Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 135114 |
| ensemblid | ENSG00000111911.7 |
| hgncid | 18468 |
| symbol | HINT3 |
| name | histidine triad nucleotide binding protein 3 |
| refseq_nuc | NM_138571.5 |
| refseq_prot | NP_612638.3 |
| ensembl_nuc | ENST00000229633.7 |
| ensembl_prot | ENSP00000229633.5 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 125956770 |
| end | 125980244 |
| strand | + |
| ver | v1.2 |
| region | chr6:125956770-125980244 |
| region5000 | chr6:125951770-125985244 |
| regionname0 | HINT3_chr6_125956770_125980244 |
| regionname5000 | HINT3_chr6_125951770_125985244 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 182 | 166 | 58 | 27 | 57 | 9 | 14 | 36 | HINT3_chr6_125951770_125985244 | HINT3 | MAEEQ others(177): Show |
chr6 | 125951770 | 125985244 |
| a0002 | 1/0 | 182 | 101 | 33 | 29 | 11 | 9 | 18 | 8 | HINT3_chr6_125951770_125985244 | HINT3 | MAEEQ others(177): Show |
chr6 | 125951770 | 125985244 |
| a0003 | 0/0 | 182 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | MAEEQ others(177): Show |
chr6 | 125951770 | 125985244 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 546 | 165 | 57 | 27 | 57 | 9 | 14 | HINT3_chr6_125951770_125985244 | HINT3 | ATGGC others(541): Show |
chr6 | 125951770 | 125985244 | ||
| a0001c0004 | 0/0 | 546 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | ATGGC others(541): Show |
chr6 | 125951770 | 125985244 | ||
| a0002c0002 | 1/0 | 546 | 100 | 33 | 29 | 11 | 9 | 17 | HINT3_chr6_125951770_125985244 | HINT3 | ATGGC others(541): Show |
chr6 | 125951770 | 125985244 | ||
| a0002c0005 | 0/0 | 546 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | ATGGC others(541): Show |
chr6 | 125951770 | 125985244 | ||
| a0003c0003 | 0/0 | 546 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | ATGGC others(541): Show |
chr6 | 125951770 | 125985244 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3327 | 131 | 28 | 23 | 56 | 9 | 14 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0001c0001t0003 | 0/0 | 3327 | 17 | 17 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0001c0001t0004 | 0/0 | 3327 | 5 | 5 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0001c0001t0005 | 0/0 | 3327 | 3 | 3 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0001c0001t0008 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0001c0001t0010 | 0/0 | 3327 | 2 | 0 | 2 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0001c0001t0011 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0001c0001t0012 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0001c0001t0014 | 0/0 | 3327 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0001c0001t0016 | 0/0 | 3327 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0001c0001t0018 | 0/0 | 3327 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0001c0004t0001 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0002c0002t0001 | 0/0 | 3327 | 20 | 4 | 8 | 0 | 3 | 5 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0002c0002t0002 | 1/0 | 3325 | 66 | 22 | 17 | 11 | 5 | 10 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3320): Show |
chr6 | 125951770 | 125985244 |
| a0002c0002t0004 | 0/0 | 3327 | 5 | 4 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0002c0002t0006 | 0/0 | 3325 | 2 | 0 | 1 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3320): Show |
chr6 | 125951770 | 125985244 |
| a0002c0002t0007 | 0/0 | 3325 | 2 | 0 | 0 | 0 | 0 | 2 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3320): Show |
chr6 | 125951770 | 125985244 |
| a0002c0002t0009 | 0/0 | 3325 | 2 | 1 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3320): Show |
chr6 | 125951770 | 125985244 |
| a0002c0002t0013 | 0/0 | 3327 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0002c0002t0015 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0002c0002t0017 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| a0002c0005t0002 | 0/0 | 3325 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3320): Show |
chr6 | 125951770 | 125985244 |
| a0003c0003t0003 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | CTCTA others(3322): Show |
chr6 | 125951770 | 125985244 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 0 | 5 | 5 | 1 | 2 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 0 | 2 | 3 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0010g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0010g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0011g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0012g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0014g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0001t0018g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0001c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0006 | 0/0 | 5 | 2 | 1 | 0 | 0 | 2 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0021 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0002 | 0/0 | 8 | 0 | 2 | 1 | 3 | 2 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0003 | 0/0 | 7 | 0 | 4 | 0 | 0 | 3 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0017 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0006g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0007g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0009g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0013g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0015g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0002t0017g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0002c0005t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| a0003c0003t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0021 | EUR | GBR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0017 | EUR | GBR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0033 | EUR | FIN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | FIN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0076 | EUR | FIN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0050 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0033 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00642 | hp2 | a0002 | c0002 | t0009 | g0049 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0046 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0179 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0074 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01109 | hp2 | a0002 | c0002 | t0006 | g0002 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01192 | hp1 | a0002 | c0002 | t0004 | g0029 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0072 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01243 | hp1 | a0001 | c0001 | t0018 | g0034 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01256 | hp1 | a0001 | c0001 | t0010 | g0004 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0044 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0019 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01258 | hp2 | a0001 | c0001 | t0010 | g0013 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01358 | hp2 | a0002 | c0002 | t0013 | g0183 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01516 | hp1 | a0002 | c0002 | t0006 | g0002 | EUR | IBS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01943 | hp1 | a0001 | c0001 | t0014 | g0035 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0042 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0068 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0045 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02055 | hp2 | a0002 | c0002 | t0004 | g0169 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | CDX | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0161 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0059 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02451 | hp2 | a0002 | c0002 | t0015 | g0069 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02572 | hp1 | a0002 | c0002 | t0009 | g0048 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0177 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02615 | hp2 | a0002 | c0002 | t0004 | g0028 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0018 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02683 | hp2 | a0002 | c0005 | t0002 | g0003 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02698 | hp1 | a0002 | c0002 | t0007 | g0032 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0053 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0054 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02723 | hp1 | a0002 | c0002 | t0017 | g0029 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0080 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0066 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02976 | hp1 | a0002 | c0002 | t0004 | g0028 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0077 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0064 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0058 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0162 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0181 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03453 | hp1 | a0001 | c0001 | t0012 | g0041 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0078 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0065 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03540 | hp2 | a0003 | c0003 | t0003 | g0015 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0082 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0154 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0075 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03669 | hp2 | a0002 | c0002 | t0007 | g0032 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0060 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0061 | SAS | BEB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0071 | SAS | STU | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | YRI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | YRI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19003 | hp2 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | LWK | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0081 | AFR | LWK | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0043 | AFR | YRI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | YRI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0051 | AFR | ASW | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ASW | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | TSI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | TSI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | GIH | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02486 | hp1 | a0002 | c0002 | t0004 | g0168 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0047 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | USA | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | USA | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | USA | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | USA | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0182 | AFR | LWK | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0055 | AFR | LWK | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0157 | REF | REF | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0017 | REF | REF | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125957084 | G | C | 2 | a0001 a0003 |
166 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(163): Show |
missense_variant | MODERATE | c.107G>C | p.Gly36Ala | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/5 | 315/3325 | 107/549 | 36/182 | chr6 | 125957084 | |||
| chr6:125966963 | T | C | 1 | a0003 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.278T>C | p.Ile93Thr | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/5 | 486/3325 | 278/549 | 93/182 | chr6 | 125966963 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125957130 | C | T | 1 | a0002c0005 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.153C>T | p.Cys51Cys | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/5 | 361/3325 | 153/549 | 51/182 | chr6 | 125957130 | |||
| chr6:125974940 | G | A | 1 | a0001c0004 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.483G>A | p.Leu161Leu | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/5 | 691/3325 | 483/549 | 161/182 | chr6 | 125974940 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125956834 | C | T | 1 | a0001c0001t0018 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-144C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/5 | 144 | chr6 | 125956834 | ||||||
| chr6:125956930 | C | T | 1 | a0001c0001t0010 | 2 | HG01256.hp1 HG01258.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-48C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/5 | chr6 | 125956930 | |||||||
| chr6:125977980 | A | T | 1 | a0001c0001t0018 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*304A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 304 | chr6 | 125977980 | ||||||
| chr6:125978071 | A | T | 1 | a0002c0002t0009 | 2 | HG00642.hp2 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*395A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 395 | chr6 | 125978071 | ||||||
| chr6:125978118 | A | T | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*442A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 442 | chr6 | 125978118 | ||||||
| chr6:125978159 | A | G | 1 | a0002c0002t0017 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*483A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 483 | chr6 | 125978159 | ||||||
| chr6:125978297 | A | T | 3 | a0001c0001t0004 a0002c0002t0004 a0002c0002t0017 |
11 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*621A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 621 | chr6 | 125978297 | ||||||
| chr6:125978562 | C | T | 1 | a0001c0001t0016 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*886C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 886 | chr6 | 125978562 | ||||||
| chr6:125978624 | T | C | 1 | a0001c0001t0011 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*948T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 948 | chr6 | 125978624 | ||||||
| chr6:125978641 | C | A | 1 | a0001c0001t0012 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*965C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 965 | chr6 | 125978641 | ||||||
| chr6:125978773 | A | G | 1 | a0001c0001t0008 | 2 | HG02976.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1097A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1097 | chr6 | 125978773 | ||||||
| chr6:125978838 | A | ACT | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*1162_*1163insCT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1163 | chr6 | 125978838 | ||||||
| chr6:125979000 | G | A | 1 | a0002c0002t0013 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1324G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1324 | chr6 | 125979000 | ||||||
| chr6:125979124 | G | A | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(13): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*1448G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1448 | chr6 | 125979124 | ||||||
| chr6:125979184 | T | C | 1 | a0001c0001t0018 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1508T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1508 | chr6 | 125979184 | ||||||
| chr6:125979272 | G | T | 2 | a0001c0001t0008 a0001c0001t0012 |
3 | HG02976.hp2 HG03453.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1596G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1596 | chr6 | 125979272 | ||||||
| chr6:125979299 | A | G | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(3): Show |
32 | HG01192.hp1 HG01891.hp2 HG02055.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1623A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1623 | chr6 | 125979299 | ||||||
| chr6:125979431 | G | A | 1 | a0002c0002t0006 | 2 | HG01109.hp2 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1755G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1755 | chr6 | 125979431 | ||||||
| chr6:125979709 | G | A | 1 | a0001c0001t0005 | 3 | HG02895.hp1 HG03579.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2033G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 2033 | chr6 | 125979709 | ||||||
| chr6:125979821 | A | G | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(14): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*2145A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 2145 | chr6 | 125979821 | ||||||
| chr6:125979907 | G | A | 1 | a0001c0001t0014 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2231G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 2231 | chr6 | 125979907 | ||||||
| chr6:125980139 | C | T | 1 | a0002c0002t0015 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2463C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 2463 | chr6 | 125980139 | ||||||
| chr6:125980219 | A | G | 1 | a0002c0002t0007 | 2 | HG02698.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2543A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 2543 | chr6 | 125980219 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125957443 | C | A | 1 | a0001c0001t0018g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.201+265C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125957443 | |||||||
| chr6:125957481 | C | T | 1 | a0002c0002t0002g0184 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.201+303C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125957481 | |||||||
| chr6:125957908 | T | A | 1 | a0001c0001t0014g0035 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.201+730T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125957908 | |||||||
| chr6:125957909 | A | T | 6 | a0002c0002t0001g0033 a0002c0002t0001g0179 a0002c0002t0001g0180 others(3): Show |
7 | HG00280.hp2 HG00642.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+731A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125957909 | |||||||
| chr6:125957912 | A | C | 1 | a0001c0001t0004g0178 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.201+734A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125957912 | |||||||
| chr6:125958041 | C | T | 2 | a0002c0002t0002g0177 a0002c0002t0007g0032 |
3 | HG02602.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.201+863C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958041 | |||||||
| chr6:125958042 | G | T | 18 | a0001c0001t0003g0015 a0001c0001t0003g0030 a0001c0001t0003g0031 others(15): Show |
22 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.201+864G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958042 | |||||||
| chr6:125958120 | AG | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
5 | HG02809.hp2 HG02970.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+944delG | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125958120 | ||||||
| chr6:125958280 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.201+1102G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958280 | |||||||
| chr6:125958428 | T | C | 1 | a0001c0001t0018g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.201+1250T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958428 | |||||||
| chr6:125958505 | A | C | 4 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0165 others(1): Show |
4 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+1327A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958505 | |||||||
| chr6:125958881 | G | A | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.201+1703G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958881 | |||||||
| chr6:125958901 | C | A | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.201+1723C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958901 | |||||||
| chr6:125959188 | C | T | 1 | a0001c0001t0011g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.201+2010C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125959188 | |||||||
| chr6:125959369 | C | T | 2 | a0001c0001t0001g0160 a0001c0004t0001g0161 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.201+2191C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125959369 | |||||||
| chr6:125959373 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(130): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.201+2195A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125959373 | |||||||
| chr6:125959486 | G | A | 41 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0085 others(38): Show |
47 | HG00741.hp1 HG01192.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.201+2308G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125959486 | |||||||
| chr6:125959880 | C | T | 2 | a0001c0001t0001g0160 a0001c0004t0001g0161 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.201+2702C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125959880 | |||||||
| chr6:125960093 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.201+2915T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960093 | |||||||
| chr6:125960113 | C | T | 18 | a0001c0001t0003g0015 a0001c0001t0003g0030 a0001c0001t0003g0031 others(15): Show |
22 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.201+2935C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960113 | |||||||
| chr6:125960320 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.201+3142G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960320 | |||||||
| chr6:125960371 | T | C | 1 | a0001c0001t0008g0077 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.201+3193T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960371 | |||||||
| chr6:125960396 | C | T | 36 | a0001c0001t0001g0012 a0001c0001t0001g0085 a0001c0001t0001g0086 others(33): Show |
42 | HG00741.hp1 HG01192.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.201+3218C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960396 | |||||||
| chr6:125960451 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0091 a0001c0001t0001g0092 |
4 | HG00408.hp1 HG02083.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+3273G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960451 | |||||||
| chr6:125960613 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.201+3435C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960613 | |||||||
| chr6:125960616 | C | T | 1 | a0002c0002t0002g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.201+3438C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960616 | |||||||
| chr6:125960655 | T | TG | 19 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0091 others(16): Show |
23 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.201+3487dupG | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125960655 | ||||||
| chr6:125960657 | G | C | 1 | a0001c0001t0001g0012 | 3 | HG02896.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.201+3479G>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960657 | |||||||
| chr6:125960665 | GA | G | 26 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0016 others(23): Show |
37 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.201+3496delA | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125960665 | ||||||
| chr6:125960666 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.201+3488A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960666 | |||||||
| chr6:125960667 | A | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0096 |
4 | HG02040.hp1 HG02040.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+3489A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960667 | |||||||
| chr6:125960667 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(99): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.201+3489A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960667 | |||||||
| chr6:125960668 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(105): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.201+3490A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960668 | |||||||
| chr6:125960669 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.201+3491A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960669 | |||||||
| chr6:125960670 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.201+3492A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960670 | |||||||
| chr6:125960671 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.201+3493A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960671 | |||||||
| chr6:125960672 | A | G | 10 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0036 others(7): Show |
12 | HG00280.hp1 HG01106.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.201+3494A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960672 | |||||||
| chr6:125960718 | A | T | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.201+3540A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960718 | |||||||
| chr6:125960929 | T | C | 1 | a0001c0001t0011g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.201+3751T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960929 | |||||||
| chr6:125960997 | A | T | 1 | a0001c0004t0001g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.201+3819A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960997 | |||||||
| chr6:125961062 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.201+3884A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961062 | |||||||
| chr6:125961111 | A | G | 1 | a0001c0001t0003g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.201+3933A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961111 | |||||||
| chr6:125961140 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.201+3962G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961140 | |||||||
| chr6:125961194 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.201+4016G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961194 | |||||||
| chr6:125961206 | C | A | 1 | a0002c0002t0002g0042 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.201+4028C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961206 | |||||||
| chr6:125961388 | A | G | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.201+4210A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961388 | |||||||
| chr6:125961459 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(144): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.201+4281T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961459 | |||||||
| chr6:125961478 | C | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0145 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.201+4300C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961478 | |||||||
| chr6:125961764 | T | C | 1 | a0002c0002t0002g0043 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.201+4586T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961764 | |||||||
| chr6:125961765 | C | T | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.201+4587C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961765 | |||||||
| chr6:125961985 | CCTGACTT others(63): Show |
C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.201+4809_202-4831d others(72): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125961985 | ||||||
| chr6:125962149 | C | CATATATA others(19): Show |
2 | a0002c0002t0002g0019 a0002c0002t0002g0020 |
4 | HG01069.hp1 HG01071.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-4702_202-4677d others(28): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962149 | ||||||
| chr6:125962155 | T | C | 2 | a0001c0001t0008g0077 a0001c0001t0008g0078 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.202-4732T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962155 | |||||||
| chr6:125962159 | TACACATA others(87): Show |
T | 2 | a0001c0001t0003g0089 a0001c0001t0003g0175 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.202-4724_202-4631d others(96): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962159 | ||||||
| chr6:125962160 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-4727A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962160 | |||||||
| chr6:125962161 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-4726C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962161 | |||||||
| chr6:125962161 | CACATAT | C | 15 | a0001c0001t0001g0008 a0002c0002t0001g0006 a0002c0002t0001g0033 others(12): Show |
20 | HG00280.hp2 HG00642.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.202-4724_202-4719d others(8): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | ||||||
| chr6:125962161 | CACATATA others(1): Show |
C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(60): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.202-4724_202-4717d others(10): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | ||||||
| chr6:125962161 | CACATATA others(3): Show |
C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(46): Show |
61 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.202-4724_202-4715d others(12): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | ||||||
| chr6:125962161 | CACATATA others(5): Show |
C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0141 |
3 | HG01515.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.202-4724_202-4713d others(14): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | ||||||
| chr6:125962161 | CACATATA others(7): Show |
C | 1 | a0001c0001t0001g0007 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.202-4724_202-4711d others(16): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | ||||||
| chr6:125962161 | CACATATA others(25): Show |
C | 10 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0018 others(7): Show |
16 | HG00609.hp1 HG00738.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.202-4724_202-4693d others(34): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | ||||||
| chr6:125962161 | CACATATA others(27): Show |
C | 1 | a0002c0002t0002g0010 | 3 | HG02965.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.202-4724_202-4691d others(36): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | ||||||
| chr6:125962161 | CACATATA others(89): Show |
C | 1 | a0001c0001t0018g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.202-4724_202-4629d others(98): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | ||||||
| chr6:125962161 | CACATATA others(146): Show |
C | 2 | a0001c0001t0001g0160 a0001c0004t0001g0161 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.202-4724_202-4572d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | ||||||
| chr6:125962163 | C | CAT | 2 | a0002c0002t0002g0002 a0002c0002t0002g0044 |
3 | HG00738.hp2 HG01167.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.202-4702_202-4701d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962163 | ||||||
| chr6:125962163 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(26): Show |
35 | HG00099.hp2 HG01074.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.202-4724C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962163 | |||||||
| chr6:125962165 | TATATATA others(17): Show |
T | 5 | a0002c0002t0002g0009 a0002c0002t0002g0059 a0002c0002t0002g0062 others(2): Show |
6 | HG02258.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-4660_202-4637d others(26): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962165 | ||||||
| chr6:125962167 | T | C | 2 | a0001c0001t0008g0077 a0001c0001t0008g0078 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.202-4720T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962167 | |||||||
| chr6:125962167 | TATATATA others(15): Show |
T | 1 | a0002c0002t0002g0009 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.202-4700_202-4679d others(24): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962167 | ||||||
| chr6:125962171 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-4716T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962171 | |||||||
| chr6:125962177 | T | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(24): Show |
33 | HG00099.hp2 HG01074.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.202-4710T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962177 | |||||||
| chr6:125962179 | T | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(24): Show |
33 | HG00099.hp2 HG01074.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.202-4708T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962179 | |||||||
| chr6:125962181 | T | C | 2 | a0001c0001t0001g0106 a0002c0002t0001g0021 |
2 | HG00099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.202-4706T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962181 | |||||||
| chr6:125962183 | T | C | 14 | a0001c0001t0001g0111 a0002c0002t0001g0006 a0002c0002t0001g0033 others(11): Show |
19 | HG00280.hp2 HG00558.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.202-4704T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962183 | |||||||
| chr6:125962183 | TATACAC | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0016 others(10): Show |
17 | HG01074.hp2 HG02080.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.202-4700_202-4695d others(8): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962183 | ||||||
| chr6:125962185 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(58): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.202-4702T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962185 | |||||||
| chr6:125962185 | TACAC | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0105 a0001c0001t0001g0106 others(6): Show |
11 | HG00099.hp2 HG02258.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.202-4700_202-4697d others(6): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962185 | ||||||
| chr6:125962185 | TACACATA others(120): Show |
T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.202-4700_202-4574d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962185 | ||||||
| chr6:125962187 | C | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0088 a0001c0001t0003g0163 others(3): Show |
6 | HG00639.hp1 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-4700C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962187 | |||||||
| chr6:125962189 | C | CAT | 2 | a0002c0002t0002g0002 a0002c0002t0002g0177 |
3 | HG01515.hp2 HG01517.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.202-4678_202-4677d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962189 | ||||||
| chr6:125962189 | C | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(59): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.202-4698C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962189 | |||||||
| chr6:125962191 | TATATATA others(15): Show |
T | 2 | a0002c0002t0002g0043 a0002c0002t0002g0058 |
2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.202-4676_202-4655d others(24): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962191 | ||||||
| chr6:125962193 | TATATATA others(13): Show |
T | 1 | a0002c0002t0002g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.202-4676_202-4657d others(22): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962193 | ||||||
| chr6:125962198 | A | G | 2 | a0001c0001t0003g0163 a0001c0001t0003g0165 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.202-4689A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962198 | |||||||
| chr6:125962199 | TATATATA others(106): Show |
T | 1 | a0001c0001t0008g0077 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.202-4676_202-4564d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962199 | ||||||
| chr6:125962201 | TATATATA others(104): Show |
T | 1 | a0001c0001t0008g0078 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.202-4676_202-4566d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962201 | ||||||
| chr6:125962203 | TATATATA others(102): Show |
T | 3 | a0001c0001t0003g0084 a0001c0001t0004g0178 a0001c0001t0012g0041 |
3 | HG02922.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.202-4676_202-4568d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962203 | ||||||
| chr6:125962205 | TATATACA others(100): Show |
T | 2 | a0002c0002t0004g0029 a0002c0002t0004g0169 |
2 | HG01192.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.202-4676_202-4570d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962205 | ||||||
| chr6:125962207 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0002c0002t0002g0056 |
4 | HG01515.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-4680T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962207 | |||||||
| chr6:125962207 | TATACACA others(98): Show |
T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0088 others(5): Show |
8 | HG02055.hp1 HG02630.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-4676_202-4572d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962207 | ||||||
| chr6:125962209 | T | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0002c0002t0002g0003 others(10): Show |
23 | HG00609.hp1 HG00738.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-4678T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962209 | |||||||
| chr6:125962209 | TACAC | T | 4 | a0001c0001t0003g0031 a0001c0001t0003g0166 a0001c0001t0003g0171 others(1): Show |
4 | HG02145.hp2 HG02647.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-4676_202-4673d others(6): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962209 | ||||||
| chr6:125962209 | TACACATA others(92): Show |
T | 5 | a0001c0001t0003g0015 a0001c0001t0003g0031 a0002c0002t0004g0028 others(2): Show |
6 | HG02486.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-4655_202-4557d others(101): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962209 | ||||||
| chr6:125962209 | TACACATA others(94): Show |
T | 2 | a0001c0001t0003g0030 a0001c0001t0004g0170 |
2 | HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.202-4674_202-4574d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962209 | ||||||
| chr6:125962209 | TACACATA others(96): Show |
T | 12 | a0001c0001t0001g0012 a0001c0001t0001g0085 a0001c0001t0003g0015 others(9): Show |
13 | HG00741.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.202-4676_202-4574d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962209 | ||||||
| chr6:125962211 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(39): Show |
56 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.202-4676C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962211 | |||||||
| chr6:125962213 | C | CAT | 4 | a0002c0002t0002g0002 a0002c0002t0002g0060 a0002c0002t0002g0076 others(1): Show |
7 | HG00323.hp2 HG02523.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-4654_202-4653d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962213 | ||||||
| chr6:125962213 | C | CATATATA others(61): Show |
1 | a0002c0002t0002g0045 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.202-4653_202-4652i others(70): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962213 | ||||||
| chr6:125962213 | C | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0002c0002t0002g0003 others(10): Show |
23 | HG00609.hp1 HG00738.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-4674C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962213 | |||||||
| chr6:125962213 | CAT | C | 4 | a0002c0002t0002g0002 a0002c0002t0002g0046 a0002c0002t0002g0053 others(1): Show |
4 | HG01074.hp1 HG02698.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-4654_202-4653d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962213 | ||||||
| chr6:125962215 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(38): Show |
56 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.202-4672T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962215 | |||||||
| chr6:125962215 | T | TATATATA others(41): Show |
1 | a0002c0002t0002g0177 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.202-4653_202-4652i others(50): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962215 | ||||||
| chr6:125962217 | TATATATA others(51): Show |
T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0145 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.202-4658_202-4601d others(60): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962217 | ||||||
| chr6:125962219 | TATATATA others(11): Show |
T | 3 | a0002c0002t0002g0011 a0002c0002t0002g0054 a0002c0002t0002g0066 |
4 | HG02717.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-4654_202-4637d others(20): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962219 | ||||||
| chr6:125962219 | TATATATA others(49): Show |
T | 4 | a0001c0001t0001g0107 a0002c0002t0001g0001 a0002c0002t0001g0006 others(1): Show |
5 | HG02257.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-4656_202-4601d others(58): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962219 | ||||||
| chr6:125962219 | TATATATA others(86): Show |
T | 2 | a0001c0001t0003g0031 a0001c0001t0003g0174 |
2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.202-4652_202-4560d others(95): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962219 | ||||||
| chr6:125962221 | TATATATA others(47): Show |
T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(59): Show |
77 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(74): Show |
intron_variant | MODIFIER | c.202-4654_202-4601d others(56): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962221 | ||||||
| chr6:125962225 | TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.202-4652_202-4641d others(14): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962225 | ||||||
| chr6:125962225 | TATATATA others(80): Show |
T | 2 | a0001c0001t0003g0166 a0001c0001t0003g0171 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.202-4652_202-4566d others(89): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962225 | ||||||
| chr6:125962227 | TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0129 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.202-4652_202-4643d others(12): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962227 | ||||||
| chr6:125962231 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0095 |
2 | HG02683.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.202-4656T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962231 | |||||||
| chr6:125962233 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(34): Show |
52 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.202-4654T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962233 | |||||||
| chr6:125962233 | T | TAC | 3 | a0002c0002t0002g0019 a0002c0002t0002g0050 a0002c0002t0002g0072 |
4 | HG00639.hp1 HG01192.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-4650_202-4649d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962233 | ||||||
| chr6:125962235 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0110 others(3): Show |
7 | HG00280.hp1 HG00323.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-4652C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962235 | |||||||
| chr6:125962235 | CACATATA others(43): Show |
C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0104 |
2 | HG02074.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.202-4648_202-4599d others(52): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962235 | ||||||
| chr6:125962237 | C | T | 1 | a0002c0002t0002g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.202-4650C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962237 | |||||||
| chr6:125962237 | CATATATA others(74): Show |
C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0141 |
3 | HG01515.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.202-4637_202-4557d others(83): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962237 | ||||||
| chr6:125962239 | T | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0110 others(4): Show |
8 | HG00280.hp1 HG00323.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-4648T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962239 | |||||||
| chr6:125962239 | T | TATATATA others(83): Show |
1 | a0002c0002t0002g0002 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.202-4637_202-4636i others(92): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962239 | ||||||
| chr6:125962239 | TATATATA others(9): Show |
T | 1 | a0002c0002t0002g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.202-4636_202-4621d others(18): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962239 | ||||||
| chr6:125962241 | TATATATA others(41): Show |
T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(30): Show |
46 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.202-4636_202-4589d others(50): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962241 | ||||||
| chr6:125962243 | TATATATA others(39): Show |
T | 1 | a0002c0002t0001g0154 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.202-4636_202-4591d others(48): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962243 | ||||||
| chr6:125962247 | TATACACA others(21): Show |
T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0110 others(3): Show |
7 | HG00280.hp1 HG00323.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-4636_202-4609d others(30): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962247 | ||||||
| chr6:125962251 | C | T | 1 | a0002c0002t0002g0002 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.202-4636C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962251 | |||||||
| chr6:125962255 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02735.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.202-4632C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962255 | |||||||
| chr6:125962255 | CAT | C | 3 | a0002c0002t0002g0044 a0002c0002t0002g0045 a0002c0002t0002g0177 |
3 | HG01256.hp2 HG01981.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.202-4618_202-4617d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962255 | ||||||
| chr6:125962257 | T | C | 1 | a0002c0002t0002g0002 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.202-4630T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962257 | |||||||
| chr6:125962269 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.202-4618T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962269 | |||||||
| chr6:125962271 | CATACATA others(38): Show |
C | 1 | a0001c0001t0001g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.202-4612_202-4568d others(47): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962271 | ||||||
| chr6:125962271 | CATACATA others(40): Show |
C | 1 | a0001c0001t0001g0137 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.202-4612_202-4566d others(49): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962271 | ||||||
| chr6:125962273 | T | C | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0003g0089 others(2): Show |
5 | HG01243.hp1 HG02735.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-4614T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962273 | |||||||
| chr6:125962279 | TATATATA others(3): Show |
T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02735.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.202-4600_202-4591d others(12): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962279 | ||||||
| chr6:125962285 | T | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(54): Show |
70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.202-4602T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962285 | |||||||
| chr6:125962289 | CAT | C | 7 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0018 others(4): Show |
14 | HG00738.hp1 HG00738.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.202-4581_202-4580d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962289 | ||||||
| chr6:125962291 | T | C | 1 | a0002c0002t0002g0052 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.202-4596T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962291 | |||||||
| chr6:125962306 | AT | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0002c0002t0001g0033 others(8): Show |
12 | HG00280.hp2 HG00642.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-4580delT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962306 | |||||||
| chr6:125962307 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-4580T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962307 | |||||||
| chr6:125962307 | TC | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(47): Show |
70 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.202-4579delC | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962307 | |||||||
| chr6:125962307 | TCAC | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0016 others(8): Show |
12 | HG01074.hp2 HG02080.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-4579_202-4577d others(5): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962307 | |||||||
| chr6:125962307 | TCACAC | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(39): Show |
50 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.202-4579_202-4575d others(7): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962307 | |||||||
| chr6:125962308 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-4579C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962308 | |||||||
| chr6:125962310 | C | T | 6 | a0001c0001t0001g0147 a0001c0001t0003g0015 a0001c0001t0003g0031 others(3): Show |
7 | HG02486.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-4577C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962310 | |||||||
| chr6:125962312 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0016 others(16): Show |
21 | HG01074.hp2 HG02080.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.202-4575C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962312 | |||||||
| chr6:125962312 | CAT | C | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0009 others(12): Show |
26 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.202-4558_202-4557d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962312 | ||||||
| chr6:125962312 | CATATAT | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(57): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.202-4562_202-4557d others(8): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962312 | ||||||
| chr6:125962316 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
59 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.202-4571T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962316 | |||||||
| chr6:125962318 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(47): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.202-4569T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962318 | |||||||
| chr6:125962320 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.202-4567T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962320 | |||||||
| chr6:125962343 | A | T | 3 | a0001c0001t0008g0077 a0001c0001t0008g0078 a0001c0001t0012g0041 |
3 | HG02976.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.202-4544A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962343 | |||||||
| chr6:125962345 | C | T | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-4542C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962345 | |||||||
| chr6:125962374 | C | T | 2 | a0001c0001t0008g0077 a0001c0001t0008g0078 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.202-4513C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962374 | |||||||
| chr6:125962396 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(144): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.202-4491G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962396 | |||||||
| chr6:125962490 | C | T | 3 | a0001c0001t0008g0077 a0001c0001t0008g0078 a0001c0001t0012g0041 |
3 | HG02976.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.202-4397C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962490 | |||||||
| chr6:125962498 | C | T | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-4389C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962498 | |||||||
| chr6:125962534 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.202-4353C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962534 | |||||||
| chr6:125962628 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.202-4259T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962628 | |||||||
| chr6:125962759 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-4128G>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962759 | |||||||
| chr6:125963067 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(183): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.202-3820A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963067 | |||||||
| chr6:125963123 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-3764A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963123 | |||||||
| chr6:125963253 | G | A | 6 | a0002c0002t0002g0019 a0002c0002t0002g0020 a0002c0002t0002g0050 others(3): Show |
8 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-3634G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963253 | |||||||
| chr6:125963255 | T | G | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-3632T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963255 | |||||||
| chr6:125963258 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-3629T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963258 | |||||||
| chr6:125963262 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-3625A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963262 | |||||||
| chr6:125963350 | A | T | 1 | a0002c0002t0002g0065 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.202-3537A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963350 | |||||||
| chr6:125963521 | C | T | 2 | a0001c0001t0008g0077 a0001c0001t0008g0078 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.202-3366C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963521 | |||||||
| chr6:125963687 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0086 others(2): Show |
7 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-3200A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963687 | |||||||
| chr6:125963709 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.202-3178A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963709 | |||||||
| chr6:125963820 | T | C | 5 | a0002c0002t0004g0028 a0002c0002t0004g0029 a0002c0002t0004g0168 others(2): Show |
6 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-3067T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963820 | |||||||
| chr6:125963942 | C | G | 1 | a0001c0001t0008g0077 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.202-2945C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963942 | |||||||
| chr6:125964064 | A | G | 1 | a0001c0001t0011g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-2823A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964064 | |||||||
| chr6:125964101 | C | A | 1 | a0002c0002t0002g0065 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.202-2786C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964101 | |||||||
| chr6:125964187 | A | G | 18 | a0001c0001t0003g0015 a0001c0001t0003g0030 a0001c0001t0003g0031 others(15): Show |
22 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.202-2700A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964187 | |||||||
| chr6:125964195 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.202-2692C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964195 | |||||||
| chr6:125964323 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.202-2564T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964323 | |||||||
| chr6:125964395 | G | GT | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(144): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.202-2491dupT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964395 | ||||||
| chr6:125964453 | A | G | 1 | a0002c0002t0001g0180 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.202-2434A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964453 | |||||||
| chr6:125964597 | A | G | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-2290A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964597 | |||||||
| chr6:125964737 | T | TAC | 4 | a0002c0002t0002g0020 a0002c0002t0002g0043 a0002c0002t0002g0050 others(1): Show |
5 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-2112_202-2111d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | ||||||
| chr6:125964737 | T | TACAC | 2 | a0002c0002t0002g0010 a0002c0002t0002g0072 |
4 | HG01192.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-2114_202-2111d others(6): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | ||||||
| chr6:125964737 | TAC | T | 10 | a0001c0001t0001g0085 a0001c0001t0001g0160 a0001c0001t0003g0089 others(7): Show |
12 | HG00609.hp1 HG00741.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-2112_202-2111d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | ||||||
| chr6:125964737 | TACAC | T | 7 | a0001c0001t0001g0145 a0001c0001t0011g0162 a0001c0001t0018g0034 others(4): Show |
13 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.202-2114_202-2111d others(6): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | ||||||
| chr6:125964737 | TACACAC | T | 19 | a0001c0001t0003g0015 a0001c0001t0003g0030 a0001c0001t0003g0031 others(16): Show |
23 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.202-2116_202-2111d others(8): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | ||||||
| chr6:125964737 | TACACACA others(1): Show |
T | 27 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0143 others(24): Show |
33 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.202-2118_202-2111d others(10): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | ||||||
| chr6:125964737 | TACACACA others(3): Show |
T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.202-2120_202-2111d others(12): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | ||||||
| chr6:125964737 | TACACACA others(5): Show |
T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0086 others(1): Show |
6 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-2122_202-2111d others(14): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | ||||||
| chr6:125964739 | CACACACA others(4): Show |
C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-2147_202-2137d others(13): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964739 | |||||||
| chr6:125964799 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.202-2088G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964799 | |||||||
| chr6:125964799 | G | T | 1 | a0001c0001t0008g0078 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.202-2088G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964799 | |||||||
| chr6:125964877 | A | G | 1 | a0001c0001t0003g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.202-2010A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964877 | |||||||
| chr6:125964969 | C | G | 1 | a0002c0002t0001g0073 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.202-1918C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964969 | |||||||
| chr6:125965026 | A | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0097 a0001c0001t0001g0126 |
4 | HG00621.hp2 HG02523.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-1861A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125965026 | |||||||
| chr6:125965427 | T | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02080.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.202-1460T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125965427 | |||||||
| chr6:125965441 | T | A | 1 | a0001c0001t0001g0103 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.202-1446T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125965441 | |||||||
| chr6:125965670 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.202-1217T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125965670 | |||||||
| chr6:125965743 | C | A | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-1144C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125965743 | |||||||
| chr6:125965909 | A | G | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-978A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125965909 | |||||||
| chr6:125966005 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(185): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.202-882T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966005 | |||||||
| chr6:125966008 | G | A | 1 | a0001c0004t0001g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.202-879G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966008 | |||||||
| chr6:125966012 | C | T | 4 | a0001c0001t0003g0084 a0001c0001t0005g0080 a0001c0001t0005g0081 others(1): Show |
4 | HG02895.hp1 HG02922.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-875C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966012 | |||||||
| chr6:125966080 | G | A | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-807G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966080 | |||||||
| chr6:125966084 | A | G | 2 | a0001c0001t0008g0077 a0001c0001t0008g0078 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.202-803A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966084 | |||||||
| chr6:125966112 | T | C | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-775T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966112 | |||||||
| chr6:125966115 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-772A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966115 | |||||||
| chr6:125966118 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-769A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966118 | |||||||
| chr6:125966291 | G | T | 3 | a0001c0001t0008g0077 a0001c0001t0008g0078 a0001c0001t0012g0041 |
3 | HG02976.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.202-596G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966291 | |||||||
| chr6:125966444 | C | T | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-443C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966444 | |||||||
| chr6:125966560 | G | GA | 3 | a0001c0001t0008g0077 a0001c0001t0008g0078 a0001c0001t0012g0041 |
3 | HG02976.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.202-327_202-326ins others(1): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966560 | |||||||
| chr6:125966582 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-305A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966582 | |||||||
| chr6:125966767 | G | T | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-120G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966767 | |||||||
| chr6:125966777 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-110A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966777 | |||||||
| chr6:125966779 | A | G | 4 | a0002c0002t0002g0011 a0002c0002t0002g0054 a0002c0002t0002g0066 others(1): Show |
6 | HG02647.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-108A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966779 | |||||||
| chr6:125966780 | T | G | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-107T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966780 | |||||||
| chr6:125966854 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-33T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966854 | |||||||
| chr6:125966855 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-32A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966855 | |||||||
| chr6:125966858 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-29A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966858 | |||||||
| chr6:125966877 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(141): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.202-10T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966877 | |||||||
| chr6:125967009 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19066.hp1 | splice_region_variant&intron_variant | LOW | c.319+5G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967009 | |||||||
| chr6:125967052 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.319+48A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967052 | |||||||
| chr6:125967221 | A | T | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.319+217A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967221 | |||||||
| chr6:125967225 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.319+221T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967225 | |||||||
| chr6:125967326 | CT | C | 9 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(6): Show |
9 | HG00099.hp1 HG00323.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.319+345delT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125967326 | ||||||
| chr6:125967326 | CTT | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(126): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.319+344_319+345del others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125967326 | ||||||
| chr6:125967326 | CTTT | C | 10 | a0001c0001t0001g0079 a0001c0001t0001g0088 a0001c0001t0001g0105 others(7): Show |
11 | HG02258.hp1 HG02615.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.319+343_319+345del others(3): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125967326 | ||||||
| chr6:125967466 | G | T | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.319+462G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967466 | |||||||
| chr6:125967524 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.319+520G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967524 | |||||||
| chr6:125967601 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0150 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.319+597G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967601 | |||||||
| chr6:125967772 | A | T | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.319+768A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967772 | |||||||
| chr6:125967880 | C | G | 1 | a0002c0002t0002g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.319+876C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967880 | |||||||
| chr6:125967993 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.319+989G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967993 | |||||||
| chr6:125968151 | C | T | 1 | a0002c0002t0002g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.319+1147C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968151 | |||||||
| chr6:125968301 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.319+1297A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968301 | |||||||
| chr6:125968324 | T | C | 1 | a0001c0001t0008g0077 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.319+1320T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968324 | |||||||
| chr6:125968366 | G | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(141): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.319+1362G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968366 | |||||||
| chr6:125968800 | C | T | 1 | a0002c0002t0002g0063 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.319+1796C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968800 | |||||||
| chr6:125968845 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.319+1841A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968845 | |||||||
| chr6:125968882 | A | G | 2 | a0001c0001t0003g0031 a0001c0001t0003g0174 |
3 | HG02622.hp1 HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.319+1878A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968882 | |||||||
| chr6:125969058 | C | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0062 a0002c0002t0002g0064 |
5 | HG02451.hp1 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.319+2054C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969058 | |||||||
| chr6:125969115 | C | T | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.319+2111C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969115 | |||||||
| chr6:125969119 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(71): Show |
107 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.319+2115A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969119 | |||||||
| chr6:125969189 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.319+2185A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969189 | |||||||
| chr6:125969263 | G | A | 1 | a0001c0001t0001g0012 | 3 | HG02896.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.319+2259G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969263 | |||||||
| chr6:125969265 | A | G | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.319+2261A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969265 | |||||||
| chr6:125969319 | A | G | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.319+2315A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969319 | |||||||
| chr6:125969396 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(138): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.319+2392T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969396 | |||||||
| chr6:125969408 | C | T | 3 | a0001c0001t0004g0172 a0001c0001t0004g0173 a0001c0001t0004g0178 |
3 | HG03041.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.319+2404C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969408 | |||||||
| chr6:125969488 | T | G | 1 | a0002c0002t0002g0184 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.319+2484T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969488 | |||||||
| chr6:125969551 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.319+2547G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969551 | |||||||
| chr6:125969573 | T | G | 1 | a0001c0001t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.319+2569T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969573 | |||||||
| chr6:125969635 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.320-2624C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969635 | |||||||
| chr6:125969636 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.320-2623A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969636 | |||||||
| chr6:125969637 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.320-2622T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969637 | |||||||
| chr6:125969644 | G | A | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.320-2615G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969644 | |||||||
| chr6:125969846 | C | T | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.320-2413C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969846 | |||||||
| chr6:125969911 | G | A | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.320-2348G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969911 | |||||||
| chr6:125970123 | A | G | 2 | a0001c0001t0008g0077 a0001c0001t0008g0078 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.320-2136A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125970123 | |||||||
| chr6:125970330 | T | C | 1 | a0002c0002t0002g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.320-1929T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125970330 | |||||||
| chr6:125970762 | G | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(143): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.320-1497G>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125970762 | |||||||
| chr6:125970950 | A | G | 4 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0165 others(1): Show |
4 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.320-1309A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125970950 | |||||||
| chr6:125970968 | A | G | 1 | a0001c0001t0011g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.320-1291A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125970968 | |||||||
| chr6:125970996 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.320-1263A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125970996 | |||||||
| chr6:125971041 | G | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(167): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.320-1218G>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971041 | |||||||
| chr6:125971155 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.320-1104C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971155 | |||||||
| chr6:125971269 | C | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0120 |
3 | HG00408.hp2 NA19066.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.320-990C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971269 | |||||||
| chr6:125971318 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(143): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.320-941T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971318 | |||||||
| chr6:125971676 | A | G | 1 | a0002c0002t0002g0010 | 3 | HG02965.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.320-583A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971676 | |||||||
| chr6:125971688 | C | G | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.320-571C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971688 | |||||||
| chr6:125971702 | C | CT | 37 | a0001c0001t0001g0079 a0001c0001t0001g0088 a0001c0001t0001g0108 others(34): Show |
42 | HG00609.hp1 HG00642.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.320-531dupT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125971702 | ||||||
| chr6:125971702 | C | CTT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(79): Show |
113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.320-532_320-531dup others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125971702 | ||||||
| chr6:125971702 | C | CTTT | 18 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0037 others(15): Show |
23 | HG00597.hp1 HG00597.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.320-533_320-531dup others(3): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125971702 | ||||||
| chr6:125971702 | C | CTTTT | 14 | a0001c0001t0001g0038 a0001c0001t0001g0106 a0001c0001t0001g0131 others(11): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.320-534_320-531dup others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125971702 | ||||||
| chr6:125971702 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0137 |
2 | HG00639.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.320-544_320-531del others(14): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125971702 | ||||||
| chr6:125971866 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.320-393C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971866 | |||||||
| chr6:125972365 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0145 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.389+37T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972365 | |||||||
| chr6:125972493 | C | T | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.389+165C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972493 | |||||||
| chr6:125972507 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.389+179A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972507 | |||||||
| chr6:125972593 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.389+265T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972593 | |||||||
| chr6:125972639 | G | T | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.389+311G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972639 | |||||||
| chr6:125972749 | G | A | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.389+421G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972749 | |||||||
| chr6:125972899 | T | C | 1 | a0002c0002t0001g0154 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.389+571T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972899 | |||||||
| chr6:125972932 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.389+604T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972932 | |||||||
| chr6:125973065 | C | CT | 7 | a0001c0001t0001g0100 a0001c0001t0001g0140 a0001c0001t0001g0156 others(4): Show |
7 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+765dupT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 125973065 | ||||||
| chr6:125973065 | C | CTT | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(66): Show |
101 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.389+764_389+765dup others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 125973065 | ||||||
| chr6:125973065 | C | CTTT | 51 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0024 others(48): Show |
63 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.389+763_389+765dup others(3): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 125973065 | ||||||
| chr6:125973065 | C | CTTTT | 15 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0001c0001t0001g0038 others(12): Show |
16 | HG01069.hp2 HG01109.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.389+762_389+765dup others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 125973065 | ||||||
| chr6:125973078 | T | G | 1 | a0002c0002t0002g0056 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.389+750T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973078 | |||||||
| chr6:125973154 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.389+826C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973154 | |||||||
| chr6:125973168 | G | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(144): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.389+840G>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973168 | |||||||
| chr6:125973217 | G | A | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.389+889G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973217 | |||||||
| chr6:125973299 | G | A | 1 | a0002c0002t0002g0046 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.389+971G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973299 | |||||||
| chr6:125973303 | T | C | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.389+975T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973303 | |||||||
| chr6:125973321 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.389+993C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973321 | |||||||
| chr6:125973361 | G | A | 1 | a0002c0002t0001g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.389+1033G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973361 | |||||||
| chr6:125973426 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(144): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.389+1098G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973426 | |||||||
| chr6:125973556 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.389+1228G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973556 | |||||||
| chr6:125973562 | A | G | 2 | a0001c0001t0001g0160 a0001c0004t0001g0161 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.389+1234A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973562 | |||||||
| chr6:125973594 | G | C | 1 | a0002c0002t0002g0060 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.390-1253G>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973594 | |||||||
| chr6:125973834 | G | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(144): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.390-1013G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973834 | |||||||
| chr6:125973882 | T | C | 1 | a0001c0001t0018g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.390-965T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973882 | |||||||
| chr6:125973951 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.390-896G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973951 | |||||||
| chr6:125974138 | G | A | 8 | a0001c0001t0003g0084 a0001c0001t0003g0163 a0001c0001t0003g0164 others(5): Show |
8 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.390-709G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974138 | |||||||
| chr6:125974153 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.390-694T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974153 | |||||||
| chr6:125974189 | A | G | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.390-658A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974189 | |||||||
| chr6:125974336 | A | C | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.390-511A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974336 | |||||||
| chr6:125974340 | C | T | 2 | a0002c0002t0009g0048 a0002c0002t0009g0049 |
2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.390-507C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974340 | |||||||
| chr6:125974365 | T | C | 2 | a0002c0002t0002g0050 a0002c0002t0002g0072 |
2 | HG00639.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.390-482T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974365 | |||||||
| chr6:125974399 | G | GA | 7 | a0001c0001t0001g0132 a0001c0001t0001g0151 a0002c0002t0004g0028 others(4): Show |
8 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.390-445dupA | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 125974399 | ||||||
| chr6:125974540 | C | A | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.390-307C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974540 | |||||||
| chr6:125974599 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(144): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.390-248T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974599 | |||||||
| chr6:125974786 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.390-61C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974786 | |||||||
| chr6:125975105 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.516+132A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975105 | |||||||
| chr6:125975178 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.516+205A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975178 | |||||||
| chr6:125975200 | C | G | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0003g0083 others(8): Show |
11 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.516+227C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975200 | |||||||
| chr6:125975463 | A | G | 3 | a0001c0001t0005g0080 a0001c0001t0005g0081 a0001c0001t0005g0082 |
3 | HG02895.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.516+490A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975463 | |||||||
| chr6:125975524 | A | G | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.516+551A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975524 | |||||||
| chr6:125975575 | T | C | 14 | a0002c0002t0001g0006 a0002c0002t0001g0021 a0002c0002t0001g0033 others(11): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.516+602T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975575 | |||||||
| chr6:125975581 | G | GT | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(128): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.516+610dupT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 125975581 | ||||||
| chr6:125975581 | G | GTT | 11 | a0001c0001t0001g0023 a0001c0001t0001g0086 a0001c0001t0001g0102 others(8): Show |
12 | HG00558.hp1 HG01175.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.516+609_516+610dup others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 125975581 | ||||||
| chr6:125975584 | G | GTTTTTTT | 5 | a0001c0001t0008g0077 a0001c0001t0008g0078 a0002c0002t0002g0011 others(2): Show |
7 | HG02647.hp1 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.516+619_516+625dup others(7): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 125975584 | ||||||
| chr6:125975584 | G | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(142): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.516+611G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975584 | |||||||
| chr6:125975586 | T | TTTGTTTT others(4): Show |
1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.516+615_516+616ins others(11): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 125975586 | ||||||
| chr6:125975656 | C | T | 2 | a0001c0001t0008g0077 a0001c0001t0008g0078 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.516+683C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975656 | |||||||
| chr6:125975728 | C | G | 1 | a0001c0001t0003g0089 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.516+755C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975728 | |||||||
| chr6:125975765 | A | G | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.516+792A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975765 | |||||||
| chr6:125976110 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.516+1137A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976110 | |||||||
| chr6:125976142 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.516+1169A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976142 | |||||||
| chr6:125976235 | C | T | 3 | a0001c0001t0008g0077 a0001c0001t0008g0078 a0001c0001t0012g0041 |
3 | HG02976.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.516+1262C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976235 | |||||||
| chr6:125976399 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.517-1245T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976399 | |||||||
| chr6:125976454 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.517-1190A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976454 | |||||||
| chr6:125976517 | G | GT | 20 | a0001c0001t0001g0037 a0001c0001t0001g0105 a0001c0001t0001g0106 others(17): Show |
20 | HG00642.hp2 HG01081.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.517-1111dupT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 125976517 | ||||||
| chr6:125976517 | GT | G | 8 | a0001c0001t0003g0015 a0001c0001t0003g0031 a0001c0001t0003g0171 others(5): Show |
10 | HG02622.hp1 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.517-1111delT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 125976517 | ||||||
| chr6:125976558 | C | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1086C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976558 | |||||||
| chr6:125976559 | T | C | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1085T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976559 | |||||||
| chr6:125976562 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1082T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976562 | |||||||
| chr6:125976565 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1079T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976565 | |||||||
| chr6:125976567 | T | A | 4 | a0001c0001t0003g0084 a0001c0001t0005g0080 a0001c0001t0005g0081 others(1): Show |
4 | HG02895.hp1 HG02922.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-1077T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976567 | |||||||
| chr6:125976585 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1059T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976585 | |||||||
| chr6:125976591 | T | C | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-1053T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976591 | |||||||
| chr6:125976593 | A | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1051A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976593 | |||||||
| chr6:125976594 | G | A | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1050G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976594 | |||||||
| chr6:125976604 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1040T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976604 | |||||||
| chr6:125976612 | A | T | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1032A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976612 | |||||||
| chr6:125976614 | A | T | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1030A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976614 | |||||||
| chr6:125976632 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1012T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976632 | |||||||
| chr6:125976634 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1010T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976634 | |||||||
| chr6:125976654 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-990T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976654 | |||||||
| chr6:125976659 | T | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(6): Show |
9 | HG00558.hp1 HG01255.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-985T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976659 | |||||||
| chr6:125976661 | A | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-983A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976661 | |||||||
| chr6:125976674 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-970T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976674 | |||||||
| chr6:125976698 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(144): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.517-946A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976698 | |||||||
| chr6:125976700 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-944T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976700 | |||||||
| chr6:125976702 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-942T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976702 | |||||||
| chr6:125976715 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-929T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976715 | |||||||
| chr6:125976722 | A | T | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-922A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976722 | |||||||
| chr6:125976724 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-920T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976724 | |||||||
| chr6:125976728 | A | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-916A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976728 | |||||||
| chr6:125976734 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-910T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976734 | |||||||
| chr6:125976737 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-907T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976737 | |||||||
| chr6:125976739 | A | T | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-905A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976739 | |||||||
| chr6:125976741 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-903T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976741 | |||||||
| chr6:125976749 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-895T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976749 | |||||||
| chr6:125976761 | T | G | 1 | a0002c0002t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-883T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976761 | |||||||
| chr6:125976823 | T | C | 1 | a0001c0001t0004g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.517-821T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976823 | |||||||
| chr6:125976922 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.517-722T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976922 | |||||||
| chr6:125976949 | G | A | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-695G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976949 | |||||||
| chr6:125977223 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(144): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.517-421T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125977223 | |||||||
| chr6:125977275 | G | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(144): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.517-369G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125977275 | |||||||
| chr6:125977368 | A | G | 1 | a0001c0001t0012g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-276A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125977368 | |||||||
| chr6:125977601 | G | T | 1 | a0001c0001t0003g0089 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.517-43G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125977601 |