Item | Value |
---|---|
geneid | 56902 |
ensemblid | ENSG00000115946.8 |
hgncid | 32790 |
symbol | PNO1 |
name | partner of NOB1 homolog |
refseq_nuc | NM_020143.4 |
refseq_prot | NP_064528.1 |
ensembl_nuc | ENST00000263657.7 |
ensembl_prot | ENSP00000263657.2 |
mane_status | MANE Select |
chr | chr2 |
start | 68157888 |
end | 68176238 |
strand | + |
ver | v1.2 |
region | chr2:68157888-68176238 |
region5000 | chr2:68152888-68181238 |
regionname0 | PNO1_chr2_68157888_68176238 |
regionname5000 | PNO1_chr2_68152888_68181238 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 252 | 303 | 87 | 58 | 118 | 9 | 31 | 88 | PNO1_chr2_68152888_68181238 | PNO1 | MESEM others(247): Show |
chr2 | 68152888 | 68181238 |
a0002 | 1/1 | 252 | 132 | 2 | 26 | 82 | 5 | 15 | 70 | PNO1_chr2_68152888_68181238 | PNO1 | MESEM others(247): Show |
chr2 | 68152888 | 68181238 |
a0003 | 0/0 | 252 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | MESEM others(247): Show |
chr2 | 68152888 | 68181238 |
a0004 | 0/0 | 252 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | MESEM others(247): Show |
chr2 | 68152888 | 68181238 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 756 | 165 | 73 | 29 | 42 | 4 | 17 | PNO1_chr2_68152888_68181238 | PNO1 | ATGGA others(751): Show |
chr2 | 68152888 | 68181238 | ||
a0001c0003 | 0/0 | 756 | 130 | 6 | 29 | 76 | 5 | 14 | PNO1_chr2_68152888_68181238 | PNO1 | ATGGA others(751): Show |
chr2 | 68152888 | 68181238 | ||
a0001c0005 | 0/0 | 756 | 8 | 8 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | ATGGA others(751): Show |
chr2 | 68152888 | 68181238 | ||
a0002c0002 | 1/1 | 756 | 132 | 2 | 26 | 82 | 5 | 15 | PNO1_chr2_68152888_68181238 | PNO1 | ATGGA others(751): Show |
chr2 | 68152888 | 68181238 | ||
a0003c0004 | 0/0 | 756 | 8 | 7 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | ATGGA others(751): Show |
chr2 | 68152888 | 68181238 | ||
a0004c0006 | 0/0 | 756 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | ATGGA others(751): Show |
chr2 | 68152888 | 68181238 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2231 | 73 | 51 | 13 | 2 | 0 | 7 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0001c0001t0003 | 0/0 | 2231 | 78 | 17 | 14 | 35 | 4 | 8 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0001c0001t0004 | 0/0 | 2231 | 3 | 0 | 1 | 0 | 0 | 2 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0001c0001t0005 | 0/0 | 2235 | 5 | 0 | 0 | 5 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2230): Show |
chr2 | 68152888 | 68181238 |
a0001c0001t0007 | 0/0 | 2231 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0001c0001t0009 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0001c0001t0010 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0001c0001t0011 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0001c0001t0012 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0001c0001t0013 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0001c0003t0001 | 0/0 | 2231 | 114 | 6 | 27 | 62 | 5 | 14 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0001c0003t0002 | 0/0 | 2242 | 2 | 0 | 2 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2237): Show |
chr2 | 68152888 | 68181238 |
a0001c0003t0004 | 0/0 | 2231 | 14 | 0 | 0 | 14 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0001c0005t0001 | 0/0 | 2231 | 6 | 6 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0001c0005t0006 | 0/0 | 2231 | 2 | 2 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0002c0002t0001 | 0/0 | 2231 | 3 | 0 | 1 | 0 | 1 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0002c0002t0002 | 1/1 | 2242 | 128 | 2 | 25 | 81 | 4 | 14 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2237): Show |
chr2 | 68152888 | 68181238 |
a0002c0002t0008 | 0/0 | 2242 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2237): Show |
chr2 | 68152888 | 68181238 |
a0003c0004t0001 | 0/0 | 2231 | 7 | 6 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0003c0004t0003 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
a0004c0006t0001 | 0/0 | 2231 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | GCAGC others(2226): Show |
chr2 | 68152888 | 68181238 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0003 | 0/0 | 17 | 1 | 3 | 12 | 1 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0020 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0042 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0005g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0007g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0009g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0011g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0001t0013g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0001 | 0/0 | 27 | 0 | 6 | 16 | 0 | 5 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0005 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0007 | 0/0 | 5 | 0 | 3 | 1 | 1 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0026 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0004g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0003t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0005t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0005t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0005t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0005t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0005t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0001c0005t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0002 | 1/0 | 25 | 0 | 2 | 18 | 0 | 4 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0010 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0002c0002t0008g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0003c0004t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0003c0004t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0003c0004t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0003c0004t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0003c0004t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0003c0004t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0003c0004t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0003c0004t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
a0004c0006t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0024 | EUR | GBR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0096 | EUR | GBR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0157 | EUR | GBR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0007 | EUR | GBR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00323 | hp1 | a0001 | c0003 | t0001 | g0022 | EUR | FIN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0188 | EUR | FIN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00408 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00423 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00438 | hp2 | a0001 | c0003 | t0001 | g0191 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00597 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00609 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00621 | hp1 | a0001 | c0003 | t0004 | g0001 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00621 | hp2 | a0001 | c0003 | t0001 | g0208 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0128 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00639 | hp2 | a0001 | c0003 | t0001 | g0271 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0223 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | CHS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00733 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0247 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0242 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0129 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0091 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01109 | hp1 | a0004 | c0006 | t0001 | g0240 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0105 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0107 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0195 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01243 | hp1 | a0003 | c0004 | t0001 | g0264 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0275 | AMR | PUR | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01255 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0220 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01257 | hp1 | a0001 | c0003 | t0002 | g0072 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0025 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01258 | hp1 | a0001 | c0003 | t0002 | g0073 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0225 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01346 | hp2 | a0001 | c0003 | t0001 | g0022 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01358 | hp1 | a0001 | c0003 | t0001 | g0183 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0258 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01361 | hp1 | a0001 | c0003 | t0001 | g0196 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0034 | EUR | IBS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0043 | EUR | IBS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0043 | EUR | IBS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0088 | EUR | IBS | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0221 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01891 | hp1 | a0003 | c0004 | t0003 | g0268 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0132 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0065 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01943 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01952 | hp1 | a0001 | c0003 | t0001 | g0238 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0130 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0069 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0228 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0071 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01993 | hp2 | a0001 | c0003 | t0001 | g0201 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02004 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02015 | hp1 | a0001 | c0003 | t0004 | g0001 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0237 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02055 | hp2 | a0003 | c0004 | t0001 | g0263 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02056 | hp1 | a0001 | c0003 | t0001 | g0226 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02071 | hp1 | a0001 | c0003 | t0001 | g0027 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02074 | hp1 | a0001 | c0003 | t0001 | g0204 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02129 | hp2 | a0001 | c0003 | t0001 | g0048 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02135 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0241 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02145 | hp2 | a0002 | c0002 | t0002 | g0125 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0150 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0198 | EAS | CDX | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0283 | EAS | CDX | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02165 | hp2 | a0001 | c0003 | t0001 | g0224 | EAS | CDX | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02273 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02293 | hp1 | a0001 | c0003 | t0001 | g0022 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0106 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0104 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02451 | hp1 | a0001 | c0001 | t0010 | g0004 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02523 | hp2 | a0001 | c0003 | t0001 | g0190 | EAS | KHV | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0248 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02615 | hp2 | a0003 | c0004 | t0001 | g0267 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02630 | hp2 | a0001 | c0001 | t0013 | g0165 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02647 | hp1 | a0001 | c0005 | t0001 | g0063 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0246 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02683 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0026 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0163 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02735 | hp2 | a0001 | c0003 | t0001 | g0048 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0186 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0187 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0189 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02922 | hp2 | a0001 | c0005 | t0001 | g0029 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0274 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03017 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0019 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | MSL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03130 | hp1 | a0003 | c0004 | t0001 | g0269 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03209 | hp1 | a0003 | c0004 | t0001 | g0266 | AFR | MSL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0156 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03239 | hp2 | a0001 | c0003 | t0001 | g0233 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | MSL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0034 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03491 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03492 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03516 | hp2 | a0001 | c0001 | t0012 | g0169 | AFR | ESN | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03540 | hp2 | a0001 | c0005 | t0001 | g0113 | AFR | GWD | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03579 | hp2 | a0001 | c0005 | t0001 | g0061 | AFR | MSL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0222 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0020 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0009 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0098 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0159 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0081 | SAS | BEB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | BEB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0212 | SAS | BEB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0026 | SAS | BEB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0016 | SAS | STU | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0016 | SAS | STU | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | BEB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0207 | SAS | STU | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0009 | SAS | STU | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0019 | SAS | STU | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG04204 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | STU | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | STU | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0181 | SAS | STU | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | YRI | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18522 | hp2 | a0001 | c0005 | t0006 | g0062 | AFR | YRI | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | CHB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18612 | hp2 | a0001 | c0003 | t0001 | g0216 | EAS | CHB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | CHB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | CHB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18941 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18943 | hp2 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18945 | hp1 | a0001 | c0003 | t0004 | g0025 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18947 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18948 | hp2 | a0001 | c0003 | t0004 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18949 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18950 | hp1 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18953 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18954 | hp2 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18956 | hp2 | a0001 | c0003 | t0001 | g0192 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18959 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18960 | hp2 | a0001 | c0003 | t0004 | g0210 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18964 | hp2 | a0001 | c0003 | t0004 | g0185 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18967 | hp2 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18972 | hp1 | a0001 | c0003 | t0004 | g0199 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18973 | hp2 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0026 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18986 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18988 | hp1 | a0001 | c0003 | t0004 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18988 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18989 | hp2 | a0001 | c0003 | t0004 | g0024 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18992 | hp2 | a0001 | c0003 | t0001 | g0194 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18993 | hp1 | a0001 | c0003 | t0001 | g0213 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18993 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0200 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18995 | hp1 | a0001 | c0003 | t0001 | g0209 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18997 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18997 | hp2 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18999 | hp1 | a0001 | c0003 | t0001 | g0211 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19001 | hp1 | a0001 | c0003 | t0001 | g0215 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19004 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19005 | hp1 | a0001 | c0003 | t0004 | g0025 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19006 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19010 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19012 | hp2 | a0001 | c0003 | t0004 | g0184 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | LWK | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19030 | hp2 | a0001 | c0005 | t0001 | g0064 | AFR | LWK | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19043 | hp1 | a0003 | c0004 | t0001 | g0265 | AFR | LWK | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19054 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19055 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19056 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19058 | hp2 | a0001 | c0003 | t0001 | g0193 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19059 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19059 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19060 | hp1 | a0001 | c0003 | t0004 | g0023 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19065 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0203 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19066 | hp2 | a0002 | c0002 | t0008 | g0016 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19072 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19072 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19075 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19075 | hp2 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19076 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19076 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19077 | hp1 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19078 | hp1 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19082 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19083 | hp2 | a0001 | c0003 | t0004 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19087 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19087 | hp2 | a0001 | c0003 | t0004 | g0005 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19089 | hp1 | a0001 | c0003 | t0001 | g0219 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19089 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19091 | hp1 | a0001 | c0003 | t0001 | g0205 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | YRI | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA19240 | hp2 | a0001 | c0005 | t0001 | g0112 | AFR | YRI | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ASW | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA20129 | hp2 | a0001 | c0005 | t0006 | g0029 | AFR | ASW | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0114 | EUR | TSI | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0136 | EUR | TSI | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0014 | EUR | TSI | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0097 | SAS | GIH | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0101 | SAS | GIH | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02559 | hp1 | a0003 | c0004 | t0001 | g0261 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0239 | AFR | USA | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | USA | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0085 | AFR | USA | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | USA | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA21309 | hp1 | a0001 | c0001 | t0011 | g0019 | AFR | LWK | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0080 | REF | REF | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0002 | REF | REF | PNO1_chr2_68152888_68181238 | PNO1 | chr2 | 68152888 | 68181238 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:68157965 | A | G | 3 | a0001 a0003 a0004 |
312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
missense_variant | MODERATE | c.31A>G | p.Arg11Gly | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 1/7 | 78/2242 | 31/759 | 11/252 | chr2 | 68157965 | |||
chr2:68158384 | G | C | 1 | a0003 | 8 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
missense_variant | MODERATE | c.212G>C | p.Gly71Ala | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/7 | 259/2242 | 212/759 | 71/252 | chr2 | 68158384 | |||
chr2:68162560 | G | A | 1 | a0004 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.517G>A | p.Gly173Arg | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/7 | 564/2242 | 517/759 | 173/252 | chr2 | 68162560 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:68158108 | C | G | 1 | a0001c0005 | 8 | HG02647.hp1 HG02922.hp2 HG03540.hp2 others(5): Show |
synonymous_variant | LOW | c.174C>G | p.Pro58Pro | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 1/7 | 221/2242 | 174/759 | 58/252 | chr2 | 68158108 | |||
chr2:68161691 | A | G | 2 | a0001c0003 a0004c0006 |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
synonymous_variant | LOW | c.366A>G | p.Lys122Lys | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 3/7 | 413/2242 | 366/759 | 122/252 | chr2 | 68161691 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:68157932 | G | C | 1 | a0001c0001t0007 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-3G>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 1/7 | 3 | chr2 | 68157932 | ||||||
chr2:68174880 | G | T | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*78G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 78 | chr2 | 68174880 | ||||||
chr2:68174991 | A | G | 1 | a0001c0001t0013 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 189 | chr2 | 68174991 | ||||||
chr2:68175021 | TA | T | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*221delA | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 221 | INFO_REALIGN_3_PRIME | chr2 | 68175021 | |||||
chr2:68175153 | A | G | 1 | a0001c0001t0012 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 351 | chr2 | 68175153 | ||||||
chr2:68175182 | T | C | 1 | a0001c0005t0006 | 2 | NA18522.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*380T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 380 | chr2 | 68175182 | ||||||
chr2:68175219 | C | A | 1 | a0001c0001t0009 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*417C>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 417 | chr2 | 68175219 | ||||||
chr2:68175228 | A | G | 4 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(1): Show |
85 | HG00140.hp1 HG00609.hp1 HG01069.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*426A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 426 | chr2 | 68175228 | ||||||
chr2:68175333 | C | T | 2 | a0001c0001t0004 a0001c0003t0004 |
17 | HG00621.hp1 HG00738.hp1 HG02015.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*531C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 531 | chr2 | 68175333 | ||||||
chr2:68175441 | T | C | 1 | a0002c0002t0008 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*639T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 639 | chr2 | 68175441 | ||||||
chr2:68175520 | C | T | 4 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(1): Show |
85 | HG00140.hp1 HG00609.hp1 HG01069.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*718C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 718 | chr2 | 68175520 | ||||||
chr2:68175654 | TTTGCAGT others(3): Show |
T | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*863_*872delTTGCAG others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 863 | INFO_REALIGN_3_PRIME | chr2 | 68175654 | |||||
chr2:68175691 | C | T | 1 | a0001c0001t0011 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*889C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 889 | chr2 | 68175691 | ||||||
chr2:68175698 | G | C | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*896G>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 896 | chr2 | 68175698 | ||||||
chr2:68175703 | A | G | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*901A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 901 | chr2 | 68175703 | ||||||
chr2:68175817 | T | C | 1 | a0001c0001t0010 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1015T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 1015 | chr2 | 68175817 | ||||||
chr2:68176206 | A | AACTT | 1 | a0001c0001t0005 | 5 | NA18973.hp1 NA18993.hp2 NA19004.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1409_*1412dupACTT | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 7/7 | 1413 | INFO_REALIGN_3_PRIME | chr2 | 68176206 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:68158186 | C | G | 1 | a0001c0003t0001g0283 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.207+45C>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 1/6 | chr2 | 68158186 | |||||||
chr2:68158199 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0053 others(6): Show |
13 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.207+58G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 1/6 | chr2 | 68158199 | |||||||
chr2:68158226 | C | T | 1 | a0002c0002t0002g0282 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.207+85C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 1/6 | chr2 | 68158226 | |||||||
chr2:68158579 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.357+50A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68158579 | |||||||
chr2:68158823 | C | T | 194 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(191): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.357+294C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68158823 | |||||||
chr2:68158835 | G | A | 1 | a0001c0003t0001g0136 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.357+306G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68158835 | |||||||
chr2:68158894 | C | T | 8 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0276 others(5): Show |
10 | HG01167.hp1 HG01243.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.357+365C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68158894 | |||||||
chr2:68159001 | T | A | 1 | a0002c0002t0002g0060 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.357+472T>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159001 | |||||||
chr2:68159019 | C | T | 1 | a0001c0001t0009g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.357+490C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159019 | |||||||
chr2:68159129 | A | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(113): Show |
175 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.357+600A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159129 | |||||||
chr2:68159146 | T | C | 3 | a0001c0001t0003g0019 a0001c0001t0003g0137 a0001c0001t0011g0019 |
4 | HG01074.hp2 HG03017.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+617T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159146 | |||||||
chr2:68159254 | ATG | A | 123 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0049 others(120): Show |
186 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.357+749_357+750del others(2): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 68159254 | ||||||
chr2:68159254 | ATGTG | A | 47 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0053 others(44): Show |
76 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.357+747_357+750del others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 68159254 | ||||||
chr2:68159256 | G | A | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.357+727G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159256 | |||||||
chr2:68159262 | G | A | 6 | a0001c0005t0001g0029 a0001c0005t0001g0061 a0001c0005t0001g0063 others(3): Show |
6 | HG02647.hp1 HG02922.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+733G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159262 | |||||||
chr2:68159274 | GTGTGTA | G | 8 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0276 others(5): Show |
10 | HG01167.hp1 HG01243.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.357+747_357+752del others(6): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 68159274 | ||||||
chr2:68159276 | GTGTA | G | 10 | a0001c0001t0001g0280 a0001c0001t0003g0021 a0001c0001t0003g0045 others(7): Show |
14 | HG02071.hp2 HG02074.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.357+749_357+752del others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 68159276 | ||||||
chr2:68159278 | G | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0050 others(110): Show |
169 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.357+749G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159278 | |||||||
chr2:68159280 | A | G | 16 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0074 others(13): Show |
18 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+751A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159280 | |||||||
chr2:68159452 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG01167.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.357+923C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159452 | |||||||
chr2:68159481 | C | T | 1 | a0001c0001t0013g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.357+952C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159481 | |||||||
chr2:68159482 | A | AG | 2 | a0001c0001t0001g0037 a0001c0001t0001g0135 |
3 | HG02109.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.357+955dupG | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 68159482 | ||||||
chr2:68159672 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.357+1143C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159672 | |||||||
chr2:68159693 | A | T | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.357+1164A>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159693 | |||||||
chr2:68159698 | G | T | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.357+1169G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159698 | |||||||
chr2:68159768 | C | A | 68 | a0001c0003t0001g0001 a0001c0003t0001g0005 a0001c0003t0001g0013 others(65): Show |
116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.357+1239C>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159768 | |||||||
chr2:68159780 | T | C | 1 | a0002c0002t0002g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.357+1251T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159780 | |||||||
chr2:68159792 | C | T | 2 | a0001c0001t0003g0043 a0001c0001t0003g0164 |
3 | HG01168.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.357+1263C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159792 | |||||||
chr2:68159946 | T | G | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.357+1417T>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159946 | |||||||
chr2:68159955 | C | G | 1 | a0001c0001t0003g0163 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.357+1426C>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159955 | |||||||
chr2:68159964 | A | AT | 74 | a0001c0001t0001g0028 a0001c0001t0001g0054 a0001c0001t0001g0055 others(71): Show |
108 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.357+1457dupT | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 68159964 | ||||||
chr2:68159964 | A | ATT | 19 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0059 others(16): Show |
25 | HG01891.hp2 HG01928.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.357+1456_357+1457d others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 68159964 | ||||||
chr2:68159964 | A | T | 3 | a0001c0001t0001g0270 a0001c0001t0003g0163 a0001c0001t0003g0180 |
3 | HG02135.hp1 HG02698.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.357+1435A>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68159964 | |||||||
chr2:68159964 | AT | A | 11 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(8): Show |
11 | HG01168.hp2 HG01975.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.357+1457delT | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 68159964 | ||||||
chr2:68160037 | C | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0053 others(6): Show |
13 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.357+1508C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68160037 | |||||||
chr2:68160336 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.358-1347C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68160336 | |||||||
chr2:68160442 | T | C | 1 | a0002c0002t0002g0071 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.358-1241T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68160442 | |||||||
chr2:68160469 | G | T | 1 | a0002c0002t0002g0060 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.358-1214G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68160469 | |||||||
chr2:68160470 | T | G | 1 | a0002c0002t0002g0060 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.358-1213T>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68160470 | |||||||
chr2:68160664 | A | G | 1 | a0001c0003t0001g0222 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.358-1019A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68160664 | |||||||
chr2:68160689 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.358-994C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68160689 | |||||||
chr2:68160698 | G | T | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.358-985G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68160698 | |||||||
chr2:68160831 | G | T | 11 | a0002c0002t0002g0011 a0002c0002t0002g0018 a0002c0002t0002g0070 others(8): Show |
16 | NA18946.hp2 NA18955.hp2 NA18961.hp2 others(13): Show |
intron_variant | MODIFIER | c.358-852G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68160831 | |||||||
chr2:68161000 | T | G | 122 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(119): Show |
183 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.358-683T>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161000 | |||||||
chr2:68161011 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.358-672G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161011 | |||||||
chr2:68161024 | C | T | 3 | a0001c0001t0003g0019 a0001c0001t0003g0137 a0001c0001t0011g0019 |
4 | HG01074.hp2 HG03017.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-659C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161024 | |||||||
chr2:68161039 | C | G | 3 | a0001c0001t0003g0019 a0001c0001t0003g0137 a0001c0001t0011g0019 |
4 | HG01074.hp2 HG03017.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-644C>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161039 | |||||||
chr2:68161061 | T | C | 2 | a0001c0001t0003g0166 a0001c0001t0003g0168 |
2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.358-622T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161061 | |||||||
chr2:68161104 | C | T | 1 | a0002c0002t0002g0115 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.358-579C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161104 | |||||||
chr2:68161112 | T | G | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.358-571T>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161112 | |||||||
chr2:68161151 | C | T | 1 | a0002c0002t0002g0114 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.358-532C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161151 | |||||||
chr2:68161254 | A | T | 1 | a0002c0002t0002g0060 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.358-429A>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161254 | |||||||
chr2:68161306 | A | G | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.358-377A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161306 | |||||||
chr2:68161307 | G | A | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.358-376G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161307 | |||||||
chr2:68161308 | A | C | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.358-375A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161308 | |||||||
chr2:68161315 | TGA | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0230 a0001c0001t0001g0235 others(2): Show |
6 | HG01884.hp1 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.358-361_358-360del others(2): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 68161315 | ||||||
chr2:68161540 | C | A | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.358-143C>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161540 | |||||||
chr2:68161559 | A | G | 1 | a0001c0003t0001g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.358-124A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 2/6 | chr2 | 68161559 | |||||||
chr2:68161814 | T | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0051 others(15): Show |
24 | HG00735.hp2 HG01167.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.441+48T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 3/6 | chr2 | 68161814 | |||||||
chr2:68161956 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0170 a0001c0001t0001g0171 others(4): Show |
8 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+190G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 3/6 | chr2 | 68161956 | |||||||
chr2:68161983 | A | G | 6 | a0001c0001t0001g0044 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
7 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+217A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 3/6 | chr2 | 68161983 | |||||||
chr2:68162034 | G | T | 2 | a0001c0003t0001g0233 a0001c0003t0001g0258 |
2 | HG01358.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.442-231G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 3/6 | chr2 | 68162034 | |||||||
chr2:68162085 | G | C | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.442-180G>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 3/6 | chr2 | 68162085 | |||||||
chr2:68162086 | C | G | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.442-179C>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 3/6 | chr2 | 68162086 | |||||||
chr2:68162095 | C | G | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.442-170C>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 3/6 | chr2 | 68162095 | |||||||
chr2:68162096 | G | C | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.442-169G>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 3/6 | chr2 | 68162096 | |||||||
chr2:68162117 | C | T | 1 | a0001c0003t0001g0220 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.442-148C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 3/6 | chr2 | 68162117 | |||||||
chr2:68162128 | G | T | 16 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(13): Show |
18 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.442-137G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 3/6 | chr2 | 68162128 | |||||||
chr2:68162144 | G | GA | 211 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(208): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.442-111dupA | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 68162144 | ||||||
chr2:68162349 | CTT | C | 68 | a0001c0003t0001g0001 a0001c0003t0001g0005 a0001c0003t0001g0013 others(65): Show |
116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.502+25_502+26delTT | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 4/6 | chr2 | 68162349 | |||||||
chr2:68162411 | G | T | 1 | a0001c0001t0001g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.502+86G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 4/6 | chr2 | 68162411 | |||||||
chr2:68162425 | T | TTA | 4 | a0001c0001t0003g0161 a0001c0003t0001g0048 a0002c0002t0002g0070 others(1): Show |
5 | HG02129.hp2 HG02735.hp2 NA19059.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-106_503-105dup others(2): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 68162425 | ||||||
chr2:68162537 | C | G | 11 | a0002c0002t0002g0011 a0002c0002t0002g0018 a0002c0002t0002g0070 others(8): Show |
16 | NA18946.hp2 NA18955.hp2 NA18961.hp2 others(13): Show |
intron_variant | MODIFIER | c.503-9C>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 4/6 | chr2 | 68162537 | |||||||
chr2:68162787 | C | T | 52 | a0001c0001t0003g0003 a0001c0001t0003g0019 a0001c0001t0003g0020 others(49): Show |
84 | HG00140.hp1 HG00609.hp1 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.620+124C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68162787 | |||||||
chr2:68162864 | G | C | 1 | a0002c0002t0002g0075 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.620+201G>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68162864 | |||||||
chr2:68162874 | G | C | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.620+211G>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68162874 | |||||||
chr2:68162875 | C | G | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.620+212C>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68162875 | |||||||
chr2:68162878 | A | G | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.620+215A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68162878 | |||||||
chr2:68163056 | A | C | 1 | a0001c0001t0001g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.620+393A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163056 | |||||||
chr2:68163104 | A | G | 52 | a0001c0001t0003g0003 a0001c0001t0003g0019 a0001c0001t0003g0020 others(49): Show |
84 | HG00140.hp1 HG00609.hp1 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.620+441A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163104 | |||||||
chr2:68163300 | G | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0051 others(15): Show |
24 | HG00735.hp2 HG01167.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.620+637G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163300 | |||||||
chr2:68163353 | GAAACCCT others(9): Show |
G | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.620+694_620+709del others(16): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68163353 | ||||||
chr2:68163377 | C | A | 77 | a0001c0003t0001g0001 a0001c0003t0001g0005 a0001c0003t0001g0007 others(74): Show |
129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.620+714C>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163377 | |||||||
chr2:68163540 | A | AATAAATA others(5): Show |
1 | a0001c0001t0009g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.620+880_620+881ins others(12): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68163540 | ||||||
chr2:68163540 | A | AATAC | 32 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0054 others(29): Show |
36 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.620+918_620+921dup others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68163540 | ||||||
chr2:68163540 | A | AATACATA others(1): Show |
4 | a0001c0001t0001g0052 a0001c0001t0001g0257 a0001c0001t0001g0272 others(1): Show |
5 | HG01243.hp2 HG01433.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.620+914_620+921dup others(8): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68163540 | ||||||
chr2:68163540 | A | AATACATA others(5): Show |
2 | a0001c0001t0001g0051 a0001c0001t0001g0280 |
3 | HG02717.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.620+910_620+921dup others(12): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68163540 | ||||||
chr2:68163540 | A | C | 7 | a0001c0001t0013g0165 a0001c0003t0001g0214 a0001c0003t0001g0215 others(4): Show |
7 | HG02630.hp2 NA18612.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.620+877A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163540 | |||||||
chr2:68163540 | AATAC | A | 2 | a0001c0003t0001g0048 a0001c0003t0001g0213 |
3 | HG02129.hp2 HG02735.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.620+918_620+921del others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68163540 | ||||||
chr2:68163540 | AATACATA others(5): Show |
A | 1 | a0001c0003t0001g0242 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.620+910_620+921del others(12): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68163540 | ||||||
chr2:68163540 | AATACATA others(9): Show |
A | 9 | a0001c0003t0002g0072 a0001c0003t0002g0073 a0002c0002t0002g0017 others(6): Show |
11 | HG01109.hp2 HG01175.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.620+906_620+921del others(16): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68163540 | ||||||
chr2:68163541 | A | ATACATAC others(5): Show |
1 | a0001c0001t0003g0143 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.620+889_620+890ins others(12): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68163541 | ||||||
chr2:68163544 | C | A | 17 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0074 others(14): Show |
19 | HG00438.hp1 HG02109.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.620+881C>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163544 | |||||||
chr2:68163549 | A | ATACG | 49 | a0001c0001t0003g0003 a0001c0001t0003g0019 a0001c0001t0003g0020 others(46): Show |
81 | HG00140.hp1 HG00609.hp1 HG01069.hp2 others(78): Show |
intron_variant | MODIFIER | c.620+889_620+890ins others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68163549 | ||||||
chr2:68163585 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.620+922T>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163585 | |||||||
chr2:68163586 | TACTC | T | 13 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0044 others(10): Show |
16 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.620+925_620+928del others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68163586 | ||||||
chr2:68163590 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.620+927C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163590 | |||||||
chr2:68163627 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.620+964A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163627 | |||||||
chr2:68163647 | TG | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0053 others(6): Show |
13 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.620+985delG | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163647 | |||||||
chr2:68163778 | G | T | 94 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0036 others(91): Show |
135 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(132): Show |
intron_variant | MODIFIER | c.620+1115G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163778 | |||||||
chr2:68163799 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.620+1136C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163799 | |||||||
chr2:68163805 | G | T | 1 | a0001c0001t0001g0278 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.620+1142G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163805 | |||||||
chr2:68163822 | C | T | 1 | a0001c0001t0013g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.620+1159C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163822 | |||||||
chr2:68163955 | A | G | 77 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0044 others(74): Show |
116 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(113): Show |
intron_variant | MODIFIER | c.620+1292A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163955 | |||||||
chr2:68163977 | A | G | 2 | a0003c0004t0001g0269 a0003c0004t0003g0268 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.620+1314A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68163977 | |||||||
chr2:68164053 | A | G | 1 | a0002c0002t0002g0103 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.620+1390A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68164053 | |||||||
chr2:68164144 | T | G | 6 | a0001c0005t0001g0029 a0001c0005t0001g0061 a0001c0005t0001g0063 others(3): Show |
6 | HG02647.hp1 HG02922.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.620+1481T>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68164144 | |||||||
chr2:68164580 | A | G | 1 | a0001c0003t0001g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.620+1917A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68164580 | |||||||
chr2:68164592 | T | C | 16 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(13): Show |
18 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.620+1929T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68164592 | |||||||
chr2:68164643 | A | G | 1 | a0001c0001t0001g0044 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.620+1980A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68164643 | |||||||
chr2:68164643 | A | T | 1 | a0001c0001t0003g0143 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.620+1980A>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68164643 | |||||||
chr2:68164746 | A | G | 1 | a0001c0001t0003g0045 | 2 | NA18999.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.620+2083A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68164746 | |||||||
chr2:68164821 | T | A | 5 | a0001c0003t0001g0186 a0001c0003t0001g0187 a0001c0003t0001g0188 others(2): Show |
5 | HG00323.hp2 HG00639.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.620+2158T>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68164821 | |||||||
chr2:68164847 | C | T | 1 | a0001c0003t0001g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.620+2184C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68164847 | |||||||
chr2:68164977 | T | G | 2 | a0003c0004t0001g0269 a0003c0004t0003g0268 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.620+2314T>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68164977 | |||||||
chr2:68165028 | C | CATT | 92 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0036 others(89): Show |
133 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(130): Show |
intron_variant | MODIFIER | c.620+2366_620+2367i others(5): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68165028 | ||||||
chr2:68165088 | G | A | 3 | a0002c0002t0002g0030 a0002c0002t0002g0082 a0002c0002t0002g0083 |
4 | NA18955.hp1 NA18979.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+2425G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165088 | |||||||
chr2:68165191 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0257 |
3 | HG02559.hp2 HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.620+2528T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165191 | |||||||
chr2:68165205 | A | C | 1 | a0001c0001t0001g0249 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.620+2542A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165205 | |||||||
chr2:68165280 | C | T | 15 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(12): Show |
17 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.620+2617C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165280 | |||||||
chr2:68165288 | C | T | 59 | a0001c0001t0001g0044 a0001c0001t0001g0170 a0001c0001t0001g0171 others(56): Show |
92 | HG00140.hp1 HG00609.hp1 HG01069.hp2 others(89): Show |
intron_variant | MODIFIER | c.620+2625C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165288 | |||||||
chr2:68165321 | G | A | 52 | a0001c0001t0003g0003 a0001c0001t0003g0019 a0001c0001t0003g0020 others(49): Show |
84 | HG00140.hp1 HG00609.hp1 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.620+2658G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165321 | |||||||
chr2:68165363 | C | CA | 6 | a0002c0002t0002g0031 a0002c0002t0002g0077 a0002c0002t0002g0082 others(3): Show |
7 | HG02300.hp1 NA18975.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.620+2716dupA | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68165363 | ||||||
chr2:68165363 | C | CAAAA | 15 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(12): Show |
19 | HG01168.hp1 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.620+2713_620+2716d others(6): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68165363 | ||||||
chr2:68165366 | AAAAAAAA others(10): Show |
A | 1 | a0002c0002t0002g0102 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.620+2718_620+2734d others(19): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68165366 | ||||||
chr2:68165377 | A | AAAAC | 63 | a0001c0001t0001g0028 a0001c0001t0001g0044 a0001c0001t0001g0049 others(60): Show |
97 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.620+2716_620+2717i others(6): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68165377 | ||||||
chr2:68165377 | A | AAAC | 132 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(129): Show |
194 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.620+2720_620+2722d others(5): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68165377 | ||||||
chr2:68165377 | A | C | 3 | a0001c0003t0001g0220 a0002c0002t0002g0015 a0002c0002t0002g0060 |
3 | HG01256.hp2 NA19059.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.620+2714A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165377 | |||||||
chr2:68165380 | C | A | 6 | a0001c0005t0001g0029 a0001c0005t0001g0061 a0001c0005t0001g0063 others(3): Show |
6 | HG02647.hp1 HG02922.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.620+2717C>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165380 | |||||||
chr2:68165383 | C | A | 7 | a0001c0005t0001g0029 a0001c0005t0001g0061 a0001c0005t0001g0063 others(4): Show |
7 | HG01928.hp1 HG02647.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.620+2720C>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165383 | |||||||
chr2:68165384 | A | C | 6 | a0001c0005t0001g0029 a0001c0005t0001g0061 a0001c0005t0001g0063 others(3): Show |
6 | HG02647.hp1 HG02922.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.620+2721A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165384 | |||||||
chr2:68165386 | A | C | 220 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(217): Show |
325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.620+2723A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165386 | |||||||
chr2:68165387 | A | C | 6 | a0001c0005t0001g0029 a0001c0005t0001g0061 a0001c0005t0001g0063 others(3): Show |
6 | HG02647.hp1 HG02922.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.620+2724A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165387 | |||||||
chr2:68165389 | A | C | 105 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0050 others(102): Show |
164 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.620+2726A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165389 | |||||||
chr2:68165390 | A | C | 6 | a0001c0005t0001g0029 a0001c0005t0001g0061 a0001c0005t0001g0063 others(3): Show |
6 | HG02647.hp1 HG02922.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.620+2727A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165390 | |||||||
chr2:68165392 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.620+2729A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165392 | |||||||
chr2:68165545 | C | CA | 158 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0050 others(155): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.620+2902dupA | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68165545 | ||||||
chr2:68165545 | C | CAA | 26 | a0001c0001t0001g0176 a0001c0001t0001g0243 a0001c0001t0003g0020 others(23): Show |
32 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.620+2901_620+2902d others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68165545 | ||||||
chr2:68165545 | CAA | C | 12 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0109 others(9): Show |
14 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.620+2901_620+2902d others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68165545 | ||||||
chr2:68165638 | T | C | 16 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(13): Show |
18 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.620+2975T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165638 | |||||||
chr2:68165662 | G | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0280 others(1): Show |
6 | HG01243.hp2 HG01433.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.620+2999G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68165662 | |||||||
chr2:68165680 | C | CA | 20 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(17): Show |
25 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(22): Show |
intron_variant | MODIFIER | c.620+3028dupA | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68165680 | ||||||
chr2:68166012 | T | A | 211 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(208): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.620+3349T>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68166012 | |||||||
chr2:68166135 | G | A | 1 | a0001c0003t0001g0190 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.620+3472G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68166135 | |||||||
chr2:68166309 | A | G | 1 | a0002c0002t0002g0103 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.620+3646A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68166309 | |||||||
chr2:68166363 | T | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0053 others(6): Show |
13 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.620+3700T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68166363 | |||||||
chr2:68166394 | A | AAAG | 221 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(218): Show |
328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.620+3733_620+3734i others(5): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68166394 | ||||||
chr2:68166559 | G | A | 3 | a0001c0001t0001g0243 a0001c0003t0001g0196 a0001c0003t0001g0225 |
3 | HG01261.hp1 HG01361.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.620+3896G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68166559 | |||||||
chr2:68166593 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.620+3930C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68166593 | |||||||
chr2:68166914 | C | A | 1 | a0001c0001t0013g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.620+4251C>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68166914 | |||||||
chr2:68166930 | T | A | 1 | a0002c0002t0002g0090 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.620+4267T>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68166930 | |||||||
chr2:68166984 | C | T | 2 | a0001c0003t0001g0233 a0001c0003t0001g0258 |
2 | HG01358.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.620+4321C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68166984 | |||||||
chr2:68167052 | C | T | 211 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(208): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.620+4389C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68167052 | |||||||
chr2:68167220 | A | G | 1 | a0001c0003t0004g0210 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.620+4557A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68167220 | |||||||
chr2:68167270 | TG | T | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(1): Show |
4 | HG01167.hp1 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+4608delG | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68167270 | |||||||
chr2:68167277 | C | T | 64 | a0001c0001t0001g0044 a0001c0001t0001g0170 a0001c0001t0001g0171 others(61): Show |
97 | HG00140.hp1 HG00609.hp1 HG01069.hp2 others(94): Show |
intron_variant | MODIFIER | c.620+4614C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68167277 | |||||||
chr2:68167602 | C | T | 1 | a0001c0001t0001g0044 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.620+4939C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68167602 | |||||||
chr2:68167662 | C | CA | 4 | a0001c0001t0001g0049 a0001c0001t0001g0074 a0001c0001t0001g0235 others(1): Show |
5 | HG01884.hp1 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.620+5005dupA | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68167662 | ||||||
chr2:68167737 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.620+5074C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68167737 | |||||||
chr2:68167805 | C | T | 6 | a0001c0005t0001g0029 a0001c0005t0001g0061 a0001c0005t0001g0063 others(3): Show |
6 | HG02647.hp1 HG02922.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.620+5142C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68167805 | |||||||
chr2:68167852 | T | C | 211 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(208): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.620+5189T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68167852 | |||||||
chr2:68167928 | T | C | 3 | a0001c0001t0003g0019 a0001c0001t0003g0137 a0001c0001t0011g0019 |
4 | HG01074.hp2 HG03017.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.620+5265T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68167928 | |||||||
chr2:68168141 | T | C | 1 | a0001c0003t0001g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.621-5206T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168141 | |||||||
chr2:68168175 | A | C | 1 | a0001c0001t0001g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.621-5172A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168175 | |||||||
chr2:68168270 | A | G | 3 | a0001c0001t0001g0050 a0001c0001t0001g0257 a0001c0001t0001g0272 |
4 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.621-5077A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168270 | |||||||
chr2:68168393 | T | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0053 others(6): Show |
13 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.621-4954T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168393 | |||||||
chr2:68168397 | G | A | 1 | a0001c0003t0001g0197 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.621-4950G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168397 | |||||||
chr2:68168432 | A | G | 3 | a0001c0003t0001g0239 a0001c0003t0001g0241 a0004c0006t0001g0240 |
3 | HG01109.hp1 HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.621-4915A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168432 | |||||||
chr2:68168499 | G | A | 211 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(208): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.621-4848G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168499 | |||||||
chr2:68168667 | A | G | 10 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(7): Show |
12 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-4680A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168667 | |||||||
chr2:68168705 | G | A | 1 | a0001c0003t0001g0198 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.621-4642G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168705 | |||||||
chr2:68168707 | C | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(6): Show |
11 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.621-4640C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168707 | |||||||
chr2:68168761 | G | C | 6 | a0001c0003t0001g0007 a0001c0003t0001g0233 a0001c0003t0001g0237 others(3): Show |
10 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.621-4586G>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168761 | |||||||
chr2:68168781 | A | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(208): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.621-4566A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168781 | |||||||
chr2:68168915 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.621-4432T>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168915 | |||||||
chr2:68168921 | C | CT | 13 | a0002c0002t0002g0006 a0002c0002t0002g0016 a0002c0002t0002g0075 others(10): Show |
18 | HG00597.hp2 HG00733.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.621-4401dupT | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68168921 | ||||||
chr2:68168921 | CT | C | 82 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0243 others(79): Show |
137 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.621-4401delT | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68168921 | ||||||
chr2:68168921 | CTT | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(60): Show |
78 | HG00099.hp1 HG00735.hp2 HG01074.hp1 others(75): Show |
intron_variant | MODIFIER | c.621-4402_621-4401d others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68168921 | ||||||
chr2:68168921 | CTTT | C | 50 | a0001c0001t0001g0231 a0001c0001t0001g0245 a0001c0001t0003g0003 others(47): Show |
82 | HG00140.hp1 HG00609.hp1 HG01074.hp2 others(79): Show |
intron_variant | MODIFIER | c.621-4403_621-4401d others(5): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68168921 | ||||||
chr2:68168929 | T | C | 1 | a0001c0003t0001g0233 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.621-4418T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168929 | |||||||
chr2:68168931 | T | C | 1 | a0001c0005t0006g0062 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.621-4416T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168931 | |||||||
chr2:68168971 | A | G | 1 | a0001c0001t0003g0137 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.621-4376A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168971 | |||||||
chr2:68168988 | G | A | 1 | a0002c0002t0002g0081 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.621-4359G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168988 | |||||||
chr2:68168998 | G | A | 1 | a0001c0001t0013g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.621-4349G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68168998 | |||||||
chr2:68169064 | A | G | 222 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(219): Show |
329 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.621-4283A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169064 | |||||||
chr2:68169162 | C | T | 1 | a0001c0003t0001g0242 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.621-4185C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169162 | |||||||
chr2:68169184 | C | G | 9 | a0001c0003t0001g0027 a0001c0003t0001g0194 a0001c0003t0001g0208 others(6): Show |
11 | HG00621.hp2 HG02071.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.621-4163C>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169184 | |||||||
chr2:68169260 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.621-4087T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169260 | |||||||
chr2:68169264 | G | A | 1 | a0001c0003t0004g0199 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.621-4083G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169264 | |||||||
chr2:68169314 | C | A | 1 | a0002c0002t0002g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.621-4033C>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169314 | |||||||
chr2:68169316 | A | T | 1 | a0002c0002t0002g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.621-4031A>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169316 | |||||||
chr2:68169319 | T | A | 1 | a0002c0002t0002g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.621-4028T>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169319 | |||||||
chr2:68169325 | G | GGACATAT others(8): Show |
1 | a0002c0002t0002g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.621-4021_621-4020i others(17): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68169325 | ||||||
chr2:68169327 | G | T | 1 | a0002c0002t0002g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.621-4020G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169327 | |||||||
chr2:68169358 | C | A | 1 | a0002c0002t0002g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.621-3989C>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169358 | |||||||
chr2:68169363 | A | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0231 a0001c0001t0001g0232 others(14): Show |
22 | HG00741.hp2 HG01074.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.621-3984A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169363 | |||||||
chr2:68169369 | A | T | 1 | a0002c0002t0002g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.621-3978A>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169369 | |||||||
chr2:68169370 | A | C | 1 | a0002c0002t0002g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.621-3977A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169370 | |||||||
chr2:68169392 | C | T | 1 | a0002c0002t0002g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.621-3955C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169392 | |||||||
chr2:68169447 | AATCAGCA others(9): Show |
A | 1 | a0002c0002t0002g0120 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.621-3885_621-3870d others(18): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68169447 | ||||||
chr2:68169480 | A | T | 1 | a0001c0003t0001g0219 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.621-3867A>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169480 | |||||||
chr2:68169509 | C | G | 1 | a0001c0001t0009g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.621-3838C>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169509 | |||||||
chr2:68169533 | G | A | 5 | a0001c0001t0003g0021 a0001c0001t0003g0045 a0001c0001t0003g0046 others(2): Show |
9 | NA18942.hp2 NA18952.hp2 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-3814G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169533 | |||||||
chr2:68169663 | G | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0053 others(6): Show |
13 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.621-3684G>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169663 | |||||||
chr2:68169667 | GTTTTAA | G | 3 | a0001c0001t0003g0139 a0001c0001t0003g0151 a0001c0001t0003g0162 |
3 | HG00609.hp1 HG04184.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.621-3673_621-3668d others(8): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68169667 | ||||||
chr2:68169714 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.621-3633G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169714 | |||||||
chr2:68169734 | C | T | 1 | a0001c0001t0003g0148 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.621-3613C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68169734 | |||||||
chr2:68170165 | A | G | 10 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(7): Show |
12 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-3182A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68170165 | |||||||
chr2:68170472 | G | T | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(4): Show |
9 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-2875G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68170472 | |||||||
chr2:68170605 | G | A | 5 | a0002c0002t0002g0006 a0002c0002t0002g0091 a0002c0002t0002g0097 others(2): Show |
9 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-2742G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68170605 | |||||||
chr2:68170621 | A | G | 1 | a0002c0002t0002g0096 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.621-2726A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68170621 | |||||||
chr2:68170685 | T | C | 10 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(7): Show |
12 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-2662T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68170685 | |||||||
chr2:68170697 | G | A | 1 | a0001c0001t0004g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.621-2650G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68170697 | |||||||
chr2:68170747 | C | CA | 84 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(81): Show |
110 | HG00140.hp2 HG00609.hp1 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.621-2578dupA | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68170747 | ||||||
chr2:68170747 | C | CAA | 65 | a0001c0001t0001g0050 a0001c0001t0001g0059 a0001c0001t0001g0249 others(62): Show |
114 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.621-2579_621-2578d others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68170747 | ||||||
chr2:68170747 | C | CAAA | 18 | a0001c0001t0004g0247 a0001c0001t0004g0248 a0001c0003t0001g0023 others(15): Show |
20 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.621-2580_621-2578d others(5): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68170747 | ||||||
chr2:68170747 | CA | C | 13 | a0001c0001t0001g0044 a0001c0001t0001g0170 a0001c0001t0001g0171 others(10): Show |
14 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.621-2578delA | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68170747 | ||||||
chr2:68170833 | T | G | 1 | a0001c0001t0009g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.621-2514T>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68170833 | |||||||
chr2:68170858 | C | T | 12 | a0001c0001t0001g0044 a0001c0001t0001g0170 a0001c0001t0001g0171 others(9): Show |
13 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.621-2489C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68170858 | |||||||
chr2:68171017 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.621-2330C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68171017 | |||||||
chr2:68171101 | C | T | 2 | a0002c0002t0002g0035 a0002c0002t0002g0088 |
3 | HG01256.hp1 HG01258.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.621-2246C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68171101 | |||||||
chr2:68171118 | C | T | 1 | a0001c0001t0003g0159 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.621-2229C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68171118 | |||||||
chr2:68171202 | G | A | 2 | a0001c0003t0001g0233 a0001c0003t0001g0258 |
2 | HG01358.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621-2145G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68171202 | |||||||
chr2:68171787 | G | C | 211 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(208): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.621-1560G>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68171787 | |||||||
chr2:68171972 | C | A | 80 | a0001c0001t0004g0246 a0001c0001t0004g0247 a0001c0001t0004g0248 others(77): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.621-1375C>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68171972 | |||||||
chr2:68172007 | C | T | 16 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(13): Show |
18 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.621-1340C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68172007 | |||||||
chr2:68172058 | C | T | 211 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(208): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.621-1289C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68172058 | |||||||
chr2:68172278 | A | AAGGCAAG | 6 | a0001c0005t0001g0029 a0001c0005t0001g0061 a0001c0005t0001g0063 others(3): Show |
6 | HG02647.hp1 HG02922.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.621-1066_621-1065i others(9): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68172278 | ||||||
chr2:68172282 | G | C | 6 | a0001c0005t0001g0029 a0001c0005t0001g0061 a0001c0005t0001g0063 others(3): Show |
6 | HG02647.hp1 HG02922.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.621-1065G>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68172282 | |||||||
chr2:68172282 | G | T | 1 | a0001c0003t0001g0206 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.621-1065G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68172282 | |||||||
chr2:68172363 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0051 others(11): Show |
20 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.621-984C>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68172363 | |||||||
chr2:68172454 | T | C | 72 | a0001c0001t0004g0246 a0001c0001t0004g0247 a0001c0001t0004g0248 others(69): Show |
122 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.621-893T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68172454 | |||||||
chr2:68172966 | G | A | 211 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(208): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.621-381G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68172966 | |||||||
chr2:68173015 | TATC | T | 6 | a0001c0001t0001g0044 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
7 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.621-329_621-327del others(3): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68173015 | ||||||
chr2:68173083 | C | CT | 31 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0272 others(28): Show |
38 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.621-240dupT | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68173083 | ||||||
chr2:68173083 | CT | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0057 a0001c0001t0001g0059 others(57): Show |
78 | HG00140.hp1 HG00609.hp1 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.621-240delT | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68173083 | ||||||
chr2:68173083 | CTT | C | 13 | a0001c0001t0001g0044 a0001c0001t0001g0170 a0001c0001t0001g0171 others(10): Show |
14 | HG01168.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.621-241_621-240del others(2): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68173083 | ||||||
chr2:68173083 | CTTTT | C | 66 | a0001c0001t0004g0246 a0001c0001t0004g0247 a0001c0001t0004g0248 others(63): Show |
116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.621-243_621-240del others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 68173083 | ||||||
chr2:68173084 | T | C | 1 | a0001c0001t0003g0003 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.621-263T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68173084 | |||||||
chr2:68173335 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0059 |
2 | HG00735.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.621-12T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 5/6 | chr2 | 68173335 | |||||||
chr2:68173507 | G | A | 11 | a0002c0002t0002g0011 a0002c0002t0002g0018 a0002c0002t0002g0070 others(8): Show |
16 | NA18946.hp2 NA18955.hp2 NA18961.hp2 others(13): Show |
intron_variant | MODIFIER | c.691+90G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68173507 | |||||||
chr2:68173568 | G | A | 1 | a0003c0004t0001g0267 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.691+151G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68173568 | |||||||
chr2:68173576 | A | AT | 120 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(117): Show |
181 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.691+181dupT | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 68173576 | ||||||
chr2:68173576 | A | ATT | 7 | a0001c0001t0013g0165 a0001c0003t0001g0026 a0001c0003t0001g0200 others(4): Show |
9 | HG01109.hp1 HG02040.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.691+180_691+181dup others(2): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 68173576 | ||||||
chr2:68173576 | A | ATTT | 9 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0053 others(6): Show |
13 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.691+179_691+181dup others(3): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 68173576 | ||||||
chr2:68173576 | AT | A | 73 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(70): Show |
107 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(104): Show |
intron_variant | MODIFIER | c.691+181delT | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 68173576 | ||||||
chr2:68173596 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.691+179T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68173596 | |||||||
chr2:68173657 | A | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0170 a0001c0001t0001g0171 others(4): Show |
8 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.691+240A>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68173657 | |||||||
chr2:68173685 | C | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
4 | HG01433.hp2 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.691+268C>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68173685 | |||||||
chr2:68173724 | A | G | 9 | a0001c0001t0001g0049 a0001c0001t0001g0074 a0001c0001t0001g0230 others(6): Show |
10 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.691+307A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68173724 | |||||||
chr2:68173729 | C | A | 10 | a0001c0001t0001g0050 a0001c0001t0001g0257 a0001c0001t0001g0272 others(7): Show |
11 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.691+312C>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68173729 | |||||||
chr2:68173824 | G | A | 211 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(208): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.691+407G>A | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68173824 | |||||||
chr2:68174005 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.691+588T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68174005 | |||||||
chr2:68174180 | G | T | 1 | a0001c0003t0001g0206 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.692-555G>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68174180 | |||||||
chr2:68174288 | GT | G | 11 | a0002c0002t0002g0011 a0002c0002t0002g0018 a0002c0002t0002g0070 others(8): Show |
16 | HG01069.hp1 NA18946.hp2 NA18955.hp2 others(13): Show |
intron_variant | MODIFIER | c.692-425delT | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 68174288 | ||||||
chr2:68174288 | GTT | G | 8 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0108 others(5): Show |
10 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.692-426_692-425del others(2): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 68174288 | ||||||
chr2:68174288 | GTTT | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0049 others(56): Show |
67 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(64): Show |
intron_variant | MODIFIER | c.692-427_692-425del others(3): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 68174288 | ||||||
chr2:68174288 | GTTTT | G | 139 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0051 others(136): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.692-428_692-425del others(4): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 68174288 | ||||||
chr2:68174288 | GTTTTT | G | 5 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0003t0001g0025 others(2): Show |
6 | HG01257.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.692-429_692-425del others(5): Show |
PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 68174288 | ||||||
chr2:68174294 | T | G | 1 | a0001c0003t0001g0228 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.692-441T>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68174294 | |||||||
chr2:68174300 | T | C | 1 | a0001c0001t0003g0161 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.692-435T>C | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68174300 | |||||||
chr2:68174310 | T | G | 2 | a0001c0003t0001g0202 a0001c0003t0001g0203 |
2 | NA19066.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.692-425T>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68174310 | |||||||
chr2:68174423 | C | G | 1 | a0001c0001t0003g0157 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.692-312C>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68174423 | |||||||
chr2:68174425 | A | G | 213 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0028 others(210): Show |
315 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.692-310A>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68174425 | |||||||
chr2:68174433 | G | GA | 10 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0053 others(7): Show |
14 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.692-294dupA | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 68174433 | ||||||
chr2:68174582 | A | T | 1 | a0001c0003t0001g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.692-153A>T | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68174582 | |||||||
chr2:68174723 | T | G | 1 | a0001c0001t0003g0149 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.692-12T>G | PNO1 | ENSG00000115946.8 | transcript | ENST00000263657.7 | protein_coding | 6/6 | chr2 | 68174723 |