2 | a0002 | c0002 | t0004 | g0007 | AFR | USA | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | LWK | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0135 | REF | REF | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0235 | REF | REF | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:24605732 | G | C | 1 | a0002 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
missense_variant | MODERATE | c.294G>C | p.Gln98His | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 384/3980 | 294/309 | 98/102 | chr1 | 24605732 | |||
| chr1:24605740 | C | T | 1 | a0003 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.302C>T | p.Thr101Met | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 392/3980 | 302/309 | 101/102 | chr1 | 24605740 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:24605741 | G | A | 1 | a0002c0002 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
synonymous_variant | LOW | c.303G>A | p.Thr101Thr | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 393/3980 | 303/309 | 101/102 | chr1 | 24605741 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:24605756 | C | T | 1 | a0001c0001t0025 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 9 | chr1 | 24605756 | ||||||
| chr1:24605760 | C | T | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*13C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 13 | chr1 | 24605760 | ||||||
| chr1:24605834 | T | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*87T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 87 | chr1 | 24605834 | ||||||
| chr1:24605872 | C | T | 1 | a0001c0001t0023 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 125 | chr1 | 24605872 | ||||||
| chr1:24605946 | C | T | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*199C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 199 | chr1 | 24605946 | ||||||
| chr1:24605953 | C | T | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*206C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 206 | chr1 | 24605953 | ||||||
| chr1:24606019 | A | G | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*272A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 272 | chr1 | 24606019 | ||||||
| chr1:24606040 | A | G | 1 | a0001c0001t0025 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*293A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 293 | chr1 | 24606040 | ||||||
| chr1:24606054 | CAGAT | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*311_*314delTAGA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 311 | INFO_REALIGN_3_PRIME | chr1 | 24606054 | |||||
| chr1:24606132 | A | C | 1 | a0001c0001t0022 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*385A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 385 | chr1 | 24606132 | ||||||
| chr1:24606157 | T | A | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*410T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 410 | chr1 | 24606157 | ||||||
| chr1:24606167 | A | G | 1 | a0001c0001t0021 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 420 | chr1 | 24606167 | ||||||
| chr1:24606219 | T | A | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*472T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 472 | chr1 | 24606219 | ||||||
| chr1:24606230 | C | T | 4 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 others(1): Show |
24 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*483C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 483 | chr1 | 24606230 | ||||||
| chr1:24606242 | A | G | 12 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(9): Show |
141 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*495A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 495 | chr1 | 24606242 | ||||||
| chr1:24606343 | T | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*596T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 596 | chr1 | 24606343 | ||||||
| chr1:24606451 | T | C | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(13): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*704T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 704 | chr1 | 24606451 | ||||||
| chr1:24606491 | C | T | 1 | a0001c0001t0006 | 15 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*744C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 744 | chr1 | 24606491 | ||||||
| chr1:24606507 | G | T | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*760G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 760 | chr1 | 24606507 | ||||||
| chr1:24606517 | T | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*770T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 770 | chr1 | 24606517 | ||||||
| chr1:24606546 | A | AC | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*800dupC | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 801 | INFO_REALIGN_3_PRIME | chr1 | 24606546 | |||||
| chr1:24606548 | G | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*801G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 801 | chr1 | 24606548 | ||||||
| chr1:24606565 | T | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*818T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 818 | chr1 | 24606565 | ||||||
| chr1:24606585 | G | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*838G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 838 | chr1 | 24606585 | ||||||
| chr1:24606619 | A | G | 1 | a0003c0003t0020 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*872A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 872 | chr1 | 24606619 | ||||||
| chr1:24606621 | G | A | 1 | a0001c0001t0015 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*874G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 874 | chr1 | 24606621 | ||||||
| chr1:24606703 | C | T | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0016 others(3): Show |
107 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*956C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 956 | chr1 | 24606703 | ||||||
| chr1:24606859 | G | C | 1 | a0001c0001t0016 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1112G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1112 | chr1 | 24606859 | ||||||
| chr1:24606881 | T | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1134T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1134 | chr1 | 24606881 | ||||||
| chr1:24606948 | T | G | 1 | a0001c0001t0006 | 15 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1201T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1201 | chr1 | 24606948 | ||||||
| chr1:24606984 | CTTTTTTC others(9): Show |
C | 1 | a0002c0002t0012 | 3 | HG02723.hp2 HG03209.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1244_*1259delCTTT others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1244 | INFO_REALIGN_3_PRIME | chr1 | 24606984 | |||||
| chr1:24606984 | CTTTTTTC others(10): Show |
C | 2 | a0002c0002t0004 a0002c0002t0024 |
20 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1244_*1260delCTTT others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1244 | INFO_REALIGN_3_PRIME | chr1 | 24606984 | |||||
| chr1:24606996 | C | CT | 10 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(7): Show |
40 | HG00558.hp1 HG01069.hp2 HG01071.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1265dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1266 | INFO_REALIGN_3_PRIME | chr1 | 24606996 | |||||
| chr1:24606996 | CT | C | 2 | a0001c0001t0001 a0001c0001t0003 |
12 | HG01168.hp1 HG02145.hp2 HG03239.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1265delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1265 | INFO_REALIGN_3_PRIME | chr1 | 24606996 | |||||
| chr1:24607069 | G | A | 4 | a0001c0001t0008 a0002c0002t0004 a0002c0002t0012 others(1): Show |
26 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1322G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1322 | chr1 | 24607069 | ||||||
| chr1:24607162 | T | A | 1 | a0001c0001t0010 | 3 | HG01891.hp1 HG02257.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1415T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1415 | chr1 | 24607162 | ||||||
| chr1:24607193 | G | A | 1 | a0003c0003t0020 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1446G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1446 | chr1 | 24607193 | ||||||
| chr1:24607221 | G | A | 1 | a0001c0001t0014 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1474G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1474 | chr1 | 24607221 | ||||||
| chr1:24607266 | G | A | 8 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(5): Show |
125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1519G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1519 | chr1 | 24607266 | ||||||
| chr1:24607267 | C | T | 1 | a0001c0001t0005 | 18 | HG00597.hp2 HG01358.hp1 HG01928.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1520C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1520 | chr1 | 24607267 | ||||||
| chr1:24607388 | CAT | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1644_*1645delAT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1644 | INFO_REALIGN_3_PRIME | chr1 | 24607388 | |||||
| chr1:24607438 | C | CAAAGAAC others(26): Show |
1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1691_*1692insAAAG others(29): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1692 | chr1 | 24607438 | ||||||
| chr1:24607440 | C | T | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1693C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1693 | chr1 | 24607440 | ||||||
| chr1:24607441 | T | G | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1694T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1694 | chr1 | 24607441 | ||||||
| chr1:24607446 | A | T | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1699A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1699 | chr1 | 24607446 | ||||||
| chr1:24607458 | T | G | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1711T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1711 | chr1 | 24607458 | ||||||
| chr1:24607465 | G | C | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1718G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1718 | chr1 | 24607465 | ||||||
| chr1:24607477 | G | T | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1730G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1730 | chr1 | 24607477 | ||||||
| chr1:24607484 | G | T | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1737G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1737 | chr1 | 24607484 | ||||||
| chr1:24607486 | T | TA | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(3): Show |
109 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*1741dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1742 | INFO_REALIGN_3_PRIME | chr1 | 24607486 | |||||
| chr1:24607489 | T | G | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1742T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1742 | chr1 | 24607489 | ||||||
| chr1:24607500 | T | C | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1753T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1753 | chr1 | 24607500 | ||||||
| chr1:24607501 | C | T | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1754C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1754 | chr1 | 24607501 | ||||||
| chr1:24607504 | T | C | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1757T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1757 | chr1 | 24607504 | ||||||
| chr1:24607505 | T | A | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1758T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1758 | chr1 | 24607505 | ||||||
| chr1:24607507 | A | T | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1760A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1760 | chr1 | 24607507 | ||||||
| chr1:24607508 | A | T | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1761A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1761 | chr1 | 24607508 | ||||||
| chr1:24607517 | C | A | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1770C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1770 | chr1 | 24607517 | ||||||
| chr1:24607522 | T | C | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1775T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1775 | chr1 | 24607522 | ||||||
| chr1:24607524 | T | A | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1777T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1777 | chr1 | 24607524 | ||||||
| chr1:24607525 | G | T | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1778G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1778 | chr1 | 24607525 | ||||||
| chr1:24607542 | T | G | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1795T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1795 | chr1 | 24607542 | ||||||
| chr1:24607584 | G | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1837G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1837 | chr1 | 24607584 | ||||||
| chr1:24607594 | G | A | 1 | a0001c0001t0006 | 15 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1847G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1847 | chr1 | 24607594 | ||||||
| chr1:24607633 | G | A | 1 | a0001c0001t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1886G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1886 | chr1 | 24607633 | ||||||
| chr1:24607636 | A | G | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1889A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1889 | chr1 | 24607636 | ||||||
| chr1:24607722 | G | T | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1975G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1975 | chr1 | 24607722 | ||||||
| chr1:24607732 | G | A | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1985G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1985 | chr1 | 24607732 | ||||||
| chr1:24607753 | A | T | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2006A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2006 | chr1 | 24607753 | ||||||
| chr1:24607775 | A | T | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2028A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2028 | chr1 | 24607775 | ||||||
| chr1:24607900 | G | A | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2153G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2153 | chr1 | 24607900 | ||||||
| chr1:24607920 | T | G | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2173T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2173 | chr1 | 24607920 | ||||||
| chr1:24607944 | T | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2197T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2197 | chr1 | 24607944 | ||||||
| chr1:24607972 | T | A | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2225T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2225 | chr1 | 24607972 | ||||||
| chr1:24607974 | G | A | 1 | a0002c0002t0012 | 3 | HG02723.hp2 HG03209.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2227G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2227 | chr1 | 24607974 | ||||||
| chr1:24608127 | T | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2380T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2380 | chr1 | 24608127 | ||||||
| chr1:24608145 | T | A | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2398T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2398 | chr1 | 24608145 | ||||||
| chr1:24608161 | G | A | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2414G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2414 | chr1 | 24608161 | ||||||
| chr1:24608183 | T | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2436T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2436 | chr1 | 24608183 | ||||||
| chr1:24608218 | G | C | 1 | a0002c0002t0024 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2471G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2471 | chr1 | 24608218 | ||||||
| chr1:24608271 | C | G | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2524C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2524 | chr1 | 24608271 | ||||||
| chr1:24608280 | T | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2533T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2533 | chr1 | 24608280 | ||||||
| chr1:24608281 | G | A | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2534G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2534 | chr1 | 24608281 | ||||||
| chr1:24608286 | A | G | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2539A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2539 | chr1 | 24608286 | ||||||
| chr1:24608353 | T | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2606T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2606 | chr1 | 24608353 | ||||||
| chr1:24608380 | T | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2633T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2633 | chr1 | 24608380 | ||||||
| chr1:24608381 | G | T | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2634G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2634 | chr1 | 24608381 | ||||||
| chr1:24608531 | C | T | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2784C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2784 | chr1 | 24608531 | ||||||
| chr1:24608590 | T | C | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2843T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2843 | chr1 | 24608590 | ||||||
| chr1:24608606 | G | T | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2859G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2859 | chr1 | 24608606 | ||||||
| chr1:24608626 | G | A | 1 | a0001c0001t0009 | 3 | HG02055.hp2 HG02280.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2879G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2879 | chr1 | 24608626 | ||||||
| chr1:24608635 | C | G | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2888C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2888 | chr1 | 24608635 | ||||||
| chr1:24608680 | G | A | 1 | a0001c0001t0018 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2933G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2933 | chr1 | 24608680 | ||||||
| chr1:24608713 | C | T | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2966C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2966 | chr1 | 24608713 | ||||||
| chr1:24608762 | A | G | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3015A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3015 | chr1 | 24608762 | ||||||
| chr1:24608850 | C | T | 1 | a0001c0001t0025 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3103C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3103 | chr1 | 24608850 | ||||||
| chr1:24608939 | G | A | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3192G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3192 | chr1 | 24608939 | ||||||
| chr1:24608950 | A | G | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3203A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3203 | chr1 | 24608950 | ||||||
| chr1:24608953 | G | C | 4 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0022 others(1): Show |
78 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*3206G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3206 | chr1 | 24608953 | ||||||
| chr1:24609035 | T | G | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3288T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3288 | chr1 | 24609035 | ||||||
| chr1:24609075 | A | T | 1 | a0001c0001t0019 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3328A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3328 | chr1 | 24609075 | ||||||
| chr1:24609079 | G | A | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3332G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3332 | chr1 | 24609079 | ||||||
| chr1:24609157 | C | T | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3410C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3410 | chr1 | 24609157 | ||||||
| chr1:24609187 | A | G | 3 | a0002c0002t0004 a0002c0002t0012 a0002c0002t0024 |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3440A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3440 | chr1 | 24609187 | ||||||
| chr1:24609232 | C | T | 1 | a0001c0001t0013 | 2 | HG02630.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3485C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3485 | chr1 | 24609232 | ||||||
| chr1:24609259 | G | A | 1 | a0001c0001t0011 | 3 | HG01069.hp2 HG01071.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3512G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3512 | chr1 | 24609259 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:24556177 | G | A | 1 | a0001c0001t0023g0004 | 1 | HG04199.hp1 | splice_region_variant&intron_variant | LOW | c.-8+8G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556177 | |||||||
| chr1:24556263 | C | T | 14 | a0001c0001t0001g0396 a0001c0001t0003g0386 a0001c0001t0003g0387 others(11): Show |
14 | HG01099.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8+94C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556263 | |||||||
| chr1:24556285 | G | A | 3 | a0001c0001t0003g0006 a0002c0002t0004g0005 a0002c0002t0004g0007 |
3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+116G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556285 | |||||||
| chr1:24556304 | C | T | 1 | a0001c0001t0006g0385 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-8+135C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556304 | |||||||
| chr1:24556314 | A | G | 69 | a0001c0001t0001g0317 a0001c0001t0001g0321 a0001c0001t0001g0322 others(66): Show |
69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-8+145A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556314 | |||||||
| chr1:24556399 | A | G | 84 | a0001c0001t0001g0317 a0001c0001t0001g0321 a0001c0001t0001g0322 others(81): Show |
84 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+230A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556399 | |||||||
| chr1:24556406 | C | T | 70 | a0001c0001t0001g0317 a0001c0001t0001g0321 a0001c0001t0001g0322 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-8+237C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556406 | |||||||
| chr1:24556436 | C | T | 45 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(42): Show |
45 | HG00280.hp1 HG00558.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.-8+267C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556436 | |||||||
| chr1:24556448 | A | C | 70 | a0001c0001t0001g0317 a0001c0001t0001g0321 a0001c0001t0001g0322 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-8+279A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556448 | |||||||
| chr1:24556473 | T | A | 1 | a0001c0001t0007g0008 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8+304T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556473 | |||||||
| chr1:24556489 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-8+320C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556489 | |||||||
| chr1:24556661 | T | C | 151 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(148): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.-8+492T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556661 | |||||||
| chr1:24556668 | A | G | 151 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(148): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.-8+499A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556668 | |||||||
| chr1:24556688 | C | A | 151 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(148): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.-8+519C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556688 | |||||||
| chr1:24556705 | G | A | 148 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(145): Show |
150 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.-8+536G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556705 | |||||||
| chr1:24556743 | C | T | 197 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(194): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-8+574C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556743 | |||||||
| chr1:24556790 | C | T | 3 | a0001c0001t0006g0152 a0001c0001t0006g0153 a0001c0001t0006g0154 |
3 | HG01168.hp2 HG01169.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-8+621C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556790 | |||||||
| chr1:24556809 | G | A | 2 | a0001c0001t0013g0009 a0001c0001t0013g0010 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-8+640G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556809 | |||||||
| chr1:24556993 | C | T | 1 | a0001c0001t0006g0315 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-8+824C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556993 | |||||||
| chr1:24557060 | G | C | 263 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(260): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-8+891G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557060 | |||||||
| chr1:24557151 | G | A | 26 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(23): Show |
26 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8+982G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557151 | |||||||
| chr1:24557374 | GGTGCATG others(9): Show |
G | 1 | a0001c0001t0002g0150 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-8+1218_-8+1233del others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24557374 | ||||||
| chr1:24557413 | TTGTGTGC others(3): Show |
T | 82 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0159 others(79): Show |
82 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-8+1257_-8+1266del others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24557413 | ||||||
| chr1:24557446 | CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0001g0381 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-8+1295_-8+1304del others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24557446 | ||||||
| chr1:24557465 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-8+1296G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557465 | |||||||
| chr1:24557578 | G | C | 2 | a0001c0001t0003g0011 a0001c0001t0003g0012 |
2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-8+1409G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557578 | |||||||
| chr1:24557599 | A | G | 1 | a0002c0002t0004g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8+1430A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557599 | |||||||
| chr1:24557626 | A | C | 1 | a0001c0001t0003g0380 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-8+1457A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557626 | |||||||
| chr1:24557726 | C | G | 1 | a0001c0001t0003g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-8+1557C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557726 | |||||||
| chr1:24557823 | C | A | 1 | a0001c0001t0007g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8+1654C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557823 | |||||||
| chr1:24557830 | C | T | 2 | a0001c0001t0010g0378 a0001c0001t0010g0379 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+1661C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557830 | |||||||
| chr1:24557831 | G | C | 3 | a0001c0001t0003g0318 a0001c0001t0003g0319 a0001c0001t0003g0320 |
3 | HG00323.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-8+1662G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557831 | |||||||
| chr1:24557834 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8+1665G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557834 | |||||||
| chr1:24557836 | G | A | 175 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(172): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.-8+1667G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557836 | |||||||
| chr1:24557839 | C | A | 3 | a0001c0001t0006g0152 a0001c0001t0006g0153 a0001c0001t0006g0154 |
3 | HG01168.hp2 HG01169.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-8+1670C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557839 | |||||||
| chr1:24557893 | GA | G | 6 | a0001c0001t0001g0396 a0001c0001t0007g0395 a0001c0001t0008g0397 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+1726delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24557893 | ||||||
| chr1:24557913 | C | T | 9 | a0001c0001t0001g0321 a0001c0001t0001g0375 a0001c0001t0001g0376 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+1744C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557913 | |||||||
| chr1:24557969 | A | G | 190 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(187): Show |
192 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.-8+1800A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557969 | |||||||
| chr1:24557988 | G | A | 4 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 others(1): Show |
4 | NA18950.hp1 NA18952.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+1819G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557988 | |||||||
| chr1:24558052 | C | T | 1 | a0001c0001t0025g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-8+1883C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558052 | |||||||
| chr1:24558168 | C | T | 9 | a0001c0001t0001g0321 a0001c0001t0001g0375 a0001c0001t0001g0376 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+1999C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558168 | |||||||
| chr1:24558225 | T | C | 2 | a0001c0001t0010g0378 a0001c0001t0010g0379 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+2056T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558225 | |||||||
| chr1:24558369 | T | A | 1 | a0001c0001t0001g0221 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-8+2200T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558369 | |||||||
| chr1:24558432 | G | C | 1 | a0001c0001t0011g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-8+2263G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558432 | |||||||
| chr1:24558625 | A | G | 3 | a0001c0001t0003g0006 a0002c0002t0004g0005 a0002c0002t0004g0007 |
3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+2456A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558625 | |||||||
| chr1:24558638 | T | C | 1 | a0001c0001t0003g0386 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+2469T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558638 | |||||||
| chr1:24558703 | C | T | 13 | a0001c0001t0001g0145 a0001c0001t0001g0321 a0001c0001t0001g0375 others(10): Show |
14 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8+2534C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558703 | |||||||
| chr1:24558766 | T | G | 3 | a0001c0001t0003g0006 a0002c0002t0004g0005 a0002c0002t0004g0007 |
3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+2597T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558766 | |||||||
| chr1:24558771 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-8+2602T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558771 | |||||||
| chr1:24558965 | T | TA | 15 | a0001c0001t0001g0157 a0001c0001t0003g0011 a0001c0001t0003g0012 others(12): Show |
16 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8+2806dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24558965 | ||||||
| chr1:24558981 | T | C | 28 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(25): Show |
28 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8+2812T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558981 | |||||||
| chr1:24559245 | A | C | 4 | a0001c0001t0001g0396 a0001c0001t0008g0397 a0001c0001t0008g0398 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+3076A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559245 | |||||||
| chr1:24559360 | C | A | 82 | a0001c0001t0001g0145 a0001c0001t0001g0317 a0001c0001t0001g0321 others(79): Show |
83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3191C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559360 | |||||||
| chr1:24559361 | C | A | 82 | a0001c0001t0001g0145 a0001c0001t0001g0317 a0001c0001t0001g0321 others(79): Show |
83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3192C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559361 | |||||||
| chr1:24559498 | A | G | 82 | a0001c0001t0001g0145 a0001c0001t0001g0317 a0001c0001t0001g0321 others(79): Show |
83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3329A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559498 | |||||||
| chr1:24559566 | C | T | 1 | a0001c0001t0003g0320 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-8+3397C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559566 | |||||||
| chr1:24559637 | C | T | 22 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(19): Show |
22 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8+3468C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559637 | |||||||
| chr1:24559645 | G | A | 82 | a0001c0001t0001g0145 a0001c0001t0001g0317 a0001c0001t0001g0321 others(79): Show |
83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3476G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559645 | |||||||
| chr1:24559669 | T | C | 82 | a0001c0001t0001g0145 a0001c0001t0001g0317 a0001c0001t0001g0321 others(79): Show |
83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3500T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559669 | |||||||
| chr1:24559691 | G | A | 4 | a0001c0001t0001g0396 a0001c0001t0008g0397 a0001c0001t0008g0398 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+3522G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559691 | |||||||
| chr1:24559747 | C | A | 1 | a0001c0001t0001g0381 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-8+3578C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559747 | |||||||
| chr1:24559889 | C | G | 1 | a0001c0001t0002g0270 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-8+3720C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559889 | |||||||
| chr1:24559936 | T | C | 82 | a0001c0001t0001g0145 a0001c0001t0001g0317 a0001c0001t0001g0321 others(79): Show |
83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3767T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559936 | |||||||
| chr1:24560002 | A | G | 82 | a0001c0001t0001g0145 a0001c0001t0001g0317 a0001c0001t0001g0321 others(79): Show |
83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3833A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560002 | |||||||
| chr1:24560018 | G | A | 2 | a0001c0001t0007g0395 a0002c0002t0004g0394 |
2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-8+3849G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560018 | |||||||
| chr1:24560086 | G | A | 130 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-8+3917G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560086 | |||||||
| chr1:24560158 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-8+3989C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560158 | |||||||
| chr1:24560160 | C | CA | 101 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(98): Show |
101 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-8+4016dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560160 | ||||||
| chr1:24560160 | C | CAA | 9 | a0001c0001t0001g0159 a0001c0001t0001g0222 a0001c0001t0002g0022 others(6): Show |
9 | HG01099.hp2 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+4015_-8+4016dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560160 | ||||||
| chr1:24560160 | CA | C | 48 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0141 others(45): Show |
49 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.-8+4016delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560160 | ||||||
| chr1:24560160 | CAAAA | C | 23 | a0001c0001t0001g0145 a0001c0001t0001g0321 a0001c0001t0001g0375 others(20): Show |
24 | HG00639.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-8+4013_-8+4016del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560160 | ||||||
| chr1:24560160 | CAAAAA | C | 55 | a0001c0001t0001g0317 a0001c0001t0001g0331 a0001c0001t0001g0332 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.-8+4012_-8+4016del others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560160 | ||||||
| chr1:24560222 | G | T | 1 | a0001c0001t0023g0004 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-8+4053G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560222 | |||||||
| chr1:24560288 | G | T | 2 | a0001c0001t0003g0372 a0001c0001t0003g0373 |
2 | HG02080.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-8+4119G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560288 | |||||||
| chr1:24560293 | A | G | 1 | a0001c0001t0003g0371 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-8+4124A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560293 | |||||||
| chr1:24560327 | G | A | 82 | a0001c0001t0001g0145 a0001c0001t0001g0317 a0001c0001t0001g0321 others(79): Show |
83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+4158G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560327 | |||||||
| chr1:24560371 | T | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | NA18954.hp2 NA18960.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-8+4202T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560371 | |||||||
| chr1:24560627 | C | G | 4 | a0001c0001t0007g0001 a0001c0001t0007g0019 a0001c0001t0007g0020 others(1): Show |
5 | HG02257.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+4458C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560627 | |||||||
| chr1:24560637 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0223 |
3 | HG00323.hp2 HG01192.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-8+4468G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560637 | |||||||
| chr1:24560747 | GA | G | 13 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(10): Show |
14 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+4590delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560747 | ||||||
| chr1:24560772 | CTT | C | 10 | a0001c0001t0001g0396 a0001c0001t0003g0392 a0001c0001t0003g0393 others(7): Show |
10 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+4606_-8+4607del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560772 | ||||||
| chr1:24560966 | C | T | 130 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-8+4797C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560966 | |||||||
| chr1:24561056 | G | A | 82 | a0001c0001t0001g0145 a0001c0001t0001g0317 a0001c0001t0001g0321 others(79): Show |
83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+4887G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561056 | |||||||
| chr1:24561108 | G | A | 1 | a0001c0001t0002g0027 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-8+4939G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561108 | |||||||
| chr1:24561130 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0221 a0001c0001t0001g0223 others(44): Show |
48 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.-8+4961C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561130 | |||||||
| chr1:24561178 | C | CA | 188 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(185): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-8+5029dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24561178 | ||||||
| chr1:24561178 | C | CAA | 62 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0052 others(59): Show |
62 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-8+5028_-8+5029dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24561178 | ||||||
| chr1:24561178 | C | CAAA | 63 | a0001c0001t0001g0159 a0001c0001t0001g0224 a0001c0001t0001g0229 others(60): Show |
63 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.-8+5027_-8+5029dup others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24561178 | ||||||
| chr1:24561178 | C | CAAAA | 20 | a0001c0001t0001g0145 a0001c0001t0001g0317 a0001c0001t0001g0331 others(17): Show |
22 | HG01109.hp2 HG01255.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-8+5026_-8+5029dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24561178 | ||||||
| chr1:24561210 | G | A | 37 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(34): Show |
37 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-8+5041G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561210 | |||||||
| chr1:24561257 | G | T | 4 | a0001c0001t0001g0145 a0001c0001t0003g0146 a0002c0002t0012g0002 others(1): Show |
5 | HG02723.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+5088G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561257 | |||||||
| chr1:24561302 | G | A | 3 | a0001c0001t0006g0152 a0001c0001t0006g0153 a0001c0001t0006g0154 |
3 | HG01168.hp2 HG01169.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-8+5133G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561302 | |||||||
| chr1:24561429 | G | A | 279 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0035 others(276): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.-8+5260G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561429 | |||||||
| chr1:24561475 | A | C | 316 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0035 others(313): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.-8+5306A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561475 | |||||||
| chr1:24561487 | A | C | 279 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0035 others(276): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.-8+5318A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561487 | |||||||
| chr1:24561529 | C | T | 3 | a0001c0001t0003g0006 a0002c0002t0004g0005 a0002c0002t0004g0007 |
3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+5360C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561529 | |||||||
| chr1:24561586 | T | C | 3 | a0001c0001t0006g0152 a0001c0001t0006g0153 a0001c0001t0006g0154 |
3 | HG01168.hp2 HG01169.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-8+5417T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561586 | |||||||
| chr1:24561633 | G | A | 13 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(10): Show |
14 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+5464G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561633 | |||||||
| chr1:24561637 | G | A | 2 | a0001c0001t0013g0009 a0001c0001t0013g0010 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-8+5468G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561637 | |||||||
| chr1:24561638 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0002g0051 |
2 | HG00438.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-8+5469C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561638 | |||||||
| chr1:24561769 | G | C | 1 | a0001c0001t0003g0333 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-8+5600G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561769 | |||||||
| chr1:24561872 | C | T | 279 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0035 others(276): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.-8+5703C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561872 | |||||||
| chr1:24561910 | CA | C | 53 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(50): Show |
54 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.-8+5756delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24561910 | ||||||
| chr1:24561910 | CAA | C | 277 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0035 others(274): Show |
279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.-8+5755_-8+5756del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24561910 | ||||||
| chr1:24562094 | C | T | 279 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0035 others(276): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.-8+5925C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562094 | |||||||
| chr1:24562260 | G | C | 279 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0035 others(276): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.-8+6091G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562260 | |||||||
| chr1:24562299 | C | G | 1 | a0001c0001t0002g0295 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-8+6130C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562299 | |||||||
| chr1:24562482 | G | C | 144 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(141): Show |
145 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.-8+6313G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562482 | |||||||
| chr1:24562525 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-8+6356A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562525 | |||||||
| chr1:24562566 | C | T | 1 | a0003c0003t0020g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-8+6397C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562566 | |||||||
| chr1:24562568 | C | T | 9 | a0001c0001t0001g0321 a0001c0001t0001g0375 a0001c0001t0001g0376 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+6399C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562568 | |||||||
| chr1:24562685 | G | T | 1 | a0001c0001t0023g0004 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-8+6516G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562685 | |||||||
| chr1:24562775 | C | T | 13 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(10): Show |
14 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+6606C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562775 | |||||||
| chr1:24562866 | A | G | 63 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0162 others(60): Show |
63 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-8+6697A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562866 | |||||||
| chr1:24562922 | C | CCT | 7 | a0001c0001t0001g0049 a0001c0001t0002g0130 a0001c0001t0002g0133 others(4): Show |
7 | HG00544.hp1 HG00621.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+6755_-8+6756dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24562922 | ||||||
| chr1:24562959 | A | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0129 a0001c0001t0001g0156 others(127): Show |
131 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-8+6790A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562959 | |||||||
| chr1:24562975 | T | TG | 38 | a0001c0001t0001g0128 a0001c0001t0001g0286 a0001c0001t0001g0287 others(35): Show |
38 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-8+6814dupG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24562975 | ||||||
| chr1:24563083 | C | T | 4 | a0001c0001t0003g0392 a0001c0001t0003g0393 a0002c0002t0004g0390 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+6914C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563083 | |||||||
| chr1:24563253 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-8+7084G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563253 | |||||||
| chr1:24563258 | GCGCCTGT others(82): Show |
G | 1 | a0001c0001t0001g0381 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-8+7091_-8+7179del others(89): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24563258 | ||||||
| chr1:24563333 | C | A | 44 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(41): Show |
45 | HG00558.hp1 HG00639.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.-8+7164C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563333 | |||||||
| chr1:24563381 | C | T | 45 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(42): Show |
46 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-8+7212C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563381 | |||||||
| chr1:24563382 | G | A | 1 | a0001c0001t0001g0383 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-8+7213G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563382 | |||||||
| chr1:24563393 | T | G | 45 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(42): Show |
46 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-8+7224T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563393 | |||||||
| chr1:24563398 | G | A | 5 | a0001c0001t0003g0239 a0001c0001t0003g0240 a0001c0001t0003g0241 others(2): Show |
5 | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+7229G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563398 | |||||||
| chr1:24563453 | C | T | 1 | a0001c0001t0001g0366 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-8+7284C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563453 | |||||||
| chr1:24563470 | C | T | 4 | a0001c0001t0001g0145 a0001c0001t0003g0146 a0002c0002t0012g0002 others(1): Show |
5 | HG02723.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+7301C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563470 | |||||||
| chr1:24563478 | C | T | 4 | a0001c0001t0001g0145 a0001c0001t0003g0146 a0002c0002t0012g0002 others(1): Show |
5 | HG02723.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+7309C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563478 | |||||||
| chr1:24563503 | C | A | 146 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(143): Show |
147 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.-8+7334C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563503 | |||||||
| chr1:24563520 | C | A | 1 | a0001c0001t0025g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-8+7351C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563520 | |||||||
| chr1:24563534 | C | CA | 136 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0049 others(133): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8+7383dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24563534 | ||||||
| chr1:24563534 | CA | C | 11 | a0001c0001t0001g0215 a0001c0001t0001g0268 a0001c0001t0001g0396 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+7383delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24563534 | ||||||
| chr1:24563534 | CAA | C | 76 | a0001c0001t0001g0145 a0001c0001t0001g0317 a0001c0001t0001g0321 others(73): Show |
77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.-8+7382_-8+7383del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24563534 | ||||||
| chr1:24563534 | CAAA | C | 28 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(25): Show |
28 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8+7381_-8+7383del others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24563534 | ||||||
| chr1:24563553 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-8+7384G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563553 | |||||||
| chr1:24563554 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-8+7385A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563554 | |||||||
| chr1:24563559 | A | G | 2 | a0001c0001t0010g0378 a0001c0001t0010g0379 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+7390A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563559 | |||||||
| chr1:24563944 | A | G | 2 | a0001c0001t0001g0312 a0001c0001t0005g0311 |
2 | NA18971.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-8+7775A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563944 | |||||||
| chr1:24564006 | C | A | 1 | a0001c0001t0007g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8+7837C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564006 | |||||||
| chr1:24564068 | T | C | 31 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(28): Show |
31 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8+7899T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564068 | |||||||
| chr1:24564367 | C | G | 48 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(45): Show |
49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+8198C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564367 | |||||||
| chr1:24564367 | C | T | 11 | a0001c0001t0001g0157 a0001c0001t0001g0204 a0001c0001t0001g0205 others(8): Show |
11 | HG00438.hp2 HG00597.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+8198C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564367 | |||||||
| chr1:24564392 | T | C | 191 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(188): Show |
193 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-8+8223T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564392 | |||||||
| chr1:24564438 | G | A | 1 | a0001c0001t0003g0239 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-8+8269G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564438 | |||||||
| chr1:24564470 | C | T | 2 | a0001c0001t0003g0386 a0001c0001t0003g0387 |
2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-8+8301C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564470 | |||||||
| chr1:24564494 | A | G | 40 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(37): Show |
40 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-8+8325A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564494 | |||||||
| chr1:24564513 | C | CA | 39 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0057 others(36): Show |
40 | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-8+8363dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564513 | ||||||
| chr1:24564513 | C | CAA | 20 | a0001c0001t0001g0029 a0001c0001t0001g0055 a0001c0001t0001g0062 others(17): Show |
20 | HG01099.hp2 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8+8362_-8+8363dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564513 | ||||||
| chr1:24564513 | C | CAAA | 51 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0052 others(48): Show |
51 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-8+8361_-8+8363dup others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564513 | ||||||
| chr1:24564513 | C | CAAAA | 32 | a0001c0001t0001g0038 a0001c0001t0001g0079 a0001c0001t0001g0080 others(29): Show |
32 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.-8+8360_-8+8363dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564513 | ||||||
| chr1:24564513 | C | CAAAAA | 11 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0048 others(8): Show |
11 | HG00738.hp2 HG01123.hp2 HG04115.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+8359_-8+8363dup others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564513 | ||||||
| chr1:24564513 | CA | C | 77 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0159 others(74): Show |
77 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-8+8363delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564513 | ||||||
| chr1:24564517 | AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0002g0027 a0001c0001t0005g0047 |
2 | NA18939.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-8+8358_-8+8373del others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564517 | ||||||
| chr1:24564527 | AAAAAAC | A | 10 | a0001c0001t0002g0277 a0001c0001t0002g0279 a0001c0001t0002g0280 others(7): Show |
10 | HG01167.hp2 HG01192.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+8364_-8+8369del others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564527 | ||||||
| chr1:24564528 | AAAAAC | A | 29 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0288 others(26): Show |
30 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-8+8364_-8+8368del others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564528 | ||||||
| chr1:24564529 | AAAAC | A | 9 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG01071.hp1 HG01106.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+8364_-8+8367del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564529 | ||||||
| chr1:24564532 | AC | A | 45 | a0001c0001t0001g0317 a0001c0001t0001g0323 a0001c0001t0001g0331 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-8+8364delC | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564532 | |||||||
| chr1:24564533 | C | A | 163 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(160): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.-8+8364C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564533 | |||||||
| chr1:24564623 | C | A | 48 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(45): Show |
49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+8454C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564623 | |||||||
| chr1:24564670 | A | G | 191 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(188): Show |
193 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-8+8501A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564670 | |||||||
| chr1:24564717 | G | C | 48 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(45): Show |
49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+8548G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564717 | |||||||
| chr1:24564730 | A | G | 48 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(45): Show |
49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+8561A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564730 | |||||||
| chr1:24564849 | C | T | 60 | a0001c0001t0001g0317 a0001c0001t0001g0322 a0001c0001t0001g0323 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-8+8680C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564849 | |||||||
| chr1:24565055 | A | T | 6 | a0001c0001t0001g0396 a0001c0001t0007g0395 a0001c0001t0008g0397 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+8886A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565055 | |||||||
| chr1:24565144 | C | CT | 69 | a0001c0001t0001g0228 a0001c0001t0001g0317 a0001c0001t0001g0322 others(66): Show |
69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-8+8990dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565144 | ||||||
| chr1:24565144 | C | T | 1 | a0001c0001t0003g0324 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-8+8975C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565144 | |||||||
| chr1:24565144 | CT | C | 52 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0056 others(49): Show |
53 | HG00408.hp2 HG00673.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.-8+8990delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565144 | ||||||
| chr1:24565144 | CTT | C | 105 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0049 others(102): Show |
106 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.-8+8989_-8+8990del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565144 | ||||||
| chr1:24565224 | T | A | 48 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(45): Show |
49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+9055T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565224 | |||||||
| chr1:24565284 | TGACAGGG others(16): Show |
T | 48 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(45): Show |
49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+9120_-8+9142del others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565284 | ||||||
| chr1:24565410 | C | CA | 191 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(188): Show |
193 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-8+9241_-8+9242ins others(1): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565410 | |||||||
| chr1:24565572 | T | TTG | 51 | a0001c0001t0001g0156 a0001c0001t0001g0159 a0001c0001t0001g0161 others(48): Show |
51 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.-8+9445_-8+9446dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | T | TTGTG | 48 | a0001c0001t0001g0003 a0001c0001t0001g0129 a0001c0001t0001g0183 others(45): Show |
49 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.-8+9443_-8+9446dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | T | TTGTGTG | 15 | a0001c0001t0001g0223 a0001c0001t0001g0236 a0001c0001t0001g0249 others(12): Show |
15 | HG00738.hp1 HG01192.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8+9441_-8+9446dup others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | T | TTGTGTGT others(1): Show |
9 | a0001c0001t0001g0229 a0001c0001t0001g0396 a0001c0001t0002g0248 others(6): Show |
9 | HG00735.hp2 HG00741.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+9439_-8+9446dup others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0250 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-8+9437_-8+9446dup others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | T | TTGTGTGT others(5): Show |
1 | a0002c0002t0004g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-8+9435_-8+9446dup others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | T | TTGTGTGT others(7): Show |
1 | a0002c0002t0012g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8+9433_-8+9446dup others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | T | TTGTGTGT others(9): Show |
2 | a0001c0001t0001g0145 a0001c0001t0003g0146 |
2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-8+9431_-8+9446dup others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | T | TTGTGTGT others(11): Show |
1 | a0002c0002t0012g0002 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-8+9429_-8+9446dup others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | TTG | T | 4 | a0001c0001t0001g0310 a0001c0001t0003g0324 a0001c0001t0003g0335 others(1): Show |
4 | HG02486.hp2 NA18964.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+9445_-8+9446del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | TTGTG | T | 53 | a0001c0001t0001g0193 a0001c0001t0001g0212 a0001c0001t0001g0317 others(50): Show |
53 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.-8+9443_-8+9446del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | TTGTGTG | T | 17 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0002g0027 others(14): Show |
17 | HG02273.hp1 HG02809.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8+9441_-8+9446del others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | TTGTGTGT others(1): Show |
T | 97 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(94): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-8+9439_-8+9446del others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | TTGTGTGT others(3): Show |
T | 15 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(12): Show |
16 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8+9437_-8+9446del others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | TTGTGTGT others(5): Show |
T | 28 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0286 others(25): Show |
28 | HG00558.hp1 HG01123.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.-8+9435_-8+9446del others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | TTGTGTGT others(7): Show |
T | 8 | a0001c0001t0001g0049 a0001c0001t0002g0130 a0001c0001t0002g0133 others(5): Show |
8 | HG00544.hp1 HG00621.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8+9433_-8+9446del others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | TTGTGTGT others(9): Show |
T | 11 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+9431_-8+9446del others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565572 | TTGTGTGT others(13): Show |
T | 2 | a0001c0001t0007g0274 a0002c0002t0004g0273 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-8+9427_-8+9446del others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | ||||||
| chr1:24565772 | AT | A | 48 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(45): Show |
49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+9611delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565772 | ||||||
| chr1:24565802 | G | C | 40 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(37): Show |
40 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-8+9633G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565802 | |||||||
| chr1:24565851 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-8+9682T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565851 | |||||||
| chr1:24565896 | A | C | 1 | a0001c0001t0002g0279 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-8+9727A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565896 | |||||||
| chr1:24565897 | T | G | 1 | a0001c0001t0002g0139 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-8+9728T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565897 | |||||||
| chr1:24565963 | A | G | 129 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-8+9794A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565963 | |||||||
| chr1:24566008 | C | T | 48 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(45): Show |
49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+9839C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566008 | |||||||
| chr1:24566044 | G | T | 48 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(45): Show |
49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+9875G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566044 | |||||||
| chr1:24566056 | C | T | 4 | a0001c0001t0001g0145 a0001c0001t0003g0146 a0002c0002t0012g0002 others(1): Show |
5 | HG02723.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+9887C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566056 | |||||||
| chr1:24566068 | C | T | 260 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(257): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.-8+9899C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566068 | |||||||
| chr1:24566325 | T | C | 260 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(257): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.-8+10156T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566325 | |||||||
| chr1:24566502 | C | T | 48 | a0001c0001t0001g0145 a0001c0001t0001g0286 a0001c0001t0001g0287 others(45): Show |
49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+10333C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566502 | |||||||
| chr1:24566956 | T | C | 1 | a0001c0001t0003g0384 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-8+10787T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566956 | |||||||
| chr1:24567005 | G | T | 1 | a0001c0001t0002g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-8+10836G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567005 | |||||||
| chr1:24567105 | C | T | 3 | a0001c0001t0003g0006 a0002c0002t0004g0005 a0002c0002t0004g0007 |
3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+10936C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567105 | |||||||
| chr1:24567178 | C | T | 14 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(11): Show |
15 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8+11009C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567178 | |||||||
| chr1:24567181 | A | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG01081.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-8+11012A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567181 | |||||||
| chr1:24567730 | C | T | 141 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(138): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-8+11561C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567730 | |||||||
| chr1:24567741 | C | G | 1 | a0001c0001t0003g0393 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-8+11572C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567741 | |||||||
| chr1:24567991 | C | G | 31 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(28): Show |
31 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8+11822C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567991 | |||||||
| chr1:24567991 | C | T | 3 | a0001c0001t0003g0006 a0002c0002t0004g0005 a0002c0002t0004g0007 |
3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+11822C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567991 | |||||||
| chr1:24568180 | C | T | 3 | a0001c0001t0007g0395 a0001c0001t0025g0316 a0002c0002t0004g0394 |
3 | HG01891.hp2 HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+12011C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568180 | |||||||
| chr1:24568242 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-8+12073G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568242 | |||||||
| chr1:24568446 | T | C | 13 | a0001c0001t0001g0029 a0001c0001t0007g0023 a0002c0002t0004g0024 others(10): Show |
13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12277T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568446 | |||||||
| chr1:24568506 | G | A | 84 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0299 others(81): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+12337G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568506 | |||||||
| chr1:24568560 | A | G | 149 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(146): Show |
151 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-8+12391A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568560 | |||||||
| chr1:24568580 | T | G | 84 | a0001c0001t0001g0029 a0001c0001t0001g0297 a0001c0001t0001g0298 others(81): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+12411T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568580 | |||||||
| chr1:24568612 | G | A | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0001c0001t0001g0377 |
3 | HG01069.hp1 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-8+12443G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568612 | |||||||
| chr1:24568619 | C | T | 13 | a0001c0001t0001g0029 a0001c0001t0007g0023 a0002c0002t0004g0024 others(10): Show |
13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12450C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568619 | |||||||
| chr1:24568696 | G | A | 1 | a0001c0001t0001g0300 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-8+12527G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568696 | |||||||
| chr1:24568762 | T | C | 248 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-8+12593T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568762 | |||||||
| chr1:24568802 | A | G | 13 | a0001c0001t0001g0029 a0001c0001t0007g0023 a0002c0002t0004g0024 others(10): Show |
13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12633A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568802 | |||||||
| chr1:24568820 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-8+12651G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568820 | |||||||
| chr1:24568820 | G | T | 1 | a0001c0001t0007g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8+12651G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568820 | |||||||
| chr1:24568903 | A | G | 283 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(280): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-8+12734A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568903 | |||||||
| chr1:24569001 | T | C | 13 | a0001c0001t0001g0029 a0001c0001t0007g0023 a0002c0002t0004g0024 others(10): Show |
13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12832T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569001 | |||||||
| chr1:24569026 | G | GT | 131 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(128): Show |
131 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-8+12866dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24569026 | ||||||
| chr1:24569026 | G | T | 2 | a0001c0001t0007g0274 a0002c0002t0004g0273 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-8+12857G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569026 | |||||||
| chr1:24569026 | GT | G | 13 | a0001c0001t0001g0029 a0001c0001t0007g0023 a0002c0002t0004g0024 others(10): Show |
13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12866delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24569026 | ||||||
| chr1:24569031 | T | G | 91 | a0001c0001t0001g0159 a0001c0001t0001g0170 a0001c0001t0001g0195 others(88): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-8+12862T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569031 | |||||||
| chr1:24569063 | C | T | 13 | a0001c0001t0001g0029 a0001c0001t0007g0023 a0002c0002t0004g0024 others(10): Show |
13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12894C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569063 | |||||||
| chr1:24569092 | C | A | 134 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(131): Show |
134 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-8+12923C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569092 | |||||||
| chr1:24569097 | A | G | 13 | a0001c0001t0001g0029 a0001c0001t0007g0023 a0002c0002t0004g0024 others(10): Show |
13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12928A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569097 | |||||||
| chr1:24569155 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-8+12986G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569155 | |||||||
| chr1:24569182 | C | T | 1 | a0001c0001t0003g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-8+13013C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569182 | |||||||
| chr1:24569238 | C | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0170 |
2 | NA18961.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-8+13069C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569238 | |||||||
| chr1:24569252 | CCAAAGTG others(5118): Show |
C | 13 | a0001c0001t0001g0029 a0001c0001t0007g0023 a0002c0002t0004g0024 others(10): Show |
13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+13115_-8+18239d others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24569252 | ||||||
| chr1:24569253 | C | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0138 |
2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-8+13084C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569253 | |||||||
| chr1:24569257 | G | A | 1 | a0001c0001t0003g0326 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-8+13088G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569257 | |||||||
| chr1:24569314 | A | G | 7 | a0001c0001t0001g0321 a0001c0001t0001g0375 a0001c0001t0001g0376 others(4): Show |
7 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+13145A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569314 | |||||||
| chr1:24569327 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-8+13158G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569327 | |||||||
| chr1:24569508 | A | C | 1 | a0001c0001t0007g0274 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8+13339A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569508 | |||||||
| chr1:24569513 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-8+13344T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569513 | |||||||
| chr1:24569535 | T | C | 1 | a0003c0003t0020g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-8+13366T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569535 | |||||||
| chr1:24569554 | T | C | 3 | a0001c0001t0007g0274 a0001c0001t0025g0316 a0002c0002t0004g0273 |
3 | HG02818.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+13385T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569554 | |||||||
| chr1:24569649 | T | G | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0001c0001t0001g0377 |
3 | HG01069.hp1 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-8+13480T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569649 | |||||||
| chr1:24569671 | C | T | 10 | a0001c0001t0001g0157 a0001c0001t0001g0204 a0001c0001t0001g0205 others(7): Show |
10 | HG00438.hp2 HG00597.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+13502C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569671 | |||||||
| chr1:24569953 | A | C | 1 | a0001c0001t0025g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-8+13784A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569953 | |||||||
| chr1:24569956 | A | T | 2 | a0001c0001t0002g0117 a0001c0001t0003g0330 |
2 | HG01255.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-8+13787A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569956 | |||||||
| chr1:24570110 | A | AT | 12 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0253 others(9): Show |
12 | HG02027.hp2 HG02135.hp1 HG03139.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8+13957dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24570110 | ||||||
| chr1:24570377 | T | C | 56 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(53): Show |
56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+14208T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24570377 | |||||||
| chr1:24570654 | T | C | 1 | a0001c0001t0003g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-8+14485T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24570654 | |||||||
| chr1:24570714 | C | T | 7 | a0001c0001t0001g0049 a0001c0001t0002g0130 a0001c0001t0002g0133 others(4): Show |
7 | HG00544.hp1 HG00621.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+14545C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24570714 | |||||||
| chr1:24570818 | C | T | 1 | a0001c0001t0003g0330 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-8+14649C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24570818 | |||||||
| chr1:24570958 | G | T | 4 | a0001c0001t0001g0080 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
4 | NA18954.hp2 NA18960.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+14789G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24570958 | |||||||
| chr1:24571076 | G | A | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0001c0001t0001g0377 |
3 | HG01069.hp1 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-8+14907G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571076 | |||||||
| chr1:24571506 | A | C | 3 | a0001c0001t0002g0081 a0001c0001t0002g0088 a0001c0001t0002g0096 |
3 | NA18963.hp2 NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-8+15337A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571506 | |||||||
| chr1:24571580 | C | T | 233 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-8+15411C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571580 | |||||||
| chr1:24571678 | C | T | 2 | a0001c0001t0011g0203 a0001c0001t0011g0216 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-8+15509C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571678 | |||||||
| chr1:24571760 | G | A | 233 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-8+15591G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571760 | |||||||
| chr1:24571856 | G | A | 1 | a0002c0002t0004g0394 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8+15687G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571856 | |||||||
| chr1:24571884 | A | C | 56 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(53): Show |
56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+15715A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571884 | |||||||
| chr1:24571886 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-8+15717G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571886 | |||||||
| chr1:24571962 | C | T | 47 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0340 others(44): Show |
47 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-8+15793C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571962 | |||||||
| chr1:24571998 | C | A | 47 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0340 others(44): Show |
47 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-8+15829C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571998 | |||||||
| chr1:24572166 | A | AAACC | 56 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(53): Show |
56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+15999_-8+16000i others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24572166 | ||||||
| chr1:24572448 | G | C | 1 | a0001c0001t0001g0249 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-8+16279G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24572448 | |||||||
| chr1:24572857 | A | G | 116 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-8+16688A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24572857 | |||||||
| chr1:24572999 | C | T | 56 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(53): Show |
56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+16830C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24572999 | |||||||
| chr1:24573039 | T | C | 135 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(132): Show |
135 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-8+16870T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573039 | |||||||
| chr1:24573120 | T | C | 1 | a0001c0001t0008g0399 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-8+16951T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573120 | |||||||
| chr1:24573408 | C | T | 44 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0340 others(41): Show |
44 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+17239C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573408 | |||||||
| chr1:24573599 | A | G | 1 | a0001c0001t0002g0277 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-8+17430A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573599 | |||||||
| chr1:24573600 | GAAACAA | G | 56 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(53): Show |
56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+17454_-8+17459d others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573600 | ||||||
| chr1:24573835 | T | C | 267 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(264): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-8+17666T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573835 | |||||||
| chr1:24573952 | C | CA | 11 | a0001c0001t0001g0038 a0001c0001t0001g0059 a0001c0001t0001g0061 others(8): Show |
11 | HG00408.hp1 HG00544.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+17802dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0323 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-8+17793_-8+17802d others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(4): Show |
16 | a0001c0001t0001g0349 a0001c0001t0001g0366 a0001c0001t0002g0336 others(13): Show |
16 | HG00099.hp1 HG01074.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8+17792_-8+17802d others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(5): Show |
17 | a0001c0001t0001g0192 a0001c0001t0001g0322 a0001c0001t0001g0340 others(14): Show |
17 | HG00673.hp1 HG01433.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8+17791_-8+17802d others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(6): Show |
7 | a0001c0001t0003g0006 a0001c0001t0003g0326 a0001c0001t0003g0348 others(4): Show |
7 | HG01106.hp1 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+17790_-8+17802d others(15): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(7): Show |
8 | a0001c0001t0001g0170 a0001c0001t0001g0208 a0001c0001t0001g0376 others(5): Show |
8 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+17789_-8+17802d others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(8): Show |
8 | a0001c0001t0001g0159 a0001c0001t0001g0321 a0001c0001t0001g0375 others(5): Show |
8 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+17788_-8+17802d others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0296 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(15): Show |
12 | a0001c0001t0001g0168 a0001c0001t0001g0181 a0001c0001t0001g0188 others(9): Show |
12 | HG00408.hp2 HG01109.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(16): Show |
21 | a0001c0001t0001g0080 a0001c0001t0001g0157 a0001c0001t0001g0161 others(18): Show |
21 | HG00642.hp2 HG00673.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(25): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(17): Show |
8 | a0001c0001t0001g0156 a0001c0001t0001g0162 a0001c0001t0001g0163 others(5): Show |
8 | HG01346.hp1 HG02040.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(26): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(18): Show |
4 | a0001c0001t0001g0193 a0001c0001t0001g0206 a0001c0001t0002g0198 others(1): Show |
4 | HG00280.hp2 HG00438.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(27): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(19): Show |
4 | a0001c0001t0001g0309 a0001c0001t0001g0312 a0001c0001t0001g0314 others(1): Show |
4 | NA18946.hp2 NA18971.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(28): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0304 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(29): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0001g0299 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(30): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0222 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(31): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0225 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(33): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0001g0310 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(38): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | CA | C | 101 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0079 others(98): Show |
101 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.-8+17802delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | CAA | C | 30 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(27): Show |
30 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8+17801_-8+17802d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573952 | CAAAAA | C | 41 | a0001c0001t0001g0317 a0001c0001t0001g0331 a0001c0001t0001g0332 others(38): Show |
43 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-8+17798_-8+17802d others(7): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | ||||||
| chr1:24573962 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0021g0160 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(25): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573962 | ||||||
| chr1:24573969 | A | AAAAAAAA others(24): Show |
3 | a0001c0001t0007g0008 a0001c0001t0011g0155 a0002c0002t0004g0202 |
3 | HG02109.hp1 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(33): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573969 | ||||||
| chr1:24573969 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(32): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573969 | ||||||
| chr1:24573969 | A | AAAAAAAA others(6): Show |
2 | a0001c0001t0011g0203 a0001c0001t0011g0216 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(15): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573969 | ||||||
| chr1:24573971 | A | AAAAAAAA others(14): Show |
1 | a0002c0002t0004g0018 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573971 | |||||||
| chr1:24573971 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0003g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(22): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573971 | |||||||
| chr1:24574024 | TCTC | T | 56 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(53): Show |
56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+17858_-8+17860d others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24574024 | ||||||
| chr1:24574078 | C | T | 233 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-8+17909C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574078 | |||||||
| chr1:24574087 | G | A | 56 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(53): Show |
56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+17918G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574087 | |||||||
| chr1:24574092 | C | T | 3 | a0001c0001t0003g0006 a0002c0002t0004g0005 a0002c0002t0004g0007 |
3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+17923C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574092 | |||||||
| chr1:24574128 | G | GT | 11 | a0001c0001t0001g0201 a0001c0001t0001g0209 a0001c0001t0001g0340 others(8): Show |
11 | HG00544.hp2 HG00673.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+17971dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24574128 | ||||||
| chr1:24574128 | GT | G | 177 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(174): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-8+17971delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24574128 | ||||||
| chr1:24574133 | T | C | 135 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(132): Show |
135 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-8+17964T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574133 | |||||||
| chr1:24574168 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-8+17999C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574168 | |||||||
| chr1:24574190 | C | A | 1 | a0001c0001t0010g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8+18021C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574190 | |||||||
| chr1:24574210 | C | A | 38 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0340 others(35): Show |
38 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.-8+18041C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574210 | |||||||
| chr1:24574230 | T | C | 2 | a0001c0001t0010g0378 a0001c0001t0010g0379 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+18061T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574230 | |||||||
| chr1:24574383 | T | C | 13 | a0001c0001t0001g0029 a0001c0001t0007g0023 a0002c0002t0004g0024 others(10): Show |
13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+18214T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574383 | |||||||
| chr1:24574389 | G | T | 6 | a0001c0001t0001g0321 a0001c0001t0001g0375 a0001c0001t0001g0376 others(3): Show |
6 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+18220G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574389 | |||||||
| chr1:24574461 | G | T | 177 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(174): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-8+18292G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574461 | |||||||
| chr1:24574574 | A | G | 6 | a0001c0001t0001g0396 a0001c0001t0007g0395 a0001c0001t0008g0397 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+18405A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574574 | |||||||
| chr1:24574626 | T | C | 69 | a0001c0001t0001g0029 a0001c0001t0001g0321 a0001c0001t0001g0322 others(66): Show |
69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-8+18457T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574626 | |||||||
| chr1:24574630 | A | C | 177 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(174): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-8+18461A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574630 | |||||||
| chr1:24574689 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-8+18520G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574689 | |||||||
| chr1:24574794 | C | CT | 42 | a0001c0001t0001g0049 a0001c0001t0001g0211 a0001c0001t0001g0286 others(39): Show |
42 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.-8+18644dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24574794 | ||||||
| chr1:24574794 | CT | C | 10 | a0001c0001t0001g0321 a0001c0001t0001g0375 a0001c0001t0001g0376 others(7): Show |
10 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+18644delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24574794 | ||||||
| chr1:24574819 | G | A | 48 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0340 others(45): Show |
48 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.-8+18650G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574819 | |||||||
| chr1:24574858 | T | C | 2 | a0001c0001t0003g0226 a0001c0001t0003g0252 |
2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-8+18689T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574858 | |||||||
| chr1:24574929 | G | A | 4 | a0001c0001t0002g0046 a0001c0001t0002g0118 a0001c0001t0002g0119 others(1): Show |
4 | NA18972.hp1 NA18986.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+18760G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574929 | |||||||
| chr1:24574941 | A | AC | 69 | a0001c0001t0001g0029 a0001c0001t0001g0321 a0001c0001t0001g0322 others(66): Show |
69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-8+18774dupC | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24574941 | ||||||
| chr1:24575005 | G | C | 47 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0340 others(44): Show |
47 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-8+18836G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575005 | |||||||
| chr1:24575015 | C | T | 44 | a0001c0001t0001g0145 a0001c0001t0001g0317 a0001c0001t0001g0331 others(41): Show |
46 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.-8+18846C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575015 | |||||||
| chr1:24575244 | C | A | 1 | a0001c0001t0003g0226 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-8+19075C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575244 | |||||||
| chr1:24575341 | T | C | 1 | a0001c0001t0007g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8+19172T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575341 | |||||||
| chr1:24575344 | C | T | 3 | a0001c0001t0002g0081 a0001c0001t0002g0088 a0001c0001t0002g0096 |
3 | NA18963.hp2 NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-8+19175C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575344 | |||||||
| chr1:24575353 | A | G | 248 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-8+19184A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575353 | |||||||
| chr1:24575359 | A | G | 69 | a0001c0001t0001g0029 a0001c0001t0001g0321 a0001c0001t0001g0322 others(66): Show |
69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-8+19190A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575359 | |||||||
| chr1:24575372 | T | G | 179 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(176): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.-8+19203T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575372 | |||||||
| chr1:24575379 | G | T | 4 | a0001c0001t0001g0396 a0001c0001t0008g0397 a0001c0001t0008g0398 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+19210G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575379 | |||||||
| chr1:24575480 | G | A | 56 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(53): Show |
56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+19311G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575480 | |||||||
| chr1:24575493 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-8+19324G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575493 | |||||||
| chr1:24575507 | T | G | 69 | a0001c0001t0001g0029 a0001c0001t0001g0321 a0001c0001t0001g0322 others(66): Show |
69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-8+19338T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575507 | |||||||
| chr1:24575535 | A | T | 4 | a0001c0001t0007g0023 a0002c0002t0004g0024 a0002c0002t0004g0026 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+19366A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575535 | |||||||
| chr1:24575552 | C | T | 249 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(246): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-8+19383C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575552 | |||||||
| chr1:24575585 | C | T | 13 | a0001c0001t0001g0029 a0001c0001t0007g0023 a0002c0002t0004g0024 others(10): Show |
13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+19416C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575585 | |||||||
| chr1:24575718 | G | A | 32 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(29): Show |
32 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.-8+19549G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575718 | |||||||
| chr1:24575760 | G | A | 281 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(278): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.-8+19591G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575760 | |||||||
| chr1:24575903 | C | T | 69 | a0001c0001t0001g0029 a0001c0001t0001g0321 a0001c0001t0001g0322 others(66): Show |
69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-19521C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575903 | |||||||
| chr1:24575915 | C | CA | 10 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0186 others(7): Show |
10 | HG01081.hp2 HG01175.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-19483dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24575915 | ||||||
| chr1:24575915 | CA | C | 180 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0049 others(177): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.-7-19483delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24575915 | ||||||
| chr1:24575915 | CAA | C | 35 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0059 others(32): Show |
35 | HG00323.hp1 HG00558.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-7-19484_-7-19483d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24575915 | ||||||
| chr1:24575915 | CAAAAAA | C | 55 | a0001c0001t0001g0029 a0001c0001t0001g0322 a0001c0001t0001g0323 others(52): Show |
55 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.-7-19488_-7-19483d others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24575915 | ||||||
| chr1:24575915 | CAAAAAAA | C | 11 | a0001c0001t0001g0321 a0001c0001t0001g0375 a0001c0001t0001g0376 others(8): Show |
11 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7-19489_-7-19483d others(9): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24575915 | ||||||
| chr1:24575915 | CAAAAAAA others(3): Show |
C | 12 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-19492_-7-19483d others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24575915 | ||||||
| chr1:24576015 | A | G | 69 | a0001c0001t0001g0029 a0001c0001t0001g0321 a0001c0001t0001g0322 others(66): Show |
69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-19409A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576015 | |||||||
| chr1:24576038 | C | T | 1 | a0001c0001t0002g0359 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-7-19386C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576038 | |||||||
| chr1:24576063 | G | A | 37 | a0001c0001t0001g0317 a0001c0001t0001g0331 a0001c0001t0001g0332 others(34): Show |
38 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-7-19361G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576063 | |||||||
| chr1:24576119 | C | T | 2 | a0001c0001t0007g0274 a0002c0002t0004g0273 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-7-19305C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576119 | |||||||
| chr1:24576209 | G | A | 69 | a0001c0001t0001g0029 a0001c0001t0001g0321 a0001c0001t0001g0322 others(66): Show |
69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-19215G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576209 | |||||||
| chr1:24576295 | A | G | 69 | a0001c0001t0001g0029 a0001c0001t0001g0321 a0001c0001t0001g0322 others(66): Show |
69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-19129A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576295 | |||||||
| chr1:24576296 | C | T | 180 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(177): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.-7-19128C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576296 | |||||||
| chr1:24576297 | G | A | 9 | a0001c0001t0001g0321 a0001c0001t0001g0375 a0001c0001t0001g0376 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-19127G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576297 | |||||||
| chr1:24576320 | C | T | 2 | a0001c0001t0010g0378 a0001c0001t0010g0379 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-19104C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576320 | |||||||
| chr1:24576343 | C | G | 69 | a0001c0001t0001g0029 a0001c0001t0001g0321 a0001c0001t0001g0322 others(66): Show |
69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-19081C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576343 | |||||||
| chr1:24576434 | C | T | 13 | a0001c0001t0001g0029 a0001c0001t0007g0023 a0002c0002t0004g0024 others(10): Show |
13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-18990C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576434 | |||||||
| chr1:24576514 | A | G | 32 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(29): Show |
32 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.-7-18910A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576514 | |||||||
| chr1:24576555 | A | G | 47 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0340 others(44): Show |
47 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-7-18869A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576555 | |||||||
| chr1:24576662 | G | T | 2 | a0001c0001t0007g0274 a0002c0002t0004g0273 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-7-18762G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576662 | |||||||
| chr1:24576745 | A | G | 1 | a0001c0001t0003g0384 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-7-18679A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576745 | |||||||
| chr1:24576752 | G | T | 1 | a0001c0001t0007g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-18672G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576752 | |||||||
| chr1:24576852 | A | G | 69 | a0001c0001t0001g0029 a0001c0001t0001g0321 a0001c0001t0001g0322 others(66): Show |
69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-18572A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576852 | |||||||
| chr1:24576866 | A | G | 69 | a0001c0001t0001g0029 a0001c0001t0001g0321 a0001c0001t0001g0322 others(66): Show |
69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-18558A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576866 | |||||||
| chr1:24576904 | G | A | 1 | a0001c0001t0003g0252 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-7-18520G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576904 | |||||||
| chr1:24576938 | G | T | 2 | a0001c0001t0003g0070 a0001c0001t0003g0075 |
2 | HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-7-18486G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576938 | |||||||
| chr1:24576981 | C | A | 179 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(176): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.-7-18443C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576981 | |||||||
| chr1:24576983 | A | C | 101 | a0001c0001t0001g0029 a0001c0001t0001g0286 a0001c0001t0001g0287 others(98): Show |
101 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.-7-18441A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576983 | |||||||
| chr1:24576999 | G | A | 1 | a0001c0001t0007g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-18425G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576999 | |||||||
| chr1:24577094 | C | T | 6 | a0001c0001t0001g0396 a0001c0001t0007g0395 a0001c0001t0008g0397 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-18330C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577094 | |||||||
| chr1:24577177 | T | A | 6 | a0001c0001t0001g0396 a0001c0001t0007g0395 a0001c0001t0008g0397 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-18247T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577177 | |||||||
| chr1:24577197 | G | T | 2 | a0001c0001t0002g0044 a0001c0001t0002g0095 |
2 | NA18983.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-7-18227G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577197 | |||||||
| chr1:24577401 | G | GT | 66 | a0001c0001t0001g0049 a0001c0001t0001g0055 a0001c0001t0001g0056 others(63): Show |
66 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.-7-17993dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577401 | ||||||
| chr1:24577401 | G | GTT | 29 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(26): Show |
30 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-7-17994_-7-17993d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577401 | ||||||
| chr1:24577401 | G | GTTT | 14 | a0001c0001t0001g0332 a0001c0001t0003g0011 a0001c0001t0003g0012 others(11): Show |
14 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-17995_-7-17993d others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577401 | ||||||
| chr1:24577401 | GT | G | 26 | a0001c0001t0001g0128 a0001c0001t0001g0157 a0001c0001t0001g0161 others(23): Show |
26 | HG00438.hp2 HG01069.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7-17993delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577401 | ||||||
| chr1:24577401 | GTT | G | 32 | a0001c0001t0001g0080 a0001c0001t0001g0163 a0001c0001t0001g0168 others(29): Show |
32 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.-7-17994_-7-17993d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577401 | ||||||
| chr1:24577401 | GTTTT | G | 12 | a0001c0001t0001g0029 a0001c0001t0001g0322 a0001c0001t0006g0325 others(9): Show |
12 | HG01099.hp2 HG01884.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-17996_-7-17993d others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577401 | ||||||
| chr1:24577404 | T | TTTTTTTG | 32 | a0001c0001t0001g0323 a0001c0001t0001g0340 a0001c0001t0001g0349 others(29): Show |
32 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-7-18014_-7-18013i others(9): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577404 | ||||||
| chr1:24577414 | T | G | 1 | a0001c0001t0007g0395 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-7-18010T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577414 | |||||||
| chr1:24577415 | T | G | 3 | a0001c0001t0001g0322 a0001c0001t0006g0325 a0001c0001t0006g0365 |
3 | HG02886.hp1 HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-7-18009T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577415 | |||||||
| chr1:24577416 | T | G | 1 | a0001c0001t0007g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-18008T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577416 | |||||||
| chr1:24577417 | T | G | 1 | a0001c0001t0001g0396 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-7-18007T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577417 | |||||||
| chr1:24577420 | T | G | 29 | a0001c0001t0001g0323 a0001c0001t0001g0340 a0001c0001t0001g0349 others(26): Show |
29 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-7-18004T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577420 | |||||||
| chr1:24577637 | T | C | 1 | a0001c0001t0001g0375 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-7-17787T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577637 | |||||||
| chr1:24577764 | G | A | 307 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(304): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.-7-17660G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577764 | |||||||
| chr1:24577883 | G | A | 1 | a0001c0001t0003g0013 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-7-17541G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577883 | |||||||
| chr1:24577919 | G | A | 198 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(195): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-7-17505G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577919 | |||||||
| chr1:24577963 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0038 others(134): Show |
138 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.-7-17461T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577963 | |||||||
| chr1:24577970 | T | G | 151 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(148): Show |
151 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.-7-17454T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577970 | |||||||
| chr1:24578012 | CAGCACTT others(4): Show |
C | 2 | a0001c0001t0013g0009 a0001c0001t0013g0010 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-7-17409_-7-17399d others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578012 | ||||||
| chr1:24578021 | G | T | 10 | a0001c0001t0001g0321 a0001c0001t0001g0375 a0001c0001t0001g0376 others(7): Show |
10 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-17403G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578021 | |||||||
| chr1:24578109 | A | G | 3 | a0001c0001t0003g0386 a0001c0001t0013g0009 a0001c0001t0013g0010 |
3 | HG02630.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-7-17315A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578109 | |||||||
| chr1:24578245 | C | CA | 153 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0126 others(150): Show |
154 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-7-17159dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578245 | ||||||
| chr1:24578245 | C | CAA | 112 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0049 others(109): Show |
112 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-7-17160_-7-17159d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578245 | ||||||
| chr1:24578245 | C | CAAA | 11 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0002g0081 others(8): Show |
11 | HG00735.hp2 HG01243.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7-17161_-7-17159d others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578245 | ||||||
| chr1:24578245 | CA | C | 22 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(19): Show |
22 | HG01175.hp1 HG01256.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7-17159delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578245 | ||||||
| chr1:24578371 | G | C | 1 | a0001c0001t0007g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-17053G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578371 | |||||||
| chr1:24578425 | C | A | 2 | a0001c0001t0001g0122 a0001c0001t0002g0214 |
2 | HG00558.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-7-16999C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578425 | |||||||
| chr1:24578469 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0003c0003t0020g0275 |
3 | HG01243.hp2 HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-7-16955G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578469 | |||||||
| chr1:24578534 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0003g0054 |
3 | HG02630.hp1 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-7-16890G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578534 | |||||||
| chr1:24578541 | G | GTTTTCT | 14 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(11): Show |
14 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-16874_-7-16869d others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578541 | ||||||
| chr1:24578551 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-7-16873T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578551 | |||||||
| chr1:24578560 | C | CT | 7 | a0001c0001t0001g0038 a0001c0001t0001g0140 a0001c0001t0001g0266 others(4): Show |
7 | HG00408.hp1 HG03490.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-16844dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578560 | ||||||
| chr1:24578560 | C | T | 12 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-16864C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578560 | |||||||
| chr1:24578560 | CT | C | 40 | a0001c0001t0001g0029 a0001c0001t0001g0105 a0001c0001t0001g0234 others(37): Show |
40 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-7-16844delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578560 | ||||||
| chr1:24578560 | CTT | C | 80 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0080 others(77): Show |
81 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.-7-16845_-7-16844d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578560 | ||||||
| chr1:24578563 | T | TC | 16 | a0001c0001t0002g0277 a0001c0001t0002g0279 a0001c0001t0002g0280 others(13): Show |
16 | HG00558.hp1 HG01167.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.-7-16861_-7-16860i others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578563 | |||||||
| chr1:24578564 | T | C | 2 | a0001c0001t0002g0282 a0001c0001t0006g0142 |
2 | HG01256.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-7-16860T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578564 | |||||||
| chr1:24578699 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0223 a0001c0001t0001g0286 others(2): Show |
6 | HG00323.hp2 HG01175.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-16725A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578699 | |||||||
| chr1:24578748 | G | C | 98 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0104 others(95): Show |
98 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-7-16676G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578748 | |||||||
| chr1:24578789 | G | A | 4 | a0001c0001t0003g0392 a0001c0001t0003g0393 a0001c0001t0007g0274 others(1): Show |
4 | HG02818.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-16635G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578789 | |||||||
| chr1:24578804 | C | A | 83 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0080 others(80): Show |
84 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.-7-16620C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578804 | |||||||
| chr1:24578844 | G | A | 15 | a0001c0001t0001g0029 a0001c0001t0007g0023 a0002c0002t0004g0024 others(12): Show |
15 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7-16580G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578844 | |||||||
| chr1:24578883 | A | G | 1 | a0001c0001t0003g0350 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-7-16541A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578883 | |||||||
| chr1:24579018 | G | A | 103 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0104 others(100): Show |
103 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-7-16406G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579018 | |||||||
| chr1:24579025 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-7-16399C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579025 | |||||||
| chr1:24579026 | G | A | 1 | a0001c0001t0003g0386 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-16398G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579026 | |||||||
| chr1:24579026 | G | T | 5 | a0001c0001t0002g0244 a0001c0001t0002g0246 a0001c0001t0002g0247 others(2): Show |
5 | HG00423.hp2 HG02080.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-16398G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579026 | |||||||
| chr1:24579038 | C | T | 1 | a0001c0001t0003g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-7-16386C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579038 | |||||||
| chr1:24579054 | G | A | 1 | a0001c0001t0003g0330 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-7-16370G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579054 | |||||||
| chr1:24579133 | G | C | 134 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0057 others(131): Show |
136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-7-16291G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579133 | |||||||
| chr1:24579169 | G | T | 2 | a0001c0001t0002g0137 a0001c0001t0002g0198 |
2 | NA18951.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-7-16255G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579169 | |||||||
| chr1:24579176 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-7-16248G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579176 | |||||||
| chr1:24579192 | TG | T | 116 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0080 others(113): Show |
118 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-7-16227delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24579192 | ||||||
| chr1:24579197 | G | GT | 7 | a0001c0001t0001g0253 a0001c0001t0002g0037 a0001c0001t0002g0046 others(4): Show |
7 | HG00544.hp2 HG02027.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-16214dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24579197 | ||||||
| chr1:24579197 | G | T | 19 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(16): Show |
19 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7-16227G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579197 | |||||||
| chr1:24579197 | GT | G | 7 | a0001c0001t0002g0118 a0001c0001t0003g0006 a0001c0001t0010g0272 others(4): Show |
7 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-16214delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24579197 | ||||||
| chr1:24579197 | GTT | G | 44 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0322 others(41): Show |
44 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-7-16215_-7-16214d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24579197 | ||||||
| chr1:24579266 | G | C | 1 | a0001c0001t0025g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-16158G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579266 | |||||||
| chr1:24579610 | C | T | 16 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(13): Show |
16 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7-15814C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579610 | |||||||
| chr1:24579648 | G | T | 4 | a0001c0001t0001g0145 a0001c0001t0003g0146 a0002c0002t0012g0002 others(1): Show |
5 | HG02723.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-15776G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579648 | |||||||
| chr1:24579829 | C | T | 12 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-15595C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579829 | |||||||
| chr1:24579838 | T | G | 4 | a0001c0001t0007g0395 a0001c0001t0013g0009 a0001c0001t0013g0010 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-15586T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579838 | |||||||
| chr1:24580002 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-7-15422G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580002 | |||||||
| chr1:24580071 | A | C | 16 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(13): Show |
16 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7-15353A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580071 | |||||||
| chr1:24580122 | G | A | 3 | a0001c0001t0001g0322 a0001c0001t0006g0325 a0001c0001t0006g0365 |
3 | HG02886.hp1 HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-7-15302G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580122 | |||||||
| chr1:24580145 | G | A | 2 | a0001c0001t0002g0336 a0001c0001t0003g0339 |
2 | HG02015.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.-7-15279G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580145 | |||||||
| chr1:24580185 | C | T | 4 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0003g0386 others(1): Show |
4 | HG02572.hp2 HG03486.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-15239C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580185 | |||||||
| chr1:24580186 | G | A | 6 | a0001c0001t0001g0321 a0001c0001t0001g0375 a0001c0001t0001g0376 others(3): Show |
6 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-15238G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580186 | |||||||
| chr1:24580220 | A | G | 302 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(299): Show |
304 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.-7-15204A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580220 | |||||||
| chr1:24580227 | A | G | 134 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0057 others(131): Show |
136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-7-15197A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580227 | |||||||
| chr1:24580398 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-7-15026C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580398 | |||||||
| chr1:24580434 | C | T | 2 | a0001c0001t0003g0372 a0001c0001t0003g0373 |
2 | HG02080.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-7-14990C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580434 | |||||||
| chr1:24580599 | C | T | 1 | a0001c0001t0002g0356 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-7-14825C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580599 | |||||||
| chr1:24580751 | G | A | 73 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0080 others(70): Show |
74 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-7-14673G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580751 | |||||||
| chr1:24580769 | T | C | 2 | a0001c0001t0003g0386 a0001c0001t0025g0316 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-7-14655T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580769 | |||||||
| chr1:24580924 | G | A | 290 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0049 others(287): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.-7-14500G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580924 | |||||||
| chr1:24580964 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-7-14460C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580964 | |||||||
| chr1:24581029 | C | T | 2 | a0001c0001t0003g0392 a0001c0001t0003g0393 |
2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-7-14395C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581029 | |||||||
| chr1:24581052 | G | C | 36 | a0001c0001t0002g0356 a0001c0001t0002g0359 a0001c0001t0003g0011 others(33): Show |
37 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.-7-14372G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581052 | |||||||
| chr1:24581122 | C | CT | 29 | a0001c0001t0001g0228 a0001c0001t0001g0321 a0001c0001t0001g0375 others(26): Show |
29 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-7-14289dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24581122 | ||||||
| chr1:24581188 | C | T | 1 | a0001c0001t0003g0374 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-7-14236C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581188 | |||||||
| chr1:24581242 | A | G | 298 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(295): Show |
300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.-7-14182A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581242 | |||||||
| chr1:24581244 | A | G | 329 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(326): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.-7-14180A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581244 | |||||||
| chr1:24581304 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-7-14120A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581304 | |||||||
| chr1:24581969 | A | G | 1 | a0001c0001t0003g0220 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-7-13455A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581969 | |||||||
| chr1:24582021 | A | T | 14 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(11): Show |
14 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-13403A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582021 | |||||||
| chr1:24582031 | G | T | 3 | a0001c0001t0010g0272 a0001c0001t0010g0378 a0001c0001t0010g0379 |
3 | HG01891.hp1 HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-13393G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582031 | |||||||
| chr1:24582044 | T | C | 45 | a0001c0001t0001g0322 a0001c0001t0002g0356 a0001c0001t0002g0359 others(42): Show |
46 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.-7-13380T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582044 | |||||||
| chr1:24582128 | T | G | 132 | a0001c0001t0001g0104 a0001c0001t0001g0122 a0001c0001t0002g0022 others(129): Show |
132 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-7-13296T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582128 | |||||||
| chr1:24582134 | A | C | 132 | a0001c0001t0001g0104 a0001c0001t0001g0122 a0001c0001t0002g0022 others(129): Show |
132 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-7-13290A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582134 | |||||||
| chr1:24582198 | C | T | 2 | a0001c0001t0003g0255 a0001c0001t0003g0263 |
2 | HG00544.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-7-13226C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582198 | |||||||
| chr1:24582292 | C | T | 261 | a0001c0001t0001g0038 a0001c0001t0001g0080 a0001c0001t0001g0104 others(258): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.-7-13132C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582292 | |||||||
| chr1:24582438 | C | T | 62 | a0001c0001t0001g0029 a0001c0001t0001g0145 a0001c0001t0001g0322 others(59): Show |
64 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.-7-12986C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582438 | |||||||
| chr1:24582468 | G | A | 155 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(152): Show |
156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.-7-12956G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582468 | |||||||
| chr1:24582596 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0141 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-7-12828C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582596 | |||||||
| chr1:24582691 | T | C | 1 | a0001c0001t0003g0330 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-7-12733T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582691 | |||||||
| chr1:24582707 | A | T | 1 | a0001c0001t0001g0224 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-7-12717A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582707 | |||||||
| chr1:24582768 | C | T | 3 | a0001c0001t0010g0272 a0001c0001t0010g0378 a0001c0001t0010g0379 |
3 | HG01891.hp1 HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-12656C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582768 | |||||||
| chr1:24582810 | G | T | 72 | a0001c0001t0001g0038 a0001c0001t0001g0080 a0001c0001t0001g0156 others(69): Show |
72 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-7-12614G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582810 | |||||||
| chr1:24582817 | T | TCCTA | 43 | a0001c0001t0001g0322 a0001c0001t0002g0356 a0001c0001t0002g0359 others(40): Show |
44 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.-7-12606_-7-12603d others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24582817 | ||||||
| chr1:24582912 | T | C | 47 | a0001c0001t0001g0349 a0001c0001t0002g0336 a0001c0001t0003g0071 others(44): Show |
47 | HG00099.hp1 HG00558.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-7-12512T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582912 | |||||||
| chr1:24583002 | A | T | 1 | a0001c0001t0003g0094 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-7-12422A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583002 | |||||||
| chr1:24583051 | C | T | 1 | a0002c0002t0004g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-7-12373C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583051 | |||||||
| chr1:24583243 | CAG | C | 101 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0056 others(98): Show |
102 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.-7-12176_-7-12175d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24583243 | ||||||
| chr1:24583287 | G | T | 1 | a0001c0001t0003g0384 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-7-12137G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583287 | |||||||
| chr1:24583466 | C | A | 3 | a0001c0001t0001g0249 a0001c0001t0001g0312 a0001c0001t0005g0311 |
3 | NA18971.hp2 NA18973.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-7-11958C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583466 | |||||||
| chr1:24583584 | C | T | 206 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0056 others(203): Show |
207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-7-11840C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583584 | |||||||
| chr1:24583717 | G | GA | 76 | a0001c0001t0001g0038 a0001c0001t0001g0080 a0001c0001t0001g0126 others(73): Show |
76 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-7-11686dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24583717 | ||||||
| chr1:24583717 | GA | G | 50 | a0001c0001t0001g0349 a0001c0001t0001g0396 a0001c0001t0002g0336 others(47): Show |
50 | HG00099.hp1 HG00558.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.-7-11686delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24583717 | ||||||
| chr1:24583717 | GAA | G | 42 | a0001c0001t0001g0322 a0001c0001t0002g0356 a0001c0001t0002g0359 others(39): Show |
43 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-7-11687_-7-11686d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24583717 | ||||||
| chr1:24583719 | A | G | 1 | a0001c0001t0003g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-7-11705A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583719 | |||||||
| chr1:24583720 | A | G | 42 | a0001c0001t0001g0322 a0001c0001t0002g0356 a0001c0001t0002g0359 others(39): Show |
43 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-7-11704A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583720 | |||||||
| chr1:24583793 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-7-11631C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583793 | |||||||
| chr1:24583828 | T | C | 207 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0056 others(204): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.-7-11596T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583828 | |||||||
| chr1:24583840 | T | A | 5 | a0001c0001t0002g0046 a0001c0001t0002g0053 a0001c0001t0002g0118 others(2): Show |
5 | NA18960.hp2 NA18972.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-11584T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583840 | |||||||
| chr1:24584096 | A | G | 1 | a0001c0001t0010g0379 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-7-11328A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584096 | |||||||
| chr1:24584176 | T | C | 5 | a0001c0001t0007g0151 a0001c0001t0007g0395 a0001c0001t0013g0009 others(2): Show |
5 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-11248T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584176 | |||||||
| chr1:24584196 | G | A | 2 | a0001c0001t0002g0036 a0001c0001t0002g0072 |
2 | NA19002.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-7-11228G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584196 | |||||||
| chr1:24584236 | A | T | 1 | a0001c0001t0003g0075 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-7-11188A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584236 | |||||||
| chr1:24584437 | G | A | 1 | a0001c0001t0002g0158 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-7-10987G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584437 | |||||||
| chr1:24584601 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0003c0003t0020g0275 |
3 | HG01243.hp2 HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-7-10823C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584601 | |||||||
| chr1:24584723 | G | T | 18 | a0001c0001t0001g0029 a0001c0001t0001g0145 a0001c0001t0007g0023 others(15): Show |
19 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7-10701G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584723 | |||||||
| chr1:24584829 | G | A | 4 | a0001c0001t0001g0396 a0001c0001t0008g0397 a0001c0001t0008g0398 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-10595G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584829 | |||||||
| chr1:24584938 | C | T | 5 | a0001c0001t0002g0046 a0001c0001t0002g0053 a0001c0001t0002g0118 others(2): Show |
5 | NA18960.hp2 NA18972.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-10486C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584938 | |||||||
| chr1:24584974 | CGGGTGGG others(9): Show |
C | 12 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0006g0142 others(9): Show |
12 | HG00558.hp1 HG01109.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7-10448_-7-10433d others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24584974 | ||||||
| chr1:24584991 | G | A | 206 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0056 others(203): Show |
207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-7-10433G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584991 | |||||||
| chr1:24584997 | G | A | 3 | a0001c0001t0003g0227 a0001c0001t0003g0324 a0001c0001t0003g0342 |
3 | HG02056.hp1 HG02135.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-7-10427G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584997 | |||||||
| chr1:24584999 | G | T | 1 | a0001c0001t0014g0014 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7-10425G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584999 | |||||||
| chr1:24585120 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0003c0003t0020g0275 |
3 | HG01243.hp2 HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-7-10304G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585120 | |||||||
| chr1:24585147 | CT | C | 3 | a0001c0001t0009g0033 a0001c0001t0009g0066 a0001c0001t0009g0068 |
3 | HG02055.hp2 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-7-10274delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24585147 | ||||||
| chr1:24585269 | G | T | 1 | a0001c0001t0025g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-10155G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585269 | |||||||
| chr1:24585434 | G | A | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0321 |
3 | HG03490.hp2 HG03492.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-7-9990G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585434 | |||||||
| chr1:24585568 | G | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0141 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-7-9856G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585568 | |||||||
| chr1:24585589 | T | G | 170 | a0001c0001t0001g0038 a0001c0001t0001g0080 a0001c0001t0001g0156 others(167): Show |
171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.-7-9835T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585589 | |||||||
| chr1:24585679 | G | A | 9 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0321 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-9745G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585679 | |||||||
| chr1:24585890 | G | A | 2 | a0001c0001t0013g0009 a0001c0001t0013g0010 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-7-9534G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585890 | |||||||
| chr1:24585978 | C | T | 37 | a0001c0001t0001g0349 a0001c0001t0002g0336 a0001c0001t0003g0071 others(34): Show |
37 | HG00099.hp1 HG01074.hp2 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.-7-9446C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585978 | |||||||
| chr1:24586037 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-7-9387C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586037 | |||||||
| chr1:24586219 | G | A | 6 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0112 others(3): Show |
6 | HG01070.hp2 HG01361.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-9205G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586219 | |||||||
| chr1:24586281 | C | A | 1 | a0001c0001t0001g0271 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-7-9143C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586281 | |||||||
| chr1:24586300 | G | T | 1 | a0001c0001t0002g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-7-9124G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586300 | |||||||
| chr1:24586393 | G | A | 62 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(59): Show |
63 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.-7-9031G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586393 | |||||||
| chr1:24586532 | G | A | 1 | a0001c0001t0002g0251 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-7-8892G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586532 | |||||||
| chr1:24586538 | G | A | 37 | a0001c0001t0001g0349 a0001c0001t0002g0336 a0001c0001t0003g0071 others(34): Show |
37 | HG00099.hp1 HG01074.hp2 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.-7-8886G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586538 | |||||||
| chr1:24586586 | C | A | 1 | a0001c0001t0003g0371 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-7-8838C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586586 | |||||||
| chr1:24586596 | A | G | 22 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(19): Show |
22 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7-8828A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586596 | |||||||
| chr1:24586619 | G | A | 1 | a0001c0001t0002g0158 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-7-8805G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586619 | |||||||
| chr1:24586737 | G | A | 141 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0056 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-7-8687G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586737 | |||||||
| chr1:24586747 | G | A | 1 | a0001c0001t0007g0274 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-8677G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586747 | |||||||
| chr1:24586759 | C | CA | 40 | a0001c0001t0001g0159 a0001c0001t0001g0170 a0001c0001t0001g0259 others(37): Show |
40 | HG00099.hp1 HG01074.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.-7-8647dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24586759 | ||||||
| chr1:24586759 | CA | C | 176 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0061 others(173): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-7-8647delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24586759 | ||||||
| chr1:24586849 | TG | T | 21 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(18): Show |
21 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-8570delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24586849 | ||||||
| chr1:24586930 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-7-8494C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586930 | |||||||
| chr1:24586972 | C | T | 318 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(315): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.-7-8452C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586972 | |||||||
| chr1:24587066 | G | T | 1 | a0001c0001t0002g0053 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-7-8358G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587066 | |||||||
| chr1:24587249 | G | C | 13 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(10): Show |
13 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-8175G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587249 | |||||||
| chr1:24587337 | T | C | 4 | a0001c0001t0001g0396 a0001c0001t0008g0397 a0001c0001t0008g0398 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-8087T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587337 | |||||||
| chr1:24587404 | T | C | 5 | a0001c0001t0007g0151 a0001c0001t0007g0395 a0001c0001t0013g0009 others(2): Show |
5 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-8020T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587404 | |||||||
| chr1:24587481 | C | A | 42 | a0001c0001t0001g0322 a0001c0001t0002g0356 a0001c0001t0002g0359 others(39): Show |
43 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-7-7943C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587481 | |||||||
| chr1:24587496 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-7-7928G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587496 | |||||||
| chr1:24587541 | A | T | 277 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(274): Show |
278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-7-7883A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587541 | |||||||
| chr1:24587588 | A | G | 75 | a0001c0001t0001g0038 a0001c0001t0001g0080 a0001c0001t0001g0156 others(72): Show |
75 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-7-7836A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587588 | |||||||
| chr1:24587666 | A | G | 1 | a0001c0001t0007g0021 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-7-7758A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587666 | |||||||
| chr1:24587749 | G | A | 1 | a0001c0001t0025g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-7675G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587749 | |||||||
| chr1:24587934 | CTTTTTCT others(5): Show |
C | 1 | a0001c0001t0025g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-7472_-7-7461del others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24587934 | ||||||
| chr1:24587985 | G | A | 21 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(18): Show |
21 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-7439G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587985 | |||||||
| chr1:24588016 | GA | G | 3 | a0001c0001t0001g0322 a0001c0001t0006g0325 a0001c0001t0006g0365 |
3 | HG02886.hp1 HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-7-7405delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24588016 | ||||||
| chr1:24588027 | A | G | 2 | a0001c0001t0003g0220 a0001c0001t0003g0348 |
2 | NA18966.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-7-7397A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24588027 | |||||||
| chr1:24588188 | T | C | 63 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(60): Show |
64 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.-7-7236T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24588188 | |||||||
| chr1:24588442 | A | G | 2 | a0001c0001t0003g0011 a0001c0001t0003g0012 |
2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-7-6982A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24588442 | |||||||
| chr1:24588460 | G | A | 1 | a0001c0001t0003g0092 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-7-6964G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24588460 | |||||||
| chr1:24588757 | G | T | 37 | a0001c0001t0002g0356 a0001c0001t0002g0359 a0001c0001t0003g0013 others(34): Show |
38 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-7-6667G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24588757 | |||||||
| chr1:24589266 | G | T | 3 | a0001c0001t0003g0006 a0002c0002t0004g0005 a0002c0002t0004g0007 |
3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-7-6158G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589266 | |||||||
| chr1:24589290 | C | G | 159 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(156): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-7-6134C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589290 | |||||||
| chr1:24589290 | CGTTTGAT others(6): Show |
C | 7 | a0001c0001t0003g0392 a0001c0001t0003g0393 a0001c0001t0007g0151 others(4): Show |
7 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-6131_-7-6119del others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24589290 | ||||||
| chr1:24589308 | T | C | 7 | a0001c0001t0003g0392 a0001c0001t0003g0393 a0001c0001t0007g0151 others(4): Show |
7 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-6116T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589308 | |||||||
| chr1:24589438 | T | A | 1 | a0001c0001t0025g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-5986T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589438 | |||||||
| chr1:24589493 | T | C | 151 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(148): Show |
153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-7-5931T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589493 | |||||||
| chr1:24589635 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0003g0054 |
3 | HG02630.hp1 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-7-5789G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589635 | |||||||
| chr1:24589731 | G | A | 1 | a0001c0001t0003g0333 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-7-5693G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589731 | |||||||
| chr1:24589734 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-7-5690G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589734 | |||||||
| chr1:24589788 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-7-5636G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589788 | |||||||
| chr1:24589818 | G | T | 1 | a0001c0001t0007g0274 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-5606G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589818 | |||||||
| chr1:24589876 | G | A | 1 | a0001c0001t0003g0220 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-7-5548G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589876 | |||||||
| chr1:24589932 | C | G | 56 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0057 others(53): Show |
57 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.-7-5492C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589932 | |||||||
| chr1:24590000 | A | T | 1 | a0001c0001t0007g0274 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-5424A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590000 | |||||||
| chr1:24590046 | C | A | 1 | a0001c0001t0003g0326 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-7-5378C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590046 | |||||||
| chr1:24590363 | C | T | 2 | a0001c0001t0007g0274 a0003c0003t0020g0275 |
2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-7-5061C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590363 | |||||||
| chr1:24590492 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-7-4932G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590492 | |||||||
| chr1:24590706 | C | G | 1 | a0003c0003t0020g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-4718C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590706 | |||||||
| chr1:24590870 | A | C | 1 | a0002c0002t0004g0018 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-7-4554A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590870 | |||||||
| chr1:24590872 | T | C | 122 | a0001c0001t0001g0104 a0001c0001t0001g0122 a0001c0001t0001g0259 others(119): Show |
122 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-7-4552T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590872 | |||||||
| chr1:24590965 | G | T | 43 | a0001c0001t0003g0071 a0001c0001t0003g0077 a0001c0001t0003g0078 others(40): Show |
43 | HG00099.hp1 HG00639.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.-7-4459G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590965 | |||||||
| chr1:24591005 | A | G | 1 | a0001c0001t0025g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-4419A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591005 | |||||||
| chr1:24591038 | G | C | 1 | a0001c0001t0006g0152 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-7-4386G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591038 | |||||||
| chr1:24591052 | A | G | 198 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(195): Show |
200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-7-4372A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591052 | |||||||
| chr1:24591053 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-7-4371C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591053 | |||||||
| chr1:24591062 | AG | A | 76 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0057 others(73): Show |
76 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.-7-4360delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24591062 | ||||||
| chr1:24591064 | G | C | 76 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0057 others(73): Show |
76 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.-7-4360G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591064 | |||||||
| chr1:24591105 | T | C | 1 | a0003c0003t0020g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-4319T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591105 | |||||||
| chr1:24591133 | C | T | 20 | a0001c0001t0001g0029 a0001c0001t0003g0392 a0001c0001t0003g0393 others(17): Show |
21 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-4291C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591133 | |||||||
| chr1:24591254 | C | T | 4 | a0001c0001t0001g0396 a0001c0001t0008g0397 a0001c0001t0008g0398 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-4170C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591254 | |||||||
| chr1:24591382 | C | T | 17 | a0001c0001t0001g0029 a0001c0001t0003g0392 a0001c0001t0003g0393 others(14): Show |
17 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-7-4042C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591382 | |||||||
| chr1:24591412 | C | T | 3 | a0001c0001t0003g0006 a0002c0002t0004g0005 a0002c0002t0004g0007 |
3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-7-4012C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591412 | |||||||
| chr1:24591515 | A | G | 3 | a0001c0001t0003g0392 a0001c0001t0003g0393 a0002c0002t0004g0018 |
3 | HG01243.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-7-3909A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591515 | |||||||
| chr1:24591575 | T | A | 1 | a0001c0001t0019g0101 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-7-3849T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591575 | |||||||
| chr1:24591712 | G | T | 15 | a0001c0001t0001g0029 a0001c0001t0007g0023 a0002c0002t0004g0024 others(12): Show |
15 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7-3712G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591712 | |||||||
| chr1:24591765 | G | T | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-7-3659G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591765 | |||||||
| chr1:24591817 | G | A | 1 | a0001c0001t0002g0270 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-7-3607G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591817 | |||||||
| chr1:24592079 | C | T | 1 | a0002c0002t0004g0018 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-7-3345C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592079 | |||||||
| chr1:24592244 | C | T | 79 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0057 others(76): Show |
79 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.-7-3180C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592244 | |||||||
| chr1:24592245 | G | A | 4 | a0001c0001t0001g0396 a0001c0001t0008g0397 a0001c0001t0008g0398 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-3179G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592245 | |||||||
| chr1:24592248 | A | G | 1 | a0001c0001t0025g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-3176A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592248 | |||||||
| chr1:24592364 | C | G | 22 | a0001c0001t0003g0075 a0001c0001t0003g0180 a0001c0001t0003g0226 others(19): Show |
22 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7-3060C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592364 | |||||||
| chr1:24592632 | A | T | 210 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(207): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.-7-2792A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592632 | |||||||
| chr1:24592745 | C | T | 9 | a0001c0001t0001g0396 a0001c0001t0007g0274 a0001c0001t0007g0395 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-2679C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592745 | |||||||
| chr1:24592812 | G | A | 6 | a0001c0001t0002g0040 a0001c0001t0002g0042 a0001c0001t0002g0116 others(3): Show |
6 | HG01081.hp1 NA18951.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-2612G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592812 | |||||||
| chr1:24592835 | C | A | 1 | a0001c0001t0003g0090 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-7-2589C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592835 | |||||||
| chr1:24592835 | C | T | 91 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(88): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-7-2589C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592835 | |||||||
| chr1:24592850 | C | T | 1 | a0001c0001t0001g0375 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-7-2574C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592850 | |||||||
| chr1:24592851 | G | A | 1 | a0001c0001t0003g0343 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-7-2573G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592851 | |||||||
| chr1:24592854 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-7-2570G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592854 | |||||||
| chr1:24592923 | T | A | 2 | a0001c0001t0003g0015 a0002c0002t0004g0018 |
2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-7-2501T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592923 | |||||||
| chr1:24593028 | A | G | 5 | a0001c0001t0001g0321 a0001c0001t0001g0375 a0001c0001t0001g0376 others(2): Show |
5 | HG00639.hp2 HG01069.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-2396A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593028 | |||||||
| chr1:24593086 | G | A | 93 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(90): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-7-2338G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593086 | |||||||
| chr1:24593115 | T | C | 2 | a0001c0001t0006g0142 a0001c0001t0006g0143 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-7-2309T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593115 | |||||||
| chr1:24593182 | GA | G | 118 | a0001c0001t0001g0065 a0001c0001t0001g0104 a0001c0001t0001g0157 others(115): Show |
118 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-7-2229delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593182 | ||||||
| chr1:24593244 | G | A | 1 | a0001c0001t0007g0274 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-2180G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593244 | |||||||
| chr1:24593266 | T | C | 1 | a0001c0001t0005g0194 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-7-2158T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593266 | |||||||
| chr1:24593271 | G | A | 1 | a0001c0001t0003g0367 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-7-2153G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593271 | |||||||
| chr1:24593321 | TA | T | 297 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(294): Show |
298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.-7-2093delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593321 | ||||||
| chr1:24593455 | T | C | 88 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0057 others(85): Show |
88 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.-7-1969T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593455 | |||||||
| chr1:24593627 | T | A | 1 | a0001c0001t0001g0332 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-7-1797T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593627 | |||||||
| chr1:24593738 | A | G | 2 | a0001c0001t0025g0316 a0003c0003t0020g0275 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7-1686A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593738 | |||||||
| chr1:24593786 | G | T | 1 | a0001c0001t0002g0136 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-7-1638G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593786 | |||||||
| chr1:24593857 | A | ATTAT | 7 | a0001c0001t0001g0123 a0001c0001t0002g0116 a0001c0001t0003g0071 others(4): Show |
7 | HG00099.hp1 HG02148.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-1524_-7-1521dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593857 | ||||||
| chr1:24593857 | ATTAT | A | 52 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0060 others(49): Show |
53 | HG00140.hp2 HG00408.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.-7-1524_-7-1521del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593857 | ||||||
| chr1:24593857 | ATTATTTA others(1): Show |
A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0056 a0001c0001t0001g0057 others(168): Show |
173 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-7-1528_-7-1521del others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593857 | ||||||
| chr1:24593857 | ATTATTTA others(5): Show |
A | 1 | a0001c0001t0025g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-1532_-7-1521del others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593857 | ||||||
| chr1:24593857 | ATTATTTA others(17): Show |
A | 12 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0006g0142 others(9): Show |
12 | HG00558.hp1 HG01109.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7-1544_-7-1521del others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593857 | ||||||
| chr1:24593921 | T | C | 1 | a0001c0001t0018g0073 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-7-1503T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593921 | |||||||
| chr1:24594035 | G | A | 76 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0057 others(73): Show |
76 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.-7-1389G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594035 | |||||||
| chr1:24594038 | CCCA | C | 107 | a0001c0001t0001g0104 a0001c0001t0002g0022 a0001c0001t0002g0027 others(104): Show |
107 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-7-1379_-7-1377del others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24594038 | ||||||
| chr1:24594107 | G | A | 1 | a0001c0001t0007g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-1317G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594107 | |||||||
| chr1:24594126 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-7-1298A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594126 | |||||||
| chr1:24594227 | G | C | 183 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0057 others(180): Show |
183 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-7-1197G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594227 | |||||||
| chr1:24594248 | A | C | 303 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(300): Show |
304 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.-7-1176A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594248 | |||||||
| chr1:24594343 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-7-1081G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594343 | |||||||
| chr1:24594490 | C | A | 97 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(94): Show |
98 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-7-934C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594490 | |||||||
| chr1:24594555 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-7-869G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594555 | |||||||
| chr1:24594556 | A | C | 3 | a0001c0001t0003g0392 a0001c0001t0003g0393 a0001c0001t0007g0151 |
3 | HG02572.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-7-868A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594556 | |||||||
| chr1:24594665 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-7-759T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594665 | |||||||
| chr1:24594778 | T | A | 1 | a0001c0001t0001g0366 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-7-646T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594778 | |||||||
| chr1:24594842 | GATTGCAC others(3): Show |
G | 1 | a0001c0001t0002g0096 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-7-581_-7-572delAT others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594842 | |||||||
| chr1:24594857 | C | T | 107 | a0001c0001t0001g0104 a0001c0001t0002g0022 a0001c0001t0002g0027 others(104): Show |
107 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-7-567C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594857 | |||||||
| chr1:24594900 | A | AT | 195 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(192): Show |
196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-7-518dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24594900 | ||||||
| chr1:24594900 | A | T | 107 | a0001c0001t0001g0104 a0001c0001t0002g0022 a0001c0001t0002g0027 others(104): Show |
107 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-7-524A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594900 | |||||||
| chr1:24594975 | T | C | 1 | a0001c0001t0002g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-7-449T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594975 | |||||||
| chr1:24595038 | GTTGA | G | 301 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(298): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.-7-381_-7-378delTT others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24595038 | ||||||
| chr1:24595083 | T | C | 4 | a0001c0001t0001g0396 a0001c0001t0008g0397 a0001c0001t0008g0398 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-341T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24595083 | |||||||
| chr1:24595116 | T | C | 1 | a0001c0001t0001g0340 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-7-308T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24595116 | |||||||
| chr1:24595174 | A | C | 2 | a0001c0001t0003g0392 a0001c0001t0003g0393 |
2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-7-250A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24595174 | |||||||
| chr1:24595237 | T | C | 1 | a0003c0003t0020g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-187T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24595237 | |||||||
| chr1:24595241 | G | A | 2 | a0001c0001t0002g0356 a0001c0001t0002g0359 |
2 | HG03239.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-7-183G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24595241 | |||||||
| chr1:24595267 | C | T | 85 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0057 others(82): Show |
85 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-7-157C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24595267 | |||||||
| chr1:24595538 | G | A | 1 | a0001c0001t0003g0384 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.82+26G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24595538 | |||||||
| chr1:24595565 | T | C | 77 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0057 others(74): Show |
77 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.82+53T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24595565 | |||||||
| chr1:24595575 | G | A | 1 | a0001c0001t0003g0326 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.82+63G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24595575 | |||||||
| chr1:24595638 | G | A | 182 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(179): Show |
183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.82+126G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24595638 | |||||||
| chr1:24595675 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.82+163A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24595675 | |||||||
| chr1:24595794 | C | CT | 60 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0050 others(57): Show |
61 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.82+303dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24595794 | ||||||
| chr1:24595794 | C | CTTT | 9 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0006g0152 others(6): Show |
9 | HG00558.hp1 HG01109.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.82+301_82+303dupTT others(1): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24595794 | ||||||
| chr1:24595794 | CT | C | 13 | a0001c0001t0001g0396 a0001c0001t0002g0053 a0001c0001t0002g0082 others(10): Show |
13 | HG01106.hp1 HG01261.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.82+303delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24595794 | ||||||
| chr1:24595794 | CTTTT | C | 97 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(94): Show |
98 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.82+300_82+303delTT others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24595794 | ||||||
| chr1:24595794 | CTTTTT | C | 78 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0057 others(75): Show |
78 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.82+299_82+303delTT others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24595794 | ||||||
| chr1:24595955 | TA | T | 179 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(176): Show |
180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.82+445delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24595955 | ||||||
| chr1:24596156 | C | T | 2 | a0001c0001t0007g0395 a0002c0002t0004g0394 |
2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.82+644C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24596156 | |||||||
| chr1:24596528 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.82+1016C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24596528 | |||||||
| chr1:24596579 | G | C | 4 | a0001c0001t0003g0006 a0001c0001t0003g0384 a0002c0002t0004g0005 others(1): Show |
4 | HG01106.hp1 HG02451.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+1067G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24596579 | |||||||
| chr1:24596626 | T | C | 1 | a0001c0001t0007g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.82+1114T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24596626 | |||||||
| chr1:24596789 | G | C | 7 | a0001c0001t0001g0322 a0001c0001t0003g0011 a0001c0001t0003g0012 others(4): Show |
7 | HG01109.hp2 HG02145.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+1277G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24596789 | |||||||
| chr1:24596927 | A | G | 3 | a0001c0001t0008g0397 a0001c0001t0008g0398 a0001c0001t0008g0399 |
3 | HG02055.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.82+1415A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24596927 | |||||||
| chr1:24597063 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.82+1551G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597063 | |||||||
| chr1:24597124 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.82+1612G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597124 | |||||||
| chr1:24597313 | C | T | 1 | a0001c0001t0001g0396 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.82+1801C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597313 | |||||||
| chr1:24597519 | A | AG | 109 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0038 others(106): Show |
111 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.82+2018dupG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597519 | ||||||
| chr1:24597519 | AG | A | 29 | a0001c0001t0001g0062 a0001c0001t0001g0296 a0001c0001t0001g0297 others(26): Show |
30 | HG00558.hp1 HG01123.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.82+2018delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597519 | ||||||
| chr1:24597519 | AGG | A | 88 | a0001c0001t0001g0104 a0001c0001t0002g0027 a0001c0001t0002g0028 others(85): Show |
88 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.82+2017_82+2018del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597519 | ||||||
| chr1:24597522 | G | T | 1 | a0001c0001t0001g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.82+2010G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597522 | |||||||
| chr1:24597527 | G | GA | 76 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0012 others(73): Show |
76 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.82+2015_82+2016ins others(1): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597527 | |||||||
| chr1:24597529 | G | A | 7 | a0001c0001t0002g0096 a0001c0001t0002g0114 a0001c0001t0002g0116 others(4): Show |
7 | HG00140.hp1 HG00544.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+2017G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597529 | |||||||
| chr1:24597530 | GA | G | 7 | a0001c0001t0002g0048 a0001c0001t0002g0096 a0001c0001t0002g0114 others(4): Show |
7 | HG00140.hp1 HG00544.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+2019delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597530 | |||||||
| chr1:24597531 | A | G | 15 | a0001c0001t0001g0049 a0001c0001t0001g0055 a0001c0001t0001g0057 others(12): Show |
15 | HG00621.hp2 HG01175.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.82+2019A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597531 | |||||||
| chr1:24597536 | G | A | 1 | a0001c0001t0002g0270 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.82+2024G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597536 | |||||||
| chr1:24597537 | A | AG | 11 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0159 others(8): Show |
11 | HG00738.hp1 HG01433.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+2030dupG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597537 | ||||||
| chr1:24597537 | A | G | 2 | a0001c0001t0001g0310 a0001c0001t0002g0270 |
2 | HG03942.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.82+2025A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597537 | |||||||
| chr1:24597546 | G | A | 1 | a0003c0003t0020g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82+2034G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597546 | |||||||
| chr1:24597555 | A | AGGGAAGG others(10): Show |
16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2046_82+2047ins others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597555 | ||||||
| chr1:24597580 | C | A | 1 | a0001c0001t0002g0136 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.82+2068C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597580 | |||||||
| chr1:24597581 | A | AAAAG | 124 | a0001c0001t0001g0104 a0001c0001t0002g0022 a0001c0001t0002g0027 others(121): Show |
124 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.82+2071_82+2074dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597581 | ||||||
| chr1:24597581 | A | G | 1 | a0001c0001t0002g0136 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.82+2069A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597581 | |||||||
| chr1:24597586 | AG | A | 5 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0273 others(2): Show |
6 | HG02723.hp2 HG02818.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+2075delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597586 | |||||||
| chr1:24597587 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.82+2075G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597587 | |||||||
| chr1:24597590 | GAA | G | 5 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0273 others(2): Show |
6 | HG02723.hp2 HG02818.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+2080_82+2081del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597590 | ||||||
| chr1:24597593 | A | AGAAGAAA others(35): Show |
4 | a0001c0001t0006g0190 a0001c0001t0006g0281 a0001c0001t0006g0283 others(1): Show |
4 | HG00558.hp1 NA18999.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+2102_82+2103ins others(42): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597593 | ||||||
| chr1:24597599 | AAGAAAGA others(11): Show |
A | 16 | a0002c0002t0004g0017 a0002c0002t0004g0018 a0002c0002t0004g0024 others(13): Show |
16 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2107_82+2124del others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597599 | ||||||
| chr1:24597601 | GAAAGAAA others(12): Show |
G | 5 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0273 others(2): Show |
6 | HG02723.hp2 HG02818.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+2092_82+2110del others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597601 | ||||||
| chr1:24597603 | A | AAGAAAGA others(11): Show |
1 | a0003c0003t0020g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82+2102_82+2103ins others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597603 | ||||||
| chr1:24597607 | AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0003g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.82+2107_82+2116del others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597607 | ||||||
| chr1:24597613 | GAAAGAGA others(1): Show |
G | 5 | a0001c0001t0001g0222 a0001c0001t0001g0225 a0001c0001t0001g0265 others(2): Show |
5 | HG02976.hp1 HG03225.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+2103_82+2110del others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597613 | ||||||
| chr1:24597613 | GAAAGAGA others(17): Show |
G | 1 | a0001c0001t0001g0157 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.82+2103_82+2126del others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597613 | ||||||
| chr1:24597613 | GAAAGAGA others(25): Show |
G | 2 | a0001c0001t0025g0316 a0002c0002t0004g0394 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.82+2103_82+2134del others(32): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597613 | ||||||
| chr1:24597615 | A | AAGAG | 25 | a0001c0001t0002g0041 a0001c0001t0002g0045 a0001c0001t0002g0069 others(22): Show |
25 | HG00733.hp2 HG01167.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.82+2105_82+2108dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597615 | ||||||
| chr1:24597615 | A | AGAGAGAG others(6): Show |
1 | a0001c0001t0002g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.82+2103_82+2104ins others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597615 | |||||||
| chr1:24597615 | A | G | 12 | a0001c0001t0003g0006 a0001c0001t0006g0142 a0001c0001t0006g0143 others(9): Show |
12 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.82+2103A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597615 | |||||||
| chr1:24597617 | G | A | 6 | a0001c0001t0002g0093 a0001c0001t0003g0006 a0001c0001t0006g0190 others(3): Show |
6 | HG00558.hp1 HG01106.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+2105G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597617 | |||||||
| chr1:24597617 | G | C | 11 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(8): Show |
11 | HG01168.hp2 HG01169.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.82+2105G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597617 | |||||||
| chr1:24597617 | G | GAAGAGAG others(4): Show |
1 | a0001c0001t0002g0285 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.82+2106_82+2107ins others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | G | GAGAA | 52 | a0001c0001t0001g0035 a0001c0001t0001g0050 a0001c0001t0001g0052 others(49): Show |
53 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.82+2159_82+2162dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | G | GAGAAAGA others(1): Show |
29 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0079 others(26): Show |
29 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.82+2155_82+2162dup others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | G | GAGAAAGA others(5): Show |
10 | a0001c0001t0001g0109 a0001c0001t0001g0191 a0001c0001t0001g0228 others(7): Show |
10 | HG00642.hp1 HG00741.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.82+2151_82+2162dup others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | G | GAGAAAGA others(9): Show |
3 | a0001c0001t0001g0236 a0001c0001t0003g0070 a0001c0001t0003g0131 |
3 | HG04184.hp2 NA19081.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.82+2147_82+2162dup others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | G | GAGAGAGA others(1): Show |
18 | a0001c0001t0001g0104 a0001c0001t0002g0044 a0001c0001t0002g0114 others(15): Show |
18 | HG00140.hp1 HG00423.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.82+2108_82+2109ins others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | G | GAGAGAGA others(5): Show |
5 | a0001c0001t0002g0022 a0001c0001t0002g0043 a0001c0001t0002g0083 others(2): Show |
5 | HG03490.hp1 HG04184.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+2108_82+2109ins others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | G | GAGAGAGA others(9): Show |
2 | a0001c0001t0002g0053 a0001c0001t0002g0095 |
2 | NA18960.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.82+2108_82+2109ins others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | G | GAGAGAGA others(13): Show |
1 | a0001c0001t0002g0158 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.82+2108_82+2109ins others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | GAGAA | G | 33 | a0001c0001t0001g0060 a0001c0001t0001g0080 a0001c0001t0001g0138 others(30): Show |
33 | HG00642.hp2 HG00733.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.82+2159_82+2162del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | GAGAAAGA others(1): Show |
G | 22 | a0001c0001t0001g0098 a0001c0001t0001g0182 a0001c0001t0001g0193 others(19): Show |
22 | HG00639.hp2 HG01256.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.82+2155_82+2162del others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | GAGAAAGA others(5): Show |
G | 12 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0055 others(9): Show |
12 | HG00408.hp1 HG01106.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.82+2151_82+2162del others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | GAGAAAGA others(9): Show |
G | 7 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(4): Show |
7 | HG00438.hp2 HG00597.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+2147_82+2162del others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | GAGAAAGA others(13): Show |
G | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.82+2143_82+2162del others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597617 | GAGAAAGA others(17): Show |
G | 1 | a0001c0001t0010g0379 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.82+2139_82+2162del others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | ||||||
| chr1:24597619 | G | A | 3 | a0001c0001t0008g0397 a0001c0001t0008g0398 a0001c0001t0008g0399 |
3 | HG02055.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.82+2107G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597619 | |||||||
| chr1:24597621 | A | C | 11 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(8): Show |
11 | HG01168.hp2 HG01169.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.82+2109A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597621 | |||||||
| chr1:24597621 | A | G | 55 | a0001c0001t0001g0301 a0001c0001t0002g0027 a0001c0001t0002g0028 others(52): Show |
55 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.82+2109A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597621 | |||||||
| chr1:24597633 | A | AAG | 4 | a0001c0001t0006g0190 a0001c0001t0006g0281 a0001c0001t0006g0283 others(1): Show |
4 | HG00558.hp1 NA18999.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+2123_82+2124dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597633 | ||||||
| chr1:24597636 | A | G | 11 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(8): Show |
11 | HG01168.hp2 HG01169.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.82+2124A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597636 | |||||||
| chr1:24597639 | GAA | G | 21 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(18): Show |
22 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.82+2129_82+2130del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597639 | ||||||
| chr1:24597640 | AAAG | A | 3 | a0001c0001t0008g0397 a0001c0001t0008g0398 a0001c0001t0008g0399 |
3 | HG02055.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.82+2131_82+2133del others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597640 | ||||||
| chr1:24597642 | A | AGAAAGAA others(1): Show |
3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0001c0001t0001g0377 |
3 | HG01069.hp1 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.82+2137_82+2138ins others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597642 | ||||||
| chr1:24597644 | A | G | 4 | a0001c0001t0006g0190 a0001c0001t0006g0281 a0001c0001t0006g0283 others(1): Show |
4 | HG00558.hp1 NA18999.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+2132A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597644 | |||||||
| chr1:24597648 | A | G | 1 | a0003c0003t0020g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82+2136A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597648 | |||||||
| chr1:24597649 | AAG | A | 3 | a0001c0001t0008g0397 a0001c0001t0008g0398 a0001c0001t0008g0399 |
3 | HG02055.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.82+2139_82+2140del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597649 | ||||||
| chr1:24597655 | G | GAA | 11 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(8): Show |
11 | HG01168.hp2 HG01169.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.82+2145_82+2146dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597655 | ||||||
| chr1:24597663 | G | GAAAAGAA | 3 | a0001c0001t0002g0028 a0001c0001t0002g0091 a0001c0001t0002g0361 |
3 | HG00280.hp2 HG00621.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.82+2154_82+2155ins others(7): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597663 | ||||||
| chr1:24597663 | GAAAGAAA others(4): Show |
G | 1 | a0001c0001t0001g0204 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.82+2153_82+2163del others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597663 | ||||||
| chr1:24597669 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.82+2157A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597669 | |||||||
| chr1:24597671 | G | A | 11 | a0001c0001t0002g0027 a0001c0001t0002g0082 a0001c0001t0002g0120 others(8): Show |
11 | HG00735.hp2 HG01261.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+2159G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597671 | |||||||
| chr1:24597671 | GAAAAGAA others(2): Show |
G | 3 | a0001c0001t0008g0397 a0001c0001t0008g0398 a0001c0001t0008g0399 |
3 | HG02055.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.82+2161_82+2169del others(9): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597671 | ||||||
| chr1:24597672 | A | AAAG | 8 | a0001c0001t0002g0028 a0001c0001t0002g0091 a0001c0001t0002g0361 others(5): Show |
8 | HG00280.hp2 HG00558.hp1 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.82+2162_82+2163ins others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597672 | ||||||
| chr1:24597672 | A | AAAGAAAG others(4): Show |
2 | a0001c0001t0001g0105 a0001c0001t0001g0111 |
2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.82+2162_82+2163ins others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597672 | ||||||
| chr1:24597672 | A | G | 11 | a0001c0001t0002g0027 a0001c0001t0002g0082 a0001c0001t0002g0120 others(8): Show |
11 | HG00735.hp2 HG01261.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+2160A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597672 | |||||||
| chr1:24597674 | A | AG | 13 | a0001c0001t0001g0258 a0001c0001t0006g0142 a0001c0001t0006g0143 others(10): Show |
13 | HG01168.hp2 HG01169.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.82+2162_82+2163ins others(1): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597674 | |||||||
| chr1:24597676 | G | A | 12 | a0001c0001t0002g0027 a0001c0001t0002g0082 a0001c0001t0002g0120 others(9): Show |
12 | HG00735.hp2 HG01261.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.82+2164G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597676 | |||||||
| chr1:24597678 | A | AAG | 4 | a0001c0001t0006g0281 a0001c0001t0006g0283 a0001c0001t0006g0315 others(1): Show |
4 | HG00558.hp1 HG03041.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+2167_82+2168ins others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597678 | ||||||
| chr1:24597678 | A | AAGAAAGG others(23): Show |
3 | a0001c0001t0006g0294 a0001c0001t0006g0365 a0001c0001t0006g0385 |
3 | HG02896.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.82+2167_82+2168ins others(30): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597678 | ||||||
| chr1:24597678 | A | AAGAAAGG others(27): Show |
7 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(4): Show |
7 | HG01168.hp2 HG01169.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+2167_82+2168ins others(34): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597678 | ||||||
| chr1:24597678 | A | AAGAAAGG others(30): Show |
1 | a0001c0001t0006g0325 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.82+2167_82+2168ins others(37): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597678 | ||||||
| chr1:24597678 | A | G | 12 | a0001c0001t0002g0027 a0001c0001t0002g0082 a0001c0001t0002g0120 others(9): Show |
12 | HG00735.hp2 HG01261.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.82+2166A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597678 | |||||||
| chr1:24597680 | A | G | 3 | a0001c0001t0002g0028 a0001c0001t0002g0091 a0001c0001t0002g0361 |
3 | HG00280.hp2 HG00621.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.82+2168A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597680 | |||||||
| chr1:24597689 | A | G | 6 | a0001c0001t0002g0028 a0001c0001t0002g0091 a0001c0001t0002g0361 others(3): Show |
6 | HG00280.hp2 HG00621.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+2177A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597689 | |||||||
| chr1:24597692 | AAG | A | 6 | a0001c0001t0002g0028 a0001c0001t0002g0091 a0001c0001t0002g0361 others(3): Show |
6 | HG00280.hp2 HG00621.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+2184_82+2185del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597692 | ||||||
| chr1:24597694 | G | GAA | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2183_82+2184ins others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597694 | ||||||
| chr1:24597694 | G | GAAAGAGA others(9): Show |
92 | a0001c0001t0001g0104 a0001c0001t0002g0022 a0001c0001t0002g0036 others(89): Show |
92 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.82+2183_82+2184ins others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597694 | ||||||
| chr1:24597694 | G | GAGAAAGA others(5): Show |
11 | a0001c0001t0002g0027 a0001c0001t0002g0082 a0001c0001t0002g0120 others(8): Show |
11 | HG00735.hp2 HG01261.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+2186_82+2197dup others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597694 | ||||||
| chr1:24597703 | G | A | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2191G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597703 | |||||||
| chr1:24597732 | T | C | 2 | a0001c0001t0003g0148 a0001c0001t0003g0276 |
2 | HG02280.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.82+2220T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597732 | |||||||
| chr1:24597742 | G | C | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2230G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597742 | |||||||
| chr1:24597745 | A | C | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2233A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597745 | |||||||
| chr1:24597818 | A | G | 3 | a0001c0001t0010g0272 a0001c0001t0010g0378 a0001c0001t0010g0379 |
3 | HG01891.hp1 HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.82+2306A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597818 | |||||||
| chr1:24597820 | C | A | 244 | a0001c0001t0001g0104 a0001c0001t0001g0201 a0001c0001t0002g0022 others(241): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.82+2308C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597820 | |||||||
| chr1:24597878 | T | C | 1 | a0001c0001t0007g0395 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.82+2366T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597878 | |||||||
| chr1:24597970 | G | C | 1 | a0001c0001t0005g0169 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.82+2458G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597970 | |||||||
| chr1:24597989 | A | G | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2477A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597989 | |||||||
| chr1:24598001 | T | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.82+2489T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598001 | |||||||
| chr1:24598038 | T | C | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2526T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598038 | |||||||
| chr1:24598101 | A | G | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2589A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598101 | |||||||
| chr1:24598210 | C | T | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2698C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598210 | |||||||
| chr1:24598225 | A | C | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2713A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598225 | |||||||
| chr1:24598287 | TG | T | 79 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0012 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.83-2650delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24598287 | ||||||
| chr1:24598319 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.83-2621G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598319 | |||||||
| chr1:24598403 | C | T | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-2537C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598403 | |||||||
| chr1:24598404 | C | A | 1 | a0001c0001t0001g0340 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.83-2536C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598404 | |||||||
| chr1:24598405 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.83-2535C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598405 | |||||||
| chr1:24598440 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.83-2500C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598440 | |||||||
| chr1:24598446 | G | A | 8 | a0001c0001t0001g0296 a0001c0001t0001g0302 a0001c0001t0001g0303 others(5): Show |
8 | NA18947.hp2 NA18951.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.83-2494G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598446 | |||||||
| chr1:24598630 | C | CT | 20 | a0001c0001t0001g0323 a0001c0001t0006g0142 a0001c0001t0006g0143 others(17): Show |
20 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.83-2300dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24598630 | ||||||
| chr1:24598826 | C | T | 1 | a0001c0001t0003g0342 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.83-2114C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598826 | |||||||
| chr1:24598918 | G | A | 5 | a0001c0001t0007g0001 a0001c0001t0007g0019 a0001c0001t0007g0020 others(2): Show |
6 | HG02257.hp2 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-2022G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598918 | |||||||
| chr1:24598928 | A | G | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-2012A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598928 | |||||||
| chr1:24598950 | T | C | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1990T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598950 | |||||||
| chr1:24598973 | T | C | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1967T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598973 | |||||||
| chr1:24599002 | G | A | 2 | a0001c0001t0001g0317 a0001c0001t0001g0331 |
2 | NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.83-1938G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599002 | |||||||
| chr1:24599108 | C | T | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1832C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599108 | |||||||
| chr1:24599228 | T | G | 1 | a0001c0001t0005g0177 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.83-1712T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599228 | |||||||
| chr1:24599240 | A | G | 5 | a0001c0001t0007g0001 a0001c0001t0007g0019 a0001c0001t0007g0020 others(2): Show |
6 | HG02257.hp2 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-1700A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599240 | |||||||
| chr1:24599280 | C | CA | 138 | a0001c0001t0001g0035 a0001c0001t0001g0064 a0001c0001t0001g0067 others(135): Show |
138 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.83-1642dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599280 | ||||||
| chr1:24599280 | C | CAA | 6 | a0001c0001t0002g0022 a0001c0001t0002g0046 a0001c0001t0002g0136 others(3): Show |
6 | HG01928.hp2 HG02486.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-1643_83-1642dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599280 | ||||||
| chr1:24599280 | CA | C | 77 | a0001c0001t0001g0210 a0001c0001t0001g0288 a0001c0001t0001g0366 others(74): Show |
77 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.83-1642delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599280 | ||||||
| chr1:24599342 | C | T | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1598C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599342 | |||||||
| chr1:24599377 | C | A | 110 | a0001c0001t0001g0104 a0001c0001t0002g0022 a0001c0001t0002g0027 others(107): Show |
110 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.83-1563C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599377 | |||||||
| chr1:24599391 | C | G | 6 | a0001c0001t0002g0022 a0001c0001t0002g0037 a0001c0001t0002g0041 others(3): Show |
6 | NA18954.hp1 NA18971.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-1549C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599391 | |||||||
| chr1:24599420 | A | AAAC | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1518_83-1516dup others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599420 | ||||||
| chr1:24599488 | C | T | 1 | a0001c0001t0023g0004 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.83-1452C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599488 | |||||||
| chr1:24599553 | A | C | 1 | a0001c0001t0001g0168 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.83-1387A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599553 | |||||||
| chr1:24599618 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.83-1322C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599618 | |||||||
| chr1:24599703 | G | C | 1 | a0001c0001t0002g0103 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.83-1237G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599703 | |||||||
| chr1:24599724 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.83-1216C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599724 | |||||||
| chr1:24599725 | A | G | 290 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0035 others(287): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.83-1215A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599725 | |||||||
| chr1:24599736 | C | A | 1 | a0001c0001t0002g0076 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.83-1204C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599736 | |||||||
| chr1:24599775 | C | A | 126 | a0001c0001t0001g0104 a0001c0001t0002g0022 a0001c0001t0002g0027 others(123): Show |
126 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.83-1165C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599775 | |||||||
| chr1:24599818 | C | T | 3 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0278 |
3 | HG01255.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.83-1122C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599818 | |||||||
| chr1:24599819 | GC | G | 19 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0115 others(16): Show |
19 | HG00642.hp1 HG01069.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.83-1101delC | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599819 | ||||||
| chr1:24599819 | GCC | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0097 others(22): Show |
26 | HG00323.hp2 HG01074.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.83-1102_83-1101del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599819 | ||||||
| chr1:24599819 | GCCC | G | 55 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0061 others(52): Show |
55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.83-1103_83-1101del others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599819 | ||||||
| chr1:24599819 | GCCCC | G | 87 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0059 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.83-1104_83-1101del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599819 | ||||||
| chr1:24599819 | GCCCCC | G | 39 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0056 others(36): Show |
39 | HG00408.hp1 HG00408.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.83-1105_83-1101del others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599819 | ||||||
| chr1:24599819 | GCCCCCC | G | 19 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0080 others(16): Show |
19 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.83-1106_83-1101del others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599819 | ||||||
| chr1:24599825 | C | T | 2 | a0001c0001t0006g0325 a0001c0001t0006g0365 |
2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.83-1115C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599825 | |||||||
| chr1:24599826 | C | A | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1114C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599826 | |||||||
| chr1:24599829 | C | A | 24 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0070 others(21): Show |
24 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.83-1111C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599829 | |||||||
| chr1:24599830 | C | A | 54 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0015 others(51): Show |
54 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.83-1110C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599830 | |||||||
| chr1:24599832 | C | A | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1108C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599832 | |||||||
| chr1:24599834 | C | CCCCCCCC others(4): Show |
3 | a0001c0001t0002g0042 a0001c0001t0002g0051 a0001c0001t0002g0359 |
3 | HG00438.hp1 HG03239.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.83-1101_83-1100ins others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599834 | ||||||
| chr1:24599834 | C | CCCCCCCC others(3): Show |
2 | a0001c0001t0002g0087 a0001c0001t0002g0137 |
2 | HG00741.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.83-1101_83-1100ins others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599834 | ||||||
| chr1:24599834 | C | CCCCCCCG | 21 | a0001c0001t0002g0028 a0001c0001t0002g0041 a0001c0001t0002g0046 others(18): Show |
21 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.83-1101_83-1100ins others(7): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599834 | ||||||
| chr1:24599834 | C | CCCCCCG | 27 | a0001c0001t0001g0104 a0001c0001t0002g0036 a0001c0001t0002g0037 others(24): Show |
27 | HG00735.hp2 HG01192.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.83-1101_83-1100ins others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599834 | ||||||
| chr1:24599834 | C | CCCCCG | 19 | a0001c0001t0002g0045 a0001c0001t0002g0076 a0001c0001t0002g0091 others(16): Show |
19 | HG00544.hp1 HG01123.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.83-1102_83-1101ins others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599834 | ||||||
| chr1:24599834 | C | CCCCG | 15 | a0001c0001t0002g0027 a0001c0001t0002g0044 a0001c0001t0002g0072 others(12): Show |
15 | HG00423.hp2 HG01167.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.83-1103_83-1102ins others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599834 | ||||||
| chr1:24599834 | CCCCCCTT | C | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1105_83-1099del others(7): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599834 | |||||||
| chr1:24599837 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.83-1103C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599837 | |||||||
| chr1:24599889 | C | T | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1051C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599889 | |||||||
| chr1:24599956 | G | C | 126 | a0001c0001t0001g0104 a0001c0001t0002g0022 a0001c0001t0002g0027 others(123): Show |
126 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.83-984G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599956 | |||||||
| chr1:24599997 | A | AT | 105 | a0001c0001t0002g0022 a0001c0001t0002g0027 a0001c0001t0002g0028 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.83-934dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599997 | ||||||
| chr1:24599997 | AT | A | 24 | a0001c0001t0001g0065 a0001c0001t0001g0309 a0001c0001t0006g0142 others(21): Show |
25 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.83-934delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599997 | ||||||
| chr1:24600006 | T | A | 2 | a0001c0001t0003g0357 a0001c0001t0003g0387 |
2 | HG00735.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.83-934T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600006 | |||||||
| chr1:24600025 | A | G | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-915A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600025 | |||||||
| chr1:24600309 | C | A | 10 | a0002c0002t0004g0018 a0002c0002t0004g0030 a0002c0002t0004g0031 others(7): Show |
10 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.83-631C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600309 | |||||||
| chr1:24600344 | G | A | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-596G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600344 | |||||||
| chr1:24600381 | T | A | 15 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(12): Show |
15 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.83-559T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600381 | |||||||
| chr1:24600393 | A | T | 1 | a0001c0001t0002g0245 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.83-547A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600393 | |||||||
| chr1:24600402 | C | T | 78 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0012 others(75): Show |
78 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.83-538C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600402 | |||||||
| chr1:24600499 | G | C | 148 | a0001c0001t0001g0129 a0001c0001t0002g0022 a0001c0001t0002g0027 others(145): Show |
149 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.83-441G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600499 | |||||||
| chr1:24600510 | G | T | 78 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0012 others(75): Show |
78 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.83-430G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600510 | |||||||
| chr1:24600512 | T | C | 5 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
5 | HG02040.hp2 NA18944.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-428T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600512 | |||||||
| chr1:24600537 | C | A | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-403C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600537 | |||||||
| chr1:24600543 | C | T | 17 | a0001c0001t0001g0201 a0001c0001t0007g0001 a0001c0001t0007g0008 others(14): Show |
18 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.83-397C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600543 | |||||||
| chr1:24600551 | T | G | 1 | a0001c0001t0002g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.83-389T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600551 | |||||||
| chr1:24600757 | G | A | 1 | a0001c0001t0001g0396 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.83-183G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600757 | |||||||
| chr1:24600778 | T | G | 1 | a0001c0001t0008g0399 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.83-162T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600778 | |||||||
| chr1:24600907 | C | T | 4 | a0001c0001t0002g0046 a0001c0001t0002g0118 a0001c0001t0002g0119 others(1): Show |
4 | NA18972.hp1 NA18986.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-33C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600907 | |||||||
| chr1:24601070 | T | C | 223 | a0001c0001t0002g0022 a0001c0001t0002g0027 a0001c0001t0002g0028 others(220): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.167+46T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601070 | |||||||
| chr1:24601100 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+76G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601100 | |||||||
| chr1:24601101 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+77G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601101 | |||||||
| chr1:24601102 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+78G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601102 | |||||||
| chr1:24601104 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+80G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601104 | |||||||
| chr1:24601106 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+82C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601106 | |||||||
| chr1:24601107 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+83C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601107 | |||||||
| chr1:24601108 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+84G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601108 | |||||||
| chr1:24601110 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+86C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601110 | |||||||
| chr1:24601113 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+89G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601113 | |||||||
| chr1:24601115 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+91G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601115 | |||||||
| chr1:24601116 | C | G | 1 | a0001c0001t0025g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.167+92C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601116 | |||||||
| chr1:24601116 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+92C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601116 | |||||||
| chr1:24601117 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+93C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601117 | |||||||
| chr1:24601119 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+95G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601119 | |||||||
| chr1:24601120 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+96G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601120 | |||||||
| chr1:24601121 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+97C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601121 | |||||||
| chr1:24601122 | A | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+98A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601122 | |||||||
| chr1:24601123 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+99G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601123 | |||||||
| chr1:24601125 | A | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+101A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601125 | |||||||
| chr1:24601127 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+103C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601127 | |||||||
| chr1:24601128 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+104C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601128 | |||||||
| chr1:24601129 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+105C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601129 | |||||||
| chr1:24601131 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+107C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601131 | |||||||
| chr1:24601132 | A | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+108A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601132 | |||||||
| chr1:24601133 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+109G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601133 | |||||||
| chr1:24601134 | C | A | 78 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0012 others(75): Show |
78 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.167+110C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601134 | |||||||
| chr1:24601134 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+110C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601134 | |||||||
| chr1:24601135 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+111C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601135 | |||||||
| chr1:24601139 | A | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+115A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601139 | |||||||
| chr1:24601140 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+116G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601140 | |||||||
| chr1:24601142 | A | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+118A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601142 | |||||||
| chr1:24601143 | A | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+119A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601143 | |||||||
| chr1:24601144 | A | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+120A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601144 | |||||||
| chr1:24601146 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+122G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601146 | |||||||
| chr1:24601147 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+123C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601147 | |||||||
| chr1:24601149 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+125C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601149 | |||||||
| chr1:24601151 | A | C | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+127A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601151 | |||||||
| chr1:24601152 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+128A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601152 | |||||||
| chr1:24601153 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+129C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601153 | |||||||
| chr1:24601154 | C | G | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+130C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601154 | |||||||
| chr1:24601155 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+131C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601155 | |||||||
| chr1:24601156 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+132T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601156 | |||||||
| chr1:24601159 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+135G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601159 | |||||||
| chr1:24601161 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+137G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601161 | |||||||
| chr1:24601162 | A | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+138A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601162 | |||||||
| chr1:24601236 | C | G | 10 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0107 others(7): Show |
10 | HG00642.hp1 HG01099.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.167+212C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601236 | |||||||
| chr1:24601236 | C | T | 125 | a0001c0001t0002g0022 a0001c0001t0002g0027 a0001c0001t0002g0028 others(122): Show |
125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.167+212C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601236 | |||||||
| chr1:24601240 | G | A | 147 | a0001c0001t0002g0022 a0001c0001t0002g0027 a0001c0001t0002g0028 others(144): Show |
148 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.167+216G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601240 | |||||||
| chr1:24601290 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.167+266T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601290 | |||||||
| chr1:24601447 | G | T | 1 | a0001c0001t0001g0396 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.167+423G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601447 | |||||||
| chr1:24601561 | A | T | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+537A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601561 | |||||||
| chr1:24601627 | C | T | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.167+603C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601627 | |||||||
| chr1:24601675 | C | T | 1 | a0001c0001t0003g0330 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.167+651C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601675 | |||||||
| chr1:24601695 | A | G | 1 | a0001c0001t0002g0069 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.167+671A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601695 | |||||||
| chr1:24601820 | A | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+796A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601820 | |||||||
| chr1:24601830 | G | A | 1 | a0001c0001t0003g0263 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.167+806G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601830 | |||||||
| chr1:24601856 | T | C | 15 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(12): Show |
15 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.167+832T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601856 | |||||||
| chr1:24601885 | G | A | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+861G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601885 | |||||||
| chr1:24601906 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.167+882C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601906 | |||||||
| chr1:24601914 | G | T | 1 | a0001c0001t0001g0340 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.167+890G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601914 | |||||||
| chr1:24601937 | A | C | 17 | a0001c0001t0001g0201 a0001c0001t0007g0001 a0001c0001t0007g0008 others(14): Show |
18 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.167+913A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601937 | |||||||
| chr1:24602030 | A | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1006A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602030 | |||||||
| chr1:24602040 | C | CA | 30 | a0001c0001t0001g0063 a0001c0001t0001g0126 a0001c0001t0001g0186 others(27): Show |
31 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.167+1030dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602040 | ||||||
| chr1:24602040 | C | CAA | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1029_167+1030d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602040 | ||||||
| chr1:24602040 | CA | C | 195 | a0001c0001t0001g0067 a0001c0001t0001g0314 a0001c0001t0002g0022 others(192): Show |
195 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.167+1030delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602040 | ||||||
| chr1:24602104 | C | A | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1080C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602104 | |||||||
| chr1:24602154 | C | T | 6 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0273 others(3): Show |
7 | HG01891.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.167+1130C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602154 | |||||||
| chr1:24602202 | A | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1178A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602202 | |||||||
| chr1:24602230 | G | A | 8 | a0001c0001t0002g0081 a0001c0001t0002g0088 a0001c0001t0002g0096 others(5): Show |
8 | HG00423.hp2 HG02080.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.167+1206G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602230 | |||||||
| chr1:24602304 | TAAGAATA others(279): Show |
T | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1298_167+1583d others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602304 | ||||||
| chr1:24602357 | C | A | 1 | a0001c0001t0023g0004 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.167+1333C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602357 | |||||||
| chr1:24602426 | C | G | 1 | a0001c0001t0005g0121 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.167+1402C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602426 | |||||||
| chr1:24602427 | G | C | 1 | a0001c0001t0005g0121 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.167+1403G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602427 | |||||||
| chr1:24602438 | T | C | 203 | a0001c0001t0002g0022 a0001c0001t0002g0027 a0001c0001t0002g0028 others(200): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.167+1414T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602438 | |||||||
| chr1:24602497 | A | G | 106 | a0001c0001t0002g0022 a0001c0001t0002g0027 a0001c0001t0002g0028 others(103): Show |
106 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.167+1473A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602497 | |||||||
| chr1:24602546 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.167+1522G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602546 | |||||||
| chr1:24602565 | A | G | 19 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(16): Show |
19 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.167+1541A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602565 | |||||||
| chr1:24602569 | C | CA | 20 | a0001c0001t0001g0061 a0001c0001t0001g0157 a0001c0001t0001g0222 others(17): Show |
20 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.167+1568dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602569 | ||||||
| chr1:24602569 | C | CAA | 86 | a0001c0001t0001g0201 a0001c0001t0002g0081 a0001c0001t0002g0139 others(83): Show |
87 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.167+1567_167+1568d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602569 | ||||||
| chr1:24602569 | C | CAAA | 104 | a0001c0001t0002g0022 a0001c0001t0002g0027 a0001c0001t0002g0028 others(101): Show |
104 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.167+1566_167+1568d others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602569 | ||||||
| chr1:24602569 | C | CAAAA | 17 | a0001c0001t0002g0042 a0001c0001t0002g0069 a0001c0001t0002g0096 others(14): Show |
17 | HG00140.hp1 HG00544.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.167+1565_167+1568d others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602569 | ||||||
| chr1:24602569 | CA | C | 12 | a0001c0001t0001g0098 a0001c0001t0001g0105 a0001c0001t0001g0138 others(9): Show |
12 | HG01069.hp1 HG01074.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.167+1568delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602569 | ||||||
| chr1:24602738 | G | GA | 16 | a0001c0001t0002g0114 a0001c0001t0003g0090 a0002c0002t0004g0005 others(13): Show |
17 | HG00140.hp1 HG01099.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.167+1726dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602738 | ||||||
| chr1:24602738 | GA | G | 17 | a0001c0001t0001g0323 a0001c0001t0006g0142 a0001c0001t0006g0143 others(14): Show |
17 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.167+1726delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602738 | ||||||
| chr1:24602781 | G | A | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1757G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602781 | |||||||
| chr1:24602794 | C | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1770C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602794 | |||||||
| chr1:24602802 | C | T | 1 | a0001c0001t0003g0345 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.167+1778C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602802 | |||||||
| chr1:24602872 | C | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1848C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602872 | |||||||
| chr1:24602971 | C | T | 3 | a0001c0001t0003g0006 a0001c0001t0003g0334 a0001c0001t0003g0386 |
3 | HG01106.hp1 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.167+1947C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602971 | |||||||
| chr1:24603059 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.167+2035A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603059 | |||||||
| chr1:24603102 | T | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+2078T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603102 | |||||||
| chr1:24603152 | T | C | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.167+2128T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603152 | |||||||
| chr1:24603185 | G | A | 244 | a0001c0001t0001g0201 a0001c0001t0002g0022 a0001c0001t0002g0027 others(241): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.167+2161G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603185 | |||||||
| chr1:24603210 | A | AT | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.167+2190dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24603210 | ||||||
| chr1:24603222 | T | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+2198T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603222 | |||||||
| chr1:24603231 | A | G | 3 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0273 |
3 | HG02818.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.167+2207A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603231 | |||||||
| chr1:24603252 | T | A | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+2228T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603252 | |||||||
| chr1:24603275 | T | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+2251T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603275 | |||||||
| chr1:24603283 | G | A | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+2259G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603283 | |||||||
| chr1:24603337 | A | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-2269A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603337 | |||||||
| chr1:24603339 | GTAA | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-2254_168-2252d others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24603339 | ||||||
| chr1:24603353 | A | T | 1 | a0001c0001t0022g0360 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.168-2253A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603353 | |||||||
| chr1:24603364 | A | G | 245 | a0001c0001t0001g0201 a0001c0001t0002g0022 a0001c0001t0002g0027 others(242): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.168-2242A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603364 | |||||||
| chr1:24603378 | A | AG | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-2228_168-2227i others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603378 | |||||||
| chr1:24603434 | A | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-2172A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603434 | |||||||
| chr1:24603488 | G | A | 1 | a0001c0001t0003g0343 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.168-2118G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603488 | |||||||
| chr1:24603533 | C | T | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-2073C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603533 | |||||||
| chr1:24603623 | A | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1983A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603623 | |||||||
| chr1:24603695 | G | T | 1 | a0003c0003t0020g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168-1911G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603695 | |||||||
| chr1:24603751 | C | T | 1 | a0002c0002t0004g0394 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168-1855C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603751 | |||||||
| chr1:24603752 | A | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1854A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603752 | |||||||
| chr1:24603802 | A | AG | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1803dupG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24603802 | ||||||
| chr1:24603869 | T | A | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1737T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603869 | |||||||
| chr1:24604044 | A | G | 2 | a0002c0002t0012g0002 a0002c0002t0012g0147 |
3 | HG02723.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.168-1562A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604044 | |||||||
| chr1:24604145 | G | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1461G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604145 | |||||||
| chr1:24604152 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.168-1454A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604152 | |||||||
| chr1:24604188 | CT | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1412delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604188 | ||||||
| chr1:24604267 | T | C | 15 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(12): Show |
15 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.168-1339T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604267 | |||||||
| chr1:24604272 | A | T | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1334A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604272 | |||||||
| chr1:24604282 | A | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1324A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604282 | |||||||
| chr1:24604325 | G | A | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1281G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604325 | |||||||
| chr1:24604353 | T | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1253T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604353 | |||||||
| chr1:24604417 | A | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1189A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604417 | |||||||
| chr1:24604439 | G | C | 1 | a0001c0001t0002g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.168-1167G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604439 | |||||||
| chr1:24604462 | C | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1144C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604462 | |||||||
| chr1:24604463 | T | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1143T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604463 | |||||||
| chr1:24604559 | AG | A | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1044delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604559 | ||||||
| chr1:24604563 | T | C | 1 | a0001c0001t0002g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.168-1043T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604563 | |||||||
| chr1:24604567 | A | ACT | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1038_168-1037d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604567 | ||||||
| chr1:24604573 | T | TA | 9 | a0001c0001t0001g0056 a0001c0001t0001g0159 a0001c0001t0001g0163 others(6): Show |
9 | HG00597.hp1 HG01257.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1000dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | ||||||
| chr1:24604573 | T | TAA | 8 | a0001c0001t0001g0098 a0001c0001t0001g0104 a0001c0001t0001g0123 others(5): Show |
8 | HG00280.hp2 HG01168.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-1001_168-1000d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | ||||||
| chr1:24604573 | TA | T | 9 | a0001c0001t0001g0204 a0001c0001t0001g0258 a0001c0001t0001g0298 others(6): Show |
9 | HG01975.hp1 NA18612.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.168-1000delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | ||||||
| chr1:24604573 | TAAAAAAA others(5): Show |
T | 2 | a0001c0001t0006g0278 a0002c0002t0004g0388 |
2 | HG01099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.168-1011_168-1000d others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | ||||||
| chr1:24604573 | TAAAAAAA others(7): Show |
T | 1 | a0002c0002t0004g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.168-1013_168-1000d others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | ||||||
| chr1:24604573 | TAAAAAAA others(9): Show |
T | 2 | a0002c0002t0004g0017 a0002c0002t0004g0018 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.168-1015_168-1000d others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | ||||||
| chr1:24604573 | TAAAAAAA others(11): Show |
T | 4 | a0002c0002t0004g0007 a0002c0002t0004g0024 a0002c0002t0004g0202 others(1): Show |
4 | HG02572.hp1 HG02809.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1017_168-1000d others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | ||||||
| chr1:24604573 | TAAAAAAA others(12): Show |
T | 1 | a0002c0002t0012g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.168-1018_168-1000d others(21): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | ||||||
| chr1:24604573 | TAAAAAAA others(13): Show |
T | 7 | a0002c0002t0004g0026 a0002c0002t0004g0030 a0002c0002t0004g0034 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-1019_168-1000d others(22): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | ||||||
| chr1:24604573 | TAAAAAAA others(14): Show |
T | 1 | a0002c0002t0012g0002 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.168-1020_168-1000d others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | ||||||
| chr1:24604573 | TAAAAAAA others(15): Show |
T | 3 | a0002c0002t0004g0031 a0002c0002t0004g0032 a0002c0002t0004g0058 |
3 | HG02647.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.168-1021_168-1000d others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | ||||||
| chr1:24604573 | TAAAAAAA others(21): Show |
T | 1 | a0002c0002t0004g0394 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168-1027_168-1000d others(30): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | ||||||
| chr1:24604574 | A | C | 1 | a0002c0002t0004g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1032A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604574 | |||||||
| chr1:24604579 | A | T | 1 | a0002c0002t0004g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1027A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604579 | |||||||
| chr1:24604581 | A | T | 1 | a0002c0002t0004g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1025A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604581 | |||||||
| chr1:24604583 | A | T | 1 | a0002c0002t0004g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1023A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604583 | |||||||
| chr1:24604585 | A | T | 1 | a0002c0002t0004g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1021A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604585 | |||||||
| chr1:24604586 | A | C | 1 | a0002c0002t0004g0388 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.168-1020A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604586 | |||||||
| chr1:24604586 | AAAAAAAA others(18): Show |
A | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.168-1018_168-994de others(26): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604586 | ||||||
| chr1:24604587 | A | T | 1 | a0002c0002t0004g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1019A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604587 | |||||||
| chr1:24604588 | A | C | 1 | a0002c0002t0004g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.168-1018A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604588 | |||||||
| chr1:24604589 | A | T | 1 | a0002c0002t0004g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1017A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604589 | |||||||
| chr1:24604589 | AAAAAAAA others(17): Show |
A | 2 | a0001c0001t0006g0142 a0001c0001t0006g0143 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.168-1015_168-992de others(25): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604589 | ||||||
| chr1:24604590 | A | C | 2 | a0002c0002t0004g0017 a0002c0002t0004g0018 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.168-1016A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604590 | |||||||
| chr1:24604591 | A | T | 2 | a0002c0002t0004g0005 a0002c0002t0004g0388 |
2 | HG01099.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.168-1015A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604591 | |||||||
| chr1:24604591 | AAAAAAAA others(27): Show |
A | 1 | a0001c0001t0003g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.168-1013_168-980de others(35): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604591 | ||||||
| chr1:24604592 | A | C | 4 | a0002c0002t0004g0007 a0002c0002t0004g0024 a0002c0002t0004g0202 others(1): Show |
4 | HG02572.hp1 HG02809.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1014A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604592 | |||||||
| chr1:24604592 | AAAAAAAA others(8): Show |
A | 2 | a0001c0001t0006g0294 a0001c0001t0006g0315 |
2 | HG03130.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.168-1012_168-998de others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604592 | ||||||
| chr1:24604592 | AAAAAAAA others(10): Show |
A | 2 | a0001c0001t0006g0293 a0001c0001t0006g0385 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.168-1012_168-996de others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604592 | ||||||
| chr1:24604592 | AAAAAAAA others(12): Show |
A | 2 | a0001c0001t0006g0152 a0001c0001t0006g0283 |
2 | HG00558.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.168-1012_168-994de others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604592 | ||||||
| chr1:24604593 | A | C | 1 | a0002c0002t0012g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.168-1013A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604593 | |||||||
| chr1:24604593 | A | T | 3 | a0002c0002t0004g0005 a0002c0002t0004g0273 a0002c0002t0004g0388 |
3 | HG01099.hp2 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.168-1013A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604593 | |||||||
| chr1:24604594 | A | C | 7 | a0002c0002t0004g0026 a0002c0002t0004g0030 a0002c0002t0004g0034 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-1012A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604594 | |||||||
| chr1:24604594 | AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0007g0395 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.168-1010_168-982de others(30): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604594 | ||||||
| chr1:24604595 | A | C | 1 | a0002c0002t0012g0002 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.168-1011A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604595 | |||||||
| chr1:24604595 | A | T | 5 | a0002c0002t0004g0005 a0002c0002t0004g0017 a0002c0002t0004g0018 others(2): Show |
5 | HG01099.hp2 HG01243.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-1011A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604595 | |||||||
| chr1:24604595 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0366 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.168-1009_168-998de others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604595 | ||||||
| chr1:24604595 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0006g0281 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.168-1009_168-996de others(15): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604595 | ||||||
| chr1:24604595 | AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0059 a0001c0001t0025g0316 |
2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.168-1009_168-992de others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604595 | ||||||
| chr1:24604595 | AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0006g0190 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.168-1009_168-990de others(21): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604595 | ||||||
| chr1:24604596 | A | C | 3 | a0002c0002t0004g0031 a0002c0002t0004g0032 a0002c0002t0004g0058 |
3 | HG02647.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.168-1010A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604596 | |||||||
| chr1:24604596 | AAAAAAAA others(8): Show |
A | 1 | a0003c0003t0020g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168-1008_168-994de others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604596 | ||||||
| chr1:24604596 | AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0003g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.168-1008_168-986de others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604596 | ||||||
| chr1:24604596 | AAAAAAAA others(20): Show |
A | 1 | a0001c0001t0010g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.168-1008_168-982de others(28): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604596 | ||||||
| chr1:24604596 | AAAAAAAA others(22): Show |
A | 2 | a0001c0001t0013g0009 a0001c0001t0013g0010 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.168-1008_168-980de others(30): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604596 | ||||||
| chr1:24604597 | A | T | 9 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(6): Show |
9 | HG01099.hp2 HG01243.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1009A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604597 | |||||||
| chr1:24604597 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0006g0365 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.168-1007_168-994de others(15): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604597 | ||||||
| chr1:24604597 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0003g0372 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.168-1007_168-992de others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604597 | ||||||
| chr1:24604597 | AAAAAAAA others(11): Show |
A | 3 | a0001c0001t0001g0322 a0001c0001t0003g0373 a0001c0001t0006g0325 |
3 | HG02080.hp2 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.168-1007_168-990de others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604597 | ||||||
| chr1:24604598 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0003g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.168-1006_168-992de others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604598 | ||||||
| chr1:24604598 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0003g0384 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.168-1006_168-990de others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604598 | ||||||
| chr1:24604598 | AAAAAAAA others(16): Show |
A | 2 | a0001c0001t0003g0054 a0001c0001t0003g0148 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.168-1006_168-984de others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604598 | ||||||
| chr1:24604598 | AAAAAAAA others(18): Show |
A | 2 | a0001c0001t0010g0378 a0001c0001t0010g0379 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.168-1006_168-982de others(26): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604598 | ||||||
| chr1:24604598 | AAAAAAAA others(20): Show |
A | 1 | a0001c0001t0007g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.168-1006_168-980de others(28): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604598 | ||||||
| chr1:24604599 | A | T | 16 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(13): Show |
16 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.168-1007A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604599 | |||||||
| chr1:24604599 | AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0376 a0001c0001t0001g0377 |
3 | HG01069.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.168-1005_168-994de others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | ||||||
| chr1:24604599 | AAAAAAAA others(9): Show |
A | 3 | a0001c0001t0002g0044 a0001c0001t0008g0397 a0001c0001t0008g0398 |
3 | HG02055.hp1 HG02486.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.168-1005_168-990de others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | ||||||
| chr1:24604599 | AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0055 a0001c0001t0003g0243 |
2 | HG00140.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.168-1005_168-988de others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | ||||||
| chr1:24604599 | AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0014g0014 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.168-1005_168-986de others(21): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | ||||||
| chr1:24604599 | AAAAAAAA others(15): Show |
A | 2 | a0001c0001t0003g0276 a0001c0001t0003g0339 |
2 | HG02027.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.168-1005_168-984de others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | ||||||
| chr1:24604599 | AAAAAAAA others(19): Show |
A | 1 | a0001c0001t0011g0216 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.168-1005_168-980de others(27): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | ||||||
| chr1:24604599 | AAAAAAAA others(21): Show |
A | 4 | a0001c0001t0001g0201 a0001c0001t0001g0221 a0001c0001t0007g0008 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1005_168-978de others(29): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | ||||||
| chr1:24604600 | AAAAAAAT others(4): Show |
A | 2 | a0001c0001t0001g0321 a0001c0001t0001g0375 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.168-1004_168-994de others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | ||||||
| chr1:24604600 | AAAAAAAT others(6): Show |
A | 1 | a0001c0001t0001g0062 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.168-1004_168-992de others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | ||||||
| chr1:24604600 | AAAAAAAT others(10): Show |
A | 4 | a0001c0001t0002g0095 a0001c0001t0002g0251 a0001c0001t0003g0226 others(1): Show |
4 | HG00735.hp2 HG01361.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1004_168-988de others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | ||||||
| chr1:24604600 | AAAAAAAT others(12): Show |
A | 2 | a0001c0001t0003g0013 a0001c0001t0003g0239 |
2 | HG02622.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.168-1004_168-986de others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | ||||||
| chr1:24604600 | AAAAAAAT others(14): Show |
A | 1 | a0001c0001t0003g0071 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.168-1004_168-984de others(22): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | ||||||
| chr1:24604600 | AAAAAAAT others(18): Show |
A | 2 | a0001c0001t0011g0155 a0001c0001t0011g0203 |
2 | HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.168-1004_168-980de others(26): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | ||||||
| chr1:24604600 | AAAAAAAT others(20): Show |
A | 4 | a0001c0001t0007g0001 a0001c0001t0007g0020 a0001c0001t0007g0023 others(1): Show |
5 | HG02145.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-1004_168-978de others(28): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | ||||||
| chr1:24604601 | A | T | 19 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(16): Show |
19 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.168-1005A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604601 | |||||||
| chr1:24604601 | AAAAAATA others(3): Show |
A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0193 |
2 | HG03130.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.168-1003_168-994de others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | ||||||
| chr1:24604601 | AAAAAATA others(5): Show |
A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0145 |
2 | HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.168-1003_168-992de others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | ||||||
| chr1:24604601 | AAAAAATA others(9): Show |
A | 1 | a0001c0001t0001g0052 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.168-1003_168-988de others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | ||||||
| chr1:24604601 | AAAAAATA others(11): Show |
A | 6 | a0001c0001t0003g0146 a0001c0001t0003g0241 a0001c0001t0003g0242 others(3): Show |
6 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-1003_168-986de others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | ||||||
| chr1:24604601 | AAAAAATA others(13): Show |
A | 2 | a0001c0001t0003g0016 a0001c0001t0023g0004 |
2 | HG02922.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.168-1003_168-984de others(21): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | ||||||
| chr1:24604601 | AAAAAATA others(19): Show |
A | 1 | a0001c0001t0001g0003 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.168-1003_168-978de others(27): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | ||||||
| chr1:24604601 | AAAAAATA others(21): Show |
A | 1 | a0001c0001t0007g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.168-1003_168-976de others(29): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | ||||||
| chr1:24604602 | A | C | 1 | a0002c0002t0004g0394 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168-1004A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604602 | |||||||
| chr1:24604602 | AAAAATAT others(4): Show |
A | 1 | a0001c0001t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.168-1002_168-992de others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604602 | ||||||
| chr1:24604602 | AAAAATAT others(6): Show |
A | 1 | a0001c0001t0001g0065 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.168-1002_168-990de others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604602 | ||||||
| chr1:24604602 | AAAAATAT others(8): Show |
A | 1 | a0001c0001t0008g0399 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.168-1002_168-988de others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604602 | ||||||
| chr1:24604602 | AAAAATAT others(10): Show |
A | 1 | a0001c0001t0003g0240 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.168-1002_168-986de others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604602 | ||||||
| chr1:24604602 | AAAAATAT others(12): Show |
A | 2 | a0001c0001t0003g0318 a0001c0001t0003g0355 |
2 | HG01169.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.168-1002_168-984de others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604602 | ||||||
| chr1:24604602 | AAAAATAT others(14): Show |
A | 2 | a0001c0001t0003g0078 a0001c0001t0003g0334 |
2 | HG02717.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.168-1002_168-982de others(22): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604602 | ||||||
| chr1:24604603 | A | T | 26 | a0001c0001t0002g0027 a0001c0001t0002g0041 a0001c0001t0002g0043 others(23): Show |
26 | HG01099.hp2 HG01243.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.168-1003A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604603 | |||||||
| chr1:24604603 | AAAATATA others(5): Show |
A | 4 | a0001c0001t0002g0028 a0001c0001t0002g0277 a0001c0001t0002g0284 others(1): Show |
4 | HG00621.hp1 HG01167.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1001_168-990de others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | ||||||
| chr1:24604603 | AAAATATA others(11): Show |
A | 8 | a0001c0001t0002g0218 a0001c0001t0003g0090 a0001c0001t0003g0252 others(5): Show |
8 | HG00323.hp1 HG01255.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.168-1001_168-984de others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | ||||||
| chr1:24604603 | AAAATATA others(13): Show |
A | 1 | a0001c0001t0003g0255 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.168-1001_168-982de others(21): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | ||||||
| chr1:24604603 | AAAATATA others(15): Show |
A | 9 | a0001c0001t0002g0219 a0001c0001t0002g0246 a0001c0001t0002g0364 others(6): Show |
9 | HG02080.hp1 HG02559.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1001_168-980de others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | ||||||
| chr1:24604603 | AAAATATA others(17): Show |
A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0207 a0001c0001t0003g0324 others(1): Show |
4 | HG00558.hp2 HG02040.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1001_168-978de others(25): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | ||||||
| chr1:24604603 | AAAATATA others(19): Show |
A | 3 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 |
3 | HG01175.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.168-1001_168-976de others(27): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | ||||||
| chr1:24604603 | AAAATATA others(23): Show |
A | 1 | a0001c0001t0002g0282 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.168-1001_168-972de others(31): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | ||||||
| chr1:24604603 | AAAATATA others(29): Show |
A | 1 | a0001c0001t0002g0165 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.168-1001_168-966de others(37): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | ||||||
| chr1:24604604 | AAATAT | A | 6 | a0001c0001t0001g0184 a0001c0001t0001g0187 a0001c0001t0001g0191 others(3): Show |
6 | HG00642.hp2 HG01081.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-1000_168-996de others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | ||||||
| chr1:24604604 | AAATATAT others(4): Show |
A | 1 | a0001c0001t0001g0292 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.168-1000_168-990de others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | ||||||
| chr1:24604604 | AAATATAT others(8): Show |
A | 1 | a0001c0001t0002g0103 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.168-1000_168-986de others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | ||||||
| chr1:24604604 | AAATATAT others(12): Show |
A | 3 | a0001c0001t0003g0070 a0001c0001t0003g0220 a0001c0001t0003g0319 |
3 | HG01167.hp1 HG04184.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.168-1000_168-982de others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | ||||||
| chr1:24604604 | AAATATAT others(14): Show |
A | 9 | a0001c0001t0002g0247 a0001c0001t0002g0363 a0001c0001t0003g0006 others(6): Show |
9 | HG00099.hp1 HG00423.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1000_168-980de others(22): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | ||||||
| chr1:24604604 | AAATATAT others(16): Show |
A | 2 | a0001c0001t0001g0050 a0001c0001t0003g0227 |
2 | HG01361.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.168-1000_168-978de others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | ||||||
| chr1:24604604 | AAATATAT others(18): Show |
A | 1 | a0001c0001t0001g0223 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.168-1000_168-976de others(26): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | ||||||
| chr1:24604604 | AAATATAT others(28): Show |
A | 1 | a0001c0001t0001g0192 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.168-1000_168-966de others(36): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | ||||||
| chr1:24604605 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0111 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.168-1000_168-999in others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0109 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.168-1000_168-999in others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0231 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.168-1000_168-999in others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | A | AAAT | 7 | a0001c0001t0001g0029 a0001c0001t0001g0257 a0001c0001t0001g0260 others(4): Show |
7 | HG02165.hp1 HG02615.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-1000_168-999in others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | A | AAATATAT others(6): Show |
1 | a0001c0001t0001g0296 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.168-1000_168-999in others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | A | AAT | 7 | a0001c0001t0001g0079 a0001c0001t0001g0106 a0001c0001t0001g0238 others(4): Show |
7 | HG00099.hp2 HG02027.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-954_168-953dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | A | ATAT | 4 | a0001c0001t0001g0162 a0001c0001t0001g0314 a0001c0001t0001g0323 others(1): Show |
4 | NA18946.hp2 NA18948.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1001_168-1000i others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604605 | |||||||
| chr1:24604605 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0306 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.168-1001_168-1000i others(15): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604605 | |||||||
| chr1:24604605 | A | T | 33 | a0001c0001t0001g0128 a0001c0001t0001g0141 a0001c0001t0001g0228 others(30): Show |
33 | HG01099.hp2 HG01243.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.168-1001A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604605 | |||||||
| chr1:24604605 | AAT | A | 9 | a0001c0001t0001g0215 a0001c0001t0001g0224 a0001c0001t0001g0236 others(6): Show |
9 | HG00597.hp2 HG00733.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-954_168-953del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | AATAT | A | 12 | a0001c0001t0001g0049 a0001c0001t0001g0170 a0001c0001t0001g0182 others(9): Show |
12 | HG00621.hp2 HG00673.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.168-956_168-953del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | AATATATA others(3): Show |
A | 1 | a0001c0001t0001g0290 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.168-962_168-953del others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | AATATATA others(7): Show |
A | 1 | a0001c0001t0001g0264 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.168-966_168-953del others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | AATATATA others(9): Show |
A | 3 | a0001c0001t0001g0107 a0001c0001t0003g0075 a0001c0001t0003g0092 |
3 | HG02300.hp1 HG04115.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.168-968_168-953del others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | AATATATA others(11): Show |
A | 5 | a0001c0001t0001g0183 a0001c0001t0002g0359 a0001c0001t0003g0077 others(2): Show |
5 | HG03239.hp2 NA18940.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-970_168-953del others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | AATATATA others(13): Show |
A | 5 | a0001c0001t0003g0346 a0001c0001t0003g0347 a0001c0001t0003g0353 others(2): Show |
5 | HG01074.hp2 HG01516.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-972_168-953del others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | AATATATA others(15): Show |
A | 1 | a0001c0001t0003g0338 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.168-974_168-953del others(22): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | AATATATA others(17): Show |
A | 2 | a0001c0001t0003g0012 a0001c0001t0003g0371 |
2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168-976_168-953del others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | AATATATA others(19): Show |
A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0259 a0001c0001t0001g0269 |
3 | HG01261.hp1 HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.168-978_168-953del others(26): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | AATATATA others(27): Show |
A | 1 | a0001c0001t0002g0069 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.168-986_168-953del others(34): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604605 | AATATATA others(29): Show |
A | 1 | a0001c0001t0002g0150 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.168-988_168-953del others(36): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | ||||||
| chr1:24604606 | AT | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0229 a0001c0001t0001g0307 others(2): Show |
5 | HG01358.hp2 HG02040.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-999delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | |||||||
| chr1:24604606 | ATAT | A | 12 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0205 others(9): Show |
12 | HG00280.hp1 HG01943.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.168-999_168-997del others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | |||||||
| chr1:24604606 | ATATAT | A | 6 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0076 others(3): Show |
6 | HG01123.hp2 HG04184.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-999_168-995del others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | |||||||
| chr1:24604606 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0002g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.168-999_168-989del others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | |||||||
| chr1:24604606 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0003g0358 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.168-999_168-983del others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | |||||||
| chr1:24604606 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0003g0263 a0001c0001t0003g0370 |
2 | HG00544.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.168-999_168-981del others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | |||||||
| chr1:24604606 | ATATATAT others(14): Show |
A | 6 | a0001c0001t0002g0117 a0001c0001t0003g0131 a0001c0001t0003g0132 others(3): Show |
6 | HG02155.hp2 NA18952.hp2 NA19063.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-999_168-979del others(21): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | |||||||
| chr1:24604606 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0003g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.168-999_168-977del others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | |||||||
| chr1:24604606 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0001g0291 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.168-999_168-969del others(31): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | |||||||
| chr1:24604607 | T | A | 19 | a0001c0001t0001g0056 a0001c0001t0001g0080 a0001c0001t0001g0098 others(16): Show |
19 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.168-999T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604607 | |||||||
| chr1:24604609 | T | A | 14 | a0001c0001t0001g0080 a0001c0001t0001g0115 a0001c0001t0001g0140 others(11): Show |
14 | HG00597.hp1 HG00597.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.168-997T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604609 | |||||||
| chr1:24604611 | T | A | 10 | a0001c0001t0001g0205 a0001c0001t0001g0215 a0001c0001t0001g0299 others(7): Show |
10 | HG00597.hp2 HG01928.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.168-995T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604611 | |||||||
| chr1:24604613 | T | A | 7 | a0001c0001t0001g0205 a0001c0001t0001g0215 a0001c0001t0001g0225 others(4): Show |
7 | HG01123.hp2 HG02074.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-993T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604613 | |||||||
| chr1:24604615 | T | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0381 a0001c0001t0002g0076 |
3 | HG00639.hp2 HG01123.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.168-991T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604615 | |||||||
| chr1:24604617 | T | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0381 |
2 | HG00639.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.168-989T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604617 | |||||||
| chr1:24604623 | T | A | 2 | a0001c0001t0001g0107 a0001c0001t0003g0092 |
2 | HG02300.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.168-983T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604623 | |||||||
| chr1:24604625 | T | A | 3 | a0001c0001t0001g0107 a0001c0001t0003g0351 a0001c0001t0005g0337 |
3 | HG02300.hp1 NA18998.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.168-981T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604625 | |||||||
| chr1:24604627 | T | A | 2 | a0001c0001t0003g0346 a0001c0001t0003g0351 |
2 | HG01516.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.168-979T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604627 | |||||||
| chr1:24604628 | A | ATGTGTGT others(41): Show |
1 | a0002c0002t0004g0394 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168-977_168-976ins others(48): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604628 | ||||||
| chr1:24604629 | T | A | 1 | a0001c0001t0003g0351 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.168-977T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604629 | |||||||
| chr1:24604630 | A | ATGTGTGT others(27): Show |
1 | a0002c0002t0012g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.168-975_168-974ins others(34): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604630 | ||||||
| chr1:24604630 | A | G | 1 | a0002c0002t0004g0394 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168-976A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604630 | |||||||
| chr1:24604632 | A | ATGTGTGT others(27): Show |
1 | a0002c0002t0012g0002 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.168-973_168-972ins others(34): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604632 | ||||||
| chr1:24604632 | A | G | 2 | a0002c0002t0004g0394 a0002c0002t0012g0147 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.168-974A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604632 | |||||||
| chr1:24604633 | T | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0269 |
2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.168-973T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604633 | |||||||
| chr1:24604634 | A | G | 3 | a0002c0002t0004g0394 a0002c0002t0012g0002 a0002c0002t0012g0147 |
4 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-972A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604634 | |||||||
| chr1:24604636 | A | G | 3 | a0002c0002t0004g0394 a0002c0002t0012g0002 a0002c0002t0012g0147 |
4 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-970A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604636 | |||||||
| chr1:24604638 | A | ATGTGTGT others(51): Show |
1 | a0002c0002t0004g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-967_168-966ins others(58): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604638 | ||||||
| chr1:24604638 | A | G | 3 | a0002c0002t0004g0394 a0002c0002t0012g0002 a0002c0002t0012g0147 |
4 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-968A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604638 | |||||||
| chr1:24604639 | T | A | 1 | a0001c0001t0001g0291 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.168-967T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604639 | |||||||
| chr1:24604641 | T | A | 1 | a0001c0001t0001g0291 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.168-965T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604641 | |||||||
| chr1:24604644 | AT | A | 4 | a0002c0002t0004g0005 a0002c0002t0004g0394 a0002c0002t0012g0002 others(1): Show |
5 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-961delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604644 | |||||||
| chr1:24604647 | T | A | 4 | a0002c0002t0004g0005 a0002c0002t0004g0394 a0002c0002t0012g0002 others(1): Show |
5 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-959T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604647 | |||||||
| chr1:24604649 | T | A | 4 | a0002c0002t0004g0005 a0002c0002t0004g0394 a0002c0002t0012g0002 others(1): Show |
5 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-957T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | |||||||
| chr1:24604649 | T | TGTGTGTG others(32): Show |
3 | a0002c0002t0004g0018 a0002c0002t0004g0026 a0002c0002t0004g0058 |
3 | HG01243.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.168-957_168-956ins others(39): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | |||||||
| chr1:24604649 | T | TGTGTGTG others(34): Show |
6 | a0002c0002t0004g0017 a0002c0002t0004g0024 a0002c0002t0004g0030 others(3): Show |
6 | HG01099.hp2 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-957_168-956ins others(41): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | |||||||
| chr1:24604649 | T | TGTGTGTG others(36): Show |
4 | a0002c0002t0004g0031 a0002c0002t0004g0032 a0002c0002t0004g0034 others(1): Show |
4 | HG02559.hp1 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-957_168-956ins others(43): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | |||||||
| chr1:24604649 | T | TGTGTGTG others(38): Show |
2 | a0002c0002t0004g0390 a0002c0002t0004g0391 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.168-957_168-956ins others(45): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | |||||||
| chr1:24604649 | T | TGTGTGTG others(42): Show |
1 | a0002c0002t0004g0389 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.168-957_168-956ins others(49): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | |||||||
| chr1:24604649 | T | TGTGTGTG others(52): Show |
1 | a0002c0002t0004g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.168-957_168-956ins others(59): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | |||||||
| chr1:24604649 | T | TGTGTGTG others(60): Show |
1 | a0002c0002t0004g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.168-957_168-956ins others(67): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | |||||||
| chr1:24604671 | C | T | 226 | a0001c0001t0002g0022 a0001c0001t0002g0027 a0001c0001t0002g0028 others(223): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.168-935C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604671 | |||||||
| chr1:24604672 | C | A | 16 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.168-934C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604672 | |||||||
| chr1:24604709 | T | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-897T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604709 | |||||||
| chr1:24604779 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.168-827G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604779 | |||||||
| chr1:24604841 | A | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-765A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604841 | |||||||
| chr1:24604872 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.168-734T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604872 | |||||||
| chr1:24604873 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.168-733G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604873 | |||||||
| chr1:24604913 | G | A | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-693G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604913 | |||||||
| chr1:24604953 | A | T | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-653A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604953 | |||||||
| chr1:24604988 | T | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-618T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604988 | |||||||
| chr1:24604989 | G | A | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-617G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604989 | |||||||
| chr1:24605010 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.168-596G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605010 | |||||||
| chr1:24605076 | A | G | 14 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(11): Show |
15 | HG01099.hp2 HG01891.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.168-530A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605076 | |||||||
| chr1:24605094 | T | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-512T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605094 | |||||||
| chr1:24605106 | A | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-500A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605106 | |||||||
| chr1:24605123 | GAA | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-473_168-472del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24605123 | ||||||
| chr1:24605220 | T | C | 1 | a0001c0001t0007g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.168-386T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605220 | |||||||
| chr1:24605360 | C | T | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-246C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605360 | |||||||
| chr1:24605376 | T | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-230T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605376 | |||||||
| chr1:24605435 | G | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-171G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605435 | |||||||
| chr1:24605448 | A | C | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-158A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605448 | |||||||
| chr1:24605503 | A | G | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-103A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605503 | |||||||
| chr1:24605539 | C | T | 1 | a0002c0002t0004g0394 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168-67C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605539 | |||||||
| chr1:24605555 | C | T | 1 | a0001c0001t0003g0326 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.168-51C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605555 | |||||||
| chr1:24605556 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0254 a0001c0001t0001g0260 |
3 | HG00423.hp1 HG02074.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.168-50G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605556 | |||||||
| chr1:24605557 | C | T | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-49C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605557 | |||||||
| chr1:24605570 | G | A | 22 | a0002c0002t0004g0005 a0002c0002t0004g0007 a0002c0002t0004g0017 others(19): Show |
23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-36G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605570 |