Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80221 |
| ensemblid | ENSG00000167107.13 |
| hgncid | 26101 |
| symbol | ACSF2 |
| name | acyl-CoA synthetase family member 2 |
| refseq_nuc | NM_025149.6 |
| refseq_prot | NP_079425.3 |
| ensembl_nuc | ENST00000300441.9 |
| ensembl_prot | ENSP00000300441.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 50426218 |
| end | 50474837 |
| strand | + |
| ver | v1.2 |
| region | chr17:50426218-50474837 |
| region5000 | chr17:50421218-50479837 |
| regionname0 | ACSF2_chr17_50426218_50474837 |
| regionname5000 | ACSF2_chr17_50421218_50479837 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 615 | 292 | 66 | 67 | 109 | 14 | 34 | 80 | ACSF2_chr17_50421218_50479837 | ACSF2 | MAVYV others(610): Show |
chr17 | 50421218 | 50479837 |
| a0002 | 0/0 | 615 | 12 | 8 | 4 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | MAVYV others(610): Show |
chr17 | 50421218 | 50479837 |
| a0003 | 0/0 | 615 | 8 | 5 | 3 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | MAVYV others(610): Show |
chr17 | 50421218 | 50479837 |
| a0004 | 0/0 | 615 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | MAVYV others(610): Show |
chr17 | 50421218 | 50479837 |
| a0005 | 0/0 | 615 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ACSF2_chr17_50421218_50479837 | ACSF2 | MAVYV others(610): Show |
chr17 | 50421218 | 50479837 |
| a0006 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | MAVYV others(610): Show |
chr17 | 50421218 | 50479837 |
| a0007 | 0/0 | 615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | MAVYV others(610): Show |
chr17 | 50421218 | 50479837 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1845 | 125 | 13 | 26 | 61 | 8 | 16 | ACSF2_chr17_50421218_50479837 | ACSF2 | ATGGC others(1840): Show |
chr17 | 50421218 | 50479837 | ||
| a0001c0002 | 0/0 | 1845 | 84 | 46 | 15 | 15 | 2 | 6 | ACSF2_chr17_50421218_50479837 | ACSF2 | ATGGC others(1840): Show |
chr17 | 50421218 | 50479837 | ||
| a0001c0003 | 0/1 | 1845 | 82 | 6 | 26 | 33 | 4 | 12 | ACSF2_chr17_50421218_50479837 | ACSF2 | ATGGC others(1840): Show |
chr17 | 50421218 | 50479837 | ||
| a0001c0009 | 0/0 | 1845 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ATGGC others(1840): Show |
chr17 | 50421218 | 50479837 | ||
| a0002c0004 | 0/0 | 1845 | 10 | 7 | 3 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ATGGC others(1840): Show |
chr17 | 50421218 | 50479837 | ||
| a0002c0008 | 0/0 | 1845 | 2 | 1 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ATGGC others(1840): Show |
chr17 | 50421218 | 50479837 | ||
| a0003c0005 | 0/0 | 1845 | 8 | 5 | 3 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ATGGC others(1840): Show |
chr17 | 50421218 | 50479837 | ||
| a0004c0006 | 0/0 | 1845 | 4 | 4 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ATGGC others(1840): Show |
chr17 | 50421218 | 50479837 | ||
| a0005c0007 | 0/0 | 1845 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ATGGC others(1840): Show |
chr17 | 50421218 | 50479837 | ||
| a0006c0011 | 0/0 | 1845 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ATGGC others(1840): Show |
chr17 | 50421218 | 50479837 | ||
| a0007c0010 | 0/0 | 1845 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ATGGC others(1840): Show |
chr17 | 50421218 | 50479837 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2177 | 125 | 13 | 26 | 61 | 8 | 16 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0001c0002t0001 | 0/0 | 2177 | 22 | 19 | 2 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0001c0002t0002 | 0/0 | 2177 | 61 | 26 | 13 | 14 | 2 | 6 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0001c0002t0003 | 0/0 | 2177 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0001c0003t0001 | 0/1 | 2177 | 81 | 6 | 26 | 32 | 4 | 12 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0001c0003t0002 | 0/0 | 2177 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0001c0009t0001 | 0/0 | 2177 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0002c0004t0002 | 0/0 | 2177 | 10 | 7 | 3 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0002c0008t0001 | 0/0 | 2177 | 2 | 1 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0003c0005t0002 | 0/0 | 2177 | 8 | 5 | 3 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0004c0006t0001 | 0/0 | 2177 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0004c0006t0002 | 0/0 | 2177 | 3 | 3 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0005c0007t0001 | 0/0 | 2177 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0006c0011t0001 | 0/0 | 2177 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| a0007c0010t0001 | 0/0 | 2177 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | ACTTT others(2172): Show |
chr17 | 50421218 | 50479837 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 2 | 4 | 6 | 0 | 2 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0003 | 0/0 | 5 | 1 | 0 | 3 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0004 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0008 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0009 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0003t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0001c0009t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0002c0004t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0002c0004t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0002c0004t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0002c0004t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0002c0004t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0002c0004t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0002c0004t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0002c0004t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0002c0004t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0002c0008t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0002c0008t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0003c0005t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0003c0005t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0003c0005t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0003c0005t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0003c0005t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0003c0005t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0003c0005t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0004c0006t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0004c0006t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0004c0006t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0004c0006t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0005c0007t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0006c0011t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| a0007c0010t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0240 | EUR | GBR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0009 | EUR | GBR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0203 | EUR | FIN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | CHS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00438 | hp2 | a0006 | c0011 | t0001 | g0091 | EAS | CHS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0213 | EAS | CHS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0224 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0171 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0195 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0205 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0023 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0215 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0177 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0223 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01069 | hp1 | a0003 | c0005 | t0002 | g0021 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0009 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0191 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0024 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01071 | hp2 | a0003 | c0005 | t0002 | g0021 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0139 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0026 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0024 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0196 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01099 | hp1 | a0003 | c0005 | t0002 | g0148 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01106 | hp2 | a0002 | c0004 | t0002 | g0046 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0144 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0207 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0212 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01167 | hp2 | a0002 | c0004 | t0002 | g0045 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0141 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0178 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01169 | hp1 | a0002 | c0004 | t0002 | g0040 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0172 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0181 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0143 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01243 | hp2 | a0002 | c0008 | t0001 | g0264 | AMR | PUR | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0023 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0193 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0230 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0175 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0185 | EUR | IBS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0182 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0160 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0248 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0218 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0026 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0194 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0217 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0216 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0231 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0235 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0211 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02145 | hp1 | a0002 | c0008 | t0001 | g0263 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0170 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0174 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0025 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CDX | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | CDX | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0258 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02451 | hp1 | a0004 | c0006 | t0002 | g0137 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02572 | hp1 | a0003 | c0005 | t0002 | g0152 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0031 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0204 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0184 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02615 | hp2 | a0002 | c0004 | t0002 | g0047 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02630 | hp1 | a0002 | c0004 | t0002 | g0043 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0210 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0226 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0155 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0142 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0004 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02809 | hp2 | a0004 | c0006 | t0002 | g0136 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0251 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02886 | hp2 | a0003 | c0005 | t0002 | g0150 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02895 | hp1 | a0002 | c0004 | t0002 | g0012 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02895 | hp2 | a0003 | c0005 | t0002 | g0151 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0131 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02970 | hp1 | a0007 | c0010 | t0001 | g0209 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02976 | hp2 | a0003 | c0005 | t0002 | g0149 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0157 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0187 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0247 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0117 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0250 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0165 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0253 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03225 | hp2 | a0002 | c0004 | t0002 | g0012 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0056 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0188 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0180 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ESN | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03540 | hp1 | a0003 | c0005 | t0002 | g0153 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03540 | hp2 | a0002 | c0004 | t0002 | g0042 | AFR | GWD | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0156 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0183 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0140 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0260 | SAS | STU | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0166 | SAS | STU | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0164 | SAS | BEB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0070 | SAS | BEB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0097 | SAS | BEB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0145 | SAS | BEB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0161 | SAS | BEB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0025 | SAS | STU | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0176 | SAS | STU | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0206 | SAS | STU | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18522 | hp2 | a0004 | c0006 | t0002 | g0138 | AFR | YRI | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0243 | EAS | CHB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | YRI | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18942 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18943 | hp1 | a0001 | c0003 | t0001 | g0200 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18945 | hp2 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18946 | hp1 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0233 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18960 | hp1 | a0005 | c0007 | t0001 | g0016 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18961 | hp2 | a0001 | c0003 | t0001 | g0237 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0225 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0201 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0245 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0199 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0208 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18989 | hp2 | a0001 | c0003 | t0001 | g0236 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18992 | hp1 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19009 | hp1 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19030 | hp2 | a0004 | c0006 | t0001 | g0135 | AFR | LWK | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0262 | AFR | LWK | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0147 | AFR | LWK | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0100 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19063 | hp1 | a0001 | c0003 | t0001 | g0259 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19063 | hp2 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19068 | hp1 | a0001 | c0003 | t0001 | g0221 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0219 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19087 | hp1 | a0001 | c0003 | t0001 | g0154 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19090 | hp1 | a0005 | c0007 | t0001 | g0016 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | ASW | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0173 | EUR | TSI | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0009 | EUR | TSI | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0179 | SAS | GIH | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | GIH | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0134 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0252 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0254 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0242 | AFR | ACB | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0249 | AFR | MSL | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG06807 | hp1 | a0001 | c0009 | t0001 | g0032 | AFR | USA | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| HG06807 | hp2 | a0002 | c0004 | t0002 | g0044 | AFR | USA | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0256 | AFR | USA | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| NA21309 | hp2 | a0002 | c0004 | t0002 | g0041 | AFR | LWK | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0146 | REF | REF | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0088 | REF | REF | ACSF2_chr17_50421218_50479837 | ACSF2 | chr17 | 50421218 | 50479837 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50426316 | G | T | 1 | a0002 | 12 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
missense_variant | MODERATE | c.55G>T | p.Gly19Trp | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/16 | 99/2177 | 55/1848 | 19/615 | chr17 | 50426316 | |||
| chr17:50426323 | T | A | 1 | a0003 | 8 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(5): Show |
missense_variant | MODERATE | c.62T>A | p.Leu21Gln | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/16 | 106/2177 | 62/1848 | 21/615 | chr17 | 50426323 | |||
| chr17:50426362 | C | T | 1 | a0004 | 4 | HG02451.hp1 HG02809.hp2 NA18522.hp2 others(1): Show |
missense_variant | MODERATE | c.101C>T | p.Ala34Val | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/16 | 145/2177 | 101/1848 | 34/615 | chr17 | 50426362 | |||
| chr17:50460756 | A | C | 1 | a0006 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.208A>C | p.Asn70His | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 2/16 | 252/2177 | 208/1848 | 70/615 | chr17 | 50460756 | |||
| chr17:50463410 | C | T | 1 | a0005 | 2 | NA18960.hp1 NA19090.hp1 |
missense_variant | MODERATE | c.904C>T | p.Arg302Trp | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 8/16 | 948/2177 | 904/1848 | 302/615 | chr17 | 50463410 | |||
| chr17:50474547 | C | A | 1 | a0007 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.1843C>A | p.Leu615Met | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 16/16 | 1887/2177 | 1843/1848 | 615/615 | chr17 | 50474547 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50426315 | G | T | 2 | a0002c0004 a0002c0008 |
12 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
synonymous_variant | LOW | c.54G>T | p.Ser18Ser | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/16 | 98/2177 | 54/1848 | 18/615 | chr17 | 50426315 | |||
| chr17:50461674 | T | C | 5 | a0001c0002 a0001c0009 a0002c0004 others(2): Show |
107 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(104): Show |
synonymous_variant | LOW | c.495T>C | p.Tyr165Tyr | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/16 | 539/2177 | 495/1848 | 165/615 | chr17 | 50461674 | |||
| chr17:50472430 | C | G | 2 | a0001c0003 a0007c0010 |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
splice_region_variant&synonymous_variant | LOW | c.1326C>G | p.Ala442Ala | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 12/16 | 1370/2177 | 1326/1848 | 442/615 | chr17 | 50472430 | |||
| chr17:50474201 | C | T | 1 | a0001c0009 | 1 | HG06807.hp1 | splice_region_variant&synonymous_variant | LOW | c.1731C>T | p.Ile577Ile | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 15/16 | 1775/2177 | 1731/1848 | 577/615 | chr17 | 50474201 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50474562 | C | G | 1 | a0001c0002t0003 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 16/16 | 10 | chr17 | 50474562 | ||||||
| chr17:50474793 | G | C | 5 | a0001c0002t0002 a0001c0003t0002 a0002c0004t0002 others(2): Show |
83 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*241G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 16/16 | 241 | chr17 | 50474793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50426560 | C | G | 2 | a0002c0008t0001g0263 a0002c0008t0001g0264 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.128+171C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50426560 | |||||||
| chr17:50426567 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | NA18971.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.128+178G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50426567 | |||||||
| chr17:50426580 | A | G | 1 | a0001c0002t0002g0262 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.128+191A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50426580 | |||||||
| chr17:50426668 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.128+279G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50426668 | |||||||
| chr17:50426751 | T | C | 1 | a0001c0002t0003g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.128+362T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50426751 | |||||||
| chr17:50426769 | A | G | 1 | a0001c0002t0003g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.128+380A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50426769 | |||||||
| chr17:50426771 | A | G | 139 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0001t0001g0228 others(136): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.128+382A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50426771 | |||||||
| chr17:50426843 | C | T | 6 | a0002c0008t0001g0263 a0002c0008t0001g0264 a0004c0006t0001g0135 others(3): Show |
6 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+454C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50426843 | |||||||
| chr17:50426853 | T | C | 1 | a0004c0006t0001g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.128+464T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50426853 | |||||||
| chr17:50426887 | A | G | 2 | a0002c0008t0001g0263 a0002c0008t0001g0264 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.128+498A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50426887 | |||||||
| chr17:50426967 | C | T | 1 | a0001c0002t0002g0262 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.128+578C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50426967 | |||||||
| chr17:50426999 | C | T | 1 | a0001c0002t0002g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.128+610C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50426999 | |||||||
| chr17:50427895 | C | G | 3 | a0001c0002t0001g0133 a0004c0006t0001g0135 a0004c0006t0002g0138 |
3 | HG02451.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.128+1506C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50427895 | |||||||
| chr17:50427920 | G | C | 1 | a0001c0002t0002g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.128+1531G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50427920 | |||||||
| chr17:50428138 | G | A | 145 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(142): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.128+1749G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50428138 | |||||||
| chr17:50428140 | C | T | 155 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(152): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.128+1751C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50428140 | |||||||
| chr17:50428194 | A | T | 1 | a0001c0001t0001g0038 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.128+1805A>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50428194 | |||||||
| chr17:50428377 | G | A | 11 | a0001c0002t0001g0039 a0001c0002t0002g0262 a0002c0004t0002g0012 others(8): Show |
12 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.128+1988G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50428377 | |||||||
| chr17:50428401 | A | G | 5 | a0001c0002t0001g0132 a0004c0006t0001g0135 a0004c0006t0002g0136 others(2): Show |
5 | HG02451.hp1 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+2012A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50428401 | |||||||
| chr17:50428489 | T | TAAATAA | 140 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0001t0001g0228 others(137): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.128+2108_128+2113d others(8): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50428489 | ||||||
| chr17:50428628 | T | C | 140 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0001t0001g0228 others(137): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.128+2239T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50428628 | |||||||
| chr17:50428679 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.128+2290G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50428679 | |||||||
| chr17:50429007 | T | C | 7 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(4): Show |
7 | HG01074.hp1 HG01109.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.128+2618T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429007 | |||||||
| chr17:50429346 | T | A | 137 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0001t0001g0228 others(134): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.128+2957T>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429346 | |||||||
| chr17:50429472 | C | T | 1 | a0001c0003t0001g0260 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.128+3083C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429472 | |||||||
| chr17:50429520 | T | A | 1 | a0001c0003t0001g0139 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.128+3131T>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429520 | |||||||
| chr17:50429521 | C | CT | 36 | a0001c0002t0001g0027 a0001c0002t0001g0039 a0001c0002t0001g0130 others(33): Show |
40 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.128+3142dupT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50429521 | ||||||
| chr17:50429532 | A | T | 166 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(163): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.128+3143A>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429532 | |||||||
| chr17:50429586 | C | A | 1 | a0001c0002t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128+3197C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429586 | |||||||
| chr17:50429665 | G | A | 30 | a0001c0002t0001g0027 a0001c0002t0001g0039 a0001c0002t0001g0130 others(27): Show |
34 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.128+3276G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429665 | |||||||
| chr17:50429668 | C | T | 13 | a0001c0002t0001g0039 a0001c0002t0001g0130 a0001c0002t0001g0131 others(10): Show |
14 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.128+3279C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429668 | |||||||
| chr17:50429673 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.128+3284C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429673 | |||||||
| chr17:50429699 | G | A | 7 | a0003c0005t0002g0021 a0003c0005t0002g0148 a0003c0005t0002g0149 others(4): Show |
8 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+3310G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429699 | |||||||
| chr17:50429778 | A | G | 1 | a0003c0005t0002g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.128+3389A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429778 | |||||||
| chr17:50429785 | TGGGATTA others(2): Show |
T | 13 | a0001c0002t0001g0039 a0001c0002t0001g0130 a0001c0002t0001g0131 others(10): Show |
14 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.128+3399_128+3407d others(11): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50429785 | ||||||
| chr17:50429788 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.128+3399G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429788 | |||||||
| chr17:50429813 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.128+3424C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429813 | |||||||
| chr17:50429886 | C | A | 1 | a0001c0002t0001g0246 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.128+3497C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50429886 | |||||||
| chr17:50430164 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG01069.hp2 HG01975.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.128+3775G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50430164 | |||||||
| chr17:50430405 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.128+4016C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50430405 | |||||||
| chr17:50430590 | G | A | 46 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0002t0001g0186 others(43): Show |
52 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.128+4201G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50430590 | |||||||
| chr17:50430614 | G | A | 6 | a0001c0003t0001g0007 a0001c0003t0001g0023 a0001c0003t0001g0193 others(3): Show |
9 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.128+4225G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50430614 | |||||||
| chr17:50430733 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.128+4344A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50430733 | |||||||
| chr17:50430878 | C | T | 2 | a0001c0002t0002g0191 a0001c0002t0002g0192 |
2 | HG01070.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.128+4489C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50430878 | |||||||
| chr17:50430890 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.128+4501G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50430890 | |||||||
| chr17:50430934 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.128+4545A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50430934 | |||||||
| chr17:50431003 | C | T | 1 | a0001c0002t0002g0190 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.128+4614C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50431003 | |||||||
| chr17:50431063 | A | C | 4 | a0001c0001t0001g0244 a0001c0003t0001g0243 a0001c0003t0001g0245 others(1): Show |
4 | NA18612.hp1 NA18979.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.128+4674A>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50431063 | |||||||
| chr17:50431110 | G | A | 1 | a0001c0003t0001g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.128+4721G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50431110 | |||||||
| chr17:50431515 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.128+5126C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50431515 | |||||||
| chr17:50431538 | A | T | 1 | a0001c0001t0001g0125 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.128+5149A>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50431538 | |||||||
| chr17:50431651 | T | C | 100 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(97): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.128+5262T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50431651 | |||||||
| chr17:50431787 | G | A | 6 | a0001c0002t0001g0130 a0001c0002t0001g0131 a0001c0002t0002g0010 others(3): Show |
8 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.128+5398G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50431787 | |||||||
| chr17:50431968 | C | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(5): Show |
8 | HG00140.hp1 HG00733.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+5579C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50431968 | |||||||
| chr17:50432101 | A | G | 8 | a0001c0003t0001g0007 a0001c0003t0001g0023 a0001c0003t0001g0056 others(5): Show |
11 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.128+5712A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50432101 | |||||||
| chr17:50432167 | G | A | 1 | a0001c0002t0002g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.128+5778G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50432167 | |||||||
| chr17:50432194 | C | T | 2 | a0001c0001t0001g0244 a0001c0003t0001g0245 |
2 | NA18979.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.128+5805C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50432194 | |||||||
| chr17:50432409 | A | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0125 a0001c0002t0001g0132 |
3 | HG00558.hp2 HG03098.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.128+6020A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50432409 | |||||||
| chr17:50432604 | T | C | 162 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0001t0001g0228 others(159): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.128+6215T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50432604 | |||||||
| chr17:50432659 | C | T | 13 | a0001c0002t0001g0039 a0001c0002t0001g0130 a0001c0002t0001g0131 others(10): Show |
14 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.128+6270C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50432659 | |||||||
| chr17:50432694 | A | G | 15 | a0001c0002t0001g0039 a0001c0002t0001g0130 a0001c0002t0001g0131 others(12): Show |
16 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.128+6305A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50432694 | |||||||
| chr17:50432741 | G | A | 69 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(66): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.128+6352G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50432741 | |||||||
| chr17:50432807 | G | A | 1 | a0001c0002t0003g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.128+6418G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50432807 | |||||||
| chr17:50432924 | A | C | 4 | a0001c0002t0002g0006 a0001c0002t0002g0190 a0001c0002t0002g0191 others(1): Show |
6 | HG01070.hp2 HG01192.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+6535A>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50432924 | |||||||
| chr17:50432936 | G | C | 1 | a0001c0002t0001g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.128+6547G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50432936 | |||||||
| chr17:50433111 | C | CT | 129 | a0001c0001t0001g0124 a0001c0001t0001g0158 a0001c0001t0001g0169 others(126): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.128+6736dupT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50433111 | ||||||
| chr17:50433131 | G | A | 1 | a0001c0003t0001g0260 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.128+6742G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50433131 | |||||||
| chr17:50433396 | C | T | 1 | a0001c0002t0002g0262 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.128+7007C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50433396 | |||||||
| chr17:50433519 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0122 a0001c0001t0001g0123 |
4 | HG00323.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.128+7130A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50433519 | |||||||
| chr17:50433679 | C | T | 4 | a0001c0002t0001g0186 a0001c0002t0001g0189 a0001c0002t0002g0187 others(1): Show |
4 | HG00741.hp1 HG01346.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.128+7290C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50433679 | |||||||
| chr17:50433823 | C | T | 1 | a0001c0002t0002g0185 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.128+7434C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50433823 | |||||||
| chr17:50433915 | G | A | 1 | a0001c0002t0002g0241 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.128+7526G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50433915 | |||||||
| chr17:50434094 | G | A | 1 | a0003c0005t0002g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.128+7705G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50434094 | |||||||
| chr17:50434214 | G | A | 26 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0002t0002g0005 others(23): Show |
32 | HG00423.hp2 HG00438.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.128+7825G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50434214 | |||||||
| chr17:50434238 | G | C | 1 | a0001c0001t0001g0014 | 2 | NA18942.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.128+7849G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50434238 | |||||||
| chr17:50434439 | C | A | 85 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(82): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.128+8050C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50434439 | |||||||
| chr17:50434453 | G | A | 17 | a0001c0002t0001g0027 a0001c0002t0001g0239 a0001c0002t0001g0246 others(14): Show |
18 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.128+8064G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50434453 | |||||||
| chr17:50434548 | T | C | 85 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(82): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.128+8159T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50434548 | |||||||
| chr17:50434550 | G | A | 1 | a0001c0002t0002g0262 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.128+8161G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50434550 | |||||||
| chr17:50434695 | A | AT | 10 | a0001c0001t0001g0121 a0002c0004t0002g0012 a0002c0004t0002g0040 others(7): Show |
11 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.128+8320dupT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50434695 | ||||||
| chr17:50434738 | G | A | 3 | a0001c0002t0001g0246 a0001c0002t0001g0247 a0001c0002t0001g0248 |
3 | HG01891.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.128+8349G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50434738 | |||||||
| chr17:50434765 | A | G | 162 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0001t0001g0228 others(159): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.128+8376A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50434765 | |||||||
| chr17:50434773 | G | T | 205 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(202): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.128+8384G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50434773 | |||||||
| chr17:50434911 | C | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(5): Show |
8 | HG00140.hp1 HG00733.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+8522C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50434911 | |||||||
| chr17:50435013 | C | G | 171 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(168): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.128+8624C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435013 | |||||||
| chr17:50435057 | A | G | 1 | a0001c0003t0001g0196 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.128+8668A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435057 | |||||||
| chr17:50435070 | A | G | 1 | a0001c0002t0002g0170 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.128+8681A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435070 | |||||||
| chr17:50435118 | T | C | 205 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(202): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.128+8729T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435118 | |||||||
| chr17:50435122 | G | A | 1 | a0001c0009t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.128+8733G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435122 | |||||||
| chr17:50435150 | G | A | 10 | a0001c0002t0002g0010 a0001c0002t0002g0241 a0001c0002t0002g0242 others(7): Show |
13 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.128+8761G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435150 | |||||||
| chr17:50435262 | G | A | 15 | a0001c0002t0001g0039 a0001c0002t0001g0130 a0001c0002t0001g0131 others(12): Show |
16 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.128+8873G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435262 | |||||||
| chr17:50435358 | C | CT | 70 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(67): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.128+8976dupT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50435358 | ||||||
| chr17:50435421 | T | A | 1 | a0001c0002t0002g0171 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.128+9032T>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435421 | |||||||
| chr17:50435511 | A | G | 1 | a0001c0003t0001g0237 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.128+9122A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435511 | |||||||
| chr17:50435601 | T | TG | 162 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0001t0001g0228 others(159): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.128+9214dupG | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50435601 | ||||||
| chr17:50435627 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.128+9238G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435627 | |||||||
| chr17:50435692 | C | G | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
5 | HG00140.hp1 HG00733.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.128+9303C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435692 | |||||||
| chr17:50435721 | T | C | 17 | a0001c0002t0001g0027 a0001c0002t0001g0239 a0001c0002t0001g0246 others(14): Show |
20 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.128+9332T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435721 | |||||||
| chr17:50435724 | C | G | 1 | a0001c0002t0002g0258 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.128+9335C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435724 | |||||||
| chr17:50435737 | T | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0228 |
2 | HG00558.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.128+9348T>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435737 | |||||||
| chr17:50435857 | A | G | 1 | a0001c0002t0002g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.128+9468A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435857 | |||||||
| chr17:50435869 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.128+9480C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435869 | |||||||
| chr17:50435878 | A | G | 1 | a0001c0002t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.128+9489A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435878 | |||||||
| chr17:50435901 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.128+9512T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50435901 | |||||||
| chr17:50436086 | C | G | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.128+9697C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436086 | |||||||
| chr17:50436097 | T | TTTGTTG | 3 | a0001c0002t0002g0010 a0001c0002t0002g0241 a0001c0002t0002g0242 |
5 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+9723_128+9728d others(8): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50436097 | ||||||
| chr17:50436097 | TTTGTTG | T | 15 | a0001c0002t0001g0039 a0001c0002t0001g0130 a0001c0002t0001g0131 others(12): Show |
16 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.128+9723_128+9728d others(8): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50436097 | ||||||
| chr17:50436222 | C | T | 1 | a0001c0002t0002g0011 | 3 | HG02922.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.128+9833C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436222 | |||||||
| chr17:50436223 | G | A | 11 | a0001c0002t0002g0171 a0001c0002t0002g0172 a0001c0002t0002g0173 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.128+9834G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436223 | |||||||
| chr17:50436275 | G | T | 1 | a0001c0002t0001g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.128+9886G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436275 | |||||||
| chr17:50436408 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.128+10019C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436408 | |||||||
| chr17:50436553 | C | G | 57 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0002t0001g0133 others(54): Show |
66 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.128+10164C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436553 | |||||||
| chr17:50436558 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.128+10169C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436558 | |||||||
| chr17:50436579 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.128+10190A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436579 | |||||||
| chr17:50436591 | A | G | 162 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0001t0001g0228 others(159): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.128+10202A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436591 | |||||||
| chr17:50436631 | G | T | 9 | a0002c0004t0002g0012 a0002c0004t0002g0040 a0002c0004t0002g0041 others(6): Show |
10 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.128+10242G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436631 | |||||||
| chr17:50436681 | A | G | 87 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(84): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.128+10292A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436681 | |||||||
| chr17:50436716 | G | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(5): Show |
8 | HG00140.hp1 HG00733.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+10327G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436716 | |||||||
| chr17:50436738 | C | CT | 9 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(6): Show |
10 | HG01175.hp1 HG01255.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.128+10365dupT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50436738 | ||||||
| chr17:50436756 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.128+10367C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436756 | |||||||
| chr17:50436903 | A | G | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.128+10514A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436903 | |||||||
| chr17:50436968 | A | G | 1 | a0006c0011t0001g0091 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.128+10579A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50436968 | |||||||
| chr17:50437002 | C | G | 3 | a0001c0002t0001g0132 a0004c0006t0001g0135 a0004c0006t0002g0138 |
3 | HG03098.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.128+10613C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50437002 | |||||||
| chr17:50437217 | C | G | 5 | a0001c0001t0001g0234 a0001c0003t0001g0026 a0001c0003t0001g0233 others(2): Show |
6 | HG01074.hp2 HG01943.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+10828C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50437217 | |||||||
| chr17:50437243 | T | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | NA18947.hp2 NA18956.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.128+10854T>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50437243 | |||||||
| chr17:50437275 | T | G | 1 | a0001c0003t0001g0139 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.128+10886T>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50437275 | |||||||
| chr17:50437326 | G | A | 7 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0001c0003t0001g0199 others(4): Show |
7 | NA18943.hp1 NA18945.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.128+10937G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50437326 | |||||||
| chr17:50437334 | G | C | 70 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(67): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.128+10945G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50437334 | |||||||
| chr17:50437604 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0002t0002g0134 |
3 | HG02109.hp1 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.128+11215C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50437604 | |||||||
| chr17:50438057 | T | C | 3 | a0001c0002t0002g0011 a0002c0008t0001g0263 a0002c0008t0001g0264 |
5 | HG01243.hp2 HG02145.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+11668T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50438057 | |||||||
| chr17:50438318 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG01175.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.128+11929A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50438318 | |||||||
| chr17:50438582 | T | G | 70 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(67): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.128+12193T>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50438582 | |||||||
| chr17:50439014 | T | C | 1 | a0001c0002t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.128+12625T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50439014 | |||||||
| chr17:50439155 | C | T | 7 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(4): Show |
7 | HG01074.hp1 HG01109.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.128+12766C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50439155 | |||||||
| chr17:50439197 | A | G | 56 | a0001c0002t0001g0186 a0001c0002t0001g0189 a0001c0002t0002g0005 others(53): Show |
67 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.128+12808A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50439197 | |||||||
| chr17:50439232 | C | CT | 36 | a0001c0001t0001g0036 a0001c0001t0001g0060 a0001c0001t0001g0090 others(33): Show |
37 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.128+12870dupT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50439232 | ||||||
| chr17:50439232 | CT | C | 6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0096 others(3): Show |
6 | HG01168.hp1 HG01361.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.128+12870delT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50439232 | ||||||
| chr17:50439233 | T | A | 1 | a0001c0002t0001g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.128+12844T>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50439233 | |||||||
| chr17:50439233 | T | C | 5 | a0001c0003t0001g0140 a0001c0003t0001g0142 a0001c0003t0001g0143 others(2): Show |
5 | HG01109.hp1 HG01192.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.128+12844T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50439233 | |||||||
| chr17:50439234 | T | C | 1 | a0001c0003t0001g0141 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.128+12845T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50439234 | |||||||
| chr17:50439317 | T | C | 70 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(67): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.128+12928T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50439317 | |||||||
| chr17:50439563 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.128+13174G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50439563 | |||||||
| chr17:50439565 | G | A | 57 | a0001c0002t0001g0133 a0001c0002t0001g0186 a0001c0002t0001g0189 others(54): Show |
68 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.128+13176G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50439565 | |||||||
| chr17:50439591 | C | T | 69 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(66): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.128+13202C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50439591 | |||||||
| chr17:50439796 | A | T | 2 | a0002c0008t0001g0263 a0002c0008t0001g0264 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.128+13407A>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50439796 | |||||||
| chr17:50439806 | T | TA | 6 | a0001c0002t0003g0031 a0001c0003t0001g0203 a0001c0003t0001g0204 others(3): Show |
6 | HG00280.hp2 HG00733.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.128+13425dupA | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50439806 | ||||||
| chr17:50439912 | T | A | 1 | a0001c0003t0001g0097 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.128+13523T>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50439912 | |||||||
| chr17:50440098 | T | C | 69 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(66): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.128+13709T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50440098 | |||||||
| chr17:50440131 | G | C | 2 | a0002c0008t0001g0263 a0002c0008t0001g0264 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.128+13742G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50440131 | |||||||
| chr17:50440132 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.128+13743G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50440132 | |||||||
| chr17:50440132 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.128+13743G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50440132 | |||||||
| chr17:50440136 | TAAGGAGC others(1): Show |
T | 9 | a0002c0004t0002g0012 a0002c0004t0002g0040 a0002c0004t0002g0041 others(6): Show |
10 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.128+13748_128+1375 others(12): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50440136 | |||||||
| chr17:50440234 | C | T | 3 | a0003c0005t0002g0150 a0003c0005t0002g0151 a0003c0005t0002g0152 |
3 | HG02572.hp1 HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.128+13845C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50440234 | |||||||
| chr17:50440365 | G | C | 3 | a0001c0002t0001g0132 a0004c0006t0001g0135 a0004c0006t0002g0138 |
3 | HG03098.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.128+13976G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50440365 | |||||||
| chr17:50440380 | C | T | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | NA18946.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.128+13991C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50440380 | |||||||
| chr17:50440501 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.128+14112C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50440501 | |||||||
| chr17:50440675 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0128 |
2 | HG01361.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.128+14286C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50440675 | |||||||
| chr17:50440713 | G | C | 69 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(66): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.128+14324G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50440713 | |||||||
| chr17:50440906 | C | A | 29 | a0001c0002t0001g0027 a0001c0002t0001g0039 a0001c0002t0001g0130 others(26): Show |
31 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.128+14517C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50440906 | |||||||
| chr17:50441076 | A | G | 8 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(5): Show |
8 | HG00140.hp1 HG00733.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+14687A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50441076 | |||||||
| chr17:50441225 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.128+14836A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50441225 | |||||||
| chr17:50441312 | A | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
4 | HG00140.hp1 HG00733.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.128+14923A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50441312 | |||||||
| chr17:50441351 | T | C | 1 | a0001c0003t0001g0208 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.128+14962T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50441351 | |||||||
| chr17:50441465 | A | G | 1 | a0001c0009t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.128+15076A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50441465 | |||||||
| chr17:50441534 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02015.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.128+15145C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50441534 | |||||||
| chr17:50441925 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.128+15536G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50441925 | |||||||
| chr17:50442325 | A | T | 1 | a0001c0003t0001g0227 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.128+15936A>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50442325 | |||||||
| chr17:50442325 | AT | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.128+15955delT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50442325 | ||||||
| chr17:50442325 | ATT | A | 8 | a0001c0001t0001g0055 a0001c0001t0001g0098 a0001c0001t0001g0099 others(5): Show |
8 | HG00323.hp2 HG00558.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.128+15954_128+1595 others(6): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50442325 | ||||||
| chr17:50442350 | G | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(61): Show |
86 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.128+15961G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50442350 | |||||||
| chr17:50442435 | T | G | 2 | a0001c0003t0001g0210 a0007c0010t0001g0209 |
2 | HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.128+16046T>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50442435 | |||||||
| chr17:50442559 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0112 a0001c0001t0001g0113 |
4 | HG02965.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.128+16170A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50442559 | |||||||
| chr17:50442970 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.128+16581C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50442970 | |||||||
| chr17:50443049 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.128+16660A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50443049 | |||||||
| chr17:50443130 | G | A | 28 | a0001c0002t0001g0027 a0001c0002t0001g0039 a0001c0002t0001g0130 others(25): Show |
30 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.128+16741G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50443130 | |||||||
| chr17:50443187 | C | T | 1 | a0001c0003t0001g0139 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.128+16798C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50443187 | |||||||
| chr17:50443199 | C | T | 2 | a0001c0002t0001g0130 a0001c0002t0001g0131 |
2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.128+16810C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50443199 | |||||||
| chr17:50443310 | A | G | 5 | a0001c0002t0001g0132 a0004c0006t0001g0135 a0004c0006t0002g0136 others(2): Show |
5 | HG02451.hp1 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+16921A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50443310 | |||||||
| chr17:50443327 | A | G | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.128+16938A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50443327 | |||||||
| chr17:50443450 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.128+17061G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50443450 | |||||||
| chr17:50443515 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.128+17126C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50443515 | |||||||
| chr17:50443842 | G | A | 71 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(68): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.129-16835G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50443842 | |||||||
| chr17:50443871 | C | G | 46 | a0001c0002t0001g0186 a0001c0002t0001g0189 a0001c0002t0002g0005 others(43): Show |
54 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.129-16806C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50443871 | |||||||
| chr17:50443919 | A | C | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.129-16758A>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50443919 | |||||||
| chr17:50444080 | C | A | 2 | a0004c0006t0001g0135 a0004c0006t0002g0138 |
2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.129-16597C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50444080 | |||||||
| chr17:50444151 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0090 a0005c0007t0001g0016 |
4 | NA18943.hp2 NA18960.hp1 NA19089.hp1 others(1): Show |
intron_variant | MODIFIER | c.129-16526C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50444151 | |||||||
| chr17:50444168 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.129-16509T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50444168 | |||||||
| chr17:50444214 | T | C | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.129-16463T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50444214 | |||||||
| chr17:50444218 | G | A | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(259): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.129-16459G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50444218 | |||||||
| chr17:50444278 | C | T | 5 | a0001c0002t0001g0132 a0004c0006t0001g0135 a0004c0006t0002g0136 others(2): Show |
5 | HG02451.hp1 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-16399C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50444278 | |||||||
| chr17:50444327 | C | T | 69 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(66): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.129-16350C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50444327 | |||||||
| chr17:50444418 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.129-16259G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50444418 | |||||||
| chr17:50444532 | C | T | 3 | a0001c0002t0002g0006 a0001c0002t0002g0191 a0001c0002t0002g0192 |
5 | HG01070.hp2 HG01192.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.129-16145C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50444532 | |||||||
| chr17:50444636 | A | AAC | 45 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(42): Show |
51 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.129-16010_129-1600 others(6): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50444636 | ||||||
| chr17:50444636 | A | AACAC | 16 | a0001c0001t0001g0065 a0001c0002t0001g0186 a0001c0002t0002g0011 others(13): Show |
19 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.129-16012_129-1600 others(8): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50444636 | ||||||
| chr17:50444636 | A | AACACAC | 5 | a0001c0002t0002g0010 a0001c0002t0002g0173 a0001c0002t0002g0241 others(2): Show |
7 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.129-16014_129-1600 others(10): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50444636 | ||||||
| chr17:50444636 | AAC | A | 71 | a0001c0001t0001g0036 a0001c0001t0001g0228 a0001c0001t0001g0229 others(68): Show |
84 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.129-16010_129-1600 others(6): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50444636 | ||||||
| chr17:50444636 | AACAC | A | 3 | a0001c0003t0001g0240 a0002c0008t0001g0263 a0002c0008t0001g0264 |
3 | HG00099.hp1 HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.129-16012_129-1600 others(8): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50444636 | ||||||
| chr17:50444679 | A | T | 3 | a0001c0002t0002g0005 a0001c0002t0002g0163 a0001c0002t0002g0168 |
6 | HG00423.hp2 HG00438.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-15998A>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50444679 | |||||||
| chr17:50444733 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.129-15944C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50444733 | |||||||
| chr17:50444904 | T | C | 1 | a0001c0003t0001g0194 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.129-15773T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50444904 | |||||||
| chr17:50445152 | G | T | 44 | a0001c0002t0001g0186 a0001c0002t0001g0189 a0001c0002t0002g0005 others(41): Show |
50 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.129-15525G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50445152 | |||||||
| chr17:50445170 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.129-15507C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50445170 | |||||||
| chr17:50445375 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.129-15302G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50445375 | |||||||
| chr17:50445532 | C | T | 2 | a0002c0008t0001g0263 a0002c0008t0001g0264 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.129-15145C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50445532 | |||||||
| chr17:50445559 | C | T | 1 | a0001c0003t0001g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.129-15118C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50445559 | |||||||
| chr17:50445641 | A | T | 2 | a0001c0002t0002g0171 a0001c0002t0002g0177 |
2 | HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.129-15036A>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50445641 | |||||||
| chr17:50445642 | T | A | 1 | a0004c0006t0001g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.129-15035T>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50445642 | |||||||
| chr17:50445806 | T | TA | 157 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(154): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.129-14855dupA | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50445806 | ||||||
| chr17:50445854 | C | G | 1 | a0001c0003t0001g0145 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.129-14823C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50445854 | |||||||
| chr17:50446139 | A | G | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.129-14538A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50446139 | |||||||
| chr17:50446173 | ATGTT | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | NA18947.hp2 NA18956.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.129-14503_129-1450 others(8): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50446173 | |||||||
| chr17:50446343 | C | T | 1 | a0001c0002t0002g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.129-14334C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50446343 | |||||||
| chr17:50446446 | C | T | 9 | a0002c0004t0002g0012 a0002c0004t0002g0040 a0002c0004t0002g0041 others(6): Show |
10 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.129-14231C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50446446 | |||||||
| chr17:50446759 | T | C | 69 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(66): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.129-13918T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50446759 | |||||||
| chr17:50446812 | T | C | 169 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(166): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.129-13865T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50446812 | |||||||
| chr17:50446813 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.129-13864G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50446813 | |||||||
| chr17:50446964 | A | G | 1 | a0001c0002t0002g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.129-13713A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50446964 | |||||||
| chr17:50447239 | G | A | 1 | a0001c0002t0002g0173 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.129-13438G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50447239 | |||||||
| chr17:50447432 | C | T | 44 | a0001c0002t0001g0186 a0001c0002t0001g0189 a0001c0002t0002g0005 others(41): Show |
52 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.129-13245C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50447432 | |||||||
| chr17:50447499 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.129-13178G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50447499 | |||||||
| chr17:50447543 | A | AAAT | 56 | a0001c0002t0001g0186 a0001c0002t0001g0189 a0001c0002t0002g0005 others(53): Show |
67 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.129-13112_129-1311 others(7): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50447543 | ||||||
| chr17:50447746 | C | T | 1 | a0001c0003t0001g0139 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.129-12931C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50447746 | |||||||
| chr17:50447812 | A | C | 2 | a0001c0002t0001g0130 a0001c0002t0001g0131 |
2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.129-12865A>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50447812 | |||||||
| chr17:50447949 | A | G | 12 | a0001c0002t0002g0011 a0001c0002t0002g0171 a0001c0002t0002g0172 others(9): Show |
14 | HG00642.hp1 HG00738.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.129-12728A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50447949 | |||||||
| chr17:50448032 | C | G | 1 | a0001c0003t0001g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.129-12645C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50448032 | |||||||
| chr17:50448054 | G | A | 1 | a0001c0002t0002g0174 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.129-12623G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50448054 | |||||||
| chr17:50448087 | T | C | 2 | a0002c0004t0002g0040 a0002c0004t0002g0045 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.129-12590T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50448087 | |||||||
| chr17:50448129 | A | AGATGGTA others(1): Show |
8 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(5): Show |
8 | HG00140.hp1 HG00733.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-12547_129-1254 others(12): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50448129 | ||||||
| chr17:50448187 | G | A | 1 | a0001c0009t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.129-12490G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50448187 | |||||||
| chr17:50448215 | A | G | 2 | a0001c0002t0002g0162 a0001c0002t0002g0167 |
2 | NA19062.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.129-12462A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50448215 | |||||||
| chr17:50448295 | A | G | 161 | a0001c0001t0001g0084 a0001c0001t0001g0228 a0001c0001t0001g0229 others(158): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.129-12382A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50448295 | |||||||
| chr17:50448453 | G | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0038 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.129-12224G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50448453 | |||||||
| chr17:50448730 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0068 |
3 | NA18942.hp2 NA19057.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.129-11947G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50448730 | |||||||
| chr17:50448890 | C | T | 2 | a0004c0006t0001g0135 a0004c0006t0002g0138 |
2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.129-11787C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50448890 | |||||||
| chr17:50448919 | A | G | 1 | a0001c0003t0001g0207 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.129-11758A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50448919 | |||||||
| chr17:50448983 | A | G | 1 | a0001c0002t0002g0053 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.129-11694A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50448983 | |||||||
| chr17:50449010 | C | CT | 20 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0060 others(17): Show |
21 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.129-11644dupT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50449010 | ||||||
| chr17:50449029 | T | C | 3 | a0001c0002t0002g0011 a0002c0008t0001g0263 a0002c0008t0001g0264 |
5 | HG01243.hp2 HG02145.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-11648T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50449029 | |||||||
| chr17:50449030 | T | C | 3 | a0001c0002t0002g0011 a0002c0008t0001g0263 a0002c0008t0001g0264 |
5 | HG01243.hp2 HG02145.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-11647T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50449030 | |||||||
| chr17:50449039 | T | C | 1 | a0001c0002t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.129-11638T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50449039 | |||||||
| chr17:50449309 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG00140.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.129-11368G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50449309 | |||||||
| chr17:50449441 | G | T | 1 | a0001c0002t0002g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.129-11236G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50449441 | |||||||
| chr17:50449466 | G | A | 4 | a0001c0002t0001g0130 a0001c0002t0001g0131 a0004c0006t0002g0136 others(1): Show |
4 | HG02451.hp1 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-11211G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50449466 | |||||||
| chr17:50449473 | C | T | 3 | a0001c0002t0001g0132 a0004c0006t0001g0135 a0004c0006t0002g0138 |
3 | HG03098.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.129-11204C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50449473 | |||||||
| chr17:50449635 | C | T | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
5 | HG00140.hp1 HG00733.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.129-11042C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50449635 | |||||||
| chr17:50449772 | T | C | 1 | a0001c0002t0003g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.129-10905T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50449772 | |||||||
| chr17:50449925 | C | T | 1 | a0001c0002t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.129-10752C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50449925 | |||||||
| chr17:50449949 | A | G | 1 | a0004c0006t0002g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.129-10728A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50449949 | |||||||
| chr17:50450035 | C | T | 1 | a0004c0006t0001g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.129-10642C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50450035 | |||||||
| chr17:50450036 | T | C | 1 | a0001c0002t0002g0117 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.129-10641T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50450036 | |||||||
| chr17:50450049 | G | A | 1 | a0001c0002t0002g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.129-10628G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50450049 | |||||||
| chr17:50450134 | A | T | 20 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(17): Show |
20 | HG00280.hp2 HG00733.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.129-10543A>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50450134 | |||||||
| chr17:50450208 | C | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0128 |
2 | HG01361.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.129-10469C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50450208 | |||||||
| chr17:50450275 | G | T | 1 | a0001c0001t0001g0029 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.129-10402G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50450275 | |||||||
| chr17:50450500 | CA | C | 86 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0129 others(83): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.129-10161delA | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50450500 | ||||||
| chr17:50450754 | C | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0009t0001g0032 |
3 | HG02965.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.129-9923C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50450754 | |||||||
| chr17:50450790 | C | T | 69 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(66): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.129-9887C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50450790 | |||||||
| chr17:50450954 | CAG | C | 69 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(66): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.129-9720_129-9719d others(4): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50450954 | ||||||
| chr17:50451029 | C | T | 3 | a0001c0002t0002g0052 a0001c0002t0002g0053 a0001c0002t0002g0054 |
3 | HG02165.hp2 HG02523.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.129-9648C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50451029 | |||||||
| chr17:50451043 | C | T | 1 | a0001c0002t0002g0161 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.129-9634C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50451043 | |||||||
| chr17:50451141 | G | A | 9 | a0002c0004t0002g0012 a0002c0004t0002g0040 a0002c0004t0002g0041 others(6): Show |
10 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.129-9536G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50451141 | |||||||
| chr17:50451191 | G | A | 68 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(65): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.129-9486G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50451191 | |||||||
| chr17:50451452 | A | T | 1 | a0001c0002t0002g0163 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.129-9225A>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50451452 | |||||||
| chr17:50451490 | C | T | 45 | a0001c0002t0001g0186 a0001c0002t0001g0189 a0001c0002t0002g0005 others(42): Show |
51 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.129-9187C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50451490 | |||||||
| chr17:50451514 | A | C | 2 | a0004c0006t0002g0136 a0004c0006t0002g0137 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.129-9163A>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50451514 | |||||||
| chr17:50451601 | A | G | 87 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0228 others(84): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.129-9076A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50451601 | |||||||
| chr17:50451622 | G | T | 1 | a0001c0001t0001g0083 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.129-9055G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50451622 | |||||||
| chr17:50451746 | A | G | 18 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0002t0001g0027 others(15): Show |
19 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.129-8931A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50451746 | |||||||
| chr17:50451970 | A | G | 1 | a0001c0003t0001g0222 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.129-8707A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50451970 | |||||||
| chr17:50452026 | T | C | 1 | a0001c0002t0002g0176 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.129-8651T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50452026 | |||||||
| chr17:50452138 | A | C | 1 | a0001c0002t0002g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.129-8539A>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50452138 | |||||||
| chr17:50452192 | G | T | 1 | a0001c0003t0001g0235 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.129-8485G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50452192 | |||||||
| chr17:50452193 | C | T | 1 | a0001c0003t0001g0144 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.129-8484C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50452193 | |||||||
| chr17:50452246 | C | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0098 a0001c0001t0001g0104 |
3 | HG00323.hp2 HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.129-8431C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50452246 | |||||||
| chr17:50452256 | T | G | 69 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(66): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.129-8421T>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50452256 | |||||||
| chr17:50452264 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.129-8413C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50452264 | |||||||
| chr17:50452293 | T | C | 3 | a0001c0002t0002g0011 a0002c0008t0001g0263 a0002c0008t0001g0264 |
5 | HG01243.hp2 HG02145.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-8384T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50452293 | |||||||
| chr17:50452526 | G | GC | 4 | a0001c0001t0001g0049 a0001c0002t0002g0168 a0001c0003t0001g0236 others(1): Show |
4 | HG00423.hp2 HG02572.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-8149dupC | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50452526 | ||||||
| chr17:50452602 | C | T | 43 | a0001c0002t0001g0186 a0001c0002t0001g0189 a0001c0002t0002g0005 others(40): Show |
49 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.129-8075C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50452602 | |||||||
| chr17:50452648 | G | A | 11 | a0001c0002t0001g0027 a0001c0002t0001g0239 a0001c0002t0001g0246 others(8): Show |
12 | HG01891.hp2 HG02559.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.129-8029G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50452648 | |||||||
| chr17:50453055 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.129-7622A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50453055 | |||||||
| chr17:50453075 | C | T | 7 | a0003c0005t0002g0021 a0003c0005t0002g0148 a0003c0005t0002g0149 others(4): Show |
8 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-7602C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50453075 | |||||||
| chr17:50453411 | T | C | 1 | a0001c0002t0003g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.129-7266T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50453411 | |||||||
| chr17:50453460 | A | G | 18 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0002t0001g0027 others(15): Show |
19 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.129-7217A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50453460 | |||||||
| chr17:50453488 | G | A | 1 | a0001c0003t0001g0026 | 2 | HG01074.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.129-7189G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50453488 | |||||||
| chr17:50453554 | C | T | 1 | a0002c0004t0002g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.129-7123C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50453554 | |||||||
| chr17:50453558 | C | G | 1 | a0001c0001t0001g0080 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.129-7119C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50453558 | |||||||
| chr17:50453759 | G | A | 68 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(65): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.129-6918G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50453759 | |||||||
| chr17:50453949 | T | TA | 4 | a0001c0001t0001g0049 a0001c0002t0002g0011 a0002c0008t0001g0263 others(1): Show |
6 | HG01243.hp2 HG02145.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.129-6715dupA | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50453949 | ||||||
| chr17:50453950 | A | T | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.129-6727A>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50453950 | |||||||
| chr17:50453977 | A | C | 10 | a0001c0002t0002g0010 a0001c0002t0002g0241 a0001c0002t0002g0242 others(7): Show |
13 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-6700A>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50453977 | |||||||
| chr17:50454058 | A | C | 2 | a0001c0003t0001g0217 a0001c0003t0001g0231 |
2 | HG02015.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.129-6619A>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50454058 | |||||||
| chr17:50454075 | G | A | 1 | a0001c0003t0001g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.129-6602G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50454075 | |||||||
| chr17:50454085 | A | G | 1 | a0001c0003t0001g0097 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.129-6592A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50454085 | |||||||
| chr17:50454169 | A | AT | 52 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0037 others(49): Show |
57 | HG00438.hp2 HG00738.hp1 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.129-6483dupT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50454169 | ||||||
| chr17:50454169 | A | ATT | 9 | a0001c0001t0001g0079 a0001c0001t0001g0115 a0001c0002t0001g0248 others(6): Show |
9 | HG01891.hp2 HG02129.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.129-6484_129-6483d others(4): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50454169 | ||||||
| chr17:50454169 | AT | A | 59 | a0001c0001t0001g0069 a0001c0001t0001g0228 a0001c0001t0001g0229 others(56): Show |
68 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.129-6483delT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50454169 | ||||||
| chr17:50454235 | C | T | 8 | a0001c0003t0001g0007 a0001c0003t0001g0023 a0001c0003t0001g0056 others(5): Show |
11 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.129-6442C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50454235 | |||||||
| chr17:50454652 | G | A | 1 | a0001c0002t0002g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.129-6025G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50454652 | |||||||
| chr17:50454858 | T | C | 7 | a0003c0005t0002g0021 a0003c0005t0002g0148 a0003c0005t0002g0149 others(4): Show |
8 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-5819T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50454858 | |||||||
| chr17:50454989 | G | A | 1 | a0001c0003t0001g0101 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.129-5688G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50454989 | |||||||
| chr17:50455107 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.129-5570C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50455107 | |||||||
| chr17:50455140 | G | A | 1 | a0001c0002t0002g0159 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.129-5537G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50455140 | |||||||
| chr17:50455432 | T | C | 167 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0228 others(164): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.129-5245T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50455432 | |||||||
| chr17:50455440 | G | A | 1 | a0001c0002t0002g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.129-5237G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50455440 | |||||||
| chr17:50455464 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.129-5213G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50455464 | |||||||
| chr17:50455792 | C | T | 7 | a0003c0005t0002g0021 a0003c0005t0002g0148 a0003c0005t0002g0149 others(4): Show |
8 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-4885C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50455792 | |||||||
| chr17:50455868 | C | T | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.129-4809C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50455868 | |||||||
| chr17:50456091 | C | G | 7 | a0003c0005t0002g0021 a0003c0005t0002g0148 a0003c0005t0002g0149 others(4): Show |
8 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-4586C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50456091 | |||||||
| chr17:50456452 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.129-4225G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50456452 | |||||||
| chr17:50456667 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.129-4010G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50456667 | |||||||
| chr17:50456719 | G | A | 47 | a0001c0002t0001g0186 a0001c0002t0001g0189 a0001c0002t0002g0005 others(44): Show |
53 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.129-3958G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50456719 | |||||||
| chr17:50456743 | GATAAAA | G | 15 | a0001c0002t0001g0027 a0001c0002t0001g0039 a0001c0002t0001g0239 others(12): Show |
16 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.129-3927_129-3922d others(8): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50456743 | ||||||
| chr17:50456890 | T | C | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.129-3787T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50456890 | |||||||
| chr17:50457405 | C | G | 21 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0002t0001g0130 others(18): Show |
24 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.129-3272C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50457405 | |||||||
| chr17:50457426 | G | A | 69 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(66): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.129-3251G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50457426 | |||||||
| chr17:50457674 | G | A | 10 | a0001c0002t0003g0031 a0002c0008t0001g0263 a0002c0008t0001g0264 others(7): Show |
11 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.129-3003G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50457674 | |||||||
| chr17:50458209 | T | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0037 |
2 | HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.129-2468T>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50458209 | |||||||
| chr17:50458343 | C | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0098 a0001c0001t0001g0104 |
3 | HG00323.hp2 HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.129-2334C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50458343 | |||||||
| chr17:50458344 | C | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0098 a0001c0001t0001g0104 |
3 | HG00323.hp2 HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.129-2333C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50458344 | |||||||
| chr17:50458345 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0098 a0001c0001t0001g0104 |
3 | HG00323.hp2 HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.129-2332C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50458345 | |||||||
| chr17:50458529 | G | A | 13 | a0001c0002t0001g0130 a0001c0002t0001g0131 a0001c0002t0002g0117 others(10): Show |
14 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.129-2148G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50458529 | |||||||
| chr17:50458535 | C | G | 1 | a0001c0002t0002g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.129-2142C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50458535 | |||||||
| chr17:50458553 | C | T | 62 | a0001c0002t0001g0027 a0001c0002t0001g0039 a0001c0002t0001g0186 others(59): Show |
69 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.129-2124C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50458553 | |||||||
| chr17:50458579 | A | T | 1 | a0001c0001t0001g0069 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.129-2098A>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50458579 | |||||||
| chr17:50458638 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.129-2039A>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50458638 | |||||||
| chr17:50458686 | T | C | 48 | a0001c0002t0001g0186 a0001c0002t0001g0189 a0001c0002t0002g0005 others(45): Show |
54 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.129-1991T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50458686 | |||||||
| chr17:50459077 | T | C | 71 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0001c0001t0001g0244 others(68): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.129-1600T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50459077 | |||||||
| chr17:50459092 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0037 |
2 | HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.129-1585C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50459092 | |||||||
| chr17:50459115 | C | T | 1 | a0001c0002t0001g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.129-1562C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50459115 | |||||||
| chr17:50459143 | G | A | 48 | a0001c0002t0001g0186 a0001c0002t0001g0189 a0001c0002t0002g0005 others(45): Show |
54 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.129-1534G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50459143 | |||||||
| chr17:50459198 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.129-1479C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50459198 | |||||||
| chr17:50459365 | G | A | 70 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0001c0002t0002g0005 others(67): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.129-1312G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50459365 | |||||||
| chr17:50459398 | AC | A | 15 | a0001c0002t0001g0130 a0001c0002t0001g0131 a0001c0002t0002g0117 others(12): Show |
16 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.129-1277delC | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50459398 | ||||||
| chr17:50459516 | G | C | 63 | a0001c0002t0001g0027 a0001c0002t0001g0039 a0001c0002t0001g0133 others(60): Show |
70 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.129-1161G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50459516 | |||||||
| chr17:50459539 | T | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0096 a0001c0001t0001g0105 |
4 | HG01496.hp2 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-1138T>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50459539 | |||||||
| chr17:50459549 | A | G | 7 | a0003c0005t0002g0021 a0003c0005t0002g0148 a0003c0005t0002g0149 others(4): Show |
8 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-1128A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50459549 | |||||||
| chr17:50459555 | C | T | 1 | a0001c0003t0001g0215 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.129-1122C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50459555 | |||||||
| chr17:50459774 | A | G | 149 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0232 others(146): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.129-903A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50459774 | |||||||
| chr17:50459842 | G | A | 1 | a0001c0002t0002g0011 | 3 | HG02922.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.129-835G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50459842 | |||||||
| chr17:50460040 | A | AT | 4 | a0001c0002t0002g0010 a0001c0002t0002g0241 a0001c0002t0002g0242 others(1): Show |
6 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.129-636dupT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 50460040 | ||||||
| chr17:50460076 | G | A | 1 | a0001c0002t0001g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.129-601G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50460076 | |||||||
| chr17:50460129 | G | A | 1 | a0001c0002t0002g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.129-548G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | chr17 | 50460129 | |||||||
| chr17:50461222 | C | T | 3 | a0001c0002t0002g0010 a0001c0002t0002g0241 a0001c0002t0002g0242 |
5 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-20C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 2/15 | chr17 | 50461222 | |||||||
| chr17:50461373 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03491.hp1 | splice_region_variant&intron_variant | LOW | c.453+3G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 3/15 | chr17 | 50461373 | |||||||
| chr17:50461393 | C | T | 1 | a0001c0002t0002g0182 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.453+23C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 3/15 | chr17 | 50461393 | |||||||
| chr17:50461471 | T | C | 1 | a0001c0003t0001g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.453+101T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 3/15 | chr17 | 50461471 | |||||||
| chr17:50461738 | T | C | 18 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0002t0001g0027 others(15): Show |
19 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.507+52T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | chr17 | 50461738 | |||||||
| chr17:50461892 | G | T | 1 | a0001c0002t0001g0186 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.507+206G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | chr17 | 50461892 | |||||||
| chr17:50461927 | G | GGT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(58): Show |
83 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.508-233_508-232dup others(2): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 50461927 | ||||||
| chr17:50461927 | G | GGTGT | 17 | a0001c0001t0001g0051 a0001c0001t0001g0098 a0001c0001t0001g0104 others(14): Show |
21 | HG00323.hp2 HG01070.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.508-235_508-232dup others(4): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 50461927 | ||||||
| chr17:50461927 | G | GGTGTGT | 34 | a0001c0002t0001g0189 a0001c0002t0002g0005 a0001c0002t0002g0011 others(31): Show |
40 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.508-237_508-232dup others(6): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 50461927 | ||||||
| chr17:50461927 | G | GGTGTGTG others(1): Show |
23 | a0001c0002t0001g0027 a0001c0002t0001g0239 a0001c0002t0001g0246 others(20): Show |
25 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.508-239_508-232dup others(8): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 50461927 | ||||||
| chr17:50461927 | G | GGTGTGTG others(3): Show |
2 | a0001c0002t0001g0132 a0001c0002t0003g0031 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.508-241_508-232dup others(10): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 50461927 | ||||||
| chr17:50461927 | G | GGTGTGTG others(5): Show |
2 | a0001c0002t0001g0133 a0001c0002t0002g0188 |
2 | HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.508-243_508-232dup others(12): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 50461927 | ||||||
| chr17:50461927 | G | GGTGTGTG others(7): Show |
1 | a0001c0002t0002g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.508-245_508-232dup others(14): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 50461927 | ||||||
| chr17:50461927 | GGT | G | 6 | a0001c0001t0001g0060 a0001c0001t0001g0129 a0001c0002t0001g0130 others(3): Show |
6 | HG02486.hp2 HG02922.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.508-233_508-232del others(2): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 50461927 | ||||||
| chr17:50461927 | GGTGTGT | G | 9 | a0002c0004t0002g0012 a0002c0004t0002g0040 a0002c0004t0002g0041 others(6): Show |
10 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.508-237_508-232del others(6): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 50461927 | ||||||
| chr17:50461951 | T | C | 2 | a0001c0001t0001g0118 a0001c0003t0001g0203 |
2 | HG00280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.508-233T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | chr17 | 50461951 | |||||||
| chr17:50461951 | T | TGTGTGTG others(11): Show |
2 | a0002c0008t0001g0263 a0002c0008t0001g0264 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.508-232_508-231ins others(18): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 50461951 | ||||||
| chr17:50461954 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
12 | HG00558.hp2 HG02083.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.508-230G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | chr17 | 50461954 | |||||||
| chr17:50461995 | G | A | 3 | a0001c0002t0002g0010 a0001c0002t0002g0241 a0001c0002t0002g0242 |
5 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-189G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | chr17 | 50461995 | |||||||
| chr17:50461997 | GGT | G | 3 | a0001c0002t0002g0156 a0001c0002t0002g0157 a0001c0002t0002g0258 |
3 | HG02258.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.508-178_508-177del others(2): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 50461997 | ||||||
| chr17:50462064 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.508-120G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | chr17 | 50462064 | |||||||
| chr17:50462085 | G | A | 1 | a0004c0006t0001g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.508-99G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | chr17 | 50462085 | |||||||
| chr17:50462172 | C | T | 1 | a0001c0003t0001g0235 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.508-12C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4/15 | chr17 | 50462172 | |||||||
| chr17:50462402 | C | A | 70 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0001c0003t0001g0004 others(67): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.627-18C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 5/15 | chr17 | 50462402 | |||||||
| chr17:50462636 | T | C | 167 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0232 others(164): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.792+51T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 6/15 | chr17 | 50462636 | |||||||
| chr17:50462806 | G | A | 15 | a0001c0002t0001g0130 a0001c0002t0001g0131 a0001c0002t0002g0117 others(12): Show |
16 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.792+221G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 6/15 | chr17 | 50462806 | |||||||
| chr17:50462812 | G | A | 2 | a0002c0008t0001g0263 a0002c0008t0001g0264 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.792+227G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 6/15 | chr17 | 50462812 | |||||||
| chr17:50463080 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.793-76G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 6/15 | chr17 | 50463080 | |||||||
| chr17:50463574 | AC | A | 6 | a0003c0005t0002g0021 a0003c0005t0002g0149 a0003c0005t0002g0150 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1046+23delC | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 8/15 | chr17 | 50463574 | |||||||
| chr17:50463599 | C | G | 165 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0232 others(162): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1046+47C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 8/15 | chr17 | 50463599 | |||||||
| chr17:50463701 | C | A | 6 | a0003c0005t0002g0021 a0003c0005t0002g0149 a0003c0005t0002g0150 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1047-117C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 8/15 | chr17 | 50463701 | |||||||
| chr17:50463747 | T | C | 1 | a0001c0002t0003g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1047-71T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 8/15 | chr17 | 50463747 | |||||||
| chr17:50464082 | G | C | 160 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0001c0002t0001g0027 others(157): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.1139-136G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 9/15 | chr17 | 50464082 | |||||||
| chr17:50464130 | A | G | 70 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0001c0003t0001g0004 others(67): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1139-88A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 9/15 | chr17 | 50464130 | |||||||
| chr17:50464324 | G | A | 1 | a0001c0002t0002g0177 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1215+30G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50464324 | |||||||
| chr17:50464346 | G | A | 166 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0232 others(163): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1215+52G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50464346 | |||||||
| chr17:50464352 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0037 |
2 | HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1215+58G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50464352 | |||||||
| chr17:50464397 | C | G | 1 | a0001c0002t0002g0238 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1215+103C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50464397 | |||||||
| chr17:50464469 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1215+175G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50464469 | |||||||
| chr17:50464528 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1215+234A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50464528 | |||||||
| chr17:50464573 | C | T | 1 | a0001c0003t0001g0139 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1215+279C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50464573 | |||||||
| chr17:50464769 | T | TG | 18 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0062 others(15): Show |
19 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1215+485dupG | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | 50464769 | ||||||
| chr17:50464769 | T | TGGG | 43 | a0001c0002t0001g0027 a0001c0002t0001g0131 a0001c0002t0001g0133 others(40): Show |
53 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.1215+483_1215+485d others(5): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | 50464769 | ||||||
| chr17:50464769 | T | TGGGG | 46 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0001c0002t0001g0130 others(43): Show |
51 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1215+482_1215+485d others(6): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | 50464769 | ||||||
| chr17:50464771 | G | GT | 3 | a0001c0002t0002g0010 a0001c0002t0002g0241 a0001c0002t0002g0242 |
5 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215+477_1215+478i others(3): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50464771 | |||||||
| chr17:50464777 | G | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0068 |
3 | NA18942.hp2 NA19057.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1215+483G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50464777 | |||||||
| chr17:50464778 | G | GT | 44 | a0001c0002t0001g0108 a0001c0002t0002g0005 a0001c0002t0002g0006 others(41): Show |
50 | HG00423.hp2 HG00438.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1215+484_1215+485i others(3): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50464778 | |||||||
| chr17:50464778 | G | T | 1 | a0004c0006t0002g0138 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1215+484G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50464778 | |||||||
| chr17:50465211 | C | G | 167 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0232 others(164): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1215+917C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50465211 | |||||||
| chr17:50465233 | C | G | 2 | a0001c0003t0001g0101 a0001c0003t0001g0107 |
2 | NA18946.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1215+939C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50465233 | |||||||
| chr17:50465329 | G | A | 3 | a0001c0002t0002g0011 a0002c0008t0001g0263 a0002c0008t0001g0264 |
5 | HG01243.hp2 HG02145.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215+1035G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50465329 | |||||||
| chr17:50465416 | C | A | 5 | a0002c0004t0002g0012 a0002c0004t0002g0040 a0002c0004t0002g0045 others(2): Show |
6 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215+1122C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50465416 | |||||||
| chr17:50465433 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1215+1139C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50465433 | |||||||
| chr17:50465508 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0037 |
2 | HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1215+1214A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50465508 | |||||||
| chr17:50465529 | C | T | 1 | a0004c0006t0002g0136 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1215+1235C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50465529 | |||||||
| chr17:50465793 | G | A | 2 | a0001c0002t0001g0186 a0001c0002t0001g0189 |
2 | HG00741.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1215+1499G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50465793 | |||||||
| chr17:50465822 | A | G | 1 | a0001c0003t0001g0101 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1215+1528A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50465822 | |||||||
| chr17:50466030 | A | C | 71 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0001c0003t0001g0004 others(68): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1215+1736A>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50466030 | |||||||
| chr17:50466073 | CT | C | 89 | a0001c0001t0001g0074 a0001c0001t0001g0232 a0001c0001t0001g0234 others(86): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1215+1795delT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | 50466073 | ||||||
| chr17:50466076 | T | C | 1 | a0001c0002t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1215+1782T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50466076 | |||||||
| chr17:50466091 | C | CT | 15 | a0001c0002t0001g0027 a0001c0002t0001g0039 a0001c0002t0001g0239 others(12): Show |
16 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1215+1810dupT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | 50466091 | ||||||
| chr17:50466092 | T | C | 1 | a0001c0003t0001g0214 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1215+1798T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50466092 | |||||||
| chr17:50466146 | G | A | 1 | a0001c0002t0002g0241 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1215+1852G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50466146 | |||||||
| chr17:50466169 | C | A | 1 | a0001c0001t0001g0106 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1215+1875C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50466169 | |||||||
| chr17:50466180 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0038 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1215+1886G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50466180 | |||||||
| chr17:50466258 | T | C | 167 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0001c0002t0001g0027 others(164): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1215+1964T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50466258 | |||||||
| chr17:50466263 | A | AT | 71 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0001c0003t0001g0004 others(68): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1215+1976dupT | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | 50466263 | ||||||
| chr17:50466319 | G | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0037 |
2 | HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1215+2025G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50466319 | |||||||
| chr17:50466418 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0229 |
2 | HG01257.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1215+2124G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50466418 | |||||||
| chr17:50466618 | G | A | 5 | a0001c0002t0002g0010 a0001c0002t0002g0241 a0001c0002t0002g0242 others(2): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1215+2324G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50466618 | |||||||
| chr17:50466696 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0037 |
2 | HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1215+2402G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50466696 | |||||||
| chr17:50466822 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0037 |
2 | HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1215+2528C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50466822 | |||||||
| chr17:50467004 | C | T | 2 | a0001c0002t0002g0173 a0001c0002t0002g0254 |
2 | HG02559.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1215+2710C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50467004 | |||||||
| chr17:50467240 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1215+2946C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50467240 | |||||||
| chr17:50467335 | C | A | 1 | a0004c0006t0001g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1215+3041C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50467335 | |||||||
| chr17:50467373 | G | A | 1 | a0001c0002t0001g0239 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1215+3079G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50467373 | |||||||
| chr17:50467556 | C | G | 1 | a0003c0005t0002g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1215+3262C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50467556 | |||||||
| chr17:50467577 | C | T | 2 | a0001c0002t0001g0130 a0001c0002t0001g0131 |
2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1215+3283C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50467577 | |||||||
| chr17:50467639 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0096 a0001c0001t0001g0105 |
4 | HG01496.hp2 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+3345A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50467639 | |||||||
| chr17:50467682 | C | T | 10 | a0001c0001t0001g0232 a0001c0003t0001g0203 a0001c0003t0001g0204 others(7): Show |
10 | HG00280.hp2 HG00733.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1216-3346C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50467682 | |||||||
| chr17:50467782 | T | A | 1 | a0001c0002t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1216-3246T>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50467782 | |||||||
| chr17:50467885 | G | A | 2 | a0002c0008t0001g0263 a0002c0008t0001g0264 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1216-3143G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50467885 | |||||||
| chr17:50467887 | C | T | 168 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0232 others(165): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1216-3141C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50467887 | |||||||
| chr17:50467951 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1216-3077C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50467951 | |||||||
| chr17:50468138 | G | A | 3 | a0001c0002t0002g0010 a0001c0002t0002g0241 a0001c0002t0002g0242 |
5 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1216-2890G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50468138 | |||||||
| chr17:50468159 | G | A | 2 | a0001c0003t0001g0204 a0001c0003t0001g0206 |
2 | HG02602.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1216-2869G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50468159 | |||||||
| chr17:50468235 | G | A | 71 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0001c0003t0001g0004 others(68): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1216-2793G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50468235 | |||||||
| chr17:50468634 | G | A | 2 | a0001c0002t0002g0162 a0001c0002t0002g0167 |
2 | NA19062.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1216-2394G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50468634 | |||||||
| chr17:50468741 | G | T | 5 | a0001c0002t0002g0010 a0001c0002t0002g0241 a0001c0002t0002g0242 others(2): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1216-2287G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50468741 | |||||||
| chr17:50468871 | G | C | 54 | a0001c0002t0001g0108 a0001c0002t0001g0132 a0001c0002t0001g0133 others(51): Show |
62 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.1216-2157G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50468871 | |||||||
| chr17:50469032 | G | A | 1 | a0001c0002t0002g0176 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1216-1996G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469032 | |||||||
| chr17:50469060 | G | C | 1 | a0001c0002t0001g0108 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1216-1968G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469060 | |||||||
| chr17:50469097 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0037 |
2 | HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1216-1931C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469097 | |||||||
| chr17:50469114 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1216-1914C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469114 | |||||||
| chr17:50469171 | G | A | 1 | a0001c0002t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1216-1857G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469171 | |||||||
| chr17:50469193 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0037 |
2 | HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1216-1835C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469193 | |||||||
| chr17:50469233 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1216-1795T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469233 | |||||||
| chr17:50469294 | T | G | 1 | a0001c0002t0002g0161 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1216-1734T>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469294 | |||||||
| chr17:50469319 | G | A | 3 | a0001c0002t0001g0130 a0001c0002t0001g0131 a0001c0002t0003g0031 |
3 | HG02486.hp2 HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1216-1709G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469319 | |||||||
| chr17:50469353 | C | A | 1 | a0001c0003t0001g0235 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1216-1675C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469353 | |||||||
| chr17:50469419 | G | T | 3 | a0001c0002t0001g0130 a0001c0002t0001g0131 a0001c0002t0003g0031 |
3 | HG02486.hp2 HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1216-1609G>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469419 | |||||||
| chr17:50469432 | A | G | 165 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0234 others(162): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1216-1596A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469432 | |||||||
| chr17:50469591 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG00140.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.1216-1437G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469591 | |||||||
| chr17:50469679 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0038 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1216-1349G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469679 | |||||||
| chr17:50469743 | T | C | 3 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 |
3 | HG01109.hp1 HG01168.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1216-1285T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469743 | |||||||
| chr17:50469897 | C | T | 1 | a0001c0002t0003g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1216-1131C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50469897 | |||||||
| chr17:50470072 | T | C | 163 | a0001c0001t0001g0234 a0001c0002t0001g0027 a0001c0002t0001g0039 others(160): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1216-956T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50470072 | |||||||
| chr17:50470103 | A | C | 1 | a0001c0003t0001g0218 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1216-925A>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50470103 | |||||||
| chr17:50470186 | G | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0019 others(21): Show |
31 | HG00140.hp1 HG00323.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.1216-842G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50470186 | |||||||
| chr17:50470449 | T | A | 1 | a0001c0002t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1216-579T>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50470449 | |||||||
| chr17:50470615 | T | G | 13 | a0001c0002t0002g0010 a0001c0002t0002g0184 a0001c0002t0002g0241 others(10): Show |
16 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1216-413T>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50470615 | |||||||
| chr17:50470681 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0128 |
2 | HG01361.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1216-347G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50470681 | |||||||
| chr17:50470736 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0084 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1216-292G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | 50470736 | |||||||
| chr17:50471174 | TCACCCAG others(8): Show |
T | 1 | a0001c0001t0001g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1323+52_1323+66del others(15): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 50471174 | ||||||
| chr17:50471336 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1323+201T>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 11/15 | chr17 | 50471336 | |||||||
| chr17:50471743 | G | C | 1 | a0001c0001t0001g0062 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1323+608G>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 11/15 | chr17 | 50471743 | |||||||
| chr17:50471744 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1323+609C>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 11/15 | chr17 | 50471744 | |||||||
| chr17:50471806 | A | G | 167 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0002t0001g0027 others(164): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1324-622A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 11/15 | chr17 | 50471806 | |||||||
| chr17:50472019 | T | TC | 8 | a0001c0002t0002g0184 a0003c0005t0002g0021 a0003c0005t0002g0148 others(5): Show |
9 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1324-408dupC | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 50472019 | ||||||
| chr17:50472096 | C | T | 71 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0003t0001g0004 others(68): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1324-332C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 11/15 | chr17 | 50472096 | |||||||
| chr17:50472692 | C | A | 3 | a0001c0002t0001g0130 a0001c0002t0001g0131 a0001c0002t0003g0031 |
3 | HG02486.hp2 HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1475+113C>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 12/15 | chr17 | 50472692 | |||||||
| chr17:50472912 | G | A | 3 | a0001c0002t0001g0130 a0001c0002t0001g0131 a0001c0002t0003g0031 |
3 | HG02486.hp2 HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1475+333G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 12/15 | chr17 | 50472912 | |||||||
| chr17:50472989 | C | T | 1 | a0004c0006t0002g0136 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1475+410C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 12/15 | chr17 | 50472989 | |||||||
| chr17:50473042 | A | G | 3 | a0001c0002t0001g0130 a0001c0002t0001g0131 a0001c0002t0003g0031 |
3 | HG02486.hp2 HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1475+463A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 12/15 | chr17 | 50473042 | |||||||
| chr17:50473177 | T | A | 1 | a0001c0001t0001g0244 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1476-488T>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 12/15 | chr17 | 50473177 | |||||||
| chr17:50473306 | T | C | 1 | a0004c0006t0002g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1476-359T>C | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 12/15 | chr17 | 50473306 | |||||||
| chr17:50473833 | C | T | 2 | a0001c0002t0001g0130 a0001c0002t0001g0131 |
2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1617+27C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 13/15 | chr17 | 50473833 | |||||||
| chr17:50474031 | A | G | 2 | a0001c0002t0001g0132 a0001c0002t0001g0133 |
2 | HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1728+27A>G | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 14/15 | chr17 | 50474031 | |||||||
| chr17:50474146 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1729-53C>T | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 14/15 | chr17 | 50474146 | |||||||
| chr17:50474379 | G | A | 5 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0071 others(2): Show |
5 | HG02040.hp2 HG02165.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.1797+112G>A | ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 15/15 | chr17 | 50474379 |