Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55620 |
| ensemblid | ENSG00000178078.12 |
| hgncid | 30430 |
| symbol | STAP2 |
| name | signal transducing adaptor family member 2 |
| refseq_nuc | NM_001013841.2 |
| refseq_prot | NP_001013863.1 |
| ensembl_nuc | ENST00000594605.6 |
| ensembl_prot | ENSP00000471052.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 4324043 |
| end | 4338827 |
| strand | - |
| ver | v1.2 |
| region | chr19:4324043-4338827 |
| region5000 | chr19:4319043-4343827 |
| regionname0 | STAP2_chr19_4324043_4338827 |
| regionname5000 | STAP2_chr19_4319043_4343827 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 403 | 256 | 71 | 49 | 97 | 8 | 30 | 71 | STAP2_chr19_4319043_4343827 | STAP2 | MASAL others(398): Show |
chr19 | 4319043 | 4343827 |
| a0002 | 1/0 | 403 | 127 | 24 | 28 | 54 | 6 | 14 | 36 | STAP2_chr19_4319043_4343827 | STAP2 | MASAL others(398): Show |
chr19 | 4319043 | 4343827 |
| a0003 | 0/0 | 168 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | MASAL others(163): Show |
chr19 | 4319043 | 4343827 |
| a0004 | 0/0 | 403 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | MASAL others(398): Show |
chr19 | 4319043 | 4343827 |
| a0005 | 0/0 | 403 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | MASAL others(398): Show |
chr19 | 4319043 | 4343827 |
| a0006 | 0/0 | 403 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | MASAL others(398): Show |
chr19 | 4319043 | 4343827 |
| a0007 | 0/0 | 403 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | MASAL others(398): Show |
chr19 | 4319043 | 4343827 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1209 | 200 | 51 | 35 | 84 | 7 | 22 | STAP2_chr19_4319043_4343827 | STAP2 | ATGGC others(1204): Show |
chr19 | 4319043 | 4343827 | ||
| a0001c0003 | 0/0 | 1209 | 56 | 20 | 14 | 13 | 1 | 8 | STAP2_chr19_4319043_4343827 | STAP2 | ATGGC others(1204): Show |
chr19 | 4319043 | 4343827 | ||
| a0002c0002 | 1/0 | 1209 | 118 | 24 | 26 | 48 | 6 | 13 | STAP2_chr19_4319043_4343827 | STAP2 | ATGGC others(1204): Show |
chr19 | 4319043 | 4343827 | ||
| a0002c0004 | 0/0 | 1209 | 5 | 0 | 1 | 3 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | ATGGC others(1204): Show |
chr19 | 4319043 | 4343827 | ||
| a0002c0005 | 0/0 | 1209 | 3 | 0 | 0 | 3 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | ATGGC others(1204): Show |
chr19 | 4319043 | 4343827 | ||
| a0002c0009 | 0/0 | 1209 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | ATGGC others(1204): Show |
chr19 | 4319043 | 4343827 | ||
| a0003c0008 | 0/0 | 1209 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | ATGGC others(1204): Show |
chr19 | 4319043 | 4343827 | ||
| a0004c0007 | 0/0 | 1209 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | ATGGC others(1204): Show |
chr19 | 4319043 | 4343827 | ||
| a0005c0011 | 0/0 | 1209 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | ATGGC others(1204): Show |
chr19 | 4319043 | 4343827 | ||
| a0006c0010 | 0/0 | 1209 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | ATGGC others(1204): Show |
chr19 | 4319043 | 4343827 | ||
| a0007c0006 | 0/0 | 1209 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | ATGGC others(1204): Show |
chr19 | 4319043 | 4343827 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1376 | 200 | 51 | 35 | 84 | 7 | 22 | STAP2_chr19_4319043_4343827 | STAP2 | CTGTT others(1371): Show |
chr19 | 4319043 | 4343827 |
| a0001c0003t0001 | 0/0 | 1376 | 52 | 17 | 14 | 13 | 1 | 7 | STAP2_chr19_4319043_4343827 | STAP2 | CTGTT others(1371): Show |
chr19 | 4319043 | 4343827 |
| a0001c0003t0002 | 0/0 | 1376 | 3 | 3 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | CTGTT others(1371): Show |
chr19 | 4319043 | 4343827 |
| a0001c0003t0003 | 0/0 | 1376 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | CTGTT others(1371): Show |
chr19 | 4319043 | 4343827 |
| a0002c0002t0001 | 1/0 | 1376 | 118 | 24 | 26 | 48 | 6 | 13 | STAP2_chr19_4319043_4343827 | STAP2 | CTGTT others(1371): Show |
chr19 | 4319043 | 4343827 |
| a0002c0004t0001 | 0/0 | 1376 | 5 | 0 | 1 | 3 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | CTGTT others(1371): Show |
chr19 | 4319043 | 4343827 |
| a0002c0005t0001 | 0/0 | 1376 | 3 | 0 | 0 | 3 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | CTGTT others(1371): Show |
chr19 | 4319043 | 4343827 |
| a0002c0009t0001 | 0/0 | 1376 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | CTGTT others(1371): Show |
chr19 | 4319043 | 4343827 |
| a0003c0008t0001 | 0/0 | 1376 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | CTGTT others(1371): Show |
chr19 | 4319043 | 4343827 |
| a0004c0007t0001 | 0/0 | 1376 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | CTGTT others(1371): Show |
chr19 | 4319043 | 4343827 |
| a0005c0011t0001 | 0/0 | 1376 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | CTGTT others(1371): Show |
chr19 | 4319043 | 4343827 |
| a0006c0010t0001 | 0/0 | 1376 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | CTGTT others(1371): Show |
chr19 | 4319043 | 4343827 |
| a0007c0006t0001 | 0/0 | 1376 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | CTGTT others(1371): Show |
chr19 | 4319043 | 4343827 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 37 | 2 | 3 | 31 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0002 | 0/0 | 13 | 0 | 5 | 2 | 0 | 6 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 0 | 1 | 3 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0014 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0012 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0001c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0003 | 0/0 | 11 | 0 | 11 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0004 | 0/0 | 10 | 0 | 2 | 4 | 0 | 4 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0005 | 0/0 | 9 | 0 | 0 | 6 | 2 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0011 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0017 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0004t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0004t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0005t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0005t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0002c0009t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0003c0008t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0004c0007t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0005c0011t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0006c0010t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| a0007c0006t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0134 | EUR | GBR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | GBR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | GBR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | FIN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | FIN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0185 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0132 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0024 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0024 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0183 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0157 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01109 | hp2 | a0002 | c0004 | t0001 | g0133 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0145 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0144 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0149 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0186 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0032 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0176 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0032 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0177 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01496 | hp2 | a0003 | c0008 | t0001 | g0187 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0235 | EUR | IBS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0055 | EUR | IBS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0152 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01981 | hp2 | a0002 | c0009 | t0001 | g0112 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0059 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0113 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0155 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0227 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0158 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | CDX | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0123 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0159 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02300 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0051 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0087 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0033 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0116 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0179 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0188 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0079 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0182 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0190 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0191 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0140 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0138 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0167 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03098 | hp2 | a0001 | c0003 | t0002 | g0168 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0154 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0141 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03486 | hp2 | a0004 | c0007 | t0001 | g0206 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0072 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0170 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0012 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0169 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | ESN | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0192 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03669 | hp1 | a0002 | c0004 | t0001 | g0125 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0061 | SAS | STU | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0031 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0099 | SAS | BEB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | STU | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0128 | SAS | BEB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG04199 | hp1 | a0001 | c0003 | t0003 | g0041 | SAS | STU | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0151 | SAS | STU | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | CHB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0236 | EAS | CHB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | YRI | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | YRI | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18939 | hp2 | a0005 | c0011 | t0001 | g0146 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0171 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18954 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18957 | hp1 | a0006 | c0010 | t0001 | g0127 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0184 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18970 | hp1 | a0007 | c0006 | t0001 | g0108 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18972 | hp1 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0178 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18974 | hp2 | a0002 | c0004 | t0001 | g0027 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18999 | hp2 | a0002 | c0005 | t0001 | g0111 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19003 | hp2 | a0002 | c0005 | t0001 | g0110 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19007 | hp1 | a0002 | c0004 | t0001 | g0238 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0081 | AFR | LWK | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | LWK | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19059 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19059 | hp2 | a0002 | c0004 | t0001 | g0027 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19068 | hp2 | a0001 | c0003 | t0001 | g0174 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19089 | hp1 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19089 | hp2 | a0002 | c0005 | t0001 | g0062 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0053 | AFR | YRI | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | YRI | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0189 | AFR | ASW | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0117 | EUR | TSI | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0118 | EUR | TSI | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0160 | SAS | GIH | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0019 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0019 | AFR | ACB | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0153 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | USA | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0019 | AFR | USA | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | LWK | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0082 | REF | REF | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0105 | REF | REF | STAP2_chr19_4319043_4343827 | STAP2 | chr19 | 4319043 | 4343827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4327384 | T | C | 1 | a0006 | 1 | NA18957.hp1 | missense_variant&splice_region_variant | MODERATE | c.592A>G | p.Thr198Ala | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 7/13 | 666/1376 | 592/1212 | 198/403 | chr19 | 4327384 | |||
| chr19:4328706 | C | G | 1 | a0004 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.559G>C | p.Val187Leu | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/13 | 633/1376 | 559/1212 | 187/403 | chr19 | 4328706 | |||
| chr19:4328758 | G | C | 1 | a0003 | 1 | HG01496.hp2 | stop_gained | HIGH | c.507C>G | p.Tyr169* | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/13 | 581/1376 | 507/1212 | 169/403 | chr19 | 4328758 | |||
| chr19:4333714 | C | T | 4 | a0001 a0003 a0004 others(1): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
missense_variant | MODERATE | c.277G>A | p.Asp93Asn | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/13 | 351/1376 | 277/1212 | 93/403 | chr19 | 4333714 | |||
| chr19:4333716 | C | T | 1 | a0007 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.275G>A | p.Arg92Gln | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/13 | 349/1376 | 275/1212 | 92/403 | chr19 | 4333716 | |||
| chr19:4333992 | T | A | 1 | a0005 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.155A>T | p.Asn52Ile | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 2/13 | 229/1376 | 155/1212 | 52/403 | chr19 | 4333992 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4325436 | G | A | 4 | a0001c0001 a0002c0004 a0004c0007 others(1): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
synonymous_variant | LOW | c.939C>T | p.Pro313Pro | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 10/13 | 1013/1376 | 939/1212 | 313/403 | chr19 | 4325436 | |||
| chr19:4325454 | T | C | 1 | a0002c0005 | 3 | NA18999.hp2 NA19003.hp2 NA19089.hp2 |
synonymous_variant | LOW | c.921A>G | p.Glu307Glu | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 10/13 | 995/1376 | 921/1212 | 307/403 | chr19 | 4325454 | |||
| chr19:4325514 | C | T | 1 | a0002c0009 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.861G>A | p.Pro287Pro | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 10/13 | 935/1376 | 861/1212 | 287/403 | chr19 | 4325514 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4324085 | G | A | 1 | a0001c0003t0002 | 3 | HG02572.hp1 HG03098.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*48C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 13/13 | 48 | chr19 | 4324085 | ||||||
| chr19:4338815 | A | G | 1 | a0001c0003t0003 | 1 | HG04199.hp1 | 5_prime_UTR_variant | MODIFIER | c.-62T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/13 | 62 | chr19 | 4338815 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4324285 | G | C | 1 | a0001c0001t0001g0245 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1148-88C>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 12/12 | chr19 | 4324285 | |||||||
| chr19:4324366 | A | T | 8 | a0001c0003t0001g0185 a0001c0003t0001g0186 a0001c0003t0001g0188 others(5): Show |
8 | HG00642.hp1 HG01175.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1147+89T>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 12/12 | chr19 | 4324366 | |||||||
| chr19:4324393 | G | C | 5 | a0001c0003t0001g0019 a0001c0003t0001g0033 a0001c0003t0001g0190 others(2): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1147+62C>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 12/12 | chr19 | 4324393 | |||||||
| chr19:4324410 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1147+45G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 12/12 | chr19 | 4324410 | |||||||
| chr19:4324567 | C | T | 31 | a0001c0003t0001g0012 a0001c0003t0001g0019 a0001c0003t0001g0030 others(28): Show |
40 | HG01099.hp1 HG01256.hp1 HG01257.hp1 others(37): Show |
intron_variant | MODIFIER | c.1073-38G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4324567 | |||||||
| chr19:4324693 | G | A | 5 | a0001c0003t0001g0079 a0001c0003t0001g0081 a0001c0003t0001g0087 others(2): Show |
5 | HG02615.hp1 HG02818.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073-164C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4324693 | |||||||
| chr19:4324817 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1073-288G>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4324817 | |||||||
| chr19:4324862 | C | T | 5 | a0001c0003t0001g0079 a0001c0003t0001g0081 a0001c0003t0001g0087 others(2): Show |
5 | HG02615.hp1 HG02818.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073-333G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4324862 | |||||||
| chr19:4324884 | C | A | 1 | a0001c0003t0001g0175 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1072+332G>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4324884 | |||||||
| chr19:4324889 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG00738.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1072+327G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4324889 | |||||||
| chr19:4324909 | C | T | 1 | a0002c0002t0001g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1072+307G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4324909 | |||||||
| chr19:4324910 | G | A | 13 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0092 others(10): Show |
15 | HG00140.hp1 HG00639.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1072+306C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4324910 | |||||||
| chr19:4324917 | G | A | 5 | a0001c0003t0001g0079 a0001c0003t0001g0081 a0001c0003t0001g0087 others(2): Show |
5 | HG02615.hp1 HG02818.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1072+299C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4324917 | |||||||
| chr19:4325008 | G | T | 5 | a0001c0003t0001g0185 a0001c0003t0001g0186 a0001c0003t0001g0188 others(2): Show |
5 | HG00642.hp1 HG01175.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1072+208C>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4325008 | |||||||
| chr19:4325027 | T | C | 1 | a0001c0003t0001g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1072+189A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4325027 | |||||||
| chr19:4325035 | A | G | 3 | a0001c0003t0002g0051 a0001c0003t0002g0053 a0001c0003t0002g0168 |
3 | HG02572.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1072+181T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4325035 | |||||||
| chr19:4325118 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(103): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1072+98C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4325118 | |||||||
| chr19:4325136 | CA | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1072+79delT | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4325136 | |||||||
| chr19:4325136 | CAA | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(41): Show |
93 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1072+78_1072+79del others(2): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4325136 | |||||||
| chr19:4325160 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1072+56C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 11/12 | chr19 | 4325160 | |||||||
| chr19:4325330 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(118): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.980-22C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 10/12 | chr19 | 4325330 | |||||||
| chr19:4325381 | C | CTGTTCCC others(17): Show |
1 | a0001c0003t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.970_979+14dupAACCA others(19): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 10/12 | chr19 | 4325381 | |||||||
| chr19:4325550 | T | A | 3 | a0002c0002t0001g0009 a0002c0002t0001g0069 a0002c0002t0001g0071 |
7 | HG00735.hp1 HG02257.hp1 HG02647.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.830-5A>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4325550 | |||||||
| chr19:4325625 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.830-80A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4325625 | |||||||
| chr19:4325635 | C | T | 13 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0092 others(10): Show |
15 | HG00140.hp1 HG00639.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.830-90G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4325635 | |||||||
| chr19:4325699 | G | A | 1 | a0002c0002t0001g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.830-154C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4325699 | |||||||
| chr19:4325968 | C | CA | 8 | a0001c0001t0001g0089 a0001c0001t0001g0211 a0001c0003t0001g0186 others(5): Show |
8 | HG01175.hp2 HG01496.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.830-424dupT | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4325968 | |||||||
| chr19:4325968 | CA | C | 14 | a0001c0001t0001g0103 a0001c0001t0001g0198 a0001c0001t0001g0200 others(11): Show |
14 | HG00099.hp1 HG00544.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.830-424delT | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4325968 | |||||||
| chr19:4326053 | C | G | 5 | a0001c0003t0001g0079 a0001c0003t0001g0081 a0001c0003t0001g0087 others(2): Show |
5 | HG02615.hp1 HG02818.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.830-508G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326053 | |||||||
| chr19:4326060 | G | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(213): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.830-515C>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326060 | |||||||
| chr19:4326081 | G | A | 1 | a0002c0002t0001g0124 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.830-536C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326081 | |||||||
| chr19:4326136 | G | A | 5 | a0001c0003t0001g0079 a0001c0003t0001g0081 a0001c0003t0001g0087 others(2): Show |
5 | HG02615.hp1 HG02818.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.830-591C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326136 | |||||||
| chr19:4326242 | T | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(108): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.830-697A>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326242 | |||||||
| chr19:4326316 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.829+626T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326316 | |||||||
| chr19:4326488 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.829+454T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326488 | |||||||
| chr19:4326520 | G | A | 5 | a0001c0003t0001g0019 a0001c0003t0001g0033 a0001c0003t0001g0190 others(2): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.829+422C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326520 | |||||||
| chr19:4326549 | TGTCC | T | 4 | a0002c0002t0001g0070 a0002c0002t0001g0071 a0002c0002t0001g0123 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.829+389_829+392del others(4): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326549 | |||||||
| chr19:4326553 | C | T | 4 | a0001c0001t0001g0080 a0001c0003t0001g0081 a0001c0003t0001g0153 others(1): Show |
4 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.829+389G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326553 | |||||||
| chr19:4326577 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.829+365A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326577 | |||||||
| chr19:4326668 | G | A | 4 | a0001c0001t0001g0080 a0001c0003t0001g0081 a0001c0003t0001g0153 others(1): Show |
4 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.829+274C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326668 | |||||||
| chr19:4326678 | C | T | 1 | a0001c0003t0001g0167 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.829+264G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326678 | |||||||
| chr19:4326683 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.829+259G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326683 | |||||||
| chr19:4326722 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.829+220G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326722 | |||||||
| chr19:4326784 | A | C | 18 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0092 others(15): Show |
19 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.829+158T>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326784 | |||||||
| chr19:4326803 | A | G | 1 | a0002c0002t0001g0136 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.829+139T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326803 | |||||||
| chr19:4326865 | C | T | 1 | a0001c0003t0001g0190 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.829+77G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326865 | |||||||
| chr19:4326901 | C | G | 21 | a0001c0003t0001g0012 a0001c0003t0001g0030 a0001c0003t0001g0031 others(18): Show |
27 | HG01099.hp1 HG01256.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.829+41G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 9/12 | chr19 | 4326901 | |||||||
| chr19:4327079 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.763+45C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 8/12 | chr19 | 4327079 | |||||||
| chr19:4327567 | TCCCGGAG others(11): Show |
T | 1 | a0001c0003t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.591-200_591-183del others(18): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4327567 | |||||||
| chr19:4327781 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.591-396C>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4327781 | |||||||
| chr19:4327879 | C | T | 4 | a0002c0002t0001g0059 a0002c0002t0001g0121 a0002c0002t0001g0122 others(1): Show |
4 | HG00544.hp1 HG02004.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.591-494G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4327879 | |||||||
| chr19:4327890 | G | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0214 a0001c0001t0001g0247 others(1): Show |
5 | HG00639.hp2 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.591-505C>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4327890 | |||||||
| chr19:4328008 | T | A | 4 | a0001c0001t0001g0080 a0001c0003t0001g0081 a0001c0003t0001g0153 others(1): Show |
4 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.591-623A>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4328008 | |||||||
| chr19:4328047 | C | T | 23 | a0001c0003t0001g0012 a0001c0003t0001g0030 a0001c0003t0001g0031 others(20): Show |
29 | HG01099.hp1 HG01256.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.590+628G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4328047 | |||||||
| chr19:4328052 | C | T | 1 | a0002c0002t0001g0141 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.590+623G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4328052 | |||||||
| chr19:4328281 | G | T | 3 | a0002c0005t0001g0062 a0002c0005t0001g0110 a0002c0005t0001g0111 |
3 | NA18999.hp2 NA19003.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.590+394C>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4328281 | |||||||
| chr19:4328377 | C | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0020 others(31): Show |
55 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.590+298G>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4328377 | |||||||
| chr19:4328409 | T | TCGCCCAG others(57): Show |
1 | a0001c0003t0001g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.590+202_590+265dup others(64): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4328409 | |||||||
| chr19:4328418 | CCAGCTCT others(57): Show |
C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(86): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.590+193_590+256del others(64): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4328418 | |||||||
| chr19:4328516 | A | G | 23 | a0001c0003t0001g0012 a0001c0003t0001g0030 a0001c0003t0001g0031 others(20): Show |
29 | HG01099.hp1 HG01256.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.590+159T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4328516 | |||||||
| chr19:4328542 | G | C | 6 | a0001c0001t0001g0080 a0001c0003t0001g0081 a0001c0003t0001g0153 others(3): Show |
6 | HG01109.hp1 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.590+133C>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4328542 | |||||||
| chr19:4328575 | A | G | 4 | a0001c0001t0001g0080 a0001c0003t0001g0081 a0001c0003t0001g0153 others(1): Show |
4 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.590+100T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4328575 | |||||||
| chr19:4328605 | G | C | 1 | a0001c0003t0002g0168 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.590+70C>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4328605 | |||||||
| chr19:4328619 | G | A | 1 | a0001c0003t0001g0167 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.590+56C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4328619 | |||||||
| chr19:4328662 | C | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0049 others(11): Show |
18 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.590+13G>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 6/12 | chr19 | 4328662 | |||||||
| chr19:4328840 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.456-31G>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4328840 | |||||||
| chr19:4328863 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(144): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.456-54A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4328863 | |||||||
| chr19:4328924 | C | T | 1 | a0002c0002t0001g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.456-115G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4328924 | |||||||
| chr19:4329007 | G | GT | 6 | a0001c0001t0001g0006 a0001c0001t0001g0065 a0001c0001t0001g0075 others(3): Show |
11 | HG02109.hp1 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.456-199dupA | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329007 | |||||||
| chr19:4329009 | T | G | 1 | a0001c0003t0001g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.456-200A>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329009 | |||||||
| chr19:4329110 | C | G | 2 | a0001c0003t0001g0176 a0001c0003t0001g0177 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.456-301G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329110 | |||||||
| chr19:4329171 | G | C | 19 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0021 others(16): Show |
29 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.456-362C>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329171 | |||||||
| chr19:4329172 | T | C | 19 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0021 others(16): Show |
29 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.456-363A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329172 | |||||||
| chr19:4329177 | C | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0021 others(16): Show |
29 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.456-368G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329177 | |||||||
| chr19:4329185 | A | G | 19 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0021 others(16): Show |
29 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.456-376T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329185 | |||||||
| chr19:4329192 | C | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0021 others(16): Show |
29 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.456-383G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329192 | |||||||
| chr19:4329193 | T | G | 19 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0021 others(16): Show |
29 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.456-384A>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329193 | |||||||
| chr19:4329198 | C | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0021 others(16): Show |
29 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.456-389G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329198 | |||||||
| chr19:4329343 | A | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0246 |
2 | HG00438.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.456-534T>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329343 | |||||||
| chr19:4329349 | C | G | 1 | a0001c0003t0001g0167 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.456-540G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329349 | |||||||
| chr19:4329380 | C | A | 4 | a0001c0001t0001g0080 a0001c0003t0001g0081 a0001c0003t0001g0153 others(1): Show |
4 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-571G>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329380 | |||||||
| chr19:4329420 | G | T | 1 | a0001c0003t0001g0171 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.455+541C>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329420 | |||||||
| chr19:4329440 | A | T | 2 | a0002c0002t0001g0029 a0002c0002t0001g0138 |
3 | HG02965.hp2 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.455+521T>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329440 | |||||||
| chr19:4329512 | A | G | 1 | a0002c0002t0001g0137 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.455+449T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329512 | |||||||
| chr19:4329788 | TC | T | 5 | a0001c0001t0001g0080 a0001c0003t0001g0081 a0001c0003t0001g0153 others(2): Show |
5 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.455+172delG | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329788 | |||||||
| chr19:4329814 | T | C | 1 | a0001c0003t0001g0175 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.455+147A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329814 | |||||||
| chr19:4329820 | T | C | 1 | a0002c0002t0001g0155 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.455+141A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 5/12 | chr19 | 4329820 | |||||||
| chr19:4330198 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.355-137C>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330198 | |||||||
| chr19:4330268 | C | T | 4 | a0001c0001t0001g0080 a0001c0003t0001g0081 a0001c0003t0001g0153 others(1): Show |
4 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-207G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330268 | |||||||
| chr19:4330279 | G | T | 1 | a0001c0003t0001g0175 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.355-218C>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330279 | |||||||
| chr19:4330286 | C | T | 4 | a0001c0001t0001g0080 a0001c0003t0001g0081 a0001c0003t0001g0153 others(1): Show |
4 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-225G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330286 | |||||||
| chr19:4330350 | G | A | 1 | a0001c0003t0001g0171 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.355-289C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330350 | |||||||
| chr19:4330381 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.355-320C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330381 | |||||||
| chr19:4330492 | C | T | 6 | a0001c0003t0001g0185 a0001c0003t0001g0186 a0001c0003t0001g0188 others(3): Show |
6 | HG00642.hp1 HG01106.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.355-431G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330492 | |||||||
| chr19:4330518 | G | A | 1 | a0001c0003t0001g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.355-457C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330518 | |||||||
| chr19:4330523 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.355-462G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330523 | |||||||
| chr19:4330532 | A | C | 4 | a0001c0001t0001g0080 a0001c0003t0001g0081 a0001c0003t0001g0153 others(1): Show |
4 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-471T>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330532 | |||||||
| chr19:4330540 | C | CA | 14 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0219 others(11): Show |
14 | HG01255.hp2 HG03098.hp2 HG03688.hp1 others(11): Show |
intron_variant | MODIFIER | c.355-480dupT | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330540 | |||||||
| chr19:4330565 | T | C | 6 | a0001c0003t0001g0185 a0001c0003t0001g0186 a0001c0003t0001g0188 others(3): Show |
6 | HG00642.hp1 HG01106.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.355-504A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330565 | |||||||
| chr19:4330639 | T | C | 4 | a0001c0001t0001g0080 a0001c0003t0001g0081 a0001c0003t0001g0153 others(1): Show |
4 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-578A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330639 | |||||||
| chr19:4330689 | G | A | 4 | a0001c0001t0001g0080 a0001c0003t0001g0081 a0001c0003t0001g0153 others(1): Show |
4 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-628C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330689 | |||||||
| chr19:4330711 | A | AT | 58 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(55): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.355-651dupA | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330711 | |||||||
| chr19:4330711 | AT | A | 28 | a0001c0001t0001g0013 a0001c0001t0001g0038 a0001c0001t0001g0050 others(25): Show |
33 | HG00323.hp1 HG00544.hp2 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.355-651delA | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330711 | |||||||
| chr19:4330871 | C | T | 1 | a0002c0005t0001g0110 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.355-810G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4330871 | |||||||
| chr19:4331003 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(172): Show |
279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.355-942T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331003 | |||||||
| chr19:4331040 | C | T | 22 | a0001c0003t0001g0012 a0001c0003t0001g0030 a0001c0003t0001g0031 others(19): Show |
28 | HG01099.hp1 HG01256.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.355-979G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331040 | |||||||
| chr19:4331069 | T | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0020 others(33): Show |
57 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.354+953A>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331069 | |||||||
| chr19:4331077 | C | T | 4 | a0001c0001t0001g0080 a0001c0003t0001g0081 a0001c0003t0001g0153 others(1): Show |
4 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+945G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331077 | |||||||
| chr19:4331119 | C | T | 8 | a0002c0002t0001g0009 a0002c0002t0001g0029 a0002c0002t0001g0048 others(5): Show |
13 | HG00735.hp1 HG01256.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.354+903G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331119 | |||||||
| chr19:4331121 | G | C | 2 | a0001c0003t0002g0053 a0001c0003t0002g0168 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.354+901C>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331121 | |||||||
| chr19:4331172 | A | T | 1 | a0001c0001t0001g0075 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.354+850T>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331172 | |||||||
| chr19:4331188 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.354+834C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331188 | |||||||
| chr19:4331213 | C | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0203 |
4 | HG02630.hp2 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+809G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331213 | |||||||
| chr19:4331505 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.354+517G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331505 | |||||||
| chr19:4331564 | A | G | 1 | a0001c0001t0001g0241 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.354+458T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331564 | |||||||
| chr19:4331623 | C | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0021 others(19): Show |
32 | HG00423.hp1 HG00558.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.354+399G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331623 | |||||||
| chr19:4331624 | T | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0021 others(19): Show |
32 | HG00423.hp1 HG00558.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.354+398A>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331624 | |||||||
| chr19:4331624 | T | C | 1 | a0002c0002t0001g0131 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.354+398A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331624 | |||||||
| chr19:4331659 | C | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(165): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.354+363G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331659 | |||||||
| chr19:4331707 | T | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0021 others(19): Show |
32 | HG00423.hp1 HG00558.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.354+315A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331707 | |||||||
| chr19:4331718 | T | G | 22 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0021 others(19): Show |
32 | HG00423.hp1 HG00558.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.354+304A>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331718 | |||||||
| chr19:4331943 | AAAAG | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(74): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.354+75_354+78delCT others(2): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 4/12 | chr19 | 4331943 | |||||||
| chr19:4332108 | A | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(70): Show |
132 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.298-30T>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332108 | |||||||
| chr19:4332193 | C | T | 1 | a0001c0003t0001g0175 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.298-115G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332193 | |||||||
| chr19:4332196 | C | CT | 17 | a0001c0001t0001g0248 a0001c0003t0001g0030 a0001c0003t0001g0031 others(14): Show |
20 | HG01099.hp1 HG01256.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.298-119dupA | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332196 | |||||||
| chr19:4332196 | C | T | 1 | a0001c0003t0001g0175 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.298-118G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332196 | |||||||
| chr19:4332196 | CT | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(97): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.298-119delA | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332196 | |||||||
| chr19:4332196 | CTT | C | 29 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0098 others(26): Show |
33 | HG00099.hp1 HG00642.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.298-120_298-119del others(2): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332196 | |||||||
| chr19:4332196 | CTTT | C | 4 | a0001c0003t0001g0019 a0001c0003t0001g0033 a0001c0003t0001g0190 others(1): Show |
7 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-121_298-119del others(3): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332196 | |||||||
| chr19:4332196 | CTTTTTTT others(3): Show |
C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(60): Show |
121 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.298-128_298-119del others(10): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332196 | |||||||
| chr19:4332196 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0001g0086 a0001c0001t0001g0148 a0001c0001t0001g0237 others(3): Show |
6 | HG01167.hp2 HG02615.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-129_298-119del others(11): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332196 | |||||||
| chr19:4332196 | CTTTTTTT others(6): Show |
C | 1 | a0001c0003t0002g0168 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.298-131_298-119del others(13): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332196 | |||||||
| chr19:4332197 | T | A | 1 | a0002c0002t0001g0016 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.298-119A>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332197 | |||||||
| chr19:4332247 | G | A | 1 | a0002c0002t0001g0161 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.298-169C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332247 | |||||||
| chr19:4332653 | G | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(70): Show |
132 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.298-575C>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332653 | |||||||
| chr19:4332666 | G | C | 5 | a0002c0002t0001g0029 a0002c0002t0001g0137 a0002c0002t0001g0138 others(2): Show |
6 | HG01884.hp2 HG02723.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-588C>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332666 | |||||||
| chr19:4332752 | C | T | 1 | a0002c0004t0001g0027 | 2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.298-674G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332752 | |||||||
| chr19:4332760 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0075 a0001c0001t0001g0076 |
8 | HG02109.hp1 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.298-682G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4332760 | |||||||
| chr19:4333021 | C | G | 1 | a0001c0001t0001g0220 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.297+673G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333021 | |||||||
| chr19:4333063 | G | A | 1 | a0002c0002t0001g0107 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.297+631C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333063 | |||||||
| chr19:4333082 | C | T | 20 | a0001c0003t0001g0012 a0001c0003t0001g0030 a0001c0003t0001g0031 others(17): Show |
26 | HG01099.hp1 HG01256.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.297+612G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333082 | |||||||
| chr19:4333178 | G | A | 1 | a0001c0003t0001g0087 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.297+516C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333178 | |||||||
| chr19:4333212 | C | T | 5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+482G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333212 | |||||||
| chr19:4333232 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.297+462G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333232 | |||||||
| chr19:4333268 | G | T | 3 | a0002c0002t0001g0157 a0002c0002t0001g0158 a0002c0002t0001g0159 |
3 | HG01106.hp2 HG02148.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.297+426C>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333268 | |||||||
| chr19:4333302 | A | G | 3 | a0002c0005t0001g0062 a0002c0005t0001g0110 a0002c0005t0001g0111 |
3 | NA18999.hp2 NA19003.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.297+392T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333302 | |||||||
| chr19:4333353 | A | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.297+341T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333353 | |||||||
| chr19:4333368 | C | T | 1 | a0001c0003t0001g0190 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.297+326G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333368 | |||||||
| chr19:4333450 | C | T | 1 | a0002c0002t0001g0109 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.297+244G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333450 | |||||||
| chr19:4333451 | G | A | 1 | a0002c0002t0001g0141 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.297+243C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333451 | |||||||
| chr19:4333506 | TAATAA | T | 3 | a0001c0001t0001g0201 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | HG02074.hp2 NA18972.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.297+183_297+187del others(5): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333506 | |||||||
| chr19:4333563 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.297+131G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333563 | |||||||
| chr19:4333628 | G | A | 36 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0040 others(33): Show |
44 | HG00639.hp2 HG00642.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.297+66C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333628 | |||||||
| chr19:4333669 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(71): Show |
133 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.297+25A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 3/12 | chr19 | 4333669 | |||||||
| chr19:4333899 | C | T | 1 | a0002c0002t0001g0107 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.174+74G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 2/12 | chr19 | 4333899 | |||||||
| chr19:4333967 | C | T | 1 | a0002c0002t0001g0106 | 1 | HG01978.hp2 | splice_region_variant&intron_variant | LOW | c.174+6G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 2/12 | chr19 | 4333967 | |||||||
| chr19:4334246 | G | T | 1 | a0005c0011t0001g0146 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.103-202C>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334246 | |||||||
| chr19:4334313 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
134 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.103-269G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334313 | |||||||
| chr19:4334322 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-278T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334322 | |||||||
| chr19:4334379 | T | A | 1 | a0005c0011t0001g0146 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.103-335A>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334379 | |||||||
| chr19:4334394 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0075 a0001c0001t0001g0076 |
8 | HG02109.hp1 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-350G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334394 | |||||||
| chr19:4334405 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(108): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.103-361G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334405 | |||||||
| chr19:4334414 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0200 |
3 | HG01243.hp2 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.103-370A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334414 | |||||||
| chr19:4334659 | G | A | 1 | a0001c0003t0003g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.103-615C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334659 | |||||||
| chr19:4334809 | T | TCATCCAT others(99): Show |
1 | a0002c0002t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.103-766_103-765ins others(106): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334809 | |||||||
| chr19:4334809 | T | TCATCCAT others(115): Show |
196 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(193): Show |
312 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.103-766_103-765ins others(122): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334809 | |||||||
| chr19:4334809 | T | TCATCCAT others(115): Show |
1 | a0001c0001t0001g0200 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.103-766_103-765ins others(122): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334809 | |||||||
| chr19:4334809 | T | TCATCCAT others(115): Show |
1 | a0001c0001t0001g0207 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.103-766_103-765ins others(122): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334809 | |||||||
| chr19:4334809 | T | TCATCCAT others(115): Show |
10 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
13 | HG02559.hp1 HG02572.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.103-766_103-765ins others(122): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334809 | |||||||
| chr19:4334816 | T | TCCATTCA others(99): Show |
36 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0020 others(33): Show |
57 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.103-773_103-772ins others(106): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334816 | |||||||
| chr19:4334817 | C | CCATTCAT others(115): Show |
1 | a0001c0003t0002g0168 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.103-774_103-773ins others(122): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334817 | |||||||
| chr19:4334953 | ATCATCCA others(9): Show |
A | 3 | a0001c0001t0001g0101 a0001c0003t0001g0144 a0001c0003t0001g0145 |
3 | HG00280.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.103-925_103-910del others(16): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4334953 | |||||||
| chr19:4335022 | C | G | 1 | a0001c0003t0001g0167 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.103-978G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335022 | |||||||
| chr19:4335115 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.103-1071G>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335115 | |||||||
| chr19:4335165 | C | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0057 a0001c0001t0001g0068 others(2): Show |
10 | HG00280.hp1 HG00735.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-1121G>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335165 | |||||||
| chr19:4335191 | ATCCATCA others(20): Show |
A | 1 | a0001c0003t0002g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.103-1174_103-1148d others(29): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335191 | |||||||
| chr19:4335247 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.103-1203G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335247 | |||||||
| chr19:4335364 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.103-1320G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335364 | |||||||
| chr19:4335410 | C | T | 1 | a0004c0007t0001g0206 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.103-1366G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335410 | |||||||
| chr19:4335439 | C | T | 1 | a0002c0002t0001g0026 | 2 | NA18993.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.103-1395G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335439 | |||||||
| chr19:4335489 | C | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(58): Show |
92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.103-1445G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335489 | |||||||
| chr19:4335505 | C | G | 1 | a0001c0001t0001g0074 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.103-1461G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335505 | |||||||
| chr19:4335507 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.103-1463G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335507 | |||||||
| chr19:4335516 | T | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(63): Show |
120 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.103-1472A>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335516 | |||||||
| chr19:4335559 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(58): Show |
92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.103-1515G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335559 | |||||||
| chr19:4335748 | C | G | 1 | a0001c0001t0001g0074 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.103-1704G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335748 | |||||||
| chr19:4335836 | T | C | 1 | a0002c0002t0001g0143 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.103-1792A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335836 | |||||||
| chr19:4335872 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(78): Show |
138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.103-1828C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335872 | |||||||
| chr19:4335978 | T | C | 1 | a0001c0003t0002g0168 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.103-1934A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4335978 | |||||||
| chr19:4336158 | C | G | 1 | a0001c0003t0002g0168 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.103-2114G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336158 | |||||||
| chr19:4336270 | C | T | 10 | a0001c0003t0001g0019 a0001c0003t0001g0033 a0001c0003t0001g0185 others(7): Show |
13 | HG00642.hp1 HG01175.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.103-2226G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336270 | |||||||
| chr19:4336275 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.103-2231T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336275 | |||||||
| chr19:4336295 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.103-2251C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336295 | |||||||
| chr19:4336314 | C | CT | 62 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): Show |
109 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.103-2271dupA | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336314 | |||||||
| chr19:4336314 | C | CTT | 31 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0040 others(28): Show |
38 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.103-2272_103-2271d others(4): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336314 | |||||||
| chr19:4336314 | C | CTTT | 7 | a0001c0001t0001g0197 a0001c0001t0001g0248 a0001c0003t0001g0019 others(4): Show |
9 | HG02145.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.103-2273_103-2271d others(5): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336314 | |||||||
| chr19:4336336 | T | G | 1 | a0002c0002t0001g0162 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.103-2292A>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336336 | |||||||
| chr19:4336374 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(98): Show |
164 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.102+2278C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336374 | |||||||
| chr19:4336381 | C | T | 1 | a0001c0003t0002g0168 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.102+2271G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336381 | |||||||
| chr19:4336382 | C | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(69): Show |
126 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.102+2270G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336382 | |||||||
| chr19:4336399 | A | AC | 15 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(12): Show |
16 | HG00673.hp2 HG02055.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.102+2252dupG | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336399 | |||||||
| chr19:4336401 | C | A | 2 | a0001c0003t0001g0144 a0001c0003t0001g0145 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.102+2251G>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336401 | |||||||
| chr19:4336521 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.102+2131G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336521 | |||||||
| chr19:4336722 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0200 |
3 | HG01243.hp2 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.102+1930G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336722 | |||||||
| chr19:4336730 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.102+1922C>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336730 | |||||||
| chr19:4336805 | T | G | 1 | a0001c0001t0001g0242 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.102+1847A>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336805 | |||||||
| chr19:4336911 | A | G | 2 | a0002c0002t0001g0058 a0002c0002t0001g0059 |
2 | HG02004.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.102+1741T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4336911 | |||||||
| chr19:4337028 | T | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(79): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.102+1624A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337028 | |||||||
| chr19:4337146 | C | G | 2 | a0001c0003t0001g0169 a0001c0003t0001g0170 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.102+1506G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337146 | |||||||
| chr19:4337420 | C | T | 5 | a0001c0003t0001g0019 a0001c0003t0001g0033 a0001c0003t0001g0190 others(2): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.102+1232G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337420 | |||||||
| chr19:4337484 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(100): Show |
166 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.102+1168T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337484 | |||||||
| chr19:4337495 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.102+1157C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337495 | |||||||
| chr19:4337548 | C | CA | 10 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0150 others(7): Show |
10 | HG00738.hp1 HG01175.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.102+1103dupT | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337548 | |||||||
| chr19:4337548 | CA | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(91): Show |
157 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.102+1103delT | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337548 | |||||||
| chr19:4337581 | T | G | 2 | a0001c0003t0001g0153 a0001c0003t0001g0154 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.102+1071A>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337581 | |||||||
| chr19:4337661 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.102+991T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337661 | |||||||
| chr19:4337673 | A | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(101): Show |
167 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.102+979T>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337673 | |||||||
| chr19:4337713 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(79): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.102+939G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337713 | |||||||
| chr19:4337714 | G | A | 2 | a0001c0003t0001g0153 a0001c0003t0001g0154 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.102+938C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337714 | |||||||
| chr19:4337738 | G | A | 8 | a0002c0002t0001g0018 a0002c0002t0001g0155 a0002c0002t0001g0156 others(5): Show |
10 | HG00741.hp1 HG01106.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.102+914C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337738 | |||||||
| chr19:4337750 | C | T | 1 | a0002c0002t0001g0055 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.102+902G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337750 | |||||||
| chr19:4337758 | G | A | 1 | a0001c0003t0002g0168 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.102+894C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337758 | |||||||
| chr19:4337775 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(103): Show |
169 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.102+877A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337775 | |||||||
| chr19:4337847 | T | C | 5 | a0001c0003t0001g0019 a0001c0003t0001g0033 a0001c0003t0001g0190 others(2): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.102+805A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337847 | |||||||
| chr19:4337859 | A | T | 2 | a0001c0003t0001g0169 a0001c0003t0001g0170 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.102+793T>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337859 | |||||||
| chr19:4337887 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.102+765C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4337887 | |||||||
| chr19:4338063 | G | A | 1 | a0001c0003t0002g0168 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.102+589C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338063 | |||||||
| chr19:4338120 | G | GCA | 33 | a0001c0003t0001g0012 a0001c0003t0001g0019 a0001c0003t0001g0030 others(30): Show |
42 | HG00642.hp1 HG01099.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.102+530_102+531dup others(2): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338120 | |||||||
| chr19:4338120 | G | GCACA | 68 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(65): Show |
121 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.102+528_102+531dup others(4): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338120 | |||||||
| chr19:4338120 | G | GCACACA | 3 | a0001c0001t0001g0040 a0001c0001t0001g0247 a0001c0001t0001g0248 |
4 | HG00639.hp2 HG02818.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+526_102+531dup others(6): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338120 | |||||||
| chr19:4338176 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(64): Show |
121 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.102+476T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338176 | |||||||
| chr19:4338187 | G | A | 1 | a0002c0002t0001g0166 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.102+465C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338187 | |||||||
| chr19:4338264 | G | A | 20 | a0001c0003t0001g0012 a0001c0003t0001g0030 a0001c0003t0001g0031 others(17): Show |
26 | HG01099.hp1 HG01256.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.102+388C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338264 | |||||||
| chr19:4338264 | G | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+388C>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338264 | |||||||
| chr19:4338304 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(100): Show |
166 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.102+348T>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338304 | |||||||
| chr19:4338326 | T | C | 10 | a0001c0003t0001g0019 a0001c0003t0001g0033 a0001c0003t0001g0185 others(7): Show |
13 | HG00642.hp1 HG01175.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.102+326A>G | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338326 | |||||||
| chr19:4338364 | C | G | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0052 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+288G>C | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338364 | |||||||
| chr19:4338419 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(95): Show |
161 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.102+233C>T | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338419 | |||||||
| chr19:4338483 | C | T | 1 | a0002c0002t0001g0048 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.102+169G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338483 | |||||||
| chr19:4338528 | C | T | 6 | a0002c0002t0001g0015 a0002c0002t0001g0043 a0002c0002t0001g0044 others(3): Show |
8 | HG02132.hp1 NA18939.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.102+124G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338528 | |||||||
| chr19:4338558 | C | T | 1 | a0001c0003t0003g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.102+94G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338558 | |||||||
| chr19:4338589 | CAGAG | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(64): Show |
121 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.102+59_102+62delCT others(2): Show |
STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338589 | |||||||
| chr19:4338646 | C | T | 1 | a0002c0002t0001g0042 | 1 | HG00673.hp1 | splice_region_variant&intron_variant | LOW | c.102+6G>A | STAP2 | ENSG00000178078.12 | transcript | ENST00000594605.6 | protein_coding | 1/12 | chr19 | 4338646 |