Item | Value |
---|---|
geneid | 666 |
ensemblid | ENSG00000176720.6 |
hgncid | 1087 |
symbol | BOK |
name | BCL2 family apoptosis regulator BOK |
refseq_nuc | NM_032515.5 |
refseq_prot | NP_115904.1 |
ensembl_nuc | ENST00000318407.5 |
ensembl_prot | ENSP00000314132.3 |
mane_status | MANE Select |
chr | chr2 |
start | 241558745 |
end | 241574131 |
strand | + |
ver | v1.2 |
region | chr2:241558745-241574131 |
region5000 | chr2:241553745-241579131 |
regionname0 | BOK_chr2_241558745_241574131 |
regionname5000 | BOK_chr2_241553745_241579131 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 212 | 426 | 93 | 77 | 192 | 14 | 48 | 143 | BOK_chr2_241553745_241579131 | BOK | MEVLR others(207): Show |
chr2 | 241553745 | 241579131 |
a0002 | 0/0 | 212 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | MEVLR others(207): Show |
chr2 | 241553745 | 241579131 |
a0003 | 0/0 | 212 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BOK_chr2_241553745_241579131 | BOK | MEVLR others(207): Show |
chr2 | 241553745 | 241579131 |
a0004 | 0/0 | 36 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | MEVLR others(31): Show |
chr2 | 241553745 | 241579131 |
a0005 | 0/0 | 212 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | MEVLR others(207): Show |
chr2 | 241553745 | 241579131 |
a0006 | 0/0 | 212 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | MEVLR others(207): Show |
chr2 | 241553745 | 241579131 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 636 | 409 | 77 | 76 | 192 | 14 | 48 | BOK_chr2_241553745_241579131 | BOK | ATGGA others(631): Show |
chr2 | 241553745 | 241579131 | ||
a0001c0002 | 0/0 | 636 | 14 | 13 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | ATGGA others(631): Show |
chr2 | 241553745 | 241579131 | ||
a0001c0007 | 0/0 | 636 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | ATGGA others(631): Show |
chr2 | 241553745 | 241579131 | ||
a0001c0008 | 0/0 | 636 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | ATGGA others(631): Show |
chr2 | 241553745 | 241579131 | ||
a0001c0009 | 0/0 | 636 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | ATGGA others(631): Show |
chr2 | 241553745 | 241579131 | ||
a0002c0003 | 0/0 | 636 | 3 | 0 | 1 | 0 | 2 | 0 | BOK_chr2_241553745_241579131 | BOK | ATGGA others(631): Show |
chr2 | 241553745 | 241579131 | ||
a0003c0004 | 0/0 | 636 | 2 | 0 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | ATGGA others(631): Show |
chr2 | 241553745 | 241579131 | ||
a0004c0010 | 0/0 | 636 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | ATGGA others(631): Show |
chr2 | 241553745 | 241579131 | ||
a0005c0006 | 0/0 | 636 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | ATGGA others(631): Show |
chr2 | 241553745 | 241579131 | ||
a0006c0005 | 0/0 | 636 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | ATGGA others(631): Show |
chr2 | 241553745 | 241579131 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2666 | 136 | 33 | 23 | 64 | 5 | 10 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0002 | 0/0 | 2666 | 81 | 6 | 11 | 51 | 0 | 13 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0003 | 1/0 | 2626 | 26 | 2 | 13 | 2 | 4 | 4 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0004 | 0/0 | 2615 | 27 | 0 | 10 | 12 | 1 | 4 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2610): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0005 | 0/0 | 2626 | 20 | 0 | 2 | 17 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0006 | 0/0 | 2546 | 18 | 2 | 2 | 9 | 0 | 5 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2541): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0007 | 0/0 | 2666 | 14 | 5 | 0 | 9 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0008 | 0/0 | 2626 | 7 | 0 | 0 | 7 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0009 | 0/0 | 2546 | 5 | 1 | 4 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2541): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0010 | 0/0 | 2626 | 6 | 0 | 0 | 4 | 2 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0011 | 0/0 | 2626 | 4 | 4 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0012 | 0/0 | 2655 | 5 | 0 | 1 | 1 | 1 | 2 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2650): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0013 | 0/0 | 2666 | 4 | 0 | 0 | 4 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0014 | 0/0 | 2666 | 4 | 0 | 0 | 4 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0015 | 0/0 | 2667 | 4 | 2 | 1 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2662): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0016 | 0/0 | 2615 | 4 | 0 | 0 | 0 | 0 | 4 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2610): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0017 | 0/0 | 2655 | 4 | 3 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2650): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0018 | 0/0 | 2626 | 3 | 3 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0019 | 0/0 | 2666 | 3 | 0 | 2 | 0 | 1 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0020 | 0/0 | 2666 | 3 | 3 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0021 | 0/0 | 2546 | 3 | 3 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2541): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0022 | 0/0 | 2546 | 2 | 1 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2541): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0023 | 0/0 | 2666 | 2 | 0 | 1 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0024 | 0/0 | 2626 | 2 | 0 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0025 | 0/0 | 2627 | 2 | 2 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2622): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0027 | 0/0 | 2666 | 2 | 2 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0028 | 0/0 | 2666 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0029 | 0/0 | 2626 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0031 | 0/0 | 2666 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0032 | 0/0 | 2666 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0033 | 0/0 | 2665 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2660): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0034 | 0/0 | 2666 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0035 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2620): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0036 | 0/0 | 2827 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2822): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0037 | 0/0 | 2666 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0038 | 0/0 | 2626 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0039 | 0/0 | 2546 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2541): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0040 | 0/0 | 2666 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0041 | 0/0 | 2626 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0042 | 0/0 | 2533 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2528): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0043 | 0/0 | 2615 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2610): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0044 | 0/0 | 2615 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2610): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0045 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2530): Show |
chr2 | 241553745 | 241579131 |
a0001c0001t0046 | 0/0 | 2655 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2650): Show |
chr2 | 241553745 | 241579131 |
a0001c0002t0001 | 0/0 | 2666 | 11 | 11 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0002t0009 | 0/0 | 2546 | 2 | 1 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2541): Show |
chr2 | 241553745 | 241579131 |
a0001c0002t0011 | 0/0 | 2626 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0001c0007t0030 | 0/0 | 2585 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2580): Show |
chr2 | 241553745 | 241579131 |
a0001c0008t0002 | 0/0 | 2666 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0001c0009t0001 | 0/0 | 2666 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0002c0003t0003 | 0/0 | 2626 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0002c0003t0026 | 0/0 | 2747 | 2 | 0 | 0 | 0 | 2 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2742): Show |
chr2 | 241553745 | 241579131 |
a0003c0004t0005 | 0/0 | 2626 | 2 | 0 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0004c0010t0002 | 0/0 | 2666 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
a0005c0006t0003 | 0/0 | 2626 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2621): Show |
chr2 | 241553745 | 241579131 |
a0006c0005t0007 | 0/0 | 2666 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | CTCTC others(2661): Show |
chr2 | 241553745 | 241579131 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 27 | 2 | 0 | 25 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0002 | 0/0 | 23 | 0 | 3 | 18 | 1 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0012 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0024 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0003 | 0/0 | 10 | 2 | 0 | 8 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0007 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0011 | 0/0 | 4 | 1 | 0 | 0 | 2 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0048 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0010 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0006g0004 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0006g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0007g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0007g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0007g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0008g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0008g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0009g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0009g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0009g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0009g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0010g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0010g0057 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0010g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0010g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0011g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0011g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0011g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0012g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0012g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0012g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0012g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0012g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0013g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0013g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0014g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0014g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0015g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0015g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0015g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0015g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0016g0009 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0017g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0017g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0017g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0017g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0018g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0018g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0018g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0019g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0019g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0020g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0020g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0021g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0021g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0021g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0022g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0023g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0023g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0024g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0025g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0027g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0027g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0028g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0029g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0031g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0032g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0033g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0034g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0035g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0036g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0037g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0038g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0039g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0040g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0041g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0042g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0043g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0044g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0045g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0001t0046g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0002t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0002t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0002t0009g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0002t0011g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0007t0030g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0008t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0001c0009t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0002c0003t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0002c0003t0026g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0003c0004t0005g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0004c0010t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0005c0006t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
a0006c0005t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00099 | hp2 | a0001 | c0001 | t0012 | g0084 | EUR | GBR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | FIN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00280 | hp2 | a0001 | c0001 | t0010 | g0057 | EUR | FIN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00323 | hp2 | a0001 | c0001 | t0010 | g0057 | EUR | FIN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00423 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0131 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00544 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00597 | hp1 | a0001 | c0001 | t0008 | g0018 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00621 | hp2 | a0001 | c0001 | t0008 | g0113 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0205 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00642 | hp2 | a0001 | c0002 | t0009 | g0025 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00673 | hp1 | a0001 | c0001 | t0010 | g0055 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0097 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0207 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01074 | hp1 | a0001 | c0001 | t0019 | g0038 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01074 | hp2 | a0001 | c0001 | t0023 | g0206 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01081 | hp2 | a0001 | c0001 | t0009 | g0071 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01099 | hp1 | a0001 | c0001 | t0042 | g0030 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01106 | hp2 | a0001 | c0001 | t0017 | g0090 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01109 | hp2 | a0001 | c0001 | t0015 | g0241 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0266 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0107 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01243 | hp1 | a0001 | c0001 | t0022 | g0052 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01258 | hp1 | a0002 | c0003 | t0003 | g0035 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01261 | hp1 | a0001 | c0001 | t0046 | g0092 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01261 | hp2 | a0001 | c0001 | t0009 | g0058 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0101 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01358 | hp2 | a0001 | c0001 | t0028 | g0051 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | IBS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0228 | EUR | IBS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01516 | hp1 | a0002 | c0003 | t0026 | g0036 | EUR | IBS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01517 | hp1 | a0002 | c0003 | t0026 | g0036 | EUR | IBS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0011 | EUR | IBS | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0184 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01891 | hp2 | a0001 | c0008 | t0002 | g0128 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01934 | hp1 | a0001 | c0001 | t0019 | g0172 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0265 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0109 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02004 | hp2 | a0001 | c0001 | t0009 | g0235 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0200 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02015 | hp2 | a0001 | c0001 | t0008 | g0167 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02027 | hp2 | a0001 | c0001 | t0015 | g0176 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02040 | hp1 | a0004 | c0010 | t0002 | g0130 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02055 | hp1 | a0001 | c0001 | t0017 | g0106 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02055 | hp2 | a0001 | c0001 | t0043 | g0099 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02056 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0267 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02080 | hp2 | a0001 | c0001 | t0010 | g0275 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02129 | hp1 | a0001 | c0001 | t0005 | g0263 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02132 | hp1 | a0001 | c0001 | t0006 | g0203 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02132 | hp2 | a0001 | c0001 | t0010 | g0274 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02135 | hp1 | a0001 | c0001 | t0008 | g0168 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02135 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02148 | hp1 | a0001 | c0001 | t0004 | g0105 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02148 | hp2 | a0001 | c0001 | t0012 | g0108 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CDX | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02155 | hp2 | a0001 | c0001 | t0008 | g0166 | EAS | CDX | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | CDX | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0257 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02257 | hp2 | a0001 | c0001 | t0020 | g0003 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0256 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02293 | hp2 | a0001 | c0001 | t0005 | g0268 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02300 | hp2 | a0001 | c0001 | t0044 | g0096 | AMR | PEL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0277 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02523 | hp2 | a0001 | c0001 | t0007 | g0008 | EAS | KHV | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0072 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02615 | hp1 | a0001 | c0001 | t0015 | g0162 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0062 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0065 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02630 | hp2 | a0001 | c0001 | t0041 | g0239 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02647 | hp1 | a0001 | c0001 | t0017 | g0091 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02723 | hp1 | a0001 | c0001 | t0020 | g0177 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0215 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02818 | hp1 | a0001 | c0001 | t0018 | g0147 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02886 | hp2 | a0001 | c0001 | t0018 | g0145 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02896 | hp2 | a0001 | c0001 | t0011 | g0181 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02922 | hp2 | a0001 | c0001 | t0021 | g0187 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02965 | hp1 | a0001 | c0001 | t0011 | g0190 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02970 | hp2 | a0001 | c0002 | t0009 | g0025 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02976 | hp1 | a0001 | c0007 | t0030 | g0115 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03041 | hp1 | a0001 | c0001 | t0015 | g0242 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03041 | hp2 | a0001 | c0001 | t0031 | g0232 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | MSL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03130 | hp2 | a0001 | c0001 | t0018 | g0146 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0183 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0165 | AFR | MSL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03209 | hp2 | a0001 | c0001 | t0027 | g0178 | AFR | MSL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | MSL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03239 | hp1 | a0001 | c0001 | t0006 | g0004 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03453 | hp1 | a0001 | c0001 | t0025 | g0026 | AFR | MSL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03490 | hp1 | a0001 | c0001 | t0016 | g0009 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03490 | hp2 | a0001 | c0001 | t0039 | g0227 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0010 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03492 | hp1 | a0001 | c0001 | t0016 | g0009 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03516 | hp1 | a0001 | c0001 | t0022 | g0052 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0276 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | MSL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03669 | hp1 | a0001 | c0001 | t0034 | g0116 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0236 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03688 | hp1 | a0001 | c0001 | t0012 | g0100 | SAS | STU | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0083 | SAS | STU | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03704 | hp1 | a0001 | c0001 | t0029 | g0061 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0230 | SAS | PJL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | BEB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03834 | hp2 | a0001 | c0001 | t0037 | g0210 | SAS | BEB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03927 | hp1 | a0001 | c0001 | t0006 | g0216 | SAS | BEB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03927 | hp2 | a0001 | c0001 | t0016 | g0009 | SAS | BEB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0110 | SAS | BEB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | STU | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | STU | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG04184 | hp1 | a0001 | c0001 | t0016 | g0009 | SAS | BEB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | BEB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG04199 | hp1 | a0001 | c0001 | t0023 | g0111 | SAS | STU | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0221 | SAS | STU | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0094 | SAS | STU | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0048 | SAS | STU | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG04228 | hp1 | a0001 | c0001 | t0012 | g0095 | SAS | STU | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18522 | hp1 | a0001 | c0001 | t0020 | g0003 | AFR | YRI | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18522 | hp2 | a0001 | c0001 | t0011 | g0080 | AFR | YRI | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | CHB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | CHB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18906 | hp1 | a0001 | c0001 | t0027 | g0153 | AFR | YRI | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | YRI | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18940 | hp2 | a0001 | c0001 | t0024 | g0028 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18941 | hp1 | a0001 | c0001 | t0040 | g0008 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18941 | hp2 | a0001 | c0001 | t0005 | g0264 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18942 | hp2 | a0003 | c0004 | t0005 | g0054 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18945 | hp2 | a0001 | c0001 | t0013 | g0225 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18948 | hp1 | a0001 | c0001 | t0024 | g0028 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18948 | hp2 | a0005 | c0006 | t0003 | g0163 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18954 | hp1 | a0001 | c0001 | t0007 | g0259 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18957 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18959 | hp1 | a0001 | c0001 | t0007 | g0258 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18959 | hp2 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18962 | hp1 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18965 | hp1 | a0001 | c0001 | t0038 | g0123 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18966 | hp2 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18969 | hp1 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18969 | hp2 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18971 | hp2 | a0001 | c0001 | t0005 | g0269 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18975 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18977 | hp2 | a0001 | c0001 | t0007 | g0217 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18984 | hp2 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18987 | hp2 | a0001 | c0001 | t0033 | g0041 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18992 | hp2 | a0001 | c0001 | t0014 | g0017 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18993 | hp1 | a0001 | c0001 | t0035 | g0088 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18997 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18998 | hp1 | a0001 | c0001 | t0014 | g0017 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18998 | hp2 | a0001 | c0001 | t0006 | g0137 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19000 | hp1 | a0003 | c0004 | t0005 | g0054 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19000 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19003 | hp1 | a0001 | c0001 | t0014 | g0017 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19007 | hp1 | a0001 | c0001 | t0007 | g0056 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19009 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19011 | hp1 | a0001 | c0001 | t0036 | g0003 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19012 | hp1 | a0001 | c0001 | t0006 | g0208 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19030 | hp1 | a0001 | c0001 | t0017 | g0086 | AFR | LWK | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | LWK | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19043 | hp2 | a0001 | c0001 | t0045 | g0085 | AFR | LWK | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19056 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19059 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19064 | hp1 | a0001 | c0001 | t0010 | g0055 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19067 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19068 | hp1 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0260 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19070 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19074 | hp1 | a0001 | c0001 | t0014 | g0160 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19085 | hp1 | a0001 | c0001 | t0012 | g0098 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19086 | hp1 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19087 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19240 | hp1 | a0001 | c0001 | t0011 | g0182 | AFR | YRI | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA19240 | hp2 | a0001 | c0001 | t0021 | g0185 | AFR | YRI | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ASW | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ASW | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0169 | EUR | TSI | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0030 | EUR | TSI | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA20805 | hp1 | a0001 | c0001 | t0019 | g0038 | EUR | TSI | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | GIH | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | GIH | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01123 | hp1 | a0001 | c0001 | t0009 | g0073 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02109 | hp1 | a0001 | c0001 | t0021 | g0186 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG03471 | hp2 | a0001 | c0001 | t0025 | g0026 | AFR | MSL | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG06807 | hp1 | a0001 | c0002 | t0011 | g0175 | AFR | USA | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
HG06807 | hp2 | a0001 | c0001 | t0032 | g0231 | AFR | USA | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA18955 | hp2 | a0001 | c0001 | t0007 | g0056 | EAS | JPT | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | USA | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | USA | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA21309 | hp1 | a0006 | c0005 | t0007 | g0188 | AFR | LWK | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
NA21309 | hp2 | a0001 | c0009 | t0001 | g0139 | AFR | LWK | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0012 | REF | REF | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0048 | REF | REF | BOK_chr2_241553745_241579131 | BOK | chr2 | 241553745 | 241579131 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241559569 | C | G | 1 | a0002 | 3 | HG01258.hp1 HG01516.hp1 HG01517.hp1 |
missense_variant | MODERATE | c.86C>G | p.Ala29Gly | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/5 | 364/2626 | 86/639 | 29/212 | chr2 | 241559569 | |||
chr2:241559587 | G | C | 1 | a0006 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.104G>C | p.Gly35Ala | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/5 | 382/2626 | 104/639 | 35/212 | chr2 | 241559587 | |||
chr2:241559592 | G | T | 1 | a0004 | 1 | HG02040.hp1 | stop_gained | HIGH | c.109G>T | p.Glu37* | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/5 | 387/2626 | 109/639 | 37/212 | chr2 | 241559592 | |||
chr2:241562459 | G | A | 1 | a0005 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.332G>A | p.Gly111Asp | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/5 | 610/2626 | 332/639 | 111/212 | chr2 | 241562459 | |||
chr2:241570278 | G | A | 1 | a0003 | 2 | NA18942.hp2 NA19000.hp1 |
missense_variant | MODERATE | c.503G>A | p.Arg168His | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/5 | 781/2626 | 503/639 | 168/212 | chr2 | 241570278 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241562388 | C | T | 1 | a0001c0009 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.261C>T | p.Asn87Asn | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/5 | 539/2626 | 261/639 | 87/212 | chr2 | 241562388 | |||
chr2:241562413 | C | T | 1 | a0001c0008 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.286C>T | p.Leu96Leu | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/5 | 564/2626 | 286/639 | 96/212 | chr2 | 241562413 | |||
chr2:241562436 | C | G | 1 | a0001c0002 | 14 | HG00642.hp2 HG02486.hp1 HG02615.hp2 others(11): Show |
synonymous_variant | LOW | c.309C>G | p.Thr103Thr | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/5 | 587/2626 | 309/639 | 103/212 | chr2 | 241562436 | |||
chr2:241570132 | G | A | 1 | a0001c0007 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.357G>A | p.Thr119Thr | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/5 | 635/2626 | 357/639 | 119/212 | chr2 | 241570132 | |||
chr2:241570150 | C | T | 1 | a0004c0010 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.375C>T | p.Ser125Ser | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/5 | 653/2626 | 375/639 | 125/212 | chr2 | 241570150 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241558805 | C | A | 1 | a0001c0001t0028 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-218C>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 1/5 | 679 | chr2 | 241558805 | ||||||
chr2:241558816 | C | G | 1 | a0001c0001t0046 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-207C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 1/5 | 668 | chr2 | 241558816 | ||||||
chr2:241558825 | GGGAAGCC others(4): Show |
G | 9 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0016 others(6): Show |
45 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-194_-184delAGCCCC others(5): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 1/5 | 645 | INFO_REALIGN_3_PRIME | chr2 | 241558825 | |||||
chr2:241558860 | C | T | 1 | a0001c0001t0010 | 6 | HG00280.hp2 HG00323.hp2 HG00673.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-163C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 1/5 | 624 | chr2 | 241558860 | ||||||
chr2:241572784 | G | GGGAACAC others(74): Show |
1 | a0002c0003t0026 | 2 | HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*405_*485dupGAACAC others(75): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 486 | INFO_REALIGN_3_PRIME | chr2 | 241572784 | |||||
chr2:241572824 | CG | C | 2 | a0001c0001t0016 a0001c0001t0029 |
5 | HG03490.hp1 HG03492.hp1 HG03704.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*405delG | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 405 | INFO_REALIGN_3_PRIME | chr2 | 241572824 | |||||
chr2:241572847 | A | G | 2 | a0001c0001t0016 a0001c0001t0029 |
5 | HG03490.hp1 HG03492.hp1 HG03704.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*425A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 425 | chr2 | 241572847 | ||||||
chr2:241572865 | C | T | 1 | a0001c0001t0027 | 2 | HG03209.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*443C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 443 | chr2 | 241572865 | ||||||
chr2:241572905 | C | CG | 2 | a0001c0001t0016 a0001c0001t0029 |
5 | HG03490.hp1 HG03492.hp1 HG03704.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*485dupG | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 486 | INFO_REALIGN_3_PRIME | chr2 | 241572905 | |||||
chr2:241572905 | C | T | 1 | a0001c0001t0045 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 483 | chr2 | 241572905 | ||||||
chr2:241572927 | GCCCCAGG others(75): Show |
G | 1 | a0001c0001t0042 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*524_*605delGGGAAC others(76): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 524 | INFO_REALIGN_3_PRIME | chr2 | 241572927 | |||||
chr2:241572968 | G | A | 3 | a0001c0001t0016 a0001c0001t0024 a0001c0001t0029 |
7 | HG03490.hp1 HG03492.hp1 HG03704.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*546G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 546 | chr2 | 241572968 | ||||||
chr2:241572973 | A | T | 4 | a0001c0001t0011 a0001c0001t0043 a0001c0002t0011 others(1): Show |
7 | HG02055.hp2 HG02896.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*551A>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 551 | chr2 | 241572973 | ||||||
chr2:241572986 | CG | C | 3 | a0001c0001t0016 a0001c0001t0024 a0001c0001t0029 |
7 | HG03490.hp1 HG03492.hp1 HG03704.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*567delG | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 567 | INFO_REALIGN_3_PRIME | chr2 | 241572986 | |||||
chr2:241572986 | CGGGAACA others(115): Show |
C | 4 | a0001c0001t0011 a0001c0001t0043 a0001c0002t0011 others(1): Show |
7 | HG02055.hp2 HG02896.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*567_*688del | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 567 | INFO_REALIGN_3_PRIME | chr2 | 241572986 | |||||
chr2:241573009 | A | G | 5 | a0001c0001t0016 a0001c0001t0024 a0001c0001t0025 others(2): Show |
10 | HG02630.hp2 HG03453.hp1 HG03471.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*587A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 587 | chr2 | 241573009 | ||||||
chr2:241573027 | C | CG | 2 | a0001c0001t0015 a0001c0001t0025 |
6 | HG01109.hp2 HG02027.hp2 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*605_*606insG | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 606 | chr2 | 241573027 | ||||||
chr2:241573028 | A | G | 34 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(31): Show |
204 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*606A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 606 | chr2 | 241573028 | ||||||
chr2:241573033 | A | G | 1 | a0001c0001t0025 | 2 | HG03453.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*611A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 611 | chr2 | 241573033 | ||||||
chr2:241573067 | C | CG | 4 | a0001c0001t0016 a0001c0001t0024 a0001c0001t0029 others(1): Show |
8 | HG02630.hp2 HG03490.hp1 HG03492.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*647dupG | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 648 | INFO_REALIGN_3_PRIME | chr2 | 241573067 | |||||
chr2:241573067 | C | T | 1 | a0001c0001t0034 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*645C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 645 | chr2 | 241573067 | ||||||
chr2:241573094 | A | T | 4 | a0001c0001t0016 a0001c0001t0024 a0001c0001t0029 others(1): Show |
8 | HG02630.hp2 HG03490.hp1 HG03492.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*672A>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 672 | chr2 | 241573094 | ||||||
chr2:241573107 | C | T | 1 | a0001c0001t0023 | 2 | HG01074.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*685C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 685 | chr2 | 241573107 | ||||||
chr2:241573107 | CG | C | 5 | a0001c0001t0016 a0001c0001t0024 a0001c0001t0029 others(2): Show |
9 | HG02630.hp2 HG03490.hp1 HG03492.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*688delG | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 688 | INFO_REALIGN_3_PRIME | chr2 | 241573107 | |||||
chr2:241573116 | C | T | 1 | a0001c0001t0041 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*694C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 694 | chr2 | 241573116 | ||||||
chr2:241573128 | G | C | 2 | a0001c0001t0019 a0001c0001t0023 |
5 | HG01074.hp1 HG01074.hp2 HG01934.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*706G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 706 | chr2 | 241573128 | ||||||
chr2:241573135 | T | A | 9 | a0001c0001t0011 a0001c0001t0016 a0001c0001t0024 others(6): Show |
16 | HG02055.hp2 HG02630.hp2 HG02896.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*713T>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 713 | chr2 | 241573135 | ||||||
chr2:241573135 | T | TGGTGAAG others(33): Show |
8 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0014 others(5): Show |
97 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*733_*734insCTGCTC others(34): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 734 | INFO_REALIGN_3_PRIME | chr2 | 241573135 | |||||
chr2:241573135 | T | TGGTGAAG others(194): Show |
1 | a0001c0001t0036 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*733_*734insCTGCTC others(195): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 734 | INFO_REALIGN_3_PRIME | chr2 | 241573135 | |||||
chr2:241573135 | T | TGGTGAAG others(32): Show |
1 | a0001c0001t0033 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*725_*726insGGAACA others(33): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 726 | INFO_REALIGN_3_PRIME | chr2 | 241573135 | |||||
chr2:241573156 | T | C | 26 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(23): Show |
155 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*734T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 734 | chr2 | 241573156 | ||||||
chr2:241573156 | T | TTGCTCTC others(33): Show |
17 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0013 others(14): Show |
188 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*753_*792dupAGGTGA others(34): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 793 | INFO_REALIGN_3_PRIME | chr2 | 241573156 | |||||
chr2:241573198 | GCTCTCAC others(73): Show |
G | 7 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0021 others(4): Show |
32 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*793_*872delCGGTGA others(74): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 793 | INFO_REALIGN_3_PRIME | chr2 | 241573198 | |||||
chr2:241573215 | C | A | 1 | a0001c0001t0018 | 3 | HG02818.hp1 HG02886.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*793C>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 793 | chr2 | 241573215 | ||||||
chr2:241573215 | CGGTGAAG others(73): Show |
C | 1 | a0001c0001t0035 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*814_*893delTTGCTC others(74): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 814 | INFO_REALIGN_3_PRIME | chr2 | 241573215 | |||||
chr2:241573228 | C | T | 1 | a0001c0001t0001 | 6 | HG01934.hp2 NA18960.hp2 NA19056.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*806C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 806 | chr2 | 241573228 | ||||||
chr2:241573236 | T | C | 3 | a0001c0001t0001 a0001c0001t0018 a0001c0001t0031 |
6 | HG02602.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*814T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 814 | chr2 | 241573236 | ||||||
chr2:241573238 | G | GCTCTCAC others(33): Show |
1 | a0001c0001t0002 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*859_*898dupCTCACC others(34): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 899 | INFO_REALIGN_3_PRIME | chr2 | 241573238 | |||||
chr2:241573255 | A | C | 1 | a0001c0001t0018 | 3 | HG02818.hp1 HG02886.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*833A>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 833 | chr2 | 241573255 | ||||||
chr2:241573308 | CGGAACAC others(34): Show |
C | 1 | a0001c0007t0030 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*897_*937delCTGTCA others(35): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 897 | INFO_REALIGN_3_PRIME | chr2 | 241573308 | |||||
chr2:241573317 | T | A | 2 | a0001c0001t0007 a0001c0001t0027 |
3 | HG03209.hp1 HG03209.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*895T>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 895 | chr2 | 241573317 | ||||||
chr2:241573318 | C | G | 7 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0021 others(4): Show |
32 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*896C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 896 | chr2 | 241573318 | ||||||
chr2:241573321 | G | C | 7 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0021 others(4): Show |
32 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*899G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 899 | chr2 | 241573321 | ||||||
chr2:241573349 | G | A | 2 | a0001c0001t0001 a0001c0001t0018 |
11 | HG01934.hp2 HG02602.hp2 HG02818.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*927G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 927 | chr2 | 241573349 | ||||||
chr2:241573532 | G | A | 1 | a0001c0001t0021 | 3 | HG02109.hp1 HG02922.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1110G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1110 | chr2 | 241573532 | ||||||
chr2:241573547 | G | T | 1 | a0001c0001t0013 | 4 | NA18945.hp2 NA18959.hp2 NA18969.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1125G>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1125 | chr2 | 241573547 | ||||||
chr2:241573590 | G | A | 1 | a0001c0001t0037 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1168G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1168 | chr2 | 241573590 | ||||||
chr2:241573593 | G | A | 1 | a0001c0001t0022 | 2 | HG01243.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1171G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1171 | chr2 | 241573593 | ||||||
chr2:241573595 | C | T | 1 | a0001c0001t0038 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1173C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1173 | chr2 | 241573595 | ||||||
chr2:241573704 | C | T | 1 | a0001c0001t0020 | 3 | HG02257.hp2 HG02723.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1282C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1282 | chr2 | 241573704 | ||||||
chr2:241573707 | C | T | 1 | a0001c0001t0039 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1285C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1285 | chr2 | 241573707 | ||||||
chr2:241573734 | T | A | 3 | a0001c0001t0006 a0001c0001t0022 a0001c0001t0045 |
21 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1312T>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1312 | chr2 | 241573734 | ||||||
chr2:241573737 | A | G | 1 | a0001c0001t0014 | 4 | NA18992.hp2 NA18998.hp1 NA19003.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1315A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1315 | chr2 | 241573737 | ||||||
chr2:241573738 | A | G | 4 | a0001c0001t0011 a0001c0001t0043 a0001c0002t0011 others(1): Show |
7 | HG02055.hp2 HG02896.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1316A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1316 | chr2 | 241573738 | ||||||
chr2:241573740 | C | A | 4 | a0001c0001t0011 a0001c0001t0043 a0001c0002t0011 others(1): Show |
7 | HG02055.hp2 HG02896.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1318C>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1318 | chr2 | 241573740 | ||||||
chr2:241573760 | A | G | 1 | a0001c0001t0008 | 7 | HG00597.hp1 HG00621.hp2 HG02015.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1338A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1338 | chr2 | 241573760 | ||||||
chr2:241573877 | G | A | 1 | a0001c0001t0032 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1455G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1455 | chr2 | 241573877 | ||||||
chr2:241573989 | G | A | 1 | a0001c0001t0040 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1567G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 5/5 | 1567 | chr2 | 241573989 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241559014 | G | A | 1 | a0001c0001t0009g0058 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-30+21G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 1/4 | chr2 | 241559014 | |||||||
chr2:241559031 | C | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
7 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+38C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 1/4 | chr2 | 241559031 | |||||||
chr2:241559059 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-30+66G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 1/4 | chr2 | 241559059 | |||||||
chr2:241559065 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-30+72G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 1/4 | chr2 | 241559065 | |||||||
chr2:241559082 | G | A | 148 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0033 others(145): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.-30+89G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 1/4 | chr2 | 241559082 | |||||||
chr2:241559204 | C | T | 21 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0271 others(18): Show |
25 | HG00280.hp2 HG00323.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-30+211C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 1/4 | chr2 | 241559204 | |||||||
chr2:241559730 | G | T | 1 | a0001c0002t0011g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.220+27G>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241559730 | |||||||
chr2:241559849 | G | A | 1 | a0001c0001t0015g0176 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.220+146G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241559849 | |||||||
chr2:241559972 | A | G | 1 | a0001c0001t0010g0057 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.220+269A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241559972 | |||||||
chr2:241560072 | T | A | 2 | a0001c0001t0020g0177 a0001c0001t0027g0178 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.220+369T>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241560072 | |||||||
chr2:241560075 | T | C | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG01975.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.220+372T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241560075 | |||||||
chr2:241560107 | C | T | 1 | a0001c0002t0001g0039 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.220+404C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241560107 | |||||||
chr2:241560396 | C | G | 1 | a0001c0001t0002g0174 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.220+693C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241560396 | |||||||
chr2:241560399 | G | C | 1 | a0001c0001t0002g0174 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.220+696G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241560399 | |||||||
chr2:241560736 | C | T | 12 | a0001c0001t0001g0037 a0001c0001t0003g0007 a0001c0001t0003g0011 others(9): Show |
22 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.220+1033C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241560736 | |||||||
chr2:241560874 | ACAGCT | A | 5 | a0001c0001t0003g0035 a0001c0001t0003g0169 a0001c0001t0003g0170 others(2): Show |
6 | HG01168.hp2 HG01258.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+1175_220+1179d others(7): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 241560874 | ||||||
chr2:241561135 | C | A | 180 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0027 others(177): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.221-1213C>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561135 | |||||||
chr2:241561137 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.221-1211G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561137 | |||||||
chr2:241561137 | GA | G | 180 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0027 others(177): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.221-1210delA | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561137 | |||||||
chr2:241561141 | A | T | 180 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0027 others(177): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.221-1207A>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561141 | |||||||
chr2:241561143 | C | CT | 180 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0027 others(177): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.221-1205_221-1204i others(3): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561143 | |||||||
chr2:241561146 | T | G | 180 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0027 others(177): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.221-1202T>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561146 | |||||||
chr2:241561247 | C | T | 159 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0027 others(156): Show |
216 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.221-1101C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561247 | |||||||
chr2:241561281 | T | C | 1 | a0001c0001t0029g0061 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.221-1067T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561281 | |||||||
chr2:241561311 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.221-1037G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561311 | |||||||
chr2:241561372 | A | G | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.221-976A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561372 | |||||||
chr2:241561418 | AGGGTGGC others(95): Show |
A | 15 | a0001c0001t0001g0164 a0001c0001t0002g0003 a0001c0001t0002g0034 others(12): Show |
28 | HG00438.hp2 HG02074.hp2 HG02083.hp1 others(25): Show |
intron_variant | MODIFIER | c.221-658_221-557del | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 241561418 | ||||||
chr2:241561418 | AGGGTGGC others(197): Show |
A | 23 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0002g0068 others(20): Show |
27 | HG00280.hp2 HG00323.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.221-760_221-557del | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 241561418 | ||||||
chr2:241561435 | C | CGGCCCAG others(95): Show |
2 | a0001c0001t0002g0029 a0001c0001t0002g0089 |
3 | NA18986.hp2 NA19086.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.221-812_221-811ins others(102): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 241561435 | ||||||
chr2:241561469 | C | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0069 a0001c0001t0001g0076 others(5): Show |
9 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-879C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561469 | |||||||
chr2:241561537 | C | T | 47 | a0001c0001t0001g0033 a0001c0001t0001g0114 a0001c0001t0001g0118 others(44): Show |
52 | HG00408.hp1 HG00438.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.221-811C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561537 | |||||||
chr2:241561537 | CGGCCCAG others(146): Show |
C | 1 | a0001c0001t0007g0259 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.221-760_221-608del | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 241561537 | ||||||
chr2:241561538 | G | A | 10 | a0001c0002t0001g0013 a0001c0002t0001g0039 a0001c0002t0001g0062 others(7): Show |
14 | HG00642.hp2 HG02486.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-810G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561538 | |||||||
chr2:241561571 | C | T | 14 | a0001c0001t0001g0164 a0001c0001t0002g0003 a0001c0001t0002g0034 others(11): Show |
27 | HG00438.hp2 HG02074.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.221-777C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561571 | |||||||
chr2:241561588 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0011g0190 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.221-760G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561588 | |||||||
chr2:241561639 | C | T | 1 | a0001c0007t0030g0115 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.221-709C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561639 | |||||||
chr2:241561714 | C | T | 1 | a0001c0001t0001g0053 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.221-634C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561714 | |||||||
chr2:241561843 | C | T | 1 | a0001c0001t0007g0258 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.221-505C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561843 | |||||||
chr2:241561904 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.221-444G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561904 | |||||||
chr2:241561906 | C | T | 1 | a0001c0001t0006g0257 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.221-442C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561906 | |||||||
chr2:241561947 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.221-401C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561947 | |||||||
chr2:241561959 | C | T | 15 | a0001c0001t0001g0024 a0001c0001t0001g0189 a0001c0001t0001g0278 others(12): Show |
17 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.221-389C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241561959 | |||||||
chr2:241562014 | G | A | 1 | a0001c0001t0015g0176 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.221-334G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241562014 | |||||||
chr2:241562037 | G | A | 1 | a0001c0001t0005g0070 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.221-311G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241562037 | |||||||
chr2:241562043 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0005g0015 a0001c0001t0005g0070 others(2): Show |
11 | HG00621.hp2 HG01934.hp2 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-305C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241562043 | |||||||
chr2:241562160 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.221-188C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241562160 | |||||||
chr2:241562214 | A | G | 3 | a0001c0001t0006g0256 a0001c0001t0006g0257 a0001c0001t0022g0052 |
4 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-134A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241562214 | |||||||
chr2:241562311 | C | T | 1 | a0001c0002t0001g0039 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.221-37C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241562311 | |||||||
chr2:241562312 | G | A | 1 | a0001c0001t0007g0258 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.221-36G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 2/4 | chr2 | 241562312 | |||||||
chr2:241562601 | A | G | 1 | a0001c0001t0002g0155 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.349+125A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241562601 | |||||||
chr2:241562625 | G | A | 21 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0271 others(18): Show |
25 | HG00280.hp2 HG00323.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.349+149G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241562625 | |||||||
chr2:241562875 | CA | C | 7 | a0001c0002t0001g0039 a0001c0002t0001g0063 a0001c0002t0001g0064 others(4): Show |
8 | HG02486.hp1 HG02622.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+401delA | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241562875 | ||||||
chr2:241562918 | G | T | 5 | a0001c0001t0001g0006 a0001c0001t0005g0015 a0001c0001t0005g0070 others(2): Show |
11 | HG00621.hp2 HG01934.hp2 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.349+442G>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241562918 | |||||||
chr2:241562979 | C | T | 13 | a0001c0001t0001g0037 a0001c0001t0003g0007 a0001c0001t0003g0011 others(10): Show |
23 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.349+503C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241562979 | |||||||
chr2:241563042 | C | T | 1 | a0001c0001t0004g0110 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.349+566C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241563042 | |||||||
chr2:241563105 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0033 others(61): Show |
109 | HG00280.hp1 HG00423.hp1 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.349+629C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241563105 | |||||||
chr2:241563109 | T | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(256): Show |
373 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.349+633T>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241563109 | |||||||
chr2:241563173 | G | A | 1 | a0001c0001t0005g0260 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.349+697G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241563173 | |||||||
chr2:241563227 | C | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(217): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.349+751C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241563227 | |||||||
chr2:241563377 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.349+901G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241563377 | |||||||
chr2:241563526 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.349+1050G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241563526 | |||||||
chr2:241563541 | C | T | 216 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0027 others(213): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.349+1065C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241563541 | |||||||
chr2:241563632 | C | T | 216 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0027 others(213): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.349+1156C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241563632 | |||||||
chr2:241563678 | C | T | 2 | a0001c0001t0004g0109 a0001c0001t0012g0108 |
2 | HG02004.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.349+1202C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241563678 | |||||||
chr2:241563800 | C | T | 1 | a0006c0005t0007g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349+1324C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241563800 | |||||||
chr2:241563806 | GGGGTGAC others(719): Show |
G | 1 | a0001c0001t0001g0019 | 3 | HG00741.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.349+1334_349+2059d others(2): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241563806 | ||||||
chr2:241564031 | G | A | 1 | a0001c0008t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.349+1555G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241564031 | |||||||
chr2:241564128 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0023 others(247): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.349+1652T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241564128 | |||||||
chr2:241564324 | C | T | 26 | a0001c0001t0001g0037 a0001c0001t0001g0164 a0001c0001t0002g0003 others(23): Show |
49 | HG00099.hp1 HG00438.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.349+1848C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241564324 | |||||||
chr2:241564510 | T | A | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.349+2034T>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241564510 | |||||||
chr2:241564520 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.349+2044G>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241564520 | |||||||
chr2:241564598 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.349+2122A>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241564598 | |||||||
chr2:241564729 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0037 others(78): Show |
119 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.349+2253A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241564729 | |||||||
chr2:241564767 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.349+2291G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241564767 | |||||||
chr2:241564769 | C | T | 2 | a0001c0001t0006g0256 a0001c0001t0006g0257 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.349+2293C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241564769 | |||||||
chr2:241564924 | A | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0114 |
3 | HG02451.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.349+2448A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241564924 | |||||||
chr2:241564979 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.349+2503C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241564979 | |||||||
chr2:241565077 | C | T | 1 | a0001c0001t0002g0234 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.349+2601C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241565077 | |||||||
chr2:241565129 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.349+2653G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241565129 | |||||||
chr2:241565200 | G | T | 1 | a0001c0007t0030g0115 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.349+2724G>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241565200 | |||||||
chr2:241565399 | T | C | 4 | a0001c0001t0011g0181 a0001c0001t0011g0182 a0001c0001t0011g0190 others(1): Show |
5 | HG02896.hp2 HG02965.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+2923T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241565399 | |||||||
chr2:241565574 | C | CG | 219 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0027 others(216): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.349+3100dupG | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241565574 | ||||||
chr2:241565621 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0114 |
3 | HG02451.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.349+3145C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241565621 | |||||||
chr2:241565653 | T | C | 205 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0027 others(202): Show |
275 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.349+3177T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241565653 | |||||||
chr2:241565726 | C | CGTGGGGG | 2 | a0001c0001t0001g0046 a0001c0001t0001g0237 |
3 | HG01516.hp2 HG02738.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.349+3251_349+3257d others(9): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241565726 | ||||||
chr2:241566112 | C | G | 3 | a0001c0001t0004g0107 a0001c0001t0017g0090 a0001c0001t0017g0106 |
3 | HG01106.hp2 HG01192.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.349+3636C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241566112 | |||||||
chr2:241566152 | C | G | 1 | a0001c0007t0030g0115 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.349+3676C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241566152 | |||||||
chr2:241566157 | G | A | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.349+3681G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241566157 | |||||||
chr2:241566159 | C | CTGTA | 13 | a0001c0001t0001g0037 a0001c0001t0003g0007 a0001c0001t0003g0011 others(10): Show |
23 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.349+3684_349+3687d others(6): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241566159 | ||||||
chr2:241566215 | C | T | 1 | a0001c0001t0008g0113 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.349+3739C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241566215 | |||||||
chr2:241566228 | GAGCCGAG others(1143): Show |
G | 1 | a0001c0001t0002g0218 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.349+3757_350-2743d others(2): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241566228 | ||||||
chr2:241566302 | C | CT | 197 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0033 others(194): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.350-3811dupT | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241566302 | ||||||
chr2:241566302 | C | CTT | 19 | a0001c0001t0001g0024 a0001c0001t0001g0074 a0001c0001t0001g0075 others(16): Show |
21 | HG01081.hp2 HG01123.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.350-3812_350-3811d others(4): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241566302 | ||||||
chr2:241566368 | G | A | 46 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0069 others(43): Show |
61 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.350-3757G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241566368 | |||||||
chr2:241566448 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.350-3677G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241566448 | |||||||
chr2:241566563 | C | A | 1 | a0001c0001t0002g0032 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.350-3562C>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241566563 | |||||||
chr2:241566575 | A | G | 1 | a0001c0001t0004g0102 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.350-3550A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241566575 | |||||||
chr2:241566654 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0027 others(118): Show |
187 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.350-3471T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241566654 | |||||||
chr2:241566688 | AGCTGGCC others(1221): Show |
A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0027 others(118): Show |
187 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.350-3435_350-2208d others(2): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241566688 | ||||||
chr2:241566862 | G | C | 1 | a0001c0001t0005g0015 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.350-3263G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241566862 | |||||||
chr2:241567063 | C | T | 2 | a0001c0001t0031g0232 a0001c0001t0032g0231 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.350-3062C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241567063 | |||||||
chr2:241567064 | G | A | 1 | a0001c0001t0001g0022 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.350-3061G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241567064 | |||||||
chr2:241567129 | G | A | 1 | a0001c0001t0027g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.350-2996G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241567129 | |||||||
chr2:241567144 | CT | C | 8 | a0001c0001t0002g0003 a0001c0001t0003g0087 a0001c0001t0005g0015 others(5): Show |
8 | HG00323.hp2 HG02976.hp2 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-2967delT | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241567144 | ||||||
chr2:241567161 | T | A | 1 | a0001c0001t0002g0174 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.350-2964T>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241567161 | |||||||
chr2:241567318 | G | A | 13 | a0001c0001t0001g0037 a0001c0001t0003g0007 a0001c0001t0003g0011 others(10): Show |
23 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.350-2807G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241567318 | |||||||
chr2:241567370 | G | A | 1 | a0001c0001t0001g0006 | 5 | HG01934.hp2 NA19056.hp2 NA19067.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-2755G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241567370 | |||||||
chr2:241567511 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0114 |
3 | HG02451.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.350-2614C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241567511 | |||||||
chr2:241567522 | C | T | 23 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0271 others(20): Show |
28 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.350-2603C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241567522 | |||||||
chr2:241567618 | C | T | 1 | a0001c0001t0003g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.350-2507C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241567618 | |||||||
chr2:241567917 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0027 others(118): Show |
187 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.350-2208G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241567917 | |||||||
chr2:241567919 | G | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0027 others(118): Show |
187 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.350-2206G>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241567919 | |||||||
chr2:241567922 | C | T | 1 | a0001c0001t0002g0150 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.350-2203C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241567922 | |||||||
chr2:241567976 | G | A | 15 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0271 others(12): Show |
16 | HG01192.hp1 HG01952.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.350-2149G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241567976 | |||||||
chr2:241568018 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0028g0051 |
2 | HG00280.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.350-2107C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241568018 | |||||||
chr2:241568063 | CA | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0027 others(117): Show |
186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.350-2060delA | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241568063 | ||||||
chr2:241568207 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.350-1918G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241568207 | |||||||
chr2:241568258 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.350-1867C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241568258 | |||||||
chr2:241568276 | A | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0041 others(28): Show |
62 | HG00280.hp1 HG00423.hp1 HG01099.hp2 others(59): Show |
intron_variant | MODIFIER | c.350-1849A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241568276 | |||||||
chr2:241568322 | G | A | 7 | a0001c0001t0002g0122 a0001c0001t0009g0058 a0001c0001t0009g0071 others(4): Show |
8 | HG00408.hp1 HG00673.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-1803G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241568322 | |||||||
chr2:241568542 | C | T | 3 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0156 |
3 | HG03654.hp2 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.350-1583C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241568542 | |||||||
chr2:241568543 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.350-1582G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241568543 | |||||||
chr2:241568578 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.350-1547C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241568578 | |||||||
chr2:241568651 | C | G | 12 | a0001c0001t0001g0195 a0001c0001t0001g0278 a0001c0002t0001g0013 others(9): Show |
16 | HG00642.hp2 HG02486.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.350-1474C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241568651 | |||||||
chr2:241568915 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.350-1210T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241568915 | |||||||
chr2:241568956 | AGGGACCA others(16): Show |
A | 3 | a0001c0001t0011g0181 a0001c0001t0011g0182 a0001c0002t0001g0067 |
3 | HG02896.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.350-1162_350-1140d others(25): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241568956 | ||||||
chr2:241568966 | G | A | 1 | a0001c0001t0008g0166 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.350-1159G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241568966 | |||||||
chr2:241568969 | GACTCCCT others(16): Show |
G | 1 | a0001c0001t0015g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.350-1148_350-1126d others(25): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241568969 | ||||||
chr2:241568985 | C | T | 1 | a0001c0001t0004g0105 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.350-1140C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241568985 | |||||||
chr2:241568992 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0023 others(116): Show |
177 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.350-1133A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241568992 | |||||||
chr2:241569104 | A | G | 49 | a0001c0001t0001g0050 a0001c0001t0001g0254 a0001c0001t0002g0045 others(46): Show |
62 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.350-1021A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569104 | |||||||
chr2:241569121 | T | G | 3 | a0001c0001t0007g0165 a0001c0001t0031g0232 a0001c0001t0032g0231 |
3 | HG03041.hp2 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.350-1004T>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569121 | |||||||
chr2:241569153 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.350-972C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569153 | |||||||
chr2:241569185 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0038g0123 |
2 | NA18944.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.350-940T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569185 | |||||||
chr2:241569187 | C | A | 2 | a0001c0001t0001g0138 a0001c0001t0038g0123 |
2 | NA18944.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.350-938C>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569187 | |||||||
chr2:241569192 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0027g0178 |
2 | HG03209.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.350-933G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569192 | |||||||
chr2:241569200 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.350-925A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569200 | |||||||
chr2:241569238 | T | G | 4 | a0001c0001t0011g0181 a0001c0001t0011g0182 a0001c0001t0011g0190 others(1): Show |
5 | HG02896.hp2 HG02965.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-887T>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569238 | |||||||
chr2:241569275 | G | A | 4 | a0001c0001t0005g0049 a0001c0001t0005g0260 a0001c0001t0005g0270 others(1): Show |
6 | NA18942.hp2 NA18962.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-850G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569275 | |||||||
chr2:241569277 | G | A | 1 | a0001c0001t0010g0275 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.350-848G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569277 | |||||||
chr2:241569322 | A | G | 2 | a0001c0001t0002g0135 a0001c0001t0002g0136 |
2 | HG02071.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.350-803A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569322 | |||||||
chr2:241569323 | C | CAG | 66 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0019 others(63): Show |
102 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.350-802_350-801ins others(2): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569323 | |||||||
chr2:241569323 | C | CGG | 116 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0027 others(113): Show |
163 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.350-801_350-800dup others(2): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241569323 | ||||||
chr2:241569340 | T | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0019 others(66): Show |
109 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.350-785T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569340 | |||||||
chr2:241569341 | C | G | 7 | a0001c0001t0009g0058 a0001c0001t0009g0071 a0001c0001t0009g0072 others(4): Show |
8 | HG00642.hp2 HG01081.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-784C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569341 | |||||||
chr2:241569348 | C | G | 12 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0076 others(9): Show |
14 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-777C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569348 | |||||||
chr2:241569352 | T | C | 12 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0076 others(9): Show |
14 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-773T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569352 | |||||||
chr2:241569378 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0023 others(160): Show |
243 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.350-747G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569378 | |||||||
chr2:241569382 | C | T | 7 | a0001c0001t0002g0136 a0001c0001t0002g0155 a0001c0001t0005g0265 others(4): Show |
7 | HG01981.hp1 HG02074.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-743C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569382 | |||||||
chr2:241569391 | A | G | 6 | a0001c0001t0005g0265 a0001c0001t0005g0267 a0001c0001t0005g0268 others(3): Show |
6 | HG01981.hp1 HG02074.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-734A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569391 | |||||||
chr2:241569405 | C | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(121): Show |
194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.350-720C>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569405 | |||||||
chr2:241569410 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(191): Show |
295 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.350-715C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569410 | |||||||
chr2:241569423 | G | A | 1 | a0001c0001t0019g0172 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.350-702G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569423 | |||||||
chr2:241569509 | G | A | 41 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0238 others(38): Show |
60 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.350-616G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569509 | |||||||
chr2:241569587 | T | C | 2 | a0001c0001t0002g0125 a0001c0001t0002g0126 |
2 | HG02683.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.350-538T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569587 | |||||||
chr2:241569592 | C | T | 4 | a0001c0001t0006g0256 a0001c0001t0006g0257 a0001c0001t0011g0181 others(1): Show |
4 | HG02257.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-533C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569592 | |||||||
chr2:241569597 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(174): Show |
263 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.350-528A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569597 | |||||||
chr2:241569598 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(170): Show |
256 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(253): Show |
intron_variant | MODIFIER | c.350-527C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569598 | |||||||
chr2:241569650 | C | A | 1 | a0001c0001t0001g0037 | 2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.350-475C>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569650 | |||||||
chr2:241569654 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(131): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.350-471C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569654 | |||||||
chr2:241569685 | G | T | 1 | a0001c0001t0013g0225 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.350-440G>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569685 | |||||||
chr2:241569728 | G | C | 6 | a0001c0001t0011g0181 a0001c0001t0011g0182 a0001c0001t0011g0190 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-397G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569728 | |||||||
chr2:241569786 | C | G | 1 | a0001c0001t0024g0028 | 2 | NA18940.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.350-339C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569786 | |||||||
chr2:241569920 | CAGGTGTG others(6): Show |
C | 1 | a0001c0001t0012g0100 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.350-201_350-189del others(13): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 241569920 | ||||||
chr2:241569938 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0119 |
6 | HG01934.hp2 NA18960.hp2 NA19056.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-187C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569938 | |||||||
chr2:241569995 | C | T | 28 | a0001c0001t0003g0214 a0001c0001t0005g0015 a0001c0001t0005g0049 others(25): Show |
36 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.350-130C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241569995 | |||||||
chr2:241570092 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.350-33A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 3/4 | chr2 | 241570092 | |||||||
chr2:241570310 | T | TGGGTGGG others(142): Show |
2 | a0001c0001t0001g0226 a0001c0002t0001g0064 |
2 | HG01255.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.513+160_513+161ins others(149): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570310 | ||||||
chr2:241570347 | A | G | 13 | a0001c0001t0007g0183 a0001c0001t0007g0184 a0001c0001t0007g0276 others(10): Show |
13 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.513+59A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570347 | |||||||
chr2:241570355 | G | A | 6 | a0001c0001t0011g0080 a0001c0001t0011g0181 a0001c0001t0011g0182 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+67G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570355 | |||||||
chr2:241570359 | T | C | 8 | a0001c0001t0001g0244 a0001c0001t0001g0253 a0001c0001t0011g0080 others(5): Show |
8 | HG02055.hp2 HG02896.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+71T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570359 | |||||||
chr2:241570362 | A | G | 6 | a0001c0001t0011g0080 a0001c0001t0011g0181 a0001c0001t0011g0182 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+74A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570362 | |||||||
chr2:241570384 | G | GGGGGGTG others(70): Show |
1 | a0001c0001t0039g0227 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.513+149_513+150ins others(77): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570384 | ||||||
chr2:241570413 | A | G | 1 | a0001c0001t0032g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.513+125A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570413 | |||||||
chr2:241570418 | C | CGTACGGG others(299): Show |
1 | a0001c0001t0011g0182 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.513+158_513+159ins others(306): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570418 | ||||||
chr2:241570418 | C | CGTACGGG others(1217): Show |
3 | a0001c0001t0018g0145 a0001c0001t0018g0146 a0001c0001t0018g0147 |
3 | HG02818.hp1 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.513+172_513+173ins others(1224): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570418 | ||||||
chr2:241570418 | C | G | 1 | a0001c0001t0032g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.513+130C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570418 | |||||||
chr2:241570435 | C | CGGATGGG others(219): Show |
1 | a0001c0001t0001g0079 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.513+160_513+161ins others(226): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570435 | ||||||
chr2:241570435 | C | T | 1 | a0001c0001t0032g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.513+147C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570435 | |||||||
chr2:241570438 | A | ATGGGTGA others(451): Show |
1 | a0001c0001t0003g0171 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.513+477_513+478ins others(458): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570438 | ||||||
chr2:241570438 | A | ATGGGTGA others(70): Show |
1 | a0001c0001t0021g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.513+172_513+173ins others(77): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570438 | ||||||
chr2:241570438 | A | ATGGGTGA others(529): Show |
1 | a0001c0001t0007g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.513+172_513+173ins others(536): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570438 | ||||||
chr2:241570438 | A | ATGGGTGA others(223): Show |
2 | a0001c0001t0021g0186 a0001c0001t0021g0187 |
2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.513+172_513+173ins others(230): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570438 | ||||||
chr2:241570438 | A | G | 6 | a0001c0001t0009g0058 a0001c0001t0009g0071 a0001c0001t0009g0072 others(3): Show |
6 | HG01081.hp2 HG01123.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+150A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570438 | |||||||
chr2:241570446 | G | GCGCCTGA others(70): Show |
5 | a0001c0001t0011g0080 a0001c0001t0011g0181 a0001c0001t0011g0190 others(2): Show |
5 | HG02055.hp2 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+158_513+159ins others(77): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570446 | |||||||
chr2:241570446 | GTGTC | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(76): Show |
150 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.513+161_513+164del others(4): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570446 | ||||||
chr2:241570446 | GTGTCTGA others(149): Show |
G | 3 | a0001c0001t0001g0189 a0001c0001t0015g0241 a0001c0002t0001g0066 |
3 | HG01109.hp2 HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.513+161_513+316del | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570446 | ||||||
chr2:241570448 | G | GTCTGAGC others(681): Show |
1 | a0001c0001t0009g0072 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.513+172_513+173ins others(688): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570448 | ||||||
chr2:241570448 | G | GTCTGAGC others(146): Show |
5 | a0001c0001t0019g0038 a0001c0001t0019g0172 a0001c0001t0022g0052 others(2): Show |
6 | HG01074.hp1 HG01074.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+172_513+173ins others(153): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570448 | ||||||
chr2:241570448 | G | GTCTGAGC others(298): Show |
18 | a0001c0001t0006g0004 a0001c0001t0006g0137 a0001c0001t0006g0203 others(15): Show |
24 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.513+172_513+173ins others(305): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570448 | ||||||
chr2:241570448 | G | GTCTGAGC others(680): Show |
1 | a0001c0002t0009g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.513+172_513+173ins others(687): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570448 | ||||||
chr2:241570448 | G | GTCTGAGC others(832): Show |
1 | a0001c0002t0009g0025 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.513+172_513+173ins others(839): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570448 | ||||||
chr2:241570448 | G | GTCTGAGC others(605): Show |
1 | a0001c0001t0007g0183 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.513+172_513+173ins others(612): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570448 | ||||||
chr2:241570460 | G | GT | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(189): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.513+172_513+173ins others(1): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570460 | |||||||
chr2:241570460 | G | GTGGGGGT others(376): Show |
5 | a0001c0001t0007g0008 a0001c0001t0007g0056 a0001c0001t0007g0258 others(2): Show |
9 | HG02056.hp1 HG02523.hp2 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.513+172_513+173ins others(383): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570460 | |||||||
chr2:241570460 | G | GTGGGGGT others(376): Show |
2 | a0001c0001t0007g0276 a0001c0001t0007g0277 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.513+172_513+173ins others(383): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570460 | |||||||
chr2:241570460 | G | GTGGGGGT others(377): Show |
1 | a0001c0001t0007g0217 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.513+172_513+173ins others(384): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570460 | |||||||
chr2:241570483 | G | A | 1 | a0001c0001t0011g0190 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.513+195G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570483 | |||||||
chr2:241570489 | G | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0001g0119 others(14): Show |
25 | HG01891.hp1 HG01934.hp2 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.513+201G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570489 | |||||||
chr2:241570494 | G | C | 24 | a0001c0001t0001g0079 a0001c0001t0001g0278 a0001c0001t0006g0004 others(21): Show |
32 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.513+206G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570494 | |||||||
chr2:241570494 | G | GGTACAGG others(69): Show |
27 | a0001c0001t0005g0015 a0001c0001t0005g0044 a0001c0001t0005g0049 others(24): Show |
36 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.513+210_513+211ins others(76): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570494 | ||||||
chr2:241570499 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(90): Show |
166 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.513+211G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570499 | |||||||
chr2:241570499 | G | GGGAGGGA others(146): Show |
1 | a0001c0001t0001g0164 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.513+222_513+223ins others(153): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570499 | ||||||
chr2:241570507 | G | A | 71 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0020 others(68): Show |
99 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.513+219G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570507 | |||||||
chr2:241570511 | C | CGGATGGG others(147): Show |
1 | a0001c0001t0027g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.513+235_513+236ins others(154): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570511 | ||||||
chr2:241570511 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(124): Show |
209 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.513+223C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570511 | |||||||
chr2:241570511 | CGGATGGG others(146): Show |
C | 1 | a0001c0001t0004g0107 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.513+529_513+681del | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570511 | ||||||
chr2:241570514 | A | G | 21 | a0001c0001t0006g0004 a0001c0001t0006g0137 a0001c0001t0006g0203 others(18): Show |
29 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.513+226A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570514 | |||||||
chr2:241570523 | C | T | 39 | a0001c0001t0006g0004 a0001c0001t0006g0137 a0001c0001t0006g0203 others(36): Show |
51 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.513+235C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570523 | |||||||
chr2:241570524 | C | G | 42 | a0001c0001t0006g0004 a0001c0001t0006g0137 a0001c0001t0006g0203 others(39): Show |
55 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.513+236C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570524 | |||||||
chr2:241570525 | T | C | 3 | a0001c0001t0007g0165 a0001c0001t0025g0026 a0001c0001t0027g0178 |
4 | HG03209.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+237T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570525 | |||||||
chr2:241570531 | C | T | 3 | a0001c0001t0007g0165 a0001c0001t0025g0026 a0001c0001t0027g0178 |
4 | HG03209.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+243C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570531 | |||||||
chr2:241570535 | T | C | 3 | a0001c0001t0007g0165 a0001c0001t0025g0026 a0001c0001t0027g0178 |
4 | HG03209.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+247T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570535 | |||||||
chr2:241570536 | G | GT | 109 | a0001c0001t0001g0278 a0001c0001t0002g0003 a0001c0001t0002g0016 others(106): Show |
151 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.513+248_513+249ins others(1): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570536 | |||||||
chr2:241570537 | G | T | 1 | a0001c0001t0002g0174 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.513+249G>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570537 | |||||||
chr2:241570538 | G | T | 3 | a0001c0001t0007g0165 a0001c0001t0025g0026 a0001c0001t0027g0178 |
4 | HG03209.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+250G>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570538 | |||||||
chr2:241570557 | G | A | 2 | a0001c0001t0007g0165 a0001c0001t0027g0178 |
2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.513+269G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570557 | |||||||
chr2:241570565 | A | G | 40 | a0001c0001t0001g0245 a0001c0001t0001g0278 a0001c0001t0006g0004 others(37): Show |
53 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.513+277A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570565 | |||||||
chr2:241570570 | C | G | 41 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0001g0278 others(38): Show |
58 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.513+282C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570570 | |||||||
chr2:241570570 | C | T | 1 | a0001c0001t0002g0045 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.513+282C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570570 | |||||||
chr2:241570571 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.513+283G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570571 | |||||||
chr2:241570575 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.513+287G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570575 | |||||||
chr2:241570575 | G | GGGAGGGA others(452): Show |
1 | a0001c0001t0038g0123 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.513+298_513+299ins others(459): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570575 | ||||||
chr2:241570583 | G | A | 2 | a0001c0001t0021g0185 a0001c0001t0039g0227 |
2 | HG03490.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.513+295G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570583 | |||||||
chr2:241570584 | T | C | 1 | a0001c0001t0023g0206 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.513+296T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570584 | |||||||
chr2:241570587 | C | T | 22 | a0001c0001t0001g0278 a0001c0001t0006g0004 a0001c0001t0006g0137 others(19): Show |
30 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.513+299C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570587 | |||||||
chr2:241570588 | G | A | 4 | a0001c0001t0005g0131 a0001c0001t0005g0263 a0001c0001t0010g0055 others(1): Show |
6 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+300G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570588 | |||||||
chr2:241570590 | A | G | 11 | a0001c0001t0007g0008 a0001c0001t0007g0056 a0001c0001t0007g0217 others(8): Show |
15 | HG02056.hp1 HG02451.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.513+302A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570590 | |||||||
chr2:241570599 | T | C | 72 | a0001c0001t0001g0278 a0001c0001t0002g0003 a0001c0001t0002g0016 others(69): Show |
100 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.513+311T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570599 | |||||||
chr2:241570600 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.513+312G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570600 | |||||||
chr2:241570600 | G | GTCTGAGC others(378): Show |
1 | a0001c0001t0002g0089 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.513+363_513+364ins others(385): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570600 | ||||||
chr2:241570611 | T | C | 3 | a0001c0001t0018g0145 a0001c0001t0018g0146 a0001c0001t0018g0147 |
3 | HG02818.hp1 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.513+323T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570611 | |||||||
chr2:241570612 | GT | G | 15 | a0001c0001t0001g0278 a0001c0001t0007g0008 a0001c0001t0007g0056 others(12): Show |
20 | HG01074.hp1 HG01074.hp2 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.513+325delT | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570612 | |||||||
chr2:241570613 | T | TGGGGGTG others(299): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0119 |
6 | HG01934.hp2 NA18960.hp2 NA19056.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+363_513+364ins others(306): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570613 | ||||||
chr2:241570635 | C | T | 1 | a0001c0001t0038g0123 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.513+347C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570635 | |||||||
chr2:241570642 | G | A | 52 | a0001c0001t0001g0121 a0001c0001t0001g0278 a0001c0001t0005g0015 others(49): Show |
66 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.513+354G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570642 | |||||||
chr2:241570647 | G | C | 42 | a0001c0001t0001g0121 a0001c0001t0001g0278 a0001c0001t0005g0015 others(39): Show |
56 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.513+359G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570647 | |||||||
chr2:241570652 | A | AGGAGGGA others(70): Show |
1 | a0001c0001t0001g0079 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.513+401_513+402ins others(77): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570652 | ||||||
chr2:241570652 | A | G | 133 | a0001c0001t0001g0121 a0001c0001t0001g0278 a0001c0001t0002g0003 others(130): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.513+364A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570652 | |||||||
chr2:241570652 | AGGAGGGA others(69): Show |
A | 1 | a0001c0001t0001g0076 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.513+376_513+451del others(76): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570652 | ||||||
chr2:241570652 | AGGAGGGA others(222): Show |
A | 1 | a0001c0001t0001g0152 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.513+376_513+604del | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570652 | ||||||
chr2:241570660 | G | A | 4 | a0001c0001t0002g0089 a0001c0001t0002g0125 a0001c0001t0002g0143 others(1): Show |
4 | HG02683.hp2 NA18974.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+372G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570660 | |||||||
chr2:241570664 | T | C | 100 | a0001c0001t0001g0121 a0001c0001t0001g0278 a0001c0001t0002g0003 others(97): Show |
134 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.513+376T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570664 | |||||||
chr2:241570667 | A | ATGGGTGA others(69): Show |
1 | a0001c0001t0027g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.513+434_513+435ins others(76): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570667 | ||||||
chr2:241570667 | A | G | 1 | a0001c0001t0021g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.513+379A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570667 | |||||||
chr2:241570676 | C | T | 36 | a0001c0001t0001g0121 a0001c0001t0001g0278 a0001c0001t0006g0004 others(33): Show |
45 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.513+388C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570676 | |||||||
chr2:241570677 | C | G | 37 | a0001c0001t0001g0121 a0001c0001t0001g0278 a0001c0001t0002g0209 others(34): Show |
46 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.513+389C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570677 | |||||||
chr2:241570688 | T | C | 3 | a0001c0001t0018g0145 a0001c0001t0018g0146 a0001c0001t0018g0147 |
3 | HG02818.hp1 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.513+400T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570688 | |||||||
chr2:241570689 | G | GT | 61 | a0001c0001t0001g0121 a0001c0001t0001g0278 a0001c0001t0002g0089 others(58): Show |
79 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.513+401_513+402ins others(1): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(71): Show |
1 | a0001c0001t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.513+401_513+402ins others(78): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(764): Show |
1 | a0001c0001t0002g0158 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.513+401_513+402ins others(771): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(687): Show |
4 | a0001c0001t0002g0029 a0001c0001t0002g0122 a0001c0001t0002g0141 others(1): Show |
5 | HG00408.hp1 HG02165.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+401_513+402ins others(694): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(764): Show |
2 | a0001c0001t0012g0095 a0004c0010t0002g0130 |
2 | HG02040.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.513+401_513+402ins others(771): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(765): Show |
1 | a0001c0001t0035g0088 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.513+401_513+402ins others(772): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(760): Show |
1 | a0001c0001t0002g0174 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.513+401_513+402ins others(767): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(456): Show |
1 | a0001c0008t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.513+401_513+402ins others(463): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(764): Show |
1 | a0001c0001t0002g0148 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.513+401_513+402ins others(771): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(456): Show |
3 | a0001c0001t0002g0135 a0001c0001t0002g0159 a0001c0001t0002g0243 |
3 | HG02071.hp1 HG02083.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.513+401_513+402ins others(463): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(1218): Show |
1 | a0001c0001t0002g0156 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.513+401_513+402ins others(1225): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(918): Show |
1 | a0001c0001t0002g0198 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.513+401_513+402ins others(925): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(763): Show |
1 | a0001c0001t0002g0251 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.513+401_513+402ins others(770): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(764): Show |
1 | a0001c0001t0002g0212 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.513+401_513+402ins others(771): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(764): Show |
40 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0020 others(37): Show |
64 | HG00099.hp2 HG00438.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.513+401_513+402ins others(771): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(764): Show |
1 | a0001c0001t0037g0210 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.513+401_513+402ins others(771): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(841): Show |
1 | a0001c0001t0002g0180 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.513+401_513+402ins others(848): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(456): Show |
1 | a0001c0001t0014g0160 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.513+401_513+402ins others(463): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(764): Show |
1 | a0001c0001t0014g0017 | 3 | NA18992.hp2 NA18998.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.513+401_513+402ins others(771): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(764): Show |
1 | a0001c0001t0002g0043 | 2 | NA18962.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.513+401_513+402ins others(771): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(764): Show |
1 | a0001c0001t0002g0149 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.513+401_513+402ins others(771): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570689 | G | GTGGGGGT others(841): Show |
1 | a0001c0001t0002g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.513+401_513+402ins others(848): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570689 | |||||||
chr2:241570718 | A | G | 81 | a0001c0001t0001g0121 a0001c0001t0001g0278 a0001c0001t0002g0003 others(78): Show |
115 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.513+430A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570718 | |||||||
chr2:241570723 | C | G | 71 | a0001c0001t0001g0121 a0001c0001t0001g0278 a0001c0001t0002g0003 others(68): Show |
100 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.513+435C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570723 | |||||||
chr2:241570728 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0278 |
2 | HG01255.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.513+440G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570728 | |||||||
chr2:241570728 | G | GGGAGGGA others(604): Show |
1 | a0001c0001t0005g0267 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.513+451_513+452ins others(611): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570728 | ||||||
chr2:241570740 | C | CGGATGGG others(296): Show |
1 | a0001c0001t0038g0123 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.513+465_513+466ins others(303): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570740 | ||||||
chr2:241570740 | C | CGGATGGG others(524): Show |
1 | a0001c0007t0030g0115 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.513+465_513+466ins others(531): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570740 | ||||||
chr2:241570740 | C | CGGGTGGG others(69): Show |
1 | a0001c0001t0021g0187 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.513+454_513+455ins others(76): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570740 | ||||||
chr2:241570740 | C | CGGGTGGG others(146): Show |
1 | a0001c0001t0039g0227 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.513+454_513+455ins others(153): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570740 | ||||||
chr2:241570740 | C | T | 29 | a0001c0001t0001g0121 a0001c0001t0001g0278 a0001c0001t0005g0015 others(26): Show |
38 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.513+452C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570740 | |||||||
chr2:241570740 | CGGATGGG others(70): Show |
C | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513+464_513+540del others(77): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570740 | ||||||
chr2:241570743 | A | G | 22 | a0001c0001t0006g0004 a0001c0001t0006g0137 a0001c0001t0006g0203 others(19): Show |
30 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.513+455A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570743 | |||||||
chr2:241570752 | T | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0278 a0001c0001t0002g0125 |
3 | HG01255.hp1 HG02683.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.513+464T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570752 | |||||||
chr2:241570753 | G | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0278 |
2 | HG01255.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.513+465G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570753 | |||||||
chr2:241570753 | GTCTGAGC others(70): Show |
G | 1 | a0001c0001t0001g0245 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.513+478_513+554del others(77): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570753 | ||||||
chr2:241570765 | GT | G | 31 | a0001c0001t0001g0121 a0001c0001t0001g0164 a0001c0001t0001g0278 others(28): Show |
40 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.513+478delT | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570765 | |||||||
chr2:241570766 | T | TGGGGGTG others(69): Show |
2 | a0001c0001t0001g0244 a0001c0001t0001g0253 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.513+506_513+507ins others(76): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570766 | ||||||
chr2:241570766 | T | TGGGGGTG others(223): Show |
1 | a0001c0001t0011g0080 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.513+506_513+507ins others(230): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570766 | ||||||
chr2:241570766 | T | TGGGGGTG others(528): Show |
1 | a0006c0005t0007g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.513+506_513+507ins others(535): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570766 | ||||||
chr2:241570766 | T | TGGGGGTG others(374): Show |
1 | a0001c0001t0011g0182 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.513+506_513+507ins others(381): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570766 | ||||||
chr2:241570766 | T | TGGGGGTG others(756): Show |
1 | a0001c0001t0043g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.513+506_513+507ins others(763): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570766 | ||||||
chr2:241570788 | C | CGAGGGTA others(223): Show |
1 | a0001c0001t0005g0270 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.513+506_513+507ins others(230): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570788 | ||||||
chr2:241570795 | G | A | 39 | a0001c0001t0001g0121 a0001c0001t0001g0244 a0001c0001t0001g0253 others(36): Show |
49 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.513+507G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570795 | |||||||
chr2:241570800 | G | C | 35 | a0001c0001t0001g0121 a0001c0001t0001g0244 a0001c0001t0001g0253 others(32): Show |
45 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.513+512G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570800 | |||||||
chr2:241570805 | A | AGGAGGGA others(147): Show |
1 | a0001c0001t0001g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.513+528_513+529ins others(154): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570805 | ||||||
chr2:241570805 | A | AGGAGGGA others(224): Show |
1 | a0001c0001t0001g0154 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.513+528_513+529ins others(231): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570805 | ||||||
chr2:241570805 | A | G | 161 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0001g0121 others(158): Show |
217 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.513+517A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570805 | |||||||
chr2:241570805 | AGGAGGGA others(69): Show |
A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0022 others(44): Show |
87 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.513+529_513+604del others(76): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570805 | ||||||
chr2:241570813 | G | A | 65 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0020 others(62): Show |
94 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.513+525G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570813 | |||||||
chr2:241570813 | G | GTGGCGGA others(224): Show |
1 | a0001c0001t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.513+528_513+529ins others(231): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570813 | ||||||
chr2:241570813 | G | GTGGCGGA others(1302): Show |
1 | a0001c0001t0002g0127 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.513+528_513+529ins others(1309): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570813 | ||||||
chr2:241570813 | G | GTGGCGGA others(686): Show |
3 | a0001c0001t0002g0143 a0001c0001t0002g0218 a0001c0001t0029g0061 |
3 | HG03704.hp1 NA18974.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.513+528_513+529ins others(693): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570813 | ||||||
chr2:241570817 | T | C | 110 | a0001c0001t0001g0077 a0001c0001t0001g0121 a0001c0001t0001g0244 others(107): Show |
145 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.513+529T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570817 | |||||||
chr2:241570820 | A | G | 4 | a0001c0001t0007g0165 a0001c0001t0018g0145 a0001c0001t0018g0146 others(1): Show |
4 | HG02818.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+532A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570820 | |||||||
chr2:241570829 | C | T | 30 | a0001c0001t0001g0077 a0001c0001t0001g0121 a0001c0001t0001g0244 others(27): Show |
36 | HG01074.hp1 HG01074.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.513+541C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570829 | |||||||
chr2:241570830 | C | CTCTGAGC others(222): Show |
3 | a0001c0001t0001g0164 a0001c0001t0001g0192 a0001c0001t0032g0231 |
3 | HG02559.hp2 HG02886.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.513+659_513+660ins others(229): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570830 | ||||||
chr2:241570830 | C | CTCTGAGC others(299): Show |
1 | a0001c0001t0001g0193 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.513+669_513+670ins others(306): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570830 | ||||||
chr2:241570830 | C | G | 30 | a0001c0001t0001g0077 a0001c0001t0001g0121 a0001c0001t0001g0244 others(27): Show |
36 | HG01074.hp1 HG01074.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.513+542C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570830 | |||||||
chr2:241570842 | G | GGGGGGTG others(451): Show |
1 | a0001c0001t0031g0232 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.513+659_513+660ins others(458): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570842 | ||||||
chr2:241570842 | G | GT | 79 | a0001c0001t0001g0121 a0001c0001t0001g0278 a0001c0001t0002g0003 others(76): Show |
108 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.513+554_513+555ins others(1): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570842 | |||||||
chr2:241570842 | G | GTGGGGGT others(67): Show |
1 | a0001c0001t0005g0270 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.513+554_513+555ins others(74): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570842 | |||||||
chr2:241570842 | G | GTGGGGGT others(918): Show |
1 | a0001c0001t0002g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.513+554_513+555ins others(925): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570842 | |||||||
chr2:241570842 | G | GTGGGGGT others(529): Show |
1 | a0001c0001t0002g0159 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.513+554_513+555ins others(536): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570842 | |||||||
chr2:241570842 | G | GTGGGGGT others(148): Show |
1 | a0001c0001t0014g0160 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.513+554_513+555ins others(155): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570842 | |||||||
chr2:241570842 | G | GTGGGGGT others(302): Show |
1 | a0001c0001t0002g0243 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.513+554_513+555ins others(309): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570842 | |||||||
chr2:241570842 | G | GTGGGGGT others(302): Show |
1 | a0001c0001t0002g0089 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.513+554_513+555ins others(309): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570842 | |||||||
chr2:241570871 | A | G | 15 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0001g0121 others(12): Show |
20 | HG00642.hp1 HG01255.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.513+583A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570871 | |||||||
chr2:241570876 | C | CGTACGGG others(222): Show |
1 | a0001c0001t0017g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.513+630_513+631ins others(229): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570876 | ||||||
chr2:241570876 | C | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0001g0121 others(10): Show |
18 | HG01255.hp1 HG01891.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.513+588C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570876 | |||||||
chr2:241570881 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0278 a0001c0009t0001g0139 |
3 | HG01255.hp1 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.513+593G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570881 | |||||||
chr2:241570881 | GGGAGGGA others(70): Show |
G | 1 | a0001c0001t0004g0097 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.513+670_513+746del others(77): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570881 | ||||||
chr2:241570889 | G | A | 1 | a0001c0001t0006g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.513+601G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570889 | |||||||
chr2:241570893 | C | T | 29 | a0001c0001t0005g0015 a0001c0001t0005g0044 a0001c0001t0005g0049 others(26): Show |
39 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.513+605C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570893 | |||||||
chr2:241570896 | A | G | 3 | a0001c0001t0006g0205 a0001c0001t0007g0165 a0001c0001t0021g0185 |
3 | HG00642.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.513+608A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570896 | |||||||
chr2:241570905 | T | C | 5 | a0001c0001t0005g0267 a0001c0001t0006g0205 a0001c0001t0007g0183 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+617T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570905 | |||||||
chr2:241570906 | G | C | 5 | a0001c0001t0005g0267 a0001c0001t0006g0205 a0001c0001t0007g0183 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+618G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570906 | |||||||
chr2:241570913 | C | T | 25 | a0001c0001t0005g0015 a0001c0001t0005g0044 a0001c0001t0005g0049 others(22): Show |
34 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.513+625C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570913 | |||||||
chr2:241570917 | T | C | 27 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0005g0015 others(24): Show |
40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.513+629T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570917 | |||||||
chr2:241570918 | G | A | 25 | a0001c0001t0005g0015 a0001c0001t0005g0044 a0001c0001t0005g0049 others(22): Show |
34 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.513+630G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570918 | |||||||
chr2:241570918 | G | GGGGGGTG others(68): Show |
11 | a0001c0001t0007g0008 a0001c0001t0007g0056 a0001c0001t0007g0217 others(8): Show |
16 | HG01074.hp1 HG01074.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.513+630_513+631ins others(75): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570918 | |||||||
chr2:241570918 | GT | G | 11 | a0001c0001t0006g0205 a0001c0001t0007g0183 a0001c0001t0007g0184 others(8): Show |
12 | HG00642.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.513+631delT | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570918 | |||||||
chr2:241570919 | T | G | 11 | a0001c0001t0007g0008 a0001c0001t0007g0056 a0001c0001t0007g0217 others(8): Show |
16 | HG01074.hp1 HG01074.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.513+631T>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570919 | |||||||
chr2:241570919 | T | TGGGGGTG others(145): Show |
1 | a0001c0001t0001g0154 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.513+659_513+660ins others(152): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570919 | ||||||
chr2:241570921 | G | T | 25 | a0001c0001t0005g0015 a0001c0001t0005g0044 a0001c0001t0005g0049 others(22): Show |
34 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.513+633G>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570921 | |||||||
chr2:241570948 | G | A | 35 | a0001c0001t0005g0270 a0001c0001t0006g0004 a0001c0001t0006g0137 others(32): Show |
44 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.513+660G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570948 | |||||||
chr2:241570953 | G | C | 28 | a0001c0001t0005g0270 a0001c0001t0006g0004 a0001c0001t0006g0137 others(25): Show |
36 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.513+665G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570953 | |||||||
chr2:241570958 | A | AGGAGGGA others(70): Show |
1 | a0001c0001t0001g0248 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.513+678_513+679ins others(77): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570958 | ||||||
chr2:241570958 | A | AGGAGGGA others(147): Show |
1 | a0001c0001t0001g0079 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.513+746_513+747ins others(154): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570958 | ||||||
chr2:241570958 | A | AGGAGGGA others(70): Show |
22 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0041 others(19): Show |
53 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.513+692_513+768dup others(77): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570958 | ||||||
chr2:241570958 | A | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0019 others(184): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.513+670A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570958 | |||||||
chr2:241570970 | C | T | 29 | a0001c0001t0005g0015 a0001c0001t0005g0044 a0001c0001t0005g0049 others(26): Show |
38 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.513+682C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570970 | |||||||
chr2:241570971 | G | A | 2 | a0001c0001t0002g0159 a0001c0001t0002g0271 |
2 | HG02071.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.513+683G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570971 | |||||||
chr2:241570971 | G | GGATGGGT others(70): Show |
1 | a0001c0001t0001g0249 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.513+759_513+760ins others(77): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570971 | ||||||
chr2:241570973 | A | G | 22 | a0001c0001t0006g0004 a0001c0001t0006g0137 a0001c0001t0006g0203 others(19): Show |
30 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.513+685A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570973 | |||||||
chr2:241570982 | T | C | 19 | a0001c0001t0005g0270 a0001c0001t0006g0205 a0001c0001t0007g0008 others(16): Show |
24 | HG00642.hp1 HG01074.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.513+694T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570982 | |||||||
chr2:241570983 | G | C | 19 | a0001c0001t0005g0270 a0001c0001t0006g0205 a0001c0001t0007g0008 others(16): Show |
24 | HG00642.hp1 HG01074.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.513+695G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570983 | |||||||
chr2:241570994 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0119 |
6 | HG01934.hp2 NA18960.hp2 NA19056.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+706T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570994 | |||||||
chr2:241570995 | G | GGGGGGGT others(221): Show |
1 | a0001c0001t0006g0236 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.513+707_513+708ins others(228): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570995 | |||||||
chr2:241570995 | G | GGGGGGTG others(220): Show |
1 | a0006c0005t0007g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.513+707_513+708ins others(227): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570995 | |||||||
chr2:241570995 | G | GGGGGGTG others(373): Show |
2 | a0001c0001t0021g0186 a0001c0001t0021g0187 |
2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.513+707_513+708ins others(380): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570995 | |||||||
chr2:241570995 | G | GGGGGGTG others(831): Show |
1 | a0001c0002t0011g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.513+707_513+708ins others(838): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570995 | |||||||
chr2:241570995 | G | GGGGGGTG others(221): Show |
1 | a0001c0001t0006g0004 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.513+707_513+708ins others(228): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570995 | |||||||
chr2:241570995 | G | GGGGGGTG others(220): Show |
19 | a0001c0001t0006g0004 a0001c0001t0006g0137 a0001c0001t0006g0203 others(16): Show |
26 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.513+707_513+708ins others(227): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570995 | |||||||
chr2:241570995 | GT | G | 96 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0020 others(93): Show |
130 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.513+708delT | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570995 | |||||||
chr2:241570996 | T | G | 24 | a0001c0001t0006g0004 a0001c0001t0006g0137 a0001c0001t0006g0203 others(21): Show |
32 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.513+708T>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241570996 | |||||||
chr2:241570996 | T | TGGGGGGT others(379): Show |
1 | a0001c0001t0005g0267 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.513+713_513+714ins others(386): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570996 | ||||||
chr2:241570996 | T | TGGGGGGT others(379): Show |
1 | a0001c0001t0038g0123 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.513+713_513+714ins others(386): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570996 | ||||||
chr2:241570996 | T | TGGGGGTG others(377): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0119 |
6 | HG01934.hp2 NA18960.hp2 NA19056.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+736_513+737ins others(384): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570996 | ||||||
chr2:241570996 | T | TGGGGGTG others(145): Show |
1 | a0001c0001t0007g0276 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.513+736_513+737ins others(152): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570996 | ||||||
chr2:241570996 | T | TGGGGGTG others(527): Show |
1 | a0001c0001t0021g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.513+746_513+747ins others(534): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570996 | ||||||
chr2:241570996 | T | TGGGGGTG others(1067): Show |
24 | a0001c0001t0005g0015 a0001c0001t0005g0044 a0001c0001t0005g0049 others(21): Show |
33 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.513+729_513+730ins others(1074): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241570996 | ||||||
chr2:241571018 | C | T | 1 | a0001c0001t0005g0112 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.513+730C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571018 | |||||||
chr2:241571025 | G | A | 2 | a0001c0001t0027g0153 a0001c0001t0027g0178 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.513+737G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571025 | |||||||
chr2:241571030 | G | C | 2 | a0001c0001t0027g0153 a0001c0001t0027g0178 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.513+742G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571030 | |||||||
chr2:241571035 | G | A | 1 | a0001c0001t0002g0129 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.513+747G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571035 | |||||||
chr2:241571043 | G | A | 101 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0020 others(98): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.513+755G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571043 | |||||||
chr2:241571043 | G | GTGGTGGA others(1068): Show |
1 | a0001c0001t0005g0112 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.513+758_513+759ins others(1075): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241571043 | ||||||
chr2:241571050 | A | ATGGGTGA others(1455): Show |
3 | a0001c0001t0002g0031 a0001c0001t0002g0133 a0001c0001t0012g0108 |
4 | HG00639.hp2 HG01175.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+768_513+769ins others(1462): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241571050 | ||||||
chr2:241571050 | A | ATGGGTGA others(1993): Show |
1 | a0001c0001t0002g0261 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.513+768_513+769ins others(2000): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241571050 | ||||||
chr2:241571050 | A | ATGGGTGA others(145): Show |
1 | a0001c0001t0027g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.513+768_513+769ins others(152): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241571050 | ||||||
chr2:241571050 | A | ATGGGTGA others(525): Show |
3 | a0001c0001t0011g0080 a0001c0001t0011g0181 a0001c0001t0011g0190 |
3 | HG02896.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.513+768_513+769ins others(532): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241571050 | ||||||
chr2:241571050 | A | G | 109 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0002g0003 others(106): Show |
151 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.513+762A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571050 | |||||||
chr2:241571053 | G | GGTGAGTG others(70): Show |
1 | a0001c0001t0001g0219 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.513+768_513+769ins others(77): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241571053 | ||||||
chr2:241571094 | G | C | 1 | a0001c0001t0008g0113 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.513+806G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571094 | |||||||
chr2:241571138 | C | G | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513+850C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571138 | |||||||
chr2:241571238 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.513+950C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571238 | |||||||
chr2:241571306 | C | CAGTTGCC others(42): Show |
2 | a0001c0001t0004g0083 a0001c0001t0004g0107 |
2 | HG01192.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.514-991_514-990ins others(49): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571306 | |||||||
chr2:241571331 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.514-966T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571331 | |||||||
chr2:241571333 | G | A | 3 | a0001c0001t0015g0162 a0001c0001t0015g0241 a0001c0001t0015g0242 |
3 | HG01109.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.514-964G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571333 | |||||||
chr2:241571364 | T | C | 149 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0020 others(146): Show |
200 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.514-933T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571364 | |||||||
chr2:241571413 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.514-884G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571413 | |||||||
chr2:241571427 | C | T | 3 | a0001c0001t0015g0162 a0001c0001t0015g0241 a0001c0001t0015g0242 |
3 | HG01109.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.514-870C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571427 | |||||||
chr2:241571428 | G | A | 2 | a0001c0001t0027g0153 a0001c0001t0027g0178 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.514-869G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571428 | |||||||
chr2:241571539 | A | C | 159 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0002g0003 others(156): Show |
215 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.514-758A>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571539 | |||||||
chr2:241571567 | G | A | 39 | a0001c0001t0006g0004 a0001c0001t0006g0137 a0001c0001t0006g0203 others(36): Show |
52 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.514-730G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571567 | |||||||
chr2:241571668 | C | T | 39 | a0001c0001t0006g0004 a0001c0001t0006g0137 a0001c0001t0006g0203 others(36): Show |
52 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.514-629C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571668 | |||||||
chr2:241571771 | C | T | 1 | a0001c0001t0025g0026 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.514-526C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571771 | |||||||
chr2:241571802 | G | A | 35 | a0001c0001t0006g0004 a0001c0001t0006g0137 a0001c0001t0006g0203 others(32): Show |
47 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.514-495G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571802 | |||||||
chr2:241571806 | G | A | 1 | a0001c0001t0027g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.514-491G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571806 | |||||||
chr2:241571817 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.514-480C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571817 | |||||||
chr2:241571818 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.514-479G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571818 | |||||||
chr2:241571913 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0124 a0001c0001t0001g0223 |
3 | HG00621.hp1 NA18952.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.514-384C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241571913 | |||||||
chr2:241572037 | C | G | 1 | a0001c0001t0001g0248 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.514-260C>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241572037 | |||||||
chr2:241572038 | G | C | 1 | a0001c0001t0001g0248 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.514-259G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241572038 | |||||||
chr2:241572071 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.514-226T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241572071 | |||||||
chr2:241572075 | G | A | 3 | a0001c0001t0018g0145 a0001c0001t0018g0146 a0001c0001t0018g0147 |
3 | HG02818.hp1 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.514-222G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241572075 | |||||||
chr2:241572132 | T | C | 159 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0002g0003 others(156): Show |
215 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.514-165T>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241572132 | |||||||
chr2:241572150 | G | A | 1 | a0001c0001t0008g0113 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.514-147G>A | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241572150 | |||||||
chr2:241572168 | G | C | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.514-129G>C | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241572168 | |||||||
chr2:241572191 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0114 |
2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.514-106A>G | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241572191 | |||||||
chr2:241572217 | A | ACGGTGCT others(11): Show |
1 | a0001c0001t0001g0023 | 3 | HG01099.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.514-67_514-50dupGC others(16): Show |
BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 241572217 | ||||||
chr2:241572218 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.514-79C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241572218 | |||||||
chr2:241572275 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.514-22C>T | BOK | ENSG00000176720.6 | transcript | ENST00000318407.5 | protein_coding | 4/4 | chr2 | 241572275 |