Item | Value |
---|---|
geneid | 54665 |
ensemblid | ENSG00000081019.14 |
hgncid | 25642 |
symbol | RSBN1 |
name | round spermatid basic protein 1 |
refseq_nuc | NM_018364.5 |
refseq_prot | NP_060834.2 |
ensembl_nuc | ENST00000261441.9 |
ensembl_prot | ENSP00000261441.5 |
mane_status | MANE Select |
chr | chr1 |
start | 113761832 |
end | 113812476 |
strand | - |
ver | v1.2 |
region | chr1:113761832-113812476 |
region5000 | chr1:113756832-113817476 |
regionname0 | RSBN1_chr1_113761832_113812476 |
regionname5000 | RSBN1_chr1_113756832_113817476 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 802 | 339 | 72 | 66 | 149 | 14 | 36 | 119 | RSBN1_chr1_113756832_113817476 | RSBN1 | MFISG others(797): Show |
chr1 | 113756832 | 113817476 |
a0002 | 0/0 | 802 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | MFISG others(797): Show |
chr1 | 113756832 | 113817476 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2406 | 274 | 67 | 54 | 107 | 13 | 31 | RSBN1_chr1_113756832_113817476 | RSBN1 | ATGTT others(2401): Show |
chr1 | 113756832 | 113817476 | ||
a0001c0002 | 0/0 | 2406 | 57 | 0 | 12 | 39 | 1 | 5 | RSBN1_chr1_113756832_113817476 | RSBN1 | ATGTT others(2401): Show |
chr1 | 113756832 | 113817476 | ||
a0001c0003 | 0/0 | 2406 | 3 | 3 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | ATGTT others(2401): Show |
chr1 | 113756832 | 113817476 | ||
a0001c0004 | 0/0 | 2406 | 3 | 0 | 0 | 3 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | ATGTT others(2401): Show |
chr1 | 113756832 | 113817476 | ||
a0001c0005 | 0/0 | 2406 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | ATGTT others(2401): Show |
chr1 | 113756832 | 113817476 | ||
a0002c0006 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | ATGTT others(2401): Show |
chr1 | 113756832 | 113817476 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6619 | 90 | 1 | 20 | 57 | 5 | 7 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6614): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0002 | 1/1 | 6621 | 76 | 21 | 13 | 25 | 5 | 10 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6616): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0004 | 0/0 | 6622 | 34 | 15 | 10 | 1 | 3 | 5 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6617): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0005 | 0/0 | 6622 | 15 | 5 | 1 | 4 | 0 | 5 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6617): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0006 | 0/0 | 6620 | 9 | 3 | 0 | 6 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6615): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0007 | 0/0 | 6621 | 9 | 0 | 1 | 7 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6616): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0008 | 0/0 | 6618 | 8 | 7 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6613): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0009 | 0/0 | 6617 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6612): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0010 | 0/0 | 6622 | 5 | 4 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6617): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0011 | 0/0 | 6621 | 4 | 3 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6616): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0012 | 0/0 | 6623 | 3 | 2 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6618): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0013 | 0/0 | 6622 | 3 | 0 | 1 | 0 | 0 | 2 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6617): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0014 | 0/0 | 6621 | 2 | 0 | 2 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6616): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0015 | 0/0 | 6621 | 2 | 1 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6616): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0016 | 0/0 | 6622 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6617): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0017 | 0/0 | 6623 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6618): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0018 | 0/0 | 6621 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6616): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0021 | 0/0 | 6619 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6614): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0022 | 0/0 | 6623 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6618): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0023 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6667): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0024 | 0/0 | 6621 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6616): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0025 | 0/0 | 6621 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6616): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0026 | 0/0 | 6621 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6616): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0027 | 0/0 | 6621 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6616): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0028 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6617): Show |
chr1 | 113756832 | 113817476 |
a0001c0001t0030 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6617): Show |
chr1 | 113756832 | 113817476 |
a0001c0002t0002 | 0/0 | 6621 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6616): Show |
chr1 | 113756832 | 113817476 |
a0001c0002t0003 | 0/0 | 6616 | 41 | 0 | 3 | 34 | 1 | 3 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6611): Show |
chr1 | 113756832 | 113817476 |
a0001c0002t0004 | 0/0 | 6622 | 7 | 0 | 7 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6617): Show |
chr1 | 113756832 | 113817476 |
a0001c0002t0009 | 0/0 | 6617 | 5 | 0 | 1 | 4 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6612): Show |
chr1 | 113756832 | 113817476 |
a0001c0002t0019 | 0/0 | 6616 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6611): Show |
chr1 | 113756832 | 113817476 |
a0001c0002t0029 | 0/0 | 6616 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6611): Show |
chr1 | 113756832 | 113817476 |
a0001c0002t0031 | 0/0 | 6616 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6611): Show |
chr1 | 113756832 | 113817476 |
a0001c0003t0002 | 0/0 | 6621 | 3 | 3 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6616): Show |
chr1 | 113756832 | 113817476 |
a0001c0004t0002 | 0/0 | 6621 | 3 | 0 | 0 | 3 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6616): Show |
chr1 | 113756832 | 113817476 |
a0001c0005t0003 | 0/0 | 6616 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6611): Show |
chr1 | 113756832 | 113817476 |
a0001c0005t0020 | 0/0 | 6616 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6611): Show |
chr1 | 113756832 | 113817476 |
a0002c0006t0003 | 0/0 | 6616 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | GCTTT others(6611): Show |
chr1 | 113756832 | 113817476 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0003 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0005g0006 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0006g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0007g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0007g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0007g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0008g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0008g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0009g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0010g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0010g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0010g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0011g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0011g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0012g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0012g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0013g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0013g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0013g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0014g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0014g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0015g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0016g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0016g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0017g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0018g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0021g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0022g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0023g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0024g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0025g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0026g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0027g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0028g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0001t0030g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0004 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0004g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0004g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0009g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0009g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0009g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0009g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0009g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0019g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0029g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0002t0031g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0003t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0004t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0004t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0004t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0005t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0001c0005t0020g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
a0002c0006t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0003 | g0249 | EUR | GBR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0149 | EUR | GBR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0202 | EUR | GBR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00423 | hp2 | a0001 | c0002 | t0003 | g0247 | EAS | CHS | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00597 | hp1 | a0001 | c0002 | t0003 | g0266 | EAS | CHS | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00621 | hp2 | a0001 | c0001 | t0006 | g0087 | EAS | CHS | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00642 | hp2 | a0001 | c0002 | t0004 | g0012 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00733 | hp2 | a0001 | c0002 | t0009 | g0255 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00738 | hp1 | a0001 | c0001 | t0011 | g0016 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0148 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG00741 | hp2 | a0001 | c0001 | t0012 | g0109 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01070 | hp2 | a0001 | c0002 | t0004 | g0239 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01081 | hp2 | a0001 | c0001 | t0022 | g0158 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01099 | hp1 | a0001 | c0002 | t0004 | g0248 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01099 | hp2 | a0001 | c0001 | t0015 | g0023 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0147 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01168 | hp1 | a0001 | c0001 | t0014 | g0229 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01169 | hp1 | a0001 | c0002 | t0004 | g0012 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01169 | hp2 | a0001 | c0001 | t0014 | g0226 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0177 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0175 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0176 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01243 | hp1 | a0001 | c0001 | t0025 | g0212 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01255 | hp2 | a0001 | c0002 | t0004 | g0012 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01257 | hp2 | a0001 | c0001 | t0013 | g0157 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0151 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01358 | hp2 | a0001 | c0002 | t0004 | g0042 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01433 | hp1 | a0001 | c0002 | t0019 | g0242 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01496 | hp1 | a0001 | c0002 | t0004 | g0042 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0211 | EUR | IBS | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0152 | EUR | IBS | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0032 | EUR | IBS | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0032 | EUR | IBS | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0196 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01943 | hp1 | a0001 | c0002 | t0003 | g0257 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0045 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02004 | hp1 | a0001 | c0001 | t0018 | g0199 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02015 | hp2 | a0001 | c0001 | t0010 | g0165 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02055 | hp1 | a0001 | c0001 | t0011 | g0070 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02055 | hp2 | a0001 | c0001 | t0012 | g0110 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02056 | hp2 | a0001 | c0002 | t0003 | g0267 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02071 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02074 | hp2 | a0001 | c0004 | t0002 | g0234 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02129 | hp1 | a0001 | c0002 | t0003 | g0039 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02129 | hp2 | a0001 | c0004 | t0002 | g0232 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02132 | hp2 | a0001 | c0002 | t0003 | g0039 | EAS | KHV | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02145 | hp1 | a0001 | c0001 | t0027 | g0156 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0092 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02155 | hp1 | a0001 | c0002 | t0003 | g0251 | EAS | CDX | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02300 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02451 | hp2 | a0001 | c0001 | t0030 | g0193 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0027 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02615 | hp1 | a0001 | c0001 | t0017 | g0112 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02615 | hp2 | a0001 | c0001 | t0010 | g0055 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02622 | hp1 | a0001 | c0001 | t0011 | g0016 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02630 | hp1 | a0001 | c0005 | t0003 | g0235 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0181 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02723 | hp2 | a0001 | c0003 | t0002 | g0044 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0228 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02896 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0160 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02897 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0197 | AFR | ESN | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | ESN | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ESN | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02965 | hp2 | a0001 | c0005 | t0020 | g0236 | AFR | ESN | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0195 | AFR | ESN | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0161 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03017 | hp2 | a0001 | c0001 | t0013 | g0139 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03041 | hp1 | a0001 | c0001 | t0012 | g0113 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | MSL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | MSL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | ESN | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03139 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | ESN | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | ESN | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03195 | hp2 | a0001 | c0001 | t0015 | g0023 | AFR | ESN | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03209 | hp2 | a0001 | c0001 | t0008 | g0051 | AFR | MSL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0166 | AFR | MSL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03225 | hp2 | a0001 | c0001 | t0010 | g0024 | AFR | MSL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0154 | AFR | MSL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03453 | hp2 | a0001 | c0001 | t0010 | g0138 | AFR | MSL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0198 | AFR | MSL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | MSL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0134 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | ESN | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | ESN | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03540 | hp1 | a0001 | c0001 | t0028 | g0167 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | GWD | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | STU | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03688 | hp2 | a0001 | c0002 | t0029 | g0263 | SAS | STU | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0182 | SAS | PJL | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0133 | SAS | BEB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0027 | SAS | BEB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03834 | hp2 | a0001 | c0002 | t0003 | g0254 | SAS | BEB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03927 | hp1 | a0001 | c0001 | t0013 | g0159 | SAS | BEB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0220 | SAS | BEB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | BEB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | STU | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG04115 | hp2 | a0001 | c0001 | t0023 | g0131 | SAS | STU | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG04184 | hp1 | a0001 | c0002 | t0003 | g0250 | SAS | BEB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | BEB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG04199 | hp1 | a0001 | c0002 | t0031 | g0245 | SAS | STU | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | STU | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG04204 | hp1 | a0001 | c0002 | t0003 | g0237 | SAS | STU | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0054 | SAS | STU | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0240 | EAS | CHB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | YRI | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18906 | hp2 | a0001 | c0001 | t0010 | g0024 | AFR | YRI | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18939 | hp1 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18941 | hp2 | a0001 | c0002 | t0003 | g0241 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18942 | hp2 | a0001 | c0002 | t0003 | g0243 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18943 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18944 | hp2 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18947 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18949 | hp2 | a0001 | c0002 | t0009 | g0258 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18951 | hp1 | a0002 | c0006 | t0003 | g0270 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18952 | hp2 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18953 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18959 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18960 | hp1 | a0001 | c0002 | t0009 | g0253 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18962 | hp1 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18965 | hp1 | a0001 | c0002 | t0003 | g0265 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18966 | hp1 | a0001 | c0002 | t0003 | g0041 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18967 | hp2 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18968 | hp2 | a0001 | c0001 | t0006 | g0085 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18972 | hp1 | a0001 | c0001 | t0007 | g0174 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18978 | hp2 | a0001 | c0004 | t0002 | g0233 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18980 | hp2 | a0001 | c0001 | t0016 | g0132 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18984 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18985 | hp1 | a0001 | c0001 | t0008 | g0099 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18985 | hp2 | a0001 | c0001 | t0016 | g0136 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18986 | hp1 | a0001 | c0001 | t0007 | g0144 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18987 | hp2 | a0001 | c0002 | t0003 | g0269 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18990 | hp1 | a0001 | c0001 | t0007 | g0230 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18990 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18994 | hp2 | a0001 | c0002 | t0003 | g0259 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18995 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18995 | hp2 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0135 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19002 | hp2 | a0001 | c0002 | t0003 | g0238 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19003 | hp2 | a0001 | c0001 | t0024 | g0169 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19004 | hp1 | a0001 | c0001 | t0007 | g0143 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19004 | hp2 | a0001 | c0002 | t0003 | g0268 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19006 | hp1 | a0001 | c0002 | t0009 | g0244 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19006 | hp2 | a0001 | c0001 | t0009 | g0086 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19011 | hp1 | a0001 | c0002 | t0003 | g0260 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | LWK | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | LWK | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19056 | hp2 | a0001 | c0002 | t0003 | g0038 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19060 | hp2 | a0001 | c0002 | t0003 | g0041 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19064 | hp1 | a0001 | c0002 | t0003 | g0264 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19064 | hp2 | a0001 | c0001 | t0026 | g0145 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19065 | hp1 | a0001 | c0001 | t0006 | g0097 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19065 | hp2 | a0001 | c0002 | t0003 | g0252 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19066 | hp2 | a0001 | c0002 | t0003 | g0262 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19080 | hp2 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19083 | hp2 | a0001 | c0002 | t0009 | g0246 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19085 | hp1 | a0001 | c0002 | t0003 | g0038 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19086 | hp1 | a0001 | c0002 | t0003 | g0261 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19091 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19091 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | YRI | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | YRI | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ASW | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ASW | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0209 | EUR | TSI | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0014 | EUR | TSI | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA20905 | hp1 | a0001 | c0001 | t0007 | g0170 | SAS | GIH | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0069 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0118 | AFR | ACB | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA18955 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA20300 | hp1 | a0001 | c0001 | t0021 | g0077 | AFR | USA | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | USA | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | LWK | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | LWK | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0214 | REF | REF | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0076 | REF | REF | RSBN1_chr1_113756832_113817476 | RSBN1 | chr1 | 113756832 | 113817476 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:113812188 | T | G | 1 | a0002 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.225A>C | p.Lys75Asn | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/7 | 289/6621 | 225/2409 | 75/802 | chr1 | 113812188 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:113768335 | G | A | 1 | a0001c0003 | 3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.1713C>T | p.Arg571Arg | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 5/7 | 1777/6621 | 1713/2409 | 571/802 | chr1 | 113768335 | |||
chr1:113812032 | T | C | 2 | a0001c0002 a0002c0006 |
58 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(55): Show |
synonymous_variant | LOW | c.381A>G | p.Pro127Pro | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/7 | 445/6621 | 381/2409 | 127/802 | chr1 | 113812032 | |||
chr1:113812311 | G | A | 1 | a0001c0004 | 3 | HG02074.hp2 HG02129.hp2 NA18978.hp2 |
synonymous_variant | LOW | c.102C>T | p.Asp34Asp | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/7 | 166/6621 | 102/2409 | 34/802 | chr1 | 113812311 | |||
chr1:113812320 | T | G | 3 | a0001c0002 a0001c0005 a0002c0006 |
60 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(57): Show |
synonymous_variant | LOW | c.93A>C | p.Arg31Arg | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/7 | 157/6621 | 93/2409 | 31/802 | chr1 | 113812320 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:113761899 | A | G | 4 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0022 others(1): Show |
14 | HG01081.hp2 HG01192.hp1 HG01257.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4081T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 4081 | chr1 | 113761899 | ||||||
chr1:113762496 | T | C | 1 | a0001c0001t0014 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3484A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 3484 | chr1 | 113762496 | ||||||
chr1:113762582 | A | C | 1 | a0001c0002t0019 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3398T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 3398 | chr1 | 113762582 | ||||||
chr1:113762752 | A | C | 1 | a0001c0001t0025 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3228T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 3228 | chr1 | 113762752 | ||||||
chr1:113763059 | T | C | 1 | a0001c0005t0020 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2921A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 2921 | chr1 | 113763059 | ||||||
chr1:113763286 | T | C | 1 | a0001c0001t0026 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2694A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 2694 | chr1 | 113763286 | ||||||
chr1:113763400 | T | A | 1 | a0001c0001t0021 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2580A>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 2580 | chr1 | 113763400 | ||||||
chr1:113763746 | TA | T | 5 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(2): Show |
112 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2233delT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 2233 | chr1 | 113763746 | ||||||
chr1:113763871 | A | ATGACAGA others(43): Show |
1 | a0001c0001t0023 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2059_*2108dupGATC others(46): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 2108 | chr1 | 113763871 | ||||||
chr1:113763953 | A | C | 1 | a0001c0001t0024 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2027T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 2027 | chr1 | 113763953 | ||||||
chr1:113764145 | C | A | 3 | a0001c0001t0005 a0001c0001t0016 a0001c0001t0023 |
18 | HG01175.hp2 HG02895.hp1 HG02897.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1835G>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 1835 | chr1 | 113764145 | ||||||
chr1:113764536 | T | G | 1 | a0001c0001t0027 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1444A>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 1444 | chr1 | 113764536 | ||||||
chr1:113764615 | A | AT | 11 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(8): Show |
79 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1364dupA | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 1364 | chr1 | 113764615 | ||||||
chr1:113764615 | A | ATT | 4 | a0001c0001t0011 a0001c0001t0012 a0001c0001t0017 others(1): Show |
9 | HG00738.hp1 HG00741.hp2 HG01081.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1363_*1364dupAA | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 1364 | chr1 | 113764615 | ||||||
chr1:113764615 | AT | A | 2 | a0001c0001t0008 a0001c0001t0015 |
10 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1364delA | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 1364 | chr1 | 113764615 | ||||||
chr1:113764670 | G | GA | 2 | a0001c0001t0010 a0001c0001t0015 |
7 | HG01099.hp2 HG02015.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1309dupT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 1309 | chr1 | 113764670 | ||||||
chr1:113764670 | GA | G | 5 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(2): Show |
112 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1309delT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 1309 | chr1 | 113764670 | ||||||
chr1:113764867 | TGAAAA | T | 9 | a0001c0001t0009 a0001c0002t0003 a0001c0002t0009 others(6): Show |
53 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1108_*1112delTTTT others(1): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 1108 | chr1 | 113764867 | ||||||
chr1:113765044 | A | C | 1 | a0001c0001t0018 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*936T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 936 | chr1 | 113765044 | ||||||
chr1:113765152 | T | A | 1 | a0001c0001t0028 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*828A>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 828 | chr1 | 113765152 | ||||||
chr1:113765214 | G | A | 1 | a0001c0002t0029 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*766C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 766 | chr1 | 113765214 | ||||||
chr1:113765249 | T | C | 1 | a0001c0001t0030 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*731A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 731 | chr1 | 113765249 | ||||||
chr1:113765480 | C | T | 1 | a0001c0001t0017 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*500G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 500 | chr1 | 113765480 | ||||||
chr1:113765603 | T | A | 1 | a0001c0002t0031 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377A>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 377 | chr1 | 113765603 | ||||||
chr1:113765603 | T | C | 1 | a0001c0001t0016 | 2 | NA18980.hp2 NA18985.hp2 |
3_prime_UTR_variant | MODIFIER | c.*377A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 7/7 | 377 | chr1 | 113765603 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:113766550 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(173): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1936-97G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 6/6 | chr1 | 113766550 | |||||||
chr1:113766735 | T | A | 1 | a0001c0001t0001g0049 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1936-282A>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 6/6 | chr1 | 113766735 | |||||||
chr1:113766843 | T | C | 1 | a0001c0002t0004g0239 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1935+256A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 6/6 | chr1 | 113766843 | |||||||
chr1:113766956 | G | A | 1 | a0001c0001t0006g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1935+143C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 6/6 | chr1 | 113766956 | |||||||
chr1:113766959 | C | G | 1 | a0001c0001t0001g0084 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1935+140G>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 6/6 | chr1 | 113766959 | |||||||
chr1:113767251 | T | C | 9 | a0001c0001t0007g0025 a0001c0001t0007g0142 a0001c0001t0007g0143 others(6): Show |
10 | HG01192.hp1 NA18952.hp2 NA18972.hp1 others(7): Show |
intron_variant | MODIFIER | c.1827-44A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 5/6 | chr1 | 113767251 | |||||||
chr1:113767425 | G | A | 1 | a0001c0001t0002g0028 | 2 | HG01123.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1827-218C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 5/6 | chr1 | 113767425 | |||||||
chr1:113767453 | A | G | 4 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0206 others(1): Show |
6 | HG00642.hp1 HG01928.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1827-246T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 5/6 | chr1 | 113767453 | |||||||
chr1:113767455 | T | G | 1 | a0001c0002t0003g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1827-248A>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 5/6 | chr1 | 113767455 | |||||||
chr1:113767474 | G | A | 1 | a0001c0001t0004g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1827-267C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 5/6 | chr1 | 113767474 | |||||||
chr1:113767775 | G | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0058 |
2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1826+447C>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 5/6 | chr1 | 113767775 | |||||||
chr1:113768170 | CATTGTCT others(8): Show |
C | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1826+37_1826+51del others(15): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 5/6 | chr1 | 113768170 | |||||||
chr1:113768508 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1659-119C>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113768508 | |||||||
chr1:113768525 | A | G | 1 | a0001c0001t0008g0051 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1659-136T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113768525 | |||||||
chr1:113768528 | A | G | 1 | a0001c0001t0013g0157 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1659-139T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113768528 | |||||||
chr1:113768887 | G | A | 1 | a0001c0001t0006g0087 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1659-498C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113768887 | |||||||
chr1:113768895 | TG | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(88): Show |
117 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1659-507delC | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113768895 | |||||||
chr1:113768927 | A | T | 37 | a0001c0001t0002g0192 a0001c0001t0004g0011 a0001c0001t0004g0045 others(34): Show |
46 | HG00642.hp2 HG01070.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.1659-538T>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113768927 | |||||||
chr1:113769146 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(79): Show |
106 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1659-757C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113769146 | |||||||
chr1:113769174 | C | G | 5 | a0001c0001t0004g0045 a0001c0001t0004g0147 a0001c0001t0004g0148 others(2): Show |
5 | HG00099.hp2 HG00741.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1659-785G>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113769174 | |||||||
chr1:113769315 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1659-926A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113769315 | |||||||
chr1:113769382 | C | G | 1 | a0001c0001t0004g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1659-993G>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113769382 | |||||||
chr1:113769445 | G | A | 2 | a0001c0001t0002g0047 a0001c0001t0002g0058 |
2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1659-1056C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113769445 | |||||||
chr1:113769746 | A | G | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1659-1357T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113769746 | |||||||
chr1:113769813 | G | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(65): Show |
90 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.1659-1424C>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113769813 | |||||||
chr1:113770001 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(185): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1659-1612A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113770001 | |||||||
chr1:113770251 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1659-1862T>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113770251 | |||||||
chr1:113770538 | A | G | 1 | a0001c0001t0007g0144 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1659-2149T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113770538 | |||||||
chr1:113770747 | C | A | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1659-2358G>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113770747 | |||||||
chr1:113770769 | G | A | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1659-2380C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113770769 | |||||||
chr1:113771101 | A | C | 2 | a0001c0002t0003g0252 a0001c0002t0009g0253 |
2 | NA18960.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1659-2712T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113771101 | |||||||
chr1:113771487 | C | T | 1 | a0001c0001t0004g0188 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1659-3098G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113771487 | |||||||
chr1:113771670 | T | C | 1 | a0001c0001t0004g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1659-3281A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113771670 | |||||||
chr1:113771747 | T | C | 1 | a0001c0003t0002g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1659-3358A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113771747 | |||||||
chr1:113771810 | C | CA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(93): Show |
125 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1659-3422dupT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113771810 | |||||||
chr1:113771810 | C | CAA | 11 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0102 others(8): Show |
12 | HG01891.hp2 HG02145.hp2 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.1659-3423_1659-342 others(6): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113771810 | |||||||
chr1:113771849 | G | A | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1659-3460C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113771849 | |||||||
chr1:113771924 | C | CT | 6 | a0001c0001t0002g0036 a0001c0001t0002g0046 a0001c0001t0002g0140 others(3): Show |
7 | HG00621.hp1 HG01109.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1659-3536dupA | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113771924 | |||||||
chr1:113772168 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1659-3779A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113772168 | |||||||
chr1:113772336 | T | G | 1 | a0001c0005t0020g0236 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1659-3947A>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113772336 | |||||||
chr1:113772786 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1659-4397G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113772786 | |||||||
chr1:113772871 | C | T | 37 | a0001c0001t0002g0192 a0001c0001t0004g0011 a0001c0001t0004g0014 others(34): Show |
45 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1658+4339G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113772871 | |||||||
chr1:113773014 | T | C | 1 | a0001c0002t0003g0243 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1658+4196A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113773014 | |||||||
chr1:113773262 | C | T | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1658+3948G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113773262 | |||||||
chr1:113773317 | G | A | 1 | a0001c0001t0021g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1658+3893C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113773317 | |||||||
chr1:113773397 | G | A | 1 | a0001c0001t0006g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1658+3813C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113773397 | |||||||
chr1:113773430 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1658+3780T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113773430 | |||||||
chr1:113773514 | C | T | 1 | a0001c0002t0003g0038 | 2 | NA19056.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1658+3696G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113773514 | |||||||
chr1:113773598 | G | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(65): Show |
90 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.1658+3612C>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113773598 | |||||||
chr1:113773771 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1658+3439C>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113773771 | |||||||
chr1:113773873 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1658+3337G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113773873 | |||||||
chr1:113774012 | A | T | 1 | a0001c0001t0002g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1658+3198T>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113774012 | |||||||
chr1:113774233 | G | C | 3 | a0001c0001t0004g0153 a0001c0001t0004g0194 a0001c0001t0030g0193 |
3 | HG02258.hp1 HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1658+2977C>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113774233 | |||||||
chr1:113774246 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1658+2964C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113774246 | |||||||
chr1:113774494 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1658+2716C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113774494 | |||||||
chr1:113774586 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1658+2624T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113774586 | |||||||
chr1:113774639 | C | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(251): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1658+2571G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113774639 | |||||||
chr1:113774821 | C | T | 1 | a0001c0001t0018g0199 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1658+2389G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113774821 | |||||||
chr1:113775169 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(84): Show |
112 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1658+2041G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113775169 | |||||||
chr1:113775343 | CT | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(85): Show |
113 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.1658+1866delA | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113775343 | |||||||
chr1:113775344 | T | C | 1 | a0001c0002t0003g0039 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1658+1866A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113775344 | |||||||
chr1:113775400 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(190): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1658+1810T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113775400 | |||||||
chr1:113775491 | G | A | 3 | a0001c0004t0002g0232 a0001c0004t0002g0233 a0001c0004t0002g0234 |
3 | HG02074.hp2 HG02129.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1658+1719C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113775491 | |||||||
chr1:113775864 | G | A | 1 | a0001c0001t0002g0202 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1658+1346C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113775864 | |||||||
chr1:113775893 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1658+1317G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113775893 | |||||||
chr1:113775982 | C | T | 18 | a0001c0001t0002g0192 a0001c0001t0004g0014 a0001c0001t0004g0015 others(15): Show |
21 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1658+1228G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113775982 | |||||||
chr1:113776002 | T | C | 1 | a0001c0001t0002g0036 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1658+1208A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776002 | |||||||
chr1:113776105 | C | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(130): Show |
170 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1658+1105G>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776105 | |||||||
chr1:113776213 | T | A | 1 | a0001c0001t0001g0083 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1658+997A>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776213 | |||||||
chr1:113776222 | A | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0058 |
2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1658+988T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776222 | |||||||
chr1:113776348 | G | A | 1 | a0001c0001t0006g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1658+862C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776348 | |||||||
chr1:113776415 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0123 |
2 | NA18939.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1658+795C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776415 | |||||||
chr1:113776520 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1658+690C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776520 | |||||||
chr1:113776578 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1658+632C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776578 | |||||||
chr1:113776611 | A | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(86): Show |
114 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.1658+599T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776611 | |||||||
chr1:113776666 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1658+544A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776666 | |||||||
chr1:113776767 | A | G | 2 | a0001c0005t0003g0235 a0001c0005t0020g0236 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1658+443T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776767 | |||||||
chr1:113776794 | G | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(79): Show |
106 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1658+416C>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776794 | |||||||
chr1:113776810 | C | CA | 10 | a0001c0001t0001g0190 a0001c0001t0002g0173 a0001c0001t0006g0092 others(7): Show |
11 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1658+399dupT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776810 | |||||||
chr1:113776810 | CA | C | 123 | a0001c0001t0001g0066 a0001c0001t0001g0117 a0001c0001t0002g0002 others(120): Show |
153 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(150): Show |
intron_variant | MODIFIER | c.1658+399delT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776810 | |||||||
chr1:113776891 | C | T | 37 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0031 others(34): Show |
47 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1658+319G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776891 | |||||||
chr1:113776900 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1658+310G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 4/6 | chr1 | 113776900 | |||||||
chr1:113777416 | C | G | 2 | a0001c0001t0002g0201 a0001c0001t0002g0225 |
2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1516-64G>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 3/6 | chr1 | 113777416 | |||||||
chr1:113777561 | A | C | 8 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0205 others(5): Show |
10 | HG02083.hp2 NA18955.hp1 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.1515+110T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 3/6 | chr1 | 113777561 | |||||||
chr1:113777971 | C | T | 8 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0205 others(5): Show |
10 | HG02083.hp2 NA18955.hp1 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.1378-163G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113777971 | |||||||
chr1:113778304 | TC | T | 57 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0060 others(54): Show |
74 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1378-497delG | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113778304 | |||||||
chr1:113778305 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(128): Show |
161 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1378-497G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113778305 | |||||||
chr1:113778401 | A | T | 1 | a0001c0001t0001g0021 | 2 | NA18974.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1378-593T>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113778401 | |||||||
chr1:113778424 | A | G | 1 | a0001c0001t0007g0143 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1378-616T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113778424 | |||||||
chr1:113778547 | G | A | 4 | a0001c0001t0013g0139 a0001c0001t0013g0157 a0001c0001t0013g0159 others(1): Show |
4 | HG01081.hp2 HG01257.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378-739C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113778547 | |||||||
chr1:113779070 | A | G | 1 | a0001c0002t0003g0038 | 2 | NA19056.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1378-1262T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113779070 | |||||||
chr1:113779145 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1378-1337A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113779145 | |||||||
chr1:113779438 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1378-1630G>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113779438 | |||||||
chr1:113779601 | G | A | 1 | a0001c0001t0004g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1378-1793C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113779601 | |||||||
chr1:113780028 | AAAAAGAA others(46): Show |
A | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1378-2273_1378-222 others(57): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113780028 | |||||||
chr1:113780696 | T | C | 39 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0031 others(36): Show |
48 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1378-2888A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113780696 | |||||||
chr1:113780893 | T | G | 1 | a0001c0001t0004g0059 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1378-3085A>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113780893 | |||||||
chr1:113781024 | C | A | 2 | a0001c0001t0005g0160 a0001c0001t0005g0228 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1378-3216G>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113781024 | |||||||
chr1:113781163 | T | C | 3 | a0001c0001t0002g0026 a0001c0001t0002g0056 a0001c0001t0004g0181 |
4 | HG02257.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378-3355A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113781163 | |||||||
chr1:113781391 | G | A | 4 | a0001c0001t0004g0045 a0001c0001t0004g0147 a0001c0001t0004g0148 others(1): Show |
4 | HG00099.hp2 HG00741.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378-3583C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113781391 | |||||||
chr1:113782048 | C | T | 1 | a0001c0002t0009g0246 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1378-4240G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113782048 | |||||||
chr1:113782077 | G | A | 1 | a0001c0002t0003g0265 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1378-4269C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113782077 | |||||||
chr1:113782533 | G | A | 5 | a0001c0001t0008g0029 a0001c0001t0008g0195 a0001c0001t0008g0196 others(2): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378-4725C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113782533 | |||||||
chr1:113782559 | T | A | 5 | a0001c0001t0008g0029 a0001c0001t0008g0195 a0001c0001t0008g0196 others(2): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378-4751A>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113782559 | |||||||
chr1:113782566 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1378-4758T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113782566 | |||||||
chr1:113782590 | A | G | 1 | a0001c0001t0008g0051 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1378-4782T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113782590 | |||||||
chr1:113783052 | A | C | 2 | a0001c0005t0003g0235 a0001c0005t0020g0236 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1378-5244T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113783052 | |||||||
chr1:113783290 | G | C | 4 | a0001c0001t0002g0189 a0001c0001t0004g0111 a0001c0001t0006g0092 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378-5482C>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113783290 | |||||||
chr1:113783292 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(128): Show |
164 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1378-5484T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113783292 | |||||||
chr1:113783457 | G | GA | 44 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0084 others(41): Show |
55 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1378-5650dupT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113783457 | |||||||
chr1:113783457 | GA | G | 43 | a0001c0001t0004g0183 a0001c0001t0012g0109 a0001c0001t0012g0110 others(40): Show |
55 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.1378-5650delT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113783457 | |||||||
chr1:113783850 | C | G | 1 | a0001c0001t0007g0142 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1378-6042G>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113783850 | |||||||
chr1:113784216 | C | G | 2 | a0001c0001t0002g0178 a0001c0001t0002g0179 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1378-6408G>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113784216 | |||||||
chr1:113784434 | T | G | 1 | a0001c0002t0003g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1378-6626A>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113784434 | |||||||
chr1:113784847 | T | C | 43 | a0001c0002t0002g0256 a0001c0002t0003g0004 a0001c0002t0003g0007 others(40): Show |
58 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1378-7039A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113784847 | |||||||
chr1:113785028 | GACTCTTG others(7): Show |
G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(136): Show |
179 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1378-7234_1378-722 others(18): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113785028 | |||||||
chr1:113785048 | G | A | 1 | a0001c0001t0002g0164 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1378-7240C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113785048 | |||||||
chr1:113785125 | C | CT | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(136): Show |
179 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1378-7318dupA | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113785125 | |||||||
chr1:113785184 | T | C | 1 | a0001c0003t0002g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1378-7376A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113785184 | |||||||
chr1:113785245 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1378-7437A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113785245 | |||||||
chr1:113785554 | T | C | 5 | a0001c0001t0004g0111 a0001c0001t0012g0109 a0001c0001t0012g0110 others(2): Show |
5 | HG00741.hp2 HG02055.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-7746A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113785554 | |||||||
chr1:113786299 | T | C | 37 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0031 others(34): Show |
47 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1378-8491A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113786299 | |||||||
chr1:113786589 | G | T | 6 | a0001c0001t0002g0002 a0001c0001t0002g0150 a0001c0001t0002g0164 others(3): Show |
11 | NA18943.hp2 NA18950.hp1 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.1378-8781C>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113786589 | |||||||
chr1:113786786 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(89): Show |
116 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.1378-8978G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113786786 | |||||||
chr1:113787163 | T | G | 6 | a0001c0001t0004g0111 a0001c0001t0004g0125 a0001c0001t0012g0109 others(3): Show |
6 | HG00741.hp2 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378-9355A>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113787163 | |||||||
chr1:113787580 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(91): Show |
119 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.1378-9772A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113787580 | |||||||
chr1:113787596 | G | A | 1 | a0001c0001t0004g0183 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1377+9767C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113787596 | |||||||
chr1:113787641 | G | A | 1 | a0001c0001t0004g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1377+9722C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113787641 | |||||||
chr1:113787643 | A | G | 1 | a0001c0001t0004g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1377+9720T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113787643 | |||||||
chr1:113787831 | C | T | 37 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0031 others(34): Show |
47 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1377+9532G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113787831 | |||||||
chr1:113787955 | A | G | 1 | a0001c0001t0004g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1377+9408T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113787955 | |||||||
chr1:113788150 | G | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1377+9213C>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113788150 | |||||||
chr1:113788155 | T | C | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1377+9208A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113788155 | |||||||
chr1:113788288 | A | G | 3 | a0001c0001t0011g0016 a0001c0001t0011g0069 a0001c0001t0011g0070 |
4 | HG00738.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1377+9075T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113788288 | |||||||
chr1:113788693 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(131): Show |
174 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1377+8670G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113788693 | |||||||
chr1:113788748 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1377+8615G>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113788748 | |||||||
chr1:113788764 | T | C | 2 | a0001c0001t0010g0055 a0001c0001t0010g0138 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1377+8599A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113788764 | |||||||
chr1:113789023 | T | A | 37 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0031 others(34): Show |
47 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1377+8340A>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113789023 | |||||||
chr1:113789246 | G | A | 1 | a0001c0001t0005g0134 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1377+8117C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113789246 | |||||||
chr1:113789386 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1377+7977G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113789386 | |||||||
chr1:113789430 | G | C | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1377+7933C>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113789430 | |||||||
chr1:113789992 | A | G | 1 | a0001c0001t0004g0183 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1377+7371T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113789992 | |||||||
chr1:113790203 | G | A | 3 | a0001c0001t0005g0141 a0001c0001t0011g0016 a0001c0001t0011g0070 |
4 | HG00738.hp1 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1377+7160C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113790203 | |||||||
chr1:113790390 | A | T | 5 | a0001c0001t0008g0029 a0001c0001t0008g0195 a0001c0001t0008g0196 others(2): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1377+6973T>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113790390 | |||||||
chr1:113790569 | T | A | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377+6794A>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113790569 | |||||||
chr1:113790582 | C | G | 1 | a0001c0002t0003g0260 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1377+6781G>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113790582 | |||||||
chr1:113791600 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(139): Show |
183 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1377+5763A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113791600 | |||||||
chr1:113791662 | T | C | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377+5701A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113791662 | |||||||
chr1:113791752 | CATTTT | C | 6 | a0001c0001t0004g0111 a0001c0001t0004g0125 a0001c0001t0012g0109 others(3): Show |
6 | HG00741.hp2 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1377+5606_1377+561 others(9): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113791752 | |||||||
chr1:113791813 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1377+5550T>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113791813 | |||||||
chr1:113791882 | T | C | 1 | a0001c0001t0002g0223 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1377+5481A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113791882 | |||||||
chr1:113792068 | A | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(136): Show |
179 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1377+5295T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113792068 | |||||||
chr1:113792366 | T | C | 1 | a0001c0002t0003g0250 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1377+4997A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113792366 | |||||||
chr1:113792457 | T | C | 2 | a0001c0001t0004g0166 a0001c0001t0028g0167 |
2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1377+4906A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113792457 | |||||||
chr1:113792460 | TAGG | T | 5 | a0001c0001t0004g0111 a0001c0001t0012g0109 a0001c0001t0012g0110 others(2): Show |
5 | HG00741.hp2 HG02055.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+4900_1377+490 others(7): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113792460 | |||||||
chr1:113792470 | A | G | 37 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0031 others(34): Show |
47 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1377+4893T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113792470 | |||||||
chr1:113792504 | A | G | 1 | a0001c0002t0003g0251 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1377+4859T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113792504 | |||||||
chr1:113792515 | C | T | 4 | a0001c0001t0004g0045 a0001c0001t0004g0147 a0001c0001t0004g0148 others(1): Show |
4 | HG00099.hp2 HG00741.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1377+4848G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113792515 | |||||||
chr1:113792541 | A | C | 1 | a0001c0001t0002g0046 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1377+4822T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113792541 | |||||||
chr1:113792790 | C | T | 1 | a0001c0001t0004g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1377+4573G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113792790 | |||||||
chr1:113792861 | A | T | 37 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0031 others(34): Show |
47 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1377+4502T>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113792861 | |||||||
chr1:113792877 | C | T | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377+4486G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113792877 | |||||||
chr1:113792956 | G | A | 2 | a0001c0001t0006g0074 a0001c0001t0006g0092 |
2 | HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1377+4407C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113792956 | |||||||
chr1:113792998 | C | T | 1 | a0001c0001t0021g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1377+4365G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113792998 | |||||||
chr1:113793093 | T | C | 1 | a0001c0001t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1377+4270A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113793093 | |||||||
chr1:113793166 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0108 |
2 | HG01361.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1377+4197A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113793166 | |||||||
chr1:113793304 | T | C | 1 | a0001c0001t0004g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1377+4059A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113793304 | |||||||
chr1:113793677 | CT | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(136): Show |
179 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1377+3685delA | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113793677 | |||||||
chr1:113794327 | T | C | 1 | a0001c0002t0003g0269 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1377+3036A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113794327 | |||||||
chr1:113794387 | C | T | 1 | a0001c0001t0004g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1377+2976G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113794387 | |||||||
chr1:113794529 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1377+2834T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113794529 | |||||||
chr1:113794593 | C | T | 3 | a0001c0001t0002g0026 a0001c0001t0002g0056 a0001c0001t0004g0181 |
4 | HG02257.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1377+2770G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113794593 | |||||||
chr1:113794935 | A | C | 1 | a0001c0001t0005g0135 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1377+2428T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113794935 | |||||||
chr1:113795073 | G | C | 2 | a0001c0001t0002g0178 a0001c0001t0002g0179 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1377+2290C>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113795073 | |||||||
chr1:113795179 | C | A | 1 | a0001c0002t0009g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1377+2184G>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113795179 | |||||||
chr1:113795260 | T | A | 5 | a0001c0001t0004g0111 a0001c0001t0012g0109 a0001c0001t0012g0110 others(2): Show |
5 | HG00741.hp2 HG02055.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+2103A>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113795260 | |||||||
chr1:113795409 | C | T | 3 | a0001c0001t0011g0016 a0001c0001t0011g0069 a0001c0001t0011g0070 |
4 | HG00738.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1377+1954G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113795409 | |||||||
chr1:113795614 | C | T | 186 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0026 others(183): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1377+1749G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113795614 | |||||||
chr1:113795967 | A | G | 45 | a0001c0002t0002g0256 a0001c0002t0003g0004 a0001c0002t0003g0007 others(42): Show |
60 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1377+1396T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113795967 | |||||||
chr1:113796071 | A | G | 2 | a0001c0001t0002g0033 a0001c0001t0002g0211 |
3 | HG01257.hp1 HG01258.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1377+1292T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113796071 | |||||||
chr1:113796181 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0094 |
3 | HG01255.hp1 HG01361.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1377+1182C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113796181 | |||||||
chr1:113796498 | T | TA | 5 | a0001c0001t0004g0111 a0001c0001t0012g0109 a0001c0001t0012g0110 others(2): Show |
5 | HG00741.hp2 HG02055.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+864dupT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113796498 | |||||||
chr1:113796511 | A | C | 5 | a0001c0001t0008g0029 a0001c0001t0008g0195 a0001c0001t0008g0196 others(2): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1377+852T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113796511 | |||||||
chr1:113796685 | A | G | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377+678T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113796685 | |||||||
chr1:113797010 | G | GAT | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1377+351_1377+352d others(4): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113797010 | |||||||
chr1:113797129 | A | G | 9 | a0001c0001t0007g0025 a0001c0001t0007g0142 a0001c0001t0007g0143 others(6): Show |
10 | HG01192.hp1 NA18952.hp2 NA18972.hp1 others(7): Show |
intron_variant | MODIFIER | c.1377+234T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113797129 | |||||||
chr1:113797334 | C | CTAAA | 186 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0026 others(183): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1377+28_1377+29ins others(4): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 2/6 | chr1 | 113797334 | |||||||
chr1:113798188 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.704-152A>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113798188 | |||||||
chr1:113798659 | T | A | 1 | a0001c0001t0002g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.704-623A>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113798659 | |||||||
chr1:113798710 | T | C | 37 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0031 others(34): Show |
47 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.704-674A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113798710 | |||||||
chr1:113798770 | T | G | 1 | a0001c0001t0004g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.704-734A>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113798770 | |||||||
chr1:113799227 | C | T | 2 | a0001c0001t0004g0057 a0001c0001t0004g0180 |
2 | HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.704-1191G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799227 | |||||||
chr1:113799379 | G | T | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.704-1343C>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799379 | |||||||
chr1:113799559 | A | T | 2 | a0001c0001t0004g0015 a0001c0001t0004g0059 |
3 | HG00738.hp2 HG01168.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.704-1523T>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799559 | |||||||
chr1:113799565 | T | TAC | 26 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0021 others(23): Show |
33 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.704-1531_704-1530d others(4): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799565 | |||||||
chr1:113799565 | T | TACAC | 9 | a0001c0001t0001g0022 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
11 | HG00642.hp1 HG01928.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.704-1533_704-1530d others(6): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799565 | |||||||
chr1:113799565 | T | TACACAC | 6 | a0001c0001t0001g0052 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
6 | NA18942.hp1 NA18947.hp2 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-1535_704-1530d others(8): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799565 | |||||||
chr1:113799565 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0100 a0001c0001t0001g0108 a0001c0001t0008g0099 |
3 | HG02738.hp2 HG03710.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.704-1537_704-1530d others(10): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799565 | |||||||
chr1:113799565 | TAC | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0048 others(22): Show |
31 | HG00735.hp2 HG00738.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.704-1531_704-1530d others(4): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799565 | |||||||
chr1:113799565 | TACAC | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0053 a0001c0001t0001g0063 others(20): Show |
28 | HG00733.hp2 HG00741.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.704-1533_704-1530d others(6): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799565 | |||||||
chr1:113799565 | TACACAC | T | 35 | a0001c0001t0001g0126 a0001c0001t0002g0189 a0001c0001t0004g0125 others(32): Show |
47 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.704-1535_704-1530d others(8): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799565 | |||||||
chr1:113799565 | TACACACA others(1): Show |
T | 3 | a0001c0002t0003g0037 a0001c0002t0009g0244 a0001c0002t0031g0245 |
4 | HG04199.hp1 NA18967.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-1537_704-1530d others(10): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799565 | |||||||
chr1:113799565 | TACACACA others(3): Show |
T | 1 | a0001c0002t0003g0266 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.704-1539_704-1530d others(12): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799565 | |||||||
chr1:113799565 | TACACACA others(5): Show |
T | 1 | a0001c0003t0002g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.704-1541_704-1530d others(14): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799565 | |||||||
chr1:113799565 | TACACACA others(7): Show |
T | 6 | a0001c0001t0001g0114 a0001c0001t0004g0161 a0001c0001t0004g0194 others(3): Show |
7 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-1543_704-1530d others(16): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799565 | |||||||
chr1:113799565 | TACACACA others(9): Show |
T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0026 a0001c0001t0002g0028 others(82): Show |
104 | HG00099.hp2 HG00621.hp1 HG00738.hp2 others(101): Show |
intron_variant | MODIFIER | c.704-1545_704-1530d others(18): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799565 | |||||||
chr1:113799565 | TACACACA others(11): Show |
T | 1 | a0001c0002t0003g0243 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.704-1547_704-1530d others(20): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799565 | |||||||
chr1:113799644 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.704-1608T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799644 | |||||||
chr1:113799732 | T | C | 5 | a0001c0001t0008g0029 a0001c0001t0008g0195 a0001c0001t0008g0196 others(2): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-1696A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799732 | |||||||
chr1:113799739 | T | C | 2 | a0001c0001t0002g0192 a0001c0001t0004g0162 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.704-1703A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113799739 | |||||||
chr1:113800349 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.704-2313A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113800349 | |||||||
chr1:113800632 | T | C | 2 | a0001c0002t0003g0252 a0001c0002t0009g0253 |
2 | NA18960.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.704-2596A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113800632 | |||||||
chr1:113800714 | G | A | 186 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0026 others(183): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.704-2678C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113800714 | |||||||
chr1:113800715 | T | C | 1 | a0001c0002t0003g0265 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.704-2679A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113800715 | |||||||
chr1:113800779 | G | A | 1 | a0001c0001t0004g0220 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.704-2743C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113800779 | |||||||
chr1:113800983 | A | AT | 6 | a0001c0001t0002g0140 a0001c0001t0002g0223 a0001c0001t0005g0141 others(3): Show |
6 | HG02615.hp2 HG02738.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-2948dupA | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113800983 | |||||||
chr1:113801130 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.704-3094A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113801130 | |||||||
chr1:113801210 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.704-3174A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113801210 | |||||||
chr1:113801461 | C | T | 129 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0026 others(126): Show |
159 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.704-3425G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113801461 | |||||||
chr1:113802231 | C | T | 1 | a0001c0001t0013g0139 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.704-4195G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113802231 | |||||||
chr1:113802313 | G | GA | 6 | a0001c0001t0001g0103 a0001c0001t0001g0123 a0001c0001t0006g0104 others(3): Show |
7 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-4278dupT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113802313 | |||||||
chr1:113802341 | G | T | 1 | a0001c0001t0002g0208 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.704-4305C>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113802341 | |||||||
chr1:113802796 | C | T | 128 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0026 others(125): Show |
158 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(155): Show |
intron_variant | MODIFIER | c.704-4760G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113802796 | |||||||
chr1:113802886 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.704-4850A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113802886 | |||||||
chr1:113802893 | T | C | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.704-4857A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113802893 | |||||||
chr1:113803017 | C | T | 1 | a0001c0002t0019g0242 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.704-4981G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803017 | |||||||
chr1:113803074 | G | A | 1 | a0001c0002t0003g0254 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.704-5038C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803074 | |||||||
chr1:113803084 | T | C | 4 | a0001c0001t0002g0035 a0001c0001t0002g0218 a0001c0001t0002g0219 others(1): Show |
5 | NA18966.hp2 NA18968.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-5048A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803084 | |||||||
chr1:113803128 | C | T | 186 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0026 others(183): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.704-5092G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803128 | |||||||
chr1:113803515 | T | C | 7 | a0001c0001t0004g0111 a0001c0001t0004g0125 a0001c0001t0008g0051 others(4): Show |
7 | HG00741.hp2 HG02055.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-5479A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803515 | |||||||
chr1:113803526 | G | A | 1 | a0001c0001t0002g0219 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.704-5490C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803526 | |||||||
chr1:113803538 | A | G | 45 | a0001c0002t0002g0256 a0001c0002t0003g0004 a0001c0002t0003g0007 others(42): Show |
60 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.704-5502T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803538 | |||||||
chr1:113803581 | C | T | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.704-5545G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803581 | |||||||
chr1:113803657 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.704-5621C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803657 | |||||||
chr1:113803743 | C | CT | 126 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0026 others(123): Show |
155 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(152): Show |
intron_variant | MODIFIER | c.704-5708dupA | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803743 | |||||||
chr1:113803882 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.704-5846A>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803882 | |||||||
chr1:113803939 | C | CA | 51 | a0001c0001t0001g0053 a0001c0001t0001g0106 a0001c0001t0001g0116 others(48): Show |
66 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.704-5904dupT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803939 | |||||||
chr1:113803939 | CAAAAAAA | C | 4 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0206 others(1): Show |
6 | HG00642.hp1 HG01928.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-5910_704-5904d others(9): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803939 | |||||||
chr1:113803991 | G | C | 1 | a0001c0001t0005g0134 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.704-5955C>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113803991 | |||||||
chr1:113804088 | C | T | 1 | a0001c0001t0005g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.704-6052G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113804088 | |||||||
chr1:113804109 | AC | A | 5 | a0001c0001t0008g0029 a0001c0001t0008g0195 a0001c0001t0008g0196 others(2): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-6074delG | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113804109 | |||||||
chr1:113804114 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.704-6078C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113804114 | |||||||
chr1:113804127 | A | C | 186 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0026 others(183): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.704-6091T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113804127 | |||||||
chr1:113804282 | G | A | 89 | a0001c0001t0002g0002 a0001c0001t0002g0026 a0001c0001t0002g0028 others(86): Show |
108 | HG00099.hp2 HG00621.hp1 HG00738.hp2 others(105): Show |
intron_variant | MODIFIER | c.704-6246C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113804282 | |||||||
chr1:113804338 | T | G | 1 | a0001c0001t0001g0114 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.704-6302A>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113804338 | |||||||
chr1:113804360 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.704-6324G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113804360 | |||||||
chr1:113804361 | G | A | 1 | a0001c0002t0009g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.704-6325C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113804361 | |||||||
chr1:113804773 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.704-6737A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113804773 | |||||||
chr1:113804907 | T | TA | 121 | a0001c0001t0001g0108 a0001c0001t0002g0026 a0001c0001t0002g0036 others(118): Show |
150 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.703+6802dupT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113804907 | |||||||
chr1:113804907 | T | TAA | 62 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0028 others(59): Show |
79 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.703+6801_703+6802d others(4): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113804907 | |||||||
chr1:113804985 | T | C | 6 | a0001c0001t0002g0036 a0001c0001t0002g0046 a0001c0001t0002g0227 others(3): Show |
7 | HG00621.hp1 HG01109.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+6725A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113804985 | |||||||
chr1:113805042 | T | G | 1 | a0001c0001t0002g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.703+6668A>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113805042 | |||||||
chr1:113805168 | T | C | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.703+6542A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113805168 | |||||||
chr1:113805213 | T | C | 1 | a0001c0002t0003g0257 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.703+6497A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113805213 | |||||||
chr1:113805367 | C | T | 3 | a0001c0002t0002g0256 a0001c0002t0003g0040 a0001c0002t0009g0258 |
4 | NA18944.hp2 NA18949.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+6343G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113805367 | |||||||
chr1:113805369 | C | T | 1 | a0001c0001t0007g0170 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.703+6341G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113805369 | |||||||
chr1:113805534 | T | C | 11 | a0001c0001t0002g0036 a0001c0001t0002g0046 a0001c0001t0002g0047 others(8): Show |
12 | HG00621.hp1 HG01109.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.703+6176A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113805534 | |||||||
chr1:113805582 | T | C | 7 | a0001c0001t0004g0111 a0001c0001t0004g0125 a0001c0001t0008g0051 others(4): Show |
7 | HG00741.hp2 HG02055.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+6128A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113805582 | |||||||
chr1:113805679 | T | C | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.703+6031A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113805679 | |||||||
chr1:113805856 | C | T | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.703+5854G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113805856 | |||||||
chr1:113806138 | C | G | 1 | a0001c0001t0002g0205 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.703+5572G>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113806138 | |||||||
chr1:113806267 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.703+5443C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113806267 | |||||||
chr1:113806320 | G | A | 37 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0031 others(34): Show |
47 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.703+5390C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113806320 | |||||||
chr1:113806332 | C | CA | 11 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0043 others(8): Show |
11 | HG01070.hp1 HG01175.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.703+5377dupT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113806332 | |||||||
chr1:113806664 | T | A | 1 | a0001c0001t0002g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.703+5046A>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113806664 | |||||||
chr1:113806838 | C | CA | 49 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0117 others(46): Show |
64 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.703+4871dupT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113806838 | |||||||
chr1:113806838 | C | CAA | 7 | a0001c0001t0001g0124 a0001c0001t0001g0191 a0001c0002t0003g0237 others(4): Show |
7 | HG00597.hp1 HG02056.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+4870_703+4871d others(4): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113806838 | |||||||
chr1:113806838 | CA | C | 52 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0231 others(49): Show |
64 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.703+4871delT | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113806838 | |||||||
chr1:113806838 | CAA | C | 77 | a0001c0001t0002g0002 a0001c0001t0002g0026 a0001c0001t0002g0028 others(74): Show |
95 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(92): Show |
intron_variant | MODIFIER | c.703+4870_703+4871d others(4): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113806838 | |||||||
chr1:113806856 | A | C | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.703+4854T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113806856 | |||||||
chr1:113806939 | A | G | 1 | a0001c0003t0002g0013 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.703+4771T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113806939 | |||||||
chr1:113807087 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.703+4623G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807087 | |||||||
chr1:113807207 | G | A | 1 | a0001c0001t0004g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.703+4503C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807207 | |||||||
chr1:113807244 | G | A | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.703+4466C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807244 | |||||||
chr1:113807264 | G | T | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.703+4446C>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807264 | |||||||
chr1:113807313 | C | A | 15 | a0001c0002t0002g0256 a0001c0002t0003g0004 a0001c0002t0003g0007 others(12): Show |
24 | HG00597.hp1 HG01081.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.703+4397G>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807313 | |||||||
chr1:113807319 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.703+4391T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807319 | |||||||
chr1:113807344 | C | T | 2 | a0001c0005t0003g0235 a0001c0005t0020g0236 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.703+4366G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807344 | |||||||
chr1:113807449 | A | G | 5 | a0001c0001t0004g0137 a0001c0001t0010g0024 a0001c0001t0010g0055 others(2): Show |
7 | HG01099.hp2 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+4261T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807449 | |||||||
chr1:113807481 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.703+4229G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807481 | |||||||
chr1:113807530 | C | T | 11 | a0001c0001t0005g0006 a0001c0001t0005g0130 a0001c0001t0005g0133 others(8): Show |
15 | HG03491.hp2 HG03654.hp2 HG03710.hp2 others(12): Show |
intron_variant | MODIFIER | c.703+4180G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807530 | |||||||
chr1:113807644 | C | T | 1 | a0001c0002t0004g0239 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.703+4066G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807644 | |||||||
chr1:113807755 | C | A | 1 | a0001c0001t0004g0180 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.703+3955G>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807755 | |||||||
chr1:113807773 | T | TTA | 4 | a0001c0001t0001g0126 a0001c0001t0002g0184 a0001c0001t0002g0185 others(1): Show |
4 | HG01123.hp1 HG02630.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+3935_703+3936d others(4): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807773 | |||||||
chr1:113807800 | T | TAC | 8 | a0001c0001t0002g0036 a0001c0001t0002g0184 a0001c0001t0002g0185 others(5): Show |
10 | HG02257.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+3908_703+3909d others(4): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807800 | |||||||
chr1:113807800 | T | TACAC | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0003t0002g0044 |
3 | HG01891.hp1 HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.703+3906_703+3909d others(6): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807800 | |||||||
chr1:113807800 | TAC | T | 73 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0127 others(70): Show |
94 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.703+3908_703+3909d others(4): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807800 | |||||||
chr1:113807802 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.703+3908G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807802 | |||||||
chr1:113807804 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.703+3906G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807804 | |||||||
chr1:113807867 | T | C | 38 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0001c0001t0002g0030 others(35): Show |
48 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.703+3843A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113807867 | |||||||
chr1:113808103 | G | GCAGTATC others(2): Show |
2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.703+3598_703+3606d others(11): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113808103 | |||||||
chr1:113808123 | C | T | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.703+3587G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113808123 | |||||||
chr1:113808161 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.703+3549A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113808161 | |||||||
chr1:113808389 | C | T | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.703+3321G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113808389 | |||||||
chr1:113808439 | T | C | 1 | a0001c0005t0020g0236 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.703+3271A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113808439 | |||||||
chr1:113808504 | T | G | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.703+3206A>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113808504 | |||||||
chr1:113808530 | C | T | 1 | a0001c0001t0004g0054 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.703+3180G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113808530 | |||||||
chr1:113808531 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0002g0129 |
2 | HG02572.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.703+3179T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113808531 | |||||||
chr1:113809061 | C | A | 1 | a0001c0002t0003g0268 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.703+2649G>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113809061 | |||||||
chr1:113809084 | C | A | 126 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0026 others(123): Show |
155 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(152): Show |
intron_variant | MODIFIER | c.703+2626G>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113809084 | |||||||
chr1:113809330 | G | A | 1 | a0001c0001t0004g0188 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.703+2380C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113809330 | |||||||
chr1:113809524 | G | A | 1 | a0001c0002t0003g0269 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.703+2186C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113809524 | |||||||
chr1:113809548 | G | C | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.703+2162C>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113809548 | |||||||
chr1:113809594 | T | C | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | NA18941.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.703+2116A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113809594 | |||||||
chr1:113809796 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.703+1914A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113809796 | |||||||
chr1:113809887 | T | C | 2 | a0001c0001t0004g0194 a0001c0001t0030g0193 |
2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.703+1823A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113809887 | |||||||
chr1:113810084 | G | A | 2 | a0001c0005t0003g0235 a0001c0005t0020g0236 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.703+1626C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113810084 | |||||||
chr1:113810153 | C | T | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.703+1557G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113810153 | |||||||
chr1:113810384 | A | AAC | 51 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(48): Show |
63 | HG00140.hp1 HG00621.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.703+1324_703+1325d others(4): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113810384 | |||||||
chr1:113810384 | A | AACAC | 3 | a0001c0001t0002g0047 a0001c0001t0002g0200 a0001c0001t0018g0199 |
3 | HG02004.hp1 HG03490.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703+1322_703+1325d others(6): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113810384 | |||||||
chr1:113810384 | A | AACACACA others(3): Show |
1 | a0001c0003t0002g0013 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.703+1316_703+1325d others(12): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113810384 | |||||||
chr1:113810384 | AACAC | A | 5 | a0001c0001t0008g0029 a0001c0001t0008g0195 a0001c0001t0008g0196 others(2): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+1322_703+1325d others(6): Show |
RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113810384 | |||||||
chr1:113810702 | T | C | 37 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0031 others(34): Show |
47 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.703+1008A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113810702 | |||||||
chr1:113810750 | A | G | 6 | a0001c0001t0002g0036 a0001c0001t0002g0046 a0001c0001t0002g0227 others(3): Show |
7 | HG00621.hp1 HG01109.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+960T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113810750 | |||||||
chr1:113810773 | A | C | 1 | a0001c0002t0003g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.703+937T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113810773 | |||||||
chr1:113810870 | C | T | 1 | a0001c0001t0004g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.703+840G>A | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113810870 | |||||||
chr1:113810936 | T | C | 5 | a0001c0001t0002g0036 a0001c0001t0002g0227 a0001c0001t0005g0228 others(2): Show |
6 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+774A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113810936 | |||||||
chr1:113811105 | G | C | 1 | a0001c0001t0007g0230 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.703+605C>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113811105 | |||||||
chr1:113811160 | A | G | 2 | a0001c0003t0002g0013 a0001c0003t0002g0044 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.703+550T>C | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113811160 | |||||||
chr1:113811309 | T | C | 1 | a0001c0002t0004g0042 | 2 | HG01358.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.703+401A>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113811309 | |||||||
chr1:113811558 | A | C | 1 | a0001c0001t0002g0043 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.703+152T>G | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113811558 | |||||||
chr1:113811585 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.703+125C>T | RSBN1 | ENSG00000081019.14 | transcript | ENST00000261441.9 | protein_coding | 1/6 | chr1 | 113811585 |