Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27152 |
| ensemblid | ENSG00000164066.13 |
| hgncid | 29239 |
| symbol | INTU |
| name | inturned planar cell polarity protein |
| refseq_nuc | NM_015693.4 |
| refseq_prot | NP_056508.2 |
| ensembl_nuc | ENST00000335251.11 |
| ensembl_prot | ENSP00000334003.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 127632957 |
| end | 127726737 |
| strand | + |
| ver | v1.2 |
| region | chr4:127632957-127726737 |
| region5000 | chr4:127627957-127731737 |
| regionname0 | INTU_chr4_127632957_127726737 |
| regionname5000 | INTU_chr4_127627957_127731737 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 942 | 267 | 81 | 57 | 87 | 14 | 26 | 62 | INTU_chr4_127627957_127731737 | INTU | MASVA others(937): Show |
chr4 | 127627957 | 127731737 |
| a0002 | 0/0 | 942 | 69 | 0 | 7 | 62 | 0 | 0 | 50 | INTU_chr4_127627957_127731737 | INTU | MASVA others(937): Show |
chr4 | 127627957 | 127731737 |
| a0003 | 0/0 | 942 | 10 | 0 | 0 | 10 | 0 | 0 | 9 | INTU_chr4_127627957_127731737 | INTU | MASVA others(937): Show |
chr4 | 127627957 | 127731737 |
| a0004 | 0/0 | 942 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | MASVA others(937): Show |
chr4 | 127627957 | 127731737 |
| a0005 | 0/0 | 942 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | MASVA others(937): Show |
chr4 | 127627957 | 127731737 |
| a0006 | 0/0 | 942 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | MASVA others(937): Show |
chr4 | 127627957 | 127731737 |
| a0007 | 0/0 | 942 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | MASVA others(937): Show |
chr4 | 127627957 | 127731737 |
| a0008 | 0/0 | 942 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | MASVA others(937): Show |
chr4 | 127627957 | 127731737 |
| a0009 | 0/0 | 942 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | MASVA others(937): Show |
chr4 | 127627957 | 127731737 |
| a0010 | 0/0 | 942 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | MASVA others(937): Show |
chr4 | 127627957 | 127731737 |
| a0011 | 0/0 | 942 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | MASVA others(937): Show |
chr4 | 127627957 | 127731737 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2826 | 123 | 44 | 29 | 28 | 7 | 14 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0001c0002 | 1/0 | 2826 | 117 | 16 | 24 | 58 | 7 | 11 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0001c0004 | 0/0 | 2826 | 18 | 16 | 2 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0001c0006 | 0/0 | 2826 | 6 | 5 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0001c0013 | 0/0 | 2826 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0001c0014 | 0/0 | 2826 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0001c0016 | 0/0 | 2826 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0002c0003 | 0/0 | 2826 | 69 | 0 | 7 | 62 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0003c0005 | 0/0 | 2826 | 10 | 0 | 0 | 10 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0004c0007 | 0/0 | 2826 | 3 | 3 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0005c0008 | 0/0 | 2826 | 3 | 3 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0006c0009 | 0/0 | 2826 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0007c0012 | 0/0 | 2826 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0008c0010 | 0/0 | 2826 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0009c0011 | 0/0 | 2826 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0010c0017 | 0/0 | 2826 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 | ||
| a0011c0015 | 0/0 | 2826 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | ATGGC others(2821): Show |
chr4 | 127627957 | 127731737 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/1 | 13207 | 49 | 12 | 13 | 12 | 6 | 5 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0005 | 0/0 | 13208 | 16 | 0 | 4 | 12 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0007 | 0/0 | 13210 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13205): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0008 | 0/0 | 13208 | 2 | 0 | 0 | 1 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0009 | 0/0 | 13206 | 9 | 2 | 5 | 0 | 0 | 2 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13201): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0010 | 0/0 | 13200 | 8 | 8 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13195): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0012 | 0/0 | 13209 | 4 | 4 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0015 | 0/0 | 13206 | 2 | 2 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13201): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0016 | 0/0 | 13208 | 3 | 1 | 1 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0017 | 0/0 | 13206 | 3 | 2 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13201): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0018 | 0/0 | 13200 | 3 | 3 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13195): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0023 | 0/0 | 13209 | 2 | 0 | 0 | 0 | 0 | 2 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0024 | 0/0 | 13208 | 2 | 0 | 1 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0025 | 0/0 | 13209 | 2 | 0 | 1 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0026 | 0/0 | 13201 | 2 | 1 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13196): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0027 | 0/0 | 13210 | 2 | 1 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13205): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0055 | 0/0 | 13207 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0056 | 0/0 | 13187 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13182): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0058 | 0/0 | 13208 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0059 | 0/0 | 13207 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0060 | 0/0 | 13207 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0061 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0062 | 0/0 | 13209 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0064 | 0/0 | 13207 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0065 | 0/0 | 13206 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13201): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0066 | 0/0 | 13206 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13201): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0067 | 0/0 | 13200 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13195): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0073 | 0/0 | 13208 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0001t0074 | 0/0 | 13207 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0001 | 0/0 | 13208 | 60 | 3 | 11 | 32 | 4 | 10 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0004 | 0/0 | 13208 | 22 | 0 | 7 | 15 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0006 | 1/0 | 13208 | 12 | 8 | 2 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0013 | 0/0 | 13209 | 2 | 1 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0014 | 0/0 | 13207 | 3 | 0 | 0 | 1 | 2 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0020 | 0/0 | 13208 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0022 | 0/0 | 13208 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0038 | 0/0 | 13208 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0039 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0041 | 0/0 | 13208 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0042 | 0/0 | 13208 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0043 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0044 | 0/0 | 13207 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0045 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0047 | 0/0 | 13209 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0048 | 0/0 | 13207 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0049 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0050 | 0/0 | 13209 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0051 | 0/0 | 13209 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0068 | 0/0 | 13208 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0002t0072 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0004t0002 | 0/0 | 13207 | 5 | 4 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0001c0004t0007 | 0/0 | 13210 | 9 | 9 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13205): Show |
chr4 | 127627957 | 127731737 |
| a0001c0004t0008 | 0/0 | 13208 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0004t0015 | 0/0 | 13206 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13201): Show |
chr4 | 127627957 | 127731737 |
| a0001c0004t0040 | 0/0 | 13206 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13201): Show |
chr4 | 127627957 | 127731737 |
| a0001c0004t0078 | 0/0 | 13210 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13205): Show |
chr4 | 127627957 | 127731737 |
| a0001c0006t0006 | 0/0 | 13208 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0006t0013 | 0/0 | 13209 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0001c0006t0046 | 0/0 | 13208 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0006t0053 | 0/0 | 13207 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0001c0006t0054 | 0/0 | 13206 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13201): Show |
chr4 | 127627957 | 127731737 |
| a0001c0006t0057 | 0/0 | 13206 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13201): Show |
chr4 | 127627957 | 127731737 |
| a0001c0013t0001 | 0/0 | 13208 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0001c0014t0002 | 0/0 | 13207 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0001c0016t0008 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0003 | 0/0 | 13208 | 50 | 0 | 7 | 43 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0011 | 0/0 | 13209 | 6 | 0 | 0 | 6 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0021 | 0/0 | 13209 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0030 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0031 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0032 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0033 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0034 | 0/0 | 13207 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0035 | 0/0 | 13207 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0036 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0037 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0069 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0070 | 0/0 | 13207 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0002c0003t0071 | 0/0 | 13206 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13201): Show |
chr4 | 127627957 | 127731737 |
| a0003c0005t0002 | 0/0 | 13207 | 4 | 0 | 0 | 4 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13202): Show |
chr4 | 127627957 | 127731737 |
| a0003c0005t0008 | 0/0 | 13208 | 5 | 0 | 0 | 5 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0003c0005t0063 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0004c0007t0075 | 0/0 | 13211 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13206): Show |
chr4 | 127627957 | 127731737 |
| a0004c0007t0076 | 0/0 | 13210 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13205): Show |
chr4 | 127627957 | 127731737 |
| a0004c0007t0077 | 0/0 | 13209 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13204): Show |
chr4 | 127627957 | 127731737 |
| a0005c0008t0019 | 0/0 | 13204 | 2 | 2 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13199): Show |
chr4 | 127627957 | 127731737 |
| a0005c0008t0028 | 0/0 | 13205 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13200): Show |
chr4 | 127627957 | 127731737 |
| a0006c0009t0052 | 0/0 | 13206 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13201): Show |
chr4 | 127627957 | 127731737 |
| a0007c0012t0001 | 0/0 | 13208 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0008c0010t0001 | 0/0 | 13208 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0009c0011t0029 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0010c0017t0003 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| a0011c0015t0005 | 0/0 | 13208 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | AGAGG others(13203): Show |
chr4 | 127627957 | 127731737 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0005g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0008g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0008g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0009g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0009g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0009g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0009g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0009g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0009g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0009g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0010g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0010g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0010g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0010g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0010g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0010g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0012g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0012g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0012g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0012g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0015g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0015g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0016g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0016g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0016g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0017g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0017g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0017g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0018g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0018g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0023g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0023g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0024g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0024g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0025g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0025g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0026g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0026g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0027g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0027g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0055g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0056g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0058g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0059g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0060g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0061g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0062g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0064g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0065g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0066g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0067g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0073g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0001t0074g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0006g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0006g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0006g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0013g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0013g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0014g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0014g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0014g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0020g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0020g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0022g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0038g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0039g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0041g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0042g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0043g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0044g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0045g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0047g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0048g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0049g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0050g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0051g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0068g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0002t0072g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0007g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0008g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0015g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0040g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0004t0078g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0006t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0006t0013g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0006t0046g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0006t0053g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0006t0054g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0006t0057g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0013t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0014t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0001c0016t0008g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0011g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0011g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0011g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0011g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0011g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0011g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0021g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0021g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0030g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0031g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0032g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0033g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0034g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0035g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0036g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0037g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0069g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0070g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0002c0003t0071g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0003c0005t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0003c0005t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0003c0005t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0003c0005t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0003c0005t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0003c0005t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0003c0005t0008g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0003c0005t0008g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0003c0005t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0003c0005t0063g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0004c0007t0075g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0004c0007t0076g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0004c0007t0077g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0005c0008t0019g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0005c0008t0019g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0005c0008t0028g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0006c0009t0052g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0007c0012t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0008c0010t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0009c0011t0029g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0010c0017t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| a0011c0015t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0101 | EUR | GBR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00099 | hp2 | a0001 | c0002 | t0006 | g0188 | EUR | GBR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0171 | EUR | GBR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0062 | EUR | GBR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0068 | EUR | FIN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00323 | hp2 | a0001 | c0002 | t0014 | g0225 | EUR | FIN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0094 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00423 | hp1 | a0002 | c0003 | t0021 | g0268 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00438 | hp2 | a0002 | c0003 | t0011 | g0278 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00544 | hp1 | a0002 | c0003 | t0003 | g0269 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00558 | hp1 | a0002 | c0003 | t0003 | g0265 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00597 | hp2 | a0002 | c0003 | t0003 | g0032 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00609 | hp2 | a0002 | c0003 | t0003 | g0032 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00621 | hp1 | a0002 | c0003 | t0033 | g0277 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | CHS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0230 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00735 | hp1 | a0001 | c0001 | t0026 | g0132 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00738 | hp1 | a0002 | c0003 | t0003 | g0033 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00738 | hp2 | a0001 | c0004 | t0002 | g0216 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG00741 | hp2 | a0001 | c0002 | t0013 | g0183 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0169 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01081 | hp2 | a0002 | c0003 | t0003 | g0301 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01106 | hp2 | a0001 | c0002 | t0068 | g0176 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0057 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01167 | hp1 | a0001 | c0001 | t0024 | g0149 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01167 | hp2 | a0001 | c0001 | t0009 | g0003 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01168 | hp1 | a0001 | c0001 | t0009 | g0053 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01168 | hp2 | a0001 | c0001 | t0017 | g0156 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01175 | hp1 | a0001 | c0013 | t0001 | g0164 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01175 | hp2 | a0001 | c0002 | t0006 | g0217 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01192 | hp1 | a0001 | c0001 | t0016 | g0064 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01192 | hp2 | a0001 | c0006 | t0046 | g0142 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01243 | hp1 | a0001 | c0002 | t0006 | g0017 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01243 | hp2 | a0001 | c0004 | t0008 | g0197 | AMR | PUR | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01255 | hp1 | a0001 | c0002 | t0050 | g0165 | AMR | CLM | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | CLM | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01358 | hp1 | a0002 | c0003 | t0003 | g0033 | AMR | CLM | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | CLM | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | CLM | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01361 | hp2 | a0001 | c0001 | t0009 | g0111 | AMR | CLM | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01496 | hp1 | a0001 | c0001 | t0009 | g0091 | AMR | CLM | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01496 | hp2 | a0001 | c0001 | t0027 | g0135 | AMR | CLM | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01515 | hp2 | a0001 | c0002 | t0014 | g0016 | EUR | IBS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0015 | EUR | IBS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0095 | EUR | IBS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0015 | EUR | IBS | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01884 | hp2 | a0001 | c0002 | t0006 | g0179 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0146 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01934 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01943 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0050 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0051 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01952 | hp2 | a0001 | c0002 | t0004 | g0218 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0072 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01975 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01978 | hp1 | a0001 | c0001 | t0025 | g0108 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01978 | hp2 | a0002 | c0003 | t0003 | g0302 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01981 | hp2 | a0002 | c0003 | t0003 | g0008 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01993 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0070 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02004 | hp1 | a0001 | c0001 | t0074 | g0115 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02015 | hp2 | a0003 | c0005 | t0063 | g0090 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02027 | hp2 | a0001 | c0016 | t0008 | g0084 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02055 | hp1 | a0004 | c0007 | t0075 | g0148 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02055 | hp2 | a0001 | c0002 | t0013 | g0180 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02056 | hp1 | a0002 | c0003 | t0030 | g0307 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02071 | hp2 | a0001 | c0002 | t0004 | g0191 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02074 | hp1 | a0002 | c0003 | t0003 | g0294 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02074 | hp2 | a0001 | c0002 | t0004 | g0244 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02080 | hp1 | a0001 | c0002 | t0004 | g0190 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0076 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02132 | hp2 | a0002 | c0003 | t0032 | g0306 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02135 | hp1 | a0001 | c0001 | t0061 | g0093 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02145 | hp1 | a0005 | c0008 | t0019 | g0136 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02145 | hp2 | a0001 | c0004 | t0007 | g0247 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02148 | hp1 | a0001 | c0002 | t0004 | g0187 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CDX | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | CDX | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02257 | hp2 | a0001 | c0004 | t0007 | g0248 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02258 | hp1 | a0001 | c0001 | t0009 | g0104 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02258 | hp2 | a0001 | c0001 | t0018 | g0013 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02273 | hp1 | a0001 | c0002 | t0047 | g0002 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02273 | hp2 | a0002 | c0003 | t0003 | g0008 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02280 | hp1 | a0001 | c0004 | t0040 | g0160 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02280 | hp2 | a0001 | c0004 | t0015 | g0174 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02300 | hp1 | a0002 | c0003 | t0003 | g0008 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02300 | hp2 | a0001 | c0002 | t0004 | g0186 | AMR | PEL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02451 | hp1 | a0001 | c0001 | t0065 | g0153 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02451 | hp2 | a0005 | c0008 | t0028 | g0137 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02523 | hp1 | a0002 | c0003 | t0031 | g0282 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02523 | hp2 | a0001 | c0002 | t0004 | g0020 | EAS | KHV | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02572 | hp1 | a0001 | c0004 | t0002 | g0253 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02572 | hp2 | a0001 | c0001 | t0027 | g0141 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0242 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0144 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0157 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0219 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02647 | hp1 | a0001 | c0002 | t0042 | g0178 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02647 | hp2 | a0001 | c0004 | t0007 | g0249 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0241 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02735 | hp1 | a0001 | c0014 | t0002 | g0073 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02735 | hp2 | a0001 | c0001 | t0009 | g0103 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02809 | hp1 | a0001 | c0006 | t0054 | g0256 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02809 | hp2 | a0001 | c0004 | t0007 | g0006 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02818 | hp1 | a0001 | c0004 | t0007 | g0006 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02818 | hp2 | a0001 | c0002 | t0038 | g0227 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02886 | hp1 | a0006 | c0009 | t0052 | g0254 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02886 | hp2 | a0001 | c0004 | t0007 | g0006 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02895 | hp1 | a0001 | c0004 | t0002 | g0252 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02895 | hp2 | a0001 | c0002 | t0006 | g0026 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02897 | hp2 | a0001 | c0002 | t0044 | g0026 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02922 | hp1 | a0001 | c0001 | t0026 | g0129 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02922 | hp2 | a0001 | c0001 | t0015 | g0112 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0125 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02965 | hp2 | a0001 | c0001 | t0017 | g0154 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02970 | hp1 | a0001 | c0002 | t0006 | g0173 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02970 | hp2 | a0001 | c0001 | t0066 | g0139 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02976 | hp1 | a0004 | c0007 | t0076 | g0158 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02976 | hp2 | a0001 | c0001 | t0067 | g0133 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03041 | hp1 | a0001 | c0002 | t0006 | g0182 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0128 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03098 | hp1 | a0001 | c0001 | t0010 | g0131 | AFR | MSL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03098 | hp2 | a0001 | c0002 | t0006 | g0193 | AFR | MSL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03130 | hp1 | a0001 | c0001 | t0016 | g0110 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0262 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0126 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03139 | hp2 | a0001 | c0001 | t0055 | g0045 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03209 | hp1 | a0001 | c0006 | t0006 | g0258 | AFR | MSL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03209 | hp2 | a0004 | c0007 | t0077 | g0159 | AFR | MSL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0145 | AFR | MSL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0232 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03239 | hp2 | a0001 | c0001 | t0008 | g0061 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0014 | AFR | MSL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03486 | hp2 | a0001 | c0001 | t0059 | g0114 | AFR | MSL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03490 | hp1 | a0007 | c0012 | t0001 | g0167 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03490 | hp2 | a0001 | c0001 | t0009 | g0003 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03516 | hp2 | a0001 | c0001 | t0017 | g0155 | AFR | ESN | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03540 | hp1 | a0001 | c0004 | t0007 | g0250 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03540 | hp2 | a0001 | c0002 | t0051 | g0243 | AFR | GWD | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03579 | hp1 | a0005 | c0008 | t0019 | g0138 | AFR | MSL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | MSL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0206 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03669 | hp2 | a0001 | c0001 | t0064 | g0098 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03688 | hp1 | a0001 | c0001 | t0023 | g0151 | SAS | STU | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0019 | SAS | STU | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0231 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03704 | hp2 | a0001 | c0002 | t0041 | g0223 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0203 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03710 | hp2 | a0001 | c0001 | t0073 | g0117 | SAS | PJL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03834 | hp1 | a0008 | c0010 | t0001 | g0198 | SAS | BEB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | BEB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03942 | hp1 | a0001 | c0001 | t0023 | g0152 | SAS | BEB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0199 | SAS | BEB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0236 | SAS | BEB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | BEB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0200 | SAS | STU | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | STU | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG04204 | hp1 | a0001 | c0001 | t0024 | g0150 | SAS | STU | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG04204 | hp2 | a0001 | c0001 | t0062 | g0096 | SAS | STU | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0140 | AFR | YRI | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0014 | AFR | YRI | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18747 | hp1 | a0002 | c0003 | t0003 | g0304 | EAS | CHB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | CHB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0134 | AFR | YRI | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18906 | hp2 | a0001 | c0004 | t0078 | g0245 | AFR | YRI | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18939 | hp1 | a0002 | c0003 | t0003 | g0287 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0087 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18942 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18942 | hp2 | a0002 | c0003 | t0003 | g0298 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18943 | hp1 | a0002 | c0003 | t0070 | g0035 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18943 | hp2 | a0009 | c0011 | t0029 | g0020 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18946 | hp1 | a0003 | c0005 | t0002 | g0079 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18946 | hp2 | a0002 | c0003 | t0003 | g0295 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18947 | hp1 | a0001 | c0002 | t0022 | g0025 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18947 | hp2 | a0002 | c0003 | t0003 | g0271 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18950 | hp1 | a0003 | c0005 | t0008 | g0083 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18951 | hp2 | a0002 | c0003 | t0071 | g0035 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18952 | hp1 | a0002 | c0003 | t0011 | g0296 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18954 | hp2 | a0010 | c0017 | t0003 | g0285 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18956 | hp1 | a0002 | c0003 | t0069 | g0300 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18957 | hp1 | a0002 | c0003 | t0036 | g0309 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18957 | hp2 | a0001 | c0002 | t0043 | g0018 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18959 | hp2 | a0003 | c0005 | t0002 | g0118 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18960 | hp2 | a0002 | c0003 | t0003 | g0272 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18961 | hp2 | a0002 | c0003 | t0021 | g0280 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18962 | hp1 | a0002 | c0003 | t0003 | g0283 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18964 | hp2 | a0001 | c0002 | t0049 | g0184 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18966 | hp1 | a0002 | c0003 | t0003 | g0034 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18966 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18968 | hp1 | a0001 | c0002 | t0020 | g0220 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18968 | hp2 | a0002 | c0003 | t0003 | g0290 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18969 | hp1 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18969 | hp2 | a0003 | c0005 | t0008 | g0086 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18970 | hp1 | a0001 | c0002 | t0039 | g0004 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18970 | hp2 | a0002 | c0003 | t0003 | g0036 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18971 | hp1 | a0002 | c0003 | t0003 | g0303 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18972 | hp1 | a0002 | c0003 | t0003 | g0299 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18973 | hp1 | a0003 | c0005 | t0002 | g0080 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18974 | hp1 | a0002 | c0003 | t0003 | g0289 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18974 | hp2 | a0003 | c0005 | t0002 | g0082 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18977 | hp1 | a0002 | c0003 | t0003 | g0028 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18978 | hp1 | a0001 | c0002 | t0004 | g0166 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18978 | hp2 | a0002 | c0003 | t0011 | g0266 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18981 | hp2 | a0002 | c0003 | t0034 | g0281 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18983 | hp1 | a0002 | c0003 | t0003 | g0273 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18984 | hp1 | a0002 | c0003 | t0003 | g0286 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18984 | hp2 | a0003 | c0005 | t0008 | g0085 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18985 | hp1 | a0011 | c0015 | t0005 | g0001 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18985 | hp2 | a0002 | c0003 | t0037 | g0027 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18986 | hp2 | a0002 | c0003 | t0035 | g0291 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18988 | hp1 | a0001 | c0002 | t0004 | g0189 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18988 | hp2 | a0002 | c0003 | t0003 | g0308 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18989 | hp1 | a0002 | c0003 | t0003 | g0034 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18991 | hp1 | a0001 | c0002 | t0004 | g0196 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18991 | hp2 | a0002 | c0003 | t0003 | g0274 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18994 | hp1 | a0001 | c0001 | t0025 | g0071 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18994 | hp2 | a0002 | c0003 | t0003 | g0292 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18998 | hp1 | a0001 | c0002 | t0072 | g0222 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18998 | hp2 | a0003 | c0005 | t0008 | g0089 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19000 | hp1 | a0001 | c0001 | t0008 | g0038 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19000 | hp2 | a0002 | c0003 | t0011 | g0263 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19001 | hp1 | a0001 | c0002 | t0045 | g0261 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19001 | hp2 | a0002 | c0003 | t0003 | g0030 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19004 | hp2 | a0002 | c0003 | t0003 | g0276 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19005 | hp1 | a0002 | c0003 | t0003 | g0284 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19007 | hp2 | a0002 | c0003 | t0003 | g0029 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19009 | hp1 | a0001 | c0002 | t0020 | g0208 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19009 | hp2 | a0002 | c0003 | t0003 | g0031 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19010 | hp2 | a0002 | c0003 | t0003 | g0027 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19011 | hp1 | a0002 | c0003 | t0003 | g0028 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19011 | hp2 | a0001 | c0002 | t0004 | g0194 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19030 | hp1 | a0001 | c0004 | t0002 | g0255 | AFR | LWK | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19030 | hp2 | a0001 | c0006 | t0053 | g0257 | AFR | LWK | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0226 | AFR | LWK | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19043 | hp2 | a0001 | c0006 | t0057 | g0259 | AFR | LWK | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19054 | hp1 | a0002 | c0003 | t0003 | g0293 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19054 | hp2 | a0003 | c0005 | t0008 | g0081 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19056 | hp1 | a0002 | c0003 | t0011 | g0297 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19058 | hp1 | a0001 | c0002 | t0048 | g0185 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19058 | hp2 | a0002 | c0003 | t0003 | g0275 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19062 | hp1 | a0001 | c0002 | t0014 | g0214 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19062 | hp2 | a0002 | c0003 | t0003 | g0036 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19063 | hp1 | a0002 | c0003 | t0003 | g0279 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19063 | hp2 | a0001 | c0002 | t0004 | g0170 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19065 | hp1 | a0002 | c0003 | t0003 | g0030 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19066 | hp1 | a0002 | c0003 | t0011 | g0270 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19066 | hp2 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19070 | hp1 | a0002 | c0003 | t0003 | g0305 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19074 | hp2 | a0001 | c0001 | t0060 | g0078 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19076 | hp1 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19077 | hp2 | a0002 | c0003 | t0003 | g0029 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19086 | hp2 | a0002 | c0003 | t0003 | g0031 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19087 | hp1 | a0001 | c0002 | t0004 | g0192 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19090 | hp2 | a0002 | c0003 | t0003 | g0267 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19091 | hp1 | a0001 | c0002 | t0022 | g0025 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA19091 | hp2 | a0002 | c0003 | t0003 | g0288 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA20129 | hp1 | a0001 | c0002 | t0006 | g0017 | AFR | ASW | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ASW | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0201 | EUR | TSI | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA20752 | hp2 | a0001 | c0001 | t0016 | g0067 | EUR | TSI | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02109 | hp1 | a0001 | c0001 | t0018 | g0013 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02109 | hp2 | a0001 | c0004 | t0007 | g0251 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0143 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02486 | hp2 | a0001 | c0006 | t0013 | g0147 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02559 | hp1 | a0001 | c0001 | t0058 | g0056 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03471 | hp1 | a0001 | c0001 | t0018 | g0130 | AFR | MSL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG03471 | hp2 | a0001 | c0002 | t0006 | g0161 | AFR | MSL | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG06807 | hp1 | a0001 | c0001 | t0056 | g0124 | AFR | USA | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| HG06807 | hp2 | a0001 | c0004 | t0007 | g0246 | AFR | USA | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18955 | hp1 | a0002 | c0003 | t0003 | g0264 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA20300 | hp1 | a0001 | c0001 | t0015 | g0113 | AFR | USA | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | USA | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | LWK | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0127 | AFR | LWK | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0055 | REF | REF | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0006 | g0195 | REF | REF | INTU_chr4_127627957_127731737 | INTU | chr4 | 127627957 | 127731737 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:127633138 | T | C | 1 | a0003 | 10 | HG02015.hp2 NA18946.hp1 NA18950.hp1 others(7): Show |
missense_variant | MODERATE | c.104T>C | p.Val35Ala | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/16 | 182/13208 | 104/2829 | 35/942 | chr4 | 127633138 | |||
| chr4:127687741 | A | C | 1 | a0010 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.1323A>C | p.Arg441Ser | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/16 | 1401/13208 | 1323/2829 | 441/942 | chr4 | 127687741 | |||
| chr4:127687752 | C | A | 1 | a0004 | 3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.1334C>A | p.Pro445His | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/16 | 1412/13208 | 1334/2829 | 445/942 | chr4 | 127687752 | |||
| chr4:127687772 | G | A | 1 | a0008 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1354G>A | p.Ala452Thr | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/16 | 1432/13208 | 1354/2829 | 452/942 | chr4 | 127687772 | |||
| chr4:127700013 | G | A | 1 | a0009 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.1453G>A | p.Glu485Lys | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/16 | 1531/13208 | 1453/2829 | 485/942 | chr4 | 127700013 | |||
| chr4:127706578 | A | G | 1 | a0007 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.1880A>G | p.Gln627Arg | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/16 | 1958/13208 | 1880/2829 | 627/942 | chr4 | 127706578 | |||
| chr4:127706772 | T | G | 2 | a0005 a0006 |
4 | HG02145.hp1 HG02451.hp2 HG02886.hp1 others(1): Show |
missense_variant | MODERATE | c.2074T>G | p.Cys692Gly | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/16 | 2152/13208 | 2074/2829 | 692/942 | chr4 | 127706772 | |||
| chr4:127706829 | T | C | 1 | a0005 | 3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.2131T>C | p.Cys711Arg | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/16 | 2209/13208 | 2131/2829 | 711/942 | chr4 | 127706829 | |||
| chr4:127706911 | G | A | 1 | a0011 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.2213G>A | p.Arg738Gln | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/16 | 2291/13208 | 2213/2829 | 738/942 | chr4 | 127706911 | |||
| chr4:127706945 | A | C | 2 | a0002 a0010 |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
missense_variant | MODERATE | c.2247A>C | p.Leu749Phe | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/16 | 2325/13208 | 2247/2829 | 749/942 | chr4 | 127706945 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:127643845 | A | G | 10 | a0001c0001 a0001c0006 a0001c0014 others(7): Show |
217 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
synonymous_variant | LOW | c.471A>G | p.Arg157Arg | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/16 | 549/13208 | 471/2829 | 157/942 | chr4 | 127643845 | |||
| chr4:127663425 | G | A | 11 | a0001c0001 a0001c0004 a0001c0014 others(8): Show |
230 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
synonymous_variant | LOW | c.813G>A | p.Thr271Thr | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/16 | 891/13208 | 813/2829 | 271/942 | chr4 | 127663425 | |||
| chr4:127663506 | C | T | 2 | a0002c0003 a0010c0017 |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
synonymous_variant | LOW | c.894C>T | p.Ile298Ile | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/16 | 972/13208 | 894/2829 | 298/942 | chr4 | 127663506 | |||
| chr4:127687828 | C | G | 1 | a0001c0013 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.1410C>G | p.Leu470Leu | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/16 | 1488/13208 | 1410/2829 | 470/942 | chr4 | 127687828 | |||
| chr4:127706783 | G | A | 1 | a0001c0014 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.2085G>A | p.Thr695Thr | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/16 | 2163/13208 | 2085/2829 | 695/942 | chr4 | 127706783 | |||
| chr4:127716367 | T | C | 1 | a0001c0016 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.2760T>C | p.Cys920Cys | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 2838/13208 | 2760/2829 | 920/942 | chr4 | 127716367 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:127716457 | G | C | 2 | a0005c0008t0019 a0005c0008t0028 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*21G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 21 | chr4 | 127716457 | ||||||
| chr4:127716482 | A | G | 7 | a0001c0001t0007 a0001c0001t0027 a0001c0004t0007 others(4): Show |
16 | HG01496.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*46A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 46 | chr4 | 127716482 | ||||||
| chr4:127716526 | G | C | 1 | a0001c0002t0020 | 2 | NA18968.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*90G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 90 | chr4 | 127716526 | ||||||
| chr4:127716615 | T | A | 2 | a0005c0008t0019 a0005c0008t0028 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*179T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 179 | chr4 | 127716615 | ||||||
| chr4:127716628 | T | C | 1 | a0009c0011t0029 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*192T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 192 | chr4 | 127716628 | ||||||
| chr4:127716730 | G | A | 3 | a0004c0007t0075 a0004c0007t0076 a0004c0007t0077 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*294G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 294 | chr4 | 127716730 | ||||||
| chr4:127716780 | A | G | 2 | a0001c0001t0073 a0001c0001t0074 |
2 | HG02004.hp1 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*344A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 344 | chr4 | 127716780 | ||||||
| chr4:127717083 | A | G | 1 | a0001c0002t0072 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*647A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 647 | chr4 | 127717083 | ||||||
| chr4:127717093 | CA | C | 3 | a0002c0003t0069 a0002c0003t0070 a0002c0003t0071 |
3 | NA18943.hp1 NA18951.hp2 NA18956.hp1 |
3_prime_UTR_variant | MODIFIER | c.*658delA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 658 | chr4 | 127717093 | ||||||
| chr4:127717357 | G | A | 2 | a0005c0008t0019 a0005c0008t0028 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*921G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 921 | chr4 | 127717357 | ||||||
| chr4:127717464 | T | C | 15 | a0002c0003t0003 a0002c0003t0011 a0002c0003t0021 others(12): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1028T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 1028 | chr4 | 127717464 | ||||||
| chr4:127717834 | G | A | 1 | a0001c0002t0038 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1398G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 1398 | chr4 | 127717834 | ||||||
| chr4:127717835 | T | C | 1 | a0001c0002t0039 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1399T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 1399 | chr4 | 127717835 | ||||||
| chr4:127718127 | A | G | 1 | a0001c0002t0068 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1691A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 1691 | chr4 | 127718127 | ||||||
| chr4:127718229 | T | C | 1 | a0001c0004t0040 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1793T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 1793 | chr4 | 127718229 | ||||||
| chr4:127718373 | T | C | 1 | a0002c0003t0030 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1937T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 1937 | chr4 | 127718373 | ||||||
| chr4:127718401 | T | A | 1 | a0001c0004t0078 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1965T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 1965 | chr4 | 127718401 | ||||||
| chr4:127718515 | A | G | 65 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(62): Show |
233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*2079A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 2079 | chr4 | 127718515 | ||||||
| chr4:127718554 | ACT | A | 2 | a0005c0008t0019 a0005c0008t0028 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2121_*2122delCT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 2121 | INFO_REALIGN_3_PRIME | chr4 | 127718554 | |||||
| chr4:127718599 | A | T | 1 | a0002c0003t0037 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2163A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 2163 | chr4 | 127718599 | ||||||
| chr4:127718644 | T | C | 1 | a0001c0002t0041 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2208T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 2208 | chr4 | 127718644 | ||||||
| chr4:127718753 | G | A | 1 | a0002c0003t0031 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2317G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 2317 | chr4 | 127718753 | ||||||
| chr4:127718797 | G | C | 1 | a0006c0009t0052 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2361G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 2361 | chr4 | 127718797 | ||||||
| chr4:127719215 | T | C | 2 | a0005c0008t0019 a0005c0008t0028 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2779T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 2779 | chr4 | 127719215 | ||||||
| chr4:127719245 | G | C | 2 | a0001c0006t0053 a0001c0006t0054 |
2 | HG02809.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2809G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 2809 | chr4 | 127719245 | ||||||
| chr4:127719462 | G | T | 1 | a0001c0001t0018 | 3 | HG02109.hp1 HG02258.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3026G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 3026 | chr4 | 127719462 | ||||||
| chr4:127719477 | C | G | 8 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0018 others(5): Show |
20 | HG00735.hp1 HG01168.hp2 HG02109.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3041C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 3041 | chr4 | 127719477 | ||||||
| chr4:127720083 | T | A | 3 | a0001c0001t0017 a0001c0001t0065 a0001c0001t0066 |
5 | HG01168.hp2 HG02451.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3647T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 3647 | chr4 | 127720083 | ||||||
| chr4:127720402 | G | T | 1 | a0001c0001t0064 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3966G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 3966 | chr4 | 127720402 | ||||||
| chr4:127720477 | G | C | 65 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(62): Show |
233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*4041G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 4041 | chr4 | 127720477 | ||||||
| chr4:127720514 | G | A | 1 | a0001c0001t0055 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4078G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 4078 | chr4 | 127720514 | ||||||
| chr4:127720622 | T | G | 65 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(62): Show |
233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*4186T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 4186 | chr4 | 127720622 | ||||||
| chr4:127720644 | T | A | 1 | a0002c0003t0032 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4208T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 4208 | chr4 | 127720644 | ||||||
| chr4:127721074 | GTGTATTT others(12): Show |
G | 1 | a0001c0001t0056 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4643_*4661delTTTC others(15): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 4643 | INFO_REALIGN_3_PRIME | chr4 | 127721074 | |||||
| chr4:127721090 | T | A | 1 | a0001c0001t0009 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4654T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 4654 | chr4 | 127721090 | ||||||
| chr4:127721099 | C | T | 4 | a0001c0001t0010 a0001c0001t0018 a0001c0001t0026 others(1): Show |
14 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4663C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 4663 | chr4 | 127721099 | ||||||
| chr4:127721468 | G | A | 4 | a0001c0001t0010 a0001c0001t0018 a0001c0001t0026 others(1): Show |
14 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5032G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 5032 | chr4 | 127721468 | ||||||
| chr4:127721492 | T | G | 4 | a0001c0001t0010 a0001c0001t0018 a0001c0001t0026 others(1): Show |
14 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5056T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 5056 | chr4 | 127721492 | ||||||
| chr4:127721507 | G | A | 4 | a0001c0001t0010 a0001c0001t0018 a0001c0001t0026 others(1): Show |
14 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5071G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 5071 | chr4 | 127721507 | ||||||
| chr4:127721825 | G | A | 1 | a0001c0006t0057 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5389G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 5389 | chr4 | 127721825 | ||||||
| chr4:127721933 | C | T | 1 | a0003c0005t0063 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5497C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 5497 | chr4 | 127721933 | ||||||
| chr4:127722149 | C | T | 1 | a0006c0009t0052 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5713C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 5713 | chr4 | 127722149 | ||||||
| chr4:127722185 | A | G | 2 | a0005c0008t0019 a0005c0008t0028 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5749A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 5749 | chr4 | 127722185 | ||||||
| chr4:127722262 | C | T | 7 | a0001c0001t0007 a0001c0001t0027 a0001c0004t0007 others(4): Show |
16 | HG01496.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5826C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 5826 | chr4 | 127722262 | ||||||
| chr4:127722263 | G | A | 4 | a0001c0001t0017 a0001c0001t0065 a0001c0001t0066 others(1): Show |
6 | HG01168.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5827G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 5827 | chr4 | 127722263 | ||||||
| chr4:127722320 | C | T | 1 | a0001c0001t0062 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5884C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 5884 | chr4 | 127722320 | ||||||
| chr4:127722490 | A | G | 1 | a0001c0004t0078 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6054A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 6054 | chr4 | 127722490 | ||||||
| chr4:127722606 | T | C | 2 | a0005c0008t0019 a0005c0008t0028 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6170T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 6170 | chr4 | 127722606 | ||||||
| chr4:127722652 | A | G | 1 | a0002c0003t0036 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6216A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 6216 | chr4 | 127722652 | ||||||
| chr4:127722716 | G | A | 1 | a0001c0001t0065 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6280G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 6280 | chr4 | 127722716 | ||||||
| chr4:127723082 | C | G | 1 | a0001c0001t0017 | 3 | HG01168.hp2 HG02965.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6646C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 6646 | chr4 | 127723082 | ||||||
| chr4:127723168 | C | G | 2 | a0005c0008t0019 a0005c0008t0028 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6732C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 6732 | chr4 | 127723168 | ||||||
| chr4:127723267 | A | G | 1 | a0001c0001t0012 | 4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6831A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 6831 | chr4 | 127723267 | ||||||
| chr4:127723284 | T | C | 2 | a0005c0008t0019 a0005c0008t0028 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6848T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 6848 | chr4 | 127723284 | ||||||
| chr4:127723385 | C | CT | 11 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0016 others(8): Show |
28 | HG00423.hp1 HG00735.hp1 HG01192.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*6968dupT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 6969 | INFO_REALIGN_3_PRIME | chr4 | 127723385 | |||||
| chr4:127723385 | C | CTT | 7 | a0001c0001t0007 a0001c0001t0027 a0001c0004t0007 others(4): Show |
16 | HG01496.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6967_*6968dupTT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 6969 | INFO_REALIGN_3_PRIME | chr4 | 127723385 | |||||
| chr4:127723425 | C | T | 1 | a0001c0004t0040 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6989C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 6989 | chr4 | 127723425 | ||||||
| chr4:127723972 | CA | C | 41 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(38): Show |
141 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*7547delA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 7547 | INFO_REALIGN_3_PRIME | chr4 | 127723972 | |||||
| chr4:127724037 | A | C | 1 | a0001c0002t0049 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7601A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 7601 | chr4 | 127724037 | ||||||
| chr4:127724136 | T | C | 3 | a0001c0001t0015 a0001c0001t0059 a0001c0004t0015 |
4 | HG02280.hp2 HG02922.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7700T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 7700 | chr4 | 127724136 | ||||||
| chr4:127724188 | G | A | 1 | a0001c0002t0042 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7752G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 7752 | chr4 | 127724188 | ||||||
| chr4:127724275 | C | G | 7 | a0001c0001t0058 a0001c0002t0004 a0001c0002t0039 others(4): Show |
28 | HG00621.hp2 HG01934.hp1 HG01943.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*7839C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 7839 | chr4 | 127724275 | ||||||
| chr4:127724414 | C | G | 2 | a0001c0001t0023 a0001c0001t0024 |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7978C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 7978 | chr4 | 127724414 | ||||||
| chr4:127724415 | G | A | 2 | a0001c0002t0043 a0002c0003t0033 |
2 | HG00621.hp1 NA18957.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7979G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 7979 | chr4 | 127724415 | ||||||
| chr4:127724419 | C | CA | 6 | a0001c0001t0005 a0001c0001t0025 a0001c0001t0060 others(3): Show |
22 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*8000dupA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 8001 | INFO_REALIGN_3_PRIME | chr4 | 127724419 | |||||
| chr4:127724435 | A | AT | 13 | a0002c0003t0003 a0002c0003t0011 a0002c0003t0021 others(10): Show |
68 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*7999_*8000insT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 8000 | chr4 | 127724435 | ||||||
| chr4:127724435 | A | T | 2 | a0002c0003t0034 a0002c0003t0071 |
2 | NA18951.hp2 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7999A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 7999 | chr4 | 127724435 | ||||||
| chr4:127724660 | C | T | 1 | a0001c0001t0012 | 4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8224C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 8224 | chr4 | 127724660 | ||||||
| chr4:127724726 | C | T | 1 | a0001c0006t0046 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8290C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 8290 | chr4 | 127724726 | ||||||
| chr4:127724977 | C | T | 11 | a0001c0002t0001 a0001c0002t0014 a0001c0002t0020 others(8): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*8541C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 8541 | chr4 | 127724977 | ||||||
| chr4:127725079 | C | T | 3 | a0001c0001t0007 a0001c0004t0007 a0001c0004t0078 |
11 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8643C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 8643 | chr4 | 127725079 | ||||||
| chr4:127725132 | T | TA | 14 | a0001c0001t0008 a0001c0001t0023 a0001c0001t0025 others(11): Show |
22 | HG00741.hp2 HG01243.hp2 HG01978.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*8721dupA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 8722 | INFO_REALIGN_3_PRIME | chr4 | 127725132 | |||||
| chr4:127725132 | TA | T | 32 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0015 others(29): Show |
105 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*8721delA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 8721 | INFO_REALIGN_3_PRIME | chr4 | 127725132 | |||||
| chr4:127725174 | GCAGGTGC | G | 4 | a0001c0001t0010 a0001c0001t0018 a0001c0001t0026 others(1): Show |
14 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*8740_*8746delAGGT others(3): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 8740 | INFO_REALIGN_3_PRIME | chr4 | 127725174 | |||||
| chr4:127725198 | T | A | 1 | a0001c0001t0060 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8762T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 8762 | chr4 | 127725198 | ||||||
| chr4:127725686 | G | C | 1 | a0001c0001t0067 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9250G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 9250 | chr4 | 127725686 | ||||||
| chr4:127725726 | G | A | 1 | a0001c0001t0065 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9290G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 9290 | chr4 | 127725726 | ||||||
| chr4:127725985 | T | C | 1 | a0006c0009t0052 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9549T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 9549 | chr4 | 127725985 | ||||||
| chr4:127726098 | T | G | 2 | a0005c0008t0019 a0005c0008t0028 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9662T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 9662 | chr4 | 127726098 | ||||||
| chr4:127726363 | T | C | 55 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(52): Show |
210 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*9927T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 9927 | chr4 | 127726363 | ||||||
| chr4:127726578 | T | C | 4 | a0001c0001t0017 a0001c0001t0065 a0001c0001t0066 others(1): Show |
6 | HG01168.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10142T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 16/16 | 10142 | chr4 | 127726578 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:127633249 | G | A | 107 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(104): Show |
118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.146+69G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127633249 | |||||||
| chr4:127633797 | C | T | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.146+617C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127633797 | |||||||
| chr4:127633828 | G | C | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+648G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127633828 | |||||||
| chr4:127633847 | A | G | 1 | a0001c0002t0006g0262 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.146+667A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127633847 | |||||||
| chr4:127634173 | C | T | 2 | a0001c0002t0001g0007 a0001c0002t0045g0261 |
4 | NA18960.hp1 NA19001.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+993C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127634173 | |||||||
| chr4:127634263 | A | G | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.146+1083A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127634263 | |||||||
| chr4:127634314 | T | A | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.146+1134T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127634314 | |||||||
| chr4:127634625 | TA | T | 6 | a0001c0001t0009g0125 a0001c0001t0027g0135 a0001c0001t0056g0124 others(3): Show |
6 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.146+1451delA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127634625 | ||||||
| chr4:127634665 | G | A | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.146+1485G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127634665 | |||||||
| chr4:127634701 | AAAGT | A | 4 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(1): Show |
4 | HG01192.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+1523_146+1526d others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127634701 | ||||||
| chr4:127634869 | C | G | 1 | a0001c0002t0001g0260 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.146+1689C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127634869 | |||||||
| chr4:127635087 | A | C | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.146+1907A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127635087 | |||||||
| chr4:127635092 | G | A | 1 | a0001c0001t0066g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.146+1912G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127635092 | |||||||
| chr4:127635110 | ACTGT | A | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+1931_146+1934d others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127635110 | |||||||
| chr4:127635115 | T | G | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+1935T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127635115 | |||||||
| chr4:127635163 | T | G | 2 | a0001c0006t0053g0257 a0001c0006t0054g0256 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.146+1983T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127635163 | |||||||
| chr4:127635318 | G | A | 2 | a0001c0006t0053g0257 a0001c0006t0054g0256 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.146+2138G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127635318 | |||||||
| chr4:127635761 | T | C | 5 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(2): Show |
5 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.146+2581T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127635761 | |||||||
| chr4:127635805 | T | C | 1 | a0001c0001t0010g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.146+2625T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127635805 | |||||||
| chr4:127636140 | T | C | 196 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(193): Show |
217 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.146+2960T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127636140 | |||||||
| chr4:127636191 | C | T | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+3011C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127636191 | |||||||
| chr4:127636195 | G | A | 8 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0037 others(5): Show |
10 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(7): Show |
intron_variant | MODIFIER | c.146+3015G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127636195 | |||||||
| chr4:127636305 | C | T | 95 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(92): Show |
104 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.146+3125C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127636305 | |||||||
| chr4:127636386 | A | G | 8 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(5): Show |
8 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.146+3206A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127636386 | |||||||
| chr4:127636403 | G | A | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.146+3223G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127636403 | |||||||
| chr4:127636426 | T | C | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.146+3246T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127636426 | |||||||
| chr4:127636453 | A | T | 1 | a0001c0001t0066g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.146+3273A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127636453 | |||||||
| chr4:127636468 | C | G | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+3288C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127636468 | |||||||
| chr4:127636485 | A | G | 209 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(206): Show |
232 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.146+3305A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127636485 | |||||||
| chr4:127636613 | C | CA | 66 | a0001c0001t0027g0135 a0001c0002t0001g0162 a0001c0002t0006g0161 others(63): Show |
76 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.146+3452dupA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127636613 | ||||||
| chr4:127636613 | C | CAA | 13 | a0001c0004t0007g0006 a0001c0004t0007g0246 a0001c0004t0007g0247 others(10): Show |
15 | HG00558.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.146+3451_146+3452d others(4): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127636613 | ||||||
| chr4:127636613 | CA | C | 12 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(9): Show |
12 | HG01192.hp2 HG01258.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.146+3452delA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127636613 | ||||||
| chr4:127636694 | G | A | 1 | a0001c0002t0001g0015 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.146+3514G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127636694 | |||||||
| chr4:127636835 | T | C | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+3655T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127636835 | |||||||
| chr4:127637113 | T | G | 1 | a0002c0003t0021g0268 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.146+3933T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127637113 | |||||||
| chr4:127637221 | T | C | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+4041T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127637221 | |||||||
| chr4:127637252 | C | T | 1 | a0001c0002t0051g0243 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.146+4072C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127637252 | |||||||
| chr4:127637394 | T | A | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+4214T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127637394 | |||||||
| chr4:127637439 | C | T | 1 | a0003c0005t0002g0118 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.146+4259C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127637439 | |||||||
| chr4:127637561 | C | G | 1 | a0001c0004t0002g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.146+4381C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127637561 | |||||||
| chr4:127637759 | G | T | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.146+4579G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127637759 | |||||||
| chr4:127637833 | G | A | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+4653G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127637833 | |||||||
| chr4:127637854 | C | G | 1 | a0001c0002t0001g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.146+4674C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127637854 | |||||||
| chr4:127638248 | G | T | 1 | a0001c0002t0001g0241 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.146+5068G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127638248 | |||||||
| chr4:127638406 | T | G | 2 | a0001c0001t0002g0044 a0001c0001t0055g0045 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.147-5115T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127638406 | |||||||
| chr4:127638748 | C | T | 5 | a0001c0002t0001g0237 a0001c0002t0001g0238 a0001c0002t0001g0239 others(2): Show |
5 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.147-4773C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127638748 | |||||||
| chr4:127638771 | A | G | 1 | a0001c0001t0073g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.147-4750A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127638771 | |||||||
| chr4:127638839 | G | T | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.147-4682G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127638839 | |||||||
| chr4:127638899 | G | A | 8 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(5): Show |
8 | HG01167.hp1 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.147-4622G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127638899 | |||||||
| chr4:127639247 | T | A | 8 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0037 others(5): Show |
10 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(7): Show |
intron_variant | MODIFIER | c.147-4274T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127639247 | |||||||
| chr4:127639310 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.147-4211A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127639310 | |||||||
| chr4:127639433 | A | C | 1 | a0001c0001t0074g0115 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.147-4088A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127639433 | |||||||
| chr4:127639806 | T | C | 116 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(113): Show |
127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.147-3715T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127639806 | |||||||
| chr4:127639920 | T | C | 196 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(193): Show |
217 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.147-3601T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127639920 | |||||||
| chr4:127640216 | T | C | 1 | a0001c0001t0002g0046 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.147-3305T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127640216 | |||||||
| chr4:127640538 | GATAC | G | 3 | a0001c0001t0010g0134 a0001c0001t0026g0132 a0001c0001t0067g0133 |
3 | HG00735.hp1 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.147-2979_147-2976d others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640538 | ||||||
| chr4:127640538 | GATACATA others(7): Show |
G | 1 | a0001c0001t0010g0014 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.147-2979_147-2966d others(16): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640538 | ||||||
| chr4:127640538 | GATACATA others(9): Show |
G | 1 | a0001c0001t0010g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.147-2979_147-2964d others(18): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640538 | ||||||
| chr4:127640538 | GATACATA others(31): Show |
G | 2 | a0001c0001t0018g0013 a0001c0001t0018g0130 |
3 | HG02109.hp1 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.147-2979_147-2942d others(40): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640538 | ||||||
| chr4:127640538 | GATACATA others(37): Show |
G | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.147-2979_147-2936d others(46): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640538 | ||||||
| chr4:127640542 | C | CAT | 10 | a0001c0001t0009g0125 a0001c0001t0059g0114 a0001c0002t0001g0232 others(7): Show |
10 | HG00099.hp2 HG01975.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.147-2931_147-2930d others(4): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | C | CATAT | 6 | a0001c0001t0023g0152 a0001c0002t0004g0005 a0001c0002t0041g0223 others(3): Show |
7 | HG02809.hp1 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.147-2933_147-2930d others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | C | CATATAT | 6 | a0001c0001t0017g0156 a0001c0002t0004g0005 a0001c0002t0004g0218 others(3): Show |
6 | HG00621.hp2 HG01168.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.147-2935_147-2930d others(8): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | C | CATATATA others(1): Show |
7 | a0001c0002t0004g0002 a0001c0002t0004g0005 a0001c0002t0004g0170 others(4): Show |
7 | HG01993.hp1 HG02071.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.147-2937_147-2930d others(10): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | C | CATATATA others(3): Show |
2 | a0001c0002t0001g0007 a0001c0004t0007g0247 |
2 | HG02145.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.147-2939_147-2930d others(12): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | C | CATATATA others(5): Show |
4 | a0001c0002t0001g0007 a0001c0002t0001g0230 a0001c0002t0004g0004 others(1): Show |
4 | HG00639.hp2 NA18964.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-2941_147-2930d others(14): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | C | CATATATA others(7): Show |
1 | a0001c0001t0023g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.147-2943_147-2930d others(16): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | C | CATATATA others(9): Show |
2 | a0001c0002t0001g0007 a0001c0002t0048g0185 |
2 | NA19058.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.147-2945_147-2930d others(18): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | C | CATATATA others(11): Show |
1 | a0001c0002t0039g0004 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.147-2947_147-2930d others(20): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | C | T | 3 | a0001c0001t0002g0043 a0001c0001t0010g0128 a0001c0001t0026g0129 |
3 | HG02922.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.147-2979C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127640542 | |||||||
| chr4:127640542 | CAT | C | 9 | a0001c0002t0001g0200 a0001c0002t0001g0202 a0001c0002t0001g0231 others(6): Show |
9 | HG00639.hp1 HG01515.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.147-2931_147-2930d others(4): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | CATAT | C | 22 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0002t0001g0023 others(19): Show |
25 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.147-2933_147-2930d others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | CATATAT | C | 18 | a0001c0002t0001g0019 a0001c0002t0001g0162 a0001c0002t0001g0175 others(15): Show |
18 | HG00323.hp2 HG01981.hp1 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.147-2935_147-2930d others(8): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | CATATATA others(1): Show |
C | 13 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0021 others(10): Show |
15 | HG01256.hp1 HG01258.hp2 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.147-2937_147-2930d others(10): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | CATATATA others(3): Show |
C | 12 | a0001c0002t0001g0024 a0001c0002t0001g0169 a0001c0002t0001g0177 others(9): Show |
13 | HG00738.hp2 HG01070.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.147-2939_147-2930d others(12): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | CATATATA others(5): Show |
C | 3 | a0001c0002t0001g0229 a0001c0002t0004g0186 a0001c0002t0013g0183 |
3 | HG00741.hp2 HG01361.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.147-2941_147-2930d others(14): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | CATATATA others(7): Show |
C | 1 | a0001c0013t0001g0164 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.147-2943_147-2930d others(16): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | CATATATA others(13): Show |
C | 1 | a0001c0002t0045g0261 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.147-2949_147-2930d others(22): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640542 | CATATATA others(29): Show |
C | 1 | a0001c0002t0001g0234 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.147-2965_147-2930d others(38): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640542 | ||||||
| chr4:127640556 | TATATATA others(29): Show |
T | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.147-2959_147-2924d others(38): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640556 | ||||||
| chr4:127640566 | TATATATA others(19): Show |
T | 5 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.147-2949_147-2924d others(28): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640566 | ||||||
| chr4:127640568 | TATATATA others(17): Show |
T | 1 | a0001c0001t0005g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.147-2947_147-2924d others(26): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640568 | ||||||
| chr4:127640570 | T | C | 1 | a0001c0002t0001g0022 | 2 | NA18948.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.147-2951T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127640570 | |||||||
| chr4:127640570 | TATATATA others(15): Show |
T | 3 | a0001c0001t0065g0153 a0001c0006t0006g0258 a0001c0006t0057g0259 |
3 | HG02451.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.147-2945_147-2924d others(24): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640570 | ||||||
| chr4:127640572 | TATATATA others(13): Show |
T | 2 | a0004c0007t0075g0148 a0004c0007t0076g0158 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.147-2943_147-2924d others(22): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640572 | ||||||
| chr4:127640574 | TATATATA others(11): Show |
T | 6 | a0001c0001t0002g0101 a0001c0001t0009g0111 a0001c0001t0016g0064 others(3): Show |
6 | HG00099.hp1 HG01192.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.147-2941_147-2924d others(20): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640574 | ||||||
| chr4:127640576 | TATATATA others(9): Show |
T | 30 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0044 others(27): Show |
32 | HG00140.hp2 HG00609.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.147-2939_147-2924d others(18): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640576 | ||||||
| chr4:127640578 | TATATATA others(7): Show |
T | 12 | a0001c0001t0002g0065 a0001c0001t0002g0095 a0001c0001t0002g0120 others(9): Show |
12 | HG01258.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.147-2937_147-2924d others(16): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640578 | ||||||
| chr4:127640580 | TATATATA others(5): Show |
T | 12 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0059 others(9): Show |
13 | HG01167.hp2 HG01169.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.147-2935_147-2924d others(14): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640580 | ||||||
| chr4:127640580 | TATATATA others(11): Show |
T | 3 | a0005c0008t0019g0136 a0005c0008t0019g0138 a0005c0008t0028g0137 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.147-2937_147-2920d others(20): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640580 | ||||||
| chr4:127640582 | TATATATA others(3): Show |
T | 10 | a0001c0001t0002g0046 a0001c0001t0002g0068 a0001c0001t0002g0077 others(7): Show |
10 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.147-2933_147-2924d others(12): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640582 | ||||||
| chr4:127640584 | TATATATA others(1): Show |
T | 13 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 others(10): Show |
13 | HG01109.hp1 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.147-2931_147-2924d others(10): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640584 | ||||||
| chr4:127640584 | TATATATA others(7): Show |
T | 1 | a0001c0001t0027g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.147-2933_147-2920d others(16): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640584 | ||||||
| chr4:127640586 | TATATAC | T | 10 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0058 others(7): Show |
12 | HG01074.hp2 HG01081.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-2925_147-2920d others(8): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640586 | ||||||
| chr4:127640588 | TATAC | T | 6 | a0001c0001t0009g0104 a0001c0001t0012g0144 a0001c0001t0017g0154 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.147-2929_147-2926d others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640588 | ||||||
| chr4:127640590 | T | TATATATA others(3): Show |
1 | a0001c0002t0004g0002 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.147-2930_147-2929i others(12): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640590 | ||||||
| chr4:127640590 | TAC | T | 7 | a0001c0001t0002g0037 a0001c0001t0012g0145 a0001c0001t0015g0112 others(4): Show |
7 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.147-2929_147-2928d others(4): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640590 | ||||||
| chr4:127640592 | C | T | 87 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0043 others(84): Show |
100 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.147-2929C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127640592 | |||||||
| chr4:127640592 | CATAT | C | 5 | a0001c0001t0002g0039 a0001c0001t0002g0042 a0001c0001t0002g0109 others(2): Show |
5 | HG00438.hp1 HG00544.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.147-2927_147-2924d others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127640592 | ||||||
| chr4:127640596 | T | C | 75 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(72): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.147-2925T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127640596 | |||||||
| chr4:127640598 | C | T | 4 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0235 others(1): Show |
4 | HG04184.hp1 NA19010.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-2923C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127640598 | |||||||
| chr4:127640674 | A | G | 4 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0001c0002t0001g0231 others(1): Show |
4 | HG00639.hp2 HG01361.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-2847A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127640674 | |||||||
| chr4:127641012 | CCT | C | 196 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(193): Show |
217 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.147-2493_147-2492d others(4): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127641012 | ||||||
| chr4:127641089 | A | G | 1 | a0001c0002t0001g0228 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.147-2432A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127641089 | |||||||
| chr4:127641115 | T | C | 2 | a0001c0006t0053g0257 a0001c0006t0054g0256 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.147-2406T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127641115 | |||||||
| chr4:127641151 | C | A | 6 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(3): Show |
6 | HG01168.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.147-2370C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127641151 | |||||||
| chr4:127641160 | C | T | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.147-2361C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127641160 | |||||||
| chr4:127641240 | A | G | 4 | a0001c0001t0002g0003 a0001c0001t0002g0046 a0001c0001t0009g0003 others(1): Show |
5 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-2281A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127641240 | |||||||
| chr4:127641241 | C | T | 112 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(109): Show |
123 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.147-2280C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127641241 | |||||||
| chr4:127641784 | T | C | 1 | a0001c0002t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.147-1737T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127641784 | |||||||
| chr4:127641977 | T | A | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.147-1544T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127641977 | |||||||
| chr4:127642026 | A | T | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-1495A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127642026 | |||||||
| chr4:127642028 | T | A | 1 | a0001c0013t0001g0164 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.147-1493T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127642028 | |||||||
| chr4:127642051 | TTAAG | T | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.147-1466_147-1463d others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 127642051 | ||||||
| chr4:127642336 | G | A | 1 | a0001c0002t0050g0165 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.147-1185G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127642336 | |||||||
| chr4:127642417 | T | A | 1 | a0001c0002t0004g0166 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.147-1104T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127642417 | |||||||
| chr4:127642508 | A | G | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.147-1013A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127642508 | |||||||
| chr4:127642782 | T | G | 1 | a0001c0001t0009g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.147-739T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127642782 | |||||||
| chr4:127642786 | T | C | 8 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(5): Show |
8 | HG01167.hp1 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.147-735T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127642786 | |||||||
| chr4:127642930 | T | G | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.147-591T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127642930 | |||||||
| chr4:127642983 | A | C | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-538A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127642983 | |||||||
| chr4:127643211 | T | C | 8 | a0001c0004t0007g0006 a0001c0004t0007g0246 a0001c0004t0007g0247 others(5): Show |
10 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.147-310T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127643211 | |||||||
| chr4:127643447 | C | T | 1 | a0001c0002t0038g0227 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147-74C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 1/15 | chr4 | 127643447 | |||||||
| chr4:127644211 | G | T | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.682+155G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127644211 | |||||||
| chr4:127644263 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.682+207T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127644263 | |||||||
| chr4:127644816 | G | A | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+760G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127644816 | |||||||
| chr4:127644882 | A | G | 1 | a0001c0004t0002g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.682+826A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127644882 | |||||||
| chr4:127645058 | G | T | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.682+1002G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127645058 | |||||||
| chr4:127645152 | T | C | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+1096T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127645152 | |||||||
| chr4:127645456 | A | T | 1 | a0001c0001t0056g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.682+1400A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127645456 | |||||||
| chr4:127645524 | ATTG | A | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.682+1477_682+1479d others(5): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 127645524 | ||||||
| chr4:127645844 | G | A | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.682+1788G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127645844 | |||||||
| chr4:127645878 | T | C | 1 | a0001c0001t0002g0059 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.682+1822T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127645878 | |||||||
| chr4:127645897 | G | A | 6 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0002t0001g0168 others(3): Show |
7 | HG00735.hp2 HG01074.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+1841G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127645897 | |||||||
| chr4:127645908 | C | T | 2 | a0001c0002t0001g0240 a0001c0002t0006g0262 |
2 | HG03130.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.682+1852C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127645908 | |||||||
| chr4:127646011 | C | T | 3 | a0001c0001t0012g0144 a0001c0001t0012g0145 a0001c0001t0012g0146 |
3 | HG01891.hp2 HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.682+1955C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127646011 | |||||||
| chr4:127646081 | G | A | 1 | a0002c0003t0003g0269 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.682+2025G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127646081 | |||||||
| chr4:127646114 | G | A | 1 | a0001c0002t0001g0169 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.682+2058G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127646114 | |||||||
| chr4:127646139 | G | A | 8 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(5): Show |
8 | HG01167.hp1 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+2083G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127646139 | |||||||
| chr4:127646169 | A | G | 8 | a0001c0001t0009g0057 a0001c0001t0009g0111 a0001c0001t0009g0125 others(5): Show |
8 | HG01109.hp1 HG01361.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+2113A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127646169 | |||||||
| chr4:127646184 | C | CA | 168 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(165): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.682+2145dupA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 127646184 | ||||||
| chr4:127646184 | C | CAAAA | 7 | a0001c0001t0023g0151 a0001c0001t0024g0149 a0001c0001t0024g0150 others(4): Show |
7 | HG01167.hp1 HG02809.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+2142_682+2145d others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 127646184 | ||||||
| chr4:127646184 | CA | C | 15 | a0001c0001t0027g0141 a0001c0002t0001g0169 a0001c0002t0001g0224 others(12): Show |
17 | HG00323.hp2 HG01070.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.682+2145delA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 127646184 | ||||||
| chr4:127646551 | T | G | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+2495T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127646551 | |||||||
| chr4:127646589 | A | G | 198 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(195): Show |
219 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.682+2533A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127646589 | |||||||
| chr4:127646804 | C | T | 1 | a0001c0004t0002g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.682+2748C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127646804 | |||||||
| chr4:127646862 | T | C | 1 | a0001c0004t0002g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.682+2806T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127646862 | |||||||
| chr4:127647066 | T | A | 4 | a0001c0004t0007g0006 a0001c0004t0007g0246 a0001c0004t0007g0247 others(1): Show |
6 | HG02145.hp2 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+3010T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127647066 | |||||||
| chr4:127647638 | A | G | 6 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(3): Show |
6 | HG01168.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.682+3582A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127647638 | |||||||
| chr4:127647754 | A | G | 3 | a0002c0003t0003g0008 a0002c0003t0003g0301 a0002c0003t0003g0302 |
5 | HG01081.hp2 HG01978.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+3698A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127647754 | |||||||
| chr4:127647782 | C | A | 6 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(3): Show |
6 | HG01168.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.682+3726C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127647782 | |||||||
| chr4:127647811 | C | T | 1 | a0001c0002t0041g0223 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.682+3755C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127647811 | |||||||
| chr4:127647870 | T | C | 2 | a0001c0002t0006g0017 a0001c0002t0006g0173 |
3 | HG01243.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.682+3814T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127647870 | |||||||
| chr4:127647952 | C | CAT | 209 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(206): Show |
232 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.682+3897_682+3898d others(4): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 127647952 | ||||||
| chr4:127648749 | C | T | 96 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(93): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.682+4693C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127648749 | |||||||
| chr4:127648768 | A | G | 7 | a0002c0003t0003g0298 a0002c0003t0003g0299 a0002c0003t0011g0296 others(4): Show |
7 | NA18942.hp2 NA18943.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.682+4712A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127648768 | |||||||
| chr4:127649084 | GA | G | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+5035delA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 127649084 | ||||||
| chr4:127649137 | C | T | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.682+5081C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127649137 | |||||||
| chr4:127649253 | G | A | 11 | a0001c0004t0002g0252 a0001c0004t0002g0253 a0001c0004t0002g0255 others(8): Show |
13 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.682+5197G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127649253 | |||||||
| chr4:127649341 | A | C | 11 | a0001c0004t0002g0252 a0001c0004t0002g0253 a0001c0004t0002g0255 others(8): Show |
13 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.682+5285A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127649341 | |||||||
| chr4:127649446 | C | T | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.682+5390C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127649446 | |||||||
| chr4:127649509 | A | AT | 12 | a0001c0004t0002g0252 a0001c0004t0002g0253 a0001c0004t0002g0255 others(9): Show |
14 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.682+5466dupT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 127649509 | ||||||
| chr4:127649524 | A | G | 1 | a0002c0003t0021g0268 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.682+5468A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127649524 | |||||||
| chr4:127649658 | A | G | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.682+5602A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127649658 | |||||||
| chr4:127650035 | T | G | 1 | a0001c0004t0015g0174 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.682+5979T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650035 | |||||||
| chr4:127650105 | A | G | 2 | a0001c0006t0053g0257 a0001c0006t0054g0256 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.682+6049A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650105 | |||||||
| chr4:127650193 | G | C | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+6137G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650193 | |||||||
| chr4:127650367 | TC | T | 9 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(6): Show |
11 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.683-6263delC | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 127650367 | ||||||
| chr4:127650372 | C | A | 1 | a0001c0004t0002g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.683-6264C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650372 | |||||||
| chr4:127650373 | C | T | 2 | a0001c0001t0010g0131 a0001c0001t0010g0134 |
2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-6263C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650373 | |||||||
| chr4:127650374 | T | C | 2 | a0001c0001t0010g0131 a0001c0001t0010g0134 |
2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-6262T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650374 | |||||||
| chr4:127650385 | C | A | 1 | a0001c0001t0005g0060 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.683-6251C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650385 | |||||||
| chr4:127650439 | C | G | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-6197C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650439 | |||||||
| chr4:127650452 | C | A | 3 | a0001c0002t0001g0018 a0001c0002t0001g0224 a0001c0002t0043g0018 |
3 | NA18940.hp1 NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.683-6184C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650452 | |||||||
| chr4:127650456 | G | T | 3 | a0001c0002t0001g0018 a0001c0002t0001g0224 a0001c0002t0043g0018 |
3 | NA18940.hp1 NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.683-6180G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650456 | |||||||
| chr4:127650485 | G | C | 1 | a0001c0002t0001g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.683-6151G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650485 | |||||||
| chr4:127650541 | C | G | 1 | a0002c0003t0003g0295 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.683-6095C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650541 | |||||||
| chr4:127650555 | A | T | 1 | a0001c0006t0057g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.683-6081A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650555 | |||||||
| chr4:127650760 | G | C | 1 | a0001c0002t0001g0175 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.683-5876G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650760 | |||||||
| chr4:127650840 | G | A | 1 | a0001c0002t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.683-5796G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650840 | |||||||
| chr4:127650856 | A | G | 2 | a0001c0001t0002g0010 a0001c0001t0008g0038 |
3 | NA18951.hp1 NA18986.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.683-5780A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650856 | |||||||
| chr4:127650879 | C | T | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG00099.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.683-5757C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650879 | |||||||
| chr4:127650891 | C | T | 4 | a0001c0001t0016g0110 a0001c0002t0006g0026 a0001c0002t0044g0026 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-5745C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650891 | |||||||
| chr4:127650893 | G | A | 2 | a0001c0001t0016g0110 a0001c0002t0072g0222 |
2 | HG03130.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.683-5743G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650893 | |||||||
| chr4:127650907 | G | T | 4 | a0001c0001t0002g0097 a0001c0001t0002g0099 a0001c0001t0062g0096 others(1): Show |
4 | HG01070.hp1 HG02148.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-5729G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650907 | |||||||
| chr4:127650939 | T | A | 1 | a0001c0001t0002g0059 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.683-5697T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650939 | |||||||
| chr4:127650941 | T | A | 1 | a0001c0001t0008g0061 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.683-5695T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650941 | |||||||
| chr4:127650997 | T | C | 1 | a0001c0001t0058g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.683-5639T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127650997 | |||||||
| chr4:127651073 | T | G | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-5563T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651073 | |||||||
| chr4:127651226 | G | C | 1 | a0001c0004t0002g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.683-5410G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651226 | |||||||
| chr4:127651294 | G | A | 193 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(190): Show |
214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.683-5342G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651294 | |||||||
| chr4:127651336 | GT | G | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-5295delT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 127651336 | ||||||
| chr4:127651404 | A | G | 1 | a0001c0002t0001g0168 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.683-5232A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651404 | |||||||
| chr4:127651422 | C | G | 193 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(190): Show |
214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.683-5214C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651422 | |||||||
| chr4:127651473 | G | A | 1 | a0001c0002t0001g0019 | 2 | HG02004.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.683-5163G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651473 | |||||||
| chr4:127651572 | A | T | 1 | a0001c0001t0010g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.683-5064A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651572 | |||||||
| chr4:127651584 | G | C | 1 | a0001c0002t0068g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.683-5052G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651584 | |||||||
| chr4:127651660 | A | C | 2 | a0001c0002t0001g0241 a0006c0009t0052g0254 |
2 | HG02698.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.683-4976A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651660 | |||||||
| chr4:127651688 | C | A | 1 | a0001c0001t0002g0062 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.683-4948C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651688 | |||||||
| chr4:127651699 | C | T | 1 | a0001c0001t0056g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.683-4937C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651699 | |||||||
| chr4:127651726 | C | T | 14 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(11): Show |
14 | HG01168.hp2 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.683-4910C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651726 | |||||||
| chr4:127651760 | T | G | 14 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(11): Show |
14 | HG01168.hp2 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.683-4876T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651760 | |||||||
| chr4:127651762 | A | T | 11 | a0001c0004t0002g0252 a0001c0004t0002g0253 a0001c0004t0002g0255 others(8): Show |
13 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.683-4874A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651762 | |||||||
| chr4:127651773 | T | G | 14 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(11): Show |
14 | HG01168.hp2 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.683-4863T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651773 | |||||||
| chr4:127651791 | T | A | 1 | a0001c0001t0012g0143 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.683-4845T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651791 | |||||||
| chr4:127651835 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.683-4801T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127651835 | |||||||
| chr4:127652040 | G | C | 8 | a0001c0001t0009g0057 a0001c0001t0009g0111 a0001c0001t0009g0125 others(5): Show |
8 | HG01109.hp1 HG01361.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-4596G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652040 | |||||||
| chr4:127652084 | T | C | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-4552T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652084 | |||||||
| chr4:127652100 | C | G | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-4536C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652100 | |||||||
| chr4:127652127 | A | G | 1 | a0001c0001t0066g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.683-4509A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652127 | |||||||
| chr4:127652278 | C | G | 8 | a0001c0001t0009g0057 a0001c0001t0009g0111 a0001c0001t0009g0125 others(5): Show |
8 | HG01109.hp1 HG01361.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-4358C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652278 | |||||||
| chr4:127652278 | C | T | 1 | a0001c0002t0001g0260 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.683-4358C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652278 | |||||||
| chr4:127652364 | A | C | 2 | a0002c0003t0003g0269 a0002c0003t0003g0294 |
2 | HG00544.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.683-4272A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652364 | |||||||
| chr4:127652369 | G | A | 1 | a0001c0002t0001g0229 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.683-4267G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652369 | |||||||
| chr4:127652385 | A | G | 2 | a0001c0001t0010g0140 a0001c0001t0027g0141 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.683-4251A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652385 | |||||||
| chr4:127652389 | C | T | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.683-4247C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652389 | |||||||
| chr4:127652390 | G | A | 3 | a0002c0003t0003g0008 a0002c0003t0003g0301 a0002c0003t0003g0302 |
5 | HG01081.hp2 HG01978.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-4246G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652390 | |||||||
| chr4:127652422 | T | C | 107 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(104): Show |
118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.683-4214T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652422 | |||||||
| chr4:127652432 | G | C | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-4204G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652432 | |||||||
| chr4:127652462 | G | A | 95 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(92): Show |
104 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.683-4174G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652462 | |||||||
| chr4:127652493 | C | A | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-4143C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652493 | |||||||
| chr4:127652535 | A | G | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-4101A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652535 | |||||||
| chr4:127652539 | A | G | 107 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(104): Show |
118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.683-4097A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652539 | |||||||
| chr4:127652547 | A | C | 6 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(3): Show |
6 | HG01168.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-4089A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652547 | |||||||
| chr4:127652553 | G | C | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-4083G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652553 | |||||||
| chr4:127652605 | C | G | 3 | a0005c0008t0019g0136 a0005c0008t0019g0138 a0005c0008t0028g0137 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.683-4031C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652605 | |||||||
| chr4:127652617 | T | G | 108 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(105): Show |
119 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.683-4019T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652617 | |||||||
| chr4:127652768 | A | G | 6 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(3): Show |
6 | HG01168.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-3868A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652768 | |||||||
| chr4:127652960 | A | G | 67 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(64): Show |
77 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.683-3676A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127652960 | |||||||
| chr4:127653007 | G | A | 5 | a0001c0001t0008g0061 a0001c0001t0023g0151 a0001c0001t0023g0152 others(2): Show |
5 | HG01167.hp1 HG03239.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-3629G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653007 | |||||||
| chr4:127653033 | T | C | 1 | a0001c0001t0010g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.683-3603T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653033 | |||||||
| chr4:127653045 | T | A | 1 | a0001c0001t0010g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.683-3591T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653045 | |||||||
| chr4:127653054 | A | G | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-3582A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653054 | |||||||
| chr4:127653070 | T | C | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-3566T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653070 | |||||||
| chr4:127653207 | G | T | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-3429G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653207 | |||||||
| chr4:127653222 | T | G | 1 | a0007c0012t0001g0167 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.683-3414T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653222 | |||||||
| chr4:127653253 | A | C | 128 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(125): Show |
139 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.683-3383A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653253 | |||||||
| chr4:127653396 | C | T | 1 | a0001c0001t0055g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.683-3240C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653396 | |||||||
| chr4:127653397 | G | A | 1 | a0001c0002t0072g0222 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.683-3239G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653397 | |||||||
| chr4:127653407 | T | G | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-3229T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653407 | |||||||
| chr4:127653496 | G | T | 1 | a0001c0002t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.683-3140G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653496 | |||||||
| chr4:127653569 | G | A | 1 | a0002c0003t0003g0271 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.683-3067G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653569 | |||||||
| chr4:127653621 | T | C | 3 | a0001c0002t0001g0169 a0001c0002t0001g0177 a0001c0002t0068g0176 |
3 | HG01070.hp2 HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.683-3015T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653621 | |||||||
| chr4:127653636 | T | C | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.683-3000T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653636 | |||||||
| chr4:127653642 | C | G | 65 | a0001c0002t0020g0220 a0001c0006t0013g0147 a0002c0003t0003g0008 others(62): Show |
75 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.683-2994C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653642 | |||||||
| chr4:127653740 | A | G | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-2896A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653740 | |||||||
| chr4:127653800 | C | T | 2 | a0001c0006t0053g0257 a0001c0006t0054g0256 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.683-2836C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653800 | |||||||
| chr4:127653907 | C | T | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-2729C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653907 | |||||||
| chr4:127653966 | C | A | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-2670C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127653966 | |||||||
| chr4:127654005 | T | G | 1 | a0001c0002t0072g0222 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.683-2631T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654005 | |||||||
| chr4:127654032 | C | G | 14 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(11): Show |
14 | HG01168.hp2 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.683-2604C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654032 | |||||||
| chr4:127654148 | C | T | 1 | a0001c0002t0072g0222 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.683-2488C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654148 | |||||||
| chr4:127654158 | G | T | 2 | a0001c0001t0002g0044 a0001c0001t0055g0045 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.683-2478G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654158 | |||||||
| chr4:127654161 | C | G | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-2475C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654161 | |||||||
| chr4:127654200 | C | T | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-2436C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654200 | |||||||
| chr4:127654275 | C | T | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.683-2361C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654275 | |||||||
| chr4:127654280 | G | T | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.683-2356G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654280 | |||||||
| chr4:127654289 | C | T | 1 | a0001c0002t0022g0025 | 2 | NA18947.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.683-2347C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654289 | |||||||
| chr4:127654290 | G | A | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-2346G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654290 | |||||||
| chr4:127654362 | G | A | 5 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(2): Show |
5 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-2274G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654362 | |||||||
| chr4:127654483 | G | T | 8 | a0001c0001t0009g0057 a0001c0001t0009g0111 a0001c0001t0009g0125 others(5): Show |
8 | HG01109.hp1 HG01361.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-2153G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654483 | |||||||
| chr4:127654564 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.683-2072G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654564 | |||||||
| chr4:127654589 | C | G | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-2047C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654589 | |||||||
| chr4:127654619 | A | T | 5 | a0001c0001t0002g0012 a0001c0001t0002g0063 a0001c0001t0002g0095 others(2): Show |
6 | HG00741.hp1 HG01258.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-2017A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654619 | |||||||
| chr4:127654629 | G | A | 4 | a0001c0002t0006g0179 a0001c0002t0013g0180 a0001c0002t0038g0227 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-2007G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654629 | |||||||
| chr4:127654672 | A | C | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-1964A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654672 | |||||||
| chr4:127654717 | C | T | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.683-1919C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654717 | |||||||
| chr4:127654736 | C | G | 10 | a0001c0001t0002g0042 a0001c0002t0001g0219 a0001c0002t0006g0026 others(7): Show |
10 | HG00438.hp1 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-1900C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654736 | |||||||
| chr4:127654915 | C | T | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-1721C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654915 | |||||||
| chr4:127654917 | C | T | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-1719C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654917 | |||||||
| chr4:127654918 | A | G | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-1718A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654918 | |||||||
| chr4:127654955 | C | T | 8 | a0001c0004t0007g0006 a0001c0004t0007g0246 a0001c0004t0007g0247 others(5): Show |
10 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-1681C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654955 | |||||||
| chr4:127654991 | A | G | 1 | a0004c0007t0077g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.683-1645A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127654991 | |||||||
| chr4:127655010 | T | C | 1 | a0001c0002t0001g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.683-1626T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655010 | |||||||
| chr4:127655131 | T | A | 1 | a0001c0002t0006g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.683-1505T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655131 | |||||||
| chr4:127655176 | T | C | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-1460T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655176 | |||||||
| chr4:127655195 | C | G | 114 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(111): Show |
125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.683-1441C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655195 | |||||||
| chr4:127655199 | G | A | 2 | a0001c0001t0010g0140 a0001c0001t0027g0141 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.683-1437G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655199 | |||||||
| chr4:127655223 | C | T | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-1413C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655223 | |||||||
| chr4:127655313 | T | G | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.683-1323T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655313 | |||||||
| chr4:127655391 | A | G | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.683-1245A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655391 | |||||||
| chr4:127655393 | G | T | 1 | a0001c0002t0004g0218 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.683-1243G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655393 | |||||||
| chr4:127655400 | T | C | 8 | a0001c0004t0007g0006 a0001c0004t0007g0246 a0001c0004t0007g0247 others(5): Show |
10 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-1236T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655400 | |||||||
| chr4:127655406 | G | A | 8 | a0001c0004t0007g0006 a0001c0004t0007g0246 a0001c0004t0007g0247 others(5): Show |
10 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-1230G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655406 | |||||||
| chr4:127655420 | T | G | 8 | a0001c0004t0007g0006 a0001c0004t0007g0246 a0001c0004t0007g0247 others(5): Show |
10 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-1216T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655420 | |||||||
| chr4:127655441 | A | C | 10 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(7): Show |
10 | HG01168.hp2 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-1195A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655441 | |||||||
| chr4:127655441 | A | T | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-1195A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655441 | |||||||
| chr4:127655445 | T | A | 209 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(206): Show |
232 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.683-1191T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655445 | |||||||
| chr4:127655447 | T | G | 9 | a0001c0001t0016g0064 a0001c0004t0007g0006 a0001c0004t0007g0246 others(6): Show |
11 | HG01192.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.683-1189T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655447 | |||||||
| chr4:127655474 | A | G | 3 | a0001c0002t0006g0179 a0001c0002t0013g0180 a0001c0002t0042g0178 |
3 | HG01884.hp2 HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.683-1162A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655474 | |||||||
| chr4:127655477 | C | G | 3 | a0001c0002t0006g0179 a0001c0002t0013g0180 a0001c0002t0042g0178 |
3 | HG01884.hp2 HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.683-1159C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655477 | |||||||
| chr4:127655497 | G | C | 1 | a0001c0002t0001g0233 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.683-1139G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655497 | |||||||
| chr4:127655499 | T | G | 5 | a0001c0002t0001g0016 a0001c0002t0001g0168 a0001c0002t0001g0233 others(2): Show |
5 | HG00735.hp2 HG01074.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-1137T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655499 | |||||||
| chr4:127655508 | G | A | 190 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(187): Show |
211 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.683-1128G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655508 | |||||||
| chr4:127655577 | C | T | 5 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(2): Show |
5 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-1059C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655577 | |||||||
| chr4:127655578 | A | G | 24 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(21): Show |
28 | HG00735.hp1 HG01192.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.683-1058A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655578 | |||||||
| chr4:127655590 | C | G | 1 | a0001c0001t0002g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.683-1046C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655590 | |||||||
| chr4:127655597 | C | T | 1 | a0001c0002t0006g0217 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.683-1039C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655597 | |||||||
| chr4:127655598 | G | C | 5 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(2): Show |
5 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-1038G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655598 | |||||||
| chr4:127655618 | C | T | 1 | a0001c0002t0001g0024 | 2 | NA18939.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.683-1018C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655618 | |||||||
| chr4:127655638 | G | T | 1 | a0001c0002t0001g0024 | 2 | NA18939.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.683-998G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655638 | |||||||
| chr4:127655757 | G | T | 2 | a0002c0003t0003g0036 a0002c0003t0003g0292 |
3 | NA18970.hp2 NA18994.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.683-879G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655757 | |||||||
| chr4:127655763 | TC | T | 2 | a0002c0003t0003g0036 a0002c0003t0003g0292 |
3 | NA18970.hp2 NA18994.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.683-871delC | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 127655763 | ||||||
| chr4:127655766 | T | C | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.683-870T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655766 | |||||||
| chr4:127655774 | A | T | 2 | a0002c0003t0003g0036 a0002c0003t0003g0292 |
3 | NA18970.hp2 NA18994.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.683-862A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655774 | |||||||
| chr4:127655789 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.683-847A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655789 | |||||||
| chr4:127655803 | G | C | 5 | a0001c0001t0002g0099 a0001c0006t0006g0258 a0001c0006t0053g0257 others(2): Show |
5 | HG01070.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-833G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655803 | |||||||
| chr4:127655803 | G | T | 1 | a0001c0002t0038g0227 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.683-833G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655803 | |||||||
| chr4:127655807 | C | G | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-829C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655807 | |||||||
| chr4:127655811 | C | T | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.683-825C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655811 | |||||||
| chr4:127655825 | G | A | 1 | a0001c0002t0038g0227 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.683-811G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655825 | |||||||
| chr4:127655831 | G | A | 2 | a0001c0001t0010g0140 a0001c0001t0027g0141 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.683-805G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655831 | |||||||
| chr4:127655831 | G | C | 2 | a0001c0001t0010g0127 a0001c0001t0026g0132 |
2 | HG00735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.683-805G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655831 | |||||||
| chr4:127655853 | T | A | 1 | a0001c0001t0002g0065 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.683-783T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655853 | |||||||
| chr4:127655870 | G | T | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-766G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655870 | |||||||
| chr4:127655871 | C | G | 2 | a0001c0001t0015g0113 a0001c0001t0059g0114 |
2 | HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.683-765C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655871 | |||||||
| chr4:127655881 | T | A | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-755T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655881 | |||||||
| chr4:127655883 | G | A | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-753G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655883 | |||||||
| chr4:127655886 | G | T | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-750G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655886 | |||||||
| chr4:127655891 | A | C | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-745A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655891 | |||||||
| chr4:127655892 | C | T | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-744C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655892 | |||||||
| chr4:127655893 | C | G | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-743C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655893 | |||||||
| chr4:127655907 | G | C | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-729G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655907 | |||||||
| chr4:127655908 | C | G | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-728C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655908 | |||||||
| chr4:127655917 | A | G | 48 | a0001c0001t0002g0011 a0001c0001t0002g0052 a0001c0001t0002g0054 others(45): Show |
53 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.683-719A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655917 | |||||||
| chr4:127655922 | G | C | 6 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(3): Show |
6 | HG01168.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-714G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655922 | |||||||
| chr4:127655929 | G | A | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-707G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655929 | |||||||
| chr4:127655930 | C | T | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-706C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655930 | |||||||
| chr4:127655932 | G | A | 2 | a0002c0003t0003g0272 a0002c0003t0003g0273 |
2 | NA18960.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.683-704G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655932 | |||||||
| chr4:127655932 | G | GT | 4 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-698dupT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 127655932 | ||||||
| chr4:127655935 | T | G | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-701T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655935 | |||||||
| chr4:127655937 | T | A | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-699T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655937 | |||||||
| chr4:127655941 | A | C | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-695A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655941 | |||||||
| chr4:127655942 | C | CGTCGCGA others(9): Show |
1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-694_683-693ins others(16): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655942 | |||||||
| chr4:127655947 | C | T | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-689C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655947 | |||||||
| chr4:127655948 | C | T | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.683-688C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655948 | |||||||
| chr4:127655952 | A | C | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-684A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655952 | |||||||
| chr4:127655952 | A | T | 107 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(104): Show |
118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.683-684A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655952 | |||||||
| chr4:127655955 | C | T | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-681C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655955 | |||||||
| chr4:127655956 | G | T | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-680G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655956 | |||||||
| chr4:127655964 | C | T | 1 | a0002c0003t0035g0291 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.683-672C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655964 | |||||||
| chr4:127655969 | G | A | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-667G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655969 | |||||||
| chr4:127655993 | C | T | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.683-643C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655993 | |||||||
| chr4:127655998 | G | A | 8 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0012g0143 others(5): Show |
8 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-638G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127655998 | |||||||
| chr4:127656003 | C | G | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-633C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656003 | |||||||
| chr4:127656004 | C | T | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-632C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656004 | |||||||
| chr4:127656008 | T | C | 1 | a0002c0003t0011g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.683-628T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656008 | |||||||
| chr4:127656017 | C | T | 1 | a0001c0006t0046g0142 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.683-619C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656017 | |||||||
| chr4:127656041 | T | C | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.683-595T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656041 | |||||||
| chr4:127656061 | A | G | 3 | a0001c0001t0005g0092 a0001c0001t0005g0094 a0001c0001t0061g0093 |
3 | HG00408.hp1 HG02135.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.683-575A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656061 | |||||||
| chr4:127656116 | ACTGT | A | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.683-516_683-513del others(4): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 127656116 | ||||||
| chr4:127656119 | G | C | 1 | a0001c0004t0002g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.683-517G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656119 | |||||||
| chr4:127656218 | T | G | 4 | a0002c0003t0003g0027 a0002c0003t0003g0274 a0002c0003t0003g0303 others(1): Show |
4 | NA18971.hp1 NA18985.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-418T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656218 | |||||||
| chr4:127656228 | T | C | 209 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(206): Show |
232 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.683-408T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656228 | |||||||
| chr4:127656274 | G | A | 4 | a0001c0002t0001g0016 a0001c0002t0001g0168 a0001c0002t0014g0016 others(1): Show |
4 | HG00735.hp2 HG01074.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-362G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656274 | |||||||
| chr4:127656284 | G | A | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-352G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656284 | |||||||
| chr4:127656387 | T | G | 1 | a0002c0003t0003g0028 | 2 | NA18977.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.683-249T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656387 | |||||||
| chr4:127656435 | T | G | 1 | a0001c0002t0013g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.683-201T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656435 | |||||||
| chr4:127656479 | A | G | 1 | a0001c0001t0002g0049 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.683-157A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656479 | |||||||
| chr4:127656488 | T | C | 2 | a0001c0002t0006g0026 a0001c0002t0044g0026 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.683-148T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656488 | |||||||
| chr4:127656530 | C | G | 1 | a0002c0003t0003g0290 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.683-106C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656530 | |||||||
| chr4:127656620 | G | C | 2 | a0001c0001t0010g0140 a0001c0001t0027g0141 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.683-16G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 2/15 | chr4 | 127656620 | |||||||
| chr4:127656788 | T | C | 1 | a0001c0001t0009g0111 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.768+67T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127656788 | |||||||
| chr4:127656917 | A | T | 68 | a0001c0002t0001g0007 a0001c0002t0001g0015 a0001c0002t0001g0016 others(65): Show |
77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.768+196A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127656917 | |||||||
| chr4:127656937 | C | A | 1 | a0001c0001t0002g0059 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.768+216C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127656937 | |||||||
| chr4:127656947 | C | G | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.768+226C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127656947 | |||||||
| chr4:127657016 | T | C | 1 | a0001c0004t0008g0197 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.768+295T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127657016 | |||||||
| chr4:127657069 | C | T | 1 | a0001c0002t0013g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.768+348C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127657069 | |||||||
| chr4:127657312 | G | A | 107 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(104): Show |
118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.768+591G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127657312 | |||||||
| chr4:127657438 | T | C | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.768+717T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127657438 | |||||||
| chr4:127657476 | G | C | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.768+755G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127657476 | |||||||
| chr4:127657579 | C | T | 1 | a0001c0001t0002g0011 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.768+858C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127657579 | |||||||
| chr4:127657585 | C | T | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.768+864C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127657585 | |||||||
| chr4:127657696 | C | T | 2 | a0001c0001t0002g0062 a0001c0001t0002g0116 |
2 | HG00140.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.768+975C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127657696 | |||||||
| chr4:127657785 | G | A | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.768+1064G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127657785 | |||||||
| chr4:127657814 | T | A | 1 | a0001c0001t0010g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.768+1093T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127657814 | |||||||
| chr4:127657937 | C | T | 6 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(3): Show |
6 | HG01168.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.768+1216C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127657937 | |||||||
| chr4:127658317 | C | CGAGATG | 95 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(92): Show |
104 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.768+1610_768+1615d others(8): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr4 | 127658317 | ||||||
| chr4:127658453 | G | A | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.768+1732G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127658453 | |||||||
| chr4:127658455 | G | A | 1 | a0008c0010t0001g0198 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.768+1734G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127658455 | |||||||
| chr4:127658546 | G | A | 1 | a0001c0001t0016g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.768+1825G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127658546 | |||||||
| chr4:127658852 | C | T | 1 | a0001c0001t0066g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.768+2131C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127658852 | |||||||
| chr4:127658916 | G | A | 1 | a0001c0002t0049g0184 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.768+2195G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127658916 | |||||||
| chr4:127658917 | C | T | 1 | a0001c0002t0049g0184 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.768+2196C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127658917 | |||||||
| chr4:127658918 | T | C | 1 | a0001c0002t0049g0184 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.768+2197T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127658918 | |||||||
| chr4:127658922 | A | T | 1 | a0001c0002t0049g0184 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.768+2201A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127658922 | |||||||
| chr4:127658978 | A | G | 2 | a0001c0002t0006g0026 a0001c0002t0044g0026 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.768+2257A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127658978 | |||||||
| chr4:127659195 | C | CT | 3 | a0005c0008t0019g0136 a0005c0008t0019g0138 a0005c0008t0028g0137 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.768+2475dupT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr4 | 127659195 | ||||||
| chr4:127659222 | G | A | 12 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(9): Show |
14 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.768+2501G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127659222 | |||||||
| chr4:127659345 | G | T | 1 | a0001c0002t0049g0184 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.768+2624G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127659345 | |||||||
| chr4:127659619 | C | A | 1 | a0001c0001t0009g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.768+2898C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127659619 | |||||||
| chr4:127659668 | G | A | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.768+2947G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127659668 | |||||||
| chr4:127659896 | T | C | 1 | a0001c0002t0001g0260 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.768+3175T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127659896 | |||||||
| chr4:127659920 | C | T | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.768+3199C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127659920 | |||||||
| chr4:127659945 | C | A | 14 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(11): Show |
14 | HG01168.hp2 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.768+3224C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127659945 | |||||||
| chr4:127660092 | C | G | 4 | a0001c0001t0002g0003 a0001c0001t0002g0046 a0001c0001t0009g0003 others(1): Show |
5 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.769-3289C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127660092 | |||||||
| chr4:127660139 | G | C | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.769-3242G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127660139 | |||||||
| chr4:127660148 | T | A | 1 | a0001c0001t0005g0092 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.769-3233T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127660148 | |||||||
| chr4:127660290 | G | A | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.769-3091G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127660290 | |||||||
| chr4:127660328 | A | C | 1 | a0001c0002t0004g0196 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.769-3053A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127660328 | |||||||
| chr4:127660378 | A | G | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.769-3003A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127660378 | |||||||
| chr4:127660442 | A | G | 1 | a0001c0001t0059g0114 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.769-2939A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127660442 | |||||||
| chr4:127660702 | G | A | 4 | a0001c0006t0006g0258 a0001c0006t0053g0257 a0001c0006t0054g0256 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.769-2679G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127660702 | |||||||
| chr4:127661053 | A | T | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.769-2328A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127661053 | |||||||
| chr4:127661123 | A | T | 1 | a0001c0001t0010g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.769-2258A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127661123 | |||||||
| chr4:127661141 | G | A | 2 | a0001c0001t0010g0140 a0001c0001t0027g0141 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.769-2240G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127661141 | |||||||
| chr4:127661329 | G | T | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.769-2052G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127661329 | |||||||
| chr4:127661388 | T | TATCTTTT others(1): Show |
6 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.769-1992_769-1991i others(10): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr4 | 127661388 | ||||||
| chr4:127661569 | A | G | 1 | a0004c0007t0075g0148 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.769-1812A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127661569 | |||||||
| chr4:127661644 | A | G | 6 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0002t0001g0168 others(3): Show |
7 | HG00735.hp2 HG01074.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.769-1737A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127661644 | |||||||
| chr4:127661748 | C | A | 2 | a0001c0004t0002g0252 a0001c0004t0002g0253 |
2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.769-1633C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127661748 | |||||||
| chr4:127661785 | G | A | 1 | a0008c0010t0001g0198 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.769-1596G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127661785 | |||||||
| chr4:127661850 | T | C | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.769-1531T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127661850 | |||||||
| chr4:127662389 | G | A | 2 | a0001c0001t0018g0013 a0001c0001t0018g0130 |
3 | HG02109.hp1 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.769-992G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127662389 | |||||||
| chr4:127662483 | C | T | 1 | a0001c0002t0050g0165 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.769-898C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127662483 | |||||||
| chr4:127662496 | G | T | 6 | a0002c0003t0003g0267 a0002c0003t0003g0272 a0002c0003t0003g0273 others(3): Show |
6 | NA18939.hp1 NA18960.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.769-885G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127662496 | |||||||
| chr4:127662691 | G | A | 2 | a0001c0004t0002g0226 a0001c0004t0002g0255 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.769-690G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127662691 | |||||||
| chr4:127662778 | A | T | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.769-603A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127662778 | |||||||
| chr4:127663076 | T | C | 1 | a0001c0001t0065g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.769-305T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127663076 | |||||||
| chr4:127663145 | A | G | 2 | a0002c0003t0003g0034 a0002c0003t0011g0266 |
3 | NA18966.hp1 NA18978.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.769-236A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127663145 | |||||||
| chr4:127663349 | G | A | 58 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(55): Show |
68 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.769-32G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 3/15 | chr4 | 127663349 | |||||||
| chr4:127664060 | A | G | 99 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(96): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.972+476A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127664060 | |||||||
| chr4:127664268 | A | G | 2 | a0001c0002t0001g0023 a0001c0002t0001g0215 |
3 | NA18956.hp2 NA18959.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.972+684A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127664268 | |||||||
| chr4:127664290 | G | A | 6 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(3): Show |
6 | HG01168.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.972+706G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127664290 | |||||||
| chr4:127664315 | G | C | 1 | a0001c0001t0061g0093 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.972+731G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127664315 | |||||||
| chr4:127664335 | G | A | 1 | a0001c0001t0005g0092 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.972+751G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127664335 | |||||||
| chr4:127664367 | C | A | 10 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(7): Show |
10 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.972+783C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127664367 | |||||||
| chr4:127664426 | T | C | 6 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.972+842T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127664426 | |||||||
| chr4:127664726 | C | A | 1 | a0001c0001t0027g0141 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.972+1142C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127664726 | |||||||
| chr4:127664984 | A | C | 14 | a0002c0003t0003g0027 a0002c0003t0003g0028 a0002c0003t0003g0032 others(11): Show |
17 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.972+1400A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127664984 | |||||||
| chr4:127665086 | T | C | 207 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(204): Show |
230 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.972+1502T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127665086 | |||||||
| chr4:127665330 | T | A | 1 | a0001c0002t0022g0025 | 2 | NA18947.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.972+1746T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127665330 | |||||||
| chr4:127665464 | A | G | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.972+1880A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127665464 | |||||||
| chr4:127665467 | C | A | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.972+1883C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127665467 | |||||||
| chr4:127665498 | C | A | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.972+1914C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127665498 | |||||||
| chr4:127665697 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.972+2113T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127665697 | |||||||
| chr4:127665924 | C | T | 1 | a0001c0002t0041g0223 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.972+2340C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127665924 | |||||||
| chr4:127665972 | A | C | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.972+2388A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127665972 | |||||||
| chr4:127666076 | T | C | 1 | a0001c0002t0001g0230 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.972+2492T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127666076 | |||||||
| chr4:127666195 | G | C | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.972+2611G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127666195 | |||||||
| chr4:127666204 | G | A | 6 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(3): Show |
6 | HG01168.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.972+2620G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127666204 | |||||||
| chr4:127666207 | C | G | 6 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.972+2623C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127666207 | |||||||
| chr4:127666208 | G | A | 12 | a0001c0004t0002g0226 a0001c0004t0002g0252 a0001c0004t0002g0253 others(9): Show |
14 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.972+2624G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127666208 | |||||||
| chr4:127666301 | T | A | 6 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.972+2717T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127666301 | |||||||
| chr4:127666324 | C | G | 6 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.973-2712C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127666324 | |||||||
| chr4:127666561 | G | A | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.973-2475G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127666561 | |||||||
| chr4:127666747 | G | A | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.973-2289G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127666747 | |||||||
| chr4:127666819 | A | C | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-2217A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127666819 | |||||||
| chr4:127666915 | A | C | 7 | a0002c0003t0003g0298 a0002c0003t0003g0299 a0002c0003t0011g0296 others(4): Show |
7 | NA18942.hp2 NA18943.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.973-2121A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127666915 | |||||||
| chr4:127666969 | A | T | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-2067A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127666969 | |||||||
| chr4:127667103 | A | C | 179 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(176): Show |
198 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.973-1933A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127667103 | |||||||
| chr4:127667235 | TTCTG | T | 2 | a0001c0001t0002g0010 a0001c0001t0008g0038 |
3 | NA18951.hp1 NA18986.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.973-1795_973-1792d others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 127667235 | ||||||
| chr4:127667372 | G | A | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.973-1664G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127667372 | |||||||
| chr4:127667540 | G | T | 6 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.973-1496G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127667540 | |||||||
| chr4:127667582 | A | T | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.973-1454A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127667582 | |||||||
| chr4:127667709 | A | G | 1 | a0001c0001t0018g0130 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.973-1327A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127667709 | |||||||
| chr4:127667955 | G | A | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.973-1081G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127667955 | |||||||
| chr4:127668239 | C | T | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.973-797C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127668239 | |||||||
| chr4:127668317 | A | G | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.973-719A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127668317 | |||||||
| chr4:127668425 | C | T | 1 | a0001c0002t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.973-611C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127668425 | |||||||
| chr4:127668451 | G | T | 1 | a0002c0003t0003g0283 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.973-585G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127668451 | |||||||
| chr4:127668531 | G | A | 1 | a0001c0002t0020g0220 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.973-505G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127668531 | |||||||
| chr4:127668534 | G | C | 6 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.973-502G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127668534 | |||||||
| chr4:127668607 | A | G | 98 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(95): Show |
107 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.973-429A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127668607 | |||||||
| chr4:127668651 | A | G | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-385A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127668651 | |||||||
| chr4:127668845 | G | A | 2 | a0002c0003t0003g0275 a0002c0003t0003g0276 |
2 | NA19004.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.973-191G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 4/15 | chr4 | 127668845 | |||||||
| chr4:127669219 | T | C | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091+65T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127669219 | |||||||
| chr4:127669249 | A | G | 12 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(9): Show |
14 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1091+95A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127669249 | |||||||
| chr4:127669322 | A | G | 6 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091+168A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127669322 | |||||||
| chr4:127669474 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1091+320A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127669474 | |||||||
| chr4:127669847 | G | A | 211 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(208): Show |
234 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.1091+693G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127669847 | |||||||
| chr4:127669925 | G | A | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1091+771G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127669925 | |||||||
| chr4:127670047 | A | G | 31 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(28): Show |
37 | HG00408.hp2 HG00597.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1091+893A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127670047 | |||||||
| chr4:127670132 | A | G | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091+978A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127670132 | |||||||
| chr4:127670389 | G | A | 1 | a0001c0001t0067g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1091+1235G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127670389 | |||||||
| chr4:127670421 | G | T | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1091+1267G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127670421 | |||||||
| chr4:127670602 | G | C | 28 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(25): Show |
32 | HG00735.hp1 HG01167.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1091+1448G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127670602 | |||||||
| chr4:127671027 | A | T | 1 | a0001c0002t0013g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1091+1873A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127671027 | |||||||
| chr4:127671119 | T | C | 1 | a0001c0004t0002g0252 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1091+1965T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127671119 | |||||||
| chr4:127671550 | A | G | 1 | a0001c0001t0002g0102 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1091+2396A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127671550 | |||||||
| chr4:127671586 | A | G | 99 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(96): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1091+2432A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127671586 | |||||||
| chr4:127671626 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1091+2472G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127671626 | |||||||
| chr4:127671756 | G | A | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1092-2368G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127671756 | |||||||
| chr4:127671973 | G | A | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092-2151G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127671973 | |||||||
| chr4:127672007 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1092-2117G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127672007 | |||||||
| chr4:127672011 | G | A | 7 | a0001c0001t0010g0127 a0001c0001t0010g0128 a0001c0001t0010g0131 others(4): Show |
8 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1092-2113G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127672011 | |||||||
| chr4:127672096 | A | G | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092-2028A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127672096 | |||||||
| chr4:127672467 | CT | C | 296 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(293): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1092-1641delT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 127672467 | ||||||
| chr4:127672467 | CTT | C | 7 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1092-1642_1092-164 others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 127672467 | ||||||
| chr4:127672555 | G | A | 5 | a0001c0002t0001g0171 a0001c0002t0001g0181 a0001c0002t0001g0199 others(2): Show |
5 | HG00140.hp1 HG02630.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092-1569G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127672555 | |||||||
| chr4:127672650 | T | C | 6 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-1474T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127672650 | |||||||
| chr4:127672663 | T | A | 12 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(9): Show |
14 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1092-1461T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127672663 | |||||||
| chr4:127672685 | C | T | 3 | a0001c0006t0053g0257 a0001c0006t0054g0256 a0001c0006t0057g0259 |
3 | HG02809.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1092-1439C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127672685 | |||||||
| chr4:127672696 | T | C | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1092-1428T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127672696 | |||||||
| chr4:127672706 | A | G | 100 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(97): Show |
110 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1092-1418A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127672706 | |||||||
| chr4:127672962 | C | T | 1 | a0001c0002t0001g0162 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1092-1162C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127672962 | |||||||
| chr4:127672987 | C | T | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092-1137C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127672987 | |||||||
| chr4:127673191 | T | C | 6 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-933T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127673191 | |||||||
| chr4:127673325 | G | A | 6 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-799G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127673325 | |||||||
| chr4:127673325 | G | C | 1 | a0001c0002t0001g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1092-799G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127673325 | |||||||
| chr4:127673348 | A | AT | 19 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(16): Show |
21 | HG01168.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1092-758dupT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 127673348 | ||||||
| chr4:127673348 | AT | A | 16 | a0001c0001t0005g0050 a0001c0001t0005g0070 a0001c0001t0005g0072 others(13): Show |
16 | HG01070.hp2 HG01167.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1092-758delT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 127673348 | ||||||
| chr4:127673366 | T | C | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1092-758T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127673366 | |||||||
| chr4:127673535 | G | A | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092-589G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127673535 | |||||||
| chr4:127673542 | A | G | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1092-582A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127673542 | |||||||
| chr4:127673550 | C | G | 4 | a0001c0001t0007g0157 a0001c0001t0017g0154 a0001c0001t0017g0155 others(1): Show |
4 | HG01168.hp2 HG02630.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092-574C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127673550 | |||||||
| chr4:127673865 | A | G | 110 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(107): Show |
119 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1092-259A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127673865 | |||||||
| chr4:127673921 | G | GT | 13 | a0001c0002t0001g0022 a0001c0004t0002g0226 a0001c0004t0002g0252 others(10): Show |
16 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1092-191dupT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 127673921 | ||||||
| chr4:127673975 | G | A | 17 | a0001c0001t0002g0077 a0001c0001t0005g0001 a0001c0001t0005g0050 others(14): Show |
21 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.1092-149G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | chr4 | 127673975 | |||||||
| chr4:127674099 | T | TTATTTTG others(2): Show |
3 | a0001c0001t0010g0014 a0001c0001t0026g0129 a0001c0001t0067g0133 |
4 | HG02922.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092-21_1092-13dup others(9): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 127674099 | ||||||
| chr4:127674263 | T | G | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1181+50T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127674263 | |||||||
| chr4:127674575 | G | T | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181+362G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127674575 | |||||||
| chr4:127674596 | C | T | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+383C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127674596 | |||||||
| chr4:127674921 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181+708G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127674921 | |||||||
| chr4:127674995 | A | G | 3 | a0001c0006t0053g0257 a0001c0006t0054g0256 a0001c0006t0057g0259 |
3 | HG02809.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1181+782A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127674995 | |||||||
| chr4:127675031 | A | G | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1181+818A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127675031 | |||||||
| chr4:127675034 | A | G | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02559.hp2 HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1181+821A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127675034 | |||||||
| chr4:127675076 | A | G | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1181+863A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127675076 | |||||||
| chr4:127675347 | G | A | 3 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 |
3 | HG01168.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1181+1134G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127675347 | |||||||
| chr4:127675443 | C | T | 210 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(207): Show |
233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1181+1230C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127675443 | |||||||
| chr4:127675495 | A | C | 1 | a0001c0002t0001g0023 | 2 | NA18956.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1181+1282A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127675495 | |||||||
| chr4:127675640 | T | C | 5 | a0001c0002t0004g0002 a0001c0002t0004g0186 a0001c0002t0004g0187 others(2): Show |
8 | HG01934.hp1 HG01943.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181+1427T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127675640 | |||||||
| chr4:127675793 | G | A | 4 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+1580G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127675793 | |||||||
| chr4:127675880 | T | C | 6 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(3): Show |
6 | HG01168.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181+1667T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127675880 | |||||||
| chr4:127675896 | G | A | 1 | a0001c0002t0001g0209 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1181+1683G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127675896 | |||||||
| chr4:127676147 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181+1934G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676147 | |||||||
| chr4:127676361 | G | A | 1 | a0001c0002t0013g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1181+2148G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676361 | |||||||
| chr4:127676440 | G | T | 1 | a0001c0002t0068g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1181+2227G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676440 | |||||||
| chr4:127676449 | A | G | 1 | a0003c0005t0063g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1181+2236A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676449 | |||||||
| chr4:127676476 | C | A | 15 | a0001c0001t0007g0157 a0001c0001t0010g0140 a0001c0001t0027g0141 others(12): Show |
17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1181+2263C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676476 | |||||||
| chr4:127676532 | G | A | 102 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(99): Show |
111 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1181+2319G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676532 | |||||||
| chr4:127676585 | C | CA | 10 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(7): Show |
10 | HG01168.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+2387dupA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 127676585 | ||||||
| chr4:127676600 | AG | A | 89 | a0001c0001t0002g0068 a0001c0001t0005g0001 a0001c0001t0005g0087 others(86): Show |
101 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1181+2388delG | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676600 | |||||||
| chr4:127676601 | G | A | 120 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(117): Show |
130 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1181+2388G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676601 | |||||||
| chr4:127676603 | G | A | 124 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(121): Show |
135 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1181+2390G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676603 | |||||||
| chr4:127676605 | G | A | 5 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(2): Show |
5 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181+2392G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676605 | |||||||
| chr4:127676630 | G | A | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1181+2417G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676630 | |||||||
| chr4:127676638 | A | C | 1 | a0001c0002t0001g0207 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1181+2425A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676638 | |||||||
| chr4:127676857 | G | A | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181+2644G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676857 | |||||||
| chr4:127676905 | G | A | 2 | a0001c0004t0002g0252 a0001c0004t0002g0253 |
2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1181+2692G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676905 | |||||||
| chr4:127676952 | G | T | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+2739G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676952 | |||||||
| chr4:127676956 | A | C | 3 | a0001c0006t0053g0257 a0001c0006t0054g0256 a0001c0006t0057g0259 |
3 | HG02809.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1181+2743A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676956 | |||||||
| chr4:127676974 | C | T | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181+2761C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676974 | |||||||
| chr4:127676988 | C | T | 99 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(96): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1181+2775C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127676988 | |||||||
| chr4:127677094 | G | A | 10 | a0001c0001t0009g0057 a0001c0001t0009g0104 a0001c0001t0009g0111 others(7): Show |
10 | HG01109.hp1 HG01361.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+2881G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677094 | |||||||
| chr4:127677200 | A | G | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1181+2987A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677200 | |||||||
| chr4:127677262 | T | C | 1 | a0001c0001t0009g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1181+3049T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677262 | |||||||
| chr4:127677297 | C | T | 1 | a0001c0002t0001g0240 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1181+3084C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677297 | |||||||
| chr4:127677307 | T | C | 17 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(14): Show |
19 | HG00735.hp1 HG01168.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1181+3094T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677307 | |||||||
| chr4:127677313 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1181+3100A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677313 | |||||||
| chr4:127677326 | G | A | 1 | a0001c0001t0009g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1181+3113G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677326 | |||||||
| chr4:127677352 | C | T | 10 | a0001c0001t0009g0057 a0001c0001t0009g0104 a0001c0001t0009g0111 others(7): Show |
10 | HG01109.hp1 HG01361.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+3139C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677352 | |||||||
| chr4:127677355 | T | C | 11 | a0001c0001t0009g0057 a0001c0001t0009g0104 a0001c0001t0009g0111 others(8): Show |
11 | HG00099.hp2 HG01109.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1181+3142T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677355 | |||||||
| chr4:127677361 | C | A | 10 | a0001c0001t0009g0057 a0001c0001t0009g0104 a0001c0001t0009g0111 others(7): Show |
10 | HG01109.hp1 HG01361.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+3148C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677361 | |||||||
| chr4:127677363 | G | C | 11 | a0001c0001t0009g0057 a0001c0001t0009g0104 a0001c0001t0009g0111 others(8): Show |
11 | HG00099.hp2 HG01109.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1181+3150G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677363 | |||||||
| chr4:127677375 | A | G | 1 | a0001c0001t0066g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1181+3162A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677375 | |||||||
| chr4:127677379 | A | G | 10 | a0001c0001t0009g0057 a0001c0001t0009g0104 a0001c0001t0009g0111 others(7): Show |
10 | HG01109.hp1 HG01361.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+3166A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677379 | |||||||
| chr4:127677386 | TACTCCTC others(120): Show |
T | 10 | a0001c0001t0009g0057 a0001c0001t0009g0104 a0001c0001t0009g0111 others(7): Show |
10 | HG01109.hp1 HG01361.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+3179_1181+330 others(4): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 127677386 | ||||||
| chr4:127677434 | G | A | 2 | a0001c0006t0053g0257 a0001c0006t0054g0256 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1181+3221G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677434 | |||||||
| chr4:127677443 | G | A | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1181+3230G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677443 | |||||||
| chr4:127677515 | C | T | 10 | a0001c0001t0009g0057 a0001c0001t0009g0104 a0001c0001t0009g0111 others(7): Show |
10 | HG01109.hp1 HG01361.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+3302C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677515 | |||||||
| chr4:127677540 | C | A | 10 | a0001c0001t0009g0057 a0001c0001t0009g0104 a0001c0001t0009g0111 others(7): Show |
10 | HG01109.hp1 HG01361.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+3327C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677540 | |||||||
| chr4:127677603 | A | G | 1 | a0001c0002t0001g0240 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1181+3390A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677603 | |||||||
| chr4:127677691 | T | C | 210 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(207): Show |
233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1181+3478T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677691 | |||||||
| chr4:127677708 | A | C | 1 | a0001c0002t0001g0015 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1181+3495A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677708 | |||||||
| chr4:127677726 | C | A | 1 | a0001c0006t0054g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1181+3513C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677726 | |||||||
| chr4:127677732 | C | T | 1 | a0001c0002t0006g0262 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1181+3519C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677732 | |||||||
| chr4:127677742 | C | A | 5 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(2): Show |
5 | HG01168.hp2 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181+3529C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677742 | |||||||
| chr4:127677865 | T | A | 15 | a0001c0001t0007g0157 a0001c0001t0010g0140 a0001c0001t0027g0141 others(12): Show |
17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1181+3652T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677865 | |||||||
| chr4:127677936 | G | A | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181+3723G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677936 | |||||||
| chr4:127677962 | T | C | 1 | a0004c0007t0077g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1181+3749T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127677962 | |||||||
| chr4:127678130 | G | T | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181+3917G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678130 | |||||||
| chr4:127678234 | T | G | 5 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(2): Show |
5 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181+4021T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678234 | |||||||
| chr4:127678251 | C | T | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181+4038C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678251 | |||||||
| chr4:127678300 | C | T | 1 | a0001c0002t0038g0227 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1181+4087C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678300 | |||||||
| chr4:127678315 | T | G | 3 | a0001c0002t0001g0241 a0004c0007t0075g0148 a0004c0007t0076g0158 |
3 | HG02055.hp1 HG02698.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1181+4102T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678315 | |||||||
| chr4:127678358 | C | T | 1 | a0001c0002t0001g0229 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1181+4145C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678358 | |||||||
| chr4:127678405 | G | A | 1 | a0001c0001t0010g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1181+4192G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678405 | |||||||
| chr4:127678419 | A | C | 9 | a0001c0001t0007g0157 a0001c0004t0007g0006 a0001c0004t0007g0246 others(6): Show |
11 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1181+4206A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678419 | |||||||
| chr4:127678432 | C | G | 16 | a0001c0001t0007g0157 a0001c0001t0010g0140 a0001c0001t0027g0141 others(13): Show |
18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1181+4219C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678432 | |||||||
| chr4:127678442 | A | G | 1 | a0001c0001t0010g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1181+4229A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678442 | |||||||
| chr4:127678589 | C | T | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1181+4376C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678589 | |||||||
| chr4:127678603 | A | G | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1181+4390A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678603 | |||||||
| chr4:127678631 | C | T | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+4418C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678631 | |||||||
| chr4:127678697 | C | T | 2 | a0001c0001t0010g0140 a0001c0001t0027g0141 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1181+4484C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678697 | |||||||
| chr4:127678773 | C | G | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1181+4560C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678773 | |||||||
| chr4:127678864 | G | A | 1 | a0001c0001t0009g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1181+4651G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678864 | |||||||
| chr4:127678884 | T | C | 1 | a0001c0001t0065g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1181+4671T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678884 | |||||||
| chr4:127678941 | G | A | 2 | a0001c0001t0010g0140 a0001c0001t0027g0141 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1181+4728G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127678941 | |||||||
| chr4:127679022 | G | T | 1 | a0001c0001t0027g0141 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1181+4809G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679022 | |||||||
| chr4:127679046 | G | T | 3 | a0005c0008t0019g0136 a0005c0008t0019g0138 a0005c0008t0028g0137 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1181+4833G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679046 | |||||||
| chr4:127679050 | T | G | 5 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(2): Show |
5 | HG01168.hp2 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181+4837T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679050 | |||||||
| chr4:127679053 | C | G | 58 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(55): Show |
68 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1181+4840C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679053 | |||||||
| chr4:127679082 | G | A | 1 | a0002c0003t0003g0272 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1181+4869G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679082 | |||||||
| chr4:127679179 | C | T | 4 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0235 others(1): Show |
4 | HG04184.hp1 NA19010.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1181+4966C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679179 | |||||||
| chr4:127679273 | T | C | 15 | a0001c0001t0007g0157 a0001c0001t0010g0140 a0001c0001t0027g0141 others(12): Show |
17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1181+5060T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679273 | |||||||
| chr4:127679331 | A | G | 4 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182-5078A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679331 | |||||||
| chr4:127679352 | A | G | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1182-5057A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679352 | |||||||
| chr4:127679381 | A | G | 1 | a0003c0005t0008g0089 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1182-5028A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679381 | |||||||
| chr4:127679460 | C | T | 2 | a0001c0002t0006g0188 a0001c0002t0006g0217 |
2 | HG00099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1182-4949C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679460 | |||||||
| chr4:127679461 | G | A | 2 | a0002c0003t0003g0036 a0002c0003t0003g0292 |
3 | NA18970.hp2 NA18994.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1182-4948G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679461 | |||||||
| chr4:127679555 | C | T | 1 | a0001c0001t0010g0014 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1182-4854C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679555 | |||||||
| chr4:127679716 | A | T | 8 | a0002c0003t0003g0027 a0002c0003t0003g0033 a0002c0003t0003g0264 others(5): Show |
9 | HG00558.hp1 HG00738.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1182-4693A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679716 | |||||||
| chr4:127679873 | T | A | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1182-4536T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679873 | |||||||
| chr4:127679898 | G | A | 4 | a0001c0001t0016g0110 a0004c0007t0075g0148 a0004c0007t0076g0158 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182-4511G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127679898 | |||||||
| chr4:127680076 | G | C | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182-4333G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680076 | |||||||
| chr4:127680116 | C | T | 102 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(99): Show |
111 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1182-4293C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680116 | |||||||
| chr4:127680243 | A | G | 6 | a0001c0002t0001g0018 a0001c0002t0001g0024 a0001c0002t0001g0224 others(3): Show |
7 | NA18939.hp2 NA18940.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1182-4166A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680243 | |||||||
| chr4:127680331 | T | C | 6 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0002t0001g0168 others(3): Show |
7 | HG00735.hp2 HG01074.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1182-4078T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680331 | |||||||
| chr4:127680334 | A | C | 1 | a0001c0013t0001g0164 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1182-4075A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680334 | |||||||
| chr4:127680453 | T | C | 184 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(181): Show |
205 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.1182-3956T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680453 | |||||||
| chr4:127680549 | C | T | 4 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182-3860C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680549 | |||||||
| chr4:127680603 | C | T | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1182-3806C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680603 | |||||||
| chr4:127680607 | A | AAAT | 184 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(181): Show |
205 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.1182-3799_1182-379 others(7): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 127680607 | ||||||
| chr4:127680640 | A | C | 1 | a0001c0002t0004g0187 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1182-3769A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680640 | |||||||
| chr4:127680716 | G | A | 6 | a0001c0001t0002g0059 a0001c0001t0010g0140 a0001c0001t0027g0141 others(3): Show |
8 | HG00738.hp1 HG01358.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1182-3693G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680716 | |||||||
| chr4:127680716 | G | C | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182-3693G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680716 | |||||||
| chr4:127680781 | G | T | 1 | a0001c0001t0018g0130 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1182-3628G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680781 | |||||||
| chr4:127680802 | A | C | 2 | a0001c0001t0018g0013 a0001c0001t0018g0130 |
3 | HG02109.hp1 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1182-3607A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680802 | |||||||
| chr4:127680834 | A | C | 1 | a0001c0004t0007g0251 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1182-3575A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680834 | |||||||
| chr4:127680867 | T | A | 5 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(2): Show |
5 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-3542T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127680867 | |||||||
| chr4:127681101 | G | A | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1182-3308G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681101 | |||||||
| chr4:127681158 | A | G | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1182-3251A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681158 | |||||||
| chr4:127681232 | C | T | 102 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(99): Show |
111 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1182-3177C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681232 | |||||||
| chr4:127681264 | A | T | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1182-3145A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681264 | |||||||
| chr4:127681290 | G | A | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1182-3119G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681290 | |||||||
| chr4:127681336 | T | TACCTG | 17 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(14): Show |
19 | HG00735.hp1 HG01168.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1182-3070_1182-306 others(9): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 127681336 | ||||||
| chr4:127681354 | A | T | 1 | a0001c0013t0001g0164 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1182-3055A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681354 | |||||||
| chr4:127681496 | G | A | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1182-2913G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681496 | |||||||
| chr4:127681627 | G | A | 2 | a0001c0001t0002g0047 a0001c0001t0002g0049 |
2 | HG02698.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1182-2782G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681627 | |||||||
| chr4:127681627 | G | T | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1182-2782G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681627 | |||||||
| chr4:127681725 | G | A | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1182-2684G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681725 | |||||||
| chr4:127681748 | C | G | 5 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(2): Show |
5 | HG01168.hp2 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-2661C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681748 | |||||||
| chr4:127681815 | C | A | 6 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(3): Show |
6 | HG01168.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182-2594C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681815 | |||||||
| chr4:127681841 | T | C | 5 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(2): Show |
5 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-2568T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681841 | |||||||
| chr4:127681926 | A | G | 1 | a0001c0001t0002g0059 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1182-2483A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681926 | |||||||
| chr4:127681940 | G | A | 2 | a0001c0001t0010g0140 a0001c0001t0027g0141 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1182-2469G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681940 | |||||||
| chr4:127681956 | T | C | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1182-2453T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681956 | |||||||
| chr4:127681968 | G | T | 3 | a0001c0006t0053g0257 a0001c0006t0054g0256 a0001c0006t0057g0259 |
3 | HG02809.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1182-2441G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127681968 | |||||||
| chr4:127682039 | C | CAAAACCA others(304): Show |
1 | a0001c0004t0002g0252 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1182-2361_1182-236 others(315): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 127682039 | ||||||
| chr4:127682039 | C | CAAAACCA others(305): Show |
1 | a0001c0004t0002g0253 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1182-2361_1182-236 others(316): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 127682039 | ||||||
| chr4:127682039 | C | CAAAACCA others(302): Show |
1 | a0001c0001t0027g0141 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1182-2361_1182-236 others(313): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 127682039 | ||||||
| chr4:127682039 | C | CAAAACCA others(319): Show |
1 | a0001c0001t0010g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1182-2361_1182-236 others(330): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 127682039 | ||||||
| chr4:127682039 | C | CAAAACCA others(318): Show |
1 | a0001c0004t0007g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1182-2361_1182-236 others(329): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 127682039 | ||||||
| chr4:127682039 | C | CAAAACCA others(319): Show |
7 | a0001c0001t0007g0157 a0001c0004t0002g0226 a0001c0004t0007g0006 others(4): Show |
9 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1182-2361_1182-236 others(330): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 127682039 | ||||||
| chr4:127682039 | C | CAAAACCA others(320): Show |
3 | a0001c0004t0002g0255 a0001c0004t0007g0246 a0001c0004t0007g0249 |
3 | HG02647.hp2 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1182-2361_1182-236 others(331): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 127682039 | ||||||
| chr4:127682059 | G | A | 14 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(11): Show |
16 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1182-2350G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127682059 | |||||||
| chr4:127682074 | G | C | 2 | a0002c0003t0003g0275 a0002c0003t0003g0276 |
2 | NA19004.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1182-2335G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127682074 | |||||||
| chr4:127682082 | A | G | 2 | a0001c0006t0053g0257 a0001c0006t0054g0256 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1182-2327A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127682082 | |||||||
| chr4:127682143 | T | G | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1182-2266T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127682143 | |||||||
| chr4:127682216 | A | G | 102 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(99): Show |
111 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1182-2193A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127682216 | |||||||
| chr4:127682227 | G | C | 1 | a0001c0001t0065g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1182-2182G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127682227 | |||||||
| chr4:127682245 | C | T | 102 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(99): Show |
111 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1182-2164C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127682245 | |||||||
| chr4:127682446 | C | T | 1 | a0002c0003t0003g0031 | 2 | NA19009.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1182-1963C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127682446 | |||||||
| chr4:127682489 | G | A | 102 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(99): Show |
111 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1182-1920G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127682489 | |||||||
| chr4:127682512 | G | A | 1 | a0001c0001t0009g0125 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1182-1897G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127682512 | |||||||
| chr4:127682528 | A | T | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1182-1881A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127682528 | |||||||
| chr4:127682898 | A | G | 1 | a0001c0002t0001g0233 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1182-1511A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127682898 | |||||||
| chr4:127683004 | C | T | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1182-1405C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127683004 | |||||||
| chr4:127683106 | G | A | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1182-1303G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127683106 | |||||||
| chr4:127683155 | G | T | 2 | a0001c0002t0001g0210 a0001c0002t0001g0211 |
2 | NA18971.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1182-1254G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127683155 | |||||||
| chr4:127683268 | T | C | 2 | a0001c0001t0010g0140 a0001c0001t0027g0141 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1182-1141T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127683268 | |||||||
| chr4:127683383 | G | A | 5 | a0002c0003t0003g0305 a0002c0003t0003g0308 a0002c0003t0030g0307 others(2): Show |
5 | HG02056.hp1 HG02132.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182-1026G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127683383 | |||||||
| chr4:127683628 | T | C | 4 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182-781T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127683628 | |||||||
| chr4:127683636 | A | T | 4 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182-773A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127683636 | |||||||
| chr4:127683700 | C | T | 1 | a0001c0001t0056g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1182-709C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127683700 | |||||||
| chr4:127684096 | C | A | 1 | a0001c0001t0066g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1182-313C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 6/15 | chr4 | 127684096 | |||||||
| chr4:127684618 | CCTCTT | C | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1259+134_1259+138d others(7): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr4 | 127684618 | ||||||
| chr4:127684619 | C | CTCTTCCT others(19): Show |
1 | a0002c0003t0003g0269 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1259+143_1259+168d others(28): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr4 | 127684619 | ||||||
| chr4:127684647 | C | A | 1 | a0001c0002t0001g0224 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1259+161C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127684647 | |||||||
| chr4:127684858 | C | T | 1 | a0001c0001t0073g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1259+372C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127684858 | |||||||
| chr4:127684900 | T | G | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1259+414T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127684900 | |||||||
| chr4:127684901 | G | T | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1259+415G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127684901 | |||||||
| chr4:127685276 | A | G | 1 | a0001c0002t0001g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1259+790A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127685276 | |||||||
| chr4:127685330 | T | A | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1259+844T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127685330 | |||||||
| chr4:127685347 | A | G | 1 | a0002c0003t0003g0271 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1259+861A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127685347 | |||||||
| chr4:127685823 | TTAGAG | T | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1259+1342_1259+134 others(9): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr4 | 127685823 | ||||||
| chr4:127685869 | A | C | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1259+1383A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127685869 | |||||||
| chr4:127686174 | G | C | 5 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(2): Show |
5 | HG01168.hp2 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260-1504G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127686174 | |||||||
| chr4:127686385 | C | T | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1260-1293C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127686385 | |||||||
| chr4:127686431 | C | T | 2 | a0001c0001t0023g0152 a0001c0002t0013g0180 |
2 | HG02055.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1260-1247C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127686431 | |||||||
| chr4:127686677 | T | C | 186 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(183): Show |
207 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1260-1001T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127686677 | |||||||
| chr4:127686999 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1260-679G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127686999 | |||||||
| chr4:127687642 | A | G | 10 | a0001c0001t0009g0057 a0001c0001t0009g0104 a0001c0001t0009g0111 others(7): Show |
10 | HG01109.hp1 HG01361.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1260-36A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 7/15 | chr4 | 127687642 | |||||||
| chr4:127687912 | T | G | 1 | a0002c0003t0033g0277 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1449+45T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127687912 | |||||||
| chr4:127687966 | A | G | 2 | a0001c0002t0006g0026 a0001c0002t0044g0026 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1449+99A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127687966 | |||||||
| chr4:127688206 | C | CA | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1449+352dupA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127688206 | ||||||
| chr4:127688305 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1449+438G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127688305 | |||||||
| chr4:127688522 | C | T | 4 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+655C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127688522 | |||||||
| chr4:127688716 | C | G | 1 | a0001c0001t0002g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1449+849C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127688716 | |||||||
| chr4:127688771 | C | T | 5 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(2): Show |
5 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1449+904C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127688771 | |||||||
| chr4:127688872 | A | G | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1449+1005A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127688872 | |||||||
| chr4:127688873 | T | TG | 7 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1449+1006_1449+100 others(5): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127688873 | |||||||
| chr4:127688892 | T | C | 2 | a0001c0002t0006g0026 a0001c0002t0044g0026 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1449+1025T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127688892 | |||||||
| chr4:127688939 | C | CCTTTCTT others(11): Show |
33 | a0001c0001t0002g0041 a0001c0001t0002g0059 a0001c0001t0002g0121 others(30): Show |
37 | HG00735.hp1 HG01167.hp1 HG02109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1449+1077_1449+109 others(22): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127688939 | ||||||
| chr4:127688958 | C | CTTTCTTT others(6): Show |
59 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(56): Show |
69 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1449+1094_1449+109 others(17): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127688958 | ||||||
| chr4:127688958 | CT | C | 117 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(114): Show |
126 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1449+1095delT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127688958 | ||||||
| chr4:127688962 | T | TTTTCTTT others(7): Show |
1 | a0001c0001t0060g0078 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1449+1095_1449+109 others(18): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127688962 | |||||||
| chr4:127688963 | C | CT | 59 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(56): Show |
69 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1449+1099dupT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127688963 | ||||||
| chr4:127688963 | C | T | 1 | a0001c0001t0060g0078 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1449+1096C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127688963 | |||||||
| chr4:127688971 | CT | C | 118 | a0001c0001t0002g0041 a0001c0001t0002g0059 a0001c0001t0002g0121 others(115): Show |
136 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1449+1127delT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127688971 | ||||||
| chr4:127688973 | T | TTTTCTTT others(10): Show |
103 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(100): Show |
112 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1449+1109_1449+111 others(21): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127688973 | ||||||
| chr4:127688974 | T | TTTCTTTT others(9): Show |
13 | a0001c0001t0002g0102 a0001c0001t0005g0074 a0001c0001t0012g0143 others(10): Show |
13 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1449+1109_1449+111 others(20): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127688974 | ||||||
| chr4:127688975 | T | C | 63 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(60): Show |
73 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1449+1108T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127688975 | |||||||
| chr4:127688976 | T | TCTTTTCT others(7): Show |
1 | a0002c0003t0003g0301 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1449+1109_1449+111 others(18): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127688976 | |||||||
| chr4:127688977 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1449+1110T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127688977 | |||||||
| chr4:127689020 | C | T | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1449+1153C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127689020 | |||||||
| chr4:127689024 | T | C | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1449+1157T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127689024 | |||||||
| chr4:127689082 | G | A | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1449+1215G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127689082 | |||||||
| chr4:127689121 | T | C | 1 | a0001c0002t0004g0194 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1449+1254T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127689121 | |||||||
| chr4:127689382 | G | A | 5 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(2): Show |
5 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1449+1515G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127689382 | |||||||
| chr4:127689635 | G | A | 104 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(101): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1449+1768G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127689635 | |||||||
| chr4:127689751 | G | C | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1449+1884G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127689751 | |||||||
| chr4:127689974 | C | G | 1 | a0001c0001t0027g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1449+2107C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127689974 | |||||||
| chr4:127690042 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1449+2175C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127690042 | |||||||
| chr4:127690063 | G | T | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1449+2196G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127690063 | |||||||
| chr4:127690200 | T | C | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1449+2333T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127690200 | |||||||
| chr4:127690295 | T | C | 1 | a0001c0002t0001g0200 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1449+2428T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127690295 | |||||||
| chr4:127690356 | C | T | 1 | a0001c0002t0049g0184 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1449+2489C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127690356 | |||||||
| chr4:127690458 | C | G | 1 | a0002c0003t0031g0282 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1449+2591C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127690458 | |||||||
| chr4:127690477 | T | G | 1 | a0001c0002t0041g0223 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1449+2610T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127690477 | |||||||
| chr4:127690534 | T | G | 3 | a0002c0003t0003g0028 a0002c0003t0003g0032 a0002c0003t0003g0284 |
5 | HG00597.hp2 HG00609.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+2667T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127690534 | |||||||
| chr4:127690679 | T | A | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1449+2812T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127690679 | |||||||
| chr4:127690704 | G | A | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1449+2837G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127690704 | |||||||
| chr4:127690805 | C | T | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1449+2938C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127690805 | |||||||
| chr4:127690976 | A | G | 1 | a0001c0001t0009g0111 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1449+3109A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127690976 | |||||||
| chr4:127691307 | C | G | 1 | a0001c0002t0013g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1449+3440C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127691307 | |||||||
| chr4:127691434 | G | T | 1 | a0001c0001t0002g0040 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1449+3567G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127691434 | |||||||
| chr4:127691447 | G | A | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1449+3580G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127691447 | |||||||
| chr4:127691470 | T | C | 2 | a0001c0001t0010g0140 a0001c0001t0027g0141 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1449+3603T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127691470 | |||||||
| chr4:127691562 | G | A | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1449+3695G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127691562 | |||||||
| chr4:127691592 | C | T | 1 | a0001c0002t0001g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1449+3725C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127691592 | |||||||
| chr4:127691609 | C | T | 4 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+3742C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127691609 | |||||||
| chr4:127691883 | A | G | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1449+4016A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127691883 | |||||||
| chr4:127691962 | G | GTA | 18 | a0001c0001t0010g0140 a0001c0001t0012g0143 a0001c0001t0012g0144 others(15): Show |
18 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1449+4113_1449+411 others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTATATAT others(3): Show |
1 | a0001c0001t0065g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1449+4105_1449+411 others(14): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTATATAT others(7): Show |
10 | a0002c0003t0003g0027 a0002c0003t0003g0033 a0002c0003t0003g0036 others(7): Show |
12 | HG00558.hp1 HG00738.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.1449+4101_1449+411 others(18): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTATATAT others(9): Show |
21 | a0002c0003t0003g0030 a0002c0003t0003g0031 a0002c0003t0003g0264 others(18): Show |
23 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1449+4099_1449+411 others(20): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTATATAT others(11): Show |
6 | a0002c0003t0003g0029 a0002c0003t0003g0272 a0002c0003t0003g0290 others(3): Show |
7 | HG00423.hp1 HG02523.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1449+4097_1449+411 others(22): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTATATAT others(13): Show |
12 | a0002c0003t0003g0008 a0002c0003t0003g0028 a0002c0003t0003g0032 others(9): Show |
17 | HG00597.hp2 HG00609.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1449+4114_1449+411 others(24): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTATATAT others(15): Show |
3 | a0002c0003t0003g0298 a0002c0003t0003g0299 a0002c0003t0011g0266 |
3 | NA18942.hp2 NA18972.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1449+4114_1449+411 others(26): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTATATAT others(17): Show |
1 | a0002c0003t0003g0288 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1449+4114_1449+411 others(28): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTATATAT others(19): Show |
4 | a0002c0003t0003g0302 a0002c0003t0069g0300 a0002c0003t0070g0035 others(1): Show |
4 | HG01978.hp2 NA18943.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+4114_1449+411 others(30): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTATATAT others(21): Show |
2 | a0001c0001t0017g0156 a0002c0003t0011g0297 |
2 | HG01168.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1449+4114_1449+411 others(32): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTATATAT others(23): Show |
3 | a0001c0001t0017g0155 a0001c0001t0066g0139 a0002c0003t0011g0296 |
3 | HG02970.hp2 HG03516.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1449+4114_1449+411 others(34): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTATATAT others(25): Show |
1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1449+4114_1449+411 others(36): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTATATAT others(27): Show |
1 | a0001c0001t0017g0154 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1449+4114_1449+411 others(38): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(1): Show |
14 | a0001c0001t0002g0077 a0001c0001t0005g0001 a0001c0001t0005g0050 others(11): Show |
18 | HG00558.hp2 HG00609.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(12): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(3): Show |
3 | a0001c0001t0005g0051 a0001c0001t0005g0075 a0001c0001t0005g0094 |
3 | HG00408.hp1 HG01952.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(14): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(7): Show |
1 | a0001c0001t0002g0068 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1449+4096_1449+409 others(18): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(9): Show |
3 | a0001c0001t0002g0009 a0001c0001t0002g0039 a0001c0001t0073g0117 |
4 | HG00544.hp2 HG02165.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(20): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(13): Show |
1 | a0001c0001t0059g0114 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1449+4096_1449+409 others(24): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(17): Show |
1 | a0001c0001t0055g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1449+4096_1449+409 others(28): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(19): Show |
11 | a0001c0001t0002g0012 a0001c0001t0002g0044 a0001c0001t0002g0046 others(8): Show |
12 | HG00741.hp1 HG01109.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(30): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(21): Show |
19 | a0001c0001t0002g0003 a0001c0001t0002g0037 a0001c0001t0002g0041 others(16): Show |
20 | HG00438.hp1 HG00738.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(32): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(23): Show |
13 | a0001c0001t0002g0010 a0001c0001t0002g0040 a0001c0001t0002g0054 others(10): Show |
14 | HG00423.hp2 HG01106.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(34): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(25): Show |
11 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(8): Show |
11 | HG00099.hp1 HG01070.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(36): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(27): Show |
6 | a0001c0001t0002g0049 a0001c0001t0002g0063 a0001c0001t0009g0104 others(3): Show |
6 | HG01891.hp1 HG02027.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(38): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(29): Show |
4 | a0001c0001t0002g0062 a0001c0001t0015g0113 a0003c0005t0002g0082 others(1): Show |
4 | HG00140.hp2 NA18950.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(40): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(31): Show |
2 | a0001c0001t0009g0125 a0001c0001t0074g0115 |
2 | HG02004.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(42): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(33): Show |
6 | a0001c0001t0002g0052 a0001c0014t0002g0073 a0003c0005t0002g0080 others(3): Show |
6 | HG01884.hp1 HG02735.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(44): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTATAT others(35): Show |
1 | a0003c0005t0002g0079 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1449+4096_1449+409 others(46): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTGTAT others(19): Show |
1 | a0001c0006t0057g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1449+4096_1449+409 others(30): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTGTAT others(23): Show |
2 | a0001c0001t0064g0098 a0001c0006t0054g0256 |
2 | HG02809.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(34): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTGTAT others(25): Show |
1 | a0001c0001t0002g0011 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(36): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTGTAT others(35): Show |
1 | a0001c0006t0053g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1449+4096_1449+409 others(46): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTGTGT others(15): Show |
2 | a0001c0001t0010g0014 a0001c0001t0067g0133 |
3 | HG02976.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(26): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTGTGT others(17): Show |
1 | a0001c0001t0026g0129 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1449+4096_1449+409 others(28): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTGTGT others(23): Show |
1 | a0001c0001t0010g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1449+4096_1449+409 others(34): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTGTGT others(25): Show |
1 | a0001c0001t0026g0132 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1449+4096_1449+409 others(36): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTGTGT others(29): Show |
2 | a0001c0001t0010g0134 a0001c0001t0018g0130 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(40): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTGTGT others(31): Show |
1 | a0001c0001t0010g0128 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1449+4096_1449+409 others(42): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691962 | G | GTGTGTGT others(35): Show |
3 | a0001c0001t0010g0126 a0001c0001t0010g0131 a0001c0001t0018g0013 |
4 | HG02109.hp1 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1449+4096_1449+409 others(46): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691962 | ||||||
| chr4:127691966 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1449+4099A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127691966 | |||||||
| chr4:127691978 | A | G | 1 | a0001c0001t0009g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1449+4111A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127691978 | |||||||
| chr4:127691980 | A | ATATATAT others(41): Show |
1 | a0005c0008t0019g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1449+4114_1449+411 others(52): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691980 | ||||||
| chr4:127691980 | A | ATATATAT others(39): Show |
1 | a0005c0008t0028g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1449+4114_1449+411 others(50): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691980 | ||||||
| chr4:127691980 | A | ATATATAT others(41): Show |
1 | a0001c0001t0027g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1449+4114_1449+411 others(52): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691980 | ||||||
| chr4:127691980 | A | ATATATGT others(3): Show |
1 | a0005c0008t0019g0138 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1449+4114_1449+411 others(14): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127691980 | ||||||
| chr4:127691980 | A | G | 2 | a0001c0001t0002g0046 a0001c0014t0002g0073 |
2 | HG01109.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1449+4113A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127691980 | |||||||
| chr4:127691994 | T | G | 1 | a0001c0006t0057g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1449+4127T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127691994 | |||||||
| chr4:127692024 | T | C | 4 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+4157T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127692024 | |||||||
| chr4:127692175 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1449+4308A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127692175 | |||||||
| chr4:127692250 | A | T | 3 | a0001c0002t0006g0188 a0001c0002t0006g0217 a0001c0002t0050g0165 |
3 | HG00099.hp2 HG01175.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1449+4383A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127692250 | |||||||
| chr4:127692276 | G | A | 6 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(3): Show |
6 | HG01168.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1449+4409G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127692276 | |||||||
| chr4:127692388 | CT | C | 5 | a0002c0003t0003g0305 a0002c0003t0003g0308 a0002c0003t0030g0307 others(2): Show |
5 | HG02056.hp1 HG02132.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+4525delT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127692388 | ||||||
| chr4:127692412 | C | G | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1449+4545C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127692412 | |||||||
| chr4:127692642 | G | A | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1449+4775G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127692642 | |||||||
| chr4:127692708 | T | A | 311 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(308): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1449+4841T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127692708 | |||||||
| chr4:127692740 | C | A | 9 | a0001c0001t0007g0157 a0001c0004t0007g0006 a0001c0004t0007g0246 others(6): Show |
11 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1449+4873C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127692740 | |||||||
| chr4:127692980 | G | A | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1449+5113G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127692980 | |||||||
| chr4:127693027 | T | A | 1 | a0001c0001t0005g0051 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1449+5160T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693027 | |||||||
| chr4:127693043 | A | G | 2 | a0004c0007t0075g0148 a0004c0007t0076g0158 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1449+5176A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693043 | |||||||
| chr4:127693316 | T | C | 1 | a0001c0002t0001g0204 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1449+5449T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693316 | |||||||
| chr4:127693410 | G | A | 1 | a0001c0002t0013g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1449+5543G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693410 | |||||||
| chr4:127693482 | T | C | 4 | a0001c0002t0001g0016 a0001c0002t0001g0168 a0001c0002t0014g0016 others(1): Show |
4 | HG00735.hp2 HG01074.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+5615T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693482 | |||||||
| chr4:127693513 | A | T | 1 | a0001c0002t0001g0203 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1449+5646A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693513 | |||||||
| chr4:127693661 | A | C | 5 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(2): Show |
5 | HG01168.hp2 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1449+5794A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693661 | |||||||
| chr4:127693674 | A | G | 1 | a0001c0002t0004g0166 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1449+5807A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693674 | |||||||
| chr4:127693703 | G | C | 210 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(207): Show |
233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1449+5836G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693703 | |||||||
| chr4:127693721 | G | T | 1 | a0001c0001t0002g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1449+5854G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693721 | |||||||
| chr4:127693793 | A | C | 1 | a0001c0002t0001g0228 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1449+5926A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693793 | |||||||
| chr4:127693877 | T | G | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1449+6010T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693877 | |||||||
| chr4:127693896 | C | T | 2 | a0001c0001t0010g0140 a0001c0001t0027g0141 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1449+6029C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693896 | |||||||
| chr4:127693921 | C | T | 1 | a0001c0001t0010g0128 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1449+6054C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693921 | |||||||
| chr4:127693957 | A | G | 36 | a0001c0002t0001g0007 a0001c0002t0001g0015 a0001c0002t0001g0016 others(33): Show |
42 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1450-6053A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127693957 | |||||||
| chr4:127694022 | C | G | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1450-5988C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127694022 | |||||||
| chr4:127694244 | G | A | 1 | a0001c0002t0001g0201 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1450-5766G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127694244 | |||||||
| chr4:127694272 | C | G | 2 | a0001c0001t0073g0117 a0001c0001t0074g0115 |
2 | HG02004.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1450-5738C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127694272 | |||||||
| chr4:127694374 | C | T | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1450-5636C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127694374 | |||||||
| chr4:127694667 | C | T | 1 | a0001c0001t0012g0143 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1450-5343C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127694667 | |||||||
| chr4:127694697 | A | G | 5 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(2): Show |
5 | HG01168.hp2 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1450-5313A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127694697 | |||||||
| chr4:127695049 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1450-4961T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695049 | |||||||
| chr4:127695098 | G | A | 4 | a0001c0002t0006g0188 a0001c0002t0006g0217 a0001c0002t0050g0165 others(1): Show |
4 | HG00099.hp2 HG01175.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450-4912G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695098 | |||||||
| chr4:127695192 | T | C | 3 | a0001c0002t0006g0179 a0001c0002t0013g0180 a0001c0002t0042g0178 |
3 | HG01884.hp2 HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1450-4818T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695192 | |||||||
| chr4:127695253 | A | G | 1 | a0001c0002t0013g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1450-4757A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695253 | |||||||
| chr4:127695359 | G | A | 1 | a0001c0002t0014g0225 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1450-4651G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695359 | |||||||
| chr4:127695386 | A | T | 1 | a0001c0001t0010g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1450-4624A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695386 | |||||||
| chr4:127695451 | G | A | 211 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(208): Show |
234 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.1450-4559G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695451 | |||||||
| chr4:127695489 | G | C | 186 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(183): Show |
207 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1450-4521G>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695489 | |||||||
| chr4:127695572 | G | T | 1 | a0001c0001t0002g0011 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1450-4438G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695572 | |||||||
| chr4:127695608 | A | C | 1 | a0001c0002t0001g0022 | 2 | NA18948.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1450-4402A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695608 | |||||||
| chr4:127695650 | A | G | 2 | a0001c0001t0010g0140 a0001c0001t0027g0141 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1450-4360A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695650 | |||||||
| chr4:127695684 | G | A | 4 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450-4326G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695684 | |||||||
| chr4:127695822 | G | A | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1450-4188G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695822 | |||||||
| chr4:127695953 | G | A | 1 | a0001c0006t0013g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1450-4057G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127695953 | |||||||
| chr4:127696513 | C | G | 13 | a0001c0001t0007g0157 a0001c0001t0010g0140 a0001c0001t0027g0141 others(10): Show |
15 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1450-3497C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127696513 | |||||||
| chr4:127696531 | C | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02559.hp2 HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1450-3479C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127696531 | |||||||
| chr4:127696532 | C | G | 12 | a0002c0003t0003g0267 a0002c0003t0003g0272 a0002c0003t0003g0273 others(9): Show |
12 | NA18939.hp1 NA18942.hp2 NA18943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1450-3478C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127696532 | |||||||
| chr4:127696575 | A | G | 88 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(85): Show |
97 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1450-3435A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127696575 | |||||||
| chr4:127696592 | A | G | 186 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(183): Show |
207 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1450-3418A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127696592 | |||||||
| chr4:127696639 | C | T | 1 | a0001c0001t0027g0141 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1450-3371C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127696639 | |||||||
| chr4:127696643 | G | A | 1 | a0001c0002t0013g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1450-3367G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127696643 | |||||||
| chr4:127696711 | C | T | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1450-3299C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127696711 | |||||||
| chr4:127696983 | C | T | 1 | a0001c0001t0009g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1450-3027C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127696983 | |||||||
| chr4:127697010 | G | A | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1450-3000G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127697010 | |||||||
| chr4:127697060 | T | C | 11 | a0001c0001t0007g0157 a0001c0004t0002g0226 a0001c0004t0002g0255 others(8): Show |
13 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1450-2950T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127697060 | |||||||
| chr4:127697109 | G | T | 5 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(2): Show |
5 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1450-2901G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127697109 | |||||||
| chr4:127697221 | G | A | 2 | a0002c0003t0003g0267 a0002c0003t0003g0289 |
2 | NA18974.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1450-2789G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127697221 | |||||||
| chr4:127697247 | T | C | 2 | a0001c0001t0002g0054 a0001c0001t0009g0053 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1450-2763T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127697247 | |||||||
| chr4:127697355 | G | T | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1450-2655G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127697355 | |||||||
| chr4:127697487 | ACCATTC | A | 210 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(207): Show |
233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1450-2516_1450-251 others(10): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127697487 | ||||||
| chr4:127697670 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1450-2340A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127697670 | |||||||
| chr4:127697847 | A | G | 3 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 |
3 | HG01168.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1450-2163A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127697847 | |||||||
| chr4:127697954 | C | CTACTAAA others(24): Show |
1 | a0001c0002t0001g0235 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1450-2055_1450-202 others(35): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127697954 | ||||||
| chr4:127697979 | G | T | 1 | a0001c0001t0012g0146 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1450-2031G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127697979 | |||||||
| chr4:127698068 | T | C | 204 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(201): Show |
227 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1450-1942T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127698068 | |||||||
| chr4:127698159 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1450-1851G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127698159 | |||||||
| chr4:127698279 | G | A | 1 | a0003c0005t0063g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1450-1731G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127698279 | |||||||
| chr4:127698316 | G | A | 3 | a0005c0008t0019g0136 a0005c0008t0019g0138 a0005c0008t0028g0137 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1450-1694G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127698316 | |||||||
| chr4:127698318 | C | A | 3 | a0005c0008t0019g0136 a0005c0008t0019g0138 a0005c0008t0028g0137 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1450-1692C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127698318 | |||||||
| chr4:127698329 | G | A | 104 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(101): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1450-1681G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127698329 | |||||||
| chr4:127698397 | G | A | 1 | a0001c0002t0001g0237 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1450-1613G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127698397 | |||||||
| chr4:127698590 | T | C | 1 | a0001c0002t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1450-1420T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127698590 | |||||||
| chr4:127698624 | G | A | 1 | a0001c0002t0001g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1450-1386G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127698624 | |||||||
| chr4:127698635 | C | T | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450-1375C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127698635 | |||||||
| chr4:127698972 | G | A | 1 | a0001c0001t0005g0070 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1450-1038G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127698972 | |||||||
| chr4:127699045 | A | G | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG00099.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1450-965A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127699045 | |||||||
| chr4:127699092 | C | A | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1450-918C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127699092 | |||||||
| chr4:127699203 | A | G | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1450-807A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127699203 | |||||||
| chr4:127699207 | C | A | 3 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 |
3 | HG01168.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1450-803C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127699207 | |||||||
| chr4:127699211 | C | G | 1 | a0001c0002t0006g0173 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1450-799C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127699211 | |||||||
| chr4:127699285 | G | GT | 17 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(14): Show |
19 | HG00735.hp1 HG01168.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1450-720dupT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 127699285 | ||||||
| chr4:127699306 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1450-704C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127699306 | |||||||
| chr4:127699427 | T | A | 1 | a0001c0001t0056g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1450-583T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127699427 | |||||||
| chr4:127699467 | A | G | 17 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(14): Show |
19 | HG00735.hp1 HG01168.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1450-543A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127699467 | |||||||
| chr4:127699630 | C | G | 1 | a0001c0001t0010g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1450-380C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127699630 | |||||||
| chr4:127699726 | C | A | 1 | a0001c0002t0001g0260 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1450-284C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127699726 | |||||||
| chr4:127699843 | A | G | 2 | a0001c0002t0006g0026 a0001c0002t0044g0026 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1450-167A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127699843 | |||||||
| chr4:127700001 | T | G | 3 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 |
3 | HG01168.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1450-9T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 8/15 | chr4 | 127700001 | |||||||
| chr4:127700117 | A | C | 211 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(208): Show |
234 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.1503+54A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127700117 | |||||||
| chr4:127700146 | G | A | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1503+83G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127700146 | |||||||
| chr4:127700212 | T | C | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503+149T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127700212 | |||||||
| chr4:127700247 | T | C | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503+184T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127700247 | |||||||
| chr4:127700249 | C | T | 59 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(56): Show |
69 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1503+186C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127700249 | |||||||
| chr4:127700465 | G | A | 1 | a0001c0001t0005g0076 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1503+402G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127700465 | |||||||
| chr4:127700491 | C | A | 1 | a0001c0002t0001g0235 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1503+428C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127700491 | |||||||
| chr4:127700739 | G | T | 1 | a0001c0002t0001g0235 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1503+676G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127700739 | |||||||
| chr4:127700772 | T | TA | 84 | a0001c0001t0007g0157 a0001c0001t0010g0140 a0001c0001t0012g0143 others(81): Show |
96 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1503+723dupA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 127700772 | ||||||
| chr4:127700772 | TA | T | 9 | a0001c0001t0027g0135 a0001c0002t0001g0233 a0001c0002t0001g0234 others(6): Show |
9 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1503+723delA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 127700772 | ||||||
| chr4:127700854 | A | G | 6 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0002t0001g0168 others(3): Show |
7 | HG00735.hp2 HG01074.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1503+791A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127700854 | |||||||
| chr4:127701370 | C | T | 2 | a0001c0006t0053g0257 a0001c0006t0054g0256 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1503+1307C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127701370 | |||||||
| chr4:127701528 | G | A | 3 | a0001c0002t0001g0018 a0001c0002t0001g0224 a0001c0002t0043g0018 |
3 | NA18940.hp1 NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1503+1465G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127701528 | |||||||
| chr4:127701708 | GA | G | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1503+1646delA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127701708 | |||||||
| chr4:127701857 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0041 |
2 | NA18983.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1503+1794G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127701857 | |||||||
| chr4:127701906 | A | C | 1 | a0001c0002t0001g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1503+1843A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127701906 | |||||||
| chr4:127701940 | A | G | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1503+1877A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127701940 | |||||||
| chr4:127702115 | C | T | 4 | a0001c0001t0027g0135 a0005c0008t0019g0136 a0005c0008t0019g0138 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1503+2052C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127702115 | |||||||
| chr4:127702174 | T | G | 187 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(184): Show |
208 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1504-2054T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127702174 | |||||||
| chr4:127702221 | A | T | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1504-2007A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127702221 | |||||||
| chr4:127702256 | T | C | 1 | a0002c0003t0031g0282 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1504-1972T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127702256 | |||||||
| chr4:127702417 | C | T | 2 | a0001c0002t0006g0026 a0001c0002t0044g0026 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1504-1811C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127702417 | |||||||
| chr4:127702477 | A | C | 1 | a0002c0003t0003g0301 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1504-1751A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127702477 | |||||||
| chr4:127702532 | AGGTGTTG others(8): Show |
A | 1 | a0001c0002t0001g0235 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1504-1694_1504-168 others(19): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 127702532 | ||||||
| chr4:127702826 | G | A | 1 | a0001c0001t0058g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1504-1402G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127702826 | |||||||
| chr4:127702989 | A | T | 3 | a0001c0002t0006g0188 a0001c0002t0006g0217 a0001c0002t0050g0165 |
3 | HG00099.hp2 HG01175.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1504-1239A>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127702989 | |||||||
| chr4:127703101 | T | G | 1 | a0001c0002t0001g0171 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1504-1127T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127703101 | |||||||
| chr4:127703189 | A | G | 2 | a0001c0001t0002g0068 a0001c0001t0016g0067 |
2 | HG00323.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1504-1039A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127703189 | |||||||
| chr4:127703334 | C | T | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1504-894C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127703334 | |||||||
| chr4:127703467 | T | C | 4 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1504-761T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127703467 | |||||||
| chr4:127703554 | G | A | 1 | a0001c0001t0065g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1504-674G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127703554 | |||||||
| chr4:127703605 | T | C | 1 | a0001c0002t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1504-623T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127703605 | |||||||
| chr4:127703639 | G | A | 210 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(207): Show |
233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1504-589G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127703639 | |||||||
| chr4:127704024 | T | C | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1504-204T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127704024 | |||||||
| chr4:127704120 | A | G | 6 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(3): Show |
6 | HG01168.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1504-108A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127704120 | |||||||
| chr4:127704124 | T | G | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1504-104T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127704124 | |||||||
| chr4:127704208 | A | G | 7 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1504-20A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 9/15 | chr4 | 127704208 | |||||||
| chr4:127704816 | G | GAAAA | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1566+526_1566+527i others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 10/15 | chr4 | 127704816 | |||||||
| chr4:127704818 | T | TCAGCTG | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1566+528_1566+529i others(8): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 10/15 | chr4 | 127704818 | |||||||
| chr4:127704853 | C | T | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1566+563C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 10/15 | chr4 | 127704853 | |||||||
| chr4:127704885 | C | T | 11 | a0001c0001t0007g0157 a0001c0001t0010g0140 a0001c0001t0027g0141 others(8): Show |
13 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1566+595C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 10/15 | chr4 | 127704885 | |||||||
| chr4:127704927 | A | G | 1 | a0001c0004t0002g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1566+637A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 10/15 | chr4 | 127704927 | |||||||
| chr4:127704979 | C | T | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1567-612C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 10/15 | chr4 | 127704979 | |||||||
| chr4:127705005 | T | C | 2 | a0002c0003t0003g0269 a0002c0003t0003g0294 |
2 | HG00544.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1567-586T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 10/15 | chr4 | 127705005 | |||||||
| chr4:127705391 | G | A | 1 | a0002c0003t0003g0284 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1567-200G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 10/15 | chr4 | 127705391 | |||||||
| chr4:127705895 | C | T | 111 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(108): Show |
120 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1788+83C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 11/15 | chr4 | 127705895 | |||||||
| chr4:127706074 | G | A | 1 | a0001c0001t0027g0141 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1788+262G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 11/15 | chr4 | 127706074 | |||||||
| chr4:127706440 | T | C | 1 | a0010c0017t0003g0285 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1789-47T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 11/15 | chr4 | 127706440 | |||||||
| chr4:127707244 | C | T | 5 | a0002c0003t0003g0274 a0005c0008t0019g0136 a0005c0008t0019g0138 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2271+275C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127707244 | |||||||
| chr4:127707390 | C | G | 1 | a0001c0002t0001g0175 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2271+421C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127707390 | |||||||
| chr4:127707392 | C | CA | 173 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(170): Show |
194 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.2271+448dupA | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 127707392 | ||||||
| chr4:127707392 | C | CAA | 14 | a0001c0001t0002g0063 a0001c0001t0002g0100 a0001c0001t0002g0102 others(11): Show |
14 | HG00438.hp2 HG01358.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2271+447_2271+448d others(4): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 127707392 | ||||||
| chr4:127707487 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2271+518A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127707487 | |||||||
| chr4:127707524 | T | C | 4 | a0005c0008t0019g0136 a0005c0008t0019g0138 a0005c0008t0028g0137 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2271+555T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127707524 | |||||||
| chr4:127707532 | G | A | 1 | a0001c0001t0017g0155 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2271+563G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127707532 | |||||||
| chr4:127707643 | C | CTGTG | 4 | a0005c0008t0019g0136 a0005c0008t0019g0138 a0005c0008t0028g0137 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2271+688_2271+691d others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 127707643 | ||||||
| chr4:127707659 | G | A | 1 | a0001c0002t0004g0191 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2271+690G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127707659 | |||||||
| chr4:127707689 | A | C | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2271+720A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127707689 | |||||||
| chr4:127707840 | G | A | 1 | a0001c0002t0001g0200 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2272-731G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127707840 | |||||||
| chr4:127707852 | T | C | 2 | a0001c0004t0002g0226 a0001c0004t0002g0255 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2272-719T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127707852 | |||||||
| chr4:127707890 | C | T | 1 | a0001c0002t0041g0223 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2272-681C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127707890 | |||||||
| chr4:127707905 | G | A | 5 | a0001c0001t0010g0127 a0001c0001t0010g0128 a0001c0001t0010g0131 others(2): Show |
5 | HG00735.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2272-666G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127707905 | |||||||
| chr4:127707984 | C | G | 2 | a0002c0003t0003g0036 a0002c0003t0003g0292 |
3 | NA18970.hp2 NA18994.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2272-587C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127707984 | |||||||
| chr4:127707992 | A | G | 1 | a0002c0003t0021g0268 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2272-579A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127707992 | |||||||
| chr4:127708477 | T | C | 11 | a0001c0001t0002g0052 a0003c0005t0002g0079 a0003c0005t0002g0080 others(8): Show |
11 | HG01884.hp1 HG02015.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.2272-94T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 12/15 | chr4 | 127708477 | |||||||
| chr4:127708721 | G | A | 9 | a0001c0001t0007g0157 a0001c0004t0007g0006 a0001c0004t0007g0246 others(6): Show |
11 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2369+53G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127708721 | |||||||
| chr4:127708730 | A | G | 6 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(3): Show |
6 | HG01168.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2369+62A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127708730 | |||||||
| chr4:127708842 | A | G | 1 | a0001c0006t0057g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2369+174A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127708842 | |||||||
| chr4:127709010 | T | C | 2 | a0001c0004t0002g0226 a0001c0004t0002g0255 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2369+342T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127709010 | |||||||
| chr4:127709087 | T | A | 1 | a0001c0001t0009g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2369+419T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127709087 | |||||||
| chr4:127709223 | A | G | 1 | a0001c0001t0012g0145 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2369+555A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127709223 | |||||||
| chr4:127709282 | G | A | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2369+614G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127709282 | |||||||
| chr4:127709343 | CT | C | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.2369+676delT | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127709343 | |||||||
| chr4:127709382 | G | A | 2 | a0004c0007t0075g0148 a0004c0007t0076g0158 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2369+714G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127709382 | |||||||
| chr4:127709421 | G | T | 1 | a0002c0003t0003g0264 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2369+753G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127709421 | |||||||
| chr4:127709616 | A | G | 3 | a0001c0001t0002g0077 a0001c0001t0005g0072 a0001c0001t0025g0108 |
3 | HG01934.hp2 HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.2369+948A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127709616 | |||||||
| chr4:127709711 | T | TCA | 21 | a0001c0002t0001g0007 a0001c0002t0001g0019 a0001c0002t0001g0022 others(18): Show |
25 | HG00099.hp2 HG00597.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.2369+1076_2369+107 others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127709711 | ||||||
| chr4:127709711 | T | TCACA | 10 | a0001c0001t0010g0140 a0001c0001t0012g0144 a0001c0001t0012g0145 others(7): Show |
10 | HG01891.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2369+1074_2369+107 others(8): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127709711 | ||||||
| chr4:127709711 | T | TCACACA | 37 | a0001c0001t0002g0012 a0001c0001t0002g0043 a0001c0001t0002g0063 others(34): Show |
43 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.2369+1072_2369+107 others(10): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127709711 | ||||||
| chr4:127709711 | T | TCACACAC others(1): Show |
22 | a0001c0001t0002g0047 a0001c0001t0002g0059 a0001c0001t0002g0099 others(19): Show |
22 | HG01070.hp1 HG01192.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.2369+1070_2369+107 others(12): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127709711 | ||||||
| chr4:127709711 | T | TCACACAC others(3): Show |
38 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0044 others(35): Show |
40 | HG00099.hp1 HG00621.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.2369+1068_2369+107 others(14): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127709711 | ||||||
| chr4:127709711 | T | TCACACAC others(5): Show |
59 | a0001c0001t0002g0009 a0001c0001t0002g0037 a0001c0001t0002g0039 others(56): Show |
68 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.2369+1066_2369+107 others(16): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127709711 | ||||||
| chr4:127709711 | T | TCACACAC others(7): Show |
11 | a0001c0001t0002g0010 a0001c0001t0008g0038 a0001c0001t0016g0110 others(8): Show |
14 | HG01081.hp2 HG01978.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.2369+1064_2369+107 others(18): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127709711 | ||||||
| chr4:127709711 | T | TCACACAC others(9): Show |
2 | a0001c0001t0002g0105 a0001c0001t0002g0121 |
2 | HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2369+1062_2369+107 others(20): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127709711 | ||||||
| chr4:127709711 | T | TCACACAC others(11): Show |
3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0122 |
3 | HG02257.hp1 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2369+1060_2369+107 others(22): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127709711 | ||||||
| chr4:127709711 | T | TCACACAC others(13): Show |
1 | a0001c0006t0057g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2369+1058_2369+107 others(24): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127709711 | ||||||
| chr4:127709711 | TCA | T | 21 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(18): Show |
25 | HG00621.hp2 HG00735.hp1 HG02071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2369+1076_2369+107 others(6): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127709711 | ||||||
| chr4:127709712 | C | CACACACA others(1): Show |
5 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(2): Show |
5 | HG01168.hp2 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2369+1051_2369+105 others(12): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127709712 | ||||||
| chr4:127709722 | C | G | 11 | a0001c0001t0010g0014 a0001c0001t0010g0126 a0001c0001t0010g0127 others(8): Show |
13 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2369+1054C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127709722 | |||||||
| chr4:127709744 | C | CACACACA others(3): Show |
1 | a0002c0003t0035g0291 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2369+1077_2369+107 others(14): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127709744 | ||||||
| chr4:127709837 | C | G | 1 | a0001c0001t0064g0098 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2370-1076C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127709837 | |||||||
| chr4:127709980 | G | A | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2370-933G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127709980 | |||||||
| chr4:127709999 | A | G | 1 | a0001c0002t0014g0225 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2370-914A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127709999 | |||||||
| chr4:127710146 | A | G | 1 | a0001c0001t0009g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2370-767A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127710146 | |||||||
| chr4:127710483 | T | C | 2 | a0001c0001t0009g0125 a0001c0001t0056g0124 |
2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2370-430T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127710483 | |||||||
| chr4:127710529 | A | G | 3 | a0004c0007t0075g0148 a0004c0007t0076g0158 a0004c0007t0077g0159 |
3 | HG02055.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2370-384A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127710529 | |||||||
| chr4:127710561 | C | T | 1 | a0001c0001t0027g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2370-352C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127710561 | |||||||
| chr4:127710704 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2370-209A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127710704 | |||||||
| chr4:127710868 | A | G | 47 | a0001c0001t0002g0011 a0001c0001t0002g0052 a0001c0001t0002g0054 others(44): Show |
52 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.2370-45A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | chr4 | 127710868 | |||||||
| chr4:127710886 | T | TTCTCTTT others(2): Show |
3 | a0001c0002t0001g0204 a0001c0002t0001g0205 a0001c0002t0001g0207 |
3 | NA18950.hp2 NA18973.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.2370-25_2370-17dup others(9): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 127710886 | ||||||
| chr4:127711151 | C | T | 2 | a0001c0001t0002g0068 a0001c0001t0016g0067 |
2 | HG00323.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2559+49C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127711151 | |||||||
| chr4:127711290 | C | T | 194 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(191): Show |
215 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.2559+188C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127711290 | |||||||
| chr4:127711431 | A | G | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2559+329A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127711431 | |||||||
| chr4:127711512 | A | G | 12 | a0001c0001t0007g0157 a0001c0001t0010g0140 a0001c0001t0027g0135 others(9): Show |
14 | HG01496.hp2 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2559+410A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127711512 | |||||||
| chr4:127711530 | T | C | 1 | a0001c0002t0004g0192 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2559+428T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127711530 | |||||||
| chr4:127711531 | G | T | 1 | a0001c0002t0004g0192 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2559+429G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127711531 | |||||||
| chr4:127711534 | C | G | 1 | a0001c0002t0004g0192 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2559+432C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127711534 | |||||||
| chr4:127711609 | C | G | 3 | a0005c0008t0019g0136 a0005c0008t0019g0138 a0005c0008t0028g0137 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2559+507C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127711609 | |||||||
| chr4:127711801 | G | T | 2 | a0001c0004t0002g0226 a0001c0004t0002g0255 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2559+699G>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127711801 | |||||||
| chr4:127712350 | C | A | 1 | a0001c0001t0009g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2559+1248C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127712350 | |||||||
| chr4:127712505 | C | T | 12 | a0001c0001t0007g0157 a0001c0004t0007g0006 a0001c0004t0007g0246 others(9): Show |
14 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2559+1403C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127712505 | |||||||
| chr4:127712546 | C | T | 13 | a0001c0001t0007g0157 a0001c0004t0007g0006 a0001c0004t0007g0246 others(10): Show |
15 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2560-1390C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127712546 | |||||||
| chr4:127712695 | G | A | 106 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(103): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.2560-1241G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127712695 | |||||||
| chr4:127712761 | T | G | 2 | a0001c0004t0007g0249 a0001c0004t0007g0251 |
2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2560-1175T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127712761 | |||||||
| chr4:127712837 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2560-1099G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127712837 | |||||||
| chr4:127713057 | C | T | 1 | a0001c0001t0058g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2560-879C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127713057 | |||||||
| chr4:127713382 | T | C | 1 | a0002c0003t0003g0264 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2560-554T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127713382 | |||||||
| chr4:127713610 | C | T | 4 | a0001c0001t0012g0143 a0001c0001t0012g0144 a0001c0001t0012g0145 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2560-326C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127713610 | |||||||
| chr4:127713634 | T | C | 1 | a0001c0002t0001g0015 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2560-302T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127713634 | |||||||
| chr4:127713665 | A | C | 1 | a0001c0001t0002g0065 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2560-271A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127713665 | |||||||
| chr4:127713783 | T | A | 3 | a0005c0008t0019g0136 a0005c0008t0019g0138 a0005c0008t0028g0137 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2560-153T>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127713783 | |||||||
| chr4:127713804 | T | G | 2 | a0001c0002t0006g0026 a0001c0002t0044g0026 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2560-132T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127713804 | |||||||
| chr4:127713867 | C | T | 92 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(89): Show |
101 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.2560-69C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 14/15 | chr4 | 127713867 | |||||||
| chr4:127714221 | C | T | 3 | a0005c0008t0019g0136 a0005c0008t0019g0138 a0005c0008t0028g0137 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2717+128C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127714221 | |||||||
| chr4:127714305 | TAC | T | 15 | a0001c0001t0007g0157 a0001c0001t0010g0140 a0001c0001t0027g0135 others(12): Show |
17 | HG01496.hp2 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2717+215_2717+216d others(4): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr4 | 127714305 | ||||||
| chr4:127714310 | T | G | 15 | a0001c0001t0007g0157 a0001c0001t0010g0140 a0001c0001t0027g0135 others(12): Show |
17 | HG01496.hp2 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2717+217T>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127714310 | |||||||
| chr4:127714391 | C | G | 4 | a0001c0001t0023g0151 a0001c0001t0023g0152 a0001c0001t0024g0149 others(1): Show |
4 | HG01167.hp1 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.2717+298C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127714391 | |||||||
| chr4:127714526 | C | T | 1 | a0002c0003t0021g0280 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2717+433C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127714526 | |||||||
| chr4:127714646 | C | G | 1 | a0001c0001t0074g0115 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2717+553C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127714646 | |||||||
| chr4:127714731 | C | T | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2717+638C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127714731 | |||||||
| chr4:127714733 | A | C | 1 | a0002c0003t0003g0279 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2717+640A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127714733 | |||||||
| chr4:127714739 | C | A | 1 | a0001c0001t0009g0053 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2717+646C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127714739 | |||||||
| chr4:127714740 | A | C | 1 | a0001c0001t0009g0053 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2717+647A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127714740 | |||||||
| chr4:127714826 | A | C | 1 | a0001c0004t0040g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2717+733A>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127714826 | |||||||
| chr4:127714844 | C | T | 210 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(207): Show |
233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.2717+751C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127714844 | |||||||
| chr4:127715027 | G | A | 214 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(211): Show |
237 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.2717+934G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127715027 | |||||||
| chr4:127715065 | T | C | 2 | a0001c0006t0053g0257 a0001c0006t0054g0256 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2717+972T>C | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127715065 | |||||||
| chr4:127715264 | C | A | 1 | a0002c0003t0003g0279 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2718-1061C>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127715264 | |||||||
| chr4:127715389 | C | G | 3 | a0001c0006t0053g0257 a0001c0006t0054g0256 a0001c0006t0057g0259 |
3 | HG02809.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2718-936C>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127715389 | |||||||
| chr4:127715468 | C | T | 1 | a0006c0009t0052g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2718-857C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127715468 | |||||||
| chr4:127715526 | C | T | 60 | a0002c0003t0003g0008 a0002c0003t0003g0027 a0002c0003t0003g0028 others(57): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.2718-799C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127715526 | |||||||
| chr4:127715539 | C | T | 1 | a0001c0002t0050g0165 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2718-786C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127715539 | |||||||
| chr4:127715568 | A | G | 1 | a0001c0001t0002g0123 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2718-757A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127715568 | |||||||
| chr4:127715705 | G | A | 6 | a0001c0001t0017g0154 a0001c0001t0017g0155 a0001c0001t0017g0156 others(3): Show |
6 | HG01168.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2718-620G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127715705 | |||||||
| chr4:127715714 | G | A | 1 | a0001c0001t0009g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2718-611G>A | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127715714 | |||||||
| chr4:127715863 | C | T | 1 | a0001c0004t0078g0245 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2718-462C>T | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127715863 | |||||||
| chr4:127716242 | A | G | 1 | a0001c0001t0010g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2718-83A>G | INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | chr4 | 127716242 | |||||||
| chr4:127716279 | T | TTTG | 3 | a0005c0008t0019g0136 a0005c0008t0019g0138 a0005c0008t0028g0137 |
3 | HG02145.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2718-40_2718-38dup others(3): Show |
INTU | ENSG00000164066.13 | transcript | ENST00000335251.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr4 | 127716279 |