Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 56994 |
| ensemblid | ENSG00000111666.11 |
| hgncid | 17852 |
| symbol | CHPT1 |
| name | choline phosphotransferase 1 |
| refseq_nuc | NM_020244.3 |
| refseq_prot | NP_064629.2 |
| ensembl_nuc | ENST00000229266.8 |
| ensembl_prot | ENSP00000229266.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 101697640 |
| end | 101729074 |
| strand | + |
| ver | v1.2 |
| region | chr12:101697640-101729074 |
| region5000 | chr12:101692640-101734074 |
| regionname0 | CHPT1_chr12_101697640_101729074 |
| regionname5000 | CHPT1_chr12_101692640_101734074 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 406 | 282 | 82 | 46 | 119 | 10 | 23 | 96 | CHPT1_chr12_101692640_101734074 | CHPT1 | MAAGA others(401): Show |
chr12 | 101692640 | 101734074 |
| a0002 | 0/0 | 406 | 105 | 6 | 20 | 64 | 4 | 11 | 53 | CHPT1_chr12_101692640_101734074 | CHPT1 | MAAGA others(401): Show |
chr12 | 101692640 | 101734074 |
| a0003 | 0/0 | 406 | 9 | 0 | 1 | 8 | 0 | 0 | 4 | CHPT1_chr12_101692640_101734074 | CHPT1 | MAAGA others(401): Show |
chr12 | 101692640 | 101734074 |
| a0004 | 0/0 | 406 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | MAAGA others(401): Show |
chr12 | 101692640 | 101734074 |
| a0005 | 0/0 | 406 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | MAAGA others(401): Show |
chr12 | 101692640 | 101734074 |
| a0006 | 0/0 | 406 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | MAAGA others(401): Show |
chr12 | 101692640 | 101734074 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1218 | 144 | 62 | 9 | 59 | 3 | 11 | CHPT1_chr12_101692640_101734074 | CHPT1 | ATGGC others(1213): Show |
chr12 | 101692640 | 101734074 | ||
| a0001c0003 | 1/1 | 1218 | 89 | 17 | 26 | 27 | 6 | 11 | CHPT1_chr12_101692640_101734074 | CHPT1 | ATGGC others(1213): Show |
chr12 | 101692640 | 101734074 | ||
| a0001c0004 | 0/0 | 1218 | 37 | 2 | 11 | 22 | 1 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | ATGGC others(1213): Show |
chr12 | 101692640 | 101734074 | ||
| a0001c0005 | 0/0 | 1218 | 10 | 0 | 0 | 10 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | ATGGC others(1213): Show |
chr12 | 101692640 | 101734074 | ||
| a0001c0010 | 0/0 | 1218 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | ATGGC others(1213): Show |
chr12 | 101692640 | 101734074 | ||
| a0001c0012 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | ATGGC others(1213): Show |
chr12 | 101692640 | 101734074 | ||
| a0002c0002 | 0/0 | 1218 | 104 | 6 | 20 | 63 | 4 | 11 | CHPT1_chr12_101692640_101734074 | CHPT1 | ATGGC others(1213): Show |
chr12 | 101692640 | 101734074 | ||
| a0002c0009 | 0/0 | 1218 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | ATGGC others(1213): Show |
chr12 | 101692640 | 101734074 | ||
| a0003c0006 | 0/0 | 1218 | 9 | 0 | 1 | 8 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | ATGGC others(1213): Show |
chr12 | 101692640 | 101734074 | ||
| a0004c0007 | 0/0 | 1218 | 3 | 0 | 3 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | ATGGC others(1213): Show |
chr12 | 101692640 | 101734074 | ||
| a0005c0008 | 0/0 | 1218 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | ATGGC others(1213): Show |
chr12 | 101692640 | 101734074 | ||
| a0006c0011 | 0/0 | 1218 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | ATGGC others(1213): Show |
chr12 | 101692640 | 101734074 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1572 | 117 | 55 | 7 | 47 | 1 | 7 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0001c0001t0002 | 0/0 | 1572 | 13 | 5 | 2 | 0 | 2 | 4 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCTC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0001c0001t0003 | 0/0 | 1572 | 9 | 0 | 0 | 9 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0001c0001t0004 | 0/0 | 1572 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0001c0001t0007 | 0/0 | 1572 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCTC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0001c0003t0001 | 1/1 | 1572 | 85 | 17 | 26 | 24 | 5 | 11 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0001c0003t0002 | 0/0 | 1572 | 2 | 0 | 0 | 1 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCTC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0001c0003t0005 | 0/0 | 1572 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0001c0004t0001 | 0/0 | 1572 | 37 | 2 | 11 | 22 | 1 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0001c0005t0002 | 0/0 | 1572 | 10 | 0 | 0 | 10 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCTC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0001c0010t0001 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0001c0012t0001 | 0/0 | 1572 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0002c0002t0001 | 0/0 | 1572 | 99 | 6 | 20 | 59 | 4 | 10 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0002c0002t0002 | 0/0 | 1572 | 2 | 0 | 0 | 1 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCTC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0002c0002t0004 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0002c0002t0006 | 0/0 | 1572 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0002c0009t0001 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0003c0006t0001 | 0/0 | 1572 | 8 | 0 | 1 | 7 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0003c0006t0004 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0004c0007t0001 | 0/0 | 1572 | 3 | 0 | 3 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0005c0008t0001 | 0/0 | 1572 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| a0006c0011t0001 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | GCCCC others(1567): Show |
chr12 | 101692640 | 101734074 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 15 | 0 | 0 | 14 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0047 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0003g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0003g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0001 | 0/0 | 20 | 2 | 5 | 9 | 3 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0006 | 0/0 | 8 | 1 | 4 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0015 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0048 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0011 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0010t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0012t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0002 | 0/0 | 18 | 0 | 8 | 7 | 0 | 3 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0004 | 0/0 | 16 | 1 | 1 | 11 | 0 | 3 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0009t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0004c0007t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0004c0007t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0005c0008t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0005c0008t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0006c0011t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0033 | EUR | GBR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0001 | EUR | GBR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0001 | EUR | GBR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0223 | EUR | GBR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0130 | EUR | FIN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | FIN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0001 | EUR | FIN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00408 | hp1 | a0001 | c0003 | t0002 | g0129 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00423 | hp2 | a0001 | c0005 | t0002 | g0014 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00544 | hp2 | a0001 | c0004 | t0001 | g0005 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00597 | hp1 | a0003 | c0006 | t0001 | g0005 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00609 | hp2 | a0001 | c0005 | t0002 | g0127 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00621 | hp2 | a0001 | c0005 | t0002 | g0014 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00639 | hp1 | a0004 | c0007 | t0001 | g0040 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01069 | hp1 | a0004 | c0007 | t0001 | g0148 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01069 | hp2 | a0001 | c0004 | t0001 | g0011 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01070 | hp1 | a0001 | c0004 | t0001 | g0022 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0072 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0022 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01071 | hp2 | a0004 | c0007 | t0001 | g0040 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0045 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0228 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0147 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0230 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0216 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0033 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0038 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0185 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0038 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0200 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01346 | hp1 | a0001 | c0004 | t0001 | g0011 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0166 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0198 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01358 | hp2 | a0001 | c0004 | t0001 | g0011 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0229 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0152 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01433 | hp1 | a0001 | c0004 | t0001 | g0045 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0199 | EUR | IBS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0119 | EUR | IBS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0172 | EUR | IBS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0201 | EUR | IBS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0153 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01928 | hp2 | a0003 | c0006 | t0001 | g0005 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01943 | hp1 | a0001 | c0004 | t0001 | g0022 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0011 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0225 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0070 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02027 | hp1 | a0001 | c0005 | t0002 | g0014 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02040 | hp1 | a0001 | c0005 | t0002 | g0128 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02055 | hp1 | a0005 | c0008 | t0001 | g0235 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02056 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02074 | hp2 | a0002 | c0002 | t0006 | g0174 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0167 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02080 | hp2 | a0001 | c0005 | t0002 | g0014 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0158 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0048 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02155 | hp1 | a0003 | c0006 | t0001 | g0226 | EAS | CDX | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | CDX | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02165 | hp2 | a0001 | c0003 | t0005 | g0006 | EAS | CDX | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0118 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0068 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0069 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0102 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0162 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0103 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02717 | hp1 | a0005 | c0008 | t0001 | g0236 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0131 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0224 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0156 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0170 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0105 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0239 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0015 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0205 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03209 | hp1 | a0001 | c0012 | t0001 | g0100 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0202 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0027 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0164 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03710 | hp2 | a0001 | c0004 | t0001 | g0214 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0088 | SAS | BEB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0163 | SAS | BEB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0154 | SAS | BEB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | STU | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | STU | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | STU | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | STU | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | YRI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | YRI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18612 | hp2 | a0003 | c0006 | t0001 | g0210 | EAS | CHB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18747 | hp1 | a0003 | c0006 | t0004 | g0077 | EAS | CHB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | YRI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18941 | hp1 | a0001 | c0005 | t0002 | g0126 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0159 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18944 | hp1 | a0002 | c0009 | t0001 | g0171 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18945 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18946 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18956 | hp1 | a0003 | c0006 | t0001 | g0208 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18957 | hp1 | a0001 | c0005 | t0002 | g0133 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18960 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18962 | hp2 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18966 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18968 | hp2 | a0001 | c0003 | t0005 | g0028 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18969 | hp2 | a0003 | c0006 | t0001 | g0215 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18972 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18974 | hp1 | a0001 | c0004 | t0001 | g0212 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0211 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18977 | hp1 | a0002 | c0002 | t0004 | g0095 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18977 | hp2 | a0001 | c0004 | t0001 | g0218 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18978 | hp1 | a0002 | c0002 | t0006 | g0181 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18985 | hp1 | a0001 | c0003 | t0001 | g0160 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18986 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18988 | hp2 | a0001 | c0005 | t0002 | g0124 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18992 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18993 | hp1 | a0001 | c0005 | t0002 | g0125 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18997 | hp1 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18997 | hp2 | a0001 | c0004 | t0001 | g0217 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18998 | hp2 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0221 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19001 | hp1 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19003 | hp1 | a0003 | c0006 | t0001 | g0005 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19004 | hp1 | a0006 | c0011 | t0001 | g0076 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19009 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19009 | hp2 | a0001 | c0004 | t0001 | g0046 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0115 | AFR | LWK | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0111 | AFR | LWK | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | LWK | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19065 | hp1 | a0001 | c0004 | t0001 | g0213 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19066 | hp1 | a0001 | c0010 | t0001 | g0090 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19068 | hp2 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0046 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19074 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19075 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19081 | hp1 | a0001 | c0004 | t0001 | g0219 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19081 | hp2 | a0001 | c0003 | t0001 | g0074 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19083 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19084 | hp1 | a0003 | c0006 | t0001 | g0209 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19084 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | YRI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0036 | AFR | ASW | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0043 | EUR | TSI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0157 | EUR | TSI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0011 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0104 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0027 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | USA | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | USA | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18955 | hp2 | a0001 | c0004 | t0001 | g0220 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | USA | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | USA | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0227 | AFR | LWK | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0151 | REF | REF | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0048 | REF | REF | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:101697970 | G | A | 1 | a0005 | 2 | HG02055.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.109G>A | p.Ala37Thr | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | 331/1572 | 109/1221 | 37/406 | chr12 | 101697970 | |||
| chr12:101714153 | A | G | 1 | a0006 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.337A>G | p.Ile113Val | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 2/9 | 559/1572 | 337/1221 | 113/406 | chr12 | 101714153 | |||
| chr12:101714567 | T | C | 2 | a0002 a0006 |
106 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(103): Show |
missense_variant | MODERATE | c.485T>C | p.Phe162Ser | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/9 | 707/1572 | 485/1221 | 162/406 | chr12 | 101714567 | |||
| chr12:101720157 | C | T | 1 | a0004 | 3 | HG00639.hp1 HG01069.hp1 HG01071.hp2 |
missense_variant | MODERATE | c.683C>T | p.Pro228Leu | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/9 | 905/1572 | 683/1221 | 228/406 | chr12 | 101720157 | |||
| chr12:101723803 | T | C | 1 | a0003 | 9 | HG00597.hp1 HG01928.hp2 HG02155.hp1 others(6): Show |
missense_variant | MODERATE | c.1021T>C | p.Phe341Leu | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/9 | 1243/1572 | 1021/1221 | 341/406 | chr12 | 101723803 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:101698053 | C | T | 1 | a0001c0012 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.192C>T | p.Asn64Asn | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | 414/1572 | 192/1221 | 64/406 | chr12 | 101698053 | |||
| chr12:101714523 | T | C | 3 | a0001c0004 a0001c0005 a0003c0006 |
56 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
synonymous_variant | LOW | c.441T>C | p.Ala147Ala | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/9 | 663/1572 | 441/1221 | 147/406 | chr12 | 101714523 | |||
| chr12:101723811 | C | T | 9 | a0001c0001 a0001c0004 a0001c0005 others(6): Show |
309 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(306): Show |
synonymous_variant | LOW | c.1029C>T | p.Asn343Asn | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/9 | 1251/1572 | 1029/1221 | 343/406 | chr12 | 101723811 | |||
| chr12:101726374 | C | T | 2 | a0001c0005 a0001c0010 |
11 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(8): Show |
synonymous_variant | LOW | c.1146C>T | p.Phe382Phe | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/9 | 1368/1572 | 1146/1221 | 382/406 | chr12 | 101726374 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:101697643 | C | T | 5 | a0001c0001t0002 a0001c0001t0007 a0001c0003t0002 others(2): Show |
29 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-219C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | 219 | chr12 | 101697643 | ||||||
| chr12:101697647 | C | T | 1 | a0001c0001t0007 | 2 | HG02280.hp1 NA19030.hp1 |
5_prime_UTR_variant | MODIFIER | c.-215C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | 215 | chr12 | 101697647 | ||||||
| chr12:101697682 | G | A | 3 | a0001c0001t0004 a0002c0002t0004 a0003c0006t0004 |
5 | NA18747.hp1 NA18971.hp1 NA18977.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-180G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | 180 | chr12 | 101697682 | ||||||
| chr12:101697712 | C | T | 1 | a0002c0002t0006 | 2 | HG02074.hp2 NA18978.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-150C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | chr12 | 101697712 | |||||||
| chr12:101697726 | C | T | 1 | a0001c0001t0003 | 9 | HG00609.hp1 HG00621.hp1 NA18942.hp1 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-136C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | chr12 | 101697726 | |||||||
| chr12:101728972 | T | C | 1 | a0001c0003t0005 | 2 | HG02165.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*27T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 9/9 | 27 | chr12 | 101728972 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:101698180 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.273+46G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698180 | |||||||
| chr12:101698206 | G | C | 1 | a0001c0001t0003g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.273+72G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698206 | |||||||
| chr12:101698248 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.273+114G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698248 | |||||||
| chr12:101698256 | T | G | 1 | a0001c0003t0001g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.273+122T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698256 | |||||||
| chr12:101698457 | G | T | 6 | a0001c0001t0001g0050 a0001c0001t0001g0237 a0001c0001t0001g0238 others(3): Show |
7 | HG01081.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+323G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698457 | |||||||
| chr12:101698490 | T | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(197): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.273+356T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698490 | |||||||
| chr12:101698608 | G | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
163 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.273+474G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698608 | |||||||
| chr12:101698623 | C | T | 1 | a0002c0002t0001g0044 | 2 | HG02074.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.273+489C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698623 | |||||||
| chr12:101698664 | C | G | 23 | a0001c0001t0002g0017 a0001c0001t0002g0034 a0001c0001t0002g0116 others(20): Show |
29 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(26): Show |
intron_variant | MODIFIER | c.273+530C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698664 | |||||||
| chr12:101698920 | A | T | 1 | a0001c0001t0002g0134 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.273+786A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698920 | |||||||
| chr12:101698965 | C | A | 2 | a0001c0001t0001g0135 a0002c0002t0001g0035 |
3 | HG02109.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.273+831C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698965 | |||||||
| chr12:101699054 | A | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(196): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.273+920A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699054 | |||||||
| chr12:101699173 | C | T | 7 | a0001c0001t0001g0231 a0001c0001t0003g0024 a0001c0001t0003g0049 others(4): Show |
10 | HG00609.hp1 HG00621.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+1039C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699173 | |||||||
| chr12:101699211 | C | A | 92 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0026 others(89): Show |
173 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.273+1077C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699211 | |||||||
| chr12:101699248 | C | T | 1 | a0002c0002t0001g0203 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.273+1114C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699248 | |||||||
| chr12:101699278 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(196): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.273+1144A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699278 | |||||||
| chr12:101699307 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.273+1173A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699307 | |||||||
| chr12:101699334 | G | A | 1 | a0001c0004t0001g0027 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.273+1200G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699334 | |||||||
| chr12:101699353 | TTGTCAAT others(15): Show |
T | 1 | a0001c0003t0001g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1221_273+1242d others(24): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101699353 | ||||||
| chr12:101699378 | A | T | 1 | a0001c0003t0001g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1244A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699378 | |||||||
| chr12:101699380 | G | T | 1 | a0001c0003t0001g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1246G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699380 | |||||||
| chr12:101699382 | A | T | 1 | a0001c0003t0001g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1248A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699382 | |||||||
| chr12:101699386 | C | T | 1 | a0001c0003t0001g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1252C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699386 | |||||||
| chr12:101699391 | C | CT | 87 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0026 others(84): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.273+1271dupT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101699391 | ||||||
| chr12:101699391 | C | T | 1 | a0001c0003t0001g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1257C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699391 | |||||||
| chr12:101699391 | CT | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(85): Show |
126 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.273+1271delT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101699391 | ||||||
| chr12:101699411 | A | G | 1 | a0001c0003t0001g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1277A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699411 | |||||||
| chr12:101699418 | C | T | 2 | a0001c0003t0001g0021 a0001c0003t0001g0202 |
4 | HG00738.hp1 HG00738.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+1284C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699418 | |||||||
| chr12:101699457 | G | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(115): Show |
172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.273+1323G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699457 | |||||||
| chr12:101699681 | G | A | 102 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0026 others(99): Show |
183 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.273+1547G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699681 | |||||||
| chr12:101699696 | T | C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(42): Show |
75 | HG00544.hp1 HG00597.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.273+1562T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699696 | |||||||
| chr12:101699746 | A | G | 6 | a0001c0001t0001g0050 a0001c0001t0001g0237 a0001c0001t0001g0238 others(3): Show |
7 | HG01081.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+1612A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699746 | |||||||
| chr12:101699920 | C | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(193): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.273+1786C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699920 | |||||||
| chr12:101699976 | G | A | 199 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(196): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.273+1842G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699976 | |||||||
| chr12:101700005 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.273+1871G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700005 | |||||||
| chr12:101700065 | A | G | 1 | a0001c0003t0001g0198 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.273+1931A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700065 | |||||||
| chr12:101700318 | CAT | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(52): Show |
84 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.273+2185_273+2186d others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700318 | |||||||
| chr12:101700319 | A | G | 24 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0057 others(21): Show |
35 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.273+2185A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700319 | |||||||
| chr12:101700321 | GT | G | 21 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0057 others(18): Show |
32 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.273+2188delT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700321 | |||||||
| chr12:101700322 | T | A | 1 | a0001c0003t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+2188T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700322 | |||||||
| chr12:101700323 | G | A | 22 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0057 others(19): Show |
33 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.273+2189G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700323 | |||||||
| chr12:101700323 | GA | G | 92 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0054 others(89): Show |
177 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.273+2205delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101700323 | ||||||
| chr12:101700581 | A | G | 4 | a0002c0002t0001g0043 a0002c0002t0001g0199 a0002c0002t0001g0200 others(1): Show |
5 | HG01192.hp1 HG01258.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+2447A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700581 | |||||||
| chr12:101700591 | C | T | 1 | a0001c0003t0001g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+2457C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700591 | |||||||
| chr12:101700598 | C | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0099 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.273+2464C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700598 | |||||||
| chr12:101700703 | C | A | 1 | a0001c0003t0001g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+2569C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700703 | |||||||
| chr12:101700715 | GT | G | 66 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0037 others(63): Show |
100 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.273+2583delT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101700715 | ||||||
| chr12:101700728 | G | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0193 a0002c0002t0001g0194 others(1): Show |
6 | NA18966.hp2 NA18968.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+2594G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700728 | |||||||
| chr12:101700745 | C | T | 8 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
9 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+2611C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700745 | |||||||
| chr12:101700800 | G | C | 26 | a0001c0001t0001g0207 a0001c0001t0001g0222 a0001c0003t0001g0038 others(23): Show |
47 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.273+2666G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700800 | |||||||
| chr12:101700865 | A | C | 124 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(121): Show |
192 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.273+2731A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700865 | |||||||
| chr12:101700948 | A | G | 191 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(188): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.273+2814A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700948 | |||||||
| chr12:101700994 | A | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0050 others(4): Show |
13 | HG01081.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+2860A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700994 | |||||||
| chr12:101701023 | G | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02486.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.273+2889G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701023 | |||||||
| chr12:101701097 | C | A | 2 | a0005c0008t0001g0235 a0005c0008t0001g0236 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.273+2963C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701097 | |||||||
| chr12:101701162 | A | T | 67 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0037 others(64): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.273+3028A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701162 | |||||||
| chr12:101701293 | A | G | 8 | a0001c0003t0002g0129 a0001c0005t0002g0014 a0001c0005t0002g0124 others(5): Show |
11 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.273+3159A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701293 | |||||||
| chr12:101701400 | A | G | 191 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(188): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.273+3266A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701400 | |||||||
| chr12:101701592 | T | G | 24 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0146 others(21): Show |
30 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.273+3458T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701592 | |||||||
| chr12:101701716 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.273+3582T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701716 | |||||||
| chr12:101701738 | A | G | 1 | a0002c0002t0001g0191 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.273+3604A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701738 | |||||||
| chr12:101701768 | A | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0001t0001g0099 others(6): Show |
13 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+3634A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701768 | |||||||
| chr12:101701789 | A | G | 1 | a0001c0003t0001g0167 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.273+3655A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701789 | |||||||
| chr12:101701823 | C | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(173): Show |
290 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.273+3689C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701823 | |||||||
| chr12:101701843 | G | A | 1 | a0001c0012t0001g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.273+3709G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701843 | |||||||
| chr12:101702042 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.273+3908C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702042 | |||||||
| chr12:101702120 | G | A | 1 | a0001c0001t0007g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.273+3986G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702120 | |||||||
| chr12:101702234 | A | T | 144 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0025 others(141): Show |
236 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.273+4100A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702234 | |||||||
| chr12:101702356 | C | G | 1 | a0001c0003t0001g0166 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.273+4222C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702356 | |||||||
| chr12:101702644 | CT | C | 20 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0045 others(17): Show |
34 | HG00544.hp2 HG00597.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.273+4518delT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101702644 | ||||||
| chr12:101702712 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.273+4578C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702712 | |||||||
| chr12:101702759 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.273+4625C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702759 | |||||||
| chr12:101702827 | G | T | 1 | a0002c0002t0001g0190 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.273+4693G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702827 | |||||||
| chr12:101702889 | G | A | 1 | a0001c0003t0001g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.273+4755G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702889 | |||||||
| chr12:101702924 | C | A | 24 | a0001c0001t0001g0222 a0001c0004t0001g0005 a0001c0004t0001g0010 others(21): Show |
44 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.273+4790C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702924 | |||||||
| chr12:101702998 | T | G | 30 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(27): Show |
54 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(51): Show |
intron_variant | MODIFIER | c.273+4864T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702998 | |||||||
| chr12:101703025 | A | G | 89 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(86): Show |
164 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.273+4891A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703025 | |||||||
| chr12:101703049 | G | A | 1 | a0002c0002t0001g0035 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+4915G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703049 | |||||||
| chr12:101703053 | C | T | 24 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0146 others(21): Show |
30 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.273+4919C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703053 | |||||||
| chr12:101703234 | T | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(50): Show |
86 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(83): Show |
intron_variant | MODIFIER | c.273+5100T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703234 | |||||||
| chr12:101703300 | G | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
181 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.273+5166G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703300 | |||||||
| chr12:101703363 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(98): Show |
182 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.273+5229G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703363 | |||||||
| chr12:101703419 | C | T | 1 | a0002c0002t0001g0169 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.273+5285C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703419 | |||||||
| chr12:101703504 | A | G | 2 | a0005c0008t0001g0235 a0005c0008t0001g0236 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.273+5370A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703504 | |||||||
| chr12:101703648 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0091 others(3): Show |
12 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.273+5514C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703648 | |||||||
| chr12:101703691 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0099 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.273+5557C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703691 | |||||||
| chr12:101703711 | C | G | 11 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0050 others(8): Show |
17 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.273+5577C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703711 | |||||||
| chr12:101703774 | C | T | 11 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0050 others(8): Show |
17 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.273+5640C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703774 | |||||||
| chr12:101703814 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.273+5680T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703814 | |||||||
| chr12:101704175 | AG | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0050 others(4): Show |
13 | HG01081.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+6043delG | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101704175 | ||||||
| chr12:101704177 | G | T | 4 | a0001c0001t0001g0051 a0001c0012t0001g0100 a0005c0008t0001g0235 others(1): Show |
4 | HG01167.hp1 HG02055.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+6043G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101704177 | |||||||
| chr12:101704196 | GT | G | 11 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0050 others(8): Show |
17 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.273+6070delT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101704196 | ||||||
| chr12:101704244 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0003t0001g0033 |
4 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+6110G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101704244 | |||||||
| chr12:101704404 | C | CT | 57 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0054 others(54): Show |
108 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(105): Show |
intron_variant | MODIFIER | c.273+6284dupT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101704404 | ||||||
| chr12:101704514 | G | GCCTCAGC others(655): Show |
1 | a0001c0003t0001g0032 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.273+7058_273+7719d others(664): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101704514 | ||||||
| chr12:101704514 | GCCTCAGC others(655): Show |
G | 26 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0031 others(23): Show |
35 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.273+7058_273+7719d others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101704514 | ||||||
| chr12:101704748 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.273+6614C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101704748 | |||||||
| chr12:101704903 | A | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0054 others(2): Show |
7 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+6769A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101704903 | |||||||
| chr12:101704970 | C | A | 1 | a0002c0002t0001g0179 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.273+6836C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101704970 | |||||||
| chr12:101705035 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0054 others(2): Show |
7 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+6901C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705035 | |||||||
| chr12:101705061 | G | A | 8 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
9 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+6927G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705061 | |||||||
| chr12:101705177 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0003g0234 |
2 | NA18984.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.273+7043C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705177 | |||||||
| chr12:101705224 | TGGCTAAT others(655): Show |
T | 67 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0037 others(64): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.273+7101_273+7762d others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101705224 | ||||||
| chr12:101705283 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.273+7149G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705283 | |||||||
| chr12:101705296 | C | T | 3 | a0001c0001t0001g0051 a0001c0012t0001g0100 a0002c0002t0001g0036 |
3 | HG01167.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.273+7162C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705296 | |||||||
| chr12:101705423 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.273+7289T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705423 | |||||||
| chr12:101705565 | A | T | 59 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0054 others(56): Show |
110 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(107): Show |
intron_variant | MODIFIER | c.273+7431A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705565 | |||||||
| chr12:101705664 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0078 a0001c0001t0004g0003 others(3): Show |
6 | NA18747.hp1 NA18971.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+7530A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705664 | |||||||
| chr12:101705697 | C | T | 67 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(64): Show |
121 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(118): Show |
intron_variant | MODIFIER | c.273+7563C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705697 | |||||||
| chr12:101705719 | C | G | 1 | a0001c0001t0001g0237 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.273+7585C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705719 | |||||||
| chr12:101705752 | T | TTTTG | 5 | a0001c0001t0004g0003 a0001c0001t0004g0082 a0001c0001t0004g0083 others(2): Show |
6 | HG03471.hp1 HG03579.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+7638_273+7641d others(6): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101705752 | ||||||
| chr12:101705871 | A | G | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02486.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.273+7737A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705871 | |||||||
| chr12:101705882 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.273+7748C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705882 | |||||||
| chr12:101706270 | A | C | 1 | a0005c0008t0001g0236 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.274-7820A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706270 | |||||||
| chr12:101706327 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.274-7763G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706327 | |||||||
| chr12:101706352 | GA | G | 61 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0054 others(58): Show |
112 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(109): Show |
intron_variant | MODIFIER | c.274-7726delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101706352 | ||||||
| chr12:101706395 | C | G | 1 | a0001c0001t0001g0026 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.274-7695C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706395 | |||||||
| chr12:101706458 | A | G | 1 | a0001c0004t0001g0027 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-7632A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706458 | |||||||
| chr12:101706486 | T | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(27): Show |
54 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(51): Show |
intron_variant | MODIFIER | c.274-7604T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706486 | |||||||
| chr12:101706653 | C | T | 23 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0011 others(20): Show |
43 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.274-7437C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706653 | |||||||
| chr12:101706762 | A | G | 5 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-7328A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706762 | |||||||
| chr12:101706780 | G | A | 1 | a0002c0002t0001g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.274-7310G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706780 | |||||||
| chr12:101706809 | TCTTTA | T | 8 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
9 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-7276_274-7272d others(7): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101706809 | ||||||
| chr12:101706810 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.274-7280C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706810 | |||||||
| chr12:101707112 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.274-6978G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707112 | |||||||
| chr12:101707168 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.274-6922G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707168 | |||||||
| chr12:101707409 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.274-6681C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707409 | |||||||
| chr12:101707411 | T | A | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274-6679T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707411 | |||||||
| chr12:101707615 | A | G | 1 | a0001c0012t0001g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.274-6475A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707615 | |||||||
| chr12:101707671 | A | G | 1 | a0002c0002t0001g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.274-6419A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707671 | |||||||
| chr12:101707848 | C | T | 44 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0037 others(41): Show |
58 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.274-6242C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707848 | |||||||
| chr12:101707872 | G | A | 1 | a0001c0004t0001g0027 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-6218G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707872 | |||||||
| chr12:101707949 | C | T | 3 | a0001c0004t0001g0046 a0001c0004t0001g0220 a0001c0004t0001g0221 |
4 | NA18955.hp2 NA18999.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-6141C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707949 | |||||||
| chr12:101707976 | C | T | 35 | a0001c0001t0001g0013 a0001c0001t0001g0059 a0001c0001t0001g0060 others(32): Show |
59 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.274-6114C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707976 | |||||||
| chr12:101708337 | G | T | 25 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0146 others(22): Show |
31 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.274-5753G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708337 | |||||||
| chr12:101708356 | G | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0106 a0001c0001t0001g0107 others(3): Show |
9 | HG01884.hp1 HG02145.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-5734G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708356 | |||||||
| chr12:101708492 | G | A | 2 | a0001c0001t0001g0016 a0006c0011t0001g0076 |
4 | NA18945.hp1 NA18954.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-5598G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708492 | |||||||
| chr12:101708509 | T | C | 2 | a0002c0002t0001g0172 a0002c0002t0001g0173 |
2 | HG01517.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.274-5581T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708509 | |||||||
| chr12:101708628 | GACAGGGT others(4673): Show |
G | 24 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0011 others(21): Show |
44 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.274-5457_274-778de others(1): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101708628 | ||||||
| chr12:101708642 | C | T | 2 | a0001c0001t0001g0222 a0001c0003t0001g0111 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.274-5448C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708642 | |||||||
| chr12:101708818 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0001t0001g0099 others(5): Show |
11 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-5272A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708818 | |||||||
| chr12:101708833 | G | A | 3 | a0001c0003t0001g0152 a0001c0003t0001g0153 a0001c0003t0001g0154 |
3 | HG01361.hp2 HG01928.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.274-5257G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708833 | |||||||
| chr12:101708840 | G | A | 1 | a0001c0003t0001g0068 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.274-5250G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708840 | |||||||
| chr12:101709002 | A | G | 1 | a0001c0004t0001g0027 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-5088A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709002 | |||||||
| chr12:101709210 | G | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(110): Show |
198 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(195): Show |
intron_variant | MODIFIER | c.274-4880G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709210 | |||||||
| chr12:101709388 | C | CA | 50 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0031 others(47): Show |
70 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.274-4680dupA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101709388 | ||||||
| chr12:101709388 | C | CAA | 8 | a0001c0001t0001g0029 a0001c0001t0001g0101 a0001c0001t0002g0117 others(5): Show |
9 | HG00408.hp1 HG00621.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-4681_274-4680d others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101709388 | ||||||
| chr12:101709388 | CA | C | 66 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(63): Show |
109 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.274-4680delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101709388 | ||||||
| chr12:101709410 | A | C | 1 | a0001c0003t0001g0069 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.274-4680A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709410 | |||||||
| chr12:101709481 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.274-4609A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709481 | |||||||
| chr12:101709608 | C | G | 1 | a0001c0001t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.274-4482C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709608 | |||||||
| chr12:101709710 | G | A | 1 | a0001c0004t0001g0027 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-4380G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709710 | |||||||
| chr12:101709864 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0001t0001g0099 others(5): Show |
11 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-4226G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709864 | |||||||
| chr12:101709959 | G | A | 1 | a0001c0001t0001g0003 | 4 | HG02165.hp1 NA18947.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-4131G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709959 | |||||||
| chr12:101710125 | A | G | 1 | a0002c0002t0001g0186 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.274-3965A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101710125 | |||||||
| chr12:101710557 | C | T | 4 | a0001c0001t0002g0034 a0001c0001t0002g0116 a0001c0001t0002g0122 others(1): Show |
4 | HG02257.hp1 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-3533C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101710557 | |||||||
| chr12:101710774 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274-3316G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101710774 | |||||||
| chr12:101710863 | A | G | 2 | a0001c0001t0001g0051 a0001c0012t0001g0100 |
2 | HG01167.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.274-3227A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101710863 | |||||||
| chr12:101710889 | G | A | 1 | a0001c0004t0001g0027 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-3201G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101710889 | |||||||
| chr12:101711027 | G | T | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274-3063G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711027 | |||||||
| chr12:101711179 | G | C | 11 | a0002c0002t0001g0007 a0002c0002t0001g0019 a0002c0002t0001g0041 others(8): Show |
20 | HG00735.hp2 HG01106.hp2 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.274-2911G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711179 | |||||||
| chr12:101711211 | G | T | 1 | a0002c0002t0001g0228 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.274-2879G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711211 | |||||||
| chr12:101711228 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.274-2862G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711228 | |||||||
| chr12:101711421 | C | G | 1 | a0001c0001t0002g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.274-2669C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711421 | |||||||
| chr12:101711460 | C | T | 1 | a0002c0002t0001g0004 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.274-2630C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711460 | |||||||
| chr12:101711566 | T | TACA | 30 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(27): Show |
54 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(51): Show |
intron_variant | MODIFIER | c.274-2523_274-2521d others(5): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101711566 | ||||||
| chr12:101711581 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.274-2509C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711581 | |||||||
| chr12:101711769 | C | T | 1 | a0001c0003t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.274-2321C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711769 | |||||||
| chr12:101711783 | C | T | 1 | a0001c0003t0001g0021 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.274-2307C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711783 | |||||||
| chr12:101711851 | T | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(26): Show |
53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.274-2239T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711851 | |||||||
| chr12:101712053 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(26): Show |
53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.274-2037C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712053 | |||||||
| chr12:101712122 | G | T | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274-1968G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712122 | |||||||
| chr12:101712195 | T | C | 11 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(8): Show |
13 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.274-1895T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712195 | |||||||
| chr12:101712260 | A | G | 4 | a0001c0001t0001g0113 a0001c0003t0001g0164 a0004c0007t0001g0040 others(1): Show |
5 | HG00280.hp2 HG00639.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-1830A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712260 | |||||||
| chr12:101712362 | C | T | 1 | a0002c0002t0001g0007 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.274-1728C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712362 | |||||||
| chr12:101712406 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0099 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.274-1684G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712406 | |||||||
| chr12:101712563 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.274-1527C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712563 | |||||||
| chr12:101712887 | A | G | 1 | a0001c0004t0001g0027 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-1203A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712887 | |||||||
| chr12:101712891 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.274-1199G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712891 | |||||||
| chr12:101713134 | G | C | 1 | a0001c0001t0002g0034 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.274-956G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713134 | |||||||
| chr12:101713249 | T | C | 1 | a0001c0004t0001g0027 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-841T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713249 | |||||||
| chr12:101713549 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0003g0049 a0001c0001t0003g0233 others(1): Show |
5 | HG00609.hp1 NA18943.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-541A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713549 | |||||||
| chr12:101713556 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0106 a0001c0001t0001g0107 others(3): Show |
9 | HG01884.hp1 HG02145.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-534A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713556 | |||||||
| chr12:101713600 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0003g0024 a0001c0001t0003g0052 others(1): Show |
7 | HG00621.hp1 NA18942.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-490C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713600 | |||||||
| chr12:101713650 | T | G | 4 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 others(1): Show |
4 | NA18612.hp2 NA18747.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-440T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713650 | |||||||
| chr12:101713687 | A | AATCTAGT others(14): Show |
24 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0011 others(21): Show |
44 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.274-396_274-395ins others(21): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101713687 | ||||||
| chr12:101713847 | A | G | 12 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(9): Show |
14 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.274-243A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713847 | |||||||
| chr12:101713955 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02486.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.274-135C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713955 | |||||||
| chr12:101713956 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274-134G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713956 | |||||||
| chr12:101713971 | G | A | 3 | a0001c0003t0001g0152 a0001c0003t0001g0153 a0001c0003t0001g0154 |
3 | HG01361.hp2 HG01928.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.274-119G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713971 | |||||||
| chr12:101714414 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.422-90C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 2/8 | chr12 | 101714414 | |||||||
| chr12:101714486 | A | T | 2 | a0001c0003t0001g0163 a0001c0003t0001g0198 |
2 | HG01358.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.422-18A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 2/8 | chr12 | 101714486 | |||||||
| chr12:101714683 | A | G | 1 | a0001c0003t0001g0088 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.563+38A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101714683 | |||||||
| chr12:101714764 | C | T | 1 | a0002c0002t0001g0189 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.563+119C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101714764 | |||||||
| chr12:101714807 | C | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
252 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.563+162C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101714807 | |||||||
| chr12:101714966 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.563+321C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101714966 | |||||||
| chr12:101714996 | G | A | 123 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(120): Show |
207 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.563+351G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101714996 | |||||||
| chr12:101715168 | T | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0054 others(4): Show |
9 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.563+523T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101715168 | |||||||
| chr12:101715497 | A | ACATGTTT others(1): Show |
6 | a0001c0001t0001g0013 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.563+853_563+860dup others(8): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 101715497 | ||||||
| chr12:101715569 | TG | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0139 others(4): Show |
10 | HG01496.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.563+927delG | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 101715569 | ||||||
| chr12:101715663 | A | G | 1 | a0002c0002t0001g0035 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.563+1018A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101715663 | |||||||
| chr12:101715708 | T | A | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.564-1020T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101715708 | |||||||
| chr12:101715951 | C | A | 1 | a0001c0001t0002g0116 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.564-777C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101715951 | |||||||
| chr12:101716026 | G | A | 1 | a0001c0003t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.564-702G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716026 | |||||||
| chr12:101716097 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.564-631A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716097 | |||||||
| chr12:101716115 | T | C | 33 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0011 others(30): Show |
57 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.564-613T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716115 | |||||||
| chr12:101716231 | C | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
7 | HG01884.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.564-497C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716231 | |||||||
| chr12:101716291 | T | A | 12 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0146 others(9): Show |
14 | HG00323.hp1 HG00408.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.564-437T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716291 | |||||||
| chr12:101716327 | A | G | 147 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(144): Show |
242 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.564-401A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716327 | |||||||
| chr12:101716523 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.564-205G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716523 | |||||||
| chr12:101716557 | T | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(152): Show |
251 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.564-171T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716557 | |||||||
| chr12:101716698 | C | T | 1 | a0001c0010t0001g0090 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.564-30C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716698 | |||||||
| chr12:101716835 | A | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(26): Show |
53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.648+23A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101716835 | |||||||
| chr12:101716914 | A | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | NA18991.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.648+102A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101716914 | |||||||
| chr12:101716914 | AT | A | 100 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0025 others(97): Show |
167 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(164): Show |
intron_variant | MODIFIER | c.648+114delT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101716914 | ||||||
| chr12:101716914 | ATT | A | 28 | a0001c0001t0001g0013 a0001c0001t0001g0097 a0001c0001t0001g0098 others(25): Show |
35 | HG00323.hp1 HG00408.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.648+113_648+114del others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101716914 | ||||||
| chr12:101717106 | T | C | 1 | a0002c0002t0006g0174 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.648+294T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717106 | |||||||
| chr12:101717145 | T | A | 18 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0037 others(15): Show |
26 | HG00609.hp1 HG00621.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.648+333T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717145 | |||||||
| chr12:101717364 | T | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0099 a0001c0001t0001g0222 |
3 | HG02451.hp1 HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.648+552T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717364 | |||||||
| chr12:101717395 | G | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(186): Show |
309 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.648+583G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717395 | |||||||
| chr12:101717639 | G | T | 2 | a0001c0003t0001g0153 a0001c0003t0001g0154 |
2 | HG01928.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.648+827G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717639 | |||||||
| chr12:101717652 | G | A | 32 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0011 others(29): Show |
55 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.648+840G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717652 | |||||||
| chr12:101717924 | T | C | 8 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
9 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.648+1112T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717924 | |||||||
| chr12:101717969 | A | G | 2 | a0001c0004t0001g0010 a0001c0004t0001g0219 |
6 | NA18945.hp2 NA18946.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.648+1157A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717969 | |||||||
| chr12:101717976 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.648+1164T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717976 | |||||||
| chr12:101718072 | G | T | 18 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0037 others(15): Show |
26 | HG00609.hp1 HG00621.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.648+1260G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718072 | |||||||
| chr12:101718092 | A | G | 1 | a0001c0003t0001g0170 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.648+1280A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718092 | |||||||
| chr12:101718233 | T | A | 1 | a0002c0002t0001g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.648+1421T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718233 | |||||||
| chr12:101718289 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.648+1477G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718289 | |||||||
| chr12:101718513 | A | T | 32 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0011 others(29): Show |
55 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.649-1610A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718513 | |||||||
| chr12:101718529 | A | G | 3 | a0001c0001t0002g0116 a0001c0001t0002g0122 a0001c0001t0002g0123 |
3 | HG02257.hp1 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.649-1594A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718529 | |||||||
| chr12:101718565 | C | T | 1 | a0002c0002t0001g0187 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.649-1558C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718565 | |||||||
| chr12:101718606 | G | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(26): Show |
53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.649-1517G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718606 | |||||||
| chr12:101718664 | T | TA | 7 | a0001c0001t0001g0063 a0001c0001t0001g0099 a0001c0001t0001g0231 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-1441dupA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101718664 | ||||||
| chr12:101718664 | TA | T | 19 | a0001c0001t0001g0051 a0001c0001t0001g0085 a0001c0001t0001g0098 others(16): Show |
19 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.649-1441delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101718664 | ||||||
| chr12:101718687 | T | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG02486.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-1436T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718687 | |||||||
| chr12:101718739 | C | T | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG02486.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-1384C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718739 | |||||||
| chr12:101718775 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.649-1348A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718775 | |||||||
| chr12:101719021 | G | T | 1 | a0001c0003t0001g0103 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.649-1102G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719021 | |||||||
| chr12:101719148 | C | T | 1 | a0001c0003t0001g0158 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.649-975C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719148 | |||||||
| chr12:101719156 | G | GA | 68 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0037 others(65): Show |
102 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.649-946dupA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101719156 | ||||||
| chr12:101719156 | G | GAA | 76 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(73): Show |
138 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.649-947_649-946dup others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101719156 | ||||||
| chr12:101719156 | G | GAAA | 33 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(30): Show |
44 | HG00735.hp2 HG01081.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.649-948_649-946dup others(3): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101719156 | ||||||
| chr12:101719156 | G | GAAAA | 7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(4): Show |
8 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.649-949_649-946dup others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101719156 | ||||||
| chr12:101719156 | G | GGAA | 7 | a0002c0002t0001g0007 a0002c0002t0001g0020 a0002c0002t0001g0042 others(4): Show |
17 | NA18944.hp1 NA18954.hp2 NA18956.hp2 others(14): Show |
intron_variant | MODIFIER | c.649-967_649-966ins others(3): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719156 | |||||||
| chr12:101719413 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.649-710A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719413 | |||||||
| chr12:101719474 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0099 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.649-649T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719474 | |||||||
| chr12:101719524 | T | C | 7 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0050 others(4): Show |
13 | HG01081.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.649-599T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719524 | |||||||
| chr12:101719558 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.649-565A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719558 | |||||||
| chr12:101719844 | G | T | 2 | a0001c0005t0002g0128 a0001c0010t0001g0090 |
2 | HG02040.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.649-279G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719844 | |||||||
| chr12:101719954 | T | TTAAA | 159 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(156): Show |
254 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.649-168_649-165dup others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101719954 | ||||||
| chr12:101719959 | A | T | 1 | a0003c0006t0001g0210 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.649-164A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719959 | |||||||
| chr12:101720007 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.649-116T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101720007 | |||||||
| chr12:101720023 | G | T | 1 | a0001c0004t0001g0216 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.649-100G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101720023 | |||||||
| chr12:101720053 | T | A | 1 | a0001c0001t0001g0030 | 2 | HG02056.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.649-70T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101720053 | |||||||
| chr12:101720424 | T | A | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.780+170T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101720424 | |||||||
| chr12:101720659 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.780+405A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101720659 | |||||||
| chr12:101720886 | C | A | 1 | a0001c0003t0001g0038 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.780+632C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101720886 | |||||||
| chr12:101720965 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(26): Show |
53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.780+711C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101720965 | |||||||
| chr12:101720997 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.780+743C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101720997 | |||||||
| chr12:101721004 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0003t0001g0033 |
4 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+750G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721004 | |||||||
| chr12:101721036 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.780+782A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721036 | |||||||
| chr12:101721101 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0003t0001g0033 |
4 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+847G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721101 | |||||||
| chr12:101721114 | G | A | 1 | a0001c0004t0001g0218 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.780+860G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721114 | |||||||
| chr12:101721184 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.780+930G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721184 | |||||||
| chr12:101721242 | G | T | 18 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0146 others(15): Show |
21 | HG00323.hp1 HG00408.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.780+988G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721242 | |||||||
| chr12:101721455 | C | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(26): Show |
53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.780+1201C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721455 | |||||||
| chr12:101721487 | C | T | 2 | a0001c0001t0004g0082 a0001c0001t0004g0083 |
2 | NA18971.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.780+1233C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721487 | |||||||
| chr12:101721511 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.780+1257T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721511 | |||||||
| chr12:101721650 | T | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0238 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.780+1396T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721650 | |||||||
| chr12:101721710 | G | A | 2 | a0002c0002t0001g0094 a0002c0002t0001g0178 |
2 | NA18951.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.780+1456G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721710 | |||||||
| chr12:101721991 | G | A | 1 | a0001c0003t0001g0038 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.781-1177G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721991 | |||||||
| chr12:101722036 | G | C | 1 | a0001c0001t0001g0237 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.781-1132G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101722036 | |||||||
| chr12:101722058 | C | CA | 33 | a0001c0001t0001g0063 a0001c0001t0001g0099 a0001c0001t0001g0222 others(30): Show |
52 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.781-1098dupA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722058 | ||||||
| chr12:101722058 | C | CAA | 2 | a0001c0004t0001g0010 a0001c0005t0002g0126 |
6 | NA18941.hp1 NA18945.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.781-1099_781-1098d others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722058 | ||||||
| chr12:101722058 | CA | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0110 a0001c0003t0001g0032 others(1): Show |
9 | HG01243.hp1 HG01257.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.781-1098delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722058 | ||||||
| chr12:101722315 | A | C | 1 | a0002c0002t0001g0177 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.781-853A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101722315 | |||||||
| chr12:101722591 | G | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0050 others(10): Show |
19 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.781-577G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101722591 | |||||||
| chr12:101722707 | T | TA | 6 | a0001c0001t0001g0093 a0001c0001t0001g0099 a0001c0003t0001g0153 others(3): Show |
7 | HG01928.hp1 HG02451.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.781-442dupA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722707 | ||||||
| chr12:101722707 | T | TAA | 12 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0050 others(9): Show |
18 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.781-443_781-442dup others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722707 | ||||||
| chr12:101722707 | TA | T | 14 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0091 others(11): Show |
19 | HG00609.hp2 HG00639.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.781-442delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722707 | ||||||
| chr12:101722707 | TAA | T | 19 | a0001c0001t0001g0057 a0001c0001t0001g0097 a0001c0001t0001g0098 others(16): Show |
22 | HG00323.hp1 HG00408.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.781-443_781-442del others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722707 | ||||||
| chr12:101722707 | TAAA | T | 76 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0026 others(73): Show |
135 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.781-444_781-442del others(3): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722707 | ||||||
| chr12:101722707 | TAAAAAAA | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
8 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-448_781-442del others(7): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722707 | ||||||
| chr12:101722878 | G | A | 190 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(187): Show |
309 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.781-290G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101722878 | |||||||
| chr12:101722973 | T | A | 1 | a0002c0002t0001g0177 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.781-195T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101722973 | |||||||
| chr12:101723014 | G | A | 98 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0026 others(95): Show |
160 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.781-154G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101723014 | |||||||
| chr12:101723371 | G | A | 18 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0146 others(15): Show |
21 | HG00323.hp1 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.939+45G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 6/8 | chr12 | 101723371 | |||||||
| chr12:101723448 | T | A | 2 | a0001c0001t0004g0082 a0001c0001t0004g0083 |
2 | NA18971.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.939+122T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 6/8 | chr12 | 101723448 | |||||||
| chr12:101723470 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.939+144G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 6/8 | chr12 | 101723470 | |||||||
| chr12:101723472 | TAA | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0003t0001g0074 |
3 | HG02486.hp2 HG03486.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.939+147_939+148del others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 6/8 | chr12 | 101723472 | |||||||
| chr12:101723942 | C | A | 2 | a0001c0001t0007g0115 a0001c0001t0007g0118 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1065+95C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101723942 | |||||||
| chr12:101724150 | C | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0197 |
2 | HG00280.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1065+303C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101724150 | |||||||
| chr12:101724218 | C | CA | 38 | a0001c0001t0001g0013 a0001c0001t0001g0066 a0001c0001t0001g0080 others(35): Show |
59 | HG01099.hp2 HG01192.hp1 HG01243.hp2 others(56): Show |
intron_variant | MODIFIER | c.1065+387dupA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 101724218 | ||||||
| chr12:101724490 | C | T | 32 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0011 others(29): Show |
55 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1065+643C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101724490 | |||||||
| chr12:101724744 | C | T | 1 | a0001c0003t0001g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1065+897C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101724744 | |||||||
| chr12:101724754 | A | ATAGATAT | 111 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0025 others(108): Show |
179 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1065+909_1065+910i others(9): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 101724754 | ||||||
| chr12:101724809 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(26): Show |
53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.1065+962C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101724809 | |||||||
| chr12:101724841 | T | C | 53 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0007 others(50): Show |
102 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1065+994T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101724841 | |||||||
| chr12:101725021 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(26): Show |
53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.1065+1174C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725021 | |||||||
| chr12:101725061 | T | G | 5 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1065+1214T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725061 | |||||||
| chr12:101725095 | G | T | 237 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(234): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1066-1199G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725095 | |||||||
| chr12:101725100 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1066-1194A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725100 | |||||||
| chr12:101725156 | G | A | 17 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0146 others(14): Show |
20 | HG00323.hp1 HG00741.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1066-1138G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725156 | |||||||
| chr12:101725236 | T | G | 59 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0054 others(56): Show |
110 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(107): Show |
intron_variant | MODIFIER | c.1066-1058T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725236 | |||||||
| chr12:101725293 | C | T | 2 | a0002c0002t0006g0174 a0002c0002t0006g0181 |
2 | HG02074.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1066-1001C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725293 | |||||||
| chr12:101725294 | G | A | 1 | a0001c0001t0004g0082 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1066-1000G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725294 | |||||||
| chr12:101725338 | A | G | 1 | a0001c0003t0001g0070 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1066-956A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725338 | |||||||
| chr12:101725441 | T | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0050 others(4): Show |
13 | HG01081.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1066-853T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725441 | |||||||
| chr12:101725508 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1066-786T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725508 | |||||||
| chr12:101725535 | G | A | 2 | a0001c0005t0002g0128 a0001c0010t0001g0090 |
2 | HG02040.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1066-759G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725535 | |||||||
| chr12:101725565 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1066-729G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725565 | |||||||
| chr12:101725623 | CA | C | 52 | a0001c0001t0001g0013 a0001c0001t0001g0059 a0001c0001t0001g0060 others(49): Show |
79 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1066-654delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 101725623 | ||||||
| chr12:101725623 | CAAAAAAA others(2): Show |
C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(26): Show |
53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.1066-662_1066-654d others(11): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 101725623 | ||||||
| chr12:101725629 | A | C | 111 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0025 others(108): Show |
179 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1066-665A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725629 | |||||||
| chr12:101725630 | A | C | 50 | a0001c0001t0001g0013 a0001c0001t0001g0059 a0001c0001t0001g0060 others(47): Show |
77 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1066-664A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725630 | |||||||
| chr12:101725638 | A | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(26): Show |
53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.1066-656A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725638 | |||||||
| chr12:101725648 | A | G | 30 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(27): Show |
54 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(51): Show |
intron_variant | MODIFIER | c.1066-646A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725648 | |||||||
| chr12:101725671 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1066-623A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725671 | |||||||
| chr12:101725868 | G | A | 3 | a0001c0004t0001g0045 a0001c0004t0001g0214 a0001c0004t0001g0216 |
4 | HG01106.hp1 HG01175.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066-426G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725868 | |||||||
| chr12:101726109 | A | G | 1 | a0003c0006t0001g0209 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1066-185A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101726109 | |||||||
| chr12:101726131 | A | T | 1 | a0001c0001t0001g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1066-163A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101726131 | |||||||
| chr12:101726144 | A | G | 1 | a0001c0005t0002g0126 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1066-150A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101726144 | |||||||
| chr12:101726200 | G | A | 3 | a0001c0003t0001g0156 a0001c0003t0001g0163 a0001c0003t0001g0198 |
3 | HG01358.hp1 HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1066-94G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101726200 | |||||||
| chr12:101726222 | A | G | 12 | a0001c0001t0001g0051 a0001c0001t0001g0059 a0001c0001t0001g0060 others(9): Show |
12 | HG00280.hp2 HG00741.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1066-72A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101726222 | |||||||
| chr12:101726418 | TTGAC | T | 6 | a0001c0003t0001g0021 a0001c0003t0001g0033 a0001c0003t0001g0088 others(3): Show |
9 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1176+20_1176+23del others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101726418 | ||||||
| chr12:101726427 | T | TAATA | 12 | a0001c0001t0001g0051 a0001c0001t0001g0059 a0001c0001t0001g0060 others(9): Show |
12 | HG00280.hp2 HG00741.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1176+24_1176+27dup others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101726427 | ||||||
| chr12:101726447 | G | T | 1 | a0001c0003t0001g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1176+43G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101726447 | |||||||
| chr12:101726511 | C | A | 94 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0026 others(91): Show |
156 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.1176+107C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101726511 | |||||||
| chr12:101726585 | C | T | 32 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0011 others(29): Show |
55 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1176+181C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101726585 | |||||||
| chr12:101726586 | A | G | 241 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(238): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1176+182A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101726586 | |||||||
| chr12:101726630 | C | A | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1176+226C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101726630 | |||||||
| chr12:101726883 | TTC | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(77): Show |
131 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1176+481_1176+482d others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101726883 | ||||||
| chr12:101727196 | AACTT | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(186): Show |
308 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.1176+797_1176+800d others(6): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101727196 | ||||||
| chr12:101727278 | G | A | 7 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG00280.hp2 HG00741.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1176+874G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727278 | |||||||
| chr12:101727315 | T | G | 37 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(34): Show |
61 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1176+911T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727315 | |||||||
| chr12:101727408 | A | G | 1 | a0002c0002t0001g0149 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1176+1004A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727408 | |||||||
| chr12:101727488 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0139 others(5): Show |
11 | HG01496.hp2 HG01891.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1176+1084G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727488 | |||||||
| chr12:101727496 | CAAA | C | 108 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0025 others(105): Show |
176 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.1176+1104_1176+110 others(7): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101727496 | ||||||
| chr12:101727496 | CAAAA | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(76): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.1176+1103_1176+110 others(8): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101727496 | ||||||
| chr12:101727509 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1176+1105A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727509 | |||||||
| chr12:101727512 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1176+1108G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727512 | |||||||
| chr12:101727881 | T | C | 19 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0097 others(16): Show |
22 | HG00323.hp1 HG00741.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1177-1020T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727881 | |||||||
| chr12:101728090 | A | G | 17 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0146 others(14): Show |
20 | HG00323.hp1 HG00741.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1177-811A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728090 | |||||||
| chr12:101728264 | C | T | 7 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG00280.hp2 HG00741.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1177-637C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728264 | |||||||
| chr12:101728352 | CATT | C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0037 others(15): Show |
26 | HG00609.hp1 HG00621.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.1177-546_1177-544d others(5): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101728352 | ||||||
| chr12:101728378 | T | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0050 others(9): Show |
18 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1177-523T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728378 | |||||||
| chr12:101728466 | A | T | 1 | a0002c0002t0001g0182 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1177-435A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728466 | |||||||
| chr12:101728527 | A | T | 1 | a0002c0002t0001g0182 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1177-374A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728527 | |||||||
| chr12:101728578 | TAAAG | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0139 a0001c0001t0001g0141 others(2): Show |
7 | HG01496.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1177-320_1177-317d others(6): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101728578 | ||||||
| chr12:101728722 | C | T | 2 | a0001c0004t0001g0011 a0001c0004t0001g0022 |
8 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1177-179C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728722 | |||||||
| chr12:101728744 | T | C | 5 | a0001c0001t0001g0051 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01167.hp1 HG02486.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1177-157T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728744 | |||||||
| chr12:101728760 | C | G | 1 | a0001c0003t0001g0159 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1177-141C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728760 | |||||||
| chr12:101728876 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1177-25G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728876 |