Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64151 |
| ensemblid | ENSG00000109805.10 |
| hgncid | 24304 |
| symbol | NCAPG |
| name | non-SMC condensin I complex subunit G |
| refseq_nuc | NM_022346.5 |
| refseq_prot | NP_071741.2 |
| ensembl_nuc | ENST00000251496.7 |
| ensembl_prot | ENSP00000251496.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 17810979 |
| end | 17844865 |
| strand | + |
| ver | v1.2 |
| region | chr4:17810979-17844865 |
| region5000 | chr4:17805979-17849865 |
| regionname0 | NCAPG_chr4_17810979_17844865 |
| regionname5000 | NCAPG_chr4_17805979_17849865 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1015 | 314 | 84 | 57 | 134 | 6 | 33 | 112 | NCAPG_chr4_17805979_17849865 | NCAPG | MGAER others(1010): Show |
chr4 | 17805979 | 17849865 |
| a0002 | 0/0 | 1015 | 47 | 4 | 14 | 18 | 2 | 9 | 9 | NCAPG_chr4_17805979_17849865 | NCAPG | MGAER others(1010): Show |
chr4 | 17805979 | 17849865 |
| a0003 | 0/0 | 1015 | 20 | 0 | 0 | 20 | 0 | 0 | 13 | NCAPG_chr4_17805979_17849865 | NCAPG | MGAER others(1010): Show |
chr4 | 17805979 | 17849865 |
| a0004 | 0/0 | 1015 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | NCAPG_chr4_17805979_17849865 | NCAPG | MGAER others(1010): Show |
chr4 | 17805979 | 17849865 |
| a0005 | 0/0 | 1015 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | MGAER others(1010): Show |
chr4 | 17805979 | 17849865 |
| a0006 | 0/0 | 1015 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | MGAER others(1010): Show |
chr4 | 17805979 | 17849865 |
| a0007 | 0/0 | 1015 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | MGAER others(1010): Show |
chr4 | 17805979 | 17849865 |
| a0008 | 0/0 | 1015 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | MGAER others(1010): Show |
chr4 | 17805979 | 17849865 |
| a0009 | 0/0 | 1015 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | MGAER others(1010): Show |
chr4 | 17805979 | 17849865 |
| a0010 | 0/0 | 1015 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | MGAER others(1010): Show |
chr4 | 17805979 | 17849865 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3045 | 177 | 64 | 32 | 67 | 3 | 11 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 | ||
| a0001c0002 | 0/0 | 3045 | 108 | 15 | 23 | 52 | 3 | 15 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 | ||
| a0001c0004 | 0/0 | 3045 | 28 | 5 | 1 | 15 | 0 | 7 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 | ||
| a0001c0010 | 0/0 | 3045 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 | ||
| a0002c0003 | 0/0 | 3045 | 46 | 3 | 14 | 18 | 2 | 9 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 | ||
| a0002c0014 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 | ||
| a0003c0005 | 0/0 | 3045 | 20 | 0 | 0 | 20 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 | ||
| a0004c0006 | 0/0 | 3045 | 4 | 0 | 0 | 4 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 | ||
| a0005c0007 | 0/0 | 3045 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 | ||
| a0006c0008 | 0/0 | 3045 | 2 | 0 | 0 | 0 | 0 | 2 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 | ||
| a0007c0012 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 | ||
| a0008c0011 | 0/0 | 3045 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 | ||
| a0009c0009 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 | ||
| a0010c0013 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | ATGGG others(3040): Show |
chr4 | 17805979 | 17849865 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4587 | 113 | 11 | 30 | 60 | 1 | 11 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0001c0001t0004 | 0/0 | 4587 | 21 | 15 | 2 | 4 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0001c0001t0005 | 0/0 | 4587 | 2 | 1 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0001c0001t0006 | 0/0 | 4588 | 11 | 11 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4583): Show |
chr4 | 17805979 | 17849865 |
| a0001c0001t0008 | 0/0 | 4587 | 12 | 12 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0001c0001t0009 | 0/0 | 4588 | 10 | 10 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4583): Show |
chr4 | 17805979 | 17849865 |
| a0001c0001t0010 | 0/0 | 4587 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0001c0001t0012 | 0/0 | 4587 | 2 | 0 | 0 | 0 | 2 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0001c0001t0015 | 0/0 | 4587 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0001c0001t0016 | 0/0 | 4587 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0001c0001t0020 | 0/0 | 4588 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4583): Show |
chr4 | 17805979 | 17849865 |
| a0001c0002t0002 | 0/0 | 4587 | 105 | 13 | 22 | 52 | 3 | 15 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0001c0002t0013 | 0/0 | 4587 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0001c0002t0018 | 0/0 | 4587 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0001c0004t0005 | 0/0 | 4587 | 22 | 2 | 0 | 14 | 0 | 6 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0001c0004t0006 | 0/0 | 4588 | 5 | 3 | 1 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4583): Show |
chr4 | 17805979 | 17849865 |
| a0001c0004t0019 | 0/0 | 4587 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0001c0010t0002 | 0/0 | 4587 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0002c0003t0003 | 0/0 | 4587 | 43 | 3 | 14 | 17 | 2 | 7 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0002c0003t0004 | 0/0 | 4587 | 3 | 0 | 0 | 1 | 0 | 2 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0002c0014t0003 | 0/0 | 4587 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0003c0005t0007 | 0/0 | 4588 | 15 | 0 | 0 | 15 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4583): Show |
chr4 | 17805979 | 17849865 |
| a0003c0005t0011 | 0/0 | 4587 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0003c0005t0014 | 0/0 | 4587 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0004c0006t0002 | 0/0 | 4587 | 4 | 0 | 0 | 4 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0005c0007t0001 | 0/0 | 4587 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0006c0008t0003 | 0/0 | 4587 | 2 | 0 | 0 | 0 | 0 | 2 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0007c0012t0004 | 0/0 | 4587 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0008c0011t0001 | 0/0 | 4587 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0009c0009t0017 | 0/0 | 4587 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4582): Show |
chr4 | 17805979 | 17849865 |
| a0010c0013t0009 | 0/0 | 4588 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | GTCAT others(4583): Show |
chr4 | 17805979 | 17849865 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 50 | 0 | 6 | 38 | 0 | 6 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 7 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0014 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0006g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0006g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0008g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0008g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0009g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0009g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0009g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0010g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0012g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0015g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0016g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0001t0020g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0002 | 0/0 | 43 | 2 | 9 | 24 | 2 | 6 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0008 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0013g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0013g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0002t0018g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0005g0011 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0005g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0005g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0005g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0005g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0005g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0006g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0006g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0004t0019g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0001c0010t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0003 | 0/0 | 14 | 0 | 9 | 2 | 2 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0006 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0017 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0003t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0002c0014t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0003c0005t0007g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0003c0005t0007g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0003c0005t0007g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0003c0005t0007g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0003c0005t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0003c0005t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0003c0005t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0003c0005t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0003c0005t0011g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0003c0005t0011g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0003c0005t0014g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0004c0006t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0005c0007t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0005c0007t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0006c0008t0003g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0006c0008t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0007c0012t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0008c0011t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0009c0009t0017g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| a0010c0013t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0120 | EUR | FIN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00423 | hp1 | a0003 | c0005 | t0007 | g0109 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00423 | hp2 | a0002 | c0003 | t0003 | g0056 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00438 | hp2 | a0003 | c0005 | t0007 | g0007 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00544 | hp2 | a0003 | c0005 | t0014 | g0039 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0119 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00639 | hp2 | a0002 | c0003 | t0003 | g0006 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0130 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00673 | hp2 | a0001 | c0004 | t0005 | g0078 | EAS | CHS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00735 | hp1 | a0002 | c0003 | t0003 | g0003 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00738 | hp2 | a0002 | c0003 | t0003 | g0003 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0141 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0042 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0123 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01099 | hp1 | a0002 | c0003 | t0003 | g0066 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0118 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0136 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0036 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01168 | hp2 | a0002 | c0003 | t0003 | g0003 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01169 | hp1 | a0002 | c0003 | t0003 | g0003 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01175 | hp2 | a0002 | c0003 | t0003 | g0003 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01192 | hp1 | a0002 | c0003 | t0003 | g0070 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0122 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01243 | hp1 | a0002 | c0003 | t0003 | g0065 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0036 | AMR | PUR | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01256 | hp1 | a0002 | c0003 | t0003 | g0003 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01258 | hp2 | a0002 | c0003 | t0003 | g0003 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01261 | hp1 | a0002 | c0003 | t0003 | g0003 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0129 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01346 | hp2 | a0002 | c0003 | t0003 | g0003 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01358 | hp1 | a0001 | c0002 | t0018 | g0124 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01358 | hp2 | a0001 | c0004 | t0006 | g0084 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01515 | hp1 | a0002 | c0003 | t0003 | g0003 | EUR | IBS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01516 | hp2 | a0001 | c0001 | t0012 | g0001 | EUR | IBS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01517 | hp1 | a0001 | c0001 | t0012 | g0001 | EUR | IBS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01517 | hp2 | a0002 | c0003 | t0003 | g0003 | EUR | IBS | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0116 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01891 | hp1 | a0007 | c0012 | t0004 | g0111 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01891 | hp2 | a0005 | c0007 | t0001 | g0165 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0133 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01952 | hp2 | a0002 | c0003 | t0003 | g0006 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01981 | hp2 | a0008 | c0011 | t0001 | g0004 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02027 | hp2 | a0002 | c0003 | t0003 | g0062 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02040 | hp1 | a0002 | c0003 | t0004 | g0057 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0179 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0140 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02056 | hp1 | a0002 | c0003 | t0003 | g0003 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0135 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02071 | hp1 | a0003 | c0005 | t0011 | g0007 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02083 | hp2 | a0002 | c0003 | t0003 | g0006 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02129 | hp1 | a0002 | c0003 | t0003 | g0003 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02132 | hp1 | a0002 | c0003 | t0003 | g0023 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02132 | hp2 | a0003 | c0005 | t0007 | g0037 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02135 | hp1 | a0002 | c0003 | t0003 | g0055 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02135 | hp2 | a0002 | c0003 | t0003 | g0006 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02145 | hp1 | a0001 | c0001 | t0020 | g0053 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | CDX | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | CDX | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CDX | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02165 | hp2 | a0003 | c0005 | t0011 | g0007 | EAS | CDX | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02257 | hp1 | a0002 | c0003 | t0003 | g0059 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02293 | hp1 | a0001 | c0010 | t0002 | g0105 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02451 | hp2 | a0001 | c0004 | t0006 | g0030 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02523 | hp1 | a0003 | c0005 | t0014 | g0039 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02572 | hp2 | a0002 | c0014 | t0003 | g0058 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02602 | hp1 | a0001 | c0004 | t0005 | g0011 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02602 | hp2 | a0006 | c0008 | t0003 | g0003 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0176 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0113 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02622 | hp2 | a0002 | c0003 | t0003 | g0074 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02630 | hp2 | a0001 | c0004 | t0005 | g0028 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0052 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0051 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02683 | hp2 | a0001 | c0004 | t0006 | g0085 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0132 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02717 | hp1 | a0001 | c0002 | t0013 | g0139 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02717 | hp2 | a0005 | c0007 | t0001 | g0049 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0121 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0182 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02886 | hp2 | a0009 | c0009 | t0017 | g0152 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0145 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0029 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0178 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02965 | hp1 | a0001 | c0002 | t0013 | g0117 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0051 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02976 | hp1 | a0001 | c0001 | t0010 | g0021 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0163 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03017 | hp1 | a0001 | c0004 | t0005 | g0076 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | MSL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0021 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0148 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03139 | hp1 | a0001 | c0004 | t0005 | g0028 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0075 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03209 | hp1 | a0001 | c0004 | t0006 | g0083 | AFR | MSL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | MSL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0052 | AFR | MSL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0181 | AFR | MSL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | MSL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03490 | hp1 | a0002 | c0003 | t0003 | g0024 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03490 | hp2 | a0001 | c0004 | t0005 | g0027 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03491 | hp1 | a0002 | c0003 | t0003 | g0017 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03492 | hp1 | a0002 | c0003 | t0003 | g0017 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03492 | hp2 | a0001 | c0004 | t0005 | g0027 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03516 | hp1 | a0001 | c0004 | t0006 | g0030 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0158 | AFR | GWD | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | MSL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03654 | hp1 | a0001 | c0004 | t0005 | g0080 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0131 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03669 | hp1 | a0002 | c0003 | t0003 | g0024 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03710 | hp1 | a0002 | c0003 | t0003 | g0003 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0042 | SAS | PJL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03831 | hp1 | a0002 | c0003 | t0003 | g0017 | SAS | BEB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03831 | hp2 | a0002 | c0003 | t0004 | g0071 | SAS | BEB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03927 | hp2 | a0001 | c0004 | t0005 | g0079 | SAS | BEB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03942 | hp1 | a0006 | c0008 | t0003 | g0069 | SAS | BEB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03942 | hp2 | a0002 | c0003 | t0004 | g0067 | SAS | BEB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG04115 | hp1 | a0002 | c0003 | t0003 | g0061 | SAS | STU | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0142 | SAS | STU | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0045 | SAS | STU | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | STU | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0072 | AFR | YRI | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18522 | hp2 | a0002 | c0003 | t0003 | g0073 | AFR | YRI | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | YRI | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0021 | AFR | YRI | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18939 | hp1 | a0001 | c0004 | t0019 | g0077 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18939 | hp2 | a0001 | c0004 | t0005 | g0018 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18941 | hp2 | a0001 | c0004 | t0005 | g0013 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18946 | hp1 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18949 | hp1 | a0001 | c0004 | t0005 | g0025 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18951 | hp2 | a0003 | c0005 | t0011 | g0110 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18959 | hp1 | a0001 | c0004 | t0005 | g0013 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18959 | hp2 | a0001 | c0001 | t0015 | g0005 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18966 | hp1 | a0003 | c0005 | t0007 | g0020 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18968 | hp2 | a0002 | c0003 | t0003 | g0060 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18970 | hp2 | a0001 | c0004 | t0005 | g0013 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18977 | hp1 | a0003 | c0005 | t0007 | g0038 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18978 | hp1 | a0003 | c0005 | t0007 | g0172 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18982 | hp2 | a0003 | c0005 | t0007 | g0108 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18984 | hp2 | a0001 | c0004 | t0005 | g0025 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18986 | hp1 | a0001 | c0001 | t0016 | g0019 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18988 | hp2 | a0003 | c0005 | t0007 | g0020 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18990 | hp1 | a0001 | c0004 | t0005 | g0011 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18991 | hp2 | a0001 | c0004 | t0005 | g0011 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19002 | hp1 | a0002 | c0003 | t0003 | g0064 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19003 | hp2 | a0001 | c0004 | t0005 | g0018 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19004 | hp1 | a0003 | c0005 | t0007 | g0020 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19005 | hp1 | a0002 | c0003 | t0003 | g0022 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19007 | hp2 | a0004 | c0006 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19010 | hp2 | a0002 | c0003 | t0003 | g0022 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19012 | hp1 | a0001 | c0004 | t0005 | g0082 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0167 | AFR | LWK | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | LWK | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0180 | AFR | LWK | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19056 | hp1 | a0003 | c0005 | t0007 | g0007 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19056 | hp2 | a0002 | c0003 | t0003 | g0023 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19060 | hp1 | a0004 | c0006 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19060 | hp2 | a0003 | c0005 | t0007 | g0007 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19063 | hp2 | a0004 | c0006 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19066 | hp1 | a0004 | c0006 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19068 | hp1 | a0002 | c0003 | t0003 | g0063 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19070 | hp1 | a0003 | c0005 | t0007 | g0007 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19072 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19076 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19078 | hp2 | a0001 | c0004 | t0005 | g0011 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19079 | hp2 | a0003 | c0005 | t0007 | g0038 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19082 | hp2 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19083 | hp1 | a0003 | c0005 | t0007 | g0173 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19085 | hp1 | a0003 | c0005 | t0007 | g0037 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19086 | hp1 | a0002 | c0003 | t0003 | g0068 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19089 | hp1 | a0001 | c0004 | t0005 | g0013 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19091 | hp1 | a0001 | c0004 | t0005 | g0011 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | YRI | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | YRI | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA20129 | hp1 | a0010 | c0013 | t0009 | g0175 | AFR | ASW | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA20129 | hp2 | a0005 | c0007 | t0001 | g0049 | AFR | ASW | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0043 | SAS | GIH | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | CLM | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0138 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0115 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | MSL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0053 | AFR | MSL | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0168 | AFR | USA | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | USA | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | USA | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0177 | AFR | USA | NCAPG_chr4_17805979_17849865 | NCAPG | chr4 | 17805979 | 17849865 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17812248 | G | A | 1 | a0004 | 4 | NA19007.hp2 NA19060.hp1 NA19063.hp2 others(1): Show |
missense_variant | MODERATE | c.139G>A | p.Glu47Lys | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 2/21 | 238/4587 | 139/3048 | 47/1015 | chr4 | 17812248 | |||
| chr4:17813140 | T | C | 1 | a0009 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.539T>C | p.Val180Ala | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/21 | 638/4587 | 539/3048 | 180/1015 | chr4 | 17813140 | |||
| chr4:17817353 | G | A | 1 | a0006 | 2 | HG02602.hp2 HG03942.hp1 |
missense_variant | MODERATE | c.868G>A | p.Val290Ile | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 6/21 | 967/4587 | 868/3048 | 290/1015 | chr4 | 17817353 | |||
| chr4:17818069 | T | C | 1 | a0008 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1099T>C | p.Tyr367His | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/21 | 1198/4587 | 1099/3048 | 367/1015 | chr4 | 17818069 | |||
| chr4:17818072 | G | A | 1 | a0003 | 20 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(17): Show |
missense_variant | MODERATE | c.1102G>A | p.Ala368Thr | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/21 | 1201/4587 | 1102/3048 | 368/1015 | chr4 | 17818072 | |||
| chr4:17828367 | G | C | 2 | a0002 a0006 |
49 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
missense_variant | MODERATE | c.1743G>C | p.Met581Ile | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/21 | 1842/4587 | 1743/3048 | 581/1015 | chr4 | 17828367 | |||
| chr4:17837650 | A | G | 1 | a0005 | 3 | HG01891.hp2 HG02717.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.2315A>G | p.Glu772Gly | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/21 | 2414/4587 | 2315/3048 | 772/1015 | chr4 | 17837650 | |||
| chr4:17840648 | A | G | 1 | a0010 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.2809A>G | p.Lys937Glu | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 19/21 | 2908/4587 | 2809/3048 | 937/1015 | chr4 | 17840648 | |||
| chr4:17842325 | C | T | 1 | a0007 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.2870C>T | p.Thr957Ile | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 20/21 | 2969/4587 | 2870/3048 | 957/1015 | chr4 | 17842325 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17811173 | C | T | 1 | a0001c0004 | 28 | HG00673.hp2 HG01358.hp2 HG02451.hp2 others(25): Show |
synonymous_variant | LOW | c.96C>T | p.Ser32Ser | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/21 | 195/4587 | 96/3048 | 32/1015 | chr4 | 17811173 | |||
| chr4:17812934 | C | T | 1 | a0002c0014 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.333C>T | p.Ser111Ser | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/21 | 432/4587 | 333/3048 | 111/1015 | chr4 | 17812934 | |||
| chr4:17817262 | T | C | 3 | a0001c0002 a0001c0010 a0004c0006 |
114 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(111): Show |
splice_region_variant&synonymous_variant | LOW | c.777T>C | p.Asp259Asp | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 6/21 | 876/4587 | 777/3048 | 259/1015 | chr4 | 17817262 | |||
| chr4:17839789 | T | C | 1 | a0001c0010 | 1 | HG02293.hp1 | synonymous_variant | LOW | c.2580T>C | p.Ser860Ser | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 17/21 | 2679/4587 | 2580/3048 | 860/1015 | chr4 | 17839789 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17810992 | A | C | 22 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(19): Show |
258 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(255): Show |
5_prime_UTR_variant | MODIFIER | c.-86A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/21 | 86 | chr4 | 17810992 | ||||||
| chr4:17811014 | G | T | 3 | a0003c0005t0007 a0003c0005t0011 a0003c0005t0014 |
20 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-64G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/21 | 64 | chr4 | 17811014 | ||||||
| chr4:17811040 | A | T | 3 | a0001c0001t0009 a0001c0001t0020 a0010c0013t0009 |
12 | HG02055.hp1 HG02145.hp1 HG02647.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-38A>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/21 | 38 | chr4 | 17811040 | ||||||
| chr4:17843555 | G | A | 1 | a0001c0002t0018 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*130G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 130 | chr4 | 17843555 | ||||||
| chr4:17843615 | G | C | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(22): Show |
269 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*190G>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 190 | chr4 | 17843615 | ||||||
| chr4:17843618 | C | T | 3 | a0002c0003t0003 a0002c0014t0003 a0006c0008t0003 |
46 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*193C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 193 | chr4 | 17843618 | ||||||
| chr4:17843840 | A | G | 1 | a0001c0001t0020 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 415 | chr4 | 17843840 | ||||||
| chr4:17843847 | C | T | 4 | a0001c0001t0005 a0001c0004t0005 a0001c0004t0019 others(1): Show |
26 | HG00673.hp2 HG02602.hp1 HG02630.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*422C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 422 | chr4 | 17843847 | ||||||
| chr4:17843866 | T | TA | 1 | a0003c0005t0007 | 15 | HG00423.hp1 HG00438.hp2 HG02132.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*442dupA | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 443 | INFO_REALIGN_3_PRIME | chr4 | 17843866 | |||||
| chr4:17843869 | C | G | 3 | a0003c0005t0007 a0003c0005t0011 a0003c0005t0014 |
20 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*444C>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 444 | chr4 | 17843869 | ||||||
| chr4:17843979 | A | C | 1 | a0001c0001t0016 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*554A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 554 | chr4 | 17843979 | ||||||
| chr4:17843994 | T | G | 1 | a0003c0005t0014 | 2 | HG00544.hp2 HG02523.hp1 |
3_prime_UTR_variant | MODIFIER | c.*569T>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 569 | chr4 | 17843994 | ||||||
| chr4:17844107 | G | A | 1 | a0001c0004t0019 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*682G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 682 | chr4 | 17844107 | ||||||
| chr4:17844110 | A | G | 1 | a0001c0001t0010 | 3 | HG02976.hp1 HG03130.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*685A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 685 | chr4 | 17844110 | ||||||
| chr4:17844145 | G | A | 1 | a0001c0002t0013 | 2 | HG02717.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*720G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 720 | chr4 | 17844145 | ||||||
| chr4:17844198 | C | T | 3 | a0001c0001t0009 a0001c0001t0020 a0010c0013t0009 |
12 | HG02055.hp1 HG02145.hp1 HG02647.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*773C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 773 | chr4 | 17844198 | ||||||
| chr4:17844295 | T | C | 1 | a0001c0001t0015 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*870T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 870 | chr4 | 17844295 | ||||||
| chr4:17844501 | T | C | 1 | a0001c0001t0012 | 2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1076T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 1076 | chr4 | 17844501 | ||||||
| chr4:17844662 | T | TA | 5 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0020 others(2): Show |
28 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1240dupA | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 21/21 | 1241 | INFO_REALIGN_3_PRIME | chr4 | 17844662 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17811528 | C | CA | 28 | a0001c0001t0005g0072 a0001c0002t0002g0054 a0002c0003t0003g0003 others(25): Show |
51 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.111+343dupA | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 17811528 | ||||||
| chr4:17811541 | G | T | 2 | a0002c0003t0003g0073 a0002c0003t0003g0074 |
2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.111+353G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/20 | chr4 | 17811541 | |||||||
| chr4:17811555 | G | T | 12 | a0001c0001t0006g0176 a0001c0001t0006g0181 a0001c0001t0009g0051 others(9): Show |
14 | HG02055.hp1 HG02145.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.111+367G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/20 | chr4 | 17811555 | |||||||
| chr4:17811596 | T | A | 33 | a0001c0001t0004g0026 a0001c0001t0004g0081 a0001c0001t0005g0018 others(30): Show |
49 | HG00673.hp2 HG01358.hp2 HG02055.hp1 others(46): Show |
intron_variant | MODIFIER | c.111+408T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/20 | chr4 | 17811596 | |||||||
| chr4:17811606 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.111+418A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/20 | chr4 | 17811606 | |||||||
| chr4:17811700 | C | T | 2 | a0003c0005t0007g0172 a0003c0005t0007g0173 |
2 | NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.111+512C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/20 | chr4 | 17811700 | |||||||
| chr4:17811728 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.112-493C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/20 | chr4 | 17811728 | |||||||
| chr4:17811909 | G | A | 1 | a0002c0003t0003g0022 | 2 | NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.112-312G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/20 | chr4 | 17811909 | |||||||
| chr4:17812037 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.112-184G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/20 | chr4 | 17812037 | |||||||
| chr4:17812088 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(28): Show |
99 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.112-133T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 1/20 | chr4 | 17812088 | |||||||
| chr4:17812487 | G | T | 4 | a0001c0004t0006g0030 a0001c0004t0006g0083 a0001c0004t0006g0084 others(1): Show |
5 | HG01358.hp2 HG02451.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+63G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 2/20 | chr4 | 17812487 | |||||||
| chr4:17812512 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0102 |
3 | HG02723.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.315+88T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 2/20 | chr4 | 17812512 | |||||||
| chr4:17812836 | G | A | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-81G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 2/20 | chr4 | 17812836 | |||||||
| chr4:17812842 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0016g0019 |
3 | NA18973.hp1 NA18986.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.316-75A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 2/20 | chr4 | 17812842 | |||||||
| chr4:17812853 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.316-64A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 2/20 | chr4 | 17812853 | |||||||
| chr4:17813397 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.544+252T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/20 | chr4 | 17813397 | |||||||
| chr4:17813400 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.544+255C>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/20 | chr4 | 17813400 | |||||||
| chr4:17813628 | A | G | 1 | a0001c0001t0006g0029 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.544+483A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/20 | chr4 | 17813628 | |||||||
| chr4:17813677 | T | C | 2 | a0001c0001t0004g0036 a0001c0001t0004g0103 |
3 | HG01109.hp2 HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.544+532T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/20 | chr4 | 17813677 | |||||||
| chr4:17814086 | A | C | 1 | a0001c0002t0002g0168 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.545-767A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/20 | chr4 | 17814086 | |||||||
| chr4:17814184 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
11 | HG01070.hp2 HG01074.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.545-669C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/20 | chr4 | 17814184 | |||||||
| chr4:17814266 | C | G | 16 | a0001c0001t0004g0026 a0001c0001t0004g0081 a0001c0001t0005g0018 others(13): Show |
28 | HG00673.hp2 HG02602.hp1 HG02630.hp2 others(25): Show |
intron_variant | MODIFIER | c.545-587C>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/20 | chr4 | 17814266 | |||||||
| chr4:17814400 | C | T | 1 | a0001c0002t0002g0050 | 2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.545-453C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/20 | chr4 | 17814400 | |||||||
| chr4:17814488 | G | C | 1 | a0010c0013t0009g0175 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.545-365G>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/20 | chr4 | 17814488 | |||||||
| chr4:17814558 | C | T | 1 | a0001c0002t0002g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.545-295C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/20 | chr4 | 17814558 | |||||||
| chr4:17814645 | TA | T | 5 | a0001c0001t0006g0075 a0001c0004t0006g0030 a0001c0004t0006g0083 others(2): Show |
6 | HG01358.hp2 HG02451.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.545-207delA | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/20 | chr4 | 17814645 | |||||||
| chr4:17814755 | C | T | 29 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(26): Show |
53 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.545-98C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/20 | chr4 | 17814755 | |||||||
| chr4:17814783 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.545-70G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 3/20 | chr4 | 17814783 | |||||||
| chr4:17815227 | A | T | 1 | a0001c0001t0005g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.691-47A>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 4/20 | chr4 | 17815227 | |||||||
| chr4:17815242 | G | A | 1 | a0001c0010t0002g0105 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.691-32G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 4/20 | chr4 | 17815242 | |||||||
| chr4:17815526 | G | GAT | 18 | a0001c0001t0006g0029 a0001c0001t0006g0075 a0001c0001t0006g0176 others(15): Show |
22 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.775+179_775+180dup others(2): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 17815526 | ||||||
| chr4:17815548 | A | G | 29 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(26): Show |
53 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.775+190A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17815548 | |||||||
| chr4:17815743 | C | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0169 others(6): Show |
14 | HG01081.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.775+385C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17815743 | |||||||
| chr4:17815744 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.775+386G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17815744 | |||||||
| chr4:17815815 | C | T | 1 | a0001c0001t0004g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.775+457C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17815815 | |||||||
| chr4:17815870 | T | A | 1 | a0001c0004t0005g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.775+512T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17815870 | |||||||
| chr4:17815964 | TA | T | 5 | a0001c0001t0004g0015 a0001c0001t0006g0015 a0001c0001t0006g0158 others(2): Show |
7 | HG02145.hp2 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.775+616delA | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 17815964 | ||||||
| chr4:17815983 | C | T | 12 | a0001c0001t0006g0176 a0001c0001t0006g0181 a0001c0001t0009g0051 others(9): Show |
14 | HG02055.hp1 HG02145.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.775+625C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17815983 | |||||||
| chr4:17816061 | C | T | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+703C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17816061 | |||||||
| chr4:17816064 | AT | A | 26 | a0002c0003t0003g0003 a0002c0003t0003g0006 a0002c0003t0003g0017 others(23): Show |
49 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.775+719delT | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 17816064 | ||||||
| chr4:17816071 | T | A | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+713T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17816071 | |||||||
| chr4:17816102 | T | G | 1 | a0001c0001t0004g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.775+744T>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17816102 | |||||||
| chr4:17816116 | G | C | 11 | a0003c0005t0007g0007 a0003c0005t0007g0020 a0003c0005t0007g0037 others(8): Show |
20 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.775+758G>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17816116 | |||||||
| chr4:17816333 | C | T | 1 | a0001c0001t0006g0029 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.776-928C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17816333 | |||||||
| chr4:17816413 | T | C | 1 | a0002c0003t0003g0055 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.776-848T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17816413 | |||||||
| chr4:17816533 | A | G | 1 | a0001c0002t0002g0047 | 2 | NA18991.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.776-728A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17816533 | |||||||
| chr4:17816642 | A | G | 29 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(26): Show |
53 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.776-619A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17816642 | |||||||
| chr4:17816854 | G | A | 1 | a0007c0012t0004g0111 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.776-407G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17816854 | |||||||
| chr4:17816909 | C | T | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.776-352C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17816909 | |||||||
| chr4:17817027 | C | T | 1 | a0002c0003t0003g0017 | 3 | HG03491.hp1 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.776-234C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17817027 | |||||||
| chr4:17817095 | G | C | 1 | a0001c0002t0002g0112 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.776-166G>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | chr4 | 17817095 | |||||||
| chr4:17817116 | A | AAT | 5 | a0001c0001t0006g0075 a0001c0004t0006g0030 a0001c0004t0006g0083 others(2): Show |
6 | HG01358.hp2 HG02451.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.776-135_776-134dup others(2): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 17817116 | ||||||
| chr4:17817512 | T | A | 26 | a0002c0003t0003g0003 a0002c0003t0003g0006 a0002c0003t0003g0017 others(23): Show |
49 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.968+59T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 6/20 | chr4 | 17817512 | |||||||
| chr4:17817540 | A | G | 1 | a0001c0001t0009g0182 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.968+87A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 6/20 | chr4 | 17817540 | |||||||
| chr4:17817692 | C | T | 1 | a0001c0002t0002g0157 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.968+239C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 6/20 | chr4 | 17817692 | |||||||
| chr4:17818165 | T | A | 3 | a0001c0004t0005g0013 a0001c0004t0005g0025 a0001c0004t0019g0077 |
7 | NA18939.hp1 NA18941.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.1118+77T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17818165 | |||||||
| chr4:17818382 | A | T | 1 | a0001c0001t0006g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1118+294A>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17818382 | |||||||
| chr4:17818398 | C | T | 18 | a0001c0001t0006g0029 a0001c0001t0006g0075 a0001c0001t0006g0176 others(15): Show |
22 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1118+310C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17818398 | |||||||
| chr4:17818740 | G | A | 1 | a0001c0002t0002g0113 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1118+652G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17818740 | |||||||
| chr4:17818749 | T | G | 2 | a0001c0004t0006g0030 a0001c0004t0006g0083 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1118+661T>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17818749 | |||||||
| chr4:17818894 | T | A | 26 | a0002c0003t0003g0003 a0002c0003t0003g0006 a0002c0003t0003g0017 others(23): Show |
49 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1118+806T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17818894 | |||||||
| chr4:17819085 | A | G | 5 | a0001c0002t0002g0010 a0001c0002t0002g0153 a0001c0002t0002g0154 others(2): Show |
10 | NA18955.hp1 NA18956.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.1118+997A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17819085 | |||||||
| chr4:17819171 | A | G | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1118+1083A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17819171 | |||||||
| chr4:17819307 | G | A | 1 | a0002c0003t0003g0022 | 2 | NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1118+1219G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17819307 | |||||||
| chr4:17819376 | A | G | 1 | a0001c0001t0009g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1118+1288A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17819376 | |||||||
| chr4:17819407 | A | AT | 28 | a0001c0001t0001g0099 a0002c0003t0003g0003 a0002c0003t0003g0006 others(25): Show |
51 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1118+1332dupT | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 17819407 | ||||||
| chr4:17819407 | AT | A | 12 | a0001c0002t0002g0114 a0003c0005t0007g0007 a0003c0005t0007g0020 others(9): Show |
21 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.1118+1332delT | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 17819407 | ||||||
| chr4:17819442 | G | A | 1 | a0002c0003t0003g0056 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1118+1354G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17819442 | |||||||
| chr4:17819492 | C | T | 1 | a0001c0001t0001g0046 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1118+1404C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17819492 | |||||||
| chr4:17819551 | G | A | 2 | a0001c0001t0004g0036 a0001c0001t0004g0103 |
3 | HG01109.hp2 HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1118+1463G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17819551 | |||||||
| chr4:17819554 | T | A | 47 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(44): Show |
75 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1118+1466T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17819554 | |||||||
| chr4:17819705 | T | C | 2 | a0001c0002t0002g0115 a0001c0002t0002g0116 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1118+1617T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17819705 | |||||||
| chr4:17819765 | T | TA | 29 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(26): Show |
53 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1118+1678dupA | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 17819765 | ||||||
| chr4:17819876 | A | C | 1 | a0001c0002t0002g0045 | 2 | HG00639.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1118+1788A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17819876 | |||||||
| chr4:17820049 | G | A | 5 | a0001c0001t0006g0075 a0001c0004t0006g0030 a0001c0004t0006g0083 others(2): Show |
6 | HG01358.hp2 HG02451.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1118+1961G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17820049 | |||||||
| chr4:17820320 | G | A | 51 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0010 others(48): Show |
114 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1118+2232G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17820320 | |||||||
| chr4:17820383 | C | T | 26 | a0002c0003t0003g0003 a0002c0003t0003g0006 a0002c0003t0003g0017 others(23): Show |
49 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1118+2295C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17820383 | |||||||
| chr4:17820399 | A | C | 1 | a0001c0002t0002g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1118+2311A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17820399 | |||||||
| chr4:17820557 | G | A | 26 | a0002c0003t0003g0003 a0002c0003t0003g0006 a0002c0003t0003g0017 others(23): Show |
49 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1119-2426G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17820557 | |||||||
| chr4:17820726 | C | A | 1 | a0001c0001t0004g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1119-2257C>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17820726 | |||||||
| chr4:17820996 | A | G | 1 | a0002c0003t0004g0071 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1119-1987A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17820996 | |||||||
| chr4:17821112 | A | C | 1 | a0001c0004t0006g0085 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1119-1871A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17821112 | |||||||
| chr4:17821145 | C | T | 3 | a0001c0002t0002g0042 a0001c0002t0002g0043 a0001c0002t0002g0141 |
5 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119-1838C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17821145 | |||||||
| chr4:17821157 | C | T | 1 | a0001c0001t0006g0160 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1119-1826C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17821157 | |||||||
| chr4:17821236 | G | A | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119-1747G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17821236 | |||||||
| chr4:17821296 | T | A | 2 | a0001c0002t0002g0042 a0001c0002t0002g0141 |
3 | HG01069.hp1 HG01071.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1119-1687T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17821296 | |||||||
| chr4:17821305 | C | A | 1 | a0001c0001t0004g0026 | 2 | NA18986.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1119-1678C>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17821305 | |||||||
| chr4:17821446 | G | T | 2 | a0001c0001t0005g0018 a0001c0004t0005g0018 |
3 | NA18939.hp2 NA19003.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1119-1537G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17821446 | |||||||
| chr4:17821457 | C | CT | 22 | a0001c0001t0001g0034 a0001c0001t0001g0098 a0001c0001t0001g0099 others(19): Show |
26 | HG01192.hp1 HG01261.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.1119-1504dupT | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 17821457 | ||||||
| chr4:17821457 | CT | C | 92 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0004g0015 others(89): Show |
193 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(190): Show |
intron_variant | MODIFIER | c.1119-1504delT | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 17821457 | ||||||
| chr4:17821457 | CTT | C | 11 | a0001c0002t0002g0118 a0001c0002t0002g0119 a0001c0002t0013g0117 others(8): Show |
19 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1119-1505_1119-150 others(6): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 17821457 | ||||||
| chr4:17821763 | CGACATTT others(2): Show |
C | 57 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(54): Show |
94 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1119-1210_1119-120 others(13): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 17821763 | ||||||
| chr4:17821839 | C | T | 1 | a0001c0002t0002g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1119-1144C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17821839 | |||||||
| chr4:17822028 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1119-955A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17822028 | |||||||
| chr4:17822110 | T | C | 1 | a0001c0001t0006g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1119-873T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17822110 | |||||||
| chr4:17822134 | A | G | 2 | a0001c0001t0004g0036 a0001c0001t0004g0103 |
3 | HG01109.hp2 HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1119-849A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17822134 | |||||||
| chr4:17822159 | GAA | G | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119-823_1119-822d others(4): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17822159 | |||||||
| chr4:17822190 | C | CT | 9 | a0001c0001t0001g0044 a0001c0001t0001g0151 a0001c0001t0004g0036 others(6): Show |
11 | HG00735.hp2 HG01109.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1119-772dupT | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 17822190 | ||||||
| chr4:17822190 | CT | C | 10 | a0001c0001t0001g0089 a0001c0001t0001g0146 a0001c0001t0008g0145 others(7): Show |
15 | HG00280.hp2 HG01069.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1119-772delT | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 17822190 | ||||||
| chr4:17822190 | CTTTTTTT others(4): Show |
C | 1 | a0002c0003t0004g0057 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1119-782_1119-772d others(13): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 17822190 | ||||||
| chr4:17822263 | G | A | 1 | a0002c0014t0003g0058 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1119-720G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17822263 | |||||||
| chr4:17822279 | T | C | 47 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(44): Show |
75 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1119-704T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17822279 | |||||||
| chr4:17822418 | C | T | 5 | a0001c0001t0004g0015 a0001c0001t0006g0015 a0001c0001t0006g0158 others(2): Show |
7 | HG02145.hp2 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1119-565C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17822418 | |||||||
| chr4:17822441 | C | T | 18 | a0001c0001t0004g0026 a0001c0001t0004g0081 a0001c0001t0005g0018 others(15): Show |
30 | HG00673.hp2 HG01891.hp1 HG02602.hp1 others(27): Show |
intron_variant | MODIFIER | c.1119-542C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17822441 | |||||||
| chr4:17822593 | T | A | 1 | a0001c0001t0004g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1119-390T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17822593 | |||||||
| chr4:17822608 | A | T | 1 | a0001c0002t0002g0137 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1119-375A>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17822608 | |||||||
| chr4:17822650 | A | T | 1 | a0001c0002t0002g0136 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1119-333A>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17822650 | |||||||
| chr4:17822699 | A | C | 1 | a0001c0001t0006g0029 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1119-284A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 7/20 | chr4 | 17822699 | |||||||
| chr4:17823156 | G | T | 1 | a0001c0001t0004g0144 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1259+33G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 8/20 | chr4 | 17823156 | |||||||
| chr4:17823159 | C | T | 1 | a0001c0001t0004g0164 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1259+36C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 8/20 | chr4 | 17823159 | |||||||
| chr4:17823207 | C | T | 1 | a0002c0003t0003g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1259+84C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 8/20 | chr4 | 17823207 | |||||||
| chr4:17823467 | T | G | 1 | a0001c0001t0004g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1260-180T>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 8/20 | chr4 | 17823467 | |||||||
| chr4:17823470 | T | G | 3 | a0001c0001t0008g0012 a0001c0001t0008g0145 a0001c0001t0008g0148 |
7 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1260-177T>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 8/20 | chr4 | 17823470 | |||||||
| chr4:17823536 | C | T | 17 | a0001c0001t0006g0075 a0001c0001t0006g0176 a0001c0001t0006g0181 others(14): Show |
20 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1260-111C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 8/20 | chr4 | 17823536 | |||||||
| chr4:17824001 | G | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0016g0019 |
5 | NA18973.hp1 NA18986.hp1 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.1383+231G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 9/20 | chr4 | 17824001 | |||||||
| chr4:17824201 | T | C | 2 | a0001c0004t0005g0078 a0001c0004t0005g0079 |
2 | HG00673.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1383+431T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 9/20 | chr4 | 17824201 | |||||||
| chr4:17824633 | G | A | 18 | a0001c0001t0006g0029 a0001c0001t0006g0075 a0001c0001t0006g0176 others(15): Show |
22 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1384-335G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 9/20 | chr4 | 17824633 | |||||||
| chr4:17824743 | C | T | 1 | a0001c0001t0006g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1384-225C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 9/20 | chr4 | 17824743 | |||||||
| chr4:17824787 | ATTGTT | A | 36 | a0001c0001t0009g0051 a0001c0001t0009g0052 a0001c0001t0009g0053 others(33): Show |
61 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.1384-168_1384-164d others(7): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 17824787 | ||||||
| chr4:17825177 | T | C | 1 | a0001c0002t0002g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1473+120T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 10/20 | chr4 | 17825177 | |||||||
| chr4:17825237 | C | G | 26 | a0002c0003t0003g0003 a0002c0003t0003g0006 a0002c0003t0003g0017 others(23): Show |
49 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1474-145C>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 10/20 | chr4 | 17825237 | |||||||
| chr4:17825283 | T | C | 1 | a0001c0001t0009g0177 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1474-99T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 10/20 | chr4 | 17825283 | |||||||
| chr4:17825341 | A | C | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1474-41A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 10/20 | chr4 | 17825341 | |||||||
| chr4:17825596 | G | A | 3 | a0001c0001t0009g0051 a0001c0001t0009g0177 a0010c0013t0009g0175 |
4 | HG02647.hp2 HG02965.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1653+35G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17825596 | |||||||
| chr4:17825926 | A | C | 58 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(55): Show |
95 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1653+365A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17825926 | |||||||
| chr4:17826078 | C | T | 1 | a0001c0002t0002g0135 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1653+517C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17826078 | |||||||
| chr4:17826092 | G | C | 29 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(26): Show |
53 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1653+531G>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17826092 | |||||||
| chr4:17826144 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(28): Show |
99 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1653+583T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17826144 | |||||||
| chr4:17826160 | T | A | 1 | a0007c0012t0004g0111 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1653+599T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17826160 | |||||||
| chr4:17826194 | C | A | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1653+633C>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17826194 | |||||||
| chr4:17826347 | A | G | 1 | a0001c0002t0002g0134 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1653+786A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17826347 | |||||||
| chr4:17826384 | G | A | 1 | a0002c0003t0003g0023 | 2 | HG02132.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1653+823G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17826384 | |||||||
| chr4:17826414 | A | T | 1 | a0001c0001t0006g0176 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1653+853A>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17826414 | |||||||
| chr4:17826486 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1653+925C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17826486 | |||||||
| chr4:17826622 | C | T | 26 | a0002c0003t0003g0003 a0002c0003t0003g0006 a0002c0003t0003g0017 others(23): Show |
49 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1653+1061C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17826622 | |||||||
| chr4:17826710 | G | C | 1 | a0001c0001t0004g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1653+1149G>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17826710 | |||||||
| chr4:17826835 | C | A | 1 | a0002c0003t0003g0059 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1653+1274C>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17826835 | |||||||
| chr4:17827253 | C | T | 1 | a0001c0001t0005g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1654-1025C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17827253 | |||||||
| chr4:17827519 | G | A | 1 | a0003c0005t0007g0173 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1654-759G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17827519 | |||||||
| chr4:17827558 | A | G | 1 | a0002c0003t0003g0073 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1654-720A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17827558 | |||||||
| chr4:17827592 | G | C | 2 | a0001c0002t0013g0117 a0001c0002t0013g0139 |
2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1654-686G>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17827592 | |||||||
| chr4:17827749 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0087 |
3 | NA18964.hp1 NA19070.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1654-529G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17827749 | |||||||
| chr4:17827760 | G | GT | 8 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0009g0180 others(5): Show |
10 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1654-505dupT | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr4 | 17827760 | ||||||
| chr4:17827791 | A | G | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1654-487A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17827791 | |||||||
| chr4:17827803 | G | C | 1 | a0001c0001t0004g0144 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1654-475G>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17827803 | |||||||
| chr4:17827805 | C | CT | 14 | a0001c0001t0001g0032 a0001c0001t0004g0048 a0001c0002t0002g0167 others(11): Show |
25 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1654-455dupT | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr4 | 17827805 | ||||||
| chr4:17827805 | CTT | C | 27 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(24): Show |
51 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1654-456_1654-455d others(4): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr4 | 17827805 | ||||||
| chr4:17827898 | C | T | 1 | a0001c0001t0006g0160 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1654-380C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17827898 | |||||||
| chr4:17828065 | T | C | 1 | a0001c0004t0005g0078 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1654-213T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17828065 | |||||||
| chr4:17828181 | G | C | 2 | a0001c0004t0006g0030 a0001c0004t0006g0083 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1654-97G>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17828181 | |||||||
| chr4:17828185 | G | A | 1 | a0001c0002t0002g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1654-93G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 11/20 | chr4 | 17828185 | |||||||
| chr4:17828429 | T | G | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1764+41T>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17828429 | |||||||
| chr4:17828623 | A | G | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1764+235A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17828623 | |||||||
| chr4:17828624 | T | C | 3 | a0001c0002t0002g0042 a0001c0002t0002g0043 a0001c0002t0002g0141 |
5 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.1764+236T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17828624 | |||||||
| chr4:17828718 | A | G | 7 | a0001c0001t0004g0015 a0001c0001t0004g0107 a0001c0001t0004g0147 others(4): Show |
9 | HG02145.hp2 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1764+330A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17828718 | |||||||
| chr4:17828727 | G | A | 1 | a0001c0001t0006g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1764+339G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17828727 | |||||||
| chr4:17828741 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1764+353C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17828741 | |||||||
| chr4:17828948 | A | T | 1 | a0002c0003t0003g0064 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1764+560A>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17828948 | |||||||
| chr4:17828950 | A | G | 12 | a0001c0001t0006g0176 a0001c0001t0006g0181 a0001c0001t0009g0051 others(9): Show |
14 | HG02055.hp1 HG02145.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1764+562A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17828950 | |||||||
| chr4:17829054 | T | C | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1764+666T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17829054 | |||||||
| chr4:17829184 | TTTG | T | 2 | a0001c0001t0004g0036 a0001c0001t0004g0103 |
3 | HG01109.hp2 HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1764+811_1764+813d others(5): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 17829184 | ||||||
| chr4:17829555 | TAC | T | 10 | a0003c0005t0007g0007 a0003c0005t0007g0020 a0003c0005t0007g0037 others(7): Show |
18 | HG00423.hp1 HG00438.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1764+1169_1764+117 others(6): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 17829555 | ||||||
| chr4:17829858 | C | G | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1765-1139C>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17829858 | |||||||
| chr4:17830156 | A | G | 1 | a0001c0001t0006g0029 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1765-841A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17830156 | |||||||
| chr4:17830163 | G | A | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1765-834G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17830163 | |||||||
| chr4:17830184 | G | A | 1 | a0001c0001t0006g0029 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1765-813G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17830184 | |||||||
| chr4:17830198 | C | T | 18 | a0001c0001t0006g0029 a0001c0001t0006g0075 a0001c0001t0006g0176 others(15): Show |
22 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1765-799C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17830198 | |||||||
| chr4:17830553 | C | CTTTT | 6 | a0001c0001t0006g0075 a0001c0001t0009g0178 a0001c0004t0006g0030 others(3): Show |
7 | HG01358.hp2 HG02451.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.1765-431_1765-428d others(6): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 17830553 | ||||||
| chr4:17830553 | C | CTTTTT | 7 | a0001c0001t0004g0104 a0001c0001t0009g0052 a0001c0001t0009g0179 others(4): Show |
8 | HG01099.hp1 HG02055.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1765-432_1765-428d others(7): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 17830553 | ||||||
| chr4:17830553 | C | CTTTTTT | 32 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0006g0176 others(29): Show |
57 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.1765-433_1765-428d others(8): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 17830553 | ||||||
| chr4:17830714 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1765-283T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17830714 | |||||||
| chr4:17830783 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1765-214A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17830783 | |||||||
| chr4:17830795 | T | C | 26 | a0002c0003t0003g0003 a0002c0003t0003g0006 a0002c0003t0003g0017 others(23): Show |
49 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1765-202T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 12/20 | chr4 | 17830795 | |||||||
| chr4:17831301 | C | T | 1 | a0001c0001t0006g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1884+185C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17831301 | |||||||
| chr4:17831357 | C | T | 1 | a0001c0001t0004g0081 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1884+241C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17831357 | |||||||
| chr4:17831358 | G | T | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1884+242G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17831358 | |||||||
| chr4:17831361 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1884+245T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17831361 | |||||||
| chr4:17831413 | G | A | 2 | a0001c0001t0004g0143 a0001c0001t0004g0144 |
2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1884+297G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17831413 | |||||||
| chr4:17831426 | T | G | 1 | a0001c0004t0005g0027 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1884+310T>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17831426 | |||||||
| chr4:17831436 | T | C | 1 | a0001c0002t0002g0121 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1884+320T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17831436 | |||||||
| chr4:17831640 | A | G | 2 | a0001c0002t0002g0131 a0001c0002t0002g0132 |
2 | HG02698.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1884+524A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17831640 | |||||||
| chr4:17831687 | T | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0169 others(6): Show |
14 | HG01081.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1884+571T>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17831687 | |||||||
| chr4:17831749 | G | A | 26 | a0002c0003t0003g0003 a0002c0003t0003g0006 a0002c0003t0003g0017 others(23): Show |
49 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1884+633G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17831749 | |||||||
| chr4:17831753 | G | T | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1884+637G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17831753 | |||||||
| chr4:17831924 | T | C | 58 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(55): Show |
95 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1884+808T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17831924 | |||||||
| chr4:17832084 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1884+968T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17832084 | |||||||
| chr4:17832265 | AG | A | 3 | a0003c0005t0007g0037 a0003c0005t0007g0038 a0003c0005t0007g0109 |
5 | HG00423.hp1 HG02132.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884+1151delG | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 17832265 | ||||||
| chr4:17832267 | G | T | 3 | a0003c0005t0007g0037 a0003c0005t0007g0038 a0003c0005t0007g0109 |
5 | HG00423.hp1 HG02132.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884+1151G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17832267 | |||||||
| chr4:17832292 | C | T | 1 | a0001c0004t0006g0030 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1884+1176C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17832292 | |||||||
| chr4:17832350 | C | T | 1 | a0001c0002t0002g0130 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1884+1234C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17832350 | |||||||
| chr4:17832393 | A | G | 29 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(26): Show |
53 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1884+1277A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17832393 | |||||||
| chr4:17832394 | T | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0171 a0001c0001t0015g0005 |
9 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1884+1278T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17832394 | |||||||
| chr4:17832434 | C | T | 1 | a0001c0004t0005g0028 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1884+1318C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17832434 | |||||||
| chr4:17832726 | G | A | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1885-1573G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17832726 | |||||||
| chr4:17832831 | C | T | 1 | a0001c0002t0002g0129 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1885-1468C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17832831 | |||||||
| chr4:17832879 | G | A | 58 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(55): Show |
95 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1885-1420G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17832879 | |||||||
| chr4:17833182 | C | T | 1 | a0002c0003t0004g0067 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1885-1117C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833182 | |||||||
| chr4:17833384 | G | A | 50 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0010 others(47): Show |
113 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1885-915G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833384 | |||||||
| chr4:17833415 | C | T | 1 | a0002c0003t0003g0063 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1885-884C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833415 | |||||||
| chr4:17833440 | C | T | 47 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(44): Show |
75 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1885-859C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833440 | |||||||
| chr4:17833458 | CA | C | 3 | a0001c0001t0010g0021 a0001c0002t0002g0126 a0002c0003t0003g0017 |
7 | HG02976.hp1 HG03130.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.1885-829delA | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 17833458 | ||||||
| chr4:17833467 | A | AT | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1885-832_1885-831i others(3): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833467 | |||||||
| chr4:17833469 | A | AT | 3 | a0001c0001t0001g0098 a0001c0001t0001g0151 a0001c0004t0005g0080 |
3 | HG01123.hp1 HG03654.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1885-830_1885-829i others(3): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833469 | |||||||
| chr4:17833469 | A | T | 66 | a0001c0001t0004g0016 a0001c0001t0004g0036 a0001c0001t0004g0048 others(63): Show |
111 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1885-830A>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833469 | |||||||
| chr4:17833471 | T | A | 2 | a0001c0001t0001g0091 a0001c0001t0008g0148 |
2 | HG03130.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1885-828T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833471 | |||||||
| chr4:17833482 | A | ATATTT | 12 | a0001c0001t0006g0029 a0001c0001t0006g0181 a0001c0001t0009g0051 others(9): Show |
15 | HG02055.hp1 HG02145.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1885-816_1885-815i others(7): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 17833482 | ||||||
| chr4:17833482 | A | ATATTTTT others(1): Show |
5 | a0001c0001t0006g0075 a0001c0004t0006g0030 a0001c0004t0006g0083 others(2): Show |
6 | HG01358.hp2 HG02451.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1885-816_1885-815i others(10): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 17833482 | ||||||
| chr4:17833482 | A | T | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1885-817A>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833482 | |||||||
| chr4:17833484 | T | A | 1 | a0002c0003t0003g0017 | 3 | HG03491.hp1 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1885-815T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833484 | |||||||
| chr4:17833485 | T | G | 17 | a0001c0001t0006g0029 a0001c0001t0006g0075 a0001c0001t0006g0181 others(14): Show |
21 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1885-814T>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833485 | |||||||
| chr4:17833485 | T | TGTTG | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1885-814_1885-813i others(6): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833485 | |||||||
| chr4:17833485 | T | TTTG | 15 | a0001c0001t0004g0026 a0001c0001t0004g0081 a0001c0001t0005g0018 others(12): Show |
26 | HG00673.hp2 HG02602.hp1 HG02630.hp2 others(23): Show |
intron_variant | MODIFIER | c.1885-790_1885-788d others(5): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 17833485 | ||||||
| chr4:17833485 | T | TTTGTTG | 3 | a0001c0001t0006g0176 a0003c0005t0007g0037 a0003c0005t0014g0039 |
5 | HG00544.hp2 HG02132.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1885-793_1885-788d others(8): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 17833485 | ||||||
| chr4:17833485 | T | TTTGTTGT others(2): Show |
8 | a0003c0005t0007g0007 a0003c0005t0007g0020 a0003c0005t0007g0108 others(5): Show |
14 | HG00423.hp1 HG00438.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1885-796_1885-788d others(11): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 17833485 | ||||||
| chr4:17833485 | T | TTTGTTGT others(5): Show |
1 | a0003c0005t0007g0038 | 2 | NA18977.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1885-799_1885-788d others(14): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 17833485 | ||||||
| chr4:17833485 | TTTGTTG | T | 5 | a0001c0001t0004g0015 a0001c0001t0006g0015 a0001c0001t0006g0158 others(2): Show |
7 | HG02145.hp2 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1885-793_1885-788d others(8): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 17833485 | ||||||
| chr4:17833485 | TTTGTTGT others(2): Show |
T | 25 | a0002c0003t0003g0003 a0002c0003t0003g0006 a0002c0003t0003g0022 others(22): Show |
46 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1885-796_1885-788d others(11): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 17833485 | ||||||
| chr4:17833487 | TGTTGTTG | T | 1 | a0002c0003t0003g0017 | 3 | HG03491.hp1 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1885-811_1885-805d others(9): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833487 | |||||||
| chr4:17833488 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1885-811G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833488 | |||||||
| chr4:17833662 | G | A | 7 | a0002c0003t0003g0006 a0002c0003t0003g0023 a0002c0003t0003g0060 others(4): Show |
13 | HG00639.hp2 HG01192.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1885-637G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833662 | |||||||
| chr4:17833914 | A | G | 18 | a0001c0001t0006g0029 a0001c0001t0006g0075 a0001c0001t0006g0176 others(15): Show |
22 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1885-385A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17833914 | |||||||
| chr4:17834098 | G | A | 26 | a0002c0003t0003g0003 a0002c0003t0003g0006 a0002c0003t0003g0017 others(23): Show |
49 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1885-201G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17834098 | |||||||
| chr4:17834132 | T | A | 26 | a0002c0003t0003g0003 a0002c0003t0003g0006 a0002c0003t0003g0017 others(23): Show |
49 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1885-167T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 13/20 | chr4 | 17834132 | |||||||
| chr4:17834541 | C | T | 12 | a0001c0001t0006g0176 a0001c0001t0006g0181 a0001c0001t0009g0051 others(9): Show |
14 | HG02055.hp1 HG02145.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2109+18C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17834541 | |||||||
| chr4:17834609 | G | C | 58 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(55): Show |
95 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2109+86G>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17834609 | |||||||
| chr4:17834627 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2109+104A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17834627 | |||||||
| chr4:17834739 | C | A | 1 | a0007c0012t0004g0111 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2109+216C>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17834739 | |||||||
| chr4:17834748 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2109+225C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17834748 | |||||||
| chr4:17835110 | C | T | 1 | a0001c0001t0004g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2109+587C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17835110 | |||||||
| chr4:17835169 | G | A | 4 | a0002c0003t0003g0065 a0002c0003t0004g0057 a0002c0003t0004g0071 others(1): Show |
4 | HG01243.hp1 HG02040.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2109+646G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17835169 | |||||||
| chr4:17835264 | T | C | 1 | a0001c0004t0019g0077 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2109+741T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17835264 | |||||||
| chr4:17835388 | C | T | 18 | a0001c0001t0006g0029 a0001c0001t0006g0075 a0001c0001t0006g0176 others(15): Show |
22 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2109+865C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17835388 | |||||||
| chr4:17835453 | GAGTGCTG others(7): Show |
G | 1 | a0001c0001t0006g0029 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2109+932_2109+945d others(16): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr4 | 17835453 | ||||||
| chr4:17835468 | A | C | 1 | a0001c0001t0006g0029 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2109+945A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17835468 | |||||||
| chr4:17835484 | G | T | 1 | a0001c0002t0002g0125 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2109+961G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17835484 | |||||||
| chr4:17835539 | C | A | 26 | a0002c0003t0003g0003 a0002c0003t0003g0006 a0002c0003t0003g0017 others(23): Show |
49 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.2109+1016C>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17835539 | |||||||
| chr4:17835960 | G | T | 29 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(26): Show |
53 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2110-1199G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17835960 | |||||||
| chr4:17836302 | G | T | 2 | a0003c0005t0007g0020 a0003c0005t0007g0108 |
4 | NA18966.hp1 NA18982.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.2110-857G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17836302 | |||||||
| chr4:17836888 | A | G | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.2110-271A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17836888 | |||||||
| chr4:17836913 | G | A | 58 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(55): Show |
95 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2110-246G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17836913 | |||||||
| chr4:17837084 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2110-75G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 14/20 | chr4 | 17837084 | |||||||
| chr4:17837920 | A | T | 12 | a0001c0001t0006g0176 a0001c0001t0006g0181 a0001c0001t0009g0051 others(9): Show |
14 | HG02055.hp1 HG02145.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2466+119A>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17837920 | |||||||
| chr4:17838072 | A | T | 12 | a0001c0001t0006g0176 a0001c0001t0006g0181 a0001c0001t0009g0051 others(9): Show |
14 | HG02055.hp1 HG02145.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2466+271A>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17838072 | |||||||
| chr4:17838100 | C | G | 1 | a0002c0003t0003g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2466+299C>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17838100 | |||||||
| chr4:17838497 | G | A | 1 | a0001c0001t0004g0092 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2466+696G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17838497 | |||||||
| chr4:17838530 | A | G | 1 | a0002c0003t0003g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2466+729A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17838530 | |||||||
| chr4:17838568 | G | A | 2 | a0001c0004t0006g0030 a0001c0004t0006g0083 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2466+767G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17838568 | |||||||
| chr4:17838603 | G | A | 2 | a0001c0001t0009g0178 a0001c0001t0009g0179 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2466+802G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17838603 | |||||||
| chr4:17838686 | T | C | 1 | a0001c0001t0006g0029 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2466+885T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17838686 | |||||||
| chr4:17839122 | G | A | 1 | a0001c0001t0004g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2467-554G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17839122 | |||||||
| chr4:17839235 | C | T | 1 | a0001c0001t0004g0163 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2467-441C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17839235 | |||||||
| chr4:17839300 | G | A | 2 | a0001c0001t0004g0036 a0001c0001t0004g0103 |
3 | HG01109.hp2 HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.2467-376G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17839300 | |||||||
| chr4:17839363 | C | T | 1 | a0002c0003t0003g0062 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2467-313C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17839363 | |||||||
| chr4:17839385 | G | C | 1 | a0001c0002t0002g0040 | 2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2467-291G>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17839385 | |||||||
| chr4:17839386 | G | C | 2 | a0001c0001t0004g0036 a0001c0001t0004g0103 |
3 | HG01109.hp2 HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.2467-290G>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17839386 | |||||||
| chr4:17839463 | A | T | 1 | a0001c0002t0018g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2467-213A>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 16/20 | chr4 | 17839463 | |||||||
| chr4:17839842 | A | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(28): Show |
99 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(96): Show |
splice_region_variant&intron_variant | LOW | c.2628+5A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 17/20 | chr4 | 17839842 | |||||||
| chr4:17839857 | C | T | 1 | a0001c0002t0002g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2628+20C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 17/20 | chr4 | 17839857 | |||||||
| chr4:17839993 | C | G | 1 | a0001c0002t0002g0157 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2629-78C>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 17/20 | chr4 | 17839993 | |||||||
| chr4:17839997 | A | G | 29 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(26): Show |
53 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2629-74A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 17/20 | chr4 | 17839997 | |||||||
| chr4:17840012 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2629-59A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 17/20 | chr4 | 17840012 | |||||||
| chr4:17840022 | A | G | 1 | a0001c0001t0006g0029 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2629-49A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 17/20 | chr4 | 17840022 | |||||||
| chr4:17840034 | G | A | 1 | a0001c0001t0009g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2629-37G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 17/20 | chr4 | 17840034 | |||||||
| chr4:17840225 | A | C | 47 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(44): Show |
75 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.2767+16A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 18/20 | chr4 | 17840225 | |||||||
| chr4:17840236 | A | G | 2 | a0001c0001t0009g0052 a0001c0001t0009g0182 |
3 | HG02647.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2767+27A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 18/20 | chr4 | 17840236 | |||||||
| chr4:17840287 | C | T | 1 | a0001c0002t0002g0133 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2767+78C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 18/20 | chr4 | 17840287 | |||||||
| chr4:17840325 | T | A | 129 | a0001c0001t0004g0026 a0001c0001t0004g0036 a0001c0001t0004g0081 others(126): Show |
241 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.2767+116T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 18/20 | chr4 | 17840325 | |||||||
| chr4:17840466 | C | T | 5 | a0001c0001t0006g0075 a0001c0004t0006g0030 a0001c0004t0006g0083 others(2): Show |
6 | HG01358.hp2 HG02451.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.2768-141C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 18/20 | chr4 | 17840466 | |||||||
| chr4:17840533 | T | C | 18 | a0001c0001t0006g0029 a0001c0001t0006g0075 a0001c0001t0006g0176 others(15): Show |
22 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2768-74T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 18/20 | chr4 | 17840533 | |||||||
| chr4:17840540 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2768-67A>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 18/20 | chr4 | 17840540 | |||||||
| chr4:17840719 | T | C | 12 | a0001c0001t0006g0176 a0001c0001t0006g0181 a0001c0001t0009g0051 others(9): Show |
14 | HG02055.hp1 HG02145.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2854+26T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 19/20 | chr4 | 17840719 | |||||||
| chr4:17840801 | AT | A | 47 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(44): Show |
75 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.2854+116delT | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 17840801 | ||||||
| chr4:17840814 | T | C | 1 | a0001c0001t0004g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2854+121T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 19/20 | chr4 | 17840814 | |||||||
| chr4:17841197 | G | T | 1 | a0001c0001t0006g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2854+504G>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 19/20 | chr4 | 17841197 | |||||||
| chr4:17841225 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2854+532A>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 19/20 | chr4 | 17841225 | |||||||
| chr4:17841277 | C | T | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.2854+584C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 19/20 | chr4 | 17841277 | |||||||
| chr4:17841487 | T | C | 1 | a0001c0001t0009g0182 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2854+794T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 19/20 | chr4 | 17841487 | |||||||
| chr4:17841600 | T | C | 1 | a0001c0002t0002g0040 | 2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2855-710T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 19/20 | chr4 | 17841600 | |||||||
| chr4:17841819 | T | C | 1 | a0001c0001t0004g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2855-491T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 19/20 | chr4 | 17841819 | |||||||
| chr4:17841890 | A | G | 1 | a0001c0002t0002g0123 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2855-420A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 19/20 | chr4 | 17841890 | |||||||
| chr4:17841993 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2855-317T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 19/20 | chr4 | 17841993 | |||||||
| chr4:17842230 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2855-80A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 19/20 | chr4 | 17842230 | |||||||
| chr4:17842406 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
269 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.2924+27G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 20/20 | chr4 | 17842406 | |||||||
| chr4:17842488 | G | A | 1 | a0001c0002t0002g0122 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2924+109G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 20/20 | chr4 | 17842488 | |||||||
| chr4:17842611 | T | A | 1 | a0001c0002t0002g0041 | 2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2924+232T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 20/20 | chr4 | 17842611 | |||||||
| chr4:17842627 | T | C | 29 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 others(26): Show |
53 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2924+248T>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 20/20 | chr4 | 17842627 | |||||||
| chr4:17842661 | G | A | 1 | a0002c0003t0003g0024 | 2 | HG03490.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2924+282G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 20/20 | chr4 | 17842661 | |||||||
| chr4:17842752 | G | C | 1 | a0001c0001t0006g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2924+373G>C | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 20/20 | chr4 | 17842752 | |||||||
| chr4:17842757 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0102 |
3 | HG02723.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2924+378G>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 20/20 | chr4 | 17842757 | |||||||
| chr4:17842790 | C | CTGTT | 14 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0169 others(11): Show |
21 | HG01081.hp2 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2924+412_2924+415d others(6): Show |
NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 17842790 | ||||||
| chr4:17843057 | C | T | 2 | a0005c0007t0001g0049 a0005c0007t0001g0165 |
3 | HG01891.hp2 HG02717.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2925-245C>T | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 20/20 | chr4 | 17843057 | |||||||
| chr4:17843097 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2925-205A>G | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 20/20 | chr4 | 17843097 | |||||||
| chr4:17843144 | T | A | 3 | a0001c0001t0004g0036 a0001c0001t0004g0103 a0001c0001t0004g0104 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.2925-158T>A | NCAPG | ENSG00000109805.10 | transcript | ENST00000251496.7 | protein_coding | 20/20 | chr4 | 17843144 |