Item | Value |
---|---|
geneid | 5316 |
ensemblid | ENSG00000160199.15 |
hgncid | 9022 |
symbol | PKNOX1 |
name | PBX/knotted 1 homeobox 1 |
refseq_nuc | NM_004571.5 |
refseq_prot | NP_004562.2 |
ensembl_nuc | ENST00000291547.10 |
ensembl_prot | ENSP00000291547.4 |
mane_status | MANE Select |
chr | chr21 |
start | 42974562 |
end | 43033931 |
strand | + |
ver | v1.2 |
region | chr21:42974562-43033931 |
region5000 | chr21:42969562-43038931 |
regionname0 | PKNOX1_chr21_42974562_43033931 |
regionname5000 | PKNOX1_chr21_42969562_43038931 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 436 | 361 | 84 | 72 | 151 | 18 | 34 | 113 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | MMATQ others(431): Show |
chr21 | 42969562 | 43038931 |
a0002 | 0/0 | 436 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | MMATQ others(431): Show |
chr21 | 42969562 | 43038931 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1308 | 287 | 74 | 59 | 105 | 18 | 30 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | ATGAT others(1303): Show |
chr21 | 42969562 | 43038931 | ||
a0001c0002 | 1/0 | 1308 | 70 | 10 | 12 | 43 | 0 | 4 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | ATGAT others(1303): Show |
chr21 | 42969562 | 43038931 | ||
a0001c0003 | 0/0 | 1308 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | ATGAT others(1303): Show |
chr21 | 42969562 | 43038931 | ||
a0001c0005 | 0/0 | 1308 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | ATGAT others(1303): Show |
chr21 | 42969562 | 43038931 | ||
a0001c0006 | 0/0 | 1308 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | ATGAT others(1303): Show |
chr21 | 42969562 | 43038931 | ||
a0002c0004 | 0/0 | 1308 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | ATGAT others(1303): Show |
chr21 | 42969562 | 43038931 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5290 | 85 | 7 | 20 | 47 | 3 | 8 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0002 | 0/0 | 5290 | 63 | 24 | 7 | 27 | 3 | 2 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0004 | 0/1 | 5312 | 21 | 0 | 5 | 8 | 1 | 6 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5307): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0005 | 0/0 | 5310 | 16 | 0 | 1 | 10 | 1 | 4 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5305): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0006 | 0/0 | 5310 | 14 | 4 | 4 | 0 | 4 | 2 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5305): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0007 | 0/0 | 5290 | 14 | 14 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0008 | 0/0 | 5283 | 14 | 1 | 5 | 0 | 4 | 4 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5278): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0010 | 0/0 | 5290 | 6 | 0 | 4 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0011 | 0/0 | 5290 | 4 | 4 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0012 | 0/0 | 5290 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0013 | 0/0 | 5290 | 3 | 0 | 3 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0014 | 0/0 | 5290 | 3 | 0 | 0 | 3 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0015 | 0/0 | 5281 | 3 | 0 | 2 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5276): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0017 | 0/0 | 5298 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5293): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0019 | 0/0 | 5282 | 2 | 0 | 0 | 0 | 1 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5277): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0020 | 0/0 | 5310 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5305): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0021 | 0/0 | 5312 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5307): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0022 | 0/0 | 5290 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0023 | 0/0 | 5290 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0024 | 0/0 | 5292 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5287): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0025 | 0/0 | 5290 | 2 | 0 | 2 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0026 | 0/0 | 5290 | 2 | 1 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0027 | 0/0 | 5292 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5287): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0030 | 0/0 | 5290 | 2 | 0 | 2 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0031 | 0/0 | 5292 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5287): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0032 | 0/0 | 5282 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5277): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0033 | 0/0 | 5310 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5305): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0034 | 0/0 | 5290 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0035 | 0/0 | 5288 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5283): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0036 | 0/0 | 5288 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5283): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0037 | 0/0 | 5290 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0038 | 0/0 | 5290 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0040 | 0/0 | 5290 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0041 | 0/0 | 5290 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0042 | 0/0 | 5292 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5287): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0043 | 0/0 | 5292 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5287): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0044 | 0/0 | 5283 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5278): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0045 | 0/0 | 5290 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0046 | 0/0 | 5290 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0047 | 0/0 | 5290 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0048 | 0/0 | 5290 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0049 | 0/0 | 5292 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5287): Show |
chr21 | 42969562 | 43038931 |
a0001c0001t0050 | 0/0 | 5292 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5287): Show |
chr21 | 42969562 | 43038931 |
a0001c0002t0003 | 1/0 | 5300 | 46 | 4 | 5 | 33 | 0 | 3 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5295): Show |
chr21 | 42969562 | 43038931 |
a0001c0002t0009 | 0/0 | 5300 | 6 | 0 | 6 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5295): Show |
chr21 | 42969562 | 43038931 |
a0001c0002t0012 | 0/0 | 5290 | 3 | 3 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0002t0016 | 0/0 | 5290 | 3 | 0 | 0 | 3 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0002t0017 | 0/0 | 5298 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5293): Show |
chr21 | 42969562 | 43038931 |
a0001c0002t0018 | 0/0 | 5302 | 3 | 0 | 0 | 2 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5297): Show |
chr21 | 42969562 | 43038931 |
a0001c0002t0028 | 0/0 | 5300 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5295): Show |
chr21 | 42969562 | 43038931 |
a0001c0002t0029 | 0/0 | 5300 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5295): Show |
chr21 | 42969562 | 43038931 |
a0001c0002t0039 | 0/0 | 5290 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0002t0051 | 0/0 | 5300 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5295): Show |
chr21 | 42969562 | 43038931 |
a0001c0002t0052 | 0/0 | 5300 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5295): Show |
chr21 | 42969562 | 43038931 |
a0001c0003t0002 | 0/0 | 5290 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5285): Show |
chr21 | 42969562 | 43038931 |
a0001c0005t0003 | 0/0 | 5300 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5295): Show |
chr21 | 42969562 | 43038931 |
a0001c0006t0009 | 0/0 | 5300 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5295): Show |
chr21 | 42969562 | 43038931 |
a0002c0004t0005 | 0/0 | 5310 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | GTGTC others(5305): Show |
chr21 | 42969562 | 43038931 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0020 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0006g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0006g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0006g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0007g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0008g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0010g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0010g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0010g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0010g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0010g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0011g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0011g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0011g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0011g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0012g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0013g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0013g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0013g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0014g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0014g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0014g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0015g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0015g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0015g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0017g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0019g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0019g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0020g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0020g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0021g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0021g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0022g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0022g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0023g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0023g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0024g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0024g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0025g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0025g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0026g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0026g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0027g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0027g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0030g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0030g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0031g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0032g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0033g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0034g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0035g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0036g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0037g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0038g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0040g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0041g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0042g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0043g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0044g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0045g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0046g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0047g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0048g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0049g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0001t0050g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0001 | 1/0 | 4 | 0 | 0 | 3 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0009g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0009g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0009g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0009g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0009g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0009g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0012g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0012g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0012g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0016g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0016g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0016g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0017g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0017g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0018g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0018g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0018g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0028g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0028g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0029g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0029g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0039g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0051g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0002t0052g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0005t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0001c0006t0009g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
a0002c0004t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0026 | g0211 | EUR | GBR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0186 | EUR | GBR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0042 | EUR | GBR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00140 | hp2 | a0001 | c0001 | t0008 | g0159 | EUR | GBR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0209 | EUR | FIN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0196 | EUR | FIN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00323 | hp2 | a0001 | c0001 | t0008 | g0158 | EUR | FIN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0199 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00597 | hp1 | a0001 | c0001 | t0014 | g0093 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00597 | hp2 | a0001 | c0002 | t0003 | g0299 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00621 | hp1 | a0001 | c0002 | t0003 | g0343 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00639 | hp1 | a0001 | c0002 | t0009 | g0320 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00639 | hp2 | a0001 | c0001 | t0025 | g0018 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00642 | hp2 | a0001 | c0001 | t0025 | g0017 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00673 | hp1 | a0001 | c0001 | t0014 | g0094 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00673 | hp2 | a0001 | c0002 | t0052 | g0332 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0195 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0194 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00735 | hp2 | a0001 | c0002 | t0051 | g0308 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00738 | hp1 | a0001 | c0002 | t0009 | g0006 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG00741 | hp2 | a0001 | c0001 | t0010 | g0036 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01070 | hp2 | a0001 | c0001 | t0008 | g0156 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01071 | hp1 | a0001 | c0001 | t0008 | g0161 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01074 | hp2 | a0001 | c0001 | t0008 | g0160 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01081 | hp1 | a0001 | c0001 | t0037 | g0213 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01081 | hp2 | a0001 | c0002 | t0003 | g0312 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01099 | hp1 | a0001 | c0001 | t0008 | g0157 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01099 | hp2 | a0001 | c0001 | t0033 | g0184 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01109 | hp1 | a0001 | c0001 | t0012 | g0110 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0182 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01168 | hp2 | a0001 | c0001 | t0030 | g0082 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0049 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0048 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01192 | hp2 | a0001 | c0001 | t0010 | g0037 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01243 | hp2 | a0001 | c0001 | t0046 | g0240 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01255 | hp1 | a0001 | c0002 | t0003 | g0318 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01258 | hp1 | a0001 | c0001 | t0030 | g0119 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01261 | hp1 | a0001 | c0001 | t0006 | g0202 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0328 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01346 | hp1 | a0001 | c0002 | t0003 | g0333 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01346 | hp2 | a0001 | c0001 | t0013 | g0114 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01496 | hp2 | a0001 | c0002 | t0003 | g0315 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0274 | EUR | IBS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0208 | EUR | IBS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01516 | hp1 | a0001 | c0001 | t0008 | g0170 | EUR | IBS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01516 | hp2 | a0001 | c0001 | t0006 | g0004 | EUR | IBS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0004 | EUR | IBS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0223 | EUR | IBS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01928 | hp1 | a0001 | c0006 | t0009 | g0006 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01934 | hp2 | a0001 | c0002 | t0009 | g0309 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01943 | hp2 | a0001 | c0002 | t0009 | g0296 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01975 | hp1 | a0001 | c0001 | t0006 | g0203 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01975 | hp2 | a0001 | c0001 | t0013 | g0084 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0142 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01981 | hp2 | a0001 | c0001 | t0015 | g0165 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02004 | hp1 | a0001 | c0001 | t0013 | g0112 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02004 | hp2 | a0001 | c0001 | t0015 | g0164 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02015 | hp1 | a0001 | c0001 | t0014 | g0111 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02027 | hp1 | a0001 | c0002 | t0003 | g0342 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0327 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02055 | hp2 | a0001 | c0001 | t0044 | g0289 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02071 | hp2 | a0001 | c0002 | t0003 | g0314 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02080 | hp1 | a0001 | c0005 | t0003 | g0301 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02083 | hp2 | a0001 | c0002 | t0003 | g0326 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0185 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0109 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02148 | hp1 | a0001 | c0001 | t0010 | g0035 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02148 | hp2 | a0001 | c0002 | t0009 | g0339 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | CDX | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02165 | hp1 | a0001 | c0002 | t0003 | g0346 | EAS | CDX | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | CDX | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02258 | hp1 | a0001 | c0001 | t0049 | g0282 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02280 | hp1 | a0001 | c0002 | t0003 | g0335 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02293 | hp1 | a0001 | c0001 | t0010 | g0033 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02293 | hp2 | a0001 | c0002 | t0009 | g0307 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02572 | hp1 | a0001 | c0001 | t0011 | g0281 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0105 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02615 | hp1 | a0001 | c0002 | t0003 | g0324 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02622 | hp1 | a0001 | c0002 | t0003 | g0329 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02647 | hp1 | a0001 | c0001 | t0040 | g0009 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02647 | hp2 | a0001 | c0001 | t0011 | g0280 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02683 | hp2 | a0001 | c0002 | t0003 | g0311 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02717 | hp1 | a0001 | c0001 | t0034 | g0107 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02723 | hp1 | a0001 | c0001 | t0031 | g0121 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0023 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0272 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02738 | hp2 | a0001 | c0001 | t0017 | g0256 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02809 | hp1 | a0001 | c0001 | t0027 | g0173 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02896 | hp2 | a0001 | c0002 | t0028 | g0287 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02897 | hp1 | a0001 | c0002 | t0028 | g0288 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0190 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02965 | hp1 | a0001 | c0002 | t0039 | g0352 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03098 | hp1 | a0001 | c0002 | t0012 | g0291 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03098 | hp2 | a0001 | c0001 | t0027 | g0188 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03139 | hp2 | a0001 | c0002 | t0003 | g0336 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03195 | hp1 | a0001 | c0001 | t0045 | g0283 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03209 | hp2 | a0001 | c0001 | t0020 | g0172 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03225 | hp1 | a0001 | c0001 | t0043 | g0193 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03453 | hp1 | a0001 | c0001 | t0035 | g0052 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0106 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0050 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03490 | hp2 | a0001 | c0001 | t0008 | g0169 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0051 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03492 | hp2 | a0001 | c0001 | t0008 | g0162 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0198 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03579 | hp2 | a0001 | c0001 | t0011 | g0279 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03654 | hp1 | a0001 | c0001 | t0019 | g0286 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0180 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03688 | hp1 | a0001 | c0001 | t0008 | g0168 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0181 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03831 | hp1 | a0001 | c0001 | t0006 | g0192 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03831 | hp2 | a0001 | c0002 | t0018 | g0298 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0047 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03834 | hp2 | a0001 | c0001 | t0015 | g0163 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03927 | hp1 | a0001 | c0001 | t0050 | g0258 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0175 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0275 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG04199 | hp1 | a0001 | c0001 | t0008 | g0166 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG04204 | hp1 | a0001 | c0002 | t0003 | g0349 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | YRI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18522 | hp2 | a0001 | c0001 | t0023 | g0054 | AFR | YRI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18906 | hp1 | a0001 | c0002 | t0012 | g0353 | AFR | YRI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | YRI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18939 | hp2 | a0001 | c0002 | t0016 | g0351 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18940 | hp1 | a0002 | c0004 | t0005 | g0178 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18942 | hp1 | a0001 | c0002 | t0003 | g0325 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18944 | hp1 | a0001 | c0002 | t0029 | g0305 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18944 | hp2 | a0001 | c0001 | t0024 | g0078 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18945 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18946 | hp2 | a0001 | c0002 | t0017 | g0295 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18950 | hp1 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18950 | hp2 | a0001 | c0001 | t0010 | g0038 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0273 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18952 | hp2 | a0001 | c0002 | t0016 | g0293 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18954 | hp1 | a0001 | c0002 | t0003 | g0345 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18956 | hp2 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18960 | hp1 | a0001 | c0002 | t0003 | g0317 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18961 | hp1 | a0001 | c0002 | t0003 | g0334 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18962 | hp1 | a0001 | c0001 | t0024 | g0029 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18962 | hp2 | a0001 | c0002 | t0018 | g0306 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18963 | hp1 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18963 | hp2 | a0001 | c0001 | t0021 | g0153 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18965 | hp1 | a0001 | c0002 | t0003 | g0340 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18969 | hp2 | a0001 | c0002 | t0029 | g0303 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18970 | hp2 | a0001 | c0002 | t0003 | g0331 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18979 | hp1 | a0001 | c0002 | t0003 | g0347 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18979 | hp2 | a0001 | c0001 | t0048 | g0265 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18982 | hp2 | a0001 | c0002 | t0003 | g0337 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18988 | hp2 | a0001 | c0002 | t0003 | g0338 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18991 | hp2 | a0001 | c0002 | t0003 | g0322 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18994 | hp1 | a0001 | c0002 | t0016 | g0294 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18995 | hp1 | a0001 | c0001 | t0038 | g0077 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18995 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18998 | hp1 | a0001 | c0001 | t0036 | g0143 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18999 | hp1 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA18999 | hp2 | a0001 | c0002 | t0003 | g0304 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19009 | hp1 | a0001 | c0002 | t0003 | g0323 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19009 | hp2 | a0001 | c0002 | t0003 | g0310 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19011 | hp2 | a0001 | c0002 | t0003 | g0344 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19030 | hp1 | a0001 | c0001 | t0011 | g0278 | AFR | LWK | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19030 | hp2 | a0001 | c0001 | t0042 | g0122 | AFR | LWK | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19043 | hp1 | a0001 | c0001 | t0022 | g0053 | AFR | LWK | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | LWK | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19055 | hp1 | a0001 | c0002 | t0003 | g0319 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19057 | hp1 | a0001 | c0002 | t0003 | g0350 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19058 | hp2 | a0001 | c0002 | t0018 | g0330 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19060 | hp1 | a0001 | c0003 | t0002 | g0221 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19063 | hp1 | a0001 | c0002 | t0003 | g0302 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19063 | hp2 | a0001 | c0001 | t0010 | g0034 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19064 | hp2 | a0001 | c0002 | t0003 | g0348 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19067 | hp2 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19070 | hp1 | a0001 | c0003 | t0002 | g0229 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19074 | hp1 | a0001 | c0002 | t0003 | g0321 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19079 | hp1 | a0001 | c0001 | t0021 | g0154 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19080 | hp1 | a0001 | c0002 | t0003 | g0313 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19081 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19082 | hp1 | a0001 | c0001 | t0041 | g0059 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19085 | hp1 | a0001 | c0002 | t0003 | g0316 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19088 | hp2 | a0001 | c0002 | t0003 | g0300 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19090 | hp1 | a0001 | c0002 | t0003 | g0341 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19091 | hp1 | a0001 | c0002 | t0017 | g0292 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19240 | hp1 | a0001 | c0002 | t0012 | g0354 | AFR | YRI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | YRI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA20129 | hp1 | a0001 | c0001 | t0032 | g0290 | AFR | ASW | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0104 | AFR | ASW | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA20752 | hp1 | a0001 | c0001 | t0008 | g0171 | EUR | TSI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA20805 | hp1 | a0001 | c0001 | t0019 | g0285 | EUR | TSI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | TSI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0197 | SAS | GIH | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA20905 | hp2 | a0001 | c0002 | t0003 | g0297 | SAS | GIH | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01123 | hp1 | a0001 | c0001 | t0008 | g0167 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02109 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0201 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02486 | hp1 | a0001 | c0001 | t0026 | g0257 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0204 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02559 | hp1 | a0001 | c0001 | t0047 | g0232 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03471 | hp1 | a0001 | c0001 | t0023 | g0117 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG03471 | hp2 | a0001 | c0001 | t0020 | g0183 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | USA | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
HG06807 | hp2 | a0001 | c0001 | t0022 | g0025 | AFR | USA | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | USA | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | USA | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | LWK | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0020 | REF | REF | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0001 | REF | REF | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:43028761 | C | A | 1 | a0002 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.986C>A | p.Thr329Asn | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/11 | 1145/5300 | 986/1311 | 329/436 | chr21 | 43028761 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:43010215 | T | C | 3 | a0001c0001 a0001c0003 a0002c0004 |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
synonymous_variant | LOW | c.342T>C | p.Thr114Thr | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/11 | 501/5300 | 342/1311 | 114/436 | chr21 | 43010215 | |||
chr21:43016961 | G | A | 1 | a0001c0003 | 2 | NA19060.hp1 NA19070.hp1 |
synonymous_variant | LOW | c.576G>A | p.Pro192Pro | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/11 | 735/5300 | 576/1311 | 192/436 | chr21 | 43016961 | |||
chr21:43016985 | C | T | 1 | a0001c0006 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.600C>T | p.Asn200Asn | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/11 | 759/5300 | 600/1311 | 200/436 | chr21 | 43016985 | |||
chr21:43029972 | G | A | 1 | a0001c0005 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.1182G>A | p.Ala394Ala | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1341/5300 | 1182/1311 | 394/436 | chr21 | 43029972 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:43004334 | C | T | 1 | a0001c0001t0030 | 2 | HG01168.hp2 HG01258.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-48C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/11 | chr21 | 43004334 | |||||||
chr21:43004380 | C | A | 1 | a0001c0001t0031 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-2C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/11 | 2 | chr21 | 43004380 | ||||||
chr21:43030260 | A | AGT | 1 | a0001c0002t0018 | 3 | HG03831.hp2 NA18962.hp2 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*191_*192dupTG | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 193 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | |||||
chr21:43030260 | AGT | A | 2 | a0001c0001t0017 a0001c0002t0017 |
3 | HG02738.hp2 NA18946.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*191_*192delTG | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 191 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | |||||
chr21:43030260 | AGTGTGTG others(1): Show |
A | 7 | a0001c0001t0024 a0001c0001t0027 a0001c0001t0031 others(4): Show |
9 | HG02258.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*185_*192delTGTGTG others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 185 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | |||||
chr21:43030260 | AGTGTGTG others(3): Show |
A | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(25): Show |
222 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*183_*192delTGTGTG others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 183 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | |||||
chr21:43030260 | AGTGTGTG others(5): Show |
A | 3 | a0001c0001t0015 a0001c0001t0035 a0001c0001t0036 |
5 | HG01981.hp2 HG02004.hp2 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*181_*192delTGTGTG others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 181 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | |||||
chr21:43030260 | AGTGTGTG others(7): Show |
A | 2 | a0001c0001t0004 a0001c0001t0021 |
22 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*179_*192delTGTGTG others(8): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 179 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | |||||
chr21:43030260 | AGTGTGTG others(9): Show |
A | 5 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0020 others(2): Show |
34 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*177_*192delTGTGTG others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 177 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | |||||
chr21:43030260 | AGTGTGTG others(11): Show |
A | 2 | a0001c0001t0019 a0001c0001t0032 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*175_*192delTGTGTG others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 175 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | |||||
chr21:43030290 | T | C | 2 | a0001c0001t0034 a0001c0001t0037 |
2 | HG01081.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*189T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 189 | chr21 | 43030290 | ||||||
chr21:43030292 | T | C | 21 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(18): Show |
132 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*191T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 191 | chr21 | 43030292 | ||||||
chr21:43030302 | C | T | 1 | a0001c0001t0021 | 2 | NA18963.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*201C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 201 | chr21 | 43030302 | ||||||
chr21:43030446 | T | G | 1 | a0001c0002t0029 | 2 | NA18944.hp1 NA18969.hp2 |
3_prime_UTR_variant | MODIFIER | c.*345T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 345 | chr21 | 43030446 | ||||||
chr21:43030828 | T | C | 7 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(4): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*727T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 727 | chr21 | 43030828 | ||||||
chr21:43030870 | C | T | 1 | a0001c0001t0041 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*769C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 769 | chr21 | 43030870 | ||||||
chr21:43030890 | A | G | 1 | a0001c0001t0048 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*789A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 789 | chr21 | 43030890 | ||||||
chr21:43030947 | G | A | 6 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0015 others(3): Show |
24 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*846G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 846 | chr21 | 43030947 | ||||||
chr21:43031060 | A | G | 1 | a0001c0001t0045 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*959A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 959 | chr21 | 43031060 | ||||||
chr21:43031128 | G | A | 1 | a0001c0001t0025 | 2 | HG00639.hp2 HG00642.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1027G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1027 | chr21 | 43031128 | ||||||
chr21:43031276 | A | T | 2 | a0001c0001t0027 a0001c0001t0043 |
3 | HG02809.hp1 HG03098.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1175A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1175 | chr21 | 43031276 | ||||||
chr21:43031301 | C | T | 8 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(5): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1200C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1200 | chr21 | 43031301 | ||||||
chr21:43031306 | C | T | 1 | a0001c0001t0047 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1205C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1205 | chr21 | 43031306 | ||||||
chr21:43031318 | C | A | 2 | a0001c0001t0022 a0001c0001t0035 |
3 | HG03453.hp1 HG06807.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1217C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1217 | chr21 | 43031318 | ||||||
chr21:43031395 | T | A | 1 | a0001c0001t0043 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1294T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1294 | chr21 | 43031395 | ||||||
chr21:43031437 | C | T | 1 | a0001c0002t0028 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1336C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1336 | chr21 | 43031437 | ||||||
chr21:43031492 | G | C | 1 | a0001c0001t0038 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1391G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1391 | chr21 | 43031492 | ||||||
chr21:43031538 | T | C | 1 | a0001c0002t0028 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1437T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1437 | chr21 | 43031538 | ||||||
chr21:43031642 | C | T | 1 | a0001c0001t0040 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1541C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1541 | chr21 | 43031642 | ||||||
chr21:43031766 | G | A | 2 | a0001c0001t0004 a0001c0001t0021 |
22 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1665G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1665 | chr21 | 43031766 | ||||||
chr21:43031802 | G | A | 7 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(4): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1701G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1701 | chr21 | 43031802 | ||||||
chr21:43031825 | T | TA | 7 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(4): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1725dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1726 | INFO_REALIGN_3_PRIME | chr21 | 43031825 | |||||
chr21:43031887 | G | A | 8 | a0001c0001t0002 a0001c0001t0025 a0001c0001t0037 others(5): Show |
72 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1786G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1786 | chr21 | 43031887 | ||||||
chr21:43032080 | G | A | 1 | a0001c0001t0014 | 3 | HG00597.hp1 HG00673.hp1 HG02015.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1979G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1979 | chr21 | 43032080 | ||||||
chr21:43032109 | C | T | 3 | a0001c0001t0012 a0001c0002t0012 a0001c0002t0039 |
5 | HG01109.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2008C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2008 | chr21 | 43032109 | ||||||
chr21:43032152 | G | A | 1 | a0001c0001t0044 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2051G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2051 | chr21 | 43032152 | ||||||
chr21:43032314 | T | TTCCCTCA others(18): Show |
7 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(4): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2214_*2238dupTCCC others(21): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2239 | INFO_REALIGN_3_PRIME | chr21 | 43032314 | |||||
chr21:43032331 | G | A | 1 | a0001c0001t0032 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2230G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2230 | chr21 | 43032331 | ||||||
chr21:43032339 | G | A | 1 | a0001c0001t0046 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2238G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2238 | chr21 | 43032339 | ||||||
chr21:43032345 | T | C | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(35): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*2244T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2244 | chr21 | 43032345 | ||||||
chr21:43032365 | G | T | 1 | a0001c0002t0052 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2264G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2264 | chr21 | 43032365 | ||||||
chr21:43032540 | C | T | 1 | a0001c0001t0043 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2439C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2439 | chr21 | 43032540 | ||||||
chr21:43032653 | C | T | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(7): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2552C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2552 | chr21 | 43032653 | ||||||
chr21:43032655 | G | C | 2 | a0001c0001t0031 a0001c0001t0042 |
2 | HG02723.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2554G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2554 | chr21 | 43032655 | ||||||
chr21:43032703 | A | G | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(7): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2602A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2602 | chr21 | 43032703 | ||||||
chr21:43032728 | C | A | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(7): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2627C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2627 | chr21 | 43032728 | ||||||
chr21:43032758 | C | G | 7 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0024 others(4): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2657C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2657 | chr21 | 43032758 | ||||||
chr21:43032836 | C | T | 1 | a0001c0001t0044 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2735C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2735 | chr21 | 43032836 | ||||||
chr21:43032838 | G | C | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(7): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2737G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2737 | chr21 | 43032838 | ||||||
chr21:43032912 | G | A | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(21): Show |
194 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*2811G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2811 | chr21 | 43032912 | ||||||
chr21:43032946 | C | G | 3 | a0001c0001t0011 a0001c0001t0045 a0001c0001t0049 |
6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2845C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2845 | chr21 | 43032946 | ||||||
chr21:43033167 | C | T | 6 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(3): Show |
54 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3066C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3066 | chr21 | 43033167 | ||||||
chr21:43033168 | A | G | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(7): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3067A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3067 | chr21 | 43033168 | ||||||
chr21:43033262 | G | C | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(7): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3161G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3161 | chr21 | 43033262 | ||||||
chr21:43033429 | TTTCGTTC | T | 3 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0044 |
18 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3330_*3336delTCGT others(3): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3330 | INFO_REALIGN_3_PRIME | chr21 | 43033429 | |||||
chr21:43033645 | T | A | 2 | a0001c0002t0009 a0001c0006t0009 |
7 | HG00639.hp1 HG00738.hp1 HG01928.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3544T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3544 | chr21 | 43033645 | ||||||
chr21:43033694 | C | T | 1 | a0001c0001t0033 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3593C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3593 | chr21 | 43033694 | ||||||
chr21:43033743 | A | G | 1 | a0001c0001t0010 | 6 | HG00741.hp2 HG01192.hp2 HG02148.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3642A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3642 | chr21 | 43033743 | ||||||
chr21:43033803 | G | C | 2 | a0001c0001t0005 a0002c0004t0005 |
17 | HG00099.hp2 HG00423.hp1 HG01109.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3702G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3702 | chr21 | 43033803 | ||||||
chr21:43033908 | A | G | 3 | a0001c0001t0012 a0001c0002t0012 a0001c0002t0039 |
5 | HG01109.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3807A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3807 | chr21 | 43033908 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:42974825 | G | C | 9 | a0001c0001t0007g0002 a0001c0001t0007g0007 a0001c0001t0007g0008 others(6): Show |
10 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57+161G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42974825 | |||||||
chr21:42974856 | G | A | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-57+192G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42974856 | |||||||
chr21:42974868 | G | T | 1 | a0001c0001t0002g0284 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-57+204G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42974868 | |||||||
chr21:42974890 | C | G | 1 | a0001c0001t0002g0284 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-57+226C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42974890 | |||||||
chr21:42974897 | C | G | 17 | a0001c0001t0008g0015 a0001c0001t0008g0156 a0001c0001t0008g0157 others(14): Show |
17 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-57+233C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42974897 | |||||||
chr21:42974991 | T | C | 287 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(284): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.-57+327T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42974991 | |||||||
chr21:42975029 | G | T | 6 | a0001c0001t0011g0278 a0001c0001t0011g0279 a0001c0001t0011g0280 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+365G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975029 | |||||||
chr21:42975047 | C | CGGGGCG | 280 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(277): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.-57+390_-57+395dup others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42975047 | ||||||
chr21:42975048 | G | GGGGCGGG others(11): Show |
1 | a0001c0001t0032g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+395_-57+396ins others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42975048 | ||||||
chr21:42975052 | C | CGGGGGCG | 6 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0004g0272 others(3): Show |
6 | HG01515.hp1 HG02056.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+389_-57+395dup others(7): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42975052 | ||||||
chr21:42975163 | C | G | 14 | a0001c0001t0002g0005 a0001c0001t0002g0261 a0001c0001t0002g0262 others(11): Show |
15 | NA18954.hp2 NA18966.hp2 NA18979.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57+499C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975163 | |||||||
chr21:42975174 | C | T | 1 | a0001c0001t0044g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-57+510C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975174 | |||||||
chr21:42975182 | C | A | 2 | a0001c0001t0025g0017 a0001c0001t0025g0018 |
2 | HG00639.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.-57+518C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975182 | |||||||
chr21:42975249 | G | A | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+585G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975249 | |||||||
chr21:42975304 | G | A | 147 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(144): Show |
149 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.-57+640G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975304 | |||||||
chr21:42975372 | G | C | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+708G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975372 | |||||||
chr21:42975379 | G | A | 17 | a0001c0001t0008g0015 a0001c0001t0008g0156 a0001c0001t0008g0157 others(14): Show |
17 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-57+715G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975379 | |||||||
chr21:42975413 | G | A | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+749G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975413 | |||||||
chr21:42975526 | C | G | 1 | a0001c0001t0002g0016 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-57+862C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975526 | |||||||
chr21:42975534 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-57+870T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975534 | |||||||
chr21:42975620 | G | C | 288 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(285): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.-57+956G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975620 | |||||||
chr21:42975621 | G | C | 1 | a0001c0001t0002g0016 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-57+957G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975621 | |||||||
chr21:42975639 | G | A | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+975G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975639 | |||||||
chr21:42975686 | C | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(241): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-57+1022C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975686 | |||||||
chr21:42975718 | G | T | 3 | a0001c0001t0001g0155 a0001c0001t0021g0153 a0001c0001t0021g0154 |
3 | NA18963.hp2 NA19004.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-57+1054G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975718 | |||||||
chr21:42975936 | A | T | 1 | a0001c0002t0016g0351 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-57+1272A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975936 | |||||||
chr21:42976026 | C | A | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-57+1362C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976026 | |||||||
chr21:42976034 | C | A | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-57+1370C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976034 | |||||||
chr21:42976165 | G | A | 291 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(288): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-57+1501G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976165 | |||||||
chr21:42976192 | A | G | 6 | a0001c0001t0011g0278 a0001c0001t0011g0279 a0001c0001t0011g0280 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+1528A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976192 | |||||||
chr21:42976219 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-57+1555T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976219 | |||||||
chr21:42976220 | TAA | T | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+1558_-57+1559d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42976220 | ||||||
chr21:42976265 | GTTAA | G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+1606_-57+1609d others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42976265 | ||||||
chr21:42976337 | A | G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+1673A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976337 | |||||||
chr21:42976352 | G | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-57+1688G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976352 | |||||||
chr21:42976510 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-57+1846A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976510 | |||||||
chr21:42976609 | A | T | 1 | a0001c0002t0003g0350 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-57+1945A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976609 | |||||||
chr21:42976657 | T | A | 2 | a0001c0001t0002g0205 a0001c0001t0002g0206 |
2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-57+1993T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976657 | |||||||
chr21:42976685 | G | C | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+2021G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976685 | |||||||
chr21:42976788 | A | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-57+2124A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976788 | |||||||
chr21:42976812 | A | G | 1 | a0001c0002t0003g0349 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-57+2148A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976812 | |||||||
chr21:42976841 | C | T | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-57+2177C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976841 | |||||||
chr21:42977071 | A | G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+2407A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977071 | |||||||
chr21:42977073 | G | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+2409G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977073 | |||||||
chr21:42977104 | C | T | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+2440C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977104 | |||||||
chr21:42977119 | G | T | 1 | a0001c0001t0008g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+2455G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977119 | |||||||
chr21:42977124 | T | C | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+2460T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977124 | |||||||
chr21:42977228 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-57+2564C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977228 | |||||||
chr21:42977241 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-57+2577A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977241 | |||||||
chr21:42977380 | T | G | 6 | a0001c0001t0011g0278 a0001c0001t0011g0279 a0001c0001t0011g0280 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+2716T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977380 | |||||||
chr21:42977384 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-57+2720C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977384 | |||||||
chr21:42977448 | G | C | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+2784G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977448 | |||||||
chr21:42977465 | C | T | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-57+2801C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977465 | |||||||
chr21:42977493 | G | A | 1 | a0001c0001t0020g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+2829G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977493 | |||||||
chr21:42977537 | CT | C | 70 | a0001c0001t0002g0206 a0001c0001t0002g0259 a0001c0001t0002g0260 others(67): Show |
71 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-57+2900delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42977537 | ||||||
chr21:42977537 | CTT | C | 95 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(92): Show |
96 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-57+2899_-57+2900d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42977537 | ||||||
chr21:42977537 | CTTT | C | 156 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(153): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.-57+2898_-57+2900d others(5): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42977537 | ||||||
chr21:42977537 | CTTTT | C | 17 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(14): Show |
17 | HG01168.hp1 HG01257.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57+2897_-57+2900d others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42977537 | ||||||
chr21:42977592 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-57+2928A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977592 | |||||||
chr21:42977616 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-57+2952C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977616 | |||||||
chr21:42977617 | G | A | 1 | a0001c0001t0005g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-57+2953G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977617 | |||||||
chr21:42977671 | C | T | 1 | a0001c0002t0003g0349 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-57+3007C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977671 | |||||||
chr21:42977731 | T | C | 109 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(106): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-57+3067T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977731 | |||||||
chr21:42977737 | C | T | 1 | a0001c0001t0044g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-57+3073C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977737 | |||||||
chr21:42977776 | C | T | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+3112C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977776 | |||||||
chr21:42978000 | C | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+3336C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978000 | |||||||
chr21:42978248 | G | A | 109 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(106): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-57+3584G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978248 | |||||||
chr21:42978374 | G | A | 6 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(3): Show |
6 | HG00741.hp2 HG01192.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+3710G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978374 | |||||||
chr21:42978404 | G | A | 291 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(288): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-57+3740G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978404 | |||||||
chr21:42978428 | G | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+3764G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978428 | |||||||
chr21:42978441 | G | A | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-57+3777G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978441 | |||||||
chr21:42978463 | A | AACTTGTT others(1): Show |
109 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(106): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-57+3800_-57+3807d others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42978463 | ||||||
chr21:42978472 | T | A | 1 | a0001c0001t0002g0276 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-57+3808T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978472 | |||||||
chr21:42978473 | T | C | 1 | a0001c0001t0002g0276 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-57+3809T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978473 | |||||||
chr21:42978476 | C | G | 1 | a0001c0001t0002g0276 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-57+3812C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978476 | |||||||
chr21:42978486 | C | CT | 9 | a0001c0001t0001g0139 a0001c0001t0002g0260 a0001c0001t0004g0137 others(6): Show |
9 | HG00544.hp1 HG01975.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+3839dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42978486 | ||||||
chr21:42978486 | CT | C | 64 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0218 others(61): Show |
64 | HG00597.hp2 HG00621.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.-57+3839delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42978486 | ||||||
chr21:42978491 | T | C | 9 | a0001c0001t0002g0276 a0001c0001t0005g0176 a0001c0001t0005g0177 others(6): Show |
9 | HG02055.hp2 HG02056.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+3827T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978491 | |||||||
chr21:42978492 | T | C | 1 | a0001c0002t0003g0297 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-57+3828T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978492 | |||||||
chr21:42978496 | T | C | 1 | a0001c0001t0002g0276 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-57+3832T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978496 | |||||||
chr21:42978514 | C | T | 18 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0125 others(15): Show |
18 | HG00438.hp2 HG01358.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.-57+3850C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978514 | |||||||
chr21:42978801 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-57+4137A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978801 | |||||||
chr21:42978825 | A | G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4161A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978825 | |||||||
chr21:42978882 | A | G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4218A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978882 | |||||||
chr21:42978922 | C | T | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4258C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978922 | |||||||
chr21:42978990 | C | T | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4326C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978990 | |||||||
chr21:42979178 | G | A | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+4514G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979178 | |||||||
chr21:42979245 | T | A | 22 | a0001c0001t0001g0155 a0001c0001t0004g0022 a0001c0001t0004g0023 others(19): Show |
22 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.-57+4581T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979245 | |||||||
chr21:42979249 | C | T | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4585C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979249 | |||||||
chr21:42979303 | AACACAG | A | 6 | a0001c0001t0011g0278 a0001c0001t0011g0279 a0001c0001t0011g0280 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+4645_-57+4650d others(8): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42979303 | ||||||
chr21:42979363 | T | C | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4699T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979363 | |||||||
chr21:42979369 | A | C | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4705A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979369 | |||||||
chr21:42979381 | G | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4717G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979381 | |||||||
chr21:42979405 | G | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4741G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979405 | |||||||
chr21:42979590 | G | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4926G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979590 | |||||||
chr21:42979611 | G | A | 3 | a0001c0001t0022g0025 a0001c0001t0022g0053 a0001c0001t0035g0052 |
3 | HG03453.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57+4947G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979611 | |||||||
chr21:42979678 | C | A | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+5014C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979678 | |||||||
chr21:42979720 | T | C | 291 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(288): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-57+5056T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979720 | |||||||
chr21:42979843 | G | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+5179G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979843 | |||||||
chr21:42979869 | G | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+5205G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979869 | |||||||
chr21:42979927 | T | C | 1 | a0001c0001t0005g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-57+5263T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979927 | |||||||
chr21:42979935 | G | A | 35 | a0001c0001t0005g0175 a0001c0001t0005g0176 a0001c0001t0005g0177 others(32): Show |
36 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.-57+5271G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979935 | |||||||
chr21:42979978 | C | T | 291 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(288): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-57+5314C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979978 | |||||||
chr21:42979988 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-57+5324C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979988 | |||||||
chr21:42980005 | A | G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+5341A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980005 | |||||||
chr21:42980072 | A | G | 3 | a0001c0001t0006g0201 a0001c0001t0006g0202 a0001c0001t0006g0204 |
3 | HG01261.hp1 HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-57+5408A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980072 | |||||||
chr21:42980139 | G | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+5475G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980139 | |||||||
chr21:42980166 | A | G | 1 | a0001c0001t0026g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+5502A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980166 | |||||||
chr21:42980179 | C | T | 1 | a0001c0002t0003g0334 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-57+5515C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980179 | |||||||
chr21:42980201 | C | T | 2 | a0001c0001t0031g0121 a0001c0001t0042g0122 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-57+5537C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980201 | |||||||
chr21:42980356 | A | C | 10 | a0001c0001t0002g0207 a0001c0001t0002g0216 a0001c0001t0002g0217 others(7): Show |
10 | HG01257.hp2 HG01258.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57+5692A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980356 | |||||||
chr21:42980382 | G | GA | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-57+5727dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42980382 | ||||||
chr21:42980427 | C | T | 2 | a0001c0001t0031g0121 a0001c0001t0042g0122 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-57+5763C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980427 | |||||||
chr21:42980431 | T | G | 17 | a0001c0001t0008g0015 a0001c0001t0008g0156 a0001c0001t0008g0157 others(14): Show |
17 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-57+5767T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980431 | |||||||
chr21:42980479 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-57+5815A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980479 | |||||||
chr21:42980551 | A | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-57+5887A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980551 | |||||||
chr21:42980718 | C | G | 2 | a0001c0001t0004g0050 a0001c0001t0004g0051 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+6054C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980718 | |||||||
chr21:42980719 | G | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6055G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980719 | |||||||
chr21:42980764 | AT | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6106delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42980764 | ||||||
chr21:42980777 | C | G | 36 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0005g0176 others(33): Show |
37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.-57+6113C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980777 | |||||||
chr21:42980793 | A | T | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6129A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980793 | |||||||
chr21:42980857 | G | A | 9 | a0001c0001t0002g0005 a0001c0001t0002g0261 a0001c0001t0002g0262 others(6): Show |
10 | NA18954.hp2 NA18966.hp2 NA18979.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57+6193G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980857 | |||||||
chr21:42981014 | C | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(168): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-57+6350C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981014 | |||||||
chr21:42981015 | G | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6351G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981015 | |||||||
chr21:42981111 | C | T | 3 | a0001c0001t0022g0025 a0001c0001t0022g0053 a0001c0001t0035g0052 |
3 | HG03453.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57+6447C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981111 | |||||||
chr21:42981176 | G | A | 1 | a0001c0001t0023g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-57+6512G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981176 | |||||||
chr21:42981207 | C | T | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-57+6543C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981207 | |||||||
chr21:42981329 | G | A | 1 | a0001c0001t0026g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+6665G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981329 | |||||||
chr21:42981369 | A | G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6705A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981369 | |||||||
chr21:42981382 | G | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6718G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981382 | |||||||
chr21:42981386 | T | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-57+6722T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981386 | |||||||
chr21:42981459 | A | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-57+6795A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981459 | |||||||
chr21:42981553 | TTTAATTT others(3): Show |
T | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6892_-57+6901d others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42981553 | ||||||
chr21:42981556 | A | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-57+6892A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981556 | |||||||
chr21:42981584 | G | A | 3 | a0001c0001t0006g0201 a0001c0001t0006g0202 a0001c0001t0006g0204 |
3 | HG01261.hp1 HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-57+6920G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981584 | |||||||
chr21:42981586 | G | T | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-57+6922G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981586 | |||||||
chr21:42981700 | C | T | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7036C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981700 | |||||||
chr21:42981701 | A | G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7037A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981701 | |||||||
chr21:42981749 | T | C | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7085T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981749 | |||||||
chr21:42981856 | G | A | 1 | a0001c0001t0005g0273 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-57+7192G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981856 | |||||||
chr21:42981937 | T | C | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7273T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981937 | |||||||
chr21:42981980 | C | T | 15 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0125 others(12): Show |
15 | HG00438.hp2 HG00621.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57+7316C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981980 | |||||||
chr21:42982017 | A | G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7353A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982017 | |||||||
chr21:42982074 | C | T | 2 | a0001c0001t0027g0173 a0001c0001t0027g0188 |
2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-57+7410C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982074 | |||||||
chr21:42982137 | C | T | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7473C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982137 | |||||||
chr21:42982352 | T | G | 1 | a0001c0002t0003g0297 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-57+7688T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982352 | |||||||
chr21:42982367 | C | T | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+7703C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982367 | |||||||
chr21:42982384 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-57+7720G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982384 | |||||||
chr21:42982435 | A | C | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7771A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982435 | |||||||
chr21:42982468 | G | A | 2 | a0001c0002t0028g0287 a0001c0002t0028g0288 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-57+7804G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982468 | |||||||
chr21:42982483 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-57+7819A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982483 | |||||||
chr21:42982524 | A | G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7860A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982524 | |||||||
chr21:42982588 | G | A | 5 | a0001c0001t0014g0093 a0001c0001t0019g0285 a0001c0001t0019g0286 others(2): Show |
5 | HG00597.hp1 HG02055.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+7924G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982588 | |||||||
chr21:42982612 | T | C | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7948T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982612 | |||||||
chr21:42982686 | G | A | 3 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0002c0004t0005g0178 |
3 | NA18940.hp1 NA18999.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-57+8022G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982686 | |||||||
chr21:42982695 | C | T | 1 | a0001c0001t0030g0119 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-57+8031C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982695 | |||||||
chr21:42982731 | C | CA | 37 | a0001c0001t0001g0040 a0001c0001t0001g0118 a0001c0001t0002g0266 others(34): Show |
38 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.-57+8083dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42982731 | ||||||
chr21:42982731 | C | CAA | 235 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(232): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.-57+8082_-57+8083d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42982731 | ||||||
chr21:42982731 | C | CAAA | 7 | a0001c0001t0001g0055 a0001c0001t0002g0222 a0001c0001t0004g0041 others(4): Show |
7 | HG00609.hp2 HG00741.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+8081_-57+8083d others(5): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42982731 | ||||||
chr21:42982731 | CAAAAAAA | C | 7 | a0001c0001t0006g0201 a0001c0001t0006g0202 a0001c0001t0006g0204 others(4): Show |
7 | HG01261.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+8077_-57+8083d others(9): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42982731 | ||||||
chr21:42982805 | G | C | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+8141G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982805 | |||||||
chr21:42982820 | T | C | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+8156T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982820 | |||||||
chr21:42982848 | T | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-57+8184T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982848 | |||||||
chr21:42982914 | A | G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+8250A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982914 | |||||||
chr21:42982949 | A | G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+8285A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982949 | |||||||
chr21:42982965 | A | T | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+8301A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982965 | |||||||
chr21:42983018 | C | T | 1 | a0001c0001t0050g0258 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-57+8354C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983018 | |||||||
chr21:42983050 | G | T | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+8386G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983050 | |||||||
chr21:42983059 | T | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-57+8395T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983059 | |||||||
chr21:42983073 | G | A | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-57+8409G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983073 | |||||||
chr21:42983099 | T | G | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-57+8435T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983099 | |||||||
chr21:42983109 | CT | C | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-57+8453delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42983109 | ||||||
chr21:42983253 | C | G | 34 | a0001c0001t0005g0175 a0001c0001t0005g0176 a0001c0001t0005g0177 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+8589C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983253 | |||||||
chr21:42983309 | GA | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-57+8647delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42983309 | ||||||
chr21:42983486 | GCTGAATA | G | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+8825_-57+8831d others(9): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42983486 | ||||||
chr21:42983528 | C | T | 1 | a0001c0001t0020g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+8864C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983528 | |||||||
chr21:42983630 | A | AT | 15 | a0001c0001t0002g0215 a0001c0001t0002g0219 a0001c0001t0002g0220 others(12): Show |
15 | HG01167.hp2 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57+8973dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42983630 | ||||||
chr21:42983849 | A | C | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+9185A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983849 | |||||||
chr21:42983929 | C | T | 1 | a0001c0001t0008g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+9265C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983929 | |||||||
chr21:42983930 | A | G | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-57+9266A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983930 | |||||||
chr21:42983934 | T | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-57+9270T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983934 | |||||||
chr21:42983993 | A | G | 1 | a0001c0001t0002g0264 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-57+9329A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983993 | |||||||
chr21:42984065 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-57+9401C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984065 | |||||||
chr21:42984083 | CGT | C | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG03098.hp1 NA18906.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+9444_-57+9445d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984083 | ||||||
chr21:42984083 | CGTGT | C | 12 | a0001c0001t0001g0125 a0001c0001t0002g0005 a0001c0001t0002g0261 others(9): Show |
13 | HG02055.hp2 NA18950.hp1 NA18954.hp2 others(10): Show |
intron_variant | MODIFIER | c.-57+9442_-57+9445d others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984083 | ||||||
chr21:42984083 | CGTGTGT | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(270): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-57+9440_-57+9445d others(8): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984083 | ||||||
chr21:42984120 | CA | C | 6 | a0001c0001t0011g0278 a0001c0001t0011g0279 a0001c0001t0011g0280 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+9457delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984120 | |||||||
chr21:42984222 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-57+9558T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984222 | |||||||
chr21:42984245 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-57+9581T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984245 | |||||||
chr21:42984284 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-57+9620T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984284 | |||||||
chr21:42984483 | G | A | 1 | a0001c0001t0026g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+9819G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984483 | |||||||
chr21:42984740 | T | C | 2 | a0001c0001t0004g0137 a0001c0001t0041g0059 |
2 | NA19082.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-57+10076T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984740 | |||||||
chr21:42984909 | T | TGA | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-57+10251_-57+1025 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984909 | ||||||
chr21:42984961 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-57+10297C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984961 | |||||||
chr21:42984974 | C | CT | 14 | a0001c0001t0007g0014 a0001c0002t0003g0297 a0001c0002t0003g0329 others(11): Show |
14 | HG00621.hp1 HG00673.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.-57+10337dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984974 | ||||||
chr21:42984974 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0044g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-57+10326_-57+1033 others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984974 | ||||||
chr21:42984974 | CT | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(145): Show |
151 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-57+10337delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984974 | ||||||
chr21:42984974 | CTT | C | 112 | a0001c0001t0001g0026 a0001c0001t0001g0060 a0001c0001t0001g0149 others(109): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.-57+10336_-57+1033 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984974 | ||||||
chr21:42984974 | CTTTTTTT others(5): Show |
C | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+10326_-57+1033 others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984974 | ||||||
chr21:42984974 | CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0001c0001t0005g0179 others(1): Show |
4 | NA18940.hp1 NA18963.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+10322_-57+1033 others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984974 | ||||||
chr21:42985590 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | HG02129.hp2 HG02523.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-57+10926C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42985590 | |||||||
chr21:42985630 | C | T | 1 | a0001c0001t0013g0112 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-57+10966C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42985630 | |||||||
chr21:42985656 | G | A | 2 | a0001c0002t0028g0287 a0001c0002t0028g0288 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-57+10992G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42985656 | |||||||
chr21:42985762 | G | A | 1 | a0001c0001t0044g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-57+11098G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42985762 | |||||||
chr21:42985841 | A | C | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+11177A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42985841 | |||||||
chr21:42985872 | G | A | 1 | a0001c0001t0020g0183 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-57+11208G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42985872 | |||||||
chr21:42986002 | G | GA | 7 | a0001c0001t0007g0008 a0001c0001t0007g0010 a0001c0001t0007g0011 others(4): Show |
7 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+11353dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42986002 | ||||||
chr21:42986002 | G | GAA | 67 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0030 others(64): Show |
68 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-57+11352_-57+1135 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42986002 | ||||||
chr21:42986002 | G | GAAA | 96 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(93): Show |
97 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-57+11351_-57+1135 others(7): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42986002 | ||||||
chr21:42986017 | A | AAT | 30 | a0001c0001t0005g0175 a0001c0001t0005g0176 a0001c0001t0005g0177 others(27): Show |
31 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.-57+11353_-57+1135 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986017 | |||||||
chr21:42986017 | A | ATT | 79 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(76): Show |
80 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-57+11354_-57+1135 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42986017 | ||||||
chr21:42986020 | A | T | 75 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(72): Show |
76 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-57+11356A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986020 | |||||||
chr21:42986021 | A | T | 2 | a0001c0001t0002g0237 a0001c0001t0002g0238 |
2 | NA18951.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.-57+11357A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986021 | |||||||
chr21:42986160 | T | G | 1 | a0001c0001t0026g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+11496T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986160 | |||||||
chr21:42986228 | C | T | 3 | a0001c0001t0002g0005 a0001c0001t0002g0264 a0001c0001t0002g0266 |
4 | NA18954.hp2 NA18983.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+11564C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986228 | |||||||
chr21:42986229 | G | A | 1 | a0001c0001t0010g0033 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-57+11565G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986229 | |||||||
chr21:42986334 | C | G | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+11670C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986334 | |||||||
chr21:42986400 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-57+11736C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986400 | |||||||
chr21:42986442 | A | G | 16 | a0001c0001t0005g0175 a0001c0001t0005g0176 a0001c0001t0005g0177 others(13): Show |
16 | HG00099.hp2 HG00423.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57+11778A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986442 | |||||||
chr21:42986484 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-57+11820G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986484 | |||||||
chr21:42986760 | T | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-57+12096T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986760 | |||||||
chr21:42986774 | G | A | 2 | a0001c0001t0008g0170 a0001c0001t0008g0171 |
2 | HG01516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-57+12110G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986774 | |||||||
chr21:42986821 | ATAAATGC others(8): Show |
A | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+12160_-57+1217 others(19): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42986821 | ||||||
chr21:42986847 | T | C | 3 | a0001c0002t0003g0299 a0001c0002t0003g0300 a0001c0005t0003g0301 |
3 | HG00597.hp2 HG02080.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-57+12183T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986847 | |||||||
chr21:42986958 | C | T | 5 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(2): Show |
5 | HG02055.hp2 HG03654.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+12294C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986958 | |||||||
chr21:42987031 | G | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-57+12367G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987031 | |||||||
chr21:42987195 | A | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-57+12531A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987195 | |||||||
chr21:42987296 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-57+12632C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987296 | |||||||
chr21:42987345 | A | G | 2 | a0001c0002t0003g0328 a0001c0002t0003g0333 |
2 | HG01261.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-57+12681A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987345 | |||||||
chr21:42987382 | CA | C | 26 | a0001c0001t0001g0028 a0001c0001t0001g0074 a0001c0001t0001g0075 others(23): Show |
26 | HG00639.hp1 HG01255.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.-57+12741delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987382 | ||||||
chr21:42987382 | CAA | C | 64 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0055 others(61): Show |
64 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-57+12740_-57+1274 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987382 | ||||||
chr21:42987382 | CAAA | C | 9 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0001g0116 others(6): Show |
9 | HG01069.hp1 HG01928.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+12739_-57+1274 others(7): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987382 | ||||||
chr21:42987382 | CAAAA | C | 9 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0225 others(6): Show |
9 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+12738_-57+1274 others(8): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987382 | ||||||
chr21:42987382 | CAAAAA | C | 20 | a0001c0001t0002g0212 a0001c0001t0005g0175 a0001c0001t0005g0176 others(17): Show |
20 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.-57+12737_-57+1274 others(9): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987382 | ||||||
chr21:42987382 | CAAAAAA | C | 52 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0189 others(49): Show |
53 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.-57+12736_-57+1274 others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987382 | ||||||
chr21:42987394 | A | T | 1 | a0001c0001t0001g0026 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-57+12730A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987394 | |||||||
chr21:42987395 | A | T | 6 | a0001c0001t0011g0278 a0001c0001t0011g0279 a0001c0001t0011g0280 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+12731A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987395 | |||||||
chr21:42987396 | A | T | 1 | a0001c0001t0001g0026 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-57+12732A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987396 | |||||||
chr21:42987396 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0002g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-57+12734_-57+1274 others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987396 | ||||||
chr21:42987398 | A | AATATATA others(3): Show |
2 | a0001c0001t0008g0015 a0001c0001t0049g0282 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-57+12735_-57+1273 others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987398 | ||||||
chr21:42987398 | A | AATATATA others(7): Show |
1 | a0001c0001t0011g0279 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-57+12735_-57+1273 others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987398 | ||||||
chr21:42987398 | A | AATATATA others(9): Show |
1 | a0001c0001t0011g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57+12735_-57+1273 others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987398 | ||||||
chr21:42987398 | A | AATATATA others(11): Show |
2 | a0001c0001t0011g0278 a0001c0001t0045g0283 |
2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-57+12735_-57+1273 others(22): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987398 | ||||||
chr21:42987398 | A | AATATATA others(15): Show |
1 | a0001c0001t0011g0281 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-57+12735_-57+1273 others(26): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987398 | ||||||
chr21:42987398 | A | T | 4 | a0001c0001t0001g0026 a0001c0001t0002g0235 a0001c0001t0002g0236 others(1): Show |
4 | HG02630.hp1 HG02630.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+12734A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987398 | |||||||
chr21:42987400 | A | T | 14 | a0001c0001t0001g0026 a0001c0001t0002g0016 a0001c0001t0002g0235 others(11): Show |
14 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.-57+12736A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987400 | |||||||
chr21:42987402 | A | AATATATA others(11): Show |
2 | a0001c0001t0001g0155 a0001c0001t0004g0101 |
2 | NA19004.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-57+12739_-57+1274 others(22): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987402 | ||||||
chr21:42987402 | A | AATATATA others(13): Show |
2 | a0001c0001t0001g0102 a0001c0001t0004g0137 |
2 | HG01167.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-57+12739_-57+1274 others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987402 | ||||||
chr21:42987402 | A | ATATATAT others(12): Show |
2 | a0001c0001t0004g0048 a0001c0001t0004g0049 |
2 | HG01175.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-57+12738_-57+1273 others(23): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987402 | |||||||
chr21:42987402 | A | T | 20 | a0001c0001t0001g0026 a0001c0001t0001g0068 a0001c0001t0001g0071 others(17): Show |
20 | HG01261.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-57+12738A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987402 | |||||||
chr21:42987402 | AAAATATA others(7): Show |
A | 1 | a0001c0001t0004g0141 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-57+12740_-57+1275 others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987402 | ||||||
chr21:42987404 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0012g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(34): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(47): Show |
1 | a0001c0001t0019g0286 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(58): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(46): Show |
1 | a0001c0001t0019g0285 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(57): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(9): Show |
1 | a0001c0002t0012g0353 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0007g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(32): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(42): Show |
1 | a0001c0001t0032g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(53): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(9): Show |
3 | a0001c0002t0012g0291 a0001c0002t0012g0354 a0001c0002t0039g0352 |
3 | HG02965.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0007g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(28): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(19): Show |
1 | a0001c0001t0015g0163 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(30): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0008g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(27): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0007g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(7): Show |
2 | a0001c0001t0007g0109 a0001c0001t0008g0160 |
2 | HG01074.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(19): Show |
2 | a0001c0001t0001g0100 a0001c0001t0007g0007 |
2 | NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(30): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(21): Show |
3 | a0001c0001t0007g0002 a0001c0001t0008g0161 a0001c0001t0015g0165 |
3 | HG01071.hp1 HG01981.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(32): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(25): Show |
2 | a0001c0001t0001g0063 a0001c0001t0007g0002 |
2 | HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(36): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAA others(27): Show |
1 | a0001c0001t0001g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(38): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAT others(6): Show |
2 | a0001c0001t0007g0104 a0001c0001t0007g0106 |
2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(17): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAT others(20): Show |
2 | a0001c0001t0007g0011 a0001c0001t0008g0166 |
2 | HG04199.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(31): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAAAT others(24): Show |
1 | a0001c0001t0040g0009 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(35): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAATA others(5): Show |
1 | a0001c0001t0007g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAATA others(7): Show |
1 | a0001c0001t0034g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAATA others(13): Show |
1 | a0001c0001t0008g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAATA others(15): Show |
1 | a0001c0001t0001g0030 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(26): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAATA others(21): Show |
2 | a0001c0001t0001g0027 a0001c0001t0007g0010 |
2 | HG02559.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(32): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAATA others(23): Show |
1 | a0001c0001t0015g0164 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(34): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAATA others(25): Show |
1 | a0001c0001t0007g0012 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(36): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAAATA others(27): Show |
1 | a0001c0001t0008g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(38): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAAATAT others(14): Show |
1 | a0001c0001t0004g0045 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(25): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAATATA others(9): Show |
1 | a0001c0001t0008g0167 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAATATA others(17): Show |
1 | a0001c0001t0004g0042 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(28): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAATATA others(19): Show |
2 | a0001c0001t0008g0170 a0001c0001t0008g0171 |
2 | HG01516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(30): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAAATATA others(23): Show |
2 | a0001c0001t0007g0013 a0001c0001t0008g0158 |
2 | HG00323.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(34): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAATATAT others(18): Show |
1 | a0001c0001t0004g0047 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(29): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AAATATAT others(20): Show |
1 | a0001c0001t0008g0162 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(31): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AATATATA others(7): Show |
1 | a0001c0001t0004g0044 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-57+12751_-57+1276 others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AATATATA others(11): Show |
2 | a0001c0001t0004g0022 a0001c0001t0004g0142 |
2 | HG01168.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-57+12747_-57+1276 others(22): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AATATATA others(13): Show |
1 | a0001c0001t0021g0153 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-57+12745_-57+1276 others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AATATATA others(15): Show |
2 | a0001c0001t0004g0023 a0001c0001t0031g0121 |
2 | HG02723.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-57+12743_-57+1276 others(26): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AATATATA others(17): Show |
2 | a0001c0001t0004g0046 a0001c0001t0004g0138 |
2 | HG00544.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-57+12741_-57+1276 others(28): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AATATATA others(19): Show |
2 | a0001c0001t0004g0041 a0001c0001t0008g0169 |
2 | HG02080.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-57+12764_-57+1276 others(30): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | ||||||
chr21:42987404 | A | AT | 4 | a0001c0001t0021g0154 a0001c0002t0003g0334 a0001c0005t0003g0301 others(1): Show |
4 | HG01928.hp1 HG02080.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+12740_-57+1274 others(5): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987404 | |||||||
chr21:42987404 | A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0043 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-57+12740_-57+1274 others(19): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987404 | |||||||
chr21:42987404 | A | ATATATAT others(10): Show |
1 | a0001c0001t0004g0050 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-57+12740_-57+1274 others(21): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987404 | |||||||
chr21:42987404 | A | ATATATAT others(16): Show |
1 | a0001c0001t0004g0024 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-57+12740_-57+1274 others(27): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987404 | |||||||
chr21:42987404 | A | ATATATAT others(18): Show |
1 | a0001c0001t0004g0272 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-57+12740_-57+1274 others(29): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987404 | |||||||
chr21:42987404 | A | T | 88 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0031 others(85): Show |
88 | HG00099.hp1 HG00609.hp1 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.-57+12740A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987404 | |||||||
chr21:42987406 | T | A | 8 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0002t0003g0343 others(5): Show |
8 | HG00544.hp2 HG00621.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+12742T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987406 | |||||||
chr21:42987407 | A | G | 2 | a0001c0001t0019g0286 a0001c0001t0032g0290 |
2 | HG03654.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-57+12743A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987407 | |||||||
chr21:42987408 | T | A | 5 | a0001c0001t0001g0021 a0001c0001t0023g0054 a0001c0001t0044g0289 others(2): Show |
5 | HG01496.hp1 HG02055.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+12744T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987408 | |||||||
chr21:42987409 | A | C | 1 | a0001c0001t0004g0049 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-57+12745A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987409 | |||||||
chr21:42987409 | A | G | 1 | a0001c0001t0019g0285 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-57+12745A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987409 | |||||||
chr21:42987410 | T | A | 3 | a0001c0001t0023g0054 a0001c0002t0028g0287 a0001c0002t0028g0288 |
3 | HG02896.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-57+12746T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987410 | |||||||
chr21:42987449 | T | G | 1 | a0001c0001t0020g0183 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-57+12785T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987449 | |||||||
chr21:42987450 | C | A | 1 | a0001c0001t0020g0183 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-57+12786C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987450 | |||||||
chr21:42987467 | G | A | 2 | a0001c0002t0028g0287 a0001c0002t0028g0288 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-57+12803G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987467 | |||||||
chr21:42987496 | A | T | 1 | a0001c0001t0026g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+12832A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987496 | |||||||
chr21:42987553 | A | T | 1 | a0001c0001t0032g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+12889A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987553 | |||||||
chr21:42987557 | C | A | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+12893C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987557 | |||||||
chr21:42987618 | CT | C | 206 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(203): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.-57+12971delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987618 | ||||||
chr21:42987680 | G | A | 1 | a0001c0001t0026g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+13016G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987680 | |||||||
chr21:42987779 | T | G | 1 | a0001c0001t0008g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+13115T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987779 | |||||||
chr21:42988065 | TG | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(175): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.-57+13402delG | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988065 | |||||||
chr21:42988066 | G | T | 110 | a0001c0001t0001g0127 a0001c0001t0001g0218 a0001c0001t0002g0005 others(107): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-57+13402G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988066 | |||||||
chr21:42988254 | T | C | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0145 |
3 | NA18983.hp1 NA18988.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-57+13590T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988254 | |||||||
chr21:42988292 | G | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-57+13628G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988292 | |||||||
chr21:42988343 | C | G | 246 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(243): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-57+13679C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988343 | |||||||
chr21:42988659 | G | A | 1 | a0001c0001t0008g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-57+13995G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988659 | |||||||
chr21:42988774 | G | A | 1 | a0001c0002t0003g0350 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-57+14110G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988774 | |||||||
chr21:42988949 | T | A | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+14285T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988949 | |||||||
chr21:42989079 | C | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0098 |
3 | HG01074.hp1 HG01243.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-57+14415C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989079 | |||||||
chr21:42989129 | C | T | 1 | a0001c0001t0008g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+14465C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989129 | |||||||
chr21:42989130 | G | A | 1 | a0001c0001t0026g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+14466G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989130 | |||||||
chr21:42989285 | CA | C | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+14623delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42989285 | ||||||
chr21:42989290 | T | C | 74 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(71): Show |
75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-57+14626T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989290 | |||||||
chr21:42989308 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-57+14644T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989308 | |||||||
chr21:42989318 | T | C | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+14654T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989318 | |||||||
chr21:42989564 | G | A | 1 | a0001c0001t0004g0050 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-56-14762G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989564 | |||||||
chr21:42989575 | C | T | 1 | a0001c0001t0006g0203 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-56-14751C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989575 | |||||||
chr21:42989577 | C | T | 1 | a0001c0001t0005g0185 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-56-14749C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989577 | |||||||
chr21:42989654 | A | G | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-14672A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989654 | |||||||
chr21:42989691 | T | C | 1 | a0001c0001t0002g0267 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-56-14635T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989691 | |||||||
chr21:42989699 | G | A | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG03654.hp1 NA18960.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-14627G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989699 | |||||||
chr21:42989713 | C | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01074.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-56-14613C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989713 | |||||||
chr21:42989716 | G | C | 1 | a0001c0001t0006g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-56-14610G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989716 | |||||||
chr21:42989877 | T | C | 3 | a0001c0001t0022g0025 a0001c0001t0022g0053 a0001c0001t0035g0052 |
3 | HG03453.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-14449T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989877 | |||||||
chr21:42989958 | G | A | 104 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0205 others(101): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-56-14368G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989958 | |||||||
chr21:42989992 | C | T | 2 | a0001c0002t0028g0287 a0001c0002t0028g0288 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-56-14334C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989992 | |||||||
chr21:42990076 | A | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-56-14250A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990076 | |||||||
chr21:42990096 | CA | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-56-14217delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42990096 | ||||||
chr21:42990107 | A | T | 11 | a0001c0001t0001g0218 a0001c0001t0002g0222 a0001c0001t0002g0234 others(8): Show |
11 | HG00609.hp2 HG01496.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56-14219A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990107 | |||||||
chr21:42990292 | C | T | 35 | a0001c0001t0005g0175 a0001c0001t0005g0176 a0001c0001t0005g0177 others(32): Show |
36 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.-56-14034C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990292 | |||||||
chr21:42990299 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-56-14027C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990299 | |||||||
chr21:42990312 | G | A | 1 | a0001c0001t0030g0082 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-56-14014G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990312 | |||||||
chr21:42990388 | T | C | 1 | a0001c0001t0044g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-13938T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990388 | |||||||
chr21:42990615 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-56-13711C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990615 | |||||||
chr21:42990796 | A | G | 1 | a0001c0001t0004g0049 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-56-13530A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990796 | |||||||
chr21:42990984 | G | A | 3 | a0001c0001t0002g0228 a0001c0003t0002g0221 a0001c0003t0002g0229 |
3 | HG02040.hp2 NA19060.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-56-13342G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990984 | |||||||
chr21:42991209 | G | A | 1 | a0001c0002t0003g0315 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-56-13117G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991209 | |||||||
chr21:42991285 | G | A | 3 | a0001c0001t0005g0191 a0001c0001t0005g0200 a0001c0001t0005g0273 |
3 | NA18950.hp1 NA18951.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.-56-13041G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991285 | |||||||
chr21:42991369 | C | G | 1 | a0001c0002t0003g0314 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-56-12957C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991369 | |||||||
chr21:42991443 | T | G | 1 | a0001c0001t0043g0193 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-56-12883T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991443 | |||||||
chr21:42991510 | A | C | 110 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(107): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-56-12816A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991510 | |||||||
chr21:42991645 | G | A | 16 | a0001c0001t0001g0056 a0001c0001t0001g0083 a0001c0001t0001g0115 others(13): Show |
16 | HG00741.hp2 HG01168.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.-56-12681G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991645 | |||||||
chr21:42991660 | G | A | 1 | a0001c0001t0006g0194 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-56-12666G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991660 | |||||||
chr21:42991733 | CA | C | 287 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(284): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.-56-12580delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42991733 | ||||||
chr21:42992082 | G | A | 1 | a0001c0001t0044g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-12244G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992082 | |||||||
chr21:42992148 | A | G | 1 | a0001c0001t0002g0189 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-56-12178A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992148 | |||||||
chr21:42992329 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-56-11997A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992329 | |||||||
chr21:42992566 | C | T | 33 | a0001c0001t0005g0175 a0001c0001t0005g0176 a0001c0001t0005g0177 others(30): Show |
34 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.-56-11760C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992566 | |||||||
chr21:42992625 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-56-11701C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992625 | |||||||
chr21:42992699 | A | G | 10 | a0001c0001t0006g0004 a0001c0001t0006g0192 a0001c0001t0006g0194 others(7): Show |
11 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.-56-11627A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992699 | |||||||
chr21:42992714 | TTCACAGC others(13): Show |
T | 5 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0225 others(2): Show |
5 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-11596_-56-1157 others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42992714 | ||||||
chr21:42992769 | G | A | 1 | a0001c0001t0005g0186 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-56-11557G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992769 | |||||||
chr21:42992828 | GGGGGCCT others(33): Show |
G | 1 | a0001c0001t0001g0097 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-56-11493_-56-1145 others(44): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42992828 | ||||||
chr21:42992843 | G | A | 287 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(284): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.-56-11483G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992843 | |||||||
chr21:42992888 | T | C | 1 | a0001c0001t0004g0049 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-56-11438T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992888 | |||||||
chr21:42992943 | T | G | 1 | a0001c0001t0044g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-11383T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992943 | |||||||
chr21:42992991 | A | C | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-11335A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992991 | |||||||
chr21:42993000 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-56-11326C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993000 | |||||||
chr21:42993073 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-56-11253G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993073 | |||||||
chr21:42993291 | G | A | 1 | a0001c0001t0005g0187 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-56-11035G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993291 | |||||||
chr21:42993347 | G | A | 6 | a0001c0001t0006g0004 a0001c0001t0006g0194 a0001c0001t0006g0195 others(3): Show |
7 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-10979G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993347 | |||||||
chr21:42993351 | C | T | 1 | a0001c0001t0023g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-56-10975C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993351 | |||||||
chr21:42993381 | C | T | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10945C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993381 | |||||||
chr21:42993396 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG03688.hp2 HG03942.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-56-10930C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993396 | |||||||
chr21:42993521 | CT | C | 7 | a0001c0001t0001g0074 a0001c0001t0001g0085 a0001c0001t0001g0115 others(4): Show |
7 | HG02602.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-10791delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993521 | ||||||
chr21:42993548 | A | G | 1 | a0001c0001t0004g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-56-10778A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993548 | |||||||
chr21:42993603 | C | G | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10723C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993603 | |||||||
chr21:42993607 | C | T | 1 | a0001c0001t0008g0166 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-56-10719C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993607 | |||||||
chr21:42993646 | CTTTGTTT others(2): Show |
C | 32 | a0001c0001t0005g0175 a0001c0001t0005g0176 a0001c0001t0005g0177 others(29): Show |
33 | HG00323.hp1 HG00423.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-56-10667_-56-1065 others(13): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993646 | ||||||
chr21:42993650 | GTTTTTTT others(3): Show |
G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10667_-56-1065 others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993650 | ||||||
chr21:42993651 | TTTTTTTT others(1): Show |
T | 167 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(164): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.-56-10667_-56-1066 others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993651 | ||||||
chr21:42993652 | TTTTTTTG | T | 78 | a0001c0001t0001g0030 a0001c0001t0001g0075 a0001c0001t0001g0083 others(75): Show |
78 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-56-10667_-56-1066 others(11): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993652 | ||||||
chr21:42993659 | G | GT | 7 | a0001c0002t0003g0312 a0001c0002t0003g0313 a0001c0002t0003g0324 others(4): Show |
7 | HG01081.hp2 HG02027.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-10652dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993659 | ||||||
chr21:42993714 | A | G | 1 | a0001c0001t0008g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-10612A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993714 | |||||||
chr21:42993723 | CTCTTTTT others(3): Show |
C | 251 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(248): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-56-10591_-56-1058 others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993723 | ||||||
chr21:42993725 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0075 a0001c0001t0001g0118 a0001c0001t0002g0268 others(1): Show |
4 | HG01516.hp1 NA18942.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10591_-56-1058 others(15): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993725 | ||||||
chr21:42993726 | TTTTTTTT others(2): Show |
T | 26 | a0001c0001t0001g0032 a0001c0001t0001g0128 a0001c0001t0001g0129 others(23): Show |
27 | HG00423.hp1 HG00735.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.-56-10591_-56-1058 others(13): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993726 | ||||||
chr21:42993733 | TTC | T | 7 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(4): Show |
7 | HG03098.hp1 HG03654.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-10591_-56-1059 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993733 | ||||||
chr21:42993734 | TC | T | 53 | a0001c0002t0003g0299 a0001c0002t0003g0300 a0001c0002t0003g0310 others(50): Show |
53 | HG00597.hp2 HG00621.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-56-10591delC | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993734 | |||||||
chr21:42993735 | C | T | 4 | a0001c0001t0044g0289 a0001c0002t0003g0297 a0001c0002t0003g0304 others(1): Show |
4 | HG02055.hp2 NA18944.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-10591C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993735 | |||||||
chr21:42993819 | G | A | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10507G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993819 | |||||||
chr21:42993826 | G | A | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-56-10500G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993826 | |||||||
chr21:42993857 | G | A | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-56-10469G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993857 | |||||||
chr21:42993978 | T | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-56-10348T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993978 | |||||||
chr21:42993996 | T | C | 1 | a0001c0001t0011g0278 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-56-10330T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993996 | |||||||
chr21:42994018 | C | T | 1 | a0001c0001t0024g0078 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-56-10308C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994018 | |||||||
chr21:42994023 | C | T | 1 | a0001c0001t0013g0114 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-56-10303C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994023 | |||||||
chr21:42994031 | C | CT | 6 | a0001c0001t0007g0109 a0001c0002t0003g0311 a0001c0002t0003g0314 others(3): Show |
6 | HG01496.hp2 HG02071.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-10273dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994031 | ||||||
chr21:42994031 | CT | C | 163 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(160): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-56-10273delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994031 | ||||||
chr21:42994031 | CTT | C | 106 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(103): Show |
108 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-56-10274_-56-1027 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994031 | ||||||
chr21:42994194 | T | C | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-56-10132T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994194 | |||||||
chr21:42994294 | A | AGCCTCCC others(2141): Show |
1 | a0001c0001t0001g0125 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2152): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2167): Show |
1 | a0001c0001t0006g0194 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2178): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2166): Show |
1 | a0001c0001t0006g0203 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2177): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2162): Show |
1 | a0001c0001t0002g0263 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2173): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2162): Show |
1 | a0001c0001t0046g0240 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2173): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2164): Show |
1 | a0001c0001t0005g0180 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2175): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2163): Show |
1 | a0001c0001t0006g0196 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2174): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2162): Show |
1 | a0001c0001t0006g0195 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2173): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2163): Show |
3 | a0001c0001t0006g0004 a0001c0001t0006g0197 a0001c0001t0006g0274 |
4 | HG01515.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2174): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2164): Show |
1 | a0001c0001t0006g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2175): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2164): Show |
1 | a0001c0001t0006g0198 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2175): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2163): Show |
1 | a0001c0001t0005g0179 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2174): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2164): Show |
3 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0002c0004t0005g0178 |
3 | NA18940.hp1 NA18999.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2175): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2166): Show |
1 | a0001c0001t0005g0191 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2177): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2164): Show |
1 | a0001c0001t0005g0200 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2175): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2166): Show |
1 | a0001c0001t0037g0213 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2177): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2169): Show |
1 | a0001c0001t0002g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2180): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2155): Show |
1 | a0001c0001t0002g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2166): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2164): Show |
1 | a0001c0001t0002g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2175): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2159): Show |
1 | a0001c0001t0002g0276 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2170): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2162): Show |
1 | a0001c0001t0026g0211 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2173): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2156): Show |
1 | a0001c0001t0002g0235 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2167): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2158): Show |
1 | a0001c0001t0002g0266 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2169): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2159): Show |
1 | a0001c0001t0002g0236 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2170): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2160): Show |
1 | a0001c0001t0002g0230 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2171): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2157): Show |
5 | a0001c0001t0002g0214 a0001c0001t0002g0228 a0001c0001t0002g0237 others(2): Show |
5 | HG02040.hp2 HG02886.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2168): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2158): Show |
20 | a0001c0001t0002g0005 a0001c0001t0002g0189 a0001c0001t0002g0212 others(17): Show |
21 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2169): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2159): Show |
2 | a0001c0001t0002g0255 a0001c0001t0002g0270 |
2 | HG02818.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2170): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2160): Show |
1 | a0001c0001t0047g0232 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2171): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2158): Show |
6 | a0001c0001t0001g0218 a0001c0001t0002g0205 a0001c0001t0002g0206 others(3): Show |
6 | HG02145.hp1 HG02602.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2169): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2160): Show |
1 | a0001c0001t0017g0256 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2171): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2158): Show |
2 | a0001c0001t0002g0251 a0001c0001t0002g0252 |
2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2169): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2162): Show |
1 | a0001c0001t0005g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2173): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2159): Show |
1 | a0001c0001t0033g0184 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2170): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2162): Show |
1 | a0001c0001t0005g0185 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2173): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2160): Show |
1 | a0001c0001t0005g0273 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2171): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2161): Show |
1 | a0001c0001t0005g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2172): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2153): Show |
1 | a0001c0001t0043g0193 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2157): Show |
1 | a0001c0001t0006g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2168): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2160): Show |
2 | a0001c0001t0005g0186 a0001c0001t0005g0275 |
2 | HG00099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2171): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2154): Show |
1 | a0001c0001t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2165): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2154): Show |
1 | a0001c0001t0002g0016 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2165): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2153): Show |
1 | a0001c0001t0002g0269 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2154): Show |
12 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0001c0001t0002g0239 others(9): Show |
12 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2165): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2155): Show |
1 | a0001c0001t0050g0258 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2166): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2153): Show |
1 | a0001c0001t0004g0023 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2154): Show |
11 | a0001c0001t0001g0155 a0001c0001t0002g0217 a0001c0001t0002g0220 others(8): Show |
11 | HG02056.hp1 HG02071.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2165): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2152): Show |
1 | a0001c0001t0007g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2163): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2153): Show |
2 | a0001c0001t0007g0105 a0001c0001t0007g0109 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2154): Show |
1 | a0001c0001t0007g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2165): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2160): Show |
1 | a0001c0001t0005g0182 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2171): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2153): Show |
1 | a0001c0001t0006g0201 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2157): Show |
2 | a0001c0001t0005g0187 a0001c0001t0005g0199 |
2 | HG00423.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2168): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2151): Show |
1 | a0001c0001t0020g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2162): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2148): Show |
1 | a0001c0001t0020g0183 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2159): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2150): Show |
1 | a0001c0001t0027g0173 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2150): Show |
1 | a0001c0001t0027g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2153): Show |
1 | a0001c0001t0006g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2155): Show |
1 | a0001c0001t0006g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2166): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2151): Show |
2 | a0001c0001t0004g0142 a0001c0001t0023g0117 |
2 | HG01981.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2162): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2152): Show |
2 | a0001c0001t0001g0027 a0001c0001t0004g0141 |
2 | HG02965.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2163): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2153): Show |
2 | a0001c0001t0002g0207 a0001c0001t0002g0216 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2149): Show |
2 | a0001c0001t0001g0075 a0001c0001t0004g0022 |
2 | HG01168.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2160): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2150): Show |
14 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0144 others(11): Show |
14 | HG01175.hp1 HG01361.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2151): Show |
3 | a0001c0001t0001g0098 a0001c0001t0002g0259 a0001c0001t0004g0048 |
3 | HG01192.hp1 HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2162): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2148): Show |
1 | a0001c0001t0031g0121 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2159): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2150): Show |
4 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG00544.hp1 HG00609.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2151): Show |
1 | a0001c0001t0001g0079 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2162): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2149): Show |
1 | a0001c0001t0034g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2160): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2150): Show |
4 | a0001c0001t0001g0116 a0001c0001t0001g0120 a0001c0001t0004g0137 others(1): Show |
4 | HG02027.hp2 NA18522.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2150): Show |
2 | a0001c0001t0001g0058 a0001c0001t0001g0086 |
2 | HG01123.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2152): Show |
1 | a0001c0001t0005g0174 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2163): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2146): Show |
1 | a0001c0001t0001g0087 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2147): Show |
1 | a0001c0001t0041g0059 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2158): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2145): Show |
2 | a0001c0001t0022g0053 a0001c0001t0035g0052 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2156): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2146): Show |
1 | a0001c0001t0001g0074 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2148): Show |
1 | a0001c0001t0001g0130 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2159): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2146): Show |
8 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0062 others(5): Show |
9 | HG01168.hp2 HG01258.hp1 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2147): Show |
2 | a0001c0001t0001g0102 a0001c0001t0001g0131 |
2 | HG01167.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2158): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2148): Show |
4 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0140 others(1): Show |
4 | HG01109.hp1 HG02602.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2159): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2149): Show |
1 | a0001c0001t0001g0056 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2160): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2150): Show |
2 | a0001c0001t0001g0088 a0001c0001t0001g0099 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2145): Show |
3 | a0001c0001t0001g0089 a0001c0001t0001g0145 a0001c0001t0010g0034 |
3 | HG00733.hp1 NA19063.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2156): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2146): Show |
26 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0055 others(23): Show |
26 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2147): Show |
6 | a0001c0001t0007g0002 a0001c0001t0007g0010 a0001c0001t0007g0011 others(3): Show |
7 | HG02280.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2158): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2149): Show |
1 | a0001c0001t0001g0127 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2160): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2145): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0149 |
2 | HG01358.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2156): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2146): Show |
21 | a0001c0001t0001g0031 a0001c0001t0001g0057 a0001c0001t0001g0067 others(18): Show |
21 | HG00597.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2147): Show |
5 | a0001c0001t0001g0030 a0001c0001t0001g0071 a0001c0001t0001g0096 others(2): Show |
5 | HG02258.hp2 HG02897.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2158): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2145): Show |
1 | a0001c0001t0001g0115 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2156): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2145): Show |
1 | a0001c0001t0001g0118 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2156): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2146): Show |
5 | a0001c0001t0001g0060 a0001c0001t0001g0139 a0001c0001t0001g0146 others(2): Show |
5 | HG02015.hp1 NA18965.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2146): Show |
1 | a0001c0001t0042g0122 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2146): Show |
1 | a0001c0001t0001g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2146): Show |
1 | a0001c0001t0001g0147 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2153): Show |
1 | a0001c0001t0008g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2146): Show |
3 | a0001c0001t0008g0157 a0001c0001t0008g0159 a0001c0001t0008g0167 |
3 | HG00140.hp2 HG01099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2145): Show |
3 | a0001c0001t0008g0156 a0001c0001t0008g0168 a0001c0001t0008g0169 |
3 | HG01070.hp2 HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2156): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2146): Show |
7 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(4): Show |
7 | HG00323.hp2 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2147): Show |
3 | a0001c0001t0008g0166 a0001c0001t0015g0164 a0001c0001t0015g0165 |
3 | HG01981.hp2 HG02004.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2158): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2152): Show |
1 | a0001c0001t0026g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2163): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2144): Show |
1 | a0001c0001t0001g0026 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2155): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2142): Show |
2 | a0001c0001t0001g0021 a0001c0001t0011g0279 |
2 | HG01496.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2153): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2140): Show |
4 | a0001c0001t0011g0278 a0001c0001t0011g0280 a0001c0001t0045g0283 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2151): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2140): Show |
1 | a0001c0001t0011g0281 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2151): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2124): Show |
6 | a0001c0002t0003g0312 a0001c0002t0003g0329 a0001c0002t0003g0335 others(3): Show |
6 | HG00621.hp1 HG01081.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2125): Show |
2 | a0001c0002t0003g0297 a0001c0002t0003g0314 |
2 | HG02071.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2136): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2126): Show |
1 | a0001c0002t0003g0341 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2137): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2123): Show |
3 | a0001c0002t0009g0296 a0001c0002t0028g0287 a0001c0002t0028g0288 |
3 | HG01943.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2134): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2124): Show |
40 | a0001c0002t0003g0299 a0001c0002t0003g0300 a0001c0002t0003g0302 others(37): Show |
40 | HG00597.hp2 HG00639.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2122): Show |
4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2133): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2124): Show |
2 | a0001c0002t0003g0310 a0001c0002t0003g0313 |
2 | NA19009.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2124): Show |
1 | a0001c0002t0003g0340 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2130): Show |
1 | a0001c0002t0016g0293 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2141): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2124): Show |
2 | a0001c0002t0016g0294 a0001c0002t0016g0351 |
2 | NA18939.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2127): Show |
2 | a0001c0001t0019g0285 a0001c0001t0032g0290 |
2 | NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2138): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2125): Show |
1 | a0001c0001t0019g0286 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2136): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2139): Show |
1 | a0001c0001t0044g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2150): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2124): Show |
1 | a0001c0002t0003g0324 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2137): Show |
1 | a0001c0001t0022g0025 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2148): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2124): Show |
1 | a0001c0005t0003g0301 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994294 | A | AGCCTCCC others(2146): Show |
1 | a0001c0001t0013g0112 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | ||||||
chr21:42994330 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-56-9996C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994330 | |||||||
chr21:42994901 | T | C | 1 | a0001c0001t0002g0269 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-56-9425T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994901 | |||||||
chr21:42994911 | C | G | 1 | a0001c0001t0001g0026 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-56-9415C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994911 | |||||||
chr21:42994918 | C | CT | 144 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(141): Show |
146 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.-56-9387dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994918 | ||||||
chr21:42994918 | C | CTT | 16 | a0001c0001t0004g0049 a0001c0001t0008g0156 a0001c0001t0008g0157 others(13): Show |
16 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-56-9388_-56-9387d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994918 | ||||||
chr21:42994918 | CT | C | 84 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(81): Show |
85 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-56-9387delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994918 | ||||||
chr21:42994918 | CTT | C | 31 | a0001c0001t0002g0237 a0001c0001t0002g0266 a0001c0001t0002g0269 others(28): Show |
32 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.-56-9388_-56-9387d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994918 | ||||||
chr21:42994945 | A | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-56-9381A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994945 | |||||||
chr21:42994980 | G | A | 1 | a0001c0001t0020g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-9346G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994980 | |||||||
chr21:42994983 | G | A | 154 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(151): Show |
156 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-56-9343G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994983 | |||||||
chr21:42995111 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-56-9215G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995111 | |||||||
chr21:42995161 | G | A | 291 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(288): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-56-9165G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995161 | |||||||
chr21:42995222 | G | A | 7 | a0001c0002t0003g0315 a0001c0002t0003g0316 a0001c0002t0003g0331 others(4): Show |
7 | HG01496.hp2 NA18939.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-9104G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995222 | |||||||
chr21:42995235 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-56-9091T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995235 | |||||||
chr21:42995241 | A | C | 1 | a0001c0001t0001g0021 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-56-9085A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995241 | |||||||
chr21:42995356 | T | C | 36 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0005g0176 others(33): Show |
37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.-56-8970T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995356 | |||||||
chr21:42995529 | T | TTAGCCAG others(19): Show |
17 | a0001c0001t0008g0015 a0001c0001t0008g0156 a0001c0001t0008g0157 others(14): Show |
17 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-56-8793_-56-8768d others(28): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42995529 | ||||||
chr21:42995532 | G | A | 110 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(107): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-56-8794G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995532 | |||||||
chr21:42995726 | G | A | 1 | a0001c0001t0004g0141 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-56-8600G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995726 | |||||||
chr21:42995774 | C | A | 1 | a0001c0001t0020g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-8552C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995774 | |||||||
chr21:42995775 | G | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(168): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-56-8551G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995775 | |||||||
chr21:42995799 | A | G | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-8527A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995799 | |||||||
chr21:42995800 | C | T | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-8526C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995800 | |||||||
chr21:42995852 | G | A | 3 | a0001c0001t0027g0173 a0001c0001t0027g0188 a0001c0001t0043g0193 |
3 | HG02809.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-56-8474G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995852 | |||||||
chr21:42995872 | T | C | 5 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0225 others(2): Show |
5 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-8454T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995872 | |||||||
chr21:42995902 | T | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(168): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-56-8424T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995902 | |||||||
chr21:42995951 | T | A | 291 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(288): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-56-8375T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995951 | |||||||
chr21:42995989 | C | T | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-8337C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995989 | |||||||
chr21:42996251 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-56-8075G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996251 | |||||||
chr21:42996314 | A | G | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-8012A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996314 | |||||||
chr21:42996317 | G | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(168): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-56-8009G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996317 | |||||||
chr21:42996442 | A | AT | 36 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0005g0176 others(33): Show |
37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.-56-7883dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42996442 | ||||||
chr21:42996540 | T | TAAAAATG others(142): Show |
1 | a0001c0001t0002g0241 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-56-7769_-56-7768i others(151): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42996540 | ||||||
chr21:42996540 | T | TAAAAATG others(143): Show |
1 | a0001c0001t0002g0220 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-56-7769_-56-7768i others(152): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42996540 | ||||||
chr21:42996540 | T | TAAAAATG others(148): Show |
1 | a0001c0001t0002g0244 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-56-7769_-56-7768i others(157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42996540 | ||||||
chr21:42996547 | G | A | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-7779G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996547 | |||||||
chr21:42996730 | A | G | 1 | a0001c0001t0020g0183 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-56-7596A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996730 | |||||||
chr21:42996819 | T | C | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-7507T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996819 | |||||||
chr21:42996891 | A | AT | 202 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(199): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.-56-7422dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42996891 | ||||||
chr21:42996943 | C | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(168): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-56-7383C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996943 | |||||||
chr21:42996949 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-56-7377C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996949 | |||||||
chr21:42997077 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0044g0289 |
2 | HG02055.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-56-7249C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997077 | |||||||
chr21:42997304 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-56-7022C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997304 | |||||||
chr21:42997422 | C | T | 2 | a0001c0001t0010g0034 a0001c0001t0010g0038 |
2 | NA18950.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-56-6904C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997422 | |||||||
chr21:42997454 | A | G | 147 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(144): Show |
149 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.-56-6872A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997454 | |||||||
chr21:42997513 | A | G | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-6813A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997513 | |||||||
chr21:42997539 | TTTG | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0090 others(2): Show |
5 | HG00423.hp2 HG01257.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-6785_-56-6783d others(5): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42997539 | ||||||
chr21:42997654 | A | G | 291 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(288): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-56-6672A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997654 | |||||||
chr21:42997855 | G | A | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-6471G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997855 | |||||||
chr21:42997871 | C | T | 1 | a0001c0001t0002g0241 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-56-6455C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997871 | |||||||
chr21:42997909 | G | T | 6 | a0001c0001t0011g0278 a0001c0001t0011g0279 a0001c0001t0011g0280 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-6417G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997909 | |||||||
chr21:42998211 | A | G | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-56-6115A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998211 | |||||||
chr21:42998326 | C | T | 36 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0005g0176 others(33): Show |
37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.-56-6000C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998326 | |||||||
chr21:42998542 | T | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-56-5784T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998542 | |||||||
chr21:42998650 | A | G | 1 | a0001c0002t0009g0309 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-56-5676A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998650 | |||||||
chr21:42998803 | G | C | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-5523G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998803 | |||||||
chr21:42998810 | G | A | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-56-5516G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998810 | |||||||
chr21:42998895 | A | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | HG02129.hp2 HG02523.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-56-5431A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998895 | |||||||
chr21:42999021 | G | A | 2 | a0001c0001t0023g0054 a0001c0001t0023g0117 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-56-5305G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999021 | |||||||
chr21:42999031 | G | C | 1 | a0001c0002t0016g0293 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-56-5295G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999031 | |||||||
chr21:42999040 | G | A | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-56-5286G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999040 | |||||||
chr21:42999048 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0126 |
2 | NA18939.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-56-5278A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999048 | |||||||
chr21:42999074 | C | T | 2 | a0001c0002t0003g0335 a0001c0002t0003g0336 |
2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-56-5252C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999074 | |||||||
chr21:42999157 | T | C | 296 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(293): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-56-5169T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999157 | |||||||
chr21:42999474 | ATTTTC | A | 74 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(71): Show |
75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-56-4842_-56-4838d others(7): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42999474 | ||||||
chr21:42999484 | C | T | 10 | a0001c0001t0006g0004 a0001c0001t0006g0192 a0001c0001t0006g0194 others(7): Show |
11 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.-56-4842C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999484 | |||||||
chr21:42999545 | A | G | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-4781A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999545 | |||||||
chr21:42999592 | C | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(168): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-56-4734C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999592 | |||||||
chr21:42999666 | A | G | 4 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 others(1): Show |
4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-4660A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999666 | |||||||
chr21:43000275 | C | G | 9 | a0001c0001t0007g0002 a0001c0001t0007g0007 a0001c0001t0007g0008 others(6): Show |
10 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-56-4051C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000275 | |||||||
chr21:43000360 | G | A | 2 | a0001c0001t0027g0173 a0001c0001t0027g0188 |
2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-56-3966G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000360 | |||||||
chr21:43000419 | G | T | 1 | a0001c0001t0008g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-3907G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000419 | |||||||
chr21:43000504 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-56-3822A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000504 | |||||||
chr21:43000576 | G | A | 1 | a0001c0002t0003g0349 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-56-3750G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000576 | |||||||
chr21:43000651 | C | T | 6 | a0001c0001t0011g0278 a0001c0001t0011g0279 a0001c0001t0011g0280 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-3675C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000651 | |||||||
chr21:43000729 | AT | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(168): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-56-3594delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 43000729 | ||||||
chr21:43000782 | C | T | 1 | a0001c0002t0003g0349 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-56-3544C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000782 | |||||||
chr21:43000816 | G | A | 1 | a0001c0001t0002g0224 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-56-3510G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000816 | |||||||
chr21:43000856 | C | G | 1 | a0001c0001t0008g0167 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-56-3470C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000856 | |||||||
chr21:43000937 | A | G | 22 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(19): Show |
22 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.-56-3389A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000937 | |||||||
chr21:43001057 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-56-3269G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001057 | |||||||
chr21:43001123 | C | T | 1 | a0001c0002t0012g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-3203C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001123 | |||||||
chr21:43001136 | G | A | 9 | a0001c0001t0007g0002 a0001c0001t0007g0007 a0001c0001t0007g0008 others(6): Show |
10 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-56-3190G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001136 | |||||||
chr21:43001408 | A | ACTCTTCC others(15): Show |
1 | a0001c0001t0027g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-56-2898_-56-2877d others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 43001408 | ||||||
chr21:43001498 | C | T | 1 | a0001c0001t0005g0275 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-56-2828C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001498 | |||||||
chr21:43001540 | G | T | 1 | a0001c0002t0003g0349 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-56-2786G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001540 | |||||||
chr21:43001654 | A | G | 4 | a0001c0001t0001g0061 a0001c0001t0001g0068 a0001c0001t0001g0069 others(1): Show |
4 | HG00609.hp1 HG02132.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-2672A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001654 | |||||||
chr21:43001703 | A | G | 291 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(288): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-56-2623A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001703 | |||||||
chr21:43001720 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-56-2606G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001720 | |||||||
chr21:43001756 | C | G | 1 | a0001c0001t0007g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-56-2570C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001756 | |||||||
chr21:43001756 | C | T | 1 | a0001c0001t0044g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-2570C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001756 | |||||||
chr21:43001827 | G | A | 109 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(106): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-56-2499G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001827 | |||||||
chr21:43001916 | G | A | 1 | a0001c0001t0004g0272 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-56-2410G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001916 | |||||||
chr21:43001917 | C | T | 17 | a0001c0001t0008g0015 a0001c0001t0008g0156 a0001c0001t0008g0157 others(14): Show |
17 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-56-2409C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001917 | |||||||
chr21:43001955 | C | T | 1 | a0001c0001t0007g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-56-2371C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001955 | |||||||
chr21:43001960 | C | CAAAT | 275 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0026 others(272): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-56-2342_-56-2339d others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 43001960 | ||||||
chr21:43001960 | C | CAAATAAA others(1): Show |
5 | a0001c0001t0001g0021 a0001c0001t0004g0044 a0001c0001t0006g0204 others(2): Show |
5 | HG01496.hp1 HG02486.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-2346_-56-2339d others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 43001960 | ||||||
chr21:43001984 | T | C | 1 | a0001c0005t0003g0301 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-56-2342T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001984 | |||||||
chr21:43002073 | A | G | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-56-2253A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002073 | |||||||
chr21:43002126 | A | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-56-2200A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002126 | |||||||
chr21:43002161 | G | A | 1 | a0001c0001t0005g0200 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-56-2165G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002161 | |||||||
chr21:43002163 | G | A | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-56-2163G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002163 | |||||||
chr21:43002186 | C | T | 37 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0005g0176 others(34): Show |
38 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.-56-2140C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002186 | |||||||
chr21:43002404 | G | GC | 6 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0225 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-1917dupC | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 43002404 | ||||||
chr21:43002405 | C | A | 1 | a0001c0001t0044g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-1921C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002405 | |||||||
chr21:43002409 | CT | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(223): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.-56-1916delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002409 | |||||||
chr21:43002410 | T | C | 62 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0189 others(59): Show |
63 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.-56-1916T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002410 | |||||||
chr21:43002485 | C | G | 35 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0005g0176 others(32): Show |
36 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.-56-1841C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002485 | |||||||
chr21:43003172 | T | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(242): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.-56-1154T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003172 | |||||||
chr21:43003255 | C | T | 3 | a0001c0001t0002g0230 a0001c0001t0002g0236 a0001c0001t0047g0232 |
3 | HG02559.hp1 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-56-1071C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003255 | |||||||
chr21:43003259 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-56-1067C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003259 | |||||||
chr21:43003271 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | HG01358.hp1 HG01928.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-1055C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003271 | |||||||
chr21:43003420 | G | A | 2 | a0001c0002t0003g0312 a0001c0002t0003g0324 |
2 | HG01081.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-56-906G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003420 | |||||||
chr21:43003457 | C | T | 1 | a0001c0001t0004g0044 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-56-869C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003457 | |||||||
chr21:43003543 | C | T | 74 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(71): Show |
75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-56-783C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003543 | |||||||
chr21:43003552 | C | T | 109 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(106): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-56-774C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003552 | |||||||
chr21:43003561 | A | G | 2 | a0001c0001t0027g0173 a0001c0001t0027g0188 |
2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-56-765A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003561 | |||||||
chr21:43003576 | C | G | 2 | a0001c0002t0028g0287 a0001c0002t0028g0288 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-56-750C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003576 | |||||||
chr21:43003693 | G | A | 1 | a0001c0001t0008g0160 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-56-633G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003693 | |||||||
chr21:43003931 | G | T | 36 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0005g0176 others(33): Show |
37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.-56-395G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003931 | |||||||
chr21:43004027 | C | T | 1 | a0001c0001t0002g0262 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-56-299C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43004027 | |||||||
chr21:43004035 | C | T | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-291C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43004035 | |||||||
chr21:43004038 | G | A | 21 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(18): Show |
21 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.-56-288G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43004038 | |||||||
chr21:43004045 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-56-281C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43004045 | |||||||
chr21:43004223 | G | A | 7 | a0001c0001t0011g0278 a0001c0001t0011g0279 a0001c0001t0011g0280 others(4): Show |
7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-103G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43004223 | |||||||
chr21:43004489 | G | A | 1 | a0001c0001t0043g0193 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.51+57G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004489 | |||||||
chr21:43004571 | C | T | 1 | a0001c0001t0006g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+139C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004571 | |||||||
chr21:43004579 | G | GA | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.51+154dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr21 | 43004579 | ||||||
chr21:43004776 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.51+344G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004776 | |||||||
chr21:43004864 | T | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.51+432T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004864 | |||||||
chr21:43004877 | A | G | 1 | a0001c0001t0008g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.51+445A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004877 | |||||||
chr21:43004924 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.51+492C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004924 | |||||||
chr21:43004927 | G | A | 281 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.51+495G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004927 | |||||||
chr21:43005091 | T | C | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.51+659T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005091 | |||||||
chr21:43005232 | G | A | 1 | a0001c0001t0008g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.51+800G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005232 | |||||||
chr21:43005249 | C | T | 1 | a0001c0001t0015g0163 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.51+817C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005249 | |||||||
chr21:43005278 | C | T | 2 | a0001c0001t0027g0173 a0001c0001t0027g0188 |
2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.51+846C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005278 | |||||||
chr21:43005289 | C | T | 243 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(240): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.51+857C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005289 | |||||||
chr21:43005413 | G | A | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.51+981G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005413 | |||||||
chr21:43005431 | G | GT | 269 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(266): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.51+1008dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr21 | 43005431 | ||||||
chr21:43005534 | CT | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(183): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.51+1116delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr21 | 43005534 | ||||||
chr21:43005659 | C | T | 2 | a0001c0002t0028g0287 a0001c0002t0028g0288 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.51+1227C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005659 | |||||||
chr21:43005939 | C | G | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.51+1507C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005939 | |||||||
chr21:43006024 | C | G | 1 | a0001c0001t0020g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.52-1467C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006024 | |||||||
chr21:43006160 | G | T | 1 | a0001c0001t0002g0224 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.52-1331G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006160 | |||||||
chr21:43006177 | G | A | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.52-1314G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006177 | |||||||
chr21:43006369 | G | A | 35 | a0001c0001t0005g0175 a0001c0001t0005g0176 a0001c0001t0005g0177 others(32): Show |
36 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.52-1122G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006369 | |||||||
chr21:43006613 | A | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.52-878A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006613 | |||||||
chr21:43006617 | G | A | 16 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(13): Show |
16 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.52-874G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006617 | |||||||
chr21:43006717 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.52-774C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006717 | |||||||
chr21:43006774 | C | T | 14 | a0001c0001t0002g0005 a0001c0001t0002g0261 a0001c0001t0002g0262 others(11): Show |
15 | NA18954.hp2 NA18966.hp2 NA18979.hp2 others(12): Show |
intron_variant | MODIFIER | c.52-717C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006774 | |||||||
chr21:43007083 | T | C | 1 | a0001c0001t0044g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.52-408T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43007083 | |||||||
chr21:43007090 | C | T | 2 | a0001c0002t0028g0287 a0001c0002t0028g0288 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.52-401C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43007090 | |||||||
chr21:43007400 | A | G | 1 | a0001c0001t0026g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.52-91A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43007400 | |||||||
chr21:43007449 | A | T | 1 | a0001c0001t0014g0111 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.52-42A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43007449 | |||||||
chr21:43007705 | G | A | 1 | a0001c0001t0002g0271 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.179+87G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43007705 | |||||||
chr21:43007909 | C | T | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.179+291C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43007909 | |||||||
chr21:43007988 | G | C | 2 | a0001c0001t0021g0153 a0001c0001t0021g0154 |
2 | NA18963.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.179+370G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43007988 | |||||||
chr21:43008002 | T | G | 1 | a0001c0001t0023g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.179+384T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008002 | |||||||
chr21:43008052 | A | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.179+434A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008052 | |||||||
chr21:43008061 | T | TCA | 12 | a0001c0001t0002g0238 a0001c0001t0002g0248 a0001c0001t0002g0250 others(9): Show |
12 | HG00735.hp2 HG02056.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.179+478_179+479dup others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCACA | 52 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0205 others(49): Show |
53 | HG00438.hp1 HG00609.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.179+476_179+479dup others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCACACA | 14 | a0001c0001t0002g0016 a0001c0001t0002g0208 a0001c0001t0002g0209 others(11): Show |
14 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.179+474_179+479dup others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCACACAC others(1): Show |
3 | a0001c0001t0002g0189 a0001c0001t0023g0117 a0001c0001t0025g0017 |
3 | HG00642.hp2 HG03471.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.179+472_179+479dup others(8): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCA | 16 | a0001c0001t0007g0002 a0001c0001t0007g0007 a0001c0001t0007g0008 others(13): Show |
17 | HG00140.hp2 HG01074.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCACA | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0049 others(2): Show |
5 | HG01168.hp1 HG01175.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCACAC others(1): Show |
13 | a0001c0001t0001g0103 a0001c0001t0007g0104 a0001c0001t0007g0105 others(10): Show |
13 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(8): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCACAC others(3): Show |
27 | a0001c0001t0001g0030 a0001c0001t0004g0024 a0001c0001t0004g0042 others(24): Show |
27 | HG00140.hp1 HG00544.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCACAC others(5): Show |
8 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0001g0100 others(5): Show |
8 | HG00642.hp1 HG01167.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCACAC others(7): Show |
4 | a0001c0001t0006g0202 a0001c0001t0006g0204 a0001c0001t0027g0173 others(1): Show |
4 | HG01261.hp1 HG02486.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCACAC others(9): Show |
2 | a0001c0001t0001g0140 a0001c0001t0008g0015 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.179+444_179+445ins others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCTCAC others(3): Show |
4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCTCAC others(5): Show |
3 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0002c0004t0005g0178 |
3 | NA18940.hp1 NA18999.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.179+444_179+445ins others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCTCAC others(7): Show |
3 | a0001c0001t0006g0197 a0001c0001t0006g0198 a0001c0001t0033g0184 |
3 | HG01099.hp2 HG03579.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.179+444_179+445ins others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCTCAC others(9): Show |
8 | a0001c0001t0005g0174 a0001c0001t0005g0179 a0001c0001t0005g0181 others(5): Show |
8 | HG00099.hp2 HG00423.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCTCAC others(11): Show |
3 | a0001c0001t0005g0175 a0001c0001t0005g0182 a0001c0001t0005g0187 |
3 | HG01109.hp2 HG03942.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.179+444_179+445ins others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCTCAC others(13): Show |
2 | a0001c0001t0005g0180 a0001c0001t0005g0185 |
2 | HG02132.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.179+444_179+445ins others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCTCAC others(15): Show |
2 | a0001c0001t0006g0190 a0001c0001t0006g0192 |
2 | HG02922.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.179+444_179+445ins others(22): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | T | TCTCTCTC others(9): Show |
1 | a0001c0001t0005g0273 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.179+444_179+445ins others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | TCA | T | 19 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0080 others(16): Show |
19 | HG00280.hp1 HG00323.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.179+478_179+479del others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | TCACA | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(89): Show |
94 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.179+476_179+479del others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | TCACACAC others(3): Show |
T | 1 | a0001c0001t0002g0249 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.179+470_179+479del others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008061 | TCACACAC others(5): Show |
T | 1 | a0001c0003t0002g0229 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.179+468_179+479del others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | ||||||
chr21:43008063 | A | T | 3 | a0001c0001t0008g0157 a0001c0001t0019g0285 a0001c0001t0019g0286 |
3 | HG01099.hp1 HG03654.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.179+445A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008063 | |||||||
chr21:43008065 | A | T | 16 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0080 others(13): Show |
16 | HG00280.hp1 HG00323.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.179+447A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008065 | |||||||
chr21:43008067 | A | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(89): Show |
94 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.179+449A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008067 | |||||||
chr21:43008069 | A | T | 2 | a0001c0001t0006g0194 a0001c0001t0006g0203 |
2 | HG00735.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.179+451A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008069 | |||||||
chr21:43008158 | C | T | 1 | a0001c0001t0008g0158 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.179+540C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008158 | |||||||
chr21:43008237 | G | A | 36 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0005g0176 others(33): Show |
37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.179+619G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008237 | |||||||
chr21:43008424 | A | G | 154 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(151): Show |
156 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.179+806A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008424 | |||||||
chr21:43008622 | T | C | 2 | a0001c0001t0002g0233 a0001c0001t0002g0276 |
2 | HG00438.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.179+1004T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008622 | |||||||
chr21:43008678 | C | T | 6 | a0001c0001t0007g0104 a0001c0001t0007g0105 a0001c0001t0007g0106 others(3): Show |
6 | HG02145.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.179+1060C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008678 | |||||||
chr21:43008770 | G | A | 2 | a0001c0001t0006g0198 a0001c0001t0033g0184 |
2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.179+1152G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008770 | |||||||
chr21:43008780 | C | CA | 21 | a0001c0001t0001g0113 a0001c0001t0001g0147 a0001c0001t0008g0156 others(18): Show |
21 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.179+1174dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008780 | ||||||
chr21:43008919 | C | T | 1 | a0001c0002t0003g0334 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.180-1134C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008919 | |||||||
chr21:43009118 | A | C | 1 | a0001c0002t0003g0336 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.180-935A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009118 | |||||||
chr21:43009226 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.180-827T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009226 | |||||||
chr21:43009280 | T | TCTA | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.180-772_180-770dup others(3): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43009280 | ||||||
chr21:43009286 | G | A | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.180-767G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009286 | |||||||
chr21:43009335 | C | G | 3 | a0001c0001t0022g0025 a0001c0001t0022g0053 a0001c0001t0035g0052 |
3 | HG03453.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.180-718C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009335 | |||||||
chr21:43009604 | C | A | 1 | a0001c0001t0017g0256 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.180-449C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009604 | |||||||
chr21:43009610 | C | CA | 34 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0005g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.180-423dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43009610 | ||||||
chr21:43009610 | C | CAA | 155 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(152): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.180-424_180-423dup others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43009610 | ||||||
chr21:43009610 | C | CAAA | 27 | a0001c0001t0001g0072 a0001c0001t0001g0096 a0001c0001t0001g0113 others(24): Show |
27 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.180-425_180-423dup others(3): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43009610 | ||||||
chr21:43009610 | C | CAAAA | 71 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0189 others(68): Show |
72 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.180-426_180-423dup others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43009610 | ||||||
chr21:43009749 | G | A | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.180-304G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009749 | |||||||
chr21:43009800 | G | A | 1 | a0001c0001t0008g0160 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.180-253G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009800 | |||||||
chr21:43009974 | G | A | 1 | a0001c0001t0045g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.180-79G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009974 | |||||||
chr21:43010029 | T | C | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.180-24T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43010029 | |||||||
chr21:43010039 | T | C | 1 | a0001c0002t0003g0326 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.180-14T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43010039 | |||||||
chr21:43010267 | T | C | 1 | a0001c0001t0004g0050 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.351+43T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010267 | |||||||
chr21:43010478 | C | T | 16 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(13): Show |
16 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.351+254C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010478 | |||||||
chr21:43010489 | A | C | 3 | a0001c0001t0002g0226 a0001c0001t0025g0017 a0001c0001t0025g0018 |
3 | HG00639.hp2 HG00642.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.351+265A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010489 | |||||||
chr21:43010599 | C | T | 2 | a0001c0001t0027g0173 a0001c0001t0027g0188 |
2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.351+375C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010599 | |||||||
chr21:43010627 | A | G | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+403A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010627 | |||||||
chr21:43010632 | A | G | 1 | a0001c0001t0020g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.351+408A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010632 | |||||||
chr21:43010648 | G | A | 1 | a0001c0001t0002g0267 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.351+424G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010648 | |||||||
chr21:43010787 | G | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.351+563G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010787 | |||||||
chr21:43010998 | T | TGTGTCTG others(14): Show |
1 | a0001c0001t0004g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.351+775_351+795dup others(21): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr21 | 43010998 | ||||||
chr21:43011066 | CT | C | 269 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(266): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.351+861delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr21 | 43011066 | ||||||
chr21:43011154 | G | A | 1 | a0001c0002t0052g0332 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.351+930G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011154 | |||||||
chr21:43011193 | G | A | 1 | a0001c0001t0006g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.351+969G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011193 | |||||||
chr21:43011248 | T | G | 36 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0005g0176 others(33): Show |
37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.351+1024T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011248 | |||||||
chr21:43011271 | G | A | 1 | a0001c0001t0044g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.351+1047G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011271 | |||||||
chr21:43011290 | C | T | 1 | a0001c0001t0026g0211 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.351+1066C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011290 | |||||||
chr21:43011291 | G | A | 1 | a0001c0001t0020g0183 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.351+1067G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011291 | |||||||
chr21:43011361 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.351+1137G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011361 | |||||||
chr21:43011372 | G | A | 6 | a0001c0001t0011g0278 a0001c0001t0011g0279 a0001c0001t0011g0280 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+1148G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011372 | |||||||
chr21:43011438 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.351+1214C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011438 | |||||||
chr21:43011504 | T | C | 110 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(107): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.351+1280T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011504 | |||||||
chr21:43011573 | C | T | 2 | a0001c0002t0028g0287 a0001c0002t0028g0288 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.351+1349C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011573 | |||||||
chr21:43011613 | G | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(142): Show |
147 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.351+1389G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011613 | |||||||
chr21:43011841 | C | T | 1 | a0001c0002t0003g0300 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.352-1227C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011841 | |||||||
chr21:43012052 | TTTGACAC others(3): Show |
T | 1 | a0001c0001t0007g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.352-1015_352-1006d others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012052 | |||||||
chr21:43012140 | A | G | 1 | a0001c0001t0023g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.352-928A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012140 | |||||||
chr21:43012259 | T | C | 1 | a0001c0001t0008g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.352-809T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012259 | |||||||
chr21:43012605 | A | G | 17 | a0001c0001t0008g0015 a0001c0001t0008g0156 a0001c0001t0008g0157 others(14): Show |
17 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.352-463A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012605 | |||||||
chr21:43012638 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.352-430C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012638 | |||||||
chr21:43012742 | G | T | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-326G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012742 | |||||||
chr21:43012770 | G | C | 36 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0005g0176 others(33): Show |
37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.352-298G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012770 | |||||||
chr21:43012784 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.352-284G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012784 | |||||||
chr21:43012806 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.352-262C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012806 | |||||||
chr21:43013344 | C | G | 74 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(71): Show |
75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.522+106C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013344 | |||||||
chr21:43013385 | G | C | 2 | a0001c0001t0031g0121 a0001c0001t0042g0122 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.522+147G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013385 | |||||||
chr21:43013571 | A | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(173): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.522+333A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013571 | |||||||
chr21:43013611 | A | C | 1 | a0001c0001t0020g0183 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.522+373A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013611 | |||||||
chr21:43013669 | A | G | 1 | a0001c0001t0002g0249 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.522+431A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013669 | |||||||
chr21:43013859 | C | A | 113 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(110): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.522+621C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013859 | |||||||
chr21:43013890 | T | C | 2 | a0001c0001t0027g0173 a0001c0001t0027g0188 |
2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.522+652T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013890 | |||||||
chr21:43013891 | G | C | 2 | a0001c0002t0028g0287 a0001c0002t0028g0288 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.522+653G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013891 | |||||||
chr21:43013892 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.522+654A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013892 | |||||||
chr21:43013906 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.522+668T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013906 | |||||||
chr21:43013907 | A | T | 1 | a0001c0001t0008g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.522+669A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013907 | |||||||
chr21:43014019 | C | CT | 79 | a0001c0001t0001g0065 a0001c0001t0001g0128 a0001c0001t0001g0129 others(76): Show |
80 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(77): Show |
intron_variant | MODIFIER | c.522+801dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr21 | 43014019 | ||||||
chr21:43014053 | G | A | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.522+815G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014053 | |||||||
chr21:43014078 | G | A | 62 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0189 others(59): Show |
63 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.522+840G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014078 | |||||||
chr21:43014107 | C | T | 35 | a0001c0001t0005g0175 a0001c0001t0005g0176 a0001c0001t0005g0177 others(32): Show |
36 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.522+869C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014107 | |||||||
chr21:43014176 | C | T | 1 | a0001c0001t0050g0258 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.522+938C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014176 | |||||||
chr21:43014225 | A | G | 6 | a0001c0001t0001g0058 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01074.hp1 HG01123.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+987A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014225 | |||||||
chr21:43014243 | G | C | 2 | a0001c0001t0005g0187 a0001c0001t0005g0199 |
2 | HG00423.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.522+1005G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014243 | |||||||
chr21:43014264 | G | A | 2 | a0001c0001t0005g0187 a0001c0001t0005g0199 |
2 | HG00423.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.522+1026G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014264 | |||||||
chr21:43014298 | A | T | 1 | a0001c0001t0002g0276 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.522+1060A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014298 | |||||||
chr21:43014301 | A | G | 1 | a0001c0001t0002g0276 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.522+1063A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014301 | |||||||
chr21:43014341 | T | C | 5 | a0001c0001t0002g0250 a0001c0001t0002g0251 a0001c0001t0002g0252 others(2): Show |
5 | HG02257.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+1103T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014341 | |||||||
chr21:43014345 | A | AT | 10 | a0001c0001t0006g0004 a0001c0001t0006g0192 a0001c0001t0006g0194 others(7): Show |
11 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.522+1116dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr21 | 43014345 | ||||||
chr21:43014385 | T | C | 18 | a0001c0001t0008g0015 a0001c0001t0008g0156 a0001c0001t0008g0157 others(15): Show |
18 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.522+1147T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014385 | |||||||
chr21:43014478 | CTT | C | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.522+1244_522+1245d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr21 | 43014478 | ||||||
chr21:43014501 | A | G | 1 | a0001c0002t0039g0352 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.522+1263A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014501 | |||||||
chr21:43014505 | T | C | 1 | a0001c0001t0043g0193 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.522+1267T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014505 | |||||||
chr21:43014726 | C | A | 60 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0004g0022 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.522+1488C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014726 | |||||||
chr21:43014888 | C | G | 60 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0001g0218 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.522+1650C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014888 | |||||||
chr21:43014922 | T | C | 1 | a0001c0001t0020g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.522+1684T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014922 | |||||||
chr21:43015845 | G | C | 18 | a0001c0001t0008g0015 a0001c0001t0008g0156 a0001c0001t0008g0157 others(15): Show |
18 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-1063G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43015845 | |||||||
chr21:43015995 | G | A | 3 | a0001c0001t0005g0185 a0001c0001t0005g0187 a0001c0001t0005g0199 |
3 | HG00423.hp1 HG02132.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.523-913G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43015995 | |||||||
chr21:43016039 | A | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0001g0100 |
3 | HG02965.hp2 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.523-869A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016039 | |||||||
chr21:43016067 | G | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(150): Show |
155 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.523-841G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016067 | |||||||
chr21:43016260 | A | T | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-648A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016260 | |||||||
chr21:43016398 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.523-510G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016398 | |||||||
chr21:43016510 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.523-398C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016510 | |||||||
chr21:43016609 | C | T | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.523-299C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016609 | |||||||
chr21:43016679 | G | A | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.523-229G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016679 | |||||||
chr21:43016897 | C | T | 1 | a0001c0001t0008g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.523-11C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016897 | |||||||
chr21:43017032 | A | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(114): Show |
119 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.622+25A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017032 | |||||||
chr21:43017057 | T | C | 3 | a0001c0001t0011g0278 a0001c0001t0011g0280 a0001c0001t0045g0283 |
3 | HG02647.hp2 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.622+50T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017057 | |||||||
chr21:43017066 | G | A | 1 | a0001c0001t0011g0279 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.622+59G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017066 | |||||||
chr21:43017112 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.622+105C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017112 | |||||||
chr21:43017378 | G | A | 1 | a0001c0001t0004g0042 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.622+371G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017378 | |||||||
chr21:43017481 | G | A | 1 | a0001c0001t0019g0286 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.622+474G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017481 | |||||||
chr21:43017486 | C | T | 2 | a0001c0002t0028g0287 a0001c0002t0028g0288 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.622+479C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017486 | |||||||
chr21:43017490 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(283): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.622+483A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017490 | |||||||
chr21:43017556 | G | GA | 63 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0002g0263 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.622+559dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43017556 | ||||||
chr21:43017643 | C | CTAATTTT others(4): Show |
1 | a0001c0001t0001g0147 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.623-489_623-479dup others(11): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43017643 | ||||||
chr21:43017672 | G | A | 1 | a0001c0001t0041g0059 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.623-461G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017672 | |||||||
chr21:43018047 | C | CA | 59 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0004g0022 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.623-63dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43018047 | ||||||
chr21:43018047 | C | CAA | 13 | a0001c0001t0004g0101 a0001c0001t0005g0191 a0001c0001t0005g0199 others(10): Show |
13 | HG00423.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.623-64_623-63dupAA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43018047 | ||||||
chr21:43018047 | C | CAAA | 27 | a0001c0001t0001g0073 a0001c0001t0001g0087 a0001c0001t0001g0091 others(24): Show |
27 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.623-65_623-63dupAA others(1): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43018047 | ||||||
chr21:43018047 | C | CAAAA | 162 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(159): Show |
165 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.623-66_623-63dupAA others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43018047 | ||||||
chr21:43018047 | C | CAAAAA | 30 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0070 others(27): Show |
30 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.623-67_623-63dupAA others(3): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43018047 | ||||||
chr21:43018378 | C | G | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.720+148C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018378 | |||||||
chr21:43018467 | CT | C | 5 | a0001c0001t0002g0217 a0001c0001t0002g0250 a0001c0001t0002g0251 others(2): Show |
5 | HG02886.hp2 HG02896.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+238delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018467 | |||||||
chr21:43018468 | T | G | 280 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(277): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.720+238T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018468 | |||||||
chr21:43018469 | G | C | 6 | a0001c0001t0002g0189 a0001c0001t0002g0207 a0001c0001t0002g0216 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+239G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018469 | |||||||
chr21:43018470 | C | CG | 27 | a0001c0001t0001g0088 a0001c0001t0004g0022 a0001c0001t0004g0024 others(24): Show |
27 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.720+240_720+241ins others(1): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018470 | |||||||
chr21:43018470 | CCA | C | 13 | a0001c0001t0008g0015 a0001c0001t0008g0156 a0001c0001t0008g0157 others(10): Show |
13 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.720+242_720+243del others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | ||||||
chr21:43018470 | CCACCCAC others(3): Show |
C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01074.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.720+244_720+253del others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | ||||||
chr21:43018470 | CCACCCAC others(5): Show |
C | 4 | a0001c0001t0001g0067 a0001c0001t0001g0134 a0001c0001t0001g0146 others(1): Show |
4 | HG01928.hp2 NA18522.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+244_720+255del others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | ||||||
chr21:43018470 | CCACCCAC others(7): Show |
C | 18 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0120 others(15): Show |
18 | HG00323.hp2 HG00597.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.720+244_720+257del others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | ||||||
chr21:43018470 | CCACCCAC others(9): Show |
C | 38 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0032 others(35): Show |
38 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.720+244_720+259del others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | ||||||
chr21:43018470 | CCACCCAC others(11): Show |
C | 15 | a0001c0001t0001g0031 a0001c0001t0001g0058 a0001c0001t0001g0066 others(12): Show |
15 | HG00280.hp1 HG00738.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.720+244_720+261del others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | ||||||
chr21:43018470 | CCACCCAC others(13): Show |
C | 4 | a0001c0001t0007g0010 a0001c0001t0011g0281 a0001c0001t0023g0054 others(1): Show |
4 | HG02559.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+244_720+263del others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | ||||||
chr21:43018471 | C | G | 32 | a0001c0001t0001g0099 a0001c0001t0004g0023 a0001c0001t0004g0042 others(29): Show |
33 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.720+241C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018471 | |||||||
chr21:43018472 | A | C | 195 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.720+242A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018472 | |||||||
chr21:43018474 | C | CCA | 15 | a0001c0002t0003g0299 a0001c0002t0003g0300 a0001c0002t0003g0302 others(12): Show |
15 | HG00597.hp2 HG00621.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.720+293_720+294dup others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | ||||||
chr21:43018474 | C | CCACA | 11 | a0001c0002t0003g0319 a0001c0002t0003g0321 a0001c0002t0003g0322 others(8): Show |
11 | HG02083.hp2 HG02280.hp1 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.720+291_720+294dup others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | ||||||
chr21:43018474 | C | G | 59 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(56): Show |
61 | HG00423.hp2 HG00621.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.720+244C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018474 | |||||||
chr21:43018474 | CCA | C | 3 | a0001c0002t0003g0314 a0001c0002t0003g0341 a0001c0002t0003g0350 |
3 | HG02071.hp2 NA19057.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.720+293_720+294del others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | ||||||
chr21:43018474 | CCACA | C | 3 | a0001c0002t0018g0298 a0001c0002t0028g0287 a0001c0002t0028g0288 |
3 | HG02896.hp2 HG02897.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.720+291_720+294del others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | ||||||
chr21:43018474 | CCACACAC others(7): Show |
C | 1 | a0001c0002t0009g0006 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.720+281_720+294del others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | ||||||
chr21:43018474 | CCACACAC others(11): Show |
C | 2 | a0001c0001t0019g0285 a0001c0001t0019g0286 |
2 | HG03654.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.720+277_720+294del others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | ||||||
chr21:43018474 | CCACACAC others(15): Show |
C | 2 | a0001c0001t0002g0214 a0001c0001t0017g0256 |
2 | HG02738.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.720+273_720+294del others(22): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | ||||||
chr21:43018474 | CCACACAC others(17): Show |
C | 8 | a0001c0001t0002g0205 a0001c0001t0002g0212 a0001c0001t0002g0233 others(5): Show |
8 | HG00438.hp1 HG00642.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.720+271_720+294del others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | ||||||
chr21:43018474 | CCACACAC others(19): Show |
C | 13 | a0001c0001t0002g0215 a0001c0001t0002g0220 a0001c0001t0002g0235 others(10): Show |
13 | HG00099.hp1 HG01243.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.720+269_720+294del others(26): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | ||||||
chr21:43018475 | CACACACA others(4): Show |
C | 1 | a0001c0001t0001g0087 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.720+246_720+256del others(11): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | |||||||
chr21:43018475 | CACACACA others(6): Show |
C | 9 | a0001c0001t0001g0021 a0001c0001t0001g0057 a0001c0001t0001g0064 others(6): Show |
9 | HG01070.hp1 HG01496.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.720+246_720+258del others(13): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | |||||||
chr21:43018475 | CACACACA others(8): Show |
C | 19 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0040 others(16): Show |
19 | HG00423.hp2 HG00621.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.720+246_720+260del others(15): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | |||||||
chr21:43018475 | CACACACA others(10): Show |
C | 22 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0060 others(19): Show |
23 | HG01168.hp2 HG01192.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.720+246_720+262del others(17): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | |||||||
chr21:43018475 | CACACACA others(12): Show |
C | 11 | a0001c0001t0005g0200 a0001c0001t0005g0275 a0001c0001t0006g0204 others(8): Show |
11 | HG02258.hp1 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.720+246_720+264del others(19): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | |||||||
chr21:43018475 | CACACACA others(14): Show |
C | 25 | a0001c0001t0005g0174 a0001c0001t0005g0176 a0001c0001t0005g0180 others(22): Show |
26 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.720+246_720+266del others(21): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | |||||||
chr21:43018475 | CACACACA others(16): Show |
C | 15 | a0001c0001t0001g0099 a0001c0001t0002g0207 a0001c0001t0002g0216 others(12): Show |
15 | HG00140.hp1 HG01069.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.720+246_720+268del others(23): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | |||||||
chr21:43018475 | CACACACA others(18): Show |
C | 29 | a0001c0001t0001g0218 a0001c0001t0002g0016 a0001c0001t0002g0189 others(26): Show |
29 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.720+246_720+270del others(25): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | |||||||
chr21:43018475 | CACACACA others(20): Show |
C | 2 | a0001c0001t0002g0239 a0001c0001t0002g0249 |
2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.720+246_720+272del others(27): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | |||||||
chr21:43018476 | A | C | 11 | a0001c0001t0001g0135 a0001c0001t0002g0005 a0001c0001t0002g0261 others(8): Show |
12 | HG02129.hp2 NA18966.hp2 NA18983.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+246A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018476 | |||||||
chr21:43018477 | CACACACA others(6): Show |
C | 7 | a0001c0001t0008g0157 a0001c0001t0008g0159 a0001c0001t0008g0162 others(4): Show |
7 | HG00140.hp2 HG01099.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.720+248_720+260del others(13): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018477 | |||||||
chr21:43018477 | CACACACA others(8): Show |
C | 5 | a0001c0001t0008g0015 a0001c0001t0008g0156 a0001c0001t0008g0160 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+248_720+262del others(15): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018477 | |||||||
chr21:43018477 | CACACACA others(14): Show |
C | 5 | a0001c0001t0005g0175 a0001c0001t0005g0177 a0001c0001t0005g0179 others(2): Show |
5 | HG00423.hp1 HG00733.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+248_720+268del others(21): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018477 | |||||||
chr21:43018477 | CACACACA others(16): Show |
C | 22 | a0001c0001t0001g0088 a0001c0001t0004g0022 a0001c0001t0004g0024 others(19): Show |
22 | HG00544.hp1 HG00642.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.720+248_720+270del others(23): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018477 | |||||||
chr21:43018478 | A | C | 11 | a0001c0001t0001g0135 a0001c0001t0002g0005 a0001c0001t0002g0261 others(8): Show |
12 | HG02129.hp2 NA18966.hp2 NA18983.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+248A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018478 | |||||||
chr21:43018480 | A | C | 11 | a0001c0001t0001g0135 a0001c0001t0002g0005 a0001c0001t0002g0261 others(8): Show |
12 | HG02129.hp2 NA18966.hp2 NA18983.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+250A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018480 | |||||||
chr21:43018482 | A | C | 15 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0135 others(12): Show |
16 | HG01074.hp1 HG01361.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.720+252A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018482 | |||||||
chr21:43018484 | A | C | 6 | a0001c0001t0001g0067 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG01928.hp2 HG02129.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+254A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018484 | |||||||
chr21:43018484 | A | G | 11 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0002g0005 others(8): Show |
12 | HG01074.hp1 HG01361.hp1 NA18966.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+254A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018484 | |||||||
chr21:43018485 | CACACACA others(18): Show |
C | 9 | a0001c0001t0002g0005 a0001c0001t0002g0261 a0001c0001t0002g0262 others(6): Show |
10 | NA18966.hp2 NA18983.hp2 NA18986.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+256_720+280del others(25): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018485 | |||||||
chr21:43018486 | A | C | 17 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0075 others(14): Show |
17 | HG00323.hp2 HG00597.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.720+256A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018486 | |||||||
chr21:43018486 | A | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0134 a0001c0001t0001g0146 others(2): Show |
5 | HG01928.hp2 NA18522.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+256A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018486 | |||||||
chr21:43018487 | CACACACA others(16): Show |
C | 1 | a0001c0001t0002g0284 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.720+258_720+280del others(23): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018487 | |||||||
chr21:43018488 | A | C | 47 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0032 others(44): Show |
47 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.720+258A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018488 | |||||||
chr21:43018488 | A | G | 12 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0120 others(9): Show |
12 | HG00597.hp1 HG00673.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+258A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018488 | |||||||
chr21:43018490 | A | C | 46 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0057 others(43): Show |
46 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.720+260A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018490 | |||||||
chr21:43018490 | A | G | 35 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0032 others(32): Show |
35 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.720+260A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018490 | |||||||
chr21:43018491 | CACACACA others(10): Show |
C | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.720+262_720+278del others(17): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018491 | |||||||
chr21:43018492 | A | C | 99 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0026 others(96): Show |
99 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.720+262A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018492 | |||||||
chr21:43018492 | A | G | 14 | a0001c0001t0001g0031 a0001c0001t0001g0058 a0001c0001t0001g0066 others(11): Show |
14 | HG00280.hp1 HG00738.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.720+262A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018492 | |||||||
chr21:43018494 | A | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(136): Show |
140 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.720+264A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018494 | |||||||
chr21:43018494 | A | G | 4 | a0001c0001t0007g0010 a0001c0001t0011g0281 a0001c0001t0023g0054 others(1): Show |
4 | HG02559.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+264A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018494 | |||||||
chr21:43018496 | A | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(147): Show |
152 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.720+266A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018496 | |||||||
chr21:43018498 | A | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(152): Show |
157 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.720+268A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018498 | |||||||
chr21:43018500 | A | C | 203 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(200): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.720+270A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018500 | |||||||
chr21:43018502 | A | C | 270 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(267): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.720+272A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018502 | |||||||
chr21:43018502 | A | T | 1 | a0001c0001t0007g0012 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.720+272A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018502 | |||||||
chr21:43018504 | A | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(270): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.720+274A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018504 | |||||||
chr21:43018506 | A | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(271): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.720+276A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018506 | |||||||
chr21:43018508 | A | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(265): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.720+278A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018508 | |||||||
chr21:43018508 | A | G | 4 | a0001c0001t0002g0266 a0001c0001t0002g0269 a0001c0001t0002g0277 others(1): Show |
4 | NA18954.hp2 NA18979.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+278A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018508 | |||||||
chr21:43018509 | CA | C | 4 | a0001c0001t0002g0266 a0001c0001t0002g0269 a0001c0001t0002g0277 others(1): Show |
4 | NA18954.hp2 NA18979.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+280delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018509 | |||||||
chr21:43018510 | A | C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(209): Show |
214 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.720+280A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018510 | |||||||
chr21:43018512 | A | C | 90 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0030 others(87): Show |
91 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.720+282A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018512 | |||||||
chr21:43018514 | A | C | 8 | a0001c0001t0001g0055 a0001c0001t0001g0063 a0001c0001t0001g0089 others(5): Show |
8 | HG00280.hp1 HG00733.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+284A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018514 | |||||||
chr21:43018516 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.720+286A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018516 | |||||||
chr21:43018529 | T | C | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+299T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018529 | |||||||
chr21:43018679 | A | G | 59 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0004g0022 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.720+449A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018679 | |||||||
chr21:43018726 | G | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(66): Show |
70 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.720+496G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018726 | |||||||
chr21:43018746 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.720+516C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018746 | |||||||
chr21:43018895 | C | G | 24 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0004g0022 others(21): Show |
24 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.720+665C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018895 | |||||||
chr21:43018958 | G | A | 1 | a0001c0002t0052g0332 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.720+728G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018958 | |||||||
chr21:43018994 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.720+764A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018994 | |||||||
chr21:43019063 | C | T | 1 | a0001c0002t0003g0331 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.720+833C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019063 | |||||||
chr21:43019084 | C | CA | 11 | a0001c0001t0004g0049 a0001c0001t0005g0181 a0001c0001t0005g0187 others(8): Show |
11 | HG00673.hp2 HG01175.hp1 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.720+870dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019084 | ||||||
chr21:43019084 | CA | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(216): Show |
222 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.720+870delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019084 | ||||||
chr21:43019196 | G | C | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.720+966G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019196 | |||||||
chr21:43019222 | G | A | 74 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(71): Show |
75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.720+992G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019222 | |||||||
chr21:43019234 | G | A | 296 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(293): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.720+1004G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019234 | |||||||
chr21:43019302 | G | A | 1 | a0001c0002t0009g0309 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.720+1072G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019302 | |||||||
chr21:43019306 | T | C | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.720+1076T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019306 | |||||||
chr21:43019379 | A | G | 284 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(281): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.720+1149A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019379 | |||||||
chr21:43019409 | C | CA | 244 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(241): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.720+1189dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019409 | ||||||
chr21:43019409 | C | CAA | 36 | a0001c0001t0001g0097 a0001c0001t0001g0102 a0001c0001t0001g0136 others(33): Show |
36 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.720+1188_720+1189d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019409 | ||||||
chr21:43019419 | AC | A | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+1190delC | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019419 | |||||||
chr21:43019420 | C | A | 284 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(281): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.720+1190C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019420 | |||||||
chr21:43019420 | C | CAA | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.720+1191_720+1192i others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019420 | ||||||
chr21:43019427 | T | G | 1 | a0001c0001t0017g0256 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.720+1197T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019427 | |||||||
chr21:43019468 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.720+1238T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019468 | |||||||
chr21:43019507 | T | C | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.720+1277T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019507 | |||||||
chr21:43019743 | C | T | 6 | a0001c0001t0008g0156 a0001c0001t0008g0158 a0001c0001t0008g0161 others(3): Show |
6 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+1513C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019743 | |||||||
chr21:43019762 | G | A | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.720+1532G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019762 | |||||||
chr21:43019779 | C | T | 3 | a0001c0002t0003g0302 a0001c0002t0003g0304 a0001c0002t0003g0338 |
3 | NA18988.hp2 NA18999.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.721-1524C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019779 | |||||||
chr21:43019831 | T | C | 285 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.721-1472T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019831 | |||||||
chr21:43019914 | C | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(223): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.721-1389C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019914 | |||||||
chr21:43019925 | A | AT | 6 | a0001c0002t0003g0304 a0001c0002t0003g0323 a0001c0002t0003g0334 others(3): Show |
6 | HG02080.hp1 HG02148.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-1353dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019925 | ||||||
chr21:43019925 | AT | A | 37 | a0001c0001t0002g0239 a0001c0001t0002g0250 a0001c0001t0002g0251 others(34): Show |
37 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.721-1353delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019925 | ||||||
chr21:43019925 | ATT | A | 141 | a0001c0001t0001g0040 a0001c0001t0001g0061 a0001c0001t0001g0068 others(138): Show |
143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.721-1354_721-1353d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019925 | ||||||
chr21:43019925 | ATTT | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(107): Show |
112 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.721-1355_721-1353d others(5): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019925 | ||||||
chr21:43019925 | ATTTT | A | 6 | a0001c0001t0001g0073 a0001c0001t0001g0091 a0001c0001t0001g0147 others(3): Show |
6 | HG00280.hp1 HG01074.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.721-1356_721-1353d others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019925 | ||||||
chr21:43020309 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.721-994C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020309 | |||||||
chr21:43020332 | G | A | 1 | a0001c0001t0008g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.721-971G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020332 | |||||||
chr21:43020373 | A | T | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-930A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020373 | |||||||
chr21:43020416 | C | T | 59 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0004g0022 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.721-887C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020416 | |||||||
chr21:43020532 | G | A | 1 | a0001c0002t0003g0341 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.721-771G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020532 | |||||||
chr21:43020655 | C | G | 6 | a0001c0001t0011g0278 a0001c0001t0011g0279 a0001c0001t0011g0280 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.721-648C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020655 | |||||||
chr21:43020905 | A | G | 1 | a0001c0002t0003g0297 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.721-398A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020905 | |||||||
chr21:43020929 | G | A | 1 | a0001c0001t0002g0189 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.721-374G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020929 | |||||||
chr21:43020989 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.721-314G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020989 | |||||||
chr21:43021081 | C | T | 1 | a0001c0001t0006g0194 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.721-222C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43021081 | |||||||
chr21:43021143 | G | A | 1 | a0001c0001t0006g0198 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.721-160G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43021143 | |||||||
chr21:43021182 | G | A | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-121G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43021182 | |||||||
chr21:43021549 | A | G | 3 | a0001c0001t0002g0230 a0001c0001t0002g0236 a0001c0001t0047g0232 |
3 | HG02559.hp1 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.849+118A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43021549 | |||||||
chr21:43021625 | C | T | 2 | a0001c0001t0010g0036 a0001c0001t0010g0037 |
2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.849+194C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43021625 | |||||||
chr21:43021647 | T | A | 1 | a0001c0001t0026g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.849+216T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43021647 | |||||||
chr21:43021795 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.849+364G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43021795 | |||||||
chr21:43021858 | A | C | 286 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(283): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.849+427A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43021858 | |||||||
chr21:43021871 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0155 |
2 | NA18956.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.849+440T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43021871 | |||||||
chr21:43022086 | C | G | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.849+655C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022086 | |||||||
chr21:43022204 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.849+773C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022204 | |||||||
chr21:43022229 | G | A | 2 | a0001c0001t0004g0048 a0001c0001t0008g0157 |
2 | HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.849+798G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022229 | |||||||
chr21:43022278 | G | A | 74 | a0001c0001t0001g0218 a0001c0001t0002g0005 a0001c0001t0002g0016 others(71): Show |
75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.849+847G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022278 | |||||||
chr21:43022281 | C | T | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.849+850C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022281 | |||||||
chr21:43022515 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.849+1084G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022515 | |||||||
chr21:43022776 | G | A | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+1345G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022776 | |||||||
chr21:43022792 | A | G | 1 | a0001c0001t0008g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.849+1361A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022792 | |||||||
chr21:43022799 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.849+1368T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022799 | |||||||
chr21:43022999 | A | T | 2 | a0001c0001t0023g0054 a0001c0001t0023g0117 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.849+1568A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022999 | |||||||
chr21:43023046 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.849+1615G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023046 | |||||||
chr21:43023048 | G | A | 22 | a0001c0001t0008g0015 a0001c0001t0008g0156 a0001c0001t0008g0157 others(19): Show |
22 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.849+1617G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023048 | |||||||
chr21:43023079 | C | T | 2 | a0001c0001t0004g0024 a0001c0001t0004g0046 |
2 | HG02071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.849+1648C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023079 | |||||||
chr21:43023084 | C | A | 1 | a0001c0002t0003g0350 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.849+1653C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023084 | |||||||
chr21:43023383 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.850-1488C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023383 | |||||||
chr21:43023541 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.850-1330G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023541 | |||||||
chr21:43023629 | A | AT | 195 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(192): Show |
198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.850-1230dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr21 | 43023629 | ||||||
chr21:43023641 | T | A | 1 | a0001c0002t0003g0297 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.850-1230T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023641 | |||||||
chr21:43023684 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.850-1187G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023684 | |||||||
chr21:43023700 | C | T | 54 | a0001c0001t0001g0030 a0001c0001t0004g0022 a0001c0001t0004g0023 others(51): Show |
55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.850-1171C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023700 | |||||||
chr21:43023761 | T | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.850-1110T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023761 | |||||||
chr21:43023771 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.850-1100T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023771 | |||||||
chr21:43023916 | A | AT | 12 | a0001c0001t0001g0139 a0001c0001t0001g0145 a0001c0001t0002g0266 others(9): Show |
12 | HG00423.hp1 HG02040.hp1 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.850-940dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr21 | 43023916 | ||||||
chr21:43023954 | G | A | 1 | a0001c0001t0008g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.850-917G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023954 | |||||||
chr21:43024062 | G | A | 3 | a0001c0001t0002g0230 a0001c0001t0002g0236 a0001c0001t0047g0232 |
3 | HG02559.hp1 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.850-809G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024062 | |||||||
chr21:43024068 | A | G | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.850-803A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024068 | |||||||
chr21:43024169 | C | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(115): Show |
120 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.850-702C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024169 | |||||||
chr21:43024261 | T | C | 6 | a0001c0001t0007g0104 a0001c0001t0007g0105 a0001c0001t0007g0106 others(3): Show |
6 | HG02145.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-610T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024261 | |||||||
chr21:43024421 | G | A | 1 | a0001c0002t0003g0311 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.850-450G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024421 | |||||||
chr21:43024456 | C | T | 7 | a0001c0001t0011g0278 a0001c0001t0011g0279 a0001c0001t0011g0280 others(4): Show |
7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-415C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024456 | |||||||
chr21:43024571 | C | T | 1 | a0001c0001t0007g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.850-300C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024571 | |||||||
chr21:43024623 | C | T | 1 | a0001c0001t0005g0186 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.850-248C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024623 | |||||||
chr21:43024665 | G | A | 287 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(284): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.850-206G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024665 | |||||||
chr21:43024666 | C | T | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.850-205C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024666 | |||||||
chr21:43024667 | A | G | 287 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(284): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.850-204A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024667 | |||||||
chr21:43025039 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.926+92T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025039 | |||||||
chr21:43025049 | C | G | 3 | a0001c0001t0027g0173 a0001c0001t0027g0188 a0001c0001t0043g0193 |
3 | HG02809.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.926+102C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025049 | |||||||
chr21:43025075 | C | T | 55 | a0001c0001t0001g0030 a0001c0001t0004g0022 a0001c0001t0004g0023 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.926+128C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025075 | |||||||
chr21:43025182 | C | T | 136 | a0001c0001t0001g0030 a0001c0001t0002g0005 a0001c0001t0002g0016 others(133): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.926+235C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025182 | |||||||
chr21:43025410 | G | T | 2 | a0001c0001t0031g0121 a0001c0001t0042g0122 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.926+463G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025410 | |||||||
chr21:43025452 | G | A | 1 | a0001c0001t0008g0160 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.926+505G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025452 | |||||||
chr21:43025454 | G | A | 7 | a0001c0002t0009g0006 a0001c0002t0009g0296 a0001c0002t0009g0307 others(4): Show |
7 | HG00639.hp1 HG00738.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.926+507G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025454 | |||||||
chr21:43025523 | C | T | 2 | a0001c0002t0028g0287 a0001c0002t0028g0288 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.926+576C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025523 | |||||||
chr21:43025677 | A | T | 294 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(291): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.926+730A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025677 | |||||||
chr21:43025855 | G | A | 1 | a0001c0001t0010g0035 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.926+908G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025855 | |||||||
chr21:43025920 | G | T | 57 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.926+973G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025920 | |||||||
chr21:43026231 | C | T | 1 | a0001c0002t0003g0310 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.926+1284C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026231 | |||||||
chr21:43026345 | T | A | 58 | a0001c0001t0001g0030 a0001c0001t0004g0022 a0001c0001t0004g0023 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.926+1398T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026345 | |||||||
chr21:43026485 | G | A | 4 | a0001c0001t0027g0173 a0001c0001t0027g0188 a0001c0002t0028g0287 others(1): Show |
4 | HG02809.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.926+1538G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026485 | |||||||
chr21:43026490 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.926+1543G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026490 | |||||||
chr21:43026711 | C | T | 1 | a0001c0002t0003g0313 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.926+1764C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026711 | |||||||
chr21:43026818 | C | T | 63 | a0001c0001t0001g0030 a0001c0001t0004g0022 a0001c0001t0004g0023 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.926+1871C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026818 | |||||||
chr21:43026847 | GC | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(196): Show |
202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.927-1854delC | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026847 | |||||||
chr21:43026906 | A | G | 1 | a0001c0001t0002g0214 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.927-1796A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026906 | |||||||
chr21:43026971 | A | G | 1 | a0001c0001t0020g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.927-1731A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026971 | |||||||
chr21:43027101 | C | T | 55 | a0001c0001t0001g0030 a0001c0001t0004g0022 a0001c0001t0004g0023 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.927-1601C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027101 | |||||||
chr21:43027132 | A | C | 1 | a0001c0001t0006g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.927-1570A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027132 | |||||||
chr21:43027133 | G | C | 56 | a0001c0001t0001g0030 a0001c0001t0004g0022 a0001c0001t0004g0023 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.927-1569G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027133 | |||||||
chr21:43027149 | T | C | 1 | a0001c0001t0019g0285 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.927-1553T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027149 | |||||||
chr21:43027237 | A | G | 237 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(234): Show |
240 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.927-1465A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027237 | |||||||
chr21:43027289 | C | T | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.927-1413C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027289 | |||||||
chr21:43027302 | G | A | 55 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.927-1400G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027302 | |||||||
chr21:43027678 | C | G | 55 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.927-1024C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027678 | |||||||
chr21:43027746 | C | CCT | 55 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.927-956_927-955ins others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027746 | |||||||
chr21:43027746 | C | T | 1 | a0001c0001t0014g0111 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.927-956C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027746 | |||||||
chr21:43027768 | G | T | 55 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.927-934G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027768 | |||||||
chr21:43027829 | T | A | 1 | a0001c0001t0013g0084 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.927-873T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027829 | |||||||
chr21:43027840 | C | T | 4 | a0001c0002t0012g0291 a0001c0002t0012g0353 a0001c0002t0012g0354 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.927-862C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027840 | |||||||
chr21:43027910 | C | T | 1 | a0001c0001t0043g0193 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.927-792C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027910 | |||||||
chr21:43028035 | C | T | 5 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0139 others(2): Show |
5 | HG00673.hp1 HG01934.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.927-667C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028035 | |||||||
chr21:43028217 | T | C | 3 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0032g0290 |
3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.927-485T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028217 | |||||||
chr21:43028274 | C | T | 113 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(110): Show |
115 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.927-428C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028274 | |||||||
chr21:43028298 | G | A | 1 | a0001c0001t0007g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.927-404G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028298 | |||||||
chr21:43028449 | C | CA | 238 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(235): Show |
241 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.927-242dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr21 | 43028449 | ||||||
chr21:43028449 | CA | C | 54 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(51): Show |
55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.927-242delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr21 | 43028449 | ||||||
chr21:43028470 | C | T | 3 | a0001c0001t0022g0025 a0001c0001t0022g0053 a0001c0001t0035g0052 |
3 | HG03453.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.927-232C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028470 | |||||||
chr21:43028524 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.927-178C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028524 | |||||||
chr21:43028608 | C | T | 74 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0189 others(71): Show |
75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.927-94C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028608 | |||||||
chr21:43028619 | G | A | 2 | a0001c0001t0020g0172 a0001c0001t0020g0183 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.927-83G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028619 | |||||||
chr21:43028653 | G | C | 73 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.927-49G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028653 | |||||||
chr21:43028662 | G | A | 2 | a0001c0001t0010g0036 a0001c0001t0010g0037 |
2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.927-40G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028662 | |||||||
chr21:43028665 | G | A | 73 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.927-37G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028665 | |||||||
chr21:43028918 | G | T | 1 | a0001c0001t0011g0279 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1099+44G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43028918 | |||||||
chr21:43028967 | A | AG | 3 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0067 |
3 | NA18970.hp1 NA18971.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1099+95dupG | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43028967 | ||||||
chr21:43028985 | G | A | 282 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(279): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1099+111G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43028985 | |||||||
chr21:43028990 | C | T | 1 | a0001c0001t0002g0228 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1099+116C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43028990 | |||||||
chr21:43029098 | A | G | 1 | a0001c0002t0003g0315 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1099+224A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029098 | |||||||
chr21:43029194 | G | T | 2 | a0001c0001t0019g0286 a0001c0001t0032g0290 |
2 | HG03654.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1099+320G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029194 | |||||||
chr21:43029231 | C | T | 74 | a0001c0001t0001g0103 a0001c0001t0001g0130 a0001c0001t0001g0218 others(71): Show |
75 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1099+357C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029231 | |||||||
chr21:43029279 | G | A | 72 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0002g0207 others(69): Show |
74 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1099+405G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029279 | |||||||
chr21:43029311 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1099+437C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029311 | |||||||
chr21:43029312 | G | A | 5 | a0001c0001t0008g0015 a0001c0001t0019g0285 a0001c0001t0019g0286 others(2): Show |
5 | HG02109.hp1 HG03471.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099+438G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029312 | |||||||
chr21:43029424 | G | GTTTTTTT | 33 | a0001c0001t0019g0286 a0001c0001t0032g0290 a0001c0002t0003g0300 others(30): Show |
33 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1100-451_1100-445d others(9): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | ||||||
chr21:43029424 | G | GTTTTTTT others(1): Show |
25 | a0001c0001t0001g0026 a0001c0001t0008g0156 a0001c0001t0008g0157 others(22): Show |
25 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1100-452_1100-445d others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | ||||||
chr21:43029424 | G | GTTTTTTT others(4): Show |
1 | a0001c0002t0028g0288 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1100-455_1100-445d others(13): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | ||||||
chr21:43029424 | G | GTTTTTTT others(5): Show |
2 | a0001c0001t0044g0289 a0001c0002t0028g0287 |
2 | HG02055.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1100-456_1100-445d others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | ||||||
chr21:43029424 | G | GTTTTTTT others(8): Show |
3 | a0001c0002t0003g0313 a0001c0002t0003g0316 a0001c0002t0003g0341 |
3 | NA19080.hp1 NA19085.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1100-459_1100-445d others(17): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | ||||||
chr21:43029424 | G | GTTTTTTT others(9): Show |
3 | a0001c0002t0003g0312 a0001c0002t0003g0324 a0001c0002t0003g0344 |
3 | HG01081.hp2 HG02615.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1100-460_1100-445d others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | ||||||
chr21:43029424 | G | GTTTTTTT others(10): Show |
5 | a0001c0002t0003g0297 a0001c0002t0003g0310 a0001c0002t0003g0315 others(2): Show |
5 | HG01496.hp2 HG04204.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1100-461_1100-445d others(19): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | ||||||
chr21:43029424 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0017g0256 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1100-462_1100-445d others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | ||||||
chr21:43029424 | G | GTTTTTTT others(12): Show |
1 | a0001c0002t0052g0332 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1100-463_1100-445d others(21): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | ||||||
chr21:43029424 | GTT | G | 11 | a0001c0001t0001g0031 a0001c0001t0001g0132 a0001c0001t0001g0139 others(8): Show |
11 | HG00438.hp2 HG02056.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.1100-446_1100-445d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | ||||||
chr21:43029424 | GTTT | G | 246 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(243): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1100-447_1100-445d others(5): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | ||||||
chr21:43029433 | T | G | 2 | a0001c0001t0002g0219 a0001c0001t0002g0246 |
2 | HG01167.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1100-457T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029433 | |||||||
chr21:43029561 | C | G | 55 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1100-329C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029561 | |||||||
chr21:43029580 | T | C | 5 | a0001c0001t0019g0285 a0001c0001t0019g0286 a0001c0001t0025g0017 others(2): Show |
5 | HG00639.hp2 HG00642.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1100-310T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029580 | |||||||
chr21:43029732 | A | ACCCCGCC others(11): Show |
1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-158_1100-157i others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029732 | |||||||
chr21:43029732 | A | AGAAACAG others(644): Show |
2 | a0001c0001t0019g0285 a0001c0001t0032g0290 |
2 | NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1100-148_1100-147i others(653): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029732 | ||||||
chr21:43029732 | A | AGAAACAG others(646): Show |
1 | a0001c0001t0019g0286 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1100-148_1100-147i others(655): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029732 | ||||||
chr21:43029733 | G | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-157G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029733 | |||||||
chr21:43029734 | A | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-156A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029734 | |||||||
chr21:43029735 | A | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-155A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029735 | |||||||
chr21:43029736 | A | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-154A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029736 | |||||||
chr21:43029738 | A | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-152A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029738 | |||||||
chr21:43029741 | T | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-149T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029741 | |||||||
chr21:43029744 | T | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-146T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029744 | |||||||
chr21:43029745 | T | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-145T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029745 | |||||||
chr21:43029747 | A | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-143A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029747 | |||||||
chr21:43029748 | A | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-142A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029748 | |||||||
chr21:43029749 | T | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-141T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029749 | |||||||
chr21:43029753 | T | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-137T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029753 | |||||||
chr21:43029754 | G | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-136G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029754 | |||||||
chr21:43029755 | T | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-135T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029755 | |||||||
chr21:43029763 | T | C | 1 | a0001c0002t0003g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-127T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029763 | |||||||
chr21:43029806 | C | T | 2 | a0001c0002t0028g0287 a0001c0002t0028g0288 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1100-84C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029806 | |||||||
chr21:43029807 | G | A | 55 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1100-83G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029807 |