Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51527 |
| ensemblid | ENSG00000100744.15 |
| hgncid | 20343 |
| symbol | GSKIP |
| name | GSK3B interacting protein |
| refseq_nuc | NM_016472.5 |
| refseq_prot | NP_057556.2 |
| ensembl_nuc | ENST00000555181.6 |
| ensembl_prot | ENSP00000450420.1 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 96363526 |
| end | 96387288 |
| strand | + |
| ver | v1.2 |
| region | chr14:96363526-96387288 |
| region5000 | chr14:96358526-96392288 |
| regionname0 | GSKIP_chr14_96363526_96387288 |
| regionname5000 | GSKIP_chr14_96358526_96392288 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 417 | 407 | 94 | 68 | 188 | 14 | 41 | GSKIP_chr14_96358526_96392288 | GSKIP | ATGGA others(412): Show |
chr14 | 96358526 | 96392288 | ||
| a0001c0002 | 0/0 | 417 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | ATGGA others(412): Show |
chr14 | 96358526 | 96392288 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2168 | 197 | 68 | 31 | 68 | 5 | 25 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| a0001c0001t0002 | 0/1 | 2168 | 99 | 16 | 24 | 44 | 6 | 8 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| a0001c0001t0003 | 0/0 | 2168 | 89 | 3 | 8 | 67 | 3 | 8 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| a0001c0001t0004 | 1/0 | 2168 | 7 | 0 | 2 | 4 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| a0001c0001t0005 | 0/0 | 2168 | 4 | 3 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| a0001c0001t0006 | 0/0 | 2168 | 3 | 3 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| a0001c0001t0007 | 0/0 | 2147 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2142): Show |
chr14 | 96358526 | 96392288 |
| a0001c0001t0008 | 0/0 | 2168 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| a0001c0001t0009 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| a0001c0001t0010 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| a0001c0001t0011 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| a0001c0001t0012 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| a0001c0001t0013 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| a0001c0001t0014 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| a0001c0002t0001 | 0/0 | 2168 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | AGTCG others(2163): Show |
chr14 | 96358526 | 96392288 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 41 | 9 | 8 | 16 | 4 | 4 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0004 | 0/0 | 30 | 1 | 6 | 18 | 1 | 4 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0006 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0016 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0002 | 0/0 | 45 | 2 | 8 | 26 | 3 | 6 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0007 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0029 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0001 | 0/0 | 49 | 2 | 4 | 38 | 2 | 3 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0011 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0023 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0004g0010 | 1/0 | 4 | 0 | 0 | 3 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0005g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0006g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0007g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0008g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0010g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0011g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0012g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0013g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0056 | EUR | GBR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0064 | EUR | FIN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0102 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01346 | hp2 | a0001 | c0001 | t0008 | g0012 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0103 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02293 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0046 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | YRI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18945 | hp2 | a0001 | c0001 | t0014 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19007 | hp2 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19062 | hp2 | a0001 | c0001 | t0012 | g0139 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19070 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19072 | hp2 | a0001 | c0001 | t0013 | g0153 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | YRI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ASW | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0021 | EUR | TSI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0029 | EUR | TSI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | GIH | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | USA | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | USA | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | LWK | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0029 | REF | REF | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0010 | REF | REF | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:96382298 | A | G | 1 | a0001c0002 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.51A>G | p.Glu17Glu | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/4 | 196/2169 | 51/420 | 17/139 | chr14 | 96382298 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:96363551 | A | G | 1 | a0001c0001t0014 | 1 | NA18945.hp2 | 5_prime_UTR_variant | MODIFIER | c.-120A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/4 | 18697 | chr14 | 96363551 | ||||||
| chr14:96379755 | G | A | 10 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(7): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
5_prime_UTR_variant | MODIFIER | c.-35G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/4 | 2493 | chr14 | 96379755 | ||||||
| chr14:96385734 | T | C | 3 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*50T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 50 | chr14 | 96385734 | ||||||
| chr14:96385887 | C | G | 1 | a0001c0001t0011 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*203C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 203 | chr14 | 96385887 | ||||||
| chr14:96386154 | A | G | 1 | a0001c0001t0006 | 3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*470A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 470 | chr14 | 96386154 | ||||||
| chr14:96386496 | CTGTGTTG others(14): Show |
C | 1 | a0001c0001t0007 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*818_*838delTGATTC others(15): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 818 | INFO_REALIGN_3_PRIME | chr14 | 96386496 | |||||
| chr14:96386576 | T | A | 1 | a0001c0001t0009 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*892T>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 892 | chr14 | 96386576 | ||||||
| chr14:96386587 | T | C | 1 | a0001c0001t0007 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*903T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 903 | chr14 | 96386587 | ||||||
| chr14:96386594 | T | C | 1 | a0001c0001t0012 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*910T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 910 | chr14 | 96386594 | ||||||
| chr14:96386745 | T | C | 1 | a0001c0001t0010 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1061T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 1061 | chr14 | 96386745 | ||||||
| chr14:96386957 | A | C | 1 | a0001c0001t0008 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1273A>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 1273 | chr14 | 96386957 | ||||||
| chr14:96386993 | C | T | 1 | a0001c0001t0005 | 4 | HG00642.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1309C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 1309 | chr14 | 96386993 | ||||||
| chr14:96387117 | C | T | 14 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(11): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
3_prime_UTR_variant | MODIFIER | c.*1433C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 1433 | chr14 | 96387117 | ||||||
| chr14:96387198 | T | G | 1 | a0001c0001t0013 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1514T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 1514 | chr14 | 96387198 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:96363661 | G | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(36): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.-103+93G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96363661 | |||||||
| chr14:96363696 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-103+128G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96363696 | |||||||
| chr14:96363748 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-103+180C>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96363748 | |||||||
| chr14:96363771 | C | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0156 a0001c0001t0006g0046 others(1): Show |
5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103+203C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96363771 | |||||||
| chr14:96363990 | T | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0076 |
4 | HG02886.hp2 HG03486.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+422T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96363990 | |||||||
| chr14:96364089 | G | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(38): Show |
98 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.-103+521G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364089 | |||||||
| chr14:96364104 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0047 |
3 | HG02559.hp1 HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-103+536G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364104 | |||||||
| chr14:96364147 | A | G | 1 | a0001c0001t0005g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-103+579A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364147 | |||||||
| chr14:96364197 | G | A | 4 | a0001c0001t0003g0038 a0001c0001t0003g0104 a0001c0001t0003g0105 others(1): Show |
5 | NA18948.hp1 NA18968.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+629G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364197 | |||||||
| chr14:96364378 | T | G | 1 | a0001c0001t0001g0107 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-103+810T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364378 | |||||||
| chr14:96364508 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-103+940G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364508 | |||||||
| chr14:96364646 | C | T | 3 | a0001c0001t0005g0037 a0001c0001t0005g0102 a0001c0001t0005g0103 |
4 | HG00642.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+1078C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364646 | |||||||
| chr14:96364666 | C | A | 1 | a0001c0001t0001g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-103+1098C>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364666 | |||||||
| chr14:96364794 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+1226G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364794 | |||||||
| chr14:96364855 | G | A | 1 | a0001c0001t0005g0102 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-103+1287G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364855 | |||||||
| chr14:96364855 | G | C | 1 | a0001c0001t0001g0006 | 7 | HG00642.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-103+1287G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364855 | |||||||
| chr14:96365028 | A | G | 1 | a0001c0001t0003g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-103+1460A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365028 | |||||||
| chr14:96365125 | C | T | 1 | a0001c0001t0001g0006 | 7 | HG00642.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-103+1557C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365125 | |||||||
| chr14:96365277 | T | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+1709T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365277 | |||||||
| chr14:96365584 | CT | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-103+2020delT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96365584 | ||||||
| chr14:96365606 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0113 others(4): Show |
12 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-103+2038G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365606 | |||||||
| chr14:96365613 | T | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0078 |
5 | HG01192.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+2045T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365613 | |||||||
| chr14:96365793 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0136 others(1): Show |
13 | HG00642.hp2 HG01255.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-103+2225C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365793 | |||||||
| chr14:96365848 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-103+2280A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365848 | |||||||
| chr14:96366050 | G | A | 1 | a0001c0001t0003g0104 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-103+2482G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366050 | |||||||
| chr14:96366107 | CAT | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0100 a0001c0001t0001g0134 others(1): Show |
6 | HG03927.hp1 NA18941.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+2540_-103+254 others(6): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366107 | |||||||
| chr14:96366119 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-103+2551T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366119 | |||||||
| chr14:96366365 | G | A | 3 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0050 |
3 | HG02145.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-103+2797G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366365 | |||||||
| chr14:96366482 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-103+2914C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366482 | |||||||
| chr14:96366659 | A | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+3091A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366659 | |||||||
| chr14:96366665 | G | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(19): Show |
60 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.-103+3097G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366665 | |||||||
| chr14:96366746 | TTA | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0108 others(1): Show |
6 | HG02735.hp2 HG03239.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+3179_-103+318 others(6): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366746 | |||||||
| chr14:96366752 | AAG | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0109 a0001c0001t0001g0110 |
5 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+3186_-103+318 others(6): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96366752 | ||||||
| chr14:96366754 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0108 others(1): Show |
6 | HG02735.hp2 HG03239.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+3186G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366754 | |||||||
| chr14:96366849 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-103+3281G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366849 | |||||||
| chr14:96366890 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0156 |
2 | HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-103+3322T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366890 | |||||||
| chr14:96367086 | C | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0156 a0001c0001t0006g0046 others(1): Show |
5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103+3518C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96367086 | |||||||
| chr14:96367257 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+3689G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96367257 | |||||||
| chr14:96367641 | C | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0113 others(4): Show |
12 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-103+4073C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96367641 | |||||||
| chr14:96367908 | G | C | 7 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0113 others(4): Show |
12 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-103+4340G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96367908 | |||||||
| chr14:96367914 | G | C | 1 | a0001c0001t0002g0117 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-103+4346G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96367914 | |||||||
| chr14:96368012 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-103+4444T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368012 | |||||||
| chr14:96368060 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-103+4492A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368060 | |||||||
| chr14:96368082 | A | AT | 9 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(6): Show |
13 | HG00621.hp2 HG02040.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-103+4529dupT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96368082 | ||||||
| chr14:96368097 | T | C | 1 | a0001c0001t0012g0139 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-103+4529T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368097 | |||||||
| chr14:96368184 | C | CT | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(34): Show |
85 | HG00099.hp1 HG00408.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.-103+4632dupT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96368184 | ||||||
| chr14:96368250 | G | A | 2 | a0001c0001t0006g0046 a0001c0001t0006g0157 |
3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-103+4682G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368250 | |||||||
| chr14:96368301 | C | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-103+4733C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368301 | |||||||
| chr14:96368332 | C | T | 1 | a0001c0001t0013g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-103+4764C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368332 | |||||||
| chr14:96368343 | A | AT | 6 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0114 others(3): Show |
11 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-103+4782dupT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96368343 | ||||||
| chr14:96368454 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-103+4886G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368454 | |||||||
| chr14:96368470 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-103+4902A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368470 | |||||||
| chr14:96368507 | T | C | 1 | a0001c0001t0003g0140 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-103+4939T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368507 | |||||||
| chr14:96369127 | G | A | 1 | a0001c0001t0003g0020 | 3 | HG00438.hp2 NA19005.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-103+5559G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369127 | |||||||
| chr14:96369204 | C | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0156 a0001c0001t0006g0046 others(1): Show |
5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103+5636C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369204 | |||||||
| chr14:96369251 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-103+5683T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369251 | |||||||
| chr14:96369615 | C | T | 2 | a0001c0001t0003g0150 a0001c0001t0003g0151 |
2 | NA19054.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-103+6047C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369615 | |||||||
| chr14:96369647 | A | G | 1 | a0001c0001t0003g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-103+6079A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369647 | |||||||
| chr14:96369651 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+6083G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369651 | |||||||
| chr14:96369801 | A | G | 4 | a0001c0001t0001g0075 a0001c0001t0001g0156 a0001c0001t0006g0046 others(1): Show |
5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103+6233A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369801 | |||||||
| chr14:96369956 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-103+6388A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369956 | |||||||
| chr14:96370181 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-103+6613G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370181 | |||||||
| chr14:96370227 | A | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(40): Show |
99 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.-103+6659A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370227 | |||||||
| chr14:96370458 | G | A | 3 | a0001c0001t0005g0037 a0001c0001t0005g0102 a0001c0001t0005g0103 |
4 | HG00642.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+6890G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370458 | |||||||
| chr14:96370551 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0136 others(1): Show |
13 | HG00642.hp2 HG01255.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-103+6983C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370551 | |||||||
| chr14:96370552 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0081 a0001c0001t0001g0082 |
4 | HG02572.hp2 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+6984G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370552 | |||||||
| chr14:96370587 | C | G | 39 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(36): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.-103+7019C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370587 | |||||||
| chr14:96370636 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-103+7068T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370636 | |||||||
| chr14:96370727 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-103+7159G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370727 | |||||||
| chr14:96370860 | G | C | 4 | a0001c0001t0001g0075 a0001c0001t0001g0156 a0001c0001t0006g0046 others(1): Show |
5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103+7292G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370860 | |||||||
| chr14:96370904 | A | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+7336A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370904 | |||||||
| chr14:96370944 | G | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+7376G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370944 | |||||||
| chr14:96371052 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(43): Show |
103 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.-103+7484T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371052 | |||||||
| chr14:96371371 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0109 a0001c0001t0001g0110 |
5 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+7803A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371371 | |||||||
| chr14:96371442 | C | CT | 6 | a0001c0001t0001g0042 a0001c0001t0002g0029 a0001c0001t0003g0023 others(3): Show |
10 | HG01952.hp2 HG02056.hp1 HG03669.hp1 others(7): Show |
intron_variant | MODIFIER | c.-103+7894dupT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96371442 | ||||||
| chr14:96371442 | CT | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0013 others(66): Show |
143 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-103+7894delT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96371442 | ||||||
| chr14:96371442 | CTT | C | 38 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(35): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-103+7893_-103+789 others(6): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96371442 | ||||||
| chr14:96371460 | T | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
11 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-103+7892T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371460 | |||||||
| chr14:96371470 | AGTCTCAC others(3): Show |
A | 1 | a0001c0001t0001g0032 | 2 | HG01261.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-103+7906_-103+791 others(14): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96371470 | ||||||
| chr14:96371540 | G | T | 1 | a0001c0001t0002g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-103+7972G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371540 | |||||||
| chr14:96371591 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-103+8023C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371591 | |||||||
| chr14:96371647 | A | G | 6 | a0001c0001t0002g0012 a0001c0001t0002g0051 a0001c0001t0002g0052 others(3): Show |
7 | HG01346.hp2 HG01433.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.-102-8041A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371647 | |||||||
| chr14:96371665 | A | G | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.-102-8023A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371665 | |||||||
| chr14:96372024 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0121 a0001c0001t0001g0122 |
4 | HG01168.hp2 HG01169.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-7664G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372024 | |||||||
| chr14:96372456 | C | G | 1 | a0001c0001t0002g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-102-7232C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372456 | |||||||
| chr14:96372510 | G | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0136 a0001c0001t0001g0137 |
6 | HG01255.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-102-7178G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372510 | |||||||
| chr14:96372569 | T | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-7119T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372569 | |||||||
| chr14:96372675 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-102-7013G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372675 | |||||||
| chr14:96372849 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-6839G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372849 | |||||||
| chr14:96372853 | A | G | 2 | a0001c0001t0002g0026 a0001c0001t0002g0072 |
3 | HG02280.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-102-6835A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372853 | |||||||
| chr14:96373094 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(21): Show |
62 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.-102-6594G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96373094 | |||||||
| chr14:96373193 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-102-6495A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96373193 | |||||||
| chr14:96373229 | C | CA | 40 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0130 others(37): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-102-6436dupA | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96373229 | ||||||
| chr14:96373229 | C | CAA | 7 | a0001c0001t0002g0008 a0001c0001t0002g0027 a0001c0001t0002g0053 others(4): Show |
12 | HG00438.hp1 HG01256.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.-102-6437_-102-643 others(6): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96373229 | ||||||
| chr14:96373229 | CA | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
166 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-102-6436delA | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96373229 | ||||||
| chr14:96373229 | CAA | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(6): Show |
13 | HG01169.hp1 HG02040.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.-102-6437_-102-643 others(6): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96373229 | ||||||
| chr14:96373246 | AAAAAAAG | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0115 others(2): Show |
10 | HG02717.hp2 HG02895.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-102-6438_-102-643 others(11): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96373246 | ||||||
| chr14:96373600 | TA | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0113 others(6): Show |
14 | HG02145.hp1 HG02293.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.-102-6076delA | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96373600 | ||||||
| chr14:96373993 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-102-5695A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96373993 | |||||||
| chr14:96374024 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-102-5664G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374024 | |||||||
| chr14:96374084 | A | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(40): Show |
100 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.-102-5604A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374084 | |||||||
| chr14:96374166 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-102-5522T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374166 | |||||||
| chr14:96374183 | A | G | 1 | a0001c0001t0006g0046 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-102-5505A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374183 | |||||||
| chr14:96374257 | T | A | 1 | a0001c0001t0003g0141 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-102-5431T>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374257 | |||||||
| chr14:96374258 | A | T | 1 | a0001c0001t0003g0141 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-102-5430A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374258 | |||||||
| chr14:96374482 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0130 |
3 | HG03195.hp1 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-102-5206A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374482 | |||||||
| chr14:96374771 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-102-4917A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374771 | |||||||
| chr14:96374935 | CT | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0136 others(1): Show |
13 | HG00642.hp2 HG01255.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-102-4751delT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96374935 | ||||||
| chr14:96375243 | A | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-4445A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375243 | |||||||
| chr14:96375359 | T | C | 1 | a0001c0001t0003g0142 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-102-4329T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375359 | |||||||
| chr14:96375430 | T | C | 1 | a0001c0001t0013g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-102-4258T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375430 | |||||||
| chr14:96375435 | TC | T | 26 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(23): Show |
64 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.-102-4252delC | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375435 | |||||||
| chr14:96375436 | C | CT | 16 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0113 others(13): Show |
27 | HG00438.hp1 HG00639.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.-102-4237dupT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96375436 | ||||||
| chr14:96375436 | CT | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(39): Show |
97 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-102-4237delT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96375436 | ||||||
| chr14:96375459 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-102-4229C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375459 | |||||||
| chr14:96375460 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-102-4228G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375460 | |||||||
| chr14:96375494 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-102-4194C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375494 | |||||||
| chr14:96375495 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-102-4193G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375495 | |||||||
| chr14:96375520 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-102-4168G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375520 | |||||||
| chr14:96375526 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-102-4162C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375526 | |||||||
| chr14:96375582 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-102-4106C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375582 | |||||||
| chr14:96375661 | T | C | 4 | a0001c0001t0001g0075 a0001c0001t0001g0156 a0001c0001t0006g0046 others(1): Show |
5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-102-4027T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375661 | |||||||
| chr14:96375667 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-102-4021C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375667 | |||||||
| chr14:96375787 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-102-3901A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375787 | |||||||
| chr14:96376010 | A | C | 1 | a0001c0001t0003g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-102-3678A>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376010 | |||||||
| chr14:96376308 | C | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0027 a0001c0001t0002g0067 others(1): Show |
10 | HG00438.hp1 HG00639.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.-102-3380C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376308 | |||||||
| chr14:96376339 | G | GC | 46 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0113 others(43): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-102-3348dupC | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96376339 | ||||||
| chr14:96376369 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-102-3319C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376369 | |||||||
| chr14:96376470 | A | G | 1 | a0001c0001t0003g0146 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-102-3218A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376470 | |||||||
| chr14:96376481 | G | C | 1 | a0001c0001t0001g0043 | 2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-102-3207G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376481 | |||||||
| chr14:96376510 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-3178G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376510 | |||||||
| chr14:96376627 | G | A | 2 | a0001c0001t0003g0150 a0001c0001t0003g0151 |
2 | NA19054.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-102-3061G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376627 | |||||||
| chr14:96376822 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-102-2866A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376822 | |||||||
| chr14:96376832 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-102-2856C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376832 | |||||||
| chr14:96376928 | CAAT | C | 28 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(25): Show |
67 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.-102-2759_-102-275 others(7): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376928 | |||||||
| chr14:96377029 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-102-2659A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377029 | |||||||
| chr14:96377146 | A | G | 3 | a0001c0001t0005g0037 a0001c0001t0005g0102 a0001c0001t0005g0103 |
4 | HG00642.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-102-2542A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377146 | |||||||
| chr14:96377237 | A | G | 5 | a0001c0001t0002g0007 a0001c0001t0002g0027 a0001c0001t0002g0066 others(2): Show |
11 | HG00438.hp1 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.-102-2451A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377237 | |||||||
| chr14:96377253 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(30): Show |
81 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.-102-2435G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377253 | |||||||
| chr14:96377307 | T | G | 1 | a0001c0001t0003g0143 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-102-2381T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377307 | |||||||
| chr14:96377435 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-102-2253C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377435 | |||||||
| chr14:96377475 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-102-2213G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377475 | |||||||
| chr14:96377698 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-102-1990A>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377698 | |||||||
| chr14:96377803 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-102-1885C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377803 | |||||||
| chr14:96377918 | G | A | 1 | a0001c0001t0003g0044 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-102-1770G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377918 | |||||||
| chr14:96378026 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-102-1662T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378026 | |||||||
| chr14:96378213 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(40): Show |
95 | HG00099.hp1 HG00408.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.-102-1475A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378213 | |||||||
| chr14:96378228 | C | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(40): Show |
100 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.-102-1460C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378228 | |||||||
| chr14:96378374 | T | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0060 |
2 | HG02129.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.-102-1314T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378374 | |||||||
| chr14:96378503 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-102-1185C>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378503 | |||||||
| chr14:96378595 | T | C | 7 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0113 others(4): Show |
12 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-102-1093T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378595 | |||||||
| chr14:96378645 | A | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(6): Show |
13 | HG00621.hp2 HG02040.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-102-1043A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378645 | |||||||
| chr14:96378737 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0108 |
3 | HG02735.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-102-951T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378737 | |||||||
| chr14:96378894 | C | G | 29 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(26): Show |
76 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.-102-794C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378894 | |||||||
| chr14:96378981 | G | A | 3 | a0001c0001t0005g0037 a0001c0001t0005g0102 a0001c0001t0005g0103 |
4 | HG00642.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-102-707G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378981 | |||||||
| chr14:96379069 | G | T | 1 | a0001c0001t0005g0102 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-102-619G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379069 | |||||||
| chr14:96379108 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-102-580G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379108 | |||||||
| chr14:96379196 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0129 a0001c0001t0011g0005 |
10 | NA18948.hp2 NA18956.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.-102-492C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379196 | |||||||
| chr14:96379291 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-102-397G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379291 | |||||||
| chr14:96379322 | G | T | 29 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(26): Show |
76 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.-102-366G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379322 | |||||||
| chr14:96379488 | C | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0071 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.-102-200C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379488 | |||||||
| chr14:96379590 | A | G | 1 | a0001c0001t0003g0151 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-102-98A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379590 | |||||||
| chr14:96379595 | C | T | 1 | a0001c0001t0003g0145 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-102-93C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379595 | |||||||
| chr14:96379898 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-2+110A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96379898 | |||||||
| chr14:96379944 | A | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2+156A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96379944 | |||||||
| chr14:96380090 | A | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0156 a0001c0001t0006g0046 others(1): Show |
5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+302A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96380090 | |||||||
| chr14:96380238 | T | G | 1 | a0001c0001t0001g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-2+450T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96380238 | |||||||
| chr14:96380390 | C | G | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-2+602C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96380390 | |||||||
| chr14:96380450 | CAGG | C | 3 | a0001c0001t0005g0037 a0001c0001t0005g0102 a0001c0001t0005g0103 |
4 | HG00642.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+665_-2+667delGA others(1): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 96380450 | ||||||
| chr14:96380474 | G | T | 1 | a0001c0001t0002g0058 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-2+686G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96380474 | |||||||
| chr14:96380656 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
8 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+868C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96380656 | |||||||
| chr14:96380721 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-2+933G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96380721 | |||||||
| chr14:96381003 | T | C | 40 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(37): Show |
96 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-2+1215T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381003 | |||||||
| chr14:96381220 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-1-1027T>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381220 | |||||||
| chr14:96381348 | G | T | 8 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(5): Show |
11 | HG02145.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-899G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381348 | |||||||
| chr14:96381360 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-1-887A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381360 | |||||||
| chr14:96381487 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1-760G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381487 | |||||||
| chr14:96381778 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-1-469C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381778 | |||||||
| chr14:96381805 | CTTTTTT | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
11 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-440_-1-435delTT others(4): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 96381805 | ||||||
| chr14:96381902 | C | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
11 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-345C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381902 | |||||||
| chr14:96381911 | T | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0113 others(2): Show |
14 | HG00642.hp2 HG01255.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-336T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381911 | |||||||
| chr14:96381978 | C | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
11 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-269C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381978 | |||||||
| chr14:96381980 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0130 |
3 | HG03195.hp1 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-1-267A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381980 | |||||||
| chr14:96382015 | G | T | 1 | a0001c0001t0003g0022 | 3 | NA18954.hp2 NA18989.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-1-232G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96382015 | |||||||
| chr14:96382036 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-1-211G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96382036 | |||||||
| chr14:96382140 | T | C | 7 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0113 others(4): Show |
12 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-107T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96382140 | |||||||
| chr14:96382195 | T | C | 1 | a0001c0001t0002g0053 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-1-52T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96382195 | |||||||
| chr14:96382228 | C | CT | 7 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0082 others(4): Show |
10 | HG02109.hp2 HG02486.hp2 HG02922.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.-1-5dupT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 96382228 | ||||||
| chr14:96382562 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(21): Show |
62 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.258+57A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96382562 | |||||||
| chr14:96382567 | A | C | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.258+62A>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96382567 | |||||||
| chr14:96382606 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0099 |
3 | HG01261.hp2 HG01496.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.258+101G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96382606 | |||||||
| chr14:96382753 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.258+248C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96382753 | |||||||
| chr14:96382986 | A | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(37): Show |
96 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.258+481A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96382986 | |||||||
| chr14:96383168 | G | A | 2 | a0001c0001t0003g0038 a0001c0001t0003g0104 |
3 | NA18968.hp2 NA18980.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.258+663G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383168 | |||||||
| chr14:96383212 | C | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
11 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+707C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383212 | |||||||
| chr14:96383394 | T | TA | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(21): Show |
62 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.258+904dupA | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 96383394 | ||||||
| chr14:96383394 | T | TAA | 6 | a0001c0001t0001g0107 a0001c0001t0001g0121 a0001c0001t0001g0124 others(3): Show |
6 | HG01952.hp1 NA18612.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+903_258+904dup others(2): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 96383394 | ||||||
| chr14:96383394 | TA | T | 7 | a0001c0001t0001g0075 a0001c0001t0001g0090 a0001c0001t0001g0156 others(4): Show |
8 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.258+904delA | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 96383394 | ||||||
| chr14:96383560 | T | A | 39 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(36): Show |
95 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.258+1055T>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383560 | |||||||
| chr14:96383574 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.258+1069G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383574 | |||||||
| chr14:96383724 | T | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(22): Show |
63 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.258+1219T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383724 | |||||||
| chr14:96383736 | C | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
11 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+1231C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383736 | |||||||
| chr14:96383972 | T | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.258+1467T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383972 | |||||||
| chr14:96383998 | G | C | 4 | a0001c0001t0001g0075 a0001c0001t0001g0156 a0001c0001t0006g0046 others(1): Show |
5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+1493G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383998 | |||||||
| chr14:96384035 | A | G | 40 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(37): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.259-1488A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384035 | |||||||
| chr14:96384100 | A | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(37): Show |
96 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.259-1423A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384100 | |||||||
| chr14:96384159 | T | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(21): Show |
62 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.259-1364T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384159 | |||||||
| chr14:96384215 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0136 a0001c0001t0001g0137 |
6 | HG01255.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-1308A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384215 | |||||||
| chr14:96384297 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.259-1226A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384297 | |||||||
| chr14:96384333 | A | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.259-1190A>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384333 | |||||||
| chr14:96384391 | AT | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.259-1129delT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 96384391 | ||||||
| chr14:96384403 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.259-1120A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384403 | |||||||
| chr14:96384481 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259-1042A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384481 | |||||||
| chr14:96384487 | A | C | 1 | a0001c0001t0003g0146 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.259-1036A>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384487 | |||||||
| chr14:96384747 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259-776G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384747 | |||||||
| chr14:96384774 | C | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(22): Show |
63 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.259-749C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384774 | |||||||
| chr14:96384834 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.259-689A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384834 | |||||||
| chr14:96384843 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.259-680T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384843 | |||||||
| chr14:96384983 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(21): Show |
62 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.259-540A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384983 | |||||||
| chr14:96384994 | TAAC | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0086 |
3 | HG00639.hp2 HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.259-525_259-523del others(3): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 96384994 | ||||||
| chr14:96384995 | A | G | 1 | a0001c0001t0002g0002 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.259-528A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384995 | |||||||
| chr14:96384999 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259-524A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384999 |