Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26228 |
| ensemblid | ENSG00000035720.8 |
| hgncid | 24133 |
| symbol | STAP1 |
| name | signal transducing adaptor family member 1 |
| refseq_nuc | NM_012108.4 |
| refseq_prot | NP_036240.1 |
| ensembl_nuc | ENST00000265404.7 |
| ensembl_prot | ENSP00000265404.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 67558727 |
| end | 67607337 |
| strand | + |
| ver | v1.2 |
| region | chr4:67558727-67607337 |
| region5000 | chr4:67553727-67612337 |
| regionname0 | STAP1_chr4_67558727_67607337 |
| regionname5000 | STAP1_chr4_67553727_67612337 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 295 | 378 | 86 | 78 | 163 | 14 | 35 | 119 | STAP1_chr4_67553727_67612337 | STAP1 | MMAKK others(290): Show |
chr4 | 67553727 | 67612337 |
| a0002 | 0/0 | 295 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | MTAKK others(290): Show |
chr4 | 67553727 | 67612337 |
| a0003 | 0/0 | 295 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | MMAKK others(290): Show |
chr4 | 67553727 | 67612337 |
| a0004 | 0/0 | 295 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | MMAKK others(290): Show |
chr4 | 67553727 | 67612337 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 885 | 253 | 46 | 52 | 125 | 5 | 23 | STAP1_chr4_67553727_67612337 | STAP1 | ATGAT others(880): Show |
chr4 | 67553727 | 67612337 | ||
| a0001c0002 | 0/0 | 885 | 93 | 27 | 15 | 38 | 5 | 8 | STAP1_chr4_67553727_67612337 | STAP1 | ATGAT others(880): Show |
chr4 | 67553727 | 67612337 | ||
| a0001c0003 | 0/0 | 885 | 30 | 12 | 11 | 0 | 4 | 3 | STAP1_chr4_67553727_67612337 | STAP1 | ATGAT others(880): Show |
chr4 | 67553727 | 67612337 | ||
| a0001c0005 | 0/0 | 885 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | ATGAT others(880): Show |
chr4 | 67553727 | 67612337 | ||
| a0001c0008 | 0/0 | 885 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | ATGAT others(880): Show |
chr4 | 67553727 | 67612337 | ||
| a0002c0004 | 0/0 | 885 | 2 | 0 | 0 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | ATGAC others(880): Show |
chr4 | 67553727 | 67612337 | ||
| a0003c0006 | 0/0 | 885 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | ATGAT others(880): Show |
chr4 | 67553727 | 67612337 | ||
| a0004c0007 | 0/0 | 885 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | ATGAT others(880): Show |
chr4 | 67553727 | 67612337 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1951 | 135 | 23 | 38 | 57 | 2 | 15 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0001t0002 | 0/1 | 1951 | 86 | 7 | 9 | 59 | 3 | 7 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0001t0003 | 1/0 | 1951 | 20 | 9 | 5 | 4 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0001t0004 | 0/0 | 1951 | 2 | 2 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0001t0005 | 0/0 | 1951 | 3 | 0 | 0 | 3 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0001t0006 | 0/0 | 1951 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0001t0007 | 0/0 | 1951 | 2 | 2 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0001t0008 | 0/0 | 1951 | 2 | 0 | 0 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0001t0009 | 0/0 | 1951 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0001t0010 | 0/0 | 1951 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0002t0001 | 0/0 | 1951 | 63 | 13 | 14 | 27 | 5 | 4 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0002t0002 | 0/0 | 1951 | 18 | 4 | 0 | 11 | 0 | 3 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0002t0003 | 0/0 | 1951 | 7 | 6 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0002t0004 | 0/0 | 1951 | 3 | 2 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0002t0006 | 0/0 | 1951 | 2 | 2 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0003t0001 | 0/0 | 1951 | 23 | 8 | 8 | 0 | 4 | 3 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0003t0002 | 0/0 | 1951 | 4 | 1 | 3 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0003t0003 | 0/0 | 1951 | 3 | 3 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0005t0001 | 0/0 | 1951 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0001c0008t0001 | 0/0 | 1951 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0002c0004t0001 | 0/0 | 1951 | 2 | 0 | 0 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0003c0006t0001 | 0/0 | 1951 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| a0004c0007t0002 | 0/0 | 1951 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | GAACA others(1946): Show |
chr4 | 67553727 | 67612337 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 1 | 5 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0008g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0008g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0010g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0005 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0004g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0008t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0002c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0002c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0003c0006t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0004c0007t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0013 | EUR | GBR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0342 | EUR | GBR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0352 | EUR | GBR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0234 | EUR | GBR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0205 | EUR | FIN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0335 | EUR | FIN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0313 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0324 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0289 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00735 | hp1 | a0001 | c0003 | t0002 | g0341 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0348 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0278 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0288 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0328 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0292 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0330 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0337 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0325 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0334 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0333 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0308 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0291 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0347 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0290 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0293 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0259 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0183 | EUR | IBS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0353 | EUR | IBS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0346 | EUR | IBS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0011 | EUR | IBS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0192 | EUR | IBS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0011 | EUR | IBS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0164 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0266 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0338 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02056 | hp1 | a0003 | c0006 | t0001 | g0027 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0318 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0165 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0351 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CDX | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0311 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0287 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0340 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02523 | hp2 | a0002 | c0004 | t0001 | g0042 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02572 | hp1 | a0001 | c0002 | t0003 | g0167 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0138 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02615 | hp2 | a0001 | c0002 | t0004 | g0336 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0176 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0286 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02647 | hp2 | a0001 | c0008 | t0001 | g0255 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0283 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0155 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0244 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0356 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02818 | hp1 | a0001 | c0002 | t0003 | g0159 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0339 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0153 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0175 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0285 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0295 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0284 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02976 | hp2 | a0001 | c0002 | t0006 | g0168 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0180 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0282 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0241 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0174 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0154 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03209 | hp2 | a0001 | c0003 | t0003 | g0349 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0162 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0188 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03239 | hp2 | a0001 | c0002 | t0003 | g0322 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0163 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0268 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0246 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0350 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03540 | hp2 | a0001 | c0002 | t0006 | g0166 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03579 | hp1 | a0001 | c0002 | t0004 | g0158 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0160 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0280 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0323 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0281 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03942 | hp2 | a0001 | c0005 | t0001 | g0041 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0177 | SAS | STU | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | STU | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04199 | hp2 | a0004 | c0007 | t0002 | g0210 | SAS | STU | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0211 | SAS | STU | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0114 | AFR | YRI | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | YRI | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | CHB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | YRI | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | YRI | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18942 | hp2 | a0001 | c0001 | t0008 | g0235 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18964 | hp2 | a0002 | c0004 | t0001 | g0073 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0354 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0317 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0355 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18987 | hp2 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | LWK | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | LWK | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0267 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19089 | hp2 | a0001 | c0001 | t0008 | g0203 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19240 | hp1 | a0001 | c0003 | t0003 | g0294 | AFR | YRI | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0152 | AFR | YRI | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | ASW | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0279 | AFR | ASW | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0272 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | USA | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | USA | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0232 | AFR | USA | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | USA | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0262 | REF | REF | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0047 | REF | REF | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:67558814 | T | C | 1 | a0002 | 2 | HG02523.hp2 NA18964.hp2 |
missense_variant | MODERATE | c.5T>C | p.Met2Thr | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/9 | 88/1951 | 5/888 | 2/295 | chr4 | 67558814 | |||
| chr4:67581459 | A | G | 1 | a0004 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.518A>G | p.Asn173Ser | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/9 | 601/1951 | 518/888 | 173/295 | chr4 | 67581459 | |||
| chr4:67581464 | A | G | 1 | a0003 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.523A>G | p.Met175Val | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/9 | 606/1951 | 523/888 | 175/295 | chr4 | 67581464 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:67577250 | A | G | 2 | a0001c0002 a0001c0003 |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
synonymous_variant | LOW | c.354A>G | p.Thr118Thr | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/9 | 437/1951 | 354/888 | 118/295 | chr4 | 67577250 | |||
| chr4:67581322 | C | T | 2 | a0001c0003 a0001c0008 |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
synonymous_variant | LOW | c.381C>T | p.Asn127Asn | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/9 | 464/1951 | 381/888 | 127/295 | chr4 | 67581322 | |||
| chr4:67581355 | G | C | 1 | a0001c0005 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.414G>C | p.Leu138Leu | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/9 | 497/1951 | 414/888 | 138/295 | chr4 | 67581355 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:67606562 | C | T | 3 | a0001c0001t0006 a0001c0001t0010 a0001c0002t0006 |
4 | HG02572.hp2 HG02976.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*205C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 205 | chr4 | 67606562 | ||||||
| chr4:67606710 | T | C | 7 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(4): Show |
113 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*353T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 353 | chr4 | 67606710 | ||||||
| chr4:67606732 | A | G | 1 | a0001c0001t0009 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*375A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 375 | chr4 | 67606732 | ||||||
| chr4:67606886 | T | C | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(15): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
3_prime_UTR_variant | MODIFIER | c.*529T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 529 | chr4 | 67606886 | ||||||
| chr4:67606984 | G | A | 1 | a0001c0001t0005 | 3 | NA18959.hp2 NA18987.hp2 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*627G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 627 | chr4 | 67606984 | ||||||
| chr4:67606991 | C | T | 1 | a0001c0001t0008 | 2 | NA18942.hp2 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*634C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 634 | chr4 | 67606991 | ||||||
| chr4:67607018 | G | A | 1 | a0001c0001t0007 | 2 | HG02922.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*661G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 661 | chr4 | 67607018 | ||||||
| chr4:67607258 | G | T | 1 | a0001c0001t0010 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*901G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 901 | chr4 | 67607258 | ||||||
| chr4:67607265 | A | G | 2 | a0001c0001t0004 a0001c0002t0004 |
5 | HG01167.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*908A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 908 | chr4 | 67607265 | ||||||
| chr4:67607296 | C | A | 1 | a0001c0001t0009 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*939C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 939 | chr4 | 67607296 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:67559031 | A | G | 1 | a0001c0001t0001g0357 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.120+102A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67559031 | |||||||
| chr4:67559384 | A | G | 94 | a0001c0001t0001g0012 a0001c0001t0001g0269 a0001c0001t0001g0296 others(91): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.120+455A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67559384 | |||||||
| chr4:67559536 | T | G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(9): Show |
12 | HG00408.hp1 HG02083.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.120+607T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67559536 | |||||||
| chr4:67559688 | A | C | 1 | a0001c0001t0005g0267 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.120+759A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67559688 | |||||||
| chr4:67559850 | A | G | 91 | a0001c0001t0001g0012 a0001c0001t0001g0296 a0001c0001t0001g0297 others(88): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.120+921A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67559850 | |||||||
| chr4:67560040 | C | G | 2 | a0001c0001t0001g0269 a0001c0001t0003g0270 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.120+1111C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560040 | |||||||
| chr4:67560106 | A | G | 178 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(175): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.120+1177A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560106 | |||||||
| chr4:67560168 | T | A | 2 | a0001c0001t0001g0198 a0001c0001t0003g0197 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.120+1239T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560168 | |||||||
| chr4:67560219 | A | G | 1 | a0001c0001t0002g0025 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.120+1290A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560219 | |||||||
| chr4:67560230 | TC | T | 178 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(175): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.120+1303delC | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560230 | ||||||
| chr4:67560294 | A | T | 1 | a0001c0003t0001g0356 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.120+1365A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560294 | |||||||
| chr4:67560347 | G | A | 1 | a0001c0002t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.120+1418G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560347 | |||||||
| chr4:67560454 | A | C | 199 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(196): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.120+1525A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560454 | |||||||
| chr4:67560637 | T | TGTGGGGG others(1): Show |
5 | a0001c0002t0001g0273 a0001c0002t0001g0275 a0001c0002t0001g0276 others(2): Show |
5 | HG00621.hp1 HG01123.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+1711_120+1712i others(10): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560637 | ||||||
| chr4:67560641 | T | TGG | 78 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
80 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.120+1714_120+1715d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560641 | ||||||
| chr4:67560643 | G | GGGGT | 20 | a0001c0001t0001g0243 a0001c0001t0001g0245 a0001c0001t0001g0250 others(17): Show |
21 | HG00558.hp2 HG00639.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.120+1715_120+1716i others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | ||||||
| chr4:67560643 | G | GGGGTGT | 10 | a0001c0001t0003g0259 a0001c0002t0001g0279 a0001c0003t0001g0278 others(7): Show |
10 | HG01081.hp1 HG01496.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.120+1715_120+1716i others(8): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | ||||||
| chr4:67560643 | G | GGGGTGTG others(1): Show |
61 | a0001c0001t0001g0012 a0001c0001t0001g0296 a0001c0001t0001g0297 others(58): Show |
69 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.120+1715_120+1716i others(10): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | ||||||
| chr4:67560643 | G | GGGGTGTG others(3): Show |
10 | a0001c0001t0001g0343 a0001c0001t0001g0344 a0001c0001t0001g0345 others(7): Show |
10 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.120+1715_120+1716i others(12): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | ||||||
| chr4:67560643 | G | GGGGTGTG others(5): Show |
1 | a0001c0001t0001g0351 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.120+1715_120+1716i others(14): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | ||||||
| chr4:67560643 | G | GGTGTGT | 4 | a0001c0001t0001g0198 a0001c0001t0001g0269 a0001c0001t0004g0268 others(1): Show |
4 | HG01884.hp1 HG02965.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+1717_120+1722d others(8): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | ||||||
| chr4:67560643 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0003g0270 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.120+1722_120+1723i others(12): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | ||||||
| chr4:67560643 | G | T | 6 | a0001c0002t0001g0273 a0001c0002t0001g0275 a0001c0002t0001g0276 others(3): Show |
6 | HG00621.hp1 HG01123.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+1714G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560643 | |||||||
| chr4:67560645 | T | G | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0002t0001g0176 |
3 | HG01256.hp1 HG01258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.120+1716T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560645 | |||||||
| chr4:67560650 | GTC | G | 4 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0007g0174 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+1723_120+1724d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560650 | ||||||
| chr4:67560652 | C | CTG | 5 | a0001c0001t0001g0087 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG02129.hp2 HG02132.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+1744_120+1745d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560652 | ||||||
| chr4:67560652 | C | G | 197 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(194): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.120+1723C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560652 | |||||||
| chr4:67560741 | T | A | 1 | a0001c0001t0003g0026 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.120+1812T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560741 | |||||||
| chr4:67560816 | C | A | 1 | a0003c0006t0001g0027 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.120+1887C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560816 | |||||||
| chr4:67560827 | T | A | 1 | a0001c0001t0001g0028 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.120+1898T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560827 | |||||||
| chr4:67560904 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.120+1975C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560904 | |||||||
| chr4:67560923 | AC | A | 13 | a0001c0003t0001g0011 a0001c0003t0001g0272 a0001c0003t0001g0278 others(10): Show |
14 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.120+1995delC | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560923 | |||||||
| chr4:67560930 | T | C | 2 | a0001c0003t0003g0294 a0001c0003t0003g0295 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+2001T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560930 | |||||||
| chr4:67560992 | G | A | 8 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 others(5): Show |
8 | HG00609.hp1 HG00621.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.120+2063G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560992 | |||||||
| chr4:67561178 | G | A | 1 | a0001c0003t0001g0352 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.120+2249G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561178 | |||||||
| chr4:67561543 | A | G | 26 | a0001c0001t0001g0240 a0001c0002t0001g0009 a0001c0002t0001g0176 others(23): Show |
27 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.120+2614A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561543 | |||||||
| chr4:67561722 | G | T | 1 | a0001c0001t0002g0024 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.120+2793G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561722 | |||||||
| chr4:67561729 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0003g0197 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.120+2800T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561729 | |||||||
| chr4:67561773 | A | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0257 a0001c0001t0002g0256 others(2): Show |
5 | HG02615.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+2844A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561773 | |||||||
| chr4:67561814 | A | C | 197 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(194): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.120+2885A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561814 | |||||||
| chr4:67561879 | C | T | 1 | a0001c0001t0002g0258 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.120+2950C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561879 | |||||||
| chr4:67561893 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.120+2964G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561893 | |||||||
| chr4:67561898 | C | T | 55 | a0001c0002t0001g0009 a0001c0002t0001g0176 a0001c0002t0001g0177 others(52): Show |
57 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.120+2969C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561898 | |||||||
| chr4:67562021 | G | A | 17 | a0001c0001t0001g0012 a0001c0001t0001g0297 a0001c0001t0001g0298 others(14): Show |
18 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.120+3092G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562021 | |||||||
| chr4:67562027 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.120+3098G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562027 | |||||||
| chr4:67562068 | CA | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
135 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.120+3162delA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | ||||||
| chr4:67562068 | CAA | C | 8 | a0001c0001t0001g0150 a0001c0001t0002g0151 a0001c0001t0007g0174 others(5): Show |
8 | HG01167.hp2 HG01255.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.120+3161_120+3162d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | ||||||
| chr4:67562068 | CAAA | C | 73 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(70): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.120+3160_120+3162d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | ||||||
| chr4:67562068 | CAAAA | C | 109 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(106): Show |
110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.120+3159_120+3162d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | ||||||
| chr4:67562068 | CAAAAA | C | 7 | a0001c0001t0001g0198 a0001c0001t0001g0238 a0001c0001t0001g0269 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+3158_120+3162d others(7): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | ||||||
| chr4:67562068 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0297 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.120+3153_120+3162d others(12): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | ||||||
| chr4:67562068 | CAAAAAAA others(4): Show |
C | 16 | a0001c0001t0001g0012 a0001c0001t0001g0298 a0001c0001t0001g0299 others(13): Show |
17 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.120+3152_120+3162d others(13): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | ||||||
| chr4:67562087 | A | G | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.120+3158A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562087 | |||||||
| chr4:67562088 | A | G | 62 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0310 others(59): Show |
68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.120+3159A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562088 | |||||||
| chr4:67562104 | GAAAGAAA others(8): Show |
G | 2 | a0001c0001t0007g0174 a0001c0001t0007g0175 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.120+3188_120+3202d others(17): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562104 | ||||||
| chr4:67562328 | C | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0254 a0001c0001t0001g0257 others(19): Show |
23 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.120+3399C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562328 | |||||||
| chr4:67562365 | GCTGT | G | 4 | a0001c0001t0001g0198 a0001c0001t0002g0053 a0001c0001t0002g0054 others(1): Show |
4 | HG01884.hp1 NA18948.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+3439_120+3442d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562365 | ||||||
| chr4:67562485 | G | A | 1 | a0001c0002t0002g0309 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.120+3556G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562485 | |||||||
| chr4:67562493 | T | C | 2 | a0001c0003t0001g0278 a0001c0003t0001g0288 |
2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.120+3564T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562493 | |||||||
| chr4:67562571 | C | T | 3 | a0001c0001t0002g0239 a0001c0001t0003g0237 a0001c0001t0004g0236 |
3 | HG02280.hp1 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.120+3642C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562571 | |||||||
| chr4:67562574 | G | C | 196 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(193): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.120+3645G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562574 | |||||||
| chr4:67562601 | T | TA | 163 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(160): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.120+3693dupA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562601 | ||||||
| chr4:67562601 | T | TAA | 6 | a0001c0001t0001g0204 a0001c0001t0002g0239 a0001c0001t0003g0259 others(3): Show |
6 | HG00735.hp1 HG01496.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.120+3692_120+3693d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562601 | ||||||
| chr4:67562601 | T | TAAAA | 13 | a0001c0001t0001g0012 a0001c0001t0001g0297 a0001c0001t0001g0298 others(10): Show |
14 | HG00735.hp2 HG01071.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.120+3690_120+3693d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562601 | ||||||
| chr4:67562601 | TA | T | 7 | a0001c0001t0001g0149 a0001c0001t0002g0051 a0001c0001t0002g0052 others(4): Show |
7 | HG01167.hp2 HG02015.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+3693delA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562601 | ||||||
| chr4:67562665 | A | G | 1 | a0001c0001t0002g0023 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.120+3736A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562665 | |||||||
| chr4:67562708 | C | T | 1 | a0001c0002t0001g0335 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.120+3779C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562708 | |||||||
| chr4:67562710 | T | C | 1 | a0001c0002t0001g0335 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.120+3781T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562710 | |||||||
| chr4:67562720 | G | C | 1 | a0001c0001t0001g0014 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.120+3791G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562720 | |||||||
| chr4:67562761 | G | A | 15 | a0001c0002t0001g0153 a0001c0002t0001g0157 a0001c0002t0001g0160 others(12): Show |
15 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+3832G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562761 | |||||||
| chr4:67562765 | C | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0263 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.120+3836C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562765 | |||||||
| chr4:67562918 | C | G | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.120+3989C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562918 | |||||||
| chr4:67563015 | G | T | 198 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(195): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.120+4086G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563015 | |||||||
| chr4:67563108 | C | A | 1 | a0001c0001t0002g0205 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.120+4179C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563108 | |||||||
| chr4:67563190 | G | A | 1 | a0001c0002t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.120+4261G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563190 | |||||||
| chr4:67563262 | G | T | 64 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(61): Show |
66 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.120+4333G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563262 | |||||||
| chr4:67563331 | C | A | 217 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(214): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.120+4402C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563331 | |||||||
| chr4:67563527 | G | A | 1 | a0001c0002t0002g0179 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.120+4598G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563527 | |||||||
| chr4:67563590 | G | C | 217 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(214): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.120+4661G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563590 | |||||||
| chr4:67563596 | G | A | 1 | a0001c0002t0001g0241 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.120+4667G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563596 | |||||||
| chr4:67563690 | G | A | 4 | a0001c0001t0001g0269 a0001c0001t0003g0237 a0001c0001t0003g0270 others(1): Show |
4 | HG02280.hp1 HG02965.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+4761G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563690 | |||||||
| chr4:67563818 | G | A | 1 | a0001c0001t0003g0050 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.120+4889G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563818 | |||||||
| chr4:67563844 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.120+4915A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563844 | |||||||
| chr4:67563873 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.120+4944G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563873 | |||||||
| chr4:67563939 | TA | T | 167 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(164): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.120+5025delA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67563939 | ||||||
| chr4:67563939 | TAA | T | 11 | a0001c0001t0001g0198 a0001c0001t0001g0257 a0001c0001t0001g0261 others(8): Show |
11 | HG00733.hp2 HG01167.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.120+5024_120+5025d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67563939 | ||||||
| chr4:67563962 | G | A | 2 | a0001c0001t0007g0174 a0001c0001t0007g0175 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.120+5033G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563962 | |||||||
| chr4:67564130 | C | T | 34 | a0001c0002t0001g0009 a0001c0002t0001g0241 a0001c0002t0001g0242 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.120+5201C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564130 | |||||||
| chr4:67564147 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.120+5218A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564147 | |||||||
| chr4:67564405 | C | T | 177 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(174): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.120+5476C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564405 | |||||||
| chr4:67564467 | T | G | 1 | a0001c0001t0001g0343 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.120+5538T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564467 | |||||||
| chr4:67564518 | G | A | 1 | a0001c0002t0001g0180 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.120+5589G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564518 | |||||||
| chr4:67564668 | T | C | 2 | a0001c0001t0002g0060 a0001c0001t0002g0061 |
2 | NA18959.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.120+5739T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564668 | |||||||
| chr4:67564683 | C | T | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.120+5754C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564683 | |||||||
| chr4:67564733 | T | C | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.120+5804T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564733 | |||||||
| chr4:67564774 | A | G | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.120+5845A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564774 | |||||||
| chr4:67564892 | C | T | 177 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(174): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.120+5963C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564892 | |||||||
| chr4:67564944 | A | G | 3 | a0001c0002t0001g0009 a0001c0002t0001g0241 a0001c0002t0001g0242 |
4 | HG02559.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+6015A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564944 | |||||||
| chr4:67564979 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.120+6050C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564979 | |||||||
| chr4:67565290 | T | G | 2 | a0001c0001t0001g0198 a0001c0001t0003g0197 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.121-5794T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565290 | |||||||
| chr4:67565322 | T | C | 1 | a0001c0001t0002g0056 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.121-5762T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565322 | |||||||
| chr4:67565323 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.121-5761C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565323 | |||||||
| chr4:67565324 | T | C | 1 | a0001c0001t0002g0056 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.121-5760T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565324 | |||||||
| chr4:67565412 | A | G | 22 | a0001c0001t0001g0012 a0001c0001t0001g0254 a0001c0001t0001g0257 others(19): Show |
23 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.121-5672A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565412 | |||||||
| chr4:67565725 | T | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.121-5359T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565725 | |||||||
| chr4:67565740 | C | G | 2 | a0001c0001t0001g0297 a0001c0001t0001g0307 |
2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.121-5344C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565740 | |||||||
| chr4:67565934 | C | CT | 56 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0048 others(53): Show |
57 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.121-5120dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67565934 | ||||||
| chr4:67565934 | CT | C | 42 | a0001c0001t0001g0012 a0001c0001t0001g0065 a0001c0001t0001g0066 others(39): Show |
46 | HG00544.hp2 HG00673.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.121-5120delT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67565934 | ||||||
| chr4:67565934 | CTT | C | 15 | a0001c0001t0001g0202 a0001c0001t0001g0263 a0001c0001t0003g0237 others(12): Show |
15 | HG00621.hp1 HG01109.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.121-5121_121-5120d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67565934 | ||||||
| chr4:67565934 | CTTT | C | 70 | a0001c0001t0001g0064 a0001c0001t0001g0198 a0001c0001t0001g0245 others(67): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.121-5122_121-5120d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67565934 | ||||||
| chr4:67566035 | G | A | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.121-5049G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566035 | |||||||
| chr4:67566047 | C | A | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-5037C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566047 | |||||||
| chr4:67566102 | C | T | 10 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0120 others(7): Show |
10 | HG00423.hp1 HG02071.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.121-4982C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566102 | |||||||
| chr4:67566120 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0003g0197 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.121-4964A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566120 | |||||||
| chr4:67566217 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.121-4867C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566217 | |||||||
| chr4:67566490 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.121-4594C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566490 | |||||||
| chr4:67566498 | G | A | 31 | a0001c0002t0001g0009 a0001c0002t0001g0241 a0001c0002t0001g0242 others(28): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.121-4586G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566498 | |||||||
| chr4:67566776 | C | A | 1 | a0001c0001t0003g0067 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.121-4308C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566776 | |||||||
| chr4:67566799 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.121-4285G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566799 | |||||||
| chr4:67567088 | A | G | 92 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(89): Show |
95 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.121-3996A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567088 | |||||||
| chr4:67567167 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.121-3917G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567167 | |||||||
| chr4:67567257 | T | G | 1 | a0001c0001t0002g0121 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.121-3827T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567257 | |||||||
| chr4:67567266 | C | T | 5 | a0001c0001t0001g0202 a0001c0001t0001g0245 a0001c0001t0001g0263 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-3818C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567266 | |||||||
| chr4:67567367 | C | CT | 25 | a0001c0002t0001g0009 a0001c0002t0001g0143 a0001c0002t0001g0176 others(22): Show |
26 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.121-3716dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67567367 | ||||||
| chr4:67567368 | T | TG | 85 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0245 others(82): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.121-3710dupG | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67567368 | ||||||
| chr4:67567765 | G | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(49): Show |
56 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.121-3319G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567765 | |||||||
| chr4:67567894 | C | T | 109 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0245 others(106): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.121-3190C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567894 | |||||||
| chr4:67567895 | G | A | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-3189G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567895 | |||||||
| chr4:67568136 | T | C | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-2948T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568136 | |||||||
| chr4:67568137 | C | T | 111 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0245 others(108): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.121-2947C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568137 | |||||||
| chr4:67568221 | T | C | 41 | a0001c0001t0002g0329 a0001c0002t0001g0004 a0001c0002t0001g0005 others(38): Show |
47 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.121-2863T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568221 | |||||||
| chr4:67568243 | A | G | 1 | a0001c0001t0002g0019 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.121-2841A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568243 | |||||||
| chr4:67568301 | T | C | 124 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0245 others(121): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.121-2783T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568301 | |||||||
| chr4:67568310 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.121-2774C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568310 | |||||||
| chr4:67568376 | A | C | 15 | a0001c0002t0001g0153 a0001c0002t0001g0157 a0001c0002t0001g0160 others(12): Show |
15 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.121-2708A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568376 | |||||||
| chr4:67568450 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.121-2634C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568450 | |||||||
| chr4:67568508 | T | A | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-2576T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568508 | |||||||
| chr4:67568517 | A | G | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-2567A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568517 | |||||||
| chr4:67568532 | A | C | 1 | a0001c0002t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.121-2552A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568532 | |||||||
| chr4:67568579 | T | C | 3 | a0001c0001t0005g0069 a0001c0001t0005g0070 a0001c0001t0005g0267 |
3 | NA18959.hp2 NA18987.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.121-2505T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568579 | |||||||
| chr4:67568744 | C | T | 126 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0245 others(123): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.121-2340C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568744 | |||||||
| chr4:67568754 | G | A | 126 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0245 others(123): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.121-2330G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568754 | |||||||
| chr4:67568880 | C | T | 4 | a0001c0003t0001g0011 a0001c0003t0001g0272 a0001c0003t0002g0287 others(1): Show |
5 | HG01123.hp1 HG01361.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-2204C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568880 | |||||||
| chr4:67568952 | A | G | 2 | a0001c0001t0007g0174 a0001c0001t0007g0175 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.121-2132A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568952 | |||||||
| chr4:67569011 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.121-2073A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67569011 | |||||||
| chr4:67569045 | C | T | 1 | a0001c0002t0001g0156 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.121-2039C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67569045 | |||||||
| chr4:67569058 | T | C | 4 | a0001c0002t0001g0176 a0001c0002t0001g0181 a0001c0002t0001g0182 others(1): Show |
4 | HG01243.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-2026T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67569058 | |||||||
| chr4:67569326 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.121-1758G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67569326 | |||||||
| chr4:67569480 | CTTGT | C | 42 | a0001c0001t0002g0329 a0001c0002t0001g0004 a0001c0002t0001g0005 others(39): Show |
48 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.121-1601_121-1598d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67569480 | ||||||
| chr4:67569732 | T | TTG | 35 | a0001c0002t0001g0143 a0001c0002t0001g0153 a0001c0002t0001g0157 others(32): Show |
35 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.121-1337_121-1336d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67569732 | ||||||
| chr4:67569761 | G | C | 5 | a0001c0001t0001g0202 a0001c0001t0001g0245 a0001c0001t0001g0263 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-1323G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67569761 | |||||||
| chr4:67569974 | G | A | 1 | a0001c0001t0002g0121 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.121-1110G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67569974 | |||||||
| chr4:67570010 | G | A | 124 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0245 others(121): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.121-1074G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570010 | |||||||
| chr4:67570138 | T | A | 217 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(214): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.121-946T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570138 | |||||||
| chr4:67570254 | T | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.121-830T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570254 | |||||||
| chr4:67570262 | G | A | 1 | a0001c0002t0001g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.121-822G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570262 | |||||||
| chr4:67570295 | C | T | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-789C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570295 | |||||||
| chr4:67570526 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.121-558G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570526 | |||||||
| chr4:67570576 | T | G | 4 | a0001c0001t0007g0174 a0001c0001t0007g0175 a0001c0002t0001g0156 others(1): Show |
4 | HG00733.hp2 HG02735.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-508T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570576 | |||||||
| chr4:67570608 | G | A | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-476G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570608 | |||||||
| chr4:67570665 | A | G | 37 | a0001c0002t0001g0143 a0001c0002t0001g0153 a0001c0002t0001g0157 others(34): Show |
37 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.121-419A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570665 | |||||||
| chr4:67570691 | GGAAA | G | 64 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(61): Show |
66 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.121-378_121-375del others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67570691 | ||||||
| chr4:67570711 | A | AAAGG | 5 | a0001c0001t0001g0254 a0001c0001t0001g0257 a0001c0001t0002g0256 others(2): Show |
5 | HG02615.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-356_121-353dup others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67570711 | ||||||
| chr4:67570785 | C | T | 31 | a0001c0002t0001g0009 a0001c0002t0001g0241 a0001c0002t0001g0242 others(28): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.121-299C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570785 | |||||||
| chr4:67570836 | A | G | 1 | a0001c0002t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.121-248A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570836 | |||||||
| chr4:67570858 | T | C | 103 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(100): Show |
106 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.121-226T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570858 | |||||||
| chr4:67570921 | A | G | 2 | a0001c0003t0003g0294 a0001c0003t0003g0295 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.121-163A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570921 | |||||||
| chr4:67570978 | C | T | 1 | a0001c0002t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.121-106C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570978 | |||||||
| chr4:67571165 | T | C | 218 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(215): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.192+10T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571165 | |||||||
| chr4:67571257 | T | C | 1 | a0001c0002t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.192+102T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571257 | |||||||
| chr4:67571302 | C | T | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.192+147C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571302 | |||||||
| chr4:67571415 | T | G | 53 | a0001c0002t0001g0009 a0001c0002t0001g0143 a0001c0002t0001g0176 others(50): Show |
55 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.192+260T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571415 | |||||||
| chr4:67571509 | C | T | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.192+354C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571509 | |||||||
| chr4:67571533 | C | T | 112 | a0001c0001t0002g0329 a0001c0002t0001g0004 a0001c0002t0001g0005 others(109): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.192+378C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571533 | |||||||
| chr4:67571629 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.192+474G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571629 | |||||||
| chr4:67571918 | T | G | 1 | a0001c0002t0004g0158 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.192+763T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571918 | |||||||
| chr4:67571979 | G | A | 209 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(206): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.192+824G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571979 | |||||||
| chr4:67572118 | T | A | 1 | a0001c0002t0003g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.192+963T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572118 | |||||||
| chr4:67572135 | A | G | 26 | a0001c0003t0001g0011 a0001c0003t0001g0272 a0001c0003t0001g0278 others(23): Show |
27 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.192+980A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572135 | |||||||
| chr4:67572414 | G | A | 3 | a0001c0002t0001g0009 a0001c0002t0001g0241 a0001c0002t0001g0242 |
4 | HG02559.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+1259G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572414 | |||||||
| chr4:67572530 | C | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0254 a0001c0001t0001g0257 others(19): Show |
23 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.192+1375C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572530 | |||||||
| chr4:67572673 | T | A | 1 | a0001c0002t0002g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.192+1518T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572673 | |||||||
| chr4:67572756 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.192+1601C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572756 | |||||||
| chr4:67572770 | G | A | 1 | a0001c0001t0004g0236 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.192+1615G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572770 | |||||||
| chr4:67572786 | G | T | 218 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(215): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.192+1631G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572786 | |||||||
| chr4:67572997 | TAA | T | 4 | a0001c0001t0001g0049 a0001c0001t0003g0026 a0001c0001t0003g0043 others(1): Show |
4 | NA18987.hp1 NA18995.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+1843_192+1844d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572997 | |||||||
| chr4:67573116 | C | A | 1 | a0001c0001t0001g0040 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.192+1961C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67573116 | |||||||
| chr4:67573200 | G | C | 1 | a0001c0003t0001g0338 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.192+2045G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67573200 | |||||||
| chr4:67573640 | A | G | 1 | a0001c0003t0001g0356 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.193-1745A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67573640 | |||||||
| chr4:67573652 | G | A | 1 | a0004c0007t0002g0210 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.193-1733G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67573652 | |||||||
| chr4:67574038 | G | A | 3 | a0001c0002t0001g0180 a0001c0002t0001g0183 a0001c0002t0001g0192 |
3 | HG01515.hp1 HG01517.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.193-1347G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574038 | |||||||
| chr4:67574056 | T | G | 2 | a0001c0001t0007g0174 a0001c0001t0007g0175 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.193-1329T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574056 | |||||||
| chr4:67574365 | T | C | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.193-1020T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574365 | |||||||
| chr4:67574476 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.193-909G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574476 | |||||||
| chr4:67574533 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-852C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574533 | |||||||
| chr4:67574616 | T | A | 1 | a0001c0001t0001g0087 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.193-769T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574616 | |||||||
| chr4:67574625 | T | A | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.193-760T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574625 | |||||||
| chr4:67574653 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.193-732G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574653 | |||||||
| chr4:67574909 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.193-476T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574909 | |||||||
| chr4:67575215 | G | C | 55 | a0001c0001t0001g0028 a0001c0001t0001g0040 a0001c0001t0001g0044 others(52): Show |
64 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.193-170G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67575215 | |||||||
| chr4:67575244 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0003g0197 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.193-141G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67575244 | |||||||
| chr4:67575373 | T | C | 41 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0013 others(38): Show |
47 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.193-12T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67575373 | |||||||
| chr4:67575582 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.306+84T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67575582 | |||||||
| chr4:67575713 | T | C | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.306+215T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67575713 | |||||||
| chr4:67575799 | C | T | 1 | a0001c0001t0009g0246 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.306+301C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67575799 | |||||||
| chr4:67575857 | C | T | 95 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(92): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.306+359C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67575857 | |||||||
| chr4:67575865 | T | C | 41 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0013 others(38): Show |
47 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.306+367T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67575865 | |||||||
| chr4:67575974 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.306+476A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67575974 | |||||||
| chr4:67576109 | C | A | 1 | a0001c0001t0002g0234 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.306+611C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576109 | |||||||
| chr4:67576136 | G | A | 1 | a0001c0001t0003g0067 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.306+638G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576136 | |||||||
| chr4:67576229 | C | G | 118 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0002t0001g0004 others(115): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.306+731C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576229 | |||||||
| chr4:67576424 | T | C | 41 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0013 others(38): Show |
47 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.307-779T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576424 | |||||||
| chr4:67576610 | A | G | 4 | a0001c0001t0001g0102 a0001c0001t0002g0100 a0001c0001t0002g0101 others(1): Show |
4 | NA18960.hp2 NA18992.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-593A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576610 | |||||||
| chr4:67576757 | G | C | 1 | a0001c0001t0004g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.307-446G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576757 | |||||||
| chr4:67576770 | A | G | 2 | a0001c0002t0002g0164 a0001c0002t0002g0165 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.307-433A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576770 | |||||||
| chr4:67576878 | G | A | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.307-325G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576878 | |||||||
| chr4:67576912 | A | T | 114 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0009 others(111): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.307-291A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576912 | |||||||
| chr4:67577036 | C | T | 40 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0013 others(37): Show |
46 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.307-167C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67577036 | |||||||
| chr4:67577546 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.363+287G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577546 | |||||||
| chr4:67577590 | T | G | 95 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(92): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.363+331T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577590 | |||||||
| chr4:67577635 | T | TTTTC | 70 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(67): Show |
72 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.363+392_363+395dup others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 67577635 | ||||||
| chr4:67577650 | TC | T | 67 | a0001c0002t0001g0009 a0001c0002t0001g0143 a0001c0002t0001g0153 others(64): Show |
69 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.363+392delC | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577650 | |||||||
| chr4:67577651 | C | CTTTCT | 23 | a0001c0001t0001g0012 a0001c0001t0001g0198 a0001c0001t0001g0204 others(20): Show |
24 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.363+395_363+396ins others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 67577651 | ||||||
| chr4:67577651 | C | T | 48 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0013 others(45): Show |
54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.363+392C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577651 | |||||||
| chr4:67577653 | T | C | 48 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0013 others(45): Show |
54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.363+394T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577653 | |||||||
| chr4:67577654 | T | C | 67 | a0001c0002t0001g0009 a0001c0002t0001g0143 a0001c0002t0001g0153 others(64): Show |
69 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.363+395T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577654 | |||||||
| chr4:67577779 | G | C | 2 | a0001c0001t0001g0103 a0001c0001t0003g0137 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.363+520G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577779 | |||||||
| chr4:67577853 | T | G | 2 | a0001c0001t0002g0239 a0001c0001t0004g0236 |
2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.363+594T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577853 | |||||||
| chr4:67578023 | C | T | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.363+764C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578023 | |||||||
| chr4:67578230 | T | C | 1 | a0001c0001t0001g0353 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.363+971T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578230 | |||||||
| chr4:67578233 | C | T | 5 | a0001c0002t0001g0273 a0001c0002t0001g0275 a0001c0002t0001g0276 others(2): Show |
5 | HG00621.hp1 NA18942.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+974C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578233 | |||||||
| chr4:67578384 | C | A | 28 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(25): Show |
28 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(25): Show |
intron_variant | MODIFIER | c.363+1125C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578384 | |||||||
| chr4:67578462 | G | A | 96 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(93): Show |
99 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.363+1203G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578462 | |||||||
| chr4:67578474 | G | A | 30 | a0001c0002t0004g0336 a0001c0002t0004g0337 a0001c0003t0001g0011 others(27): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.363+1215G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578474 | |||||||
| chr4:67578513 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0003g0270 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.363+1254T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578513 | |||||||
| chr4:67578539 | G | A | 210 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(207): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.363+1280G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578539 | |||||||
| chr4:67578584 | T | C | 38 | a0001c0002t0001g0143 a0001c0002t0001g0153 a0001c0002t0001g0157 others(35): Show |
38 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.363+1325T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578584 | |||||||
| chr4:67578702 | G | C | 1 | a0001c0003t0001g0280 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.363+1443G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578702 | |||||||
| chr4:67578741 | T | G | 2 | a0001c0001t0007g0174 a0001c0001t0007g0175 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.363+1482T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578741 | |||||||
| chr4:67578830 | A | AT | 95 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(92): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.363+1587dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 67578830 | ||||||
| chr4:67578830 | AT | A | 96 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0009 others(93): Show |
103 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.363+1587delT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 67578830 | ||||||
| chr4:67578880 | G | A | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0303 |
3 | HG01167.hp1 HG01169.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.363+1621G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578880 | |||||||
| chr4:67578975 | C | T | 8 | a0001c0001t0002g0008 a0001c0001t0002g0208 a0001c0001t0002g0220 others(5): Show |
9 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.363+1716C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578975 | |||||||
| chr4:67578989 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG01952.hp2 HG01981.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.363+1730C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578989 | |||||||
| chr4:67579145 | C | T | 4 | a0001c0002t0001g0184 a0001c0002t0001g0185 a0001c0002t0001g0193 others(1): Show |
4 | NA18944.hp1 NA18971.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1886C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67579145 | |||||||
| chr4:67579422 | T | A | 1 | a0001c0002t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.364-1883T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67579422 | |||||||
| chr4:67579559 | T | G | 96 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(93): Show |
99 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.364-1746T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67579559 | |||||||
| chr4:67579584 | A | G | 1 | a0001c0002t0003g0167 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.364-1721A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67579584 | |||||||
| chr4:67579989 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.364-1316C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67579989 | |||||||
| chr4:67580191 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.364-1114G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580191 | |||||||
| chr4:67580277 | C | T | 100 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0009 others(97): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.364-1028C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580277 | |||||||
| chr4:67580311 | T | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0263 a0001c0001t0003g0232 |
3 | HG01891.hp2 HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.364-994T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580311 | |||||||
| chr4:67580405 | C | T | 5 | a0001c0003t0001g0284 a0001c0003t0001g0285 a0001c0003t0001g0286 others(2): Show |
5 | HG02630.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-900C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580405 | |||||||
| chr4:67580584 | G | C | 39 | a0001c0002t0001g0143 a0001c0002t0001g0153 a0001c0002t0001g0157 others(36): Show |
39 | HG00544.hp2 HG01106.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.364-721G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580584 | |||||||
| chr4:67580594 | C | T | 30 | a0001c0003t0001g0011 a0001c0003t0001g0163 a0001c0003t0001g0272 others(27): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.364-711C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580594 | |||||||
| chr4:67580619 | C | A | 75 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0009 others(72): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.364-686C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580619 | |||||||
| chr4:67580703 | T | C | 66 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(63): Show |
68 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.364-602T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580703 | |||||||
| chr4:67580827 | T | G | 219 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(216): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.364-478T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580827 | |||||||
| chr4:67580831 | C | A | 2 | a0001c0002t0002g0164 a0001c0002t0002g0165 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.364-474C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580831 | |||||||
| chr4:67580908 | T | A | 173 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(170): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.364-397T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580908 | |||||||
| chr4:67580970 | G | A | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0303 |
3 | HG01167.hp1 HG01169.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.364-335G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580970 | |||||||
| chr4:67581041 | G | C | 3 | a0001c0003t0001g0280 a0001c0003t0001g0281 a0001c0003t0001g0282 |
3 | HG03017.hp2 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.364-264G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67581041 | |||||||
| chr4:67581042 | G | A | 5 | a0001c0003t0001g0284 a0001c0003t0001g0285 a0001c0003t0001g0286 others(2): Show |
5 | HG02630.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-263G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67581042 | |||||||
| chr4:67581482 | A | G | 83 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0009 others(80): Show |
90 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.530+11A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581482 | |||||||
| chr4:67581512 | A | G | 1 | a0001c0003t0002g0293 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.530+41A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581512 | |||||||
| chr4:67581531 | A | G | 70 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(67): Show |
72 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.530+60A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581531 | |||||||
| chr4:67581539 | G | A | 2 | a0001c0001t0001g0245 a0001c0001t0009g0246 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.530+68G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581539 | |||||||
| chr4:67581634 | A | G | 219 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(216): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.530+163A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581634 | |||||||
| chr4:67581667 | C | G | 1 | a0001c0001t0004g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.530+196C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581667 | |||||||
| chr4:67581691 | C | T | 2 | a0001c0003t0003g0294 a0001c0003t0003g0295 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.530+220C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581691 | |||||||
| chr4:67581716 | T | G | 32 | a0001c0002t0004g0336 a0001c0002t0004g0337 a0001c0003t0001g0011 others(29): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.530+245T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581716 | |||||||
| chr4:67581777 | T | G | 2 | a0001c0002t0004g0336 a0001c0002t0004g0337 |
2 | HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.530+306T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581777 | |||||||
| chr4:67581927 | A | C | 1 | a0001c0001t0002g0099 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.530+456A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581927 | |||||||
| chr4:67581958 | T | C | 2 | a0001c0001t0002g0030 a0001c0001t0002g0036 |
2 | NA19009.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.530+487T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581958 | |||||||
| chr4:67582229 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.530+758T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582229 | |||||||
| chr4:67582272 | G | A | 216 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(213): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.530+801G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582272 | |||||||
| chr4:67582303 | T | G | 1 | a0001c0001t0005g0069 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.530+832T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582303 | |||||||
| chr4:67582311 | T | TTG | 93 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(90): Show |
96 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.530+840_530+841ins others(2): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582311 | |||||||
| chr4:67582312 | G | T | 95 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(92): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.530+841G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582312 | |||||||
| chr4:67582321 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0263 a0001c0001t0003g0232 |
3 | HG01891.hp2 HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.530+850G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582321 | |||||||
| chr4:67582459 | C | G | 96 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(93): Show |
99 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.530+988C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582459 | |||||||
| chr4:67582555 | G | A | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.531-1019G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582555 | |||||||
| chr4:67582630 | G | GT | 160 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(157): Show |
170 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.531-933dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 67582630 | ||||||
| chr4:67582656 | A | G | 96 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(93): Show |
99 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.531-918A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582656 | |||||||
| chr4:67582785 | C | A | 3 | a0001c0001t0001g0198 a0001c0001t0003g0197 a0001c0001t0003g0237 |
3 | HG01884.hp1 HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.531-789C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582785 | |||||||
| chr4:67582883 | A | G | 66 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0009 others(63): Show |
73 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.531-691A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582883 | |||||||
| chr4:67582908 | A | G | 3 | a0001c0001t0001g0198 a0001c0001t0003g0197 a0001c0001t0003g0237 |
3 | HG01884.hp1 HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.531-666A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582908 | |||||||
| chr4:67583108 | A | G | 2 | a0001c0003t0001g0288 a0001c0003t0001g0292 |
2 | HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.531-466A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67583108 | |||||||
| chr4:67583199 | G | A | 1 | a0001c0001t0004g0236 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.531-375G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67583199 | |||||||
| chr4:67583389 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.531-185A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67583389 | |||||||
| chr4:67583546 | A | G | 2 | a0001c0001t0007g0174 a0001c0001t0007g0175 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.531-28A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67583546 | |||||||
| chr4:67583551 | G | GT | 26 | a0001c0002t0001g0009 a0001c0002t0001g0143 a0001c0002t0001g0176 others(23): Show |
27 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.531-16dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 67583551 | ||||||
| chr4:67583830 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.659+128G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67583830 | |||||||
| chr4:67583873 | C | T | 1 | a0001c0003t0003g0349 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.659+171C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67583873 | |||||||
| chr4:67583923 | C | T | 1 | a0001c0001t0002g0055 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.659+221C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67583923 | |||||||
| chr4:67583993 | G | A | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.659+291G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67583993 | |||||||
| chr4:67584098 | G | GA | 156 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
170 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.659+414dupA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67584098 | ||||||
| chr4:67584098 | GAA | G | 93 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(90): Show |
96 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.659+413_659+414del others(2): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67584098 | ||||||
| chr4:67584116 | A | AAAAT | 38 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0013 others(35): Show |
44 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.659+414_659+415ins others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584116 | |||||||
| chr4:67584116 | A | AAAT | 31 | a0001c0002t0001g0009 a0001c0002t0001g0176 a0001c0002t0001g0181 others(28): Show |
32 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.659+414_659+415ins others(3): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584116 | |||||||
| chr4:67584116 | A | AAT | 29 | a0001c0002t0001g0143 a0001c0002t0001g0177 a0001c0002t0001g0178 others(26): Show |
30 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.659+414_659+415ins others(2): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584116 | |||||||
| chr4:67584116 | A | T | 96 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(93): Show |
99 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.659+414A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584116 | |||||||
| chr4:67584306 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.659+604G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584306 | |||||||
| chr4:67584325 | A | G | 1 | a0001c0003t0001g0292 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.659+623A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584325 | |||||||
| chr4:67584510 | C | G | 1 | a0001c0002t0001g0185 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.659+808C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584510 | |||||||
| chr4:67584517 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.659+815A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584517 | |||||||
| chr4:67584584 | C | T | 76 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0009 others(73): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.659+882C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584584 | |||||||
| chr4:67584654 | A | T | 1 | a0001c0001t0002g0228 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.659+952A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584654 | |||||||
| chr4:67584688 | TAGA | T | 70 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(67): Show |
72 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.659+991_659+993del others(3): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67584688 | ||||||
| chr4:67584693 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.659+991G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584693 | |||||||
| chr4:67584780 | A | G | 1 | a0001c0002t0001g0326 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.659+1078A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584780 | |||||||
| chr4:67584876 | C | T | 10 | a0001c0002t0001g0157 a0001c0002t0001g0160 a0001c0002t0001g0161 others(7): Show |
10 | HG02572.hp1 HG02818.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.659+1174C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584876 | |||||||
| chr4:67584967 | A | G | 2 | a0001c0002t0001g0156 a0001c0002t0002g0155 |
2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.659+1265A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584967 | |||||||
| chr4:67585137 | C | A | 1 | a0001c0001t0001g0072 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.659+1435C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585137 | |||||||
| chr4:67585150 | G | A | 172 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(169): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.659+1448G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585150 | |||||||
| chr4:67585270 | A | G | 172 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(169): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.659+1568A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585270 | |||||||
| chr4:67585276 | A | G | 74 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0009 others(71): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.659+1574A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585276 | |||||||
| chr4:67585437 | G | C | 1 | a0004c0007t0002g0210 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.659+1735G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585437 | |||||||
| chr4:67585658 | T | C | 97 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0009 others(94): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.659+1956T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585658 | |||||||
| chr4:67585881 | A | T | 97 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0009 others(94): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.659+2179A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585881 | |||||||
| chr4:67585916 | C | T | 99 | a0001c0001t0007g0174 a0001c0001t0007g0175 a0001c0002t0001g0004 others(96): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.659+2214C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585916 | |||||||
| chr4:67586060 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.659+2358T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586060 | |||||||
| chr4:67586091 | C | A | 30 | a0001c0003t0001g0011 a0001c0003t0001g0163 a0001c0003t0001g0272 others(27): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.659+2389C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586091 | |||||||
| chr4:67586093 | T | A | 30 | a0001c0003t0001g0011 a0001c0003t0001g0163 a0001c0003t0001g0272 others(27): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.659+2391T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586093 | |||||||
| chr4:67586106 | C | T | 99 | a0001c0001t0007g0174 a0001c0001t0007g0175 a0001c0002t0001g0004 others(96): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.659+2404C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586106 | |||||||
| chr4:67586237 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.659+2535T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586237 | |||||||
| chr4:67586364 | G | A | 18 | a0001c0002t0001g0004 a0001c0002t0001g0312 a0001c0002t0001g0315 others(15): Show |
21 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.659+2662G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586364 | |||||||
| chr4:67586527 | G | A | 3 | a0001c0003t0001g0280 a0001c0003t0001g0281 a0001c0003t0001g0282 |
3 | HG03017.hp2 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.659+2825G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586527 | |||||||
| chr4:67586586 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG00544.hp1 NA18973.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.659+2884T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586586 | |||||||
| chr4:67586587 | G | A | 99 | a0001c0001t0007g0174 a0001c0001t0007g0175 a0001c0002t0001g0004 others(96): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.659+2885G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586587 | |||||||
| chr4:67586745 | T | G | 99 | a0001c0001t0007g0174 a0001c0001t0007g0175 a0001c0002t0001g0004 others(96): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.659+3043T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586745 | |||||||
| chr4:67586819 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0003g0270 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.659+3117T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586819 | |||||||
| chr4:67586842 | C | T | 99 | a0001c0001t0007g0174 a0001c0001t0007g0175 a0001c0002t0001g0004 others(96): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.659+3140C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586842 | |||||||
| chr4:67587155 | G | C | 30 | a0001c0003t0001g0011 a0001c0003t0001g0163 a0001c0003t0001g0272 others(27): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.659+3453G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587155 | |||||||
| chr4:67587159 | G | A | 2 | a0001c0002t0001g0327 a0001c0002t0001g0331 |
2 | NA19079.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.659+3457G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587159 | |||||||
| chr4:67587218 | C | CA | 3 | a0001c0001t0001g0202 a0001c0001t0001g0263 a0001c0001t0003g0232 |
3 | HG01891.hp2 HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.659+3520dupA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67587218 | ||||||
| chr4:67587264 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.659+3562A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587264 | |||||||
| chr4:67587441 | T | C | 1 | a0001c0002t0004g0158 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.660-3443T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587441 | |||||||
| chr4:67587446 | A | G | 67 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0009 others(64): Show |
74 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.660-3438A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587446 | |||||||
| chr4:67587471 | T | C | 99 | a0001c0001t0007g0174 a0001c0001t0007g0175 a0001c0002t0001g0004 others(96): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.660-3413T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587471 | |||||||
| chr4:67587478 | A | G | 2 | a0001c0001t0001g0269 a0001c0001t0003g0270 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.660-3406A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587478 | |||||||
| chr4:67587616 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.660-3268G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587616 | |||||||
| chr4:67587636 | C | A | 99 | a0001c0001t0007g0174 a0001c0001t0007g0175 a0001c0002t0001g0004 others(96): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.660-3248C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587636 | |||||||
| chr4:67587685 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-3199T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587685 | |||||||
| chr4:67587719 | CT | C | 80 | a0001c0001t0001g0028 a0001c0001t0001g0040 a0001c0001t0001g0044 others(77): Show |
89 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.660-3147delT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67587719 | ||||||
| chr4:67587719 | CTTT | C | 62 | a0001c0001t0001g0012 a0001c0001t0001g0254 a0001c0001t0001g0257 others(59): Show |
67 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.660-3149_660-3147d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67587719 | ||||||
| chr4:67587719 | CTTTT | C | 133 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(130): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.660-3150_660-3147d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67587719 | ||||||
| chr4:67587781 | C | T | 195 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(192): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.660-3103C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587781 | |||||||
| chr4:67587798 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.660-3086A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587798 | |||||||
| chr4:67587803 | T | C | 99 | a0001c0001t0007g0174 a0001c0001t0007g0175 a0001c0002t0001g0004 others(96): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.660-3081T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587803 | |||||||
| chr4:67587966 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.660-2918C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587966 | |||||||
| chr4:67588039 | T | TA | 119 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0028 others(116): Show |
132 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.660-2819dupA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | ||||||
| chr4:67588039 | T | TAA | 21 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0045 others(18): Show |
22 | HG00323.hp1 HG00733.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.660-2820_660-2819d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | ||||||
| chr4:67588039 | T | TAAAAA | 19 | a0001c0003t0001g0011 a0001c0003t0001g0278 a0001c0003t0001g0281 others(16): Show |
20 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.660-2823_660-2819d others(7): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | ||||||
| chr4:67588039 | T | TAAAAAA | 10 | a0001c0003t0001g0163 a0001c0003t0001g0272 a0001c0003t0001g0284 others(7): Show |
10 | HG00642.hp2 HG01106.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.660-2824_660-2819d others(8): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | ||||||
| chr4:67588039 | TA | T | 7 | a0001c0001t0001g0202 a0001c0001t0003g0232 a0001c0001t0009g0246 others(4): Show |
7 | HG00544.hp2 HG01891.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.660-2819delA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | ||||||
| chr4:67588039 | TAA | T | 27 | a0001c0001t0001g0012 a0001c0001t0001g0199 a0001c0001t0001g0207 others(24): Show |
28 | HG00733.hp2 HG01071.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.660-2820_660-2819d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | ||||||
| chr4:67588039 | TAAA | T | 100 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(97): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.660-2821_660-2819d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | ||||||
| chr4:67588039 | TAAAA | T | 11 | a0001c0001t0001g0223 a0001c0001t0001g0250 a0001c0001t0001g0261 others(8): Show |
11 | HG01168.hp2 HG01256.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.660-2822_660-2819d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | ||||||
| chr4:67588039 | TAAAAAAA others(3): Show |
T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0144 |
2 | NA18972.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.660-2828_660-2819d others(12): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | ||||||
| chr4:67588083 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.660-2801T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588083 | |||||||
| chr4:67588101 | A | T | 1 | a0001c0001t0001g0172 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.660-2783A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588101 | |||||||
| chr4:67588277 | G | A | 179 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.660-2607G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588277 | |||||||
| chr4:67588341 | A | AGAC | 98 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(95): Show |
101 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.660-2531_660-2529d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588341 | ||||||
| chr4:67588353 | C | CGAT | 30 | a0001c0001t0001g0202 a0001c0001t0001g0245 a0001c0001t0001g0263 others(27): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.660-2509_660-2507d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588353 | ||||||
| chr4:67588353 | CGAT | C | 44 | a0001c0001t0001g0269 a0001c0001t0002g0068 a0001c0001t0003g0270 others(41): Show |
50 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.660-2509_660-2507d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588353 | ||||||
| chr4:67588356 | T | C | 35 | a0001c0001t0001g0040 a0001c0001t0001g0059 a0001c0001t0001g0250 others(32): Show |
36 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.660-2528T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588356 | |||||||
| chr4:67588359 | T | C | 40 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0013 others(37): Show |
46 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.660-2525T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588359 | |||||||
| chr4:67588391 | T | G | 166 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(163): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.660-2493T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588391 | |||||||
| chr4:67588496 | G | A | 1 | a0001c0001t0002g0018 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.660-2388G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588496 | |||||||
| chr4:67588534 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.660-2350C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588534 | |||||||
| chr4:67588630 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.660-2254C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588630 | |||||||
| chr4:67588691 | G | A | 3 | a0001c0001t0001g0269 a0001c0001t0003g0270 a0001c0001t0004g0268 |
3 | HG02965.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.660-2193G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588691 | |||||||
| chr4:67588801 | T | C | 19 | a0001c0001t0001g0012 a0001c0001t0001g0064 a0001c0001t0001g0089 others(16): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.660-2083T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588801 | |||||||
| chr4:67588807 | G | A | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.660-2077G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588807 | |||||||
| chr4:67588932 | A | G | 353 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(350): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.660-1952A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588932 | |||||||
| chr4:67588991 | C | A | 14 | a0001c0002t0001g0153 a0001c0002t0001g0157 a0001c0002t0001g0160 others(11): Show |
14 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.660-1893C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588991 | |||||||
| chr4:67589007 | C | T | 2 | a0001c0002t0002g0179 a0001c0002t0002g0188 |
2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.660-1877C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589007 | |||||||
| chr4:67589028 | A | G | 2 | a0001c0002t0004g0336 a0001c0002t0004g0337 |
2 | HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.660-1856A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589028 | |||||||
| chr4:67589095 | C | T | 1 | a0001c0001t0002g0251 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.660-1789C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589095 | |||||||
| chr4:67589229 | A | G | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.660-1655A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589229 | |||||||
| chr4:67589486 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-1398A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589486 | |||||||
| chr4:67589538 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.660-1346T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589538 | |||||||
| chr4:67589575 | T | C | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.660-1309T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589575 | |||||||
| chr4:67589584 | C | G | 96 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(93): Show |
99 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.660-1300C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589584 | |||||||
| chr4:67589682 | G | T | 98 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(95): Show |
101 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.660-1202G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589682 | |||||||
| chr4:67589715 | C | T | 1 | a0001c0002t0002g0316 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.660-1169C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589715 | |||||||
| chr4:67589809 | A | AT | 40 | a0001c0001t0001g0141 a0001c0001t0001g0204 a0001c0001t0001g0209 others(37): Show |
41 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.660-1062dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67589809 | ||||||
| chr4:67589813 | T | C | 1 | a0001c0002t0001g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.660-1071T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589813 | |||||||
| chr4:67589863 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.660-1021G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589863 | |||||||
| chr4:67589879 | A | C | 2 | a0001c0001t0007g0174 a0001c0001t0007g0175 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.660-1005A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589879 | |||||||
| chr4:67590102 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-782T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590102 | |||||||
| chr4:67590103 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-781C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590103 | |||||||
| chr4:67590109 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-775C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590109 | |||||||
| chr4:67590111 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-773T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590111 | |||||||
| chr4:67590125 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0003g0270 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.660-759C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590125 | |||||||
| chr4:67590286 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.660-598T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590286 | |||||||
| chr4:67590338 | C | G | 1 | a0001c0001t0002g0121 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.660-546C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590338 | |||||||
| chr4:67590356 | C | T | 164 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(161): Show |
174 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.660-528C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590356 | |||||||
| chr4:67590426 | G | A | 5 | a0001c0001t0001g0202 a0001c0001t0001g0245 a0001c0001t0001g0263 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.660-458G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590426 | |||||||
| chr4:67590438 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-446A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590438 | |||||||
| chr4:67590462 | G | T | 2 | a0001c0001t0007g0174 a0001c0001t0007g0175 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.660-422G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590462 | |||||||
| chr4:67590650 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-234A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590650 | |||||||
| chr4:67590679 | A | G | 2 | a0001c0001t0001g0269 a0001c0001t0003g0270 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.660-205A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590679 | |||||||
| chr4:67590741 | A | G | 3 | a0001c0001t0001g0198 a0001c0001t0003g0197 a0001c0001t0003g0237 |
3 | HG01884.hp1 HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.660-143A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590741 | |||||||
| chr4:67590745 | A | AT | 19 | a0001c0001t0001g0084 a0001c0001t0001g0117 a0001c0001t0001g0126 others(16): Show |
19 | HG00621.hp1 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.660-119dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67590745 | ||||||
| chr4:67590745 | A | ATT | 63 | a0001c0001t0001g0089 a0001c0001t0001g0245 a0001c0001t0001g0269 others(60): Show |
70 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.660-120_660-119dup others(2): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67590745 | ||||||
| chr4:67590745 | A | ATTT | 28 | a0001c0001t0001g0012 a0001c0001t0001g0064 a0001c0001t0001g0254 others(25): Show |
29 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.660-121_660-119dup others(3): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67590745 | ||||||
| chr4:67590745 | A | ATTTT | 59 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(56): Show |
61 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.660-122_660-119dup others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67590745 | ||||||
| chr4:67590745 | A | ATTTTT | 13 | a0001c0001t0001g0204 a0001c0001t0001g0209 a0001c0001t0001g0213 others(10): Show |
13 | HG00733.hp2 HG01358.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.660-123_660-119dup others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67590745 | ||||||
| chr4:67590745 | AT | A | 9 | a0001c0001t0001g0044 a0001c0001t0001g0102 a0001c0001t0001g0139 others(6): Show |
9 | HG00438.hp2 HG00597.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.660-119delT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67590745 | ||||||
| chr4:67590801 | A | G | 1 | a0001c0005t0001g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.660-83A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590801 | |||||||
| chr4:67590840 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.660-44C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590840 | |||||||
| chr4:67591062 | A | G | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.729+109A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591062 | |||||||
| chr4:67591277 | A | C | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.729+324A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591277 | |||||||
| chr4:67591331 | T | A | 161 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(158): Show |
171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.729+378T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591331 | |||||||
| chr4:67591432 | A | G | 1 | a0001c0003t0001g0290 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.729+479A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591432 | |||||||
| chr4:67591685 | C | G | 102 | a0001c0001t0001g0012 a0001c0001t0001g0083 a0001c0001t0001g0084 others(99): Show |
110 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.729+732C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591685 | |||||||
| chr4:67591793 | C | A | 1 | a0001c0001t0001g0269 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.729+840C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591793 | |||||||
| chr4:67591847 | A | G | 1 | a0001c0002t0001g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.729+894A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591847 | |||||||
| chr4:67591936 | C | CT | 8 | a0001c0001t0001g0147 a0001c0001t0002g0113 a0001c0001t0004g0236 others(5): Show |
8 | HG01167.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.729+984dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 67591936 | ||||||
| chr4:67591977 | A | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0082 others(179): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.729+1024A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591977 | |||||||
| chr4:67592036 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0263 a0001c0001t0003g0232 |
3 | HG01891.hp2 HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.729+1083G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592036 | |||||||
| chr4:67592058 | A | T | 17 | a0001c0002t0001g0013 a0001c0002t0001g0156 a0001c0002t0001g0323 others(14): Show |
18 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.729+1105A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592058 | |||||||
| chr4:67592088 | C | T | 8 | a0001c0001t0001g0245 a0001c0001t0001g0254 a0001c0001t0001g0257 others(5): Show |
9 | HG02559.hp1 HG02615.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.729+1135C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592088 | |||||||
| chr4:67592113 | T | G | 17 | a0001c0001t0001g0103 a0001c0001t0001g0254 a0001c0001t0001g0257 others(14): Show |
17 | HG02572.hp1 HG02615.hp1 HG02818.hp1 others(14): Show |
intron_variant | MODIFIER | c.730-1147T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592113 | |||||||
| chr4:67592126 | A | AT | 306 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(303): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.730-1123dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 67592126 | ||||||
| chr4:67592126 | A | ATT | 8 | a0001c0001t0001g0245 a0001c0001t0001g0257 a0001c0001t0002g0256 others(5): Show |
9 | HG02559.hp1 HG02615.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.730-1124_730-1123d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 67592126 | ||||||
| chr4:67592126 | AT | A | 6 | a0001c0001t0001g0105 a0001c0001t0002g0104 a0001c0002t0002g0164 others(3): Show |
6 | HG01167.hp2 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.730-1123delT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 67592126 | ||||||
| chr4:67592156 | G | A | 85 | a0001c0001t0001g0012 a0001c0001t0001g0087 a0001c0001t0001g0091 others(82): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.730-1104G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592156 | |||||||
| chr4:67592253 | C | T | 5 | a0001c0001t0001g0202 a0001c0001t0001g0263 a0001c0001t0003g0232 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-1007C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592253 | |||||||
| chr4:67592286 | G | T | 1 | a0001c0001t0002g0021 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.730-974G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592286 | |||||||
| chr4:67592335 | T | C | 1 | a0001c0001t0002g0023 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.730-925T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592335 | |||||||
| chr4:67592401 | G | A | 3 | a0001c0002t0001g0176 a0001c0002t0001g0181 a0001c0002t0001g0182 |
3 | HG02622.hp2 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.730-859G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592401 | |||||||
| chr4:67592401 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.730-859G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592401 | |||||||
| chr4:67592478 | A | G | 1 | a0001c0003t0002g0283 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.730-782A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592478 | |||||||
| chr4:67592570 | C | T | 1 | a0001c0001t0002g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.730-690C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592570 | |||||||
| chr4:67592692 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0049 others(181): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.730-568T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592692 | |||||||
| chr4:67592725 | C | A | 2 | a0001c0003t0003g0294 a0001c0003t0003g0295 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.730-535C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592725 | |||||||
| chr4:67592774 | C | T | 1 | a0001c0002t0001g0335 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.730-486C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592774 | |||||||
| chr4:67592865 | G | A | 35 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0243 others(32): Show |
37 | HG00639.hp2 HG01261.hp2 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.730-395G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592865 | |||||||
| chr4:67592920 | A | G | 59 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0077 others(56): Show |
64 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.730-340A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592920 | |||||||
| chr4:67593090 | G | A | 40 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0243 others(37): Show |
42 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.730-170G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67593090 | |||||||
| chr4:67593219 | G | C | 180 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0040 others(177): Show |
197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.730-41G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67593219 | |||||||
| chr4:67593472 | T | C | 1 | a0001c0002t0001g0177 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.826+116T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67593472 | |||||||
| chr4:67593504 | T | G | 1 | a0001c0002t0002g0355 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.826+148T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67593504 | |||||||
| chr4:67593727 | C | T | 43 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0243 others(40): Show |
45 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.826+371C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67593727 | |||||||
| chr4:67593798 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.826+442T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67593798 | |||||||
| chr4:67594015 | T | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0077 others(59): Show |
67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+659T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594015 | |||||||
| chr4:67594036 | A | G | 64 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0077 others(61): Show |
69 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.826+680A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594036 | |||||||
| chr4:67594437 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.826+1081C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594437 | |||||||
| chr4:67594537 | T | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0077 others(59): Show |
67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+1181T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594537 | |||||||
| chr4:67594799 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.826+1443G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594799 | |||||||
| chr4:67594822 | T | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0077 others(59): Show |
67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+1466T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594822 | |||||||
| chr4:67594926 | G | A | 3 | a0001c0001t0002g0239 a0001c0001t0007g0174 a0001c0001t0007g0175 |
3 | HG02818.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.826+1570G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594926 | |||||||
| chr4:67594950 | A | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG02895.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.826+1594A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594950 | |||||||
| chr4:67595000 | T | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0077 others(59): Show |
67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+1644T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595000 | |||||||
| chr4:67595024 | C | A | 20 | a0001c0001t0001g0077 a0001c0001t0001g0243 a0001c0001t0003g0010 others(17): Show |
21 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.826+1668C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595024 | |||||||
| chr4:67595031 | T | G | 2 | a0001c0001t0003g0111 a0001c0001t0003g0214 |
2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.826+1675T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595031 | |||||||
| chr4:67595149 | C | T | 1 | a0001c0002t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.826+1793C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595149 | |||||||
| chr4:67595365 | G | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0077 others(59): Show |
67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+2009G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595365 | |||||||
| chr4:67595372 | C | CA | 42 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0028 others(39): Show |
42 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.826+2045dupA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | ||||||
| chr4:67595372 | C | CAA | 8 | a0001c0001t0001g0074 a0001c0001t0001g0129 a0001c0001t0002g0019 others(5): Show |
8 | HG00738.hp2 HG01361.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.826+2044_826+2045d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | ||||||
| chr4:67595372 | CA | C | 49 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0045 others(46): Show |
51 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.826+2045delA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | ||||||
| chr4:67595372 | CAA | C | 12 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0299 others(9): Show |
12 | HG01169.hp1 HG02132.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.826+2044_826+2045d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | ||||||
| chr4:67595372 | CAAA | C | 34 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0077 others(31): Show |
38 | HG00408.hp1 HG00544.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.826+2043_826+2045d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | ||||||
| chr4:67595372 | CAAAA | C | 10 | a0001c0001t0001g0243 a0001c0001t0003g0010 a0001c0001t0003g0026 others(7): Show |
11 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+2042_826+2045d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | ||||||
| chr4:67595372 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0303 |
3 | HG02145.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.826+2035_826+2045d others(13): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | ||||||
| chr4:67595372 | CAAAAAAA others(5): Show |
C | 70 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0057 others(67): Show |
76 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.826+2034_826+2045d others(14): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | ||||||
| chr4:67595372 | CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0002g0314 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.826+2032_826+2045d others(16): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | ||||||
| chr4:67595401 | A | T | 1 | a0001c0001t0002g0222 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.826+2045A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595401 | |||||||
| chr4:67595500 | C | T | 1 | a0001c0002t0001g0333 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.826+2144C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595500 | |||||||
| chr4:67595525 | C | T | 1 | a0001c0001t0007g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.826+2169C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595525 | |||||||
| chr4:67595668 | T | A | 3 | a0001c0001t0002g0239 a0001c0001t0007g0174 a0001c0001t0007g0175 |
3 | HG02818.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.826+2312T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595668 | |||||||
| chr4:67595784 | C | A | 43 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0243 others(40): Show |
45 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.826+2428C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595784 | |||||||
| chr4:67595818 | G | T | 1 | a0003c0006t0001g0027 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.826+2462G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595818 | |||||||
| chr4:67595976 | T | TTTTG | 62 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0077 others(59): Show |
67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+2621_826+2624d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595976 | ||||||
| chr4:67596082 | G | A | 1 | a0001c0001t0001g0353 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.826+2726G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596082 | |||||||
| chr4:67596148 | TG | T | 43 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0243 others(40): Show |
45 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.826+2796delG | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67596148 | ||||||
| chr4:67596160 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0102 a0001c0001t0001g0139 |
3 | HG02071.hp2 NA18993.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.826+2804G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596160 | |||||||
| chr4:67596330 | A | G | 43 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0243 others(40): Show |
45 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.826+2974A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596330 | |||||||
| chr4:67596421 | T | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0025 |
2 | NA18990.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.826+3065T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596421 | |||||||
| chr4:67596448 | A | G | 43 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0243 others(40): Show |
45 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.826+3092A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596448 | |||||||
| chr4:67596474 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.826+3118G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596474 | |||||||
| chr4:67596641 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.826+3285G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596641 | |||||||
| chr4:67596815 | T | C | 2 | a0001c0001t0007g0174 a0001c0001t0007g0175 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.826+3459T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596815 | |||||||
| chr4:67596912 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.826+3556A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596912 | |||||||
| chr4:67597074 | G | A | 2 | a0001c0001t0007g0174 a0001c0001t0007g0175 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.826+3718G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597074 | |||||||
| chr4:67597166 | T | C | 1 | a0002c0004t0001g0073 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.826+3810T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597166 | |||||||
| chr4:67597264 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0144 |
2 | NA18972.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.826+3908G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597264 | |||||||
| chr4:67597395 | G | A | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.826+4039G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597395 | |||||||
| chr4:67597484 | C | A | 1 | a0001c0002t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.826+4128C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597484 | |||||||
| chr4:67597495 | C | G | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.826+4139C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597495 | |||||||
| chr4:67597562 | T | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0077 others(59): Show |
67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+4206T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597562 | |||||||
| chr4:67597679 | G | A | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.826+4323G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597679 | |||||||
| chr4:67597691 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.826+4335T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597691 | |||||||
| chr4:67597961 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0298 a0001c0001t0001g0299 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+4605A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597961 | |||||||
| chr4:67597984 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.826+4628C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597984 | |||||||
| chr4:67598101 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0269 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.826+4745G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598101 | |||||||
| chr4:67598248 | C | T | 1 | a0001c0001t0009g0246 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.826+4892C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598248 | |||||||
| chr4:67598353 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.826+4997C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598353 | |||||||
| chr4:67598387 | A | G | 1 | a0001c0001t0002g0092 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.826+5031A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598387 | |||||||
| chr4:67598402 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0269 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.826+5046G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598402 | |||||||
| chr4:67598403 | T | C | 2 | a0001c0001t0005g0069 a0001c0001t0005g0267 |
2 | NA18987.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.826+5047T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598403 | |||||||
| chr4:67598445 | T | C | 1 | a0001c0002t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.826+5089T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598445 | |||||||
| chr4:67598476 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.826+5120A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598476 | |||||||
| chr4:67598635 | G | A | 46 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0243 others(43): Show |
48 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.826+5279G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598635 | |||||||
| chr4:67598665 | C | T | 46 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0243 others(43): Show |
48 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.826+5309C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598665 | |||||||
| chr4:67598858 | T | C | 67 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0077 others(64): Show |
72 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.826+5502T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598858 | |||||||
| chr4:67598879 | T | A | 13 | a0001c0001t0001g0077 a0001c0001t0001g0243 a0001c0001t0003g0010 others(10): Show |
14 | HG00639.hp2 HG01261.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.826+5523T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598879 | |||||||
| chr4:67598926 | C | T | 46 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0243 others(43): Show |
48 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.826+5570C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598926 | |||||||
| chr4:67598941 | T | C | 20 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0064 others(17): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.826+5585T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598941 | |||||||
| chr4:67598960 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.826+5604C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598960 | |||||||
| chr4:67599033 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.826+5677G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599033 | |||||||
| chr4:67599056 | G | A | 46 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0243 others(43): Show |
48 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.826+5700G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599056 | |||||||
| chr4:67599080 | G | A | 1 | a0001c0003t0001g0356 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.826+5724G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599080 | |||||||
| chr4:67599096 | T | C | 67 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0077 others(64): Show |
72 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.826+5740T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599096 | |||||||
| chr4:67599097 | G | A | 46 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0243 others(43): Show |
48 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.826+5741G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599097 | |||||||
| chr4:67599115 | T | C | 46 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0243 others(43): Show |
48 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.826+5759T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599115 | |||||||
| chr4:67599353 | T | C | 1 | a0001c0003t0001g0342 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.826+5997T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599353 | |||||||
| chr4:67599641 | T | C | 2 | a0001c0002t0002g0164 a0001c0002t0002g0165 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.826+6285T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599641 | |||||||
| chr4:67599683 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.826+6327C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599683 | |||||||
| chr4:67599687 | A | T | 1 | a0001c0001t0001g0200 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.826+6331A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599687 | |||||||
| chr4:67599716 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.826+6360A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599716 | |||||||
| chr4:67599736 | G | A | 23 | a0001c0001t0002g0008 a0001c0001t0002g0051 a0001c0001t0002g0054 others(20): Show |
24 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.826+6380G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599736 | |||||||
| chr4:67599861 | C | T | 2 | a0001c0001t0001g0200 a0001c0003t0001g0356 |
2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.827-6435C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599861 | |||||||
| chr4:67599928 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.827-6368C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599928 | |||||||
| chr4:67599987 | T | G | 1 | a0001c0002t0001g0321 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.827-6309T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599987 | |||||||
| chr4:67600015 | A | G | 309 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(306): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.827-6281A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600015 | |||||||
| chr4:67600071 | G | A | 3 | a0001c0001t0002g0256 a0001c0001t0002g0258 a0001c0003t0002g0283 |
3 | HG02717.hp1 HG02896.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.827-6225G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600071 | |||||||
| chr4:67600195 | T | C | 309 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(306): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.827-6101T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600195 | |||||||
| chr4:67600203 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.827-6093C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600203 | |||||||
| chr4:67600377 | C | T | 1 | a0001c0003t0002g0283 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.827-5919C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600377 | |||||||
| chr4:67600391 | T | A | 2 | a0001c0001t0002g0092 a0001c0001t0002g0133 |
2 | NA18966.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.827-5905T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600391 | |||||||
| chr4:67600548 | T | C | 2 | a0001c0003t0003g0294 a0001c0003t0003g0295 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.827-5748T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600548 | |||||||
| chr4:67600725 | C | T | 1 | a0001c0002t0003g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.827-5571C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600725 | |||||||
| chr4:67600744 | A | G | 39 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0032 others(36): Show |
48 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.827-5552A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600744 | |||||||
| chr4:67600855 | A | C | 3 | a0001c0001t0001g0087 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG02129.hp2 HG02132.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.827-5441A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600855 | |||||||
| chr4:67600912 | T | C | 1 | a0001c0003t0001g0342 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.827-5384T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600912 | |||||||
| chr4:67601080 | G | T | 1 | a0001c0002t0001g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.827-5216G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601080 | |||||||
| chr4:67601215 | G | A | 290 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(287): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.827-5081G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601215 | |||||||
| chr4:67601252 | G | T | 1 | a0001c0001t0001g0200 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.827-5044G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601252 | |||||||
| chr4:67601277 | C | A | 72 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0040 others(69): Show |
79 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.827-5019C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601277 | |||||||
| chr4:67601317 | T | A | 4 | a0001c0001t0006g0138 a0001c0001t0010g0114 a0001c0002t0006g0166 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-4979T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601317 | |||||||
| chr4:67601520 | G | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0089 |
2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.827-4776G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601520 | |||||||
| chr4:67601574 | T | C | 309 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(306): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.827-4722T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601574 | |||||||
| chr4:67601579 | A | G | 307 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(304): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.827-4717A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601579 | |||||||
| chr4:67601585 | T | C | 1 | a0001c0001t0001g0353 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.827-4711T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601585 | |||||||
| chr4:67601650 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.827-4646G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601650 | |||||||
| chr4:67601836 | G | T | 290 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(287): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.827-4460G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601836 | |||||||
| chr4:67601935 | A | G | 290 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(287): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.827-4361A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601935 | |||||||
| chr4:67601967 | T | C | 290 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(287): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.827-4329T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601967 | |||||||
| chr4:67602302 | C | T | 290 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(287): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.827-3994C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602302 | |||||||
| chr4:67602318 | C | CAT | 285 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(282): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.827-3978_827-3977i others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602318 | |||||||
| chr4:67602510 | G | A | 118 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(115): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.827-3786G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602510 | |||||||
| chr4:67602534 | G | A | 2 | a0001c0001t0007g0174 a0001c0001t0007g0175 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.827-3762G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602534 | |||||||
| chr4:67602625 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.827-3671C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602625 | |||||||
| chr4:67602727 | C | T | 1 | a0001c0001t0002g0022 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.827-3569C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602727 | |||||||
| chr4:67602737 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.827-3559G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602737 | |||||||
| chr4:67602812 | GTGCT | G | 290 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(287): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.827-3479_827-3476d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67602812 | ||||||
| chr4:67603040 | G | A | 290 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(287): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.827-3256G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603040 | |||||||
| chr4:67603280 | G | A | 288 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(285): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.827-3016G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603280 | |||||||
| chr4:67603600 | T | C | 1 | a0001c0003t0001g0356 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.827-2696T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603600 | |||||||
| chr4:67603612 | T | C | 309 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(306): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.827-2684T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603612 | |||||||
| chr4:67603657 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.827-2639G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603657 | |||||||
| chr4:67603677 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.827-2619G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603677 | |||||||
| chr4:67603864 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0304 |
2 | HG02165.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.827-2432G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603864 | |||||||
| chr4:67603907 | C | T | 1 | a0001c0001t0001g0006 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.827-2389C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603907 | |||||||
| chr4:67603937 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0144 |
2 | NA18972.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.827-2359A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603937 | |||||||
| chr4:67603950 | C | T | 3 | a0001c0001t0002g0239 a0001c0001t0007g0174 a0001c0001t0007g0175 |
3 | HG02818.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.827-2346C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603950 | |||||||
| chr4:67603991 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.827-2305G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603991 | |||||||
| chr4:67604244 | A | G | 1 | a0001c0002t0001g0319 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.827-2052A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604244 | |||||||
| chr4:67604268 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.827-2028A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604268 | |||||||
| chr4:67604272 | A | G | 2 | a0001c0002t0002g0179 a0001c0002t0002g0188 |
2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.827-2024A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604272 | |||||||
| chr4:67604330 | G | C | 1 | a0001c0001t0003g0232 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.827-1966G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604330 | |||||||
| chr4:67604416 | T | C | 309 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(306): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.827-1880T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604416 | |||||||
| chr4:67604506 | T | A | 3 | a0001c0001t0002g0239 a0001c0001t0007g0174 a0001c0001t0007g0175 |
3 | HG02818.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.827-1790T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604506 | |||||||
| chr4:67604713 | G | C | 1 | a0001c0001t0002g0022 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.827-1583G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604713 | |||||||
| chr4:67604737 | T | C | 98 | a0001c0001t0001g0254 a0001c0001t0002g0001 a0001c0001t0002g0002 others(95): Show |
108 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.827-1559T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604737 | |||||||
| chr4:67604801 | T | C | 1 | a0001c0002t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.827-1495T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604801 | |||||||
| chr4:67604804 | T | C | 116 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(113): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.827-1492T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604804 | |||||||
| chr4:67604818 | TTC | T | 116 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(113): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.827-1472_827-1471d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67604818 | ||||||
| chr4:67604887 | T | G | 36 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0032 others(33): Show |
45 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.827-1409T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604887 | |||||||
| chr4:67605034 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.827-1262G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605034 | |||||||
| chr4:67605168 | T | A | 1 | a0001c0003t0001g0356 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.827-1128T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605168 | |||||||
| chr4:67605170 | A | T | 1 | a0001c0001t0001g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.827-1126A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605170 | |||||||
| chr4:67605295 | T | C | 3 | a0001c0001t0002g0239 a0001c0001t0007g0174 a0001c0001t0007g0175 |
3 | HG02818.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.827-1001T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605295 | |||||||
| chr4:67605334 | T | C | 317 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(314): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.827-962T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605334 | |||||||
| chr4:67605388 | C | CA | 119 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(116): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.827-893dupA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67605388 | ||||||
| chr4:67605388 | C | CAA | 204 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(201): Show |
225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.827-894_827-893dup others(2): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67605388 | ||||||
| chr4:67605481 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.827-815C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605481 | |||||||
| chr4:67605482 | G | A | 1 | a0001c0001t0002g0233 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.827-814G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605482 | |||||||
| chr4:67605825 | T | A | 1 | a0001c0001t0001g0243 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.827-471T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605825 | |||||||
| chr4:67605871 | T | C | 99 | a0001c0001t0001g0254 a0001c0001t0002g0001 a0001c0001t0002g0002 others(96): Show |
109 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.827-425T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605871 |