Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4863 |
| ensemblid | ENSG00000149308.17 |
| hgncid | 7896 |
| symbol | NPAT |
| name | nuclear protein, coactivator of histone transcription |
| refseq_nuc | NM_002519.3 |
| refseq_prot | NP_002510.2 |
| ensembl_nuc | ENST00000278612.9 |
| ensembl_prot | ENSP00000278612.8 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 108157215 |
| end | 108222638 |
| strand | - |
| ver | v1.2 |
| region | chr11:108157215-108222638 |
| region5000 | chr11:108152215-108227638 |
| regionname0 | NPAT_chr11_108157215_108222638 |
| regionname5000 | NPAT_chr11_108152215_108227638 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1427 | 188 | 48 | 30 | 79 | 8 | 23 | 64 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0002 | 1/0 | 1427 | 88 | 25 | 14 | 39 | 0 | 9 | 29 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0003 | 0/0 | 1427 | 33 | 0 | 5 | 27 | 0 | 1 | 21 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0004 | 0/0 | 1427 | 15 | 13 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0005 | 0/0 | 1427 | 7 | 1 | 0 | 1 | 2 | 3 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0006 | 0/1 | 1427 | 3 | 0 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0007 | 0/0 | 1427 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0008 | 0/0 | 1427 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0009 | 0/0 | 1427 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0010 | 0/0 | 1427 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0011 | 0/0 | 1427 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0012 | 0/0 | 1427 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0013 | 0/0 | 1427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0014 | 0/0 | 1427 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0015 | 0/0 | 1427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0016 | 0/0 | 1427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0017 | 0/0 | 1427 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0018 | 0/0 | 1427 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| a0019 | 0/0 | 1427 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | MLLPS others(1422): Show |
chr11 | 108152215 | 108227638 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4281 | 182 | 44 | 30 | 77 | 8 | 23 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0001c0006 | 0/0 | 4281 | 4 | 4 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0001c0011 | 0/0 | 4281 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0001c0016 | 0/0 | 4281 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0002c0002 | 1/0 | 4281 | 86 | 23 | 14 | 39 | 0 | 9 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0002c0020 | 0/0 | 4281 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0002c0022 | 0/0 | 4281 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0003c0003 | 0/0 | 4281 | 33 | 0 | 5 | 27 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0004c0004 | 0/0 | 4281 | 15 | 13 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0005c0005 | 0/0 | 4281 | 7 | 1 | 0 | 1 | 2 | 3 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0006c0007 | 0/1 | 4281 | 3 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0007c0008 | 0/0 | 4281 | 3 | 0 | 2 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0008c0009 | 0/0 | 4281 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0009c0018 | 0/0 | 4281 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0010c0023 | 0/0 | 4281 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0011c0021 | 0/0 | 4281 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0012c0013 | 0/0 | 4281 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0013c0019 | 0/0 | 4281 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0014c0024 | 0/0 | 4281 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0015c0017 | 0/0 | 4281 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0016c0012 | 0/0 | 4281 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0017c0015 | 0/0 | 4281 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0018c0014 | 0/0 | 4281 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 | ||
| a0019c0010 | 0/0 | 4281 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | ATGTT others(4276): Show |
chr11 | 108152215 | 108227638 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6114 | 142 | 24 | 23 | 66 | 8 | 21 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| a0001c0001t0002 | 0/0 | 6113 | 18 | 16 | 1 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0001c0001t0003 | 0/0 | 6114 | 15 | 0 | 5 | 10 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| a0001c0001t0005 | 0/0 | 6114 | 4 | 3 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| a0001c0001t0008 | 0/0 | 6114 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| a0001c0001t0009 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0001c0001t0011 | 0/0 | 6114 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| a0001c0006t0001 | 0/0 | 6114 | 4 | 4 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| a0001c0011t0001 | 0/0 | 6114 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| a0001c0016t0001 | 0/0 | 6114 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| a0002c0002t0002 | 1/0 | 6113 | 78 | 18 | 13 | 37 | 0 | 9 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0002c0002t0004 | 0/0 | 6113 | 4 | 4 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0002c0002t0006 | 0/0 | 6113 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0002c0002t0007 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0002c0002t0010 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0002c0020t0002 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0002c0022t0002 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0003c0003t0002 | 0/0 | 6113 | 33 | 0 | 5 | 27 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0004c0004t0002 | 0/0 | 6113 | 15 | 13 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0005c0005t0001 | 0/0 | 6114 | 7 | 1 | 0 | 1 | 2 | 3 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| a0006c0007t0001 | 0/1 | 6114 | 3 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| a0007c0008t0001 | 0/0 | 6114 | 3 | 0 | 2 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| a0008c0009t0002 | 0/0 | 6113 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0009c0018t0002 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0010c0023t0003 | 0/0 | 6114 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| a0011c0021t0002 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0012c0013t0002 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0013c0019t0002 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0014c0024t0002 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0015c0017t0002 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0016c0012t0004 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0017c0015t0001 | 0/0 | 6114 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| a0018c0014t0002 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6108): Show |
chr11 | 108152215 | 108227638 |
| a0019c0010t0001 | 0/0 | 6114 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | AGTGC others(6109): Show |
chr11 | 108152215 | 108227638 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0003g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0008g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0001t0011g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0006t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0006t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0006t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0006t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0011t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0001c0016t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0006g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0002t0010g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0020t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0002c0022t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0003c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0004c0004t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0005c0005t0001g0012 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0005c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0005c0005t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0005c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0005c0005t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0005c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0006c0007t0001g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0006c0007t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0006c0007t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0007c0008t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0007c0008t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0007c0008t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0008c0009t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0008c0009t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0009c0018t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0010c0023t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0011c0021t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0012c0013t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0013c0019t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0014c0024t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0015c0017t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0016c0012t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0017c0015t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0018c0014t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| a0019c0010t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0005 | c0005 | t0001 | g0012 | EUR | GBR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00140 | hp1 | a0005 | c0005 | t0001 | g0071 | EUR | GBR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00140 | hp2 | a0009 | c0018 | t0002 | g0197 | EUR | GBR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00280 | hp2 | a0010 | c0023 | t0003 | g0091 | EUR | FIN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00323 | hp2 | a0011 | c0021 | t0002 | g0233 | EUR | FIN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00423 | hp1 | a0003 | c0003 | t0002 | g0282 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00544 | hp1 | a0003 | c0003 | t0002 | g0251 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00544 | hp2 | a0005 | c0005 | t0001 | g0077 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0238 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00673 | hp1 | a0003 | c0003 | t0002 | g0222 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0311 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00733 | hp2 | a0003 | c0003 | t0002 | g0245 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00735 | hp1 | a0006 | c0007 | t0001 | g0123 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00735 | hp2 | a0003 | c0003 | t0002 | g0262 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00738 | hp1 | a0007 | c0008 | t0001 | g0100 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0025 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00741 | hp1 | a0003 | c0003 | t0002 | g0206 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0191 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01070 | hp1 | a0006 | c0007 | t0001 | g0103 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01070 | hp2 | a0004 | c0004 | t0002 | g0306 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0267 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0193 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0025 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01168 | hp2 | a0003 | c0003 | t0002 | g0023 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01169 | hp1 | a0003 | c0003 | t0002 | g0023 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01175 | hp2 | a0012 | c0013 | t0002 | g0159 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01243 | hp1 | a0004 | c0004 | t0002 | g0026 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0219 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0041 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01257 | hp1 | a0007 | c0008 | t0001 | g0098 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0239 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0259 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0192 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0256 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01515 | hp1 | a0007 | c0008 | t0001 | g0065 | EUR | IBS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0266 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0089 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01975 | hp2 | a0008 | c0009 | t0002 | g0292 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0271 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02004 | hp2 | a0008 | c0009 | t0002 | g0293 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02040 | hp2 | a0002 | c0002 | t0006 | g0241 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02071 | hp1 | a0002 | c0002 | t0006 | g0278 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0273 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02129 | hp1 | a0003 | c0003 | t0002 | g0200 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02132 | hp1 | a0003 | c0003 | t0002 | g0250 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02135 | hp1 | a0003 | c0003 | t0002 | g0280 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02145 | hp2 | a0004 | c0004 | t0002 | g0303 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0257 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02257 | hp2 | a0013 | c0019 | t0002 | g0160 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02258 | hp1 | a0004 | c0004 | t0002 | g0188 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0290 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0194 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02451 | hp1 | a0002 | c0022 | t0002 | g0314 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0177 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02572 | hp2 | a0002 | c0002 | t0004 | g0215 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0316 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0289 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0291 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0310 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02647 | hp2 | a0004 | c0004 | t0002 | g0298 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0294 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02717 | hp1 | a0002 | c0002 | t0004 | g0315 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02717 | hp2 | a0002 | c0002 | t0004 | g0214 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02723 | hp1 | a0004 | c0004 | t0002 | g0302 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02735 | hp1 | a0014 | c0024 | t0002 | g0224 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0277 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02818 | hp2 | a0002 | c0002 | t0004 | g0216 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02895 | hp2 | a0001 | c0006 | t0001 | g0054 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02897 | hp2 | a0001 | c0006 | t0001 | g0055 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02922 | hp2 | a0015 | c0017 | t0002 | g0161 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02970 | hp1 | a0004 | c0004 | t0002 | g0304 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02970 | hp2 | a0016 | c0012 | t0004 | g0217 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02976 | hp2 | a0004 | c0004 | t0002 | g0309 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03098 | hp1 | a0004 | c0004 | t0002 | g0305 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0243 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0272 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0020 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03225 | hp1 | a0004 | c0004 | t0002 | g0026 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0255 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0208 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03516 | hp2 | a0004 | c0004 | t0002 | g0308 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03579 | hp1 | a0001 | c0006 | t0001 | g0051 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03654 | hp1 | a0005 | c0005 | t0001 | g0114 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03669 | hp2 | a0001 | c0001 | t0008 | g0064 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0268 | SAS | STU | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03704 | hp2 | a0005 | c0005 | t0001 | g0074 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0231 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0230 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03834 | hp2 | a0017 | c0015 | t0001 | g0072 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03927 | hp1 | a0003 | c0003 | t0002 | g0274 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03942 | hp2 | a0001 | c0001 | t0011 | g0164 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0236 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0242 | SAS | STU | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18522 | hp1 | a0004 | c0004 | t0002 | g0301 | AFR | YRI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0220 | AFR | YRI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0020 | AFR | YRI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18906 | hp2 | a0002 | c0002 | t0007 | g0027 | AFR | YRI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18939 | hp1 | a0003 | c0003 | t0002 | g0246 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18941 | hp2 | a0003 | c0003 | t0002 | g0209 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18946 | hp1 | a0003 | c0003 | t0002 | g0213 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18948 | hp1 | a0003 | c0003 | t0002 | g0212 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18954 | hp1 | a0001 | c0011 | t0001 | g0037 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18954 | hp2 | a0018 | c0014 | t0002 | g0196 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18961 | hp1 | a0003 | c0003 | t0002 | g0283 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18964 | hp2 | a0001 | c0016 | t0001 | g0132 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18970 | hp1 | a0003 | c0003 | t0002 | g0279 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0317 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18977 | hp1 | a0003 | c0003 | t0002 | g0249 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18982 | hp1 | a0003 | c0003 | t0002 | g0248 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18983 | hp1 | a0003 | c0003 | t0002 | g0287 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18984 | hp2 | a0003 | c0003 | t0002 | g0221 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18985 | hp1 | a0003 | c0003 | t0002 | g0285 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18986 | hp1 | a0003 | c0003 | t0002 | g0210 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18992 | hp2 | a0003 | c0003 | t0002 | g0211 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19003 | hp2 | a0003 | c0003 | t0002 | g0207 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19004 | hp1 | a0019 | c0010 | t0001 | g0128 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19005 | hp2 | a0003 | c0003 | t0002 | g0247 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0312 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | LWK | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | LWK | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19058 | hp1 | a0003 | c0003 | t0002 | g0254 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19067 | hp1 | a0003 | c0003 | t0002 | g0270 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19068 | hp2 | a0003 | c0003 | t0002 | g0286 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19078 | hp2 | a0003 | c0003 | t0002 | g0253 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19085 | hp2 | a0003 | c0003 | t0002 | g0252 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0313 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0244 | AFR | YRI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA19240 | hp2 | a0001 | c0006 | t0001 | g0052 | AFR | YRI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA20129 | hp1 | a0005 | c0005 | t0001 | g0012 | AFR | ASW | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0024 | AFR | ASW | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | TSI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA20905 | hp1 | a0005 | c0005 | t0001 | g0056 | SAS | GIH | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG01123 | hp2 | a0002 | c0002 | t0010 | g0281 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02109 | hp1 | a0004 | c0004 | t0002 | g0307 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0021 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02559 | hp1 | a0004 | c0004 | t0002 | g0300 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0024 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG03471 | hp2 | a0002 | c0020 | t0002 | g0201 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0021 | AFR | USA | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | USA | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18955 | hp1 | a0003 | c0003 | t0002 | g0284 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0265 | AFR | USA | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | USA | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0264 | AFR | LWK | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| NA21309 | hp2 | a0004 | c0004 | t0002 | g0299 | AFR | LWK | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| homoSapiens | chm13v2 | a0006 | c0007 | t0001 | g0092 | REF | REF | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0261 | REF | REF | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:108161506 | C | A | 1 | a0011 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.3580G>T | p.Gly1194Cys | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/18 | 3682/6113 | 3580/4284 | 1194/1427 | chr11 | 108161506 | |||
| chr11:108161887 | C | T | 1 | a0009 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.3199G>A | p.Asp1067Asn | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/18 | 3301/6113 | 3199/4284 | 1067/1427 | chr11 | 108161887 | |||
| chr11:108161949 | G | A | 1 | a0007 | 3 | HG00738.hp1 HG01257.hp1 HG01515.hp1 |
missense_variant | MODERATE | c.3137C>T | p.Pro1046Leu | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/18 | 3239/6113 | 3137/4284 | 1046/1427 | chr11 | 108161949 | |||
| chr11:108161980 | G | T | 1 | a0006 | 2 | HG00735.hp1 HG01070.hp1 |
missense_variant | MODERATE | c.3106C>A | p.Leu1036Ile | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/18 | 3208/6113 | 3106/4284 | 1036/1427 | chr11 | 108161980 | |||
| chr11:108169757 | G | T | 2 | a0005 a0017 |
8 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(5): Show |
missense_variant | MODERATE | c.2997C>A | p.Asn999Lys | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/18 | 3099/6113 | 2997/4284 | 999/1427 | chr11 | 108169757 | |||
| chr11:108169795 | C | T | 1 | a0012 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.2959G>A | p.Val987Ile | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/18 | 3061/6113 | 2959/4284 | 987/1427 | chr11 | 108169795 | |||
| chr11:108169835 | C | G | 1 | a0015 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.2919G>C | p.Leu973Phe | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/18 | 3021/6113 | 2919/4284 | 973/1427 | chr11 | 108169835 | |||
| chr11:108172566 | A | C | 1 | a0013 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.2418T>G | p.Asp806Glu | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 2520/6113 | 2418/4284 | 806/1427 | chr11 | 108172566 | |||
| chr11:108173122 | A | G | 1 | a0017 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.1862T>C | p.Val621Ala | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1964/6113 | 1862/4284 | 621/1427 | chr11 | 108173122 | |||
| chr11:108173161 | A | G | 1 | a0004 | 15 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(12): Show |
missense_variant | MODERATE | c.1823T>C | p.Val608Ala | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1925/6113 | 1823/4284 | 608/1427 | chr11 | 108173161 | |||
| chr11:108173261 | C | T | 13 | a0001 a0004 a0005 others(10): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
missense_variant | MODERATE | c.1723G>A | p.Val575Ile | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1825/6113 | 1723/4284 | 575/1427 | chr11 | 108173261 | |||
| chr11:108173364 | T | A | 2 | a0003 a0014 |
34 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(31): Show |
missense_variant | MODERATE | c.1620A>T | p.Leu540Phe | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1722/6113 | 1620/4284 | 540/1427 | chr11 | 108173364 | |||
| chr11:108173636 | A | C | 1 | a0018 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.1348T>G | p.Leu450Val | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1450/6113 | 1348/4284 | 450/1427 | chr11 | 108173636 | |||
| chr11:108173645 | C | T | 1 | a0012 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.1339G>A | p.Val447Met | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1441/6113 | 1339/4284 | 447/1427 | chr11 | 108173645 | |||
| chr11:108186499 | C | T | 1 | a0016 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.709G>A | p.Ala237Thr | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/18 | 811/6113 | 709/4284 | 237/1427 | chr11 | 108186499 | |||
| chr11:108189274 | T | C | 1 | a0010 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.388A>G | p.Thr130Ala | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/18 | 490/6113 | 388/4284 | 130/1427 | chr11 | 108189274 | |||
| chr11:108190498 | C | T | 1 | a0019 | 1 | NA19004.hp1 | missense_variant&splice_region_variant | MODERATE | c.293G>A | p.Ser98Asn | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/18 | 395/6113 | 293/4284 | 98/1427 | chr11 | 108190498 | |||
| chr11:108192127 | G | C | 1 | a0014 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.281C>G | p.Ser94Cys | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/18 | 383/6113 | 281/4284 | 94/1427 | chr11 | 108192127 | |||
| chr11:108194004 | T | C | 1 | a0008 | 2 | HG01975.hp2 HG02004.hp2 |
missense_variant | MODERATE | c.170A>G | p.Lys57Arg | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/18 | 272/6113 | 170/4284 | 57/1427 | chr11 | 108194004 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:108161153 | T | C | 1 | a0001c0006 | 4 | HG02895.hp2 HG02897.hp2 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.3933A>G | p.Pro1311Pro | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/18 | 4035/6113 | 3933/4284 | 1311/1427 | chr11 | 108161153 | |||
| chr11:108172920 | C | T | 1 | a0002c0020 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.2064G>A | p.Thr688Thr | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 2166/6113 | 2064/4284 | 688/1427 | chr11 | 108172920 | |||
| chr11:108173100 | C | T | 1 | a0001c0016 | 1 | NA18964.hp2 | synonymous_variant | LOW | c.1884G>A | p.Ser628Ser | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1986/6113 | 1884/4284 | 628/1427 | chr11 | 108173100 | |||
| chr11:108173127 | T | C | 1 | a0013c0019 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1857A>G | p.Gly619Gly | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1959/6113 | 1857/4284 | 619/1427 | chr11 | 108173127 | |||
| chr11:108185307 | A | G | 1 | a0001c0006 | 4 | HG02895.hp2 HG02897.hp2 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.831T>C | p.Ile277Ile | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/18 | 933/6113 | 831/4284 | 277/1427 | chr11 | 108185307 | |||
| chr11:108185471 | T | C | 1 | a0002c0022 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.750A>G | p.Arg250Arg | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 9/18 | 852/6113 | 750/4284 | 250/1427 | chr11 | 108185471 | |||
| chr11:108189158 | C | T | 1 | a0001c0011 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.504G>A | p.Ser168Ser | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/18 | 606/6113 | 504/4284 | 168/1427 | chr11 | 108189158 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:108157292 | T | C | 1 | a0001c0001t0009 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1650A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 1650 | chr11 | 108157292 | ||||||
| chr11:108157329 | T | C | 1 | a0001c0001t0005 | 4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1613A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 1613 | chr11 | 108157329 | ||||||
| chr11:108157433 | C | T | 1 | a0002c0002t0006 | 2 | HG02040.hp2 HG02071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1509G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 1509 | chr11 | 108157433 | ||||||
| chr11:108157943 | T | C | 2 | a0001c0001t0003 a0010c0023t0003 |
16 | HG00280.hp2 HG01496.hp1 HG01952.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*999A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 999 | chr11 | 108157943 | ||||||
| chr11:108158206 | T | C | 2 | a0002c0002t0004 a0016c0012t0004 |
5 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*736A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 736 | chr11 | 108158206 | ||||||
| chr11:108158257 | T | G | 1 | a0002c0002t0010 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*685A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 685 | chr11 | 108158257 | ||||||
| chr11:108158382 | T | TA | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(11): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*559dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 559 | chr11 | 108158382 | ||||||
| chr11:108158431 | A | G | 1 | a0001c0001t0008 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*511T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 511 | chr11 | 108158431 | ||||||
| chr11:108158813 | T | C | 1 | a0001c0001t0011 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*129A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 129 | chr11 | 108158813 | ||||||
| chr11:108222611 | C | T | 1 | a0002c0002t0007 | 1 | NA18906.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/18 | 75 | chr11 | 108222611 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:108159474 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4207-455T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159474 | |||||||
| chr11:108159630 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0058 others(5): Show |
10 | HG01934.hp2 HG02004.hp1 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.4207-611G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159630 | |||||||
| chr11:108159858 | A | C | 1 | a0012c0013t0002g0159 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4207-839T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159858 | |||||||
| chr11:108159860 | C | A | 1 | a0001c0001t0001g0011 | 2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.4207-841G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159860 | |||||||
| chr11:108159877 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4207-858C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159877 | |||||||
| chr11:108159886 | C | T | 3 | a0004c0004t0002g0306 a0004c0004t0002g0307 a0004c0004t0002g0308 |
3 | HG01070.hp2 HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4207-867G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159886 | |||||||
| chr11:108159968 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4206+912G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159968 | |||||||
| chr11:108160015 | G | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.4206+865C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160015 | |||||||
| chr11:108160106 | C | T | 1 | a0002c0002t0002g0240 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4206+774G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160106 | |||||||
| chr11:108160147 | C | CA | 21 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0073 others(18): Show |
23 | HG00408.hp2 HG00639.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.4206+732dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160147 | |||||||
| chr11:108160395 | T | C | 1 | a0001c0011t0001g0037 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4206+485A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160395 | |||||||
| chr11:108160435 | C | G | 313 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(310): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.4206+445G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160435 | |||||||
| chr11:108160567 | TC | T | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(135): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.4206+312delG | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160567 | |||||||
| chr11:108160568 | C | T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(55): Show |
63 | HG01070.hp2 HG01109.hp2 HG01123.hp1 others(60): Show |
intron_variant | MODIFIER | c.4206+312G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160568 | |||||||
| chr11:108160572 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4206+308A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160572 | |||||||
| chr11:108160649 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0038 others(13): Show |
19 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.4206+231C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160649 | |||||||
| chr11:108160684 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4206+196G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160684 | |||||||
| chr11:108162312 | T | C | 1 | a0002c0022t0002g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3011-132A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162312 | |||||||
| chr11:108162392 | T | C | 1 | a0002c0022t0002g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3011-212A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162392 | |||||||
| chr11:108162465 | C | CT | 5 | a0001c0001t0001g0016 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
6 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3011-286dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162465 | |||||||
| chr11:108162494 | G | A | 1 | a0002c0002t0002g0258 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3011-314C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162494 | |||||||
| chr11:108162555 | C | T | 1 | a0002c0022t0002g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3011-375G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162555 | |||||||
| chr11:108162685 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3011-505C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162685 | |||||||
| chr11:108162766 | A | G | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3011-586T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162766 | |||||||
| chr11:108162842 | T | C | 1 | a0002c0022t0002g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3011-662A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162842 | |||||||
| chr11:108163059 | G | GATTT | 34 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0043 others(31): Show |
36 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.3011-883_3011-880d others(6): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163059 | |||||||
| chr11:108163059 | G | GATTTATT others(1): Show |
29 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(26): Show |
33 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.3011-887_3011-880d others(10): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163059 | |||||||
| chr11:108163059 | G | GATTTATT others(5): Show |
14 | a0001c0001t0001g0152 a0001c0001t0002g0179 a0001c0001t0002g0180 others(11): Show |
14 | HG02055.hp1 HG02145.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.3011-891_3011-880d others(14): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163059 | |||||||
| chr11:108163059 | G | GATTTATT others(9): Show |
1 | a0001c0001t0002g0178 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3011-895_3011-880d others(18): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163059 | |||||||
| chr11:108163059 | GATTT | G | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3011-883_3011-880d others(6): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163059 | |||||||
| chr11:108163067 | T | C | 1 | a0003c0003t0002g0284 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3011-887A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163067 | |||||||
| chr11:108163103 | G | A | 42 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0190 others(39): Show |
46 | HG00323.hp2 HG00408.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.3011-923C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163103 | |||||||
| chr11:108163169 | TC | T | 3 | a0001c0001t0005g0008 a0001c0001t0005g0040 a0001c0001t0005g0041 |
4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3011-990delG | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163169 | |||||||
| chr11:108163228 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.3011-1048G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163228 | |||||||
| chr11:108163229 | G | A | 4 | a0002c0002t0002g0228 a0002c0002t0002g0234 a0002c0002t0002g0275 others(1): Show |
4 | NA18953.hp1 NA18960.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.3011-1049C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163229 | |||||||
| chr11:108163285 | A | G | 314 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(311): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.3011-1105T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163285 | |||||||
| chr11:108163315 | A | G | 2 | a0002c0002t0002g0229 a0002c0002t0002g0263 |
2 | NA18973.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.3011-1135T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163315 | |||||||
| chr11:108163397 | A | G | 100 | a0002c0002t0002g0002 a0002c0002t0002g0020 a0002c0002t0002g0021 others(97): Show |
108 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.3011-1217T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163397 | |||||||
| chr11:108163446 | A | G | 1 | a0001c0006t0001g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3011-1266T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163446 | |||||||
| chr11:108163572 | A | G | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3011-1392T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163572 | |||||||
| chr11:108163822 | G | GA | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.3011-1643_3011-164 others(5): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163822 | |||||||
| chr11:108164049 | T | C | 1 | a0002c0002t0007g0027 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3011-1869A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164049 | |||||||
| chr11:108164380 | T | C | 1 | a0002c0002t0002g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3011-2200A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164380 | |||||||
| chr11:108164404 | G | C | 1 | a0001c0001t0001g0150 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3011-2224C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164404 | |||||||
| chr11:108164484 | C | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0030 others(6): Show |
11 | HG01123.hp1 HG02109.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3011-2304G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164484 | |||||||
| chr11:108164617 | A | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.3011-2437T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164617 | |||||||
| chr11:108164882 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3011-2702C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164882 | |||||||
| chr11:108164925 | T | A | 1 | a0001c0001t0001g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3011-2745A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164925 | |||||||
| chr11:108164987 | C | A | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3011-2807G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164987 | |||||||
| chr11:108165346 | G | A | 17 | a0001c0001t0001g0015 a0001c0001t0001g0062 a0001c0001t0001g0080 others(14): Show |
18 | HG00438.hp2 HG02135.hp2 NA18941.hp1 others(15): Show |
intron_variant | MODIFIER | c.3011-3166C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165346 | |||||||
| chr11:108165375 | G | C | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3011-3195C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165375 | |||||||
| chr11:108165452 | T | TTA | 52 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(49): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.3011-3274_3011-327 others(6): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165452 | |||||||
| chr11:108165452 | T | TTATA | 10 | a0001c0001t0001g0058 a0001c0001t0001g0076 a0001c0001t0001g0082 others(7): Show |
10 | HG00733.hp1 HG01261.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.3011-3276_3011-327 others(8): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165452 | |||||||
| chr11:108165454 | A | T | 1 | a0012c0013t0002g0159 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3011-3274T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165454 | |||||||
| chr11:108165466 | A | AT | 4 | a0001c0001t0001g0143 a0001c0001t0001g0171 a0001c0006t0001g0054 others(1): Show |
4 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3011-3287dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165466 | |||||||
| chr11:108165468 | A | AT | 20 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0036 others(17): Show |
23 | HG01978.hp2 HG02132.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.3011-3289dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165468 | |||||||
| chr11:108165468 | A | T | 9 | a0001c0001t0001g0143 a0001c0001t0001g0163 a0001c0001t0001g0171 others(6): Show |
10 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3011-3288T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165468 | |||||||
| chr11:108165470 | A | AT | 23 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(20): Show |
27 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.3011-3291dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165470 | |||||||
| chr11:108165470 | A | ATT | 4 | a0001c0001t0002g0178 a0001c0001t0002g0199 a0001c0001t0005g0041 others(1): Show |
4 | HG01255.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3011-3291_3011-329 others(6): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165470 | |||||||
| chr11:108165470 | A | ATTT | 3 | a0001c0001t0001g0050 a0001c0001t0002g0183 a0001c0001t0002g0310 |
3 | HG02622.hp2 HG03486.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.3011-3291_3011-329 others(7): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165470 | |||||||
| chr11:108165470 | A | T | 40 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0036 others(37): Show |
44 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.3011-3290T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165470 | |||||||
| chr11:108165472 | A | AT | 32 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(29): Show |
34 | HG00438.hp1 HG00558.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.3011-3293dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | |||||||
| chr11:108165472 | A | ATAT | 11 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0149 others(8): Show |
13 | HG00558.hp2 HG00639.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.3011-3293_3011-329 others(7): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | |||||||
| chr11:108165472 | A | ATATT | 6 | a0001c0001t0002g0182 a0001c0001t0002g0189 a0001c0001t0002g0295 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3011-3293_3011-329 others(8): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | |||||||
| chr11:108165472 | A | ATT | 28 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0032 others(25): Show |
31 | HG00140.hp2 HG00438.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.3011-3294_3011-329 others(6): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | |||||||
| chr11:108165472 | A | ATTT | 7 | a0001c0001t0001g0018 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
8 | HG01081.hp2 HG02055.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.3011-3295_3011-329 others(7): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | |||||||
| chr11:108165472 | A | ATTTT | 11 | a0004c0004t0002g0026 a0004c0004t0002g0299 a0004c0004t0002g0300 others(8): Show |
12 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3011-3296_3011-329 others(8): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | |||||||
| chr11:108165472 | A | T | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
158 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.3011-3292T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | |||||||
| chr11:108165473 | T | TA | 3 | a0001c0001t0001g0117 a0006c0007t0001g0103 a0006c0007t0001g0123 |
3 | HG00735.hp1 HG01070.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.3011-3294_3011-329 others(5): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165473 | |||||||
| chr11:108165635 | T | A | 1 | a0001c0001t0001g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3011-3455A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165635 | |||||||
| chr11:108165663 | C | T | 1 | a0002c0002t0002g0208 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3011-3483G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165663 | |||||||
| chr11:108165756 | C | T | 3 | a0001c0001t0005g0008 a0001c0001t0005g0040 a0001c0001t0005g0041 |
4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3011-3576G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165756 | |||||||
| chr11:108165773 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3011-3593T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165773 | |||||||
| chr11:108165951 | T | A | 32 | a0001c0001t0001g0016 a0001c0001t0001g0138 a0001c0001t0001g0139 others(29): Show |
34 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.3011-3771A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165951 | |||||||
| chr11:108166023 | T | G | 4 | a0002c0002t0004g0214 a0002c0002t0004g0215 a0002c0002t0004g0216 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3010+3721A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166023 | |||||||
| chr11:108166065 | G | A | 3 | a0001c0001t0002g0198 a0009c0018t0002g0197 a0018c0014t0002g0196 |
3 | HG00140.hp2 NA18954.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.3010+3679C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166065 | |||||||
| chr11:108166302 | G | T | 1 | a0002c0002t0002g0297 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3010+3442C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166302 | |||||||
| chr11:108166353 | C | T | 4 | a0002c0002t0002g0025 a0002c0002t0002g0289 a0002c0002t0002g0290 others(1): Show |
5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3010+3391G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166353 | |||||||
| chr11:108166401 | T | A | 1 | a0001c0001t0002g0310 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3010+3343A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166401 | |||||||
| chr11:108166405 | A | T | 1 | a0001c0001t0002g0310 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3010+3339T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166405 | |||||||
| chr11:108166631 | T | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.3010+3113A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166631 | |||||||
| chr11:108167081 | A | G | 1 | a0002c0002t0004g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3010+2663T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167081 | |||||||
| chr11:108167353 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3010+2391A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167353 | |||||||
| chr11:108167415 | A | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(15): Show |
22 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.3010+2329T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167415 | |||||||
| chr11:108167599 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3010+2145C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167599 | |||||||
| chr11:108167750 | A | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(95): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.3010+1994T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167750 | |||||||
| chr11:108167816 | T | C | 10 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0002c0002t0004g0214 others(7): Show |
10 | HG00140.hp2 HG02451.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3010+1928A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167816 | |||||||
| chr11:108167923 | C | T | 1 | a0002c0022t0002g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3010+1821G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167923 | |||||||
| chr11:108168134 | G | A | 1 | a0014c0024t0002g0224 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3010+1610C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168134 | |||||||
| chr11:108168159 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3010+1585A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168159 | |||||||
| chr11:108168160 | ACTT | A | 11 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(8): Show |
11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3010+1581_3010+158 others(7): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168160 | |||||||
| chr11:108168209 | C | G | 1 | a0001c0001t0001g0126 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3010+1535G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168209 | |||||||
| chr11:108168211 | C | T | 3 | a0002c0002t0004g0214 a0002c0002t0004g0215 a0002c0002t0004g0216 |
3 | HG02572.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.3010+1533G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168211 | |||||||
| chr11:108168315 | T | C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0148 others(8): Show |
13 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3010+1429A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168315 | |||||||
| chr11:108168321 | A | G | 27 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(24): Show |
28 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.3010+1423T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168321 | |||||||
| chr11:108168414 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3010+1330T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168414 | |||||||
| chr11:108168557 | T | C | 2 | a0002c0002t0002g0239 a0002c0002t0002g0277 |
2 | HG01257.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.3010+1187A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168557 | |||||||
| chr11:108168705 | C | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0138 a0001c0001t0001g0139 others(11): Show |
15 | HG02132.hp2 HG02451.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.3010+1039G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168705 | |||||||
| chr11:108168773 | A | G | 8 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(5): Show |
8 | HG02055.hp1 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.3010+971T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168773 | |||||||
| chr11:108168835 | T | C | 1 | a0001c0001t0002g0310 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3010+909A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168835 | |||||||
| chr11:108168868 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3010+876A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168868 | |||||||
| chr11:108168889 | C | T | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3010+855G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168889 | |||||||
| chr11:108169254 | C | T | 1 | a0002c0022t0002g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3010+490G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108169254 | |||||||
| chr11:108169377 | A | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.3010+367T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108169377 | |||||||
| chr11:108169546 | C | T | 1 | a0001c0001t0001g0033 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3010+198G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108169546 | |||||||
| chr11:108169554 | G | A | 1 | a0012c0013t0002g0159 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3010+190C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108169554 | |||||||
| chr11:108169688 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0119 |
3 | HG02523.hp1 NA18973.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3010+56C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108169688 | |||||||
| chr11:108170521 | AG | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.2786-479delC | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108170521 | |||||||
| chr11:108170523 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG01358.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2786-480C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108170523 | |||||||
| chr11:108171089 | G | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(11): Show |
17 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.2786-1046C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171089 | |||||||
| chr11:108171114 | T | C | 1 | a0002c0002t0002g0021 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2786-1071A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171114 | |||||||
| chr11:108171124 | A | AT | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(134): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.2785+1074dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171124 | |||||||
| chr11:108171124 | A | ATT | 35 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(32): Show |
35 | HG00408.hp2 HG00642.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.2785+1073_2785+107 others(6): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171124 | |||||||
| chr11:108171124 | AT | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(10): Show |
17 | HG01123.hp1 HG02109.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.2785+1074delA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171124 | |||||||
| chr11:108171124 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2785+1064_2785+107 others(15): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171124 | |||||||
| chr11:108171170 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2785+1029T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171170 | |||||||
| chr11:108171193 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2785+1006G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171193 | |||||||
| chr11:108171240 | G | C | 2 | a0001c0001t0002g0178 a0001c0001t0009g0177 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2785+959C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171240 | |||||||
| chr11:108171312 | G | A | 3 | a0001c0001t0005g0008 a0001c0001t0005g0040 a0001c0001t0005g0041 |
4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2785+887C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171312 | |||||||
| chr11:108171368 | C | T | 1 | a0001c0001t0002g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2785+831G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171368 | |||||||
| chr11:108171473 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2785+726C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171473 | |||||||
| chr11:108171486 | G | GT | 12 | a0001c0001t0001g0005 a0001c0001t0001g0060 a0001c0001t0001g0133 others(9): Show |
14 | HG02602.hp2 HG03688.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.2785+712dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171486 | |||||||
| chr11:108171486 | GT | G | 7 | a0001c0001t0001g0081 a0001c0001t0002g0162 a0001c0001t0002g0185 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2785+712delA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171486 | |||||||
| chr11:108171692 | C | G | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2785+507G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171692 | |||||||
| chr11:108171732 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2785+467G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171732 | |||||||
| chr11:108171742 | C | T | 10 | a0001c0001t0001g0157 a0003c0003t0002g0207 a0003c0003t0002g0221 others(7): Show |
10 | HG00544.hp1 HG02735.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.2785+457G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171742 | |||||||
| chr11:108171814 | T | C | 1 | a0001c0001t0003g0078 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2785+385A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171814 | |||||||
| chr11:108171999 | C | T | 1 | a0002c0002t0002g0242 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2785+200G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171999 | |||||||
| chr11:108174007 | T | C | 4 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0009c0018t0002g0197 others(1): Show |
4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133-156A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174007 | |||||||
| chr11:108174268 | A | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(111): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1133-417T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174268 | |||||||
| chr11:108174564 | T | TA | 22 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0138 others(19): Show |
23 | HG00673.hp2 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1133-714dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174564 | |||||||
| chr11:108174564 | TA | T | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0107 others(8): Show |
11 | HG00140.hp2 HG01070.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.1133-714delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174564 | |||||||
| chr11:108174564 | TAAAAAAA others(3): Show |
T | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1133-723_1133-714d others(12): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174564 | |||||||
| chr11:108174586 | GTATGATA | G | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1133-742_1133-736d others(9): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174586 | |||||||
| chr11:108174615 | C | CT | 7 | a0001c0001t0001g0069 a0001c0001t0001g0138 a0001c0001t0001g0149 others(4): Show |
7 | HG01169.hp2 HG01517.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1133-765dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174615 | |||||||
| chr11:108174615 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
8 | NA18939.hp2 NA18953.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.1133-764G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174615 | |||||||
| chr11:108174715 | T | C | 2 | a0001c0001t0002g0178 a0001c0001t0009g0177 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1133-864A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174715 | |||||||
| chr11:108174769 | C | A | 4 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0009c0018t0002g0197 others(1): Show |
4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133-918G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174769 | |||||||
| chr11:108174770 | C | T | 4 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0009c0018t0002g0197 others(1): Show |
4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133-919G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174770 | |||||||
| chr11:108174771 | ACCACAC | A | 4 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0009c0018t0002g0197 others(1): Show |
4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133-926_1133-921d others(8): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174771 | |||||||
| chr11:108174785 | G | A | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133-934C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174785 | |||||||
| chr11:108174795 | T | C | 1 | a0002c0002t0002g0208 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1133-944A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174795 | |||||||
| chr11:108174916 | G | C | 3 | a0001c0001t0002g0162 a0013c0019t0002g0160 a0015c0017t0002g0161 |
3 | HG02257.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1133-1065C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174916 | |||||||
| chr11:108174983 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1133-1132C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174983 | |||||||
| chr11:108175226 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1132+1020A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175226 | |||||||
| chr11:108175229 | C | T | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(140): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1132+1017G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175229 | |||||||
| chr11:108175327 | G | T | 1 | a0001c0001t0003g0113 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1132+919C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175327 | |||||||
| chr11:108175425 | T | C | 3 | a0001c0001t0002g0198 a0009c0018t0002g0197 a0018c0014t0002g0196 |
3 | HG00140.hp2 NA18954.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1132+821A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175425 | |||||||
| chr11:108175462 | T | A | 1 | a0002c0002t0002g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1132+784A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175462 | |||||||
| chr11:108175498 | T | A | 314 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(311): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1132+748A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175498 | |||||||
| chr11:108175730 | T | C | 9 | a0003c0003t0002g0207 a0003c0003t0002g0221 a0003c0003t0002g0246 others(6): Show |
9 | HG00544.hp1 NA18939.hp1 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1132+516A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175730 | |||||||
| chr11:108176600 | G | C | 4 | a0002c0002t0002g0025 a0002c0002t0002g0289 a0002c0002t0002g0290 others(1): Show |
5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1004-226C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 11/17 | chr11 | 108176600 | |||||||
| chr11:108176680 | A | AT | 15 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(12): Show |
18 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.1004-307dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 11/17 | chr11 | 108176680 | |||||||
| chr11:108176702 | G | A | 1 | a0003c0003t0002g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1003+292C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 11/17 | chr11 | 108176702 | |||||||
| chr11:108176769 | A | G | 5 | a0001c0001t0002g0180 a0001c0006t0001g0051 a0001c0006t0001g0052 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1003+225T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 11/17 | chr11 | 108176769 | |||||||
| chr11:108176900 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1003+94T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 11/17 | chr11 | 108176900 | |||||||
| chr11:108176974 | GAAAT | G | 4 | a0001c0001t0003g0085 a0001c0001t0003g0088 a0001c0001t0003g0112 others(1): Show |
4 | HG02451.hp1 NA18955.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1003+16_1003+19del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 11/17 | chr11 | 108176974 | |||||||
| chr11:108177118 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.907-28A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177118 | |||||||
| chr11:108177187 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.907-97T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177187 | |||||||
| chr11:108177210 | GGTA | G | 5 | a0002c0002t0002g0025 a0002c0002t0002g0208 a0002c0002t0002g0289 others(2): Show |
6 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.907-123_907-121del others(3): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177210 | |||||||
| chr11:108177255 | A | G | 15 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(12): Show |
18 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.907-165T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177255 | |||||||
| chr11:108177494 | G | T | 1 | a0002c0002t0002g0190 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.907-404C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177494 | |||||||
| chr11:108177656 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG00280.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.907-566T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177656 | |||||||
| chr11:108177719 | CT | C | 163 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.907-630delA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177719 | |||||||
| chr11:108177814 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.907-724C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177814 | |||||||
| chr11:108177948 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.907-858A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177948 | |||||||
| chr11:108178002 | T | G | 1 | a0007c0008t0001g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.907-912A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178002 | |||||||
| chr11:108178027 | A | T | 1 | a0002c0022t0002g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.907-937T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178027 | |||||||
| chr11:108178172 | T | C | 1 | a0003c0003t0002g0023 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.907-1082A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178172 | |||||||
| chr11:108178370 | G | T | 2 | a0001c0001t0002g0178 a0001c0001t0009g0177 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.907-1280C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178370 | |||||||
| chr11:108178377 | G | A | 9 | a0001c0001t0002g0179 a0001c0001t0002g0181 a0001c0001t0002g0182 others(6): Show |
9 | HG02055.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.907-1287C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178377 | |||||||
| chr11:108178409 | C | T | 3 | a0001c0001t0002g0162 a0013c0019t0002g0160 a0015c0017t0002g0161 |
3 | HG02257.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.907-1319G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178409 | |||||||
| chr11:108178422 | T | G | 1 | a0001c0001t0002g0182 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.907-1332A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178422 | |||||||
| chr11:108178422 | T | TTG | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-1334_907-1333d others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178422 | |||||||
| chr11:108178566 | A | G | 3 | a0001c0001t0002g0162 a0013c0019t0002g0160 a0015c0017t0002g0161 |
3 | HG02257.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.907-1476T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178566 | |||||||
| chr11:108178581 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.907-1491T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178581 | |||||||
| chr11:108178770 | A | G | 4 | a0002c0002t0004g0214 a0002c0002t0004g0215 a0002c0002t0004g0216 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-1680T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178770 | |||||||
| chr11:108178932 | G | A | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-1842C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178932 | |||||||
| chr11:108179001 | G | A | 1 | a0005c0005t0001g0077 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.907-1911C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179001 | |||||||
| chr11:108179088 | G | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0168 |
2 | NA18970.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.907-1998C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179088 | |||||||
| chr11:108179206 | C | A | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.907-2116G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179206 | |||||||
| chr11:108179328 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.907-2238G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179328 | |||||||
| chr11:108179625 | C | T | 1 | a0002c0002t0002g0297 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.907-2535G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179625 | |||||||
| chr11:108179672 | G | C | 1 | a0005c0005t0001g0056 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.907-2582C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179672 | |||||||
| chr11:108179677 | G | A | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.907-2587C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179677 | |||||||
| chr11:108179724 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.907-2634C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179724 | |||||||
| chr11:108179766 | T | C | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.907-2676A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179766 | |||||||
| chr11:108179782 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.907-2692G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179782 | |||||||
| chr11:108179860 | G | A | 1 | a0001c0001t0003g0090 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.907-2770C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179860 | |||||||
| chr11:108180056 | G | A | 3 | a0002c0002t0004g0214 a0002c0002t0004g0215 a0002c0002t0004g0216 |
3 | HG02572.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.907-2966C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180056 | |||||||
| chr11:108180222 | G | A | 1 | a0001c0001t0003g0090 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.907-3132C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180222 | |||||||
| chr11:108180385 | C | T | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.907-3295G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180385 | |||||||
| chr11:108180417 | A | G | 1 | a0003c0003t0002g0247 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.907-3327T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180417 | |||||||
| chr11:108180542 | C | CAAAAAAT others(299): Show |
1 | a0001c0001t0002g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.907-3453_907-3452i others(308): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180542 | |||||||
| chr11:108180542 | C | CAAAAAAT others(300): Show |
1 | a0001c0001t0002g0178 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.907-3453_907-3452i others(309): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180542 | |||||||
| chr11:108180542 | C | CAAAAAAT others(301): Show |
1 | a0001c0001t0009g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.907-3453_907-3452i others(310): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180542 | |||||||
| chr11:108180573 | A | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.907-3483T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180573 | |||||||
| chr11:108180757 | T | C | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.907-3667A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180757 | |||||||
| chr11:108180978 | A | G | 14 | a0001c0001t0002g0310 a0004c0004t0002g0026 a0004c0004t0002g0298 others(11): Show |
15 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.907-3888T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180978 | |||||||
| chr11:108181025 | G | T | 2 | a0003c0003t0002g0285 a0003c0003t0002g0286 |
2 | NA18985.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.907-3935C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181025 | |||||||
| chr11:108181124 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.907-4034T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181124 | |||||||
| chr11:108181235 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.906+3997C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181235 | |||||||
| chr11:108181262 | G | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(93): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.906+3970C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181262 | |||||||
| chr11:108181275 | C | A | 1 | a0001c0001t0001g0152 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.906+3957G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181275 | |||||||
| chr11:108181291 | C | T | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+3941G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181291 | |||||||
| chr11:108181325 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.906+3907G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181325 | |||||||
| chr11:108181357 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.906+3875A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181357 | |||||||
| chr11:108181380 | G | A | 1 | a0002c0002t0002g0226 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.906+3852C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181380 | |||||||
| chr11:108181464 | C | CA | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(139): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.906+3767dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181464 | |||||||
| chr11:108181532 | A | C | 2 | a0001c0001t0002g0189 a0004c0004t0002g0188 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.906+3700T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181532 | |||||||
| chr11:108181547 | T | G | 1 | a0002c0002t0002g0288 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.906+3685A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181547 | |||||||
| chr11:108181572 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.906+3660A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181572 | |||||||
| chr11:108181690 | A | C | 1 | a0001c0001t0003g0112 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.906+3542T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181690 | |||||||
| chr11:108181701 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0038 others(13): Show |
19 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.906+3531C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181701 | |||||||
| chr11:108181737 | T | TA | 45 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0017 others(42): Show |
52 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.906+3494dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181737 | |||||||
| chr11:108181984 | T | C | 1 | a0003c0003t0002g0023 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.906+3248A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181984 | |||||||
| chr11:108182020 | T | C | 1 | a0004c0004t0002g0306 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.906+3212A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182020 | |||||||
| chr11:108182188 | T | G | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+3044A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182188 | |||||||
| chr11:108182202 | C | G | 1 | a0002c0002t0002g0227 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.906+3030G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182202 | |||||||
| chr11:108182261 | C | T | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.906+2971G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182261 | |||||||
| chr11:108182419 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0163 a0001c0001t0001g0167 others(6): Show |
11 | HG02602.hp2 HG03688.hp1 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.906+2813A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182419 | |||||||
| chr11:108182542 | C | T | 1 | a0001c0001t0001g0011 | 2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.906+2690G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182542 | |||||||
| chr11:108182566 | C | T | 4 | a0002c0002t0002g0025 a0002c0002t0002g0289 a0002c0002t0002g0290 others(1): Show |
5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+2666G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182566 | |||||||
| chr11:108182770 | G | A | 1 | a0002c0002t0002g0269 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.906+2462C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182770 | |||||||
| chr11:108182930 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.906+2302T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182930 | |||||||
| chr11:108182930 | AAAC | A | 4 | a0002c0002t0002g0025 a0002c0002t0002g0289 a0002c0002t0002g0290 others(1): Show |
5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+2299_906+2301d others(5): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182930 | |||||||
| chr11:108183041 | T | C | 1 | a0002c0002t0002g0297 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.906+2191A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183041 | |||||||
| chr11:108183160 | T | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(138): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.906+2072A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183160 | |||||||
| chr11:108183161 | T | A | 2 | a0001c0001t0003g0085 a0001c0001t0003g0088 |
2 | NA18955.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.906+2071A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183161 | |||||||
| chr11:108183247 | A | C | 1 | a0005c0005t0001g0071 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.906+1985T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183247 | |||||||
| chr11:108183355 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0038 others(8): Show |
13 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.906+1877T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183355 | |||||||
| chr11:108183581 | C | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0094 a0001c0001t0001g0102 |
3 | NA18950.hp2 NA19005.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.906+1651G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183581 | |||||||
| chr11:108183673 | A | C | 11 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(8): Show |
11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.906+1559T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183673 | |||||||
| chr11:108183773 | T | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.906+1459A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183773 | |||||||
| chr11:108183781 | C | A | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.906+1451G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183781 | |||||||
| chr11:108183855 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.906+1377G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183855 | |||||||
| chr11:108183871 | G | T | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.906+1361C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183871 | |||||||
| chr11:108183877 | A | G | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(203): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.906+1355T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183877 | |||||||
| chr11:108183895 | C | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
6 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.906+1337G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183895 | |||||||
| chr11:108183939 | A | G | 2 | a0001c0001t0002g0178 a0001c0001t0009g0177 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.906+1293T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183939 | |||||||
| chr11:108183973 | C | CAA | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.906+1257_906+1258d others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183973 | |||||||
| chr11:108183991 | T | G | 1 | a0002c0002t0010g0281 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.906+1241A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183991 | |||||||
| chr11:108184017 | C | A | 4 | a0002c0002t0004g0214 a0002c0002t0004g0215 a0002c0002t0004g0216 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+1215G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184017 | |||||||
| chr11:108184070 | T | A | 1 | a0001c0001t0001g0006 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.906+1162A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184070 | |||||||
| chr11:108184080 | T | C | 1 | a0002c0002t0002g0277 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.906+1152A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184080 | |||||||
| chr11:108184195 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.906+1037C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184195 | |||||||
| chr11:108184195 | G | C | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.906+1037C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184195 | |||||||
| chr11:108184344 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0030 others(5): Show |
10 | HG01123.hp1 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.906+888G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184344 | |||||||
| chr11:108184405 | G | C | 3 | a0002c0002t0002g0255 a0002c0002t0002g0256 a0002c0002t0002g0258 |
3 | HG01496.hp2 HG02523.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.906+827C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184405 | |||||||
| chr11:108184407 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.906+825C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184407 | |||||||
| chr11:108184451 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.906+781C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184451 | |||||||
| chr11:108184471 | C | CA | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(49): Show |
60 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.906+760dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184471 | |||||||
| chr11:108184471 | C | CAA | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(108): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.906+759_906+760dup others(2): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184471 | |||||||
| chr11:108184531 | A | ATCT | 200 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(197): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.906+700_906+701ins others(3): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184531 | |||||||
| chr11:108184627 | A | G | 1 | a0002c0002t0002g0294 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.906+605T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184627 | |||||||
| chr11:108184677 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.906+555A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184677 | |||||||
| chr11:108184951 | T | C | 6 | a0002c0002t0002g0021 a0002c0002t0002g0264 a0002c0002t0002g0265 others(3): Show |
7 | HG01074.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.906+281A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184951 | |||||||
| chr11:108184958 | T | C | 11 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(8): Show |
11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.906+274A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184958 | |||||||
| chr11:108185009 | T | C | 27 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(24): Show |
28 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.906+223A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108185009 | |||||||
| chr11:108185086 | T | A | 1 | a0002c0002t0002g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.906+146A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108185086 | |||||||
| chr11:108185102 | C | A | 3 | a0001c0001t0005g0008 a0001c0001t0005g0040 a0001c0001t0005g0041 |
4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+130G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108185102 | |||||||
| chr11:108185202 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.906+30G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108185202 | |||||||
| chr11:108185350 | T | C | 1 | a0001c0001t0002g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.819-31A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 9/17 | chr11 | 108185350 | |||||||
| chr11:108185753 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.727-259A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108185753 | |||||||
| chr11:108185763 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.727-269G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108185763 | |||||||
| chr11:108185764 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
6 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.727-270A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108185764 | |||||||
| chr11:108185784 | A | C | 3 | a0001c0001t0002g0198 a0009c0018t0002g0197 a0018c0014t0002g0196 |
3 | HG00140.hp2 NA18954.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.727-290T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108185784 | |||||||
| chr11:108185799 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.727-305G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108185799 | |||||||
| chr11:108185981 | A | C | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.727-487T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108185981 | |||||||
| chr11:108186171 | C | A | 1 | a0001c0001t0002g0310 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.726+311G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108186171 | |||||||
| chr11:108186205 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.726+277C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108186205 | |||||||
| chr11:108186242 | C | T | 1 | a0001c0006t0001g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.726+240G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108186242 | |||||||
| chr11:108186578 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.639-9G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108186578 | |||||||
| chr11:108186658 | A | G | 2 | a0001c0001t0002g0178 a0001c0001t0009g0177 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.639-89T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108186658 | |||||||
| chr11:108186690 | T | C | 1 | a0002c0002t0002g0020 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.639-121A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108186690 | |||||||
| chr11:108186703 | G | A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(140): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.639-134C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108186703 | |||||||
| chr11:108187096 | A | C | 1 | a0002c0002t0002g0226 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.639-527T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187096 | |||||||
| chr11:108187129 | G | A | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.639-560C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187129 | |||||||
| chr11:108187191 | C | A | 97 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(94): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.639-622G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187191 | |||||||
| chr11:108187304 | T | C | 1 | a0002c0002t0002g0208 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.639-735A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187304 | |||||||
| chr11:108187385 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.638+713C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187385 | |||||||
| chr11:108187662 | C | CACACTTT others(22): Show |
4 | a0001c0001t0002g0178 a0002c0002t0004g0214 a0002c0002t0004g0215 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.638+435_638+436ins others(29): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187662 | |||||||
| chr11:108187662 | C | CACACTTT others(51): Show |
2 | a0001c0001t0009g0177 a0016c0012t0004g0217 |
2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.638+435_638+436ins others(58): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187662 | |||||||
| chr11:108187818 | C | T | 4 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0009c0018t0002g0197 others(1): Show |
4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.638+280G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187818 | |||||||
| chr11:108187836 | T | C | 5 | a0001c0001t0001g0080 a0001c0001t0001g0134 a0001c0001t0001g0174 others(2): Show |
5 | HG00423.hp2 NA18944.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.638+262A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187836 | |||||||
| chr11:108187908 | T | C | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02132.hp2 HG03130.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.638+190A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187908 | |||||||
| chr11:108188042 | CT | C | 7 | a0001c0001t0001g0119 a0001c0001t0001g0130 a0001c0001t0002g0295 others(4): Show |
7 | HG01515.hp1 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.638+55delA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108188042 | |||||||
| chr11:108188067 | G | A | 6 | a0001c0001t0002g0162 a0002c0002t0007g0027 a0004c0004t0002g0301 others(3): Show |
6 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.638+31C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108188067 | |||||||
| chr11:108188273 | T | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(140): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.557-94A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188273 | |||||||
| chr11:108188323 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.557-144A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188323 | |||||||
| chr11:108188509 | C | T | 1 | a0003c0003t0002g0274 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.557-330G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188509 | |||||||
| chr11:108188602 | C | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0033 others(1): Show |
5 | HG01123.hp1 HG02615.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-423G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188602 | |||||||
| chr11:108188778 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.556+328G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188778 | |||||||
| chr11:108188842 | T | G | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.556+264A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188842 | |||||||
| chr11:108188893 | A | G | 1 | a0003c0003t0002g0246 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.556+213T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188893 | |||||||
| chr11:108188973 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.556+133G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188973 | |||||||
| chr11:108188975 | A | G | 1 | a0002c0002t0002g0268 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.556+131T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188975 | |||||||
| chr11:108189008 | C | G | 1 | a0001c0001t0002g0183 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.556+98G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108189008 | |||||||
| chr11:108189397 | A | G | 1 | a0003c0003t0002g0246 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.332-67T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189397 | |||||||
| chr11:108189478 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0151 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.332-148G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189478 | |||||||
| chr11:108189557 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0038 others(8): Show |
13 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.332-227A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189557 | |||||||
| chr11:108189596 | C | T | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.332-266G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189596 | |||||||
| chr11:108189597 | G | A | 34 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(31): Show |
35 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.332-267C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189597 | |||||||
| chr11:108189609 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.332-279C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189609 | |||||||
| chr11:108189645 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.332-315G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189645 | |||||||
| chr11:108189646 | G | A | 5 | a0001c0001t0001g0034 a0001c0001t0002g0198 a0001c0001t0002g0199 others(2): Show |
5 | HG00140.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-316C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189646 | |||||||
| chr11:108189652 | C | T | 3 | a0001c0001t0001g0166 a0002c0022t0002g0314 a0004c0004t0002g0309 |
3 | HG02451.hp1 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.332-322G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189652 | |||||||
| chr11:108189686 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.332-356G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189686 | |||||||
| chr11:108189742 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0111 |
3 | NA18979.hp2 NA18986.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.332-412G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189742 | |||||||
| chr11:108189795 | G | C | 1 | a0006c0007t0001g0103 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.332-465C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189795 | |||||||
| chr11:108189836 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.332-506G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189836 | |||||||
| chr11:108189869 | C | CA | 33 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0059 others(30): Show |
33 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.332-540dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189869 | |||||||
| chr11:108189885 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0163 a0001c0001t0001g0167 others(6): Show |
11 | HG02602.hp2 HG03688.hp1 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.332-555G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189885 | |||||||
| chr11:108190010 | A | T | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+450T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190010 | |||||||
| chr11:108190086 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.331+374G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190086 | |||||||
| chr11:108190295 | A | G | 1 | a0002c0002t0004g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.331+165T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190295 | |||||||
| chr11:108190300 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.331+160C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190300 | |||||||
| chr11:108190312 | CA | C | 105 | a0001c0001t0001g0084 a0001c0001t0001g0140 a0001c0001t0001g0141 others(102): Show |
113 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.331+147delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190312 | |||||||
| chr11:108190312 | CAA | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(59): Show |
70 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.331+146_331+147del others(2): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190312 | |||||||
| chr11:108190312 | CAAA | C | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(113): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.331+145_331+147del others(3): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190312 | |||||||
| chr11:108190312 | CAAAA | C | 16 | a0001c0001t0001g0045 a0001c0001t0001g0119 a0001c0001t0001g0125 others(13): Show |
17 | HG01070.hp2 HG01243.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.331+144_331+147del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190312 | |||||||
| chr11:108190518 | G | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02132.hp2 HG03130.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-18C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108190518 | |||||||
| chr11:108190562 | TTTAG | T | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-66_291-63delCT others(2): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108190562 | |||||||
| chr11:108190652 | C | T | 313 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(310): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.291-152G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108190652 | |||||||
| chr11:108190699 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0146 |
2 | NA18964.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.291-199G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108190699 | |||||||
| chr11:108190850 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.291-350T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108190850 | |||||||
| chr11:108191081 | C | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.291-581G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108191081 | |||||||
| chr11:108191391 | C | T | 1 | a0003c0003t0002g0222 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.290+727G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108191391 | |||||||
| chr11:108191582 | T | G | 1 | a0001c0001t0002g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.290+536A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108191582 | |||||||
| chr11:108191600 | T | C | 2 | a0002c0002t0006g0241 a0002c0002t0006g0278 |
2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.290+518A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108191600 | |||||||
| chr11:108191659 | T | C | 1 | a0002c0002t0002g0025 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.290+459A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108191659 | |||||||
| chr11:108191814 | G | GAATT | 3 | a0003c0003t0002g0023 a0003c0003t0002g0245 a0003c0003t0002g0262 |
4 | HG00733.hp2 HG00735.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+300_290+303dup others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108191814 | |||||||
| chr11:108192029 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
6 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+89T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108192029 | |||||||
| chr11:108192199 | T | C | 2 | a0002c0002t0002g0219 a0002c0002t0007g0027 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.218-9A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192199 | |||||||
| chr11:108192289 | T | C | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.218-99A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192289 | |||||||
| chr11:108192424 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218-234A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192424 | |||||||
| chr11:108192611 | C | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02132.hp2 HG03130.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.218-421G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192611 | |||||||
| chr11:108192659 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.218-469T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192659 | |||||||
| chr11:108192718 | G | A | 1 | a0002c0002t0002g0208 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.218-528C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192718 | |||||||
| chr11:108192803 | T | A | 255 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.218-613A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192803 | |||||||
| chr11:108192823 | G | T | 1 | a0001c0001t0001g0069 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.218-633C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192823 | |||||||
| chr11:108192961 | AAAAC | A | 13 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.218-775_218-772del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192961 | |||||||
| chr11:108193001 | T | C | 1 | a0002c0002t0002g0258 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.218-811A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193001 | |||||||
| chr11:108193047 | G | A | 2 | a0002c0002t0004g0315 a0002c0022t0002g0314 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.218-857C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193047 | |||||||
| chr11:108193167 | C | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0120 |
2 | HG01175.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.217+790G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193167 | |||||||
| chr11:108193170 | A | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0120 |
2 | HG01175.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.217+787T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193170 | |||||||
| chr11:108193658 | G | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
6 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+299C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193658 | |||||||
| chr11:108193693 | C | A | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.217+264G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193693 | |||||||
| chr11:108193880 | T | C | 3 | a0001c0001t0005g0008 a0001c0001t0005g0040 a0001c0001t0005g0041 |
4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+77A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193880 | |||||||
| chr11:108193918 | G | A | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+39C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193918 | |||||||
| chr11:108194034 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.157-17G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194034 | |||||||
| chr11:108194083 | A | G | 2 | a0003c0003t0002g0254 a0003c0003t0002g0280 |
2 | HG02135.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.157-66T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194083 | |||||||
| chr11:108194208 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.157-191T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194208 | |||||||
| chr11:108194235 | T | C | 1 | a0002c0002t0002g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.157-218A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194235 | |||||||
| chr11:108194525 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0038 others(8): Show |
13 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.157-508T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194525 | |||||||
| chr11:108194632 | G | A | 3 | a0001c0001t0005g0008 a0001c0001t0005g0040 a0001c0001t0005g0041 |
4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-615C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194632 | |||||||
| chr11:108194825 | AT | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0119 others(7): Show |
12 | HG00558.hp2 HG00639.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-809delA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194825 | |||||||
| chr11:108194889 | T | C | 1 | a0002c0002t0002g0219 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.157-872A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194889 | |||||||
| chr11:108194893 | G | A | 2 | a0001c0001t0002g0189 a0004c0004t0002g0188 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.157-876C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194893 | |||||||
| chr11:108194944 | C | T | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.157-927G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194944 | |||||||
| chr11:108194948 | C | T | 4 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0009c0018t0002g0197 others(1): Show |
4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-931G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194948 | |||||||
| chr11:108194981 | G | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.157-964C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194981 | |||||||
| chr11:108194999 | T | G | 4 | a0002c0002t0004g0214 a0002c0002t0004g0215 a0002c0002t0004g0216 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-982A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194999 | |||||||
| chr11:108195061 | A | C | 3 | a0002c0002t0002g0255 a0002c0002t0002g0256 a0002c0002t0002g0258 |
3 | HG01496.hp2 HG02523.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.157-1044T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195061 | |||||||
| chr11:108195289 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.157-1272A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195289 | |||||||
| chr11:108195333 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.157-1316G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195333 | |||||||
| chr11:108195403 | A | T | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.157-1386T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195403 | |||||||
| chr11:108195614 | A | G | 18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(15): Show |
22 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.157-1597T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195614 | |||||||
| chr11:108195635 | CT | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.157-1619delA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195635 | |||||||
| chr11:108195761 | G | A | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+1541C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195761 | |||||||
| chr11:108195983 | T | G | 2 | a0002c0002t0004g0315 a0002c0022t0002g0314 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.156+1319A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195983 | |||||||
| chr11:108196004 | C | T | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+1298G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196004 | |||||||
| chr11:108196024 | G | T | 1 | a0002c0002t0002g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.156+1278C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196024 | |||||||
| chr11:108196096 | T | C | 3 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0186 |
3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.156+1206A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196096 | |||||||
| chr11:108196193 | G | C | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.156+1109C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196193 | |||||||
| chr11:108196283 | T | C | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+1019A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196283 | |||||||
| chr11:108196507 | ATAAT | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.156+791_156+794del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196507 | |||||||
| chr11:108196670 | T | C | 1 | a0005c0005t0001g0012 | 2 | HG00099.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.156+632A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196670 | |||||||
| chr11:108196732 | T | G | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.156+570A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196732 | |||||||
| chr11:108196863 | A | G | 1 | a0002c0002t0004g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.156+439T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196863 | |||||||
| chr11:108196871 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.156+431A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196871 | |||||||
| chr11:108196893 | A | G | 1 | a0001c0001t0003g0088 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.156+409T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196893 | |||||||
| chr11:108196998 | G | A | 11 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(8): Show |
11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.156+304C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196998 | |||||||
| chr11:108197665 | A | G | 1 | a0004c0004t0002g0302 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.38-245T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108197665 | |||||||
| chr11:108198057 | T | C | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-637A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198057 | |||||||
| chr11:108198227 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.38-807A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198227 | |||||||
| chr11:108198312 | T | C | 2 | a0002c0002t0002g0191 a0002c0002t0002g0294 |
2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.38-892A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198312 | |||||||
| chr11:108198347 | G | C | 1 | a0001c0001t0002g0183 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.38-927C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198347 | |||||||
| chr11:108198424 | G | A | 1 | a0004c0004t0002g0302 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.38-1004C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198424 | |||||||
| chr11:108198512 | C | CAG | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.38-1093_38-1092ins others(2): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198512 | |||||||
| chr11:108198669 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.38-1249A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198669 | |||||||
| chr11:108198877 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.38-1457T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198877 | |||||||
| chr11:108198909 | T | A | 13 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.38-1489A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198909 | |||||||
| chr11:108199020 | G | C | 1 | a0002c0002t0002g0025 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.38-1600C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199020 | |||||||
| chr11:108199092 | C | T | 1 | a0014c0024t0002g0224 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.38-1672G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199092 | |||||||
| chr11:108199232 | G | A | 2 | a0003c0003t0002g0211 a0003c0003t0002g0213 |
2 | NA18946.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.38-1812C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199232 | |||||||
| chr11:108199234 | G | A | 1 | a0002c0002t0004g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.38-1814C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199234 | |||||||
| chr11:108199403 | C | T | 1 | a0004c0004t0002g0188 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.38-1983G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199403 | |||||||
| chr11:108199578 | C | T | 1 | a0001c0001t0003g0122 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.38-2158G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199578 | |||||||
| chr11:108199583 | G | A | 2 | a0002c0002t0002g0219 a0002c0002t0007g0027 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.38-2163C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199583 | |||||||
| chr11:108199595 | C | G | 2 | a0002c0002t0002g0219 a0002c0002t0007g0027 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.38-2175G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199595 | |||||||
| chr11:108199846 | C | T | 4 | a0002c0002t0004g0214 a0002c0002t0004g0215 a0002c0002t0004g0216 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-2426G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199846 | |||||||
| chr11:108200206 | G | A | 1 | a0002c0002t0007g0027 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.38-2786C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200206 | |||||||
| chr11:108200222 | G | C | 3 | a0004c0004t0002g0303 a0004c0004t0002g0304 a0004c0004t0002g0305 |
3 | HG02145.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.38-2802C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200222 | |||||||
| chr11:108200438 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.38-3018G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200438 | |||||||
| chr11:108200439 | G | A | 1 | a0002c0022t0002g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.38-3019C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200439 | |||||||
| chr11:108200523 | C | T | 3 | a0001c0001t0002g0198 a0009c0018t0002g0197 a0018c0014t0002g0196 |
3 | HG00140.hp2 NA18954.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.38-3103G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200523 | |||||||
| chr11:108200539 | T | C | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-3119A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200539 | |||||||
| chr11:108200694 | A | G | 2 | a0002c0002t0004g0315 a0002c0022t0002g0314 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.38-3274T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200694 | |||||||
| chr11:108200755 | C | A | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-3335G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200755 | |||||||
| chr11:108200855 | T | G | 4 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0009c0018t0002g0197 others(1): Show |
4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-3435A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200855 | |||||||
| chr11:108201517 | G | A | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-4097C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108201517 | |||||||
| chr11:108201545 | C | T | 4 | a0002c0002t0004g0214 a0002c0002t0004g0215 a0002c0002t0004g0216 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-4125G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108201545 | |||||||
| chr11:108201705 | G | A | 1 | a0002c0002t0002g0267 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.38-4285C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108201705 | |||||||
| chr11:108201781 | G | T | 3 | a0003c0003t0002g0283 a0003c0003t0002g0284 a0003c0003t0002g0287 |
3 | NA18955.hp1 NA18961.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.38-4361C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108201781 | |||||||
| chr11:108201875 | T | G | 1 | a0002c0002t0002g0263 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.38-4455A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108201875 | |||||||
| chr11:108202001 | C | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(11): Show |
17 | HG00558.hp2 HG00639.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.38-4581G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202001 | |||||||
| chr11:108202085 | T | C | 1 | a0003c0003t0002g0287 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.38-4665A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202085 | |||||||
| chr11:108202345 | G | A | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-4925C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202345 | |||||||
| chr11:108202385 | C | G | 1 | a0002c0002t0002g0313 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.38-4965G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202385 | |||||||
| chr11:108202448 | G | T | 1 | a0016c0012t0004g0217 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.38-5028C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202448 | |||||||
| chr11:108202569 | C | A | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-5149G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202569 | |||||||
| chr11:108202659 | T | C | 8 | a0002c0002t0002g0021 a0002c0002t0002g0220 a0002c0002t0002g0264 others(5): Show |
9 | HG01074.hp2 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.38-5239A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202659 | |||||||
| chr11:108202887 | T | G | 1 | a0003c0003t0002g0279 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.38-5467A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202887 | |||||||
| chr11:108203239 | A | G | 4 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0009c0018t0002g0197 others(1): Show |
4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-5819T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203239 | |||||||
| chr11:108203342 | C | T | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-5922G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203342 | |||||||
| chr11:108203464 | A | G | 1 | a0002c0002t0004g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.38-6044T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203464 | |||||||
| chr11:108203477 | G | A | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-6057C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203477 | |||||||
| chr11:108203521 | G | T | 1 | a0003c0003t0002g0274 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.38-6101C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203521 | |||||||
| chr11:108203540 | C | A | 1 | a0002c0002t0002g0273 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.38-6120G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203540 | |||||||
| chr11:108203603 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.38-6183A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203603 | |||||||
| chr11:108203620 | G | A | 1 | a0001c0001t0003g0088 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.38-6200C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203620 | |||||||
| chr11:108203726 | CAGTT | C | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-6310_38-6307del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203726 | |||||||
| chr11:108203870 | T | C | 4 | a0002c0002t0002g0025 a0002c0002t0002g0289 a0002c0002t0002g0290 others(1): Show |
5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-6450A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203870 | |||||||
| chr11:108204153 | C | A | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-6733G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204153 | |||||||
| chr11:108204175 | C | G | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.38-6755G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204175 | |||||||
| chr11:108204212 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.38-6792T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204212 | |||||||
| chr11:108204380 | T | TG | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(202): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.38-6961dupC | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204380 | |||||||
| chr11:108204434 | A | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.38-7014T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204434 | |||||||
| chr11:108204458 | T | C | 1 | a0002c0002t0004g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.38-7038A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204458 | |||||||
| chr11:108204544 | GGAACCTG others(2): Show |
G | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.38-7133_38-7125del others(9): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204544 | |||||||
| chr11:108204571 | A | C | 1 | a0002c0002t0002g0257 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.38-7151T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204571 | |||||||
| chr11:108204608 | C | T | 4 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0009c0018t0002g0197 others(1): Show |
4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-7188G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204608 | |||||||
| chr11:108204639 | G | A | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.38-7219C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204639 | |||||||
| chr11:108204963 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0050 |
3 | NA18966.hp1 NA19054.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.38-7543C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204963 | |||||||
| chr11:108205185 | T | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.38-7765A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205185 | |||||||
| chr11:108205479 | A | C | 4 | a0002c0002t0002g0025 a0002c0002t0002g0289 a0002c0002t0002g0290 others(1): Show |
5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-8059T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205479 | |||||||
| chr11:108205505 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.38-8085G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205505 | |||||||
| chr11:108205610 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.38-8190G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205610 | |||||||
| chr11:108205732 | T | C | 1 | a0001c0001t0003g0089 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.38-8312A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205732 | |||||||
| chr11:108205913 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.38-8493C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205913 | |||||||
| chr11:108205985 | C | G | 1 | a0015c0017t0002g0161 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.38-8565G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205985 | |||||||
| chr11:108206052 | C | A | 2 | a0003c0003t0002g0254 a0003c0003t0002g0280 |
2 | HG02135.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.38-8632G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206052 | |||||||
| chr11:108206275 | TTGCC | T | 4 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0009c0018t0002g0197 others(1): Show |
4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-8859_38-8856del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206275 | |||||||
| chr11:108206311 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.38-8891G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206311 | |||||||
| chr11:108206330 | G | A | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.38-8910C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206330 | |||||||
| chr11:108206425 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.38-9005G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206425 | |||||||
| chr11:108206454 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.38-9034T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206454 | |||||||
| chr11:108206467 | C | A | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-9047G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206467 | |||||||
| chr11:108206732 | G | A | 2 | a0002c0002t0002g0193 a0002c0002t0002g0194 |
2 | HG01081.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.38-9312C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206732 | |||||||
| chr11:108206809 | C | T | 1 | a0002c0002t0002g0256 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.38-9389G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206809 | |||||||
| chr11:108207035 | A | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0050 |
3 | NA18966.hp1 NA19054.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.38-9615T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207035 | |||||||
| chr11:108207129 | C | T | 1 | a0002c0002t0002g0273 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.38-9709G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207129 | |||||||
| chr11:108207130 | G | A | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.38-9710C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207130 | |||||||
| chr11:108207156 | G | C | 27 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(24): Show |
28 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.38-9736C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207156 | |||||||
| chr11:108207238 | G | A | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-9818C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207238 | |||||||
| chr11:108207542 | G | C | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.38-10122C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207542 | |||||||
| chr11:108207596 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.38-10176G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207596 | |||||||
| chr11:108207616 | C | G | 3 | a0002c0002t0004g0214 a0002c0002t0004g0215 a0002c0002t0004g0216 |
3 | HG02572.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.38-10196G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207616 | |||||||
| chr11:108207652 | G | A | 7 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0182 others(4): Show |
7 | HG02055.hp2 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.38-10232C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207652 | |||||||
| chr11:108207663 | C | T | 3 | a0001c0001t0005g0008 a0001c0001t0005g0040 a0001c0001t0005g0041 |
4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-10243G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207663 | |||||||
| chr11:108207684 | C | A | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-10264G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207684 | |||||||
| chr11:108207720 | G | C | 3 | a0002c0002t0004g0214 a0002c0002t0004g0215 a0002c0002t0004g0216 |
3 | HG02572.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.38-10300C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207720 | |||||||
| chr11:108207966 | G | T | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.38-10546C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207966 | |||||||
| chr11:108208233 | A | G | 2 | a0001c0001t0002g0178 a0001c0001t0009g0177 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-10813T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208233 | |||||||
| chr11:108208483 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.38-11063C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208483 | |||||||
| chr11:108208532 | G | A | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02132.hp2 HG03579.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-11112C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208532 | |||||||
| chr11:108208542 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG00558.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.38-11122A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208542 | |||||||
| chr11:108208544 | C | T | 1 | a0013c0019t0002g0160 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.38-11124G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208544 | |||||||
| chr11:108208588 | T | TA | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.38-11169dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208588 | |||||||
| chr11:108208603 | A | C | 1 | a0002c0002t0002g0024 | 2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.38-11183T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208603 | |||||||
| chr11:108208821 | A | G | 1 | a0002c0002t0002g0255 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.38-11401T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208821 | |||||||
| chr11:108208886 | G | C | 4 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0009c0018t0002g0197 others(1): Show |
4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-11466C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208886 | |||||||
| chr11:108209000 | C | T | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-11580G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209000 | |||||||
| chr11:108209026 | T | G | 1 | a0001c0001t0003g0113 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.38-11606A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209026 | |||||||
| chr11:108209288 | A | G | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-11868T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209288 | |||||||
| chr11:108209298 | A | T | 1 | a0001c0001t0001g0061 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.38-11878T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209298 | |||||||
| chr11:108209366 | C | T | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.38-11946G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209366 | |||||||
| chr11:108209381 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.38-11961C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209381 | |||||||
| chr11:108209401 | T | C | 1 | a0005c0005t0001g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.38-11981A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209401 | |||||||
| chr11:108209418 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.38-11998T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209418 | |||||||
| chr11:108209462 | T | C | 2 | a0002c0002t0002g0204 a0002c0002t0002g0205 |
2 | NA18979.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.38-12042A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209462 | |||||||
| chr11:108209637 | C | T | 1 | a0002c0002t0002g0202 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.38-12217G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209637 | |||||||
| chr11:108209672 | G | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.38-12252C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209672 | |||||||
| chr11:108209685 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(139): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.38-12265G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209685 | |||||||
| chr11:108209705 | T | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.38-12285A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209705 | |||||||
| chr11:108209837 | G | A | 1 | a0002c0002t0004g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.38-12417C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209837 | |||||||
| chr11:108209856 | T | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(12): Show |
18 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.38-12436A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209856 | |||||||
| chr11:108209888 | C | CA | 6 | a0001c0001t0002g0162 a0002c0002t0002g0192 a0002c0002t0002g0268 others(3): Show |
6 | HG01175.hp2 HG01346.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-12469dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209888 | |||||||
| chr11:108209888 | CA | C | 101 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(98): Show |
108 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.38-12469delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209888 | |||||||
| chr11:108209888 | CAA | C | 16 | a0002c0002t0002g0223 a0002c0002t0002g0269 a0003c0003t0002g0207 others(13): Show |
17 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.38-12470_38-12469d others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209888 | |||||||
| chr11:108209888 | CAAAAA | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(20): Show |
27 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.38-12473_38-12469d others(7): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209888 | |||||||
| chr11:108209888 | CAAAAAA | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.38-12474_38-12469d others(8): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209888 | |||||||
| chr11:108209940 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.38-12520C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209940 | |||||||
| chr11:108210419 | C | T | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+12081G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108210419 | |||||||
| chr11:108210476 | T | C | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+12024A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108210476 | |||||||
| chr11:108210696 | A | C | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+11804T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108210696 | |||||||
| chr11:108210731 | C | T | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+11769G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108210731 | |||||||
| chr11:108210903 | C | T | 1 | a0004c0004t0002g0299 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.37+11597G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108210903 | |||||||
| chr11:108211036 | T | C | 1 | a0002c0002t0004g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.37+11464A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211036 | |||||||
| chr11:108211130 | C | T | 2 | a0001c0001t0002g0178 a0001c0001t0009g0177 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+11370G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211130 | |||||||
| chr11:108211132 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.37+11368G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211132 | |||||||
| chr11:108211159 | T | C | 1 | a0002c0002t0004g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.37+11341A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211159 | |||||||
| chr11:108211170 | C | T | 2 | a0002c0002t0004g0315 a0002c0022t0002g0314 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.37+11330G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211170 | |||||||
| chr11:108211172 | C | T | 1 | a0002c0002t0002g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.37+11328G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211172 | |||||||
| chr11:108211307 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.37+11193G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211307 | |||||||
| chr11:108211453 | G | A | 27 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(24): Show |
28 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.37+11047C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211453 | |||||||
| chr11:108211546 | G | GA | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(35): Show |
43 | HG00438.hp2 HG00741.hp1 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.37+10953dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211546 | |||||||
| chr11:108211546 | GA | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0058 others(7): Show |
12 | HG00673.hp1 HG01934.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.37+10953delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211546 | |||||||
| chr11:108211623 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(15): Show |
22 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.37+10877C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211623 | |||||||
| chr11:108212036 | A | G | 1 | a0003c0003t0002g0221 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.37+10464T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212036 | |||||||
| chr11:108212046 | A | C | 1 | a0002c0022t0002g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.37+10454T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212046 | |||||||
| chr11:108212074 | TA | T | 14 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0140 others(11): Show |
14 | HG01081.hp1 HG01099.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.37+10425delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212074 | |||||||
| chr11:108212134 | A | G | 3 | a0002c0002t0004g0214 a0002c0002t0004g0215 a0002c0002t0004g0216 |
3 | HG02572.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.37+10366T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212134 | |||||||
| chr11:108212135 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
6 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.37+10365A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212135 | |||||||
| chr11:108212170 | T | C | 1 | a0002c0002t0002g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.37+10330A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212170 | |||||||
| chr11:108212291 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.37+10209C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212291 | |||||||
| chr11:108212399 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.37+10101G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212399 | |||||||
| chr11:108212422 | G | A | 1 | a0010c0023t0003g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.37+10078C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212422 | |||||||
| chr11:108212449 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.37+10051G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212449 | |||||||
| chr11:108212604 | T | A | 32 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(29): Show |
33 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.37+9896A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212604 | |||||||
| chr11:108212647 | C | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0030 others(6): Show |
11 | HG01123.hp1 HG02109.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.37+9853G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212647 | |||||||
| chr11:108212945 | C | CA | 23 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0002g0295 others(20): Show |
23 | HG00423.hp1 HG00673.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.37+9554dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212945 | |||||||
| chr11:108212945 | CA | C | 156 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.37+9554delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212945 | |||||||
| chr11:108212945 | CAA | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0148 a0001c0001t0001g0149 others(10): Show |
13 | HG00140.hp2 HG01081.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.37+9553_37+9554del others(2): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212945 | |||||||
| chr11:108212945 | CAAAA | C | 8 | a0001c0001t0002g0162 a0003c0003t0002g0210 a0003c0003t0002g0211 others(5): Show |
8 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.37+9551_37+9554del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212945 | |||||||
| chr11:108212995 | C | T | 2 | a0002c0002t0004g0315 a0002c0022t0002g0314 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.37+9505G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212995 | |||||||
| chr11:108213053 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.37+9447G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213053 | |||||||
| chr11:108213188 | G | A | 8 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(5): Show |
8 | HG02055.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.37+9312C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213188 | |||||||
| chr11:108213256 | A | C | 1 | a0003c0003t0002g0209 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.37+9244T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213256 | |||||||
| chr11:108213363 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0168 |
2 | NA18970.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.37+9137T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213363 | |||||||
| chr11:108213413 | A | G | 1 | a0001c0001t0008g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.37+9087T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213413 | |||||||
| chr11:108213487 | C | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(15): Show |
22 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.37+9013G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213487 | |||||||
| chr11:108213519 | C | T | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+8981G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213519 | |||||||
| chr11:108213520 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.37+8980C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213520 | |||||||
| chr11:108213675 | C | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.37+8825G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213675 | |||||||
| chr11:108213734 | A | G | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+8766T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213734 | |||||||
| chr11:108213786 | G | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.37+8714C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213786 | |||||||
| chr11:108213800 | A | G | 1 | a0002c0002t0007g0027 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.37+8700T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213800 | |||||||
| chr11:108213842 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.37+8658A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213842 | |||||||
| chr11:108214008 | C | G | 1 | a0002c0002t0002g0208 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.37+8492G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214008 | |||||||
| chr11:108214021 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.37+8479T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214021 | |||||||
| chr11:108214338 | A | G | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+8162T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214338 | |||||||
| chr11:108214357 | G | A | 17 | a0001c0001t0001g0015 a0001c0001t0001g0062 a0001c0001t0001g0125 others(14): Show |
18 | HG00438.hp2 HG02135.hp2 NA18941.hp1 others(15): Show |
intron_variant | MODIFIER | c.37+8143C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214357 | |||||||
| chr11:108214377 | T | C | 1 | a0002c0002t0002g0020 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.37+8123A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214377 | |||||||
| chr11:108214397 | C | T | 1 | a0002c0002t0002g0311 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.37+8103G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214397 | |||||||
| chr11:108214599 | G | A | 1 | a0002c0002t0007g0027 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.37+7901C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214599 | |||||||
| chr11:108214631 | A | AT | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(9): Show |
13 | HG01175.hp2 HG02055.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.37+7868dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214631 | |||||||
| chr11:108214658 | G | A | 1 | a0002c0002t0010g0281 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.37+7842C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214658 | |||||||
| chr11:108214665 | T | C | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+7835A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214665 | |||||||
| chr11:108214691 | G | C | 4 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0009c0018t0002g0197 others(1): Show |
4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+7809C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214691 | |||||||
| chr11:108214789 | T | C | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+7711A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214789 | |||||||
| chr11:108214958 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.37+7542C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214958 | |||||||
| chr11:108214958 | G | T | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+7542C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214958 | |||||||
| chr11:108214983 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.37+7517G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214983 | |||||||
| chr11:108215029 | C | A | 1 | a0003c0003t0002g0282 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.37+7471G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215029 | |||||||
| chr11:108215035 | T | G | 1 | a0002c0002t0007g0027 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.37+7465A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215035 | |||||||
| chr11:108215081 | T | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0038 others(10): Show |
15 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.37+7419A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215081 | |||||||
| chr11:108215098 | T | C | 6 | a0003c0003t0002g0200 a0003c0003t0002g0283 a0003c0003t0002g0284 others(3): Show |
6 | HG02129.hp1 NA18955.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.37+7402A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215098 | |||||||
| chr11:108215107 | G | A | 3 | a0001c0001t0002g0162 a0013c0019t0002g0160 a0015c0017t0002g0161 |
3 | HG02257.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.37+7393C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215107 | |||||||
| chr11:108215228 | C | G | 2 | a0001c0001t0002g0189 a0004c0004t0002g0188 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.37+7272G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215228 | |||||||
| chr11:108215274 | TAGTC | T | 5 | a0001c0001t0002g0162 a0003c0003t0002g0206 a0012c0013t0002g0159 others(2): Show |
5 | HG00741.hp1 HG01175.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+7222_37+7225del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215274 | |||||||
| chr11:108215342 | A | G | 4 | a0002c0002t0002g0025 a0002c0002t0002g0289 a0002c0002t0002g0290 others(1): Show |
5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+7158T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215342 | |||||||
| chr11:108215506 | A | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+6994T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215506 | |||||||
| chr11:108215528 | T | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+6972A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215528 | |||||||
| chr11:108215715 | C | T | 1 | a0002c0002t0004g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.37+6785G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215715 | |||||||
| chr11:108215720 | T | C | 1 | a0002c0002t0002g0288 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.37+6780A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215720 | |||||||
| chr11:108215761 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.37+6739T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215761 | |||||||
| chr11:108215852 | T | A | 1 | a0002c0002t0002g0195 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.37+6648A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215852 | |||||||
| chr11:108215875 | T | C | 4 | a0002c0002t0002g0025 a0002c0002t0002g0289 a0002c0002t0002g0290 others(1): Show |
5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+6625A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215875 | |||||||
| chr11:108216079 | C | T | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+6421G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216079 | |||||||
| chr11:108216085 | T | A | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+6415A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216085 | |||||||
| chr11:108216094 | T | TAAAAAAA others(1): Show |
13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+6405_37+6406ins others(8): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216094 | |||||||
| chr11:108216095 | C | A | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+6405G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216095 | |||||||
| chr11:108216150 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.37+6350A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216150 | |||||||
| chr11:108216253 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.37+6247A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216253 | |||||||
| chr11:108216336 | C | T | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+6164G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216336 | |||||||
| chr11:108216477 | A | G | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+6023T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216477 | |||||||
| chr11:108216491 | T | C | 1 | a0002c0002t0004g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.37+6009A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216491 | |||||||
| chr11:108216514 | CA | C | 4 | a0002c0002t0002g0202 a0002c0002t0002g0203 a0002c0002t0002g0204 others(1): Show |
4 | NA18942.hp2 NA18979.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+5985delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216514 | |||||||
| chr11:108216586 | C | T | 1 | a0005c0005t0001g0056 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.37+5914G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216586 | |||||||
| chr11:108216654 | T | TGGAAA | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.37+5845_37+5846ins others(5): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216654 | |||||||
| chr11:108216827 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.37+5673G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216827 | |||||||
| chr11:108216896 | A | T | 27 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(24): Show |
28 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.37+5604T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216896 | |||||||
| chr11:108217109 | C | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | NA18962.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.37+5391G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217109 | |||||||
| chr11:108217110 | A | G | 2 | a0002c0002t0004g0315 a0002c0022t0002g0314 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.37+5390T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217110 | |||||||
| chr11:108217120 | G | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(109): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.37+5380C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217120 | |||||||
| chr11:108217167 | ATGAG | A | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+5329_37+5332del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217167 | |||||||
| chr11:108217428 | A | C | 1 | a0002c0020t0002g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.37+5072T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217428 | |||||||
| chr11:108217758 | C | T | 27 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(24): Show |
28 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.37+4742G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217758 | |||||||
| chr11:108217766 | A | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.37+4734T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217766 | |||||||
| chr11:108218068 | T | C | 1 | a0001c0001t0001g0017 | 2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.37+4432A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218068 | |||||||
| chr11:108218173 | C | T | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.37+4327G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218173 | |||||||
| chr11:108218313 | T | A | 4 | a0001c0006t0001g0051 a0001c0006t0001g0052 a0001c0006t0001g0054 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+4187A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218313 | |||||||
| chr11:108218364 | TAA | T | 4 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0009c0018t0002g0197 others(1): Show |
4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+4134_37+4135del others(2): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218364 | |||||||
| chr11:108218404 | C | T | 1 | a0003c0003t0002g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.37+4096G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218404 | |||||||
| chr11:108218406 | C | T | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+4094G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218406 | |||||||
| chr11:108218424 | T | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(12): Show |
18 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.37+4076A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218424 | |||||||
| chr11:108218433 | TTTA | T | 8 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(5): Show |
8 | HG02055.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.37+4064_37+4066del others(3): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218433 | |||||||
| chr11:108218470 | G | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(195): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.37+4030C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218470 | |||||||
| chr11:108218478 | T | C | 2 | a0008c0009t0002g0292 a0008c0009t0002g0293 |
2 | HG01975.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.37+4022A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218478 | |||||||
| chr11:108218524 | T | C | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+3976A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218524 | |||||||
| chr11:108218595 | A | G | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+3905T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218595 | |||||||
| chr11:108218700 | T | C | 1 | a0001c0006t0001g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.37+3800A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218700 | |||||||
| chr11:108218714 | G | A | 1 | a0001c0001t0002g0310 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.37+3786C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218714 | |||||||
| chr11:108219194 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.37+3306C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219194 | |||||||
| chr11:108219282 | C | G | 1 | a0004c0004t0002g0298 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.37+3218G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219282 | |||||||
| chr11:108219335 | C | G | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+3165G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219335 | |||||||
| chr11:108219346 | C | A | 4 | a0001c0001t0002g0162 a0012c0013t0002g0159 a0013c0019t0002g0160 others(1): Show |
4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+3154G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219346 | |||||||
| chr11:108219380 | T | TG | 4 | a0001c0006t0001g0051 a0001c0006t0001g0052 a0001c0006t0001g0054 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+3119dupC | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219380 | |||||||
| chr11:108219592 | C | T | 1 | a0002c0002t0002g0195 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.37+2908G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219592 | |||||||
| chr11:108219608 | T | C | 2 | a0002c0002t0002g0191 a0002c0002t0002g0294 |
2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.37+2892A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219608 | |||||||
| chr11:108219669 | T | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0038 others(13): Show |
19 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.37+2831A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219669 | |||||||
| chr11:108219732 | A | AAAC | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(21): Show |
28 | HG01081.hp1 HG01123.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.37+2765_37+2767dup others(3): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219732 | |||||||
| chr11:108219732 | AAAC | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(145): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.37+2765_37+2767del others(3): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219732 | |||||||
| chr11:108219961 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.37+2539A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219961 | |||||||
| chr11:108219983 | A | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.37+2517T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219983 | |||||||
| chr11:108220304 | T | C | 13 | a0004c0004t0002g0026 a0004c0004t0002g0298 a0004c0004t0002g0299 others(10): Show |
14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+2196A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220304 | |||||||
| chr11:108220378 | A | C | 1 | a0001c0001t0001g0009 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.37+2122T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220378 | |||||||
| chr11:108220441 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.37+2059A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220441 | |||||||
| chr11:108220442 | A | T | 1 | a0002c0002t0002g0191 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.37+2058T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220442 | |||||||
| chr11:108220450 | C | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+2050G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220450 | |||||||
| chr11:108220533 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.37+1967G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220533 | |||||||
| chr11:108220596 | G | A | 1 | a0001c0001t0002g0310 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.37+1904C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220596 | |||||||
| chr11:108220660 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | NA18954.hp1 NA18962.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+1840G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220660 | |||||||
| chr11:108220678 | G | T | 1 | a0002c0002t0002g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.37+1822C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220678 | |||||||
| chr11:108220770 | G | T | 8 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(5): Show |
8 | HG02055.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.37+1730C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220770 | |||||||
| chr11:108221043 | G | C | 2 | a0001c0001t0002g0189 a0004c0004t0002g0188 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.37+1457C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221043 | |||||||
| chr11:108221128 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.37+1372A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221128 | |||||||
| chr11:108221216 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.37+1284A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221216 | |||||||
| chr11:108221386 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.37+1114G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221386 | |||||||
| chr11:108221437 | T | G | 3 | a0002c0002t0002g0311 a0002c0002t0002g0312 a0002c0002t0002g0313 |
3 | HG00673.hp2 NA19012.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.37+1063A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221437 | |||||||
| chr11:108221576 | C | G | 1 | a0002c0002t0002g0191 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.37+924G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221576 | |||||||
| chr11:108221601 | T | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
8 | NA18939.hp2 NA18953.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.37+899A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221601 | |||||||
| chr11:108221697 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.37+803C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221697 | |||||||
| chr11:108221820 | A | G | 1 | a0002c0002t0002g0190 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.37+680T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221820 | |||||||
| chr11:108221881 | T | G | 2 | a0002c0002t0004g0315 a0002c0022t0002g0314 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.37+619A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221881 | |||||||
| chr11:108221887 | C | T | 11 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(8): Show |
11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.37+613G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221887 | |||||||
| chr11:108221910 | G | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0038 others(13): Show |
19 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.37+590C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221910 | |||||||
| chr11:108221966 | T | C | 1 | a0002c0002t0002g0316 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.37+534A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221966 | |||||||
| chr11:108222275 | G | C | 1 | a0002c0002t0002g0317 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.37+225C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108222275 | |||||||
| chr11:108222275 | G | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0030 others(5): Show |
10 | HG01123.hp1 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.37+225C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108222275 | |||||||
| chr11:108222308 | G | T | 3 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0009g0177 |
3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+192C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108222308 | |||||||
| chr11:108222350 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG01358.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.37+150G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108222350 | |||||||
| chr11:108222434 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | NA18944.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.37+66C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108222434 | |||||||
| chr11:108222481 | A | T | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.37+19T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108222481 |