Item | Value |
---|---|
geneid | 8795 |
ensemblid | ENSG00000120889.13 |
hgncid | 11905 |
symbol | TNFRSF10B |
name | TNF receptor superfamily member 10b |
refseq_nuc | NM_003842.5 |
refseq_prot | NP_003833.4 |
ensembl_nuc | ENST00000276431.9 |
ensembl_prot | ENSP00000276431.4 |
mane_status | MANE Select |
chr | chr8 |
start | 23020133 |
end | 23069031 |
strand | - |
ver | v1.2 |
region | chr8:23020133-23069031 |
region5000 | chr8:23015133-23074031 |
regionname0 | TNFRSF10B_chr8_23020133_23069031 |
regionname5000 | TNFRSF10B_chr8_23015133_23074031 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 440 | 213 | 39 | 28 | 111 | 6 | 28 | 87 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0002 | 0/0 | 440 | 56 | 16 | 16 | 13 | 7 | 4 | 10 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0003 | 0/0 | 440 | 50 | 0 | 3 | 40 | 0 | 7 | 29 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0004 | 0/0 | 440 | 36 | 20 | 9 | 4 | 1 | 2 | 4 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0005 | 1/0 | 440 | 7 | 5 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0006 | 0/0 | 440 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0007 | 0/0 | 440 | 3 | 0 | 1 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0008 | 0/0 | 440 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0009 | 0/0 | 440 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0010 | 0/0 | 440 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0011 | 0/0 | 440 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0012 | 0/0 | 440 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0013 | 0/0 | 440 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0014 | 0/0 | 440 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0015 | 0/0 | 440 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0016 | 0/0 | 440 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
a0017 | 0/0 | 440 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | MEQRG others(435): Show |
chr8 | 23015133 | 23074031 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1320 | 213 | 39 | 28 | 111 | 6 | 28 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0002c0002 | 0/0 | 1320 | 56 | 16 | 16 | 13 | 7 | 4 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0003c0003 | 0/0 | 1320 | 49 | 0 | 3 | 39 | 0 | 7 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0003c0016 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0004c0004 | 0/0 | 1320 | 36 | 20 | 9 | 4 | 1 | 2 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0005c0005 | 1/0 | 1320 | 7 | 5 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0006c0006 | 0/0 | 1320 | 6 | 5 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0007c0008 | 0/0 | 1320 | 3 | 0 | 1 | 2 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0008c0007 | 0/0 | 1320 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0009c0009 | 0/0 | 1320 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0010c0014 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0011c0017 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0012c0011 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0013c0010 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0014c0012 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0015c0013 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0016c0018 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 | ||
a0017c0015 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | ATGGA others(1315): Show |
chr8 | 23015133 | 23074031 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3998 | 97 | 16 | 7 | 56 | 2 | 16 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0002 | 0/1 | 3998 | 57 | 5 | 9 | 33 | 3 | 6 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0003 | 0/0 | 3998 | 35 | 8 | 8 | 16 | 1 | 2 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0004 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0007 | 0/0 | 3998 | 2 | 0 | 0 | 1 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0008 | 0/0 | 3993 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3988): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0009 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0010 | 0/0 | 3998 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0011 | 0/0 | 3998 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0012 | 0/0 | 3998 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0013 | 0/0 | 3998 | 2 | 0 | 1 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0016 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0017 | 0/0 | 3998 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0018 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0019 | 0/0 | 3975 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3970): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0021 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0022 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0024 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0026 | 0/0 | 3998 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0001c0001t0027 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0002c0002t0002 | 0/0 | 3998 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0002c0002t0004 | 0/0 | 3998 | 21 | 10 | 4 | 5 | 2 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0002c0002t0005 | 0/0 | 3998 | 19 | 1 | 7 | 7 | 3 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0002c0002t0006 | 0/0 | 3998 | 10 | 1 | 4 | 1 | 2 | 2 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0002c0002t0015 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0002c0002t0028 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0002c0002t0029 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0002c0002t0031 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0002c0002t0032 | 0/0 | 3993 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3988): Show |
chr8 | 23015133 | 23074031 |
a0003c0003t0001 | 0/0 | 3998 | 16 | 0 | 1 | 10 | 0 | 5 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0003c0003t0002 | 0/0 | 3998 | 22 | 0 | 0 | 20 | 0 | 2 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0003c0003t0003 | 0/0 | 3998 | 7 | 0 | 2 | 5 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0003c0003t0007 | 0/0 | 3998 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0003c0003t0025 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0003c0016t0001 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0004c0004t0001 | 0/0 | 3998 | 33 | 17 | 9 | 4 | 1 | 2 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0004c0004t0002 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0004c0004t0009 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0004c0004t0020 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0005c0005t0001 | 1/0 | 3998 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0005c0005t0004 | 0/0 | 3998 | 6 | 5 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0006c0006t0001 | 0/0 | 3998 | 6 | 5 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0007c0008t0004 | 0/0 | 3998 | 2 | 0 | 1 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0007c0008t0030 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0008c0007t0004 | 0/0 | 3998 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0009c0009t0001 | 0/0 | 3998 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0010c0014t0001 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0011c0017t0001 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0012c0011t0006 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0013c0010t0014 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0014c0012t0023 | 0/0 | 4042 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(4037): Show |
chr8 | 23015133 | 23074031 |
a0015c0013t0001 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0016c0018t0001 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
a0017c0015t0001 | 0/0 | 3998 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | AGCCT others(3993): Show |
chr8 | 23015133 | 23074031 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0306 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0004g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0010g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0010g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0011g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0011g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0012g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0012g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0013g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0013g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0016g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0017g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0018g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0019g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0021g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0022g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0024g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0026g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0027g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0015g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0028g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0029g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0031g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0032g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0025g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0016t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0020g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0001g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0004g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0004g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0006c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0006c0006t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0006c0006t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0006c0006t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0006c0006t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0006c0006t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0007c0008t0004g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0007c0008t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0007c0008t0030g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0008c0007t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0008c0007t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0008c0007t0004g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0009c0009t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0009c0009t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0010c0014t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0011c0017t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0012c0011t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0013c0010t0014g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0014c0012t0023g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0015c0013t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0016c0018t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0017c0015t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0182 | EUR | GBR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00099 | hp2 | a0002 | c0002 | t0005 | g0334 | EUR | GBR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00140 | hp1 | a0002 | c0002 | t0005 | g0313 | EUR | GBR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0305 | EUR | GBR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0303 | EUR | FIN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00280 | hp2 | a0002 | c0002 | t0006 | g0325 | EUR | FIN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00408 | hp1 | a0003 | c0003 | t0001 | g0095 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00408 | hp2 | a0002 | c0002 | t0004 | g0360 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00423 | hp2 | a0003 | c0003 | t0002 | g0094 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00438 | hp1 | a0007 | c0008 | t0004 | g0362 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00558 | hp1 | a0003 | c0003 | t0002 | g0051 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00621 | hp2 | a0003 | c0003 | t0007 | g0113 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00639 | hp1 | a0004 | c0004 | t0001 | g0019 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00733 | hp2 | a0004 | c0004 | t0001 | g0209 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00735 | hp1 | a0002 | c0002 | t0004 | g0330 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00738 | hp1 | a0007 | c0008 | t0004 | g0338 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00738 | hp2 | a0004 | c0004 | t0001 | g0140 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01069 | hp1 | a0004 | c0004 | t0001 | g0300 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01070 | hp1 | a0004 | c0004 | t0001 | g0167 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01070 | hp2 | a0002 | c0002 | t0004 | g0010 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01071 | hp2 | a0002 | c0002 | t0004 | g0010 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0098 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01099 | hp1 | a0002 | c0002 | t0006 | g0337 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01099 | hp2 | a0010 | c0014 | t0001 | g0211 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01106 | hp1 | a0003 | c0003 | t0003 | g0265 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01106 | hp2 | a0002 | c0002 | t0005 | g0346 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01167 | hp1 | a0002 | c0002 | t0005 | g0368 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01167 | hp2 | a0009 | c0009 | t0001 | g0227 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01169 | hp1 | a0009 | c0009 | t0001 | g0206 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01169 | hp2 | a0002 | c0002 | t0006 | g0333 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01175 | hp1 | a0002 | c0002 | t0006 | g0008 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01175 | hp2 | a0004 | c0004 | t0001 | g0065 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01192 | hp1 | a0006 | c0006 | t0001 | g0130 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01243 | hp2 | a0001 | c0001 | t0011 | g0210 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01255 | hp1 | a0002 | c0002 | t0005 | g0329 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01255 | hp2 | a0002 | c0002 | t0005 | g0335 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01258 | hp2 | a0002 | c0002 | t0005 | g0009 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01261 | hp1 | a0011 | c0017 | t0001 | g0106 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01433 | hp1 | a0004 | c0004 | t0001 | g0064 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01433 | hp2 | a0002 | c0002 | t0004 | g0314 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01496 | hp2 | a0001 | c0001 | t0013 | g0311 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01515 | hp1 | a0002 | c0002 | t0004 | g0327 | EUR | IBS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0301 | EUR | IBS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01516 | hp1 | a0002 | c0002 | t0004 | g0366 | EUR | IBS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01516 | hp2 | a0004 | c0004 | t0001 | g0068 | EUR | IBS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01884 | hp2 | a0002 | c0002 | t0005 | g0009 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01891 | hp1 | a0012 | c0011 | t0006 | g0312 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01891 | hp2 | a0005 | c0005 | t0004 | g0321 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01934 | hp1 | a0004 | c0004 | t0001 | g0286 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01934 | hp2 | a0002 | c0002 | t0006 | g0008 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01978 | hp2 | a0001 | c0001 | t0021 | g0157 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01981 | hp1 | a0002 | c0002 | t0005 | g0324 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01981 | hp2 | a0004 | c0004 | t0001 | g0059 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01993 | hp1 | a0003 | c0003 | t0003 | g0108 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02004 | hp2 | a0001 | c0001 | t0024 | g0302 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02015 | hp1 | a0003 | c0003 | t0002 | g0084 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0199 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02040 | hp1 | a0003 | c0003 | t0007 | g0089 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02055 | hp2 | a0002 | c0002 | t0004 | g0353 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02056 | hp2 | a0002 | c0002 | t0004 | g0370 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02083 | hp2 | a0003 | c0003 | t0002 | g0047 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02135 | hp1 | a0003 | c0003 | t0001 | g0096 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02135 | hp2 | a0002 | c0002 | t0004 | g0345 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02145 | hp2 | a0004 | c0004 | t0001 | g0214 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02148 | hp1 | a0002 | c0002 | t0005 | g0348 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02155 | hp1 | a0003 | c0003 | t0001 | g0090 | EAS | CDX | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | CDX | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CDX | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02165 | hp2 | a0003 | c0003 | t0007 | g0072 | EAS | CDX | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02257 | hp1 | a0004 | c0004 | t0001 | g0026 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02258 | hp1 | a0005 | c0005 | t0004 | g0318 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02280 | hp1 | a0002 | c0002 | t0015 | g0012 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02280 | hp2 | a0004 | c0004 | t0001 | g0121 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0285 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02523 | hp1 | a0007 | c0008 | t0030 | g0363 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02572 | hp1 | a0005 | c0005 | t0004 | g0355 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02602 | hp1 | a0003 | c0003 | t0001 | g0062 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02615 | hp2 | a0004 | c0004 | t0001 | g0126 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02630 | hp2 | a0002 | c0002 | t0029 | g0354 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0298 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02683 | hp2 | a0002 | c0002 | t0006 | g0361 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02717 | hp1 | a0005 | c0005 | t0004 | g0364 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0217 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02723 | hp2 | a0006 | c0006 | t0001 | g0128 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02735 | hp1 | a0004 | c0004 | t0001 | g0033 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02738 | hp1 | a0003 | c0003 | t0001 | g0105 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0037 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02818 | hp1 | a0006 | c0006 | t0001 | g0224 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0125 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02886 | hp1 | a0001 | c0001 | t0012 | g0142 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02886 | hp2 | a0004 | c0004 | t0001 | g0132 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02895 | hp1 | a0002 | c0002 | t0004 | g0316 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02896 | hp2 | a0002 | c0002 | t0004 | g0349 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02897 | hp1 | a0002 | c0002 | t0004 | g0320 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02922 | hp1 | a0004 | c0004 | t0001 | g0223 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02922 | hp2 | a0004 | c0004 | t0002 | g0023 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02976 | hp1 | a0001 | c0001 | t0010 | g0207 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0120 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0373 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03041 | hp2 | a0004 | c0004 | t0001 | g0238 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03098 | hp2 | a0008 | c0007 | t0004 | g0356 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03130 | hp1 | a0008 | c0007 | t0004 | g0319 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03130 | hp2 | a0004 | c0004 | t0009 | g0042 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03139 | hp1 | a0013 | c0010 | t0014 | g0011 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03139 | hp2 | a0002 | c0002 | t0032 | g0323 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03195 | hp1 | a0004 | c0004 | t0001 | g0133 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03195 | hp2 | a0002 | c0002 | t0004 | g0372 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03209 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03225 | hp1 | a0006 | c0006 | t0001 | g0129 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03239 | hp2 | a0003 | c0003 | t0001 | g0091 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03453 | hp1 | a0008 | c0007 | t0004 | g0317 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03453 | hp2 | a0002 | c0002 | t0004 | g0352 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03486 | hp1 | a0002 | c0002 | t0004 | g0350 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03490 | hp1 | a0001 | c0001 | t0013 | g0246 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0304 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03516 | hp1 | a0002 | c0002 | t0028 | g0357 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03516 | hp2 | a0004 | c0004 | t0001 | g0131 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03540 | hp1 | a0002 | c0002 | t0004 | g0359 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03540 | hp2 | a0004 | c0004 | t0001 | g0135 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03579 | hp1 | a0005 | c0005 | t0004 | g0315 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03579 | hp2 | a0006 | c0006 | t0001 | g0031 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03669 | hp2 | a0001 | c0001 | t0007 | g0081 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03688 | hp2 | a0003 | c0003 | t0001 | g0264 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03704 | hp2 | a0014 | c0012 | t0023 | g0018 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03927 | hp2 | a0001 | c0001 | t0026 | g0028 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03942 | hp2 | a0004 | c0004 | t0001 | g0144 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04115 | hp1 | a0005 | c0005 | t0004 | g0365 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04115 | hp2 | a0003 | c0003 | t0001 | g0063 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04184 | hp2 | a0003 | c0003 | t0002 | g0097 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04204 | hp2 | a0002 | c0002 | t0005 | g0332 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04228 | hp1 | a0003 | c0003 | t0002 | g0103 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04228 | hp2 | a0002 | c0002 | t0006 | g0339 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0259 | AFR | YRI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18522 | hp2 | a0004 | c0004 | t0001 | g0141 | AFR | YRI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | CHB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18906 | hp1 | a0002 | c0002 | t0004 | g0331 | AFR | YRI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18906 | hp2 | a0001 | c0001 | t0010 | g0208 | AFR | YRI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18939 | hp2 | a0004 | c0004 | t0001 | g0281 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18942 | hp1 | a0002 | c0002 | t0005 | g0340 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18942 | hp2 | a0003 | c0003 | t0002 | g0048 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18947 | hp1 | a0003 | c0003 | t0001 | g0092 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18950 | hp1 | a0002 | c0002 | t0005 | g0343 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18954 | hp1 | a0003 | c0003 | t0002 | g0088 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18954 | hp2 | a0001 | c0001 | t0022 | g0289 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18956 | hp2 | a0003 | c0003 | t0002 | g0112 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18959 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18961 | hp1 | a0003 | c0003 | t0025 | g0073 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18961 | hp2 | a0002 | c0002 | t0005 | g0369 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18963 | hp2 | a0003 | c0003 | t0002 | g0030 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18970 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18971 | hp1 | a0003 | c0003 | t0002 | g0102 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18974 | hp2 | a0003 | c0003 | t0002 | g0107 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18980 | hp2 | a0003 | c0003 | t0002 | g0188 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18985 | hp2 | a0003 | c0003 | t0003 | g0111 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18987 | hp1 | a0003 | c0003 | t0002 | g0118 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18987 | hp2 | a0002 | c0002 | t0005 | g0344 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18990 | hp1 | a0003 | c0003 | t0001 | g0050 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18990 | hp2 | a0003 | c0003 | t0002 | g0198 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18991 | hp1 | a0003 | c0003 | t0001 | g0093 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18992 | hp2 | a0016 | c0018 | t0001 | g0085 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18995 | hp1 | a0002 | c0002 | t0005 | g0341 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19000 | hp1 | a0003 | c0003 | t0002 | g0189 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19002 | hp1 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19002 | hp2 | a0004 | c0004 | t0001 | g0149 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19003 | hp1 | a0003 | c0016 | t0001 | g0307 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19003 | hp2 | a0003 | c0003 | t0002 | g0263 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19009 | hp2 | a0003 | c0003 | t0003 | g0190 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19012 | hp2 | a0003 | c0003 | t0002 | g0087 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | LWK | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19030 | hp2 | a0004 | c0004 | t0001 | g0136 | AFR | LWK | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19043 | hp2 | a0002 | c0002 | t0006 | g0351 | AFR | LWK | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19054 | hp1 | a0001 | c0001 | t0007 | g0205 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19054 | hp2 | a0003 | c0003 | t0001 | g0260 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19056 | hp1 | a0003 | c0003 | t0002 | g0114 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19057 | hp2 | a0001 | c0001 | t0016 | g0013 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19058 | hp1 | a0001 | c0001 | t0027 | g0268 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19058 | hp2 | a0004 | c0004 | t0001 | g0150 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19062 | hp1 | a0003 | c0003 | t0001 | g0086 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19065 | hp1 | a0002 | c0002 | t0006 | g0347 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19065 | hp2 | a0002 | c0002 | t0005 | g0342 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19066 | hp1 | a0002 | c0002 | t0004 | g0371 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19068 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19074 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19079 | hp1 | a0004 | c0004 | t0001 | g0177 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19080 | hp2 | a0003 | c0003 | t0003 | g0123 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19081 | hp1 | a0002 | c0002 | t0004 | g0326 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19081 | hp2 | a0003 | c0003 | t0002 | g0049 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19084 | hp2 | a0002 | c0002 | t0005 | g0358 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19088 | hp2 | a0001 | c0001 | t0018 | g0170 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19090 | hp2 | a0001 | c0001 | t0019 | g0099 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19240 | hp1 | a0004 | c0004 | t0001 | g0124 | AFR | YRI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19240 | hp2 | a0001 | c0001 | t0012 | g0230 | AFR | YRI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20129 | hp1 | a0004 | c0004 | t0001 | g0134 | AFR | ASW | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ASW | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | TSI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20752 | hp2 | a0002 | c0002 | t0006 | g0328 | EUR | TSI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20805 | hp2 | a0002 | c0002 | t0005 | g0336 | EUR | TSI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20905 | hp1 | a0001 | c0001 | t0017 | g0053 | SAS | GIH | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20905 | hp2 | a0017 | c0015 | t0001 | g0082 | SAS | GIH | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01123 | hp2 | a0002 | c0002 | t0031 | g0367 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02109 | hp1 | a0002 | c0002 | t0004 | g0322 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02109 | hp2 | a0004 | c0004 | t0020 | g0041 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03471 | hp1 | a0004 | c0004 | t0001 | g0040 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | USA | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG06807 | hp2 | a0001 | c0001 | t0011 | g0225 | AFR | USA | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18955 | hp1 | a0015 | c0013 | t0001 | g0174 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | USA | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20300 | hp2 | a0006 | c0006 | t0001 | g0226 | AFR | USA | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA21309 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | LWK | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | LWK | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0306 | REF | REF | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
homoSapiens | grch38p0 | a0005 | c0005 | t0001 | g0014 | REF | REF | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:23022771 | G | A | 1 | a0010 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.1223C>T | p.Thr408Met | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1360/3998 | 1223/1323 | 408/440 | chr8 | 23022771 | |||
chr8:23027732 | C | T | 1 | a0016 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.770G>A | p.Arg257His | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 6/9 | 907/3998 | 770/1323 | 257/440 | chr8 | 23027732 | |||
chr8:23028412 | C | T | 1 | a0014 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.667G>A | p.Val223Ile | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/9 | 804/3998 | 667/1323 | 223/440 | chr8 | 23028412 | |||
chr8:23028414 | G | A | 1 | a0009 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.665C>T | p.Ala222Val | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/9 | 802/3998 | 665/1323 | 222/440 | chr8 | 23028414 | |||
chr8:23028417 | G | A | 1 | a0015 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.662C>T | p.Ala221Val | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/9 | 799/3998 | 662/1323 | 221/440 | chr8 | 23028417 | |||
chr8:23028487 | C | A | 1 | a0017 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.592G>T | p.Val198Leu | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/9 | 729/3998 | 592/1323 | 198/440 | chr8 | 23028487 | |||
chr8:23028489 | G | A | 2 | a0006 a0008 |
9 | HG01192.hp1 HG02723.hp2 HG02818.hp1 others(6): Show |
missense_variant | MODERATE | c.590C>T | p.Thr197Met | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/9 | 727/3998 | 590/1323 | 197/440 | chr8 | 23028489 | |||
chr8:23028507 | A | G | 10 | a0001 a0002 a0003 others(7): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
missense_variant | MODERATE | c.572T>C | p.Val191Ala | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/9 | 709/3998 | 572/1323 | 191/440 | chr8 | 23028507 | |||
chr8:23029610 | C | A | 1 | a0016 | 1 | NA18992.hp2 | missense_variant&splice_region_variant | MODERATE | c.476G>T | p.Gly159Val | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/9 | 613/3998 | 476/1323 | 159/440 | chr8 | 23029610 | |||
chr8:23043188 | G | A | 4 | a0003 a0007 a0011 others(1): Show |
55 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
missense_variant | MODERATE | c.200C>T | p.Ala67Val | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/9 | 337/3998 | 200/1323 | 67/440 | chr8 | 23043188 | |||
chr8:23068800 | G | A | 12 | a0001 a0003 a0004 others(9): Show |
313 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
missense_variant | MODERATE | c.95C>T | p.Pro32Leu | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 232/3998 | 95/1323 | 32/440 | chr8 | 23068800 | |||
chr8:23068833 | C | T | 1 | a0013 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.62G>A | p.Gly21Glu | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 199/3998 | 62/1323 | 21/440 | chr8 | 23068833 | |||
chr8:23068839 | C | T | 1 | a0012 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.56G>A | p.Gly19Asp | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 193/3998 | 56/1323 | 19/440 | chr8 | 23068839 | |||
chr8:23068851 | C | G | 1 | a0013 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.44G>C | p.Arg15Pro | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 181/3998 | 44/1323 | 15/440 | chr8 | 23068851 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:23022982 | G | A | 1 | a0003c0016 | 1 | NA19003.hp1 | splice_region_variant&synonymous_variant | LOW | c.1012C>T | p.Leu338Leu | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1149/3998 | 1012/1323 | 338/440 | chr8 | 23022982 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:23020184 | A | T | 3 | a0001c0001t0009 a0001c0001t0011 a0004c0004t0009 |
4 | HG01243.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2487T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 2487 | chr8 | 23020184 | ||||||
chr8:23020235 | T | A | 1 | a0004c0004t0020 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2436A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 2436 | chr8 | 23020235 | ||||||
chr8:23020488 | T | A | 3 | a0001c0001t0009 a0001c0001t0011 a0004c0004t0009 |
4 | HG01243.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2183A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 2183 | chr8 | 23020488 | ||||||
chr8:23020546 | G | A | 1 | a0001c0001t0012 | 2 | HG02886.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2125C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 2125 | chr8 | 23020546 | ||||||
chr8:23020657 | A | G | 1 | a0001c0001t0024 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2014T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 2014 | chr8 | 23020657 | ||||||
chr8:23020683 | T | C | 1 | a0002c0002t0031 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1988A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1988 | chr8 | 23020683 | ||||||
chr8:23020706 | TAAAAG | T | 2 | a0001c0001t0008 a0002c0002t0032 |
4 | HG02809.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1960_*1964delCTTT others(1): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1960 | chr8 | 23020706 | ||||||
chr8:23020813 | G | C | 1 | a0001c0001t0013 | 2 | HG01496.hp2 HG03490.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1858C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1858 | chr8 | 23020813 | ||||||
chr8:23021180 | CTGAGGTC others(16): Show |
C | 1 | a0001c0001t0019 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1468_*1490delTCTA others(19): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1468 | chr8 | 23021180 | ||||||
chr8:23021232 | G | A | 1 | a0001c0001t0027 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1439C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1439 | chr8 | 23021232 | ||||||
chr8:23021322 | G | A | 1 | a0001c0001t0021 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1349C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1349 | chr8 | 23021322 | ||||||
chr8:23021509 | A | G | 1 | a0001c0001t0026 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1162T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1162 | chr8 | 23021509 | ||||||
chr8:23021856 | A | G | 1 | a0001c0001t0018 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*815T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 815 | chr8 | 23021856 | ||||||
chr8:23022056 | C | T | 2 | a0001c0001t0010 a0002c0002t0029 |
3 | HG02630.hp2 HG02976.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*615G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 615 | chr8 | 23022056 | ||||||
chr8:23022167 | G | A | 1 | a0001c0001t0012 | 2 | HG02886.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*504C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 504 | chr8 | 23022167 | ||||||
chr8:23022168 | G | A | 1 | a0003c0003t0025 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*503C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 503 | chr8 | 23022168 | ||||||
chr8:23022185 | G | C | 1 | a0001c0001t0012 | 2 | HG02886.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*486C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 486 | chr8 | 23022185 | ||||||
chr8:23022221 | T | C | 12 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(9): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*450A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 450 | chr8 | 23022221 | ||||||
chr8:23022432 | G | A | 1 | a0001c0001t0022 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*239C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 239 | chr8 | 23022432 | ||||||
chr8:23022510 | T | TACAGGAT others(37): Show |
1 | a0014c0012t0023 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117_*160dupGAAACT others(38): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 160 | chr8 | 23022510 | ||||||
chr8:23022527 | A | G | 2 | a0001c0001t0009 a0004c0004t0009 |
2 | HG02723.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*144T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 144 | chr8 | 23022527 | ||||||
chr8:23022590 | C | G | 1 | a0001c0001t0017 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*81G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 81 | chr8 | 23022590 | ||||||
chr8:23022594 | C | T | 1 | a0002c0002t0028 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*77G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 77 | chr8 | 23022594 | ||||||
chr8:23022649 | G | C | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0013 others(14): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*22C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 22 | chr8 | 23022649 | ||||||
chr8:23022660 | G | A | 2 | a0001c0001t0008 a0002c0002t0032 |
4 | HG02809.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 11 | chr8 | 23022660 | ||||||
chr8:23068906 | A | T | 1 | a0013c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 12 | chr8 | 23068906 | ||||||
chr8:23068908 | G | C | 1 | a0013c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-14C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 14 | chr8 | 23068908 | ||||||
chr8:23068910 | T | G | 1 | a0013c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-16A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 16 | chr8 | 23068910 | ||||||
chr8:23068911 | C | T | 1 | a0013c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 17 | chr8 | 23068911 | ||||||
chr8:23068914 | A | C | 1 | a0013c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-20T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 20 | chr8 | 23068914 | ||||||
chr8:23068985 | G | A | 14 | a0001c0001t0004 a0002c0002t0004 a0002c0002t0005 others(11): Show |
69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-91C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | chr8 | 23068985 | |||||||
chr8:23068988 | A | T | 1 | a0001c0001t0016 | 1 | NA19057.hp2 | 5_prime_UTR_variant | MODIFIER | c.-94T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 94 | chr8 | 23068988 | ||||||
chr8:23068995 | G | T | 1 | a0013c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-101C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 101 | chr8 | 23068995 | ||||||
chr8:23069001 | C | G | 2 | a0002c0002t0015 a0013c0010t0014 |
2 | HG02280.hp1 HG03139.hp1 |
5_prime_UTR_variant | MODIFIER | c.-107G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 107 | chr8 | 23069001 | ||||||
chr8:23069002 | C | T | 1 | a0013c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-108G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 108 | chr8 | 23069002 | ||||||
chr8:23069004 | G | T | 1 | a0013c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 110 | chr8 | 23069004 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:23022988 | G | A | 1 | a0001c0001t0012g0142 | 1 | HG02886.hp1 | splice_region_variant&intron_variant | LOW | c.1010-4C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23022988 | |||||||
chr8:23023124 | G | A | 1 | a0004c0004t0001g0126 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1010-140C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023124 | |||||||
chr8:23023145 | C | T | 1 | a0004c0004t0001g0019 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1010-161G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023145 | |||||||
chr8:23023192 | CAA | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(91): Show |
98 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1010-210_1010-209d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023192 | |||||||
chr8:23023275 | A | C | 2 | a0001c0001t0012g0142 a0001c0001t0012g0230 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1010-291T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023275 | |||||||
chr8:23023310 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1010-326C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023310 | |||||||
chr8:23023460 | G | C | 1 | a0001c0001t0002g0156 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1010-476C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023460 | |||||||
chr8:23023478 | GT | G | 4 | a0001c0001t0008g0037 a0001c0001t0008g0120 a0001c0001t0008g0125 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1010-495delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023478 | |||||||
chr8:23023492 | ACT | A | 3 | a0001c0001t0010g0207 a0001c0001t0010g0208 a0002c0002t0029g0354 |
3 | HG02630.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1010-510_1010-509d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023492 | |||||||
chr8:23023629 | A | G | 1 | a0004c0004t0001g0141 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1009+559T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023629 | |||||||
chr8:23023907 | A | G | 326 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(323): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1009+281T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023907 | |||||||
chr8:23024019 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0069 a0001c0001t0001g0247 |
3 | HG02145.hp1 HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1009+169C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23024019 | |||||||
chr8:23024020 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0069 a0001c0001t0001g0247 |
3 | HG02145.hp1 HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1009+168T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23024020 | |||||||
chr8:23024126 | C | T | 2 | a0001c0001t0002g0162 a0002c0002t0031g0367 |
2 | HG00735.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1009+62G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23024126 | |||||||
chr8:23024339 | T | C | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(315): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.937-79A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23024339 | |||||||
chr8:23024524 | AT | A | 44 | a0001c0001t0001g0016 a0001c0001t0001g0215 a0001c0001t0001g0240 others(41): Show |
46 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.937-265delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23024524 | |||||||
chr8:23024696 | C | T | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(314): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.937-436G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23024696 | |||||||
chr8:23024780 | G | A | 104 | a0001c0001t0002g0007 a0001c0001t0002g0017 a0001c0001t0002g0052 others(101): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.937-520C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23024780 | |||||||
chr8:23024870 | G | A | 2 | a0002c0002t0005g0342 a0002c0002t0005g0358 |
2 | NA19065.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.937-610C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23024870 | |||||||
chr8:23024977 | AAAAATAA others(3): Show |
A | 66 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0045 others(63): Show |
67 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.937-727_937-718del others(10): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23024977 | |||||||
chr8:23025018 | G | A | 21 | a0001c0001t0003g0044 a0001c0001t0003g0071 a0001c0001t0003g0153 others(18): Show |
23 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.937-758C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23025018 | |||||||
chr8:23025234 | C | T | 4 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0220 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.937-974G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23025234 | |||||||
chr8:23025797 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.936+1336G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23025797 | |||||||
chr8:23026011 | G | T | 2 | a0001c0001t0009g0217 a0004c0004t0009g0042 |
2 | HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.936+1122C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026011 | |||||||
chr8:23026087 | T | C | 9 | a0006c0006t0001g0031 a0006c0006t0001g0128 a0006c0006t0001g0129 others(6): Show |
9 | HG01192.hp1 HG02723.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.936+1046A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026087 | |||||||
chr8:23026112 | A | T | 1 | a0003c0003t0001g0098 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.936+1021T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026112 | |||||||
chr8:23026221 | A | C | 5 | a0001c0001t0002g0156 a0001c0001t0002g0162 a0001c0001t0002g0303 others(2): Show |
5 | HG00280.hp1 HG00735.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.936+912T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026221 | |||||||
chr8:23026266 | G | GT | 112 | a0001c0001t0001g0039 a0001c0001t0001g0221 a0001c0001t0002g0007 others(109): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.936+866dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026266 | |||||||
chr8:23026266 | GT | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(91): Show |
98 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.936+866delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026266 | |||||||
chr8:23026272 | T | G | 2 | a0001c0001t0011g0210 a0001c0001t0011g0225 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.936+861A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026272 | |||||||
chr8:23026288 | T | G | 1 | a0001c0001t0003g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.936+845A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026288 | |||||||
chr8:23026462 | G | A | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(313): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.936+671C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026462 | |||||||
chr8:23026514 | T | C | 2 | a0001c0001t0009g0217 a0004c0004t0009g0042 |
2 | HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.936+619A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026514 | |||||||
chr8:23026637 | C | A | 1 | a0004c0004t0001g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.936+496G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026637 | |||||||
chr8:23026718 | T | C | 35 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0045 others(32): Show |
35 | HG00408.hp1 HG00609.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.936+415A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026718 | |||||||
chr8:23026721 | T | C | 1 | a0002c0002t0006g0361 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.936+412A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026721 | |||||||
chr8:23026765 | C | T | 2 | a0001c0001t0011g0210 a0001c0001t0011g0225 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.936+368G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026765 | |||||||
chr8:23026823 | T | C | 14 | a0001c0001t0003g0043 a0001c0001t0008g0037 a0001c0001t0008g0120 others(11): Show |
14 | HG01192.hp1 HG02615.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.936+310A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026823 | |||||||
chr8:23026995 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.936+138G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026995 | |||||||
chr8:23027075 | C | A | 65 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0045 others(62): Show |
66 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.936+58G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23027075 | |||||||
chr8:23027088 | G | C | 65 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0045 others(62): Show |
66 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.936+45C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23027088 | |||||||
chr8:23027100 | G | A | 2 | a0001c0001t0011g0210 a0001c0001t0011g0225 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.936+33C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23027100 | |||||||
chr8:23027320 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.781-32C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 6/8 | chr8 | 23027320 | |||||||
chr8:23027441 | G | A | 3 | a0001c0001t0001g0029 a0002c0002t0004g0331 a0002c0002t0028g0357 |
3 | HG03516.hp1 HG03669.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.781-153C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 6/8 | chr8 | 23027441 | |||||||
chr8:23027596 | A | G | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(322): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.780+126T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 6/8 | chr8 | 23027596 | |||||||
chr8:23027640 | G | A | 110 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0032 others(107): Show |
113 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.780+82C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 6/8 | chr8 | 23027640 | |||||||
chr8:23027641 | G | A | 217 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0032 others(214): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.780+81C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 6/8 | chr8 | 23027641 | |||||||
chr8:23027818 | A | T | 98 | a0001c0001t0002g0007 a0001c0001t0002g0017 a0001c0001t0002g0052 others(95): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.749-65T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23027818 | |||||||
chr8:23027930 | A | G | 2 | a0001c0001t0003g0168 a0002c0002t0006g0337 |
2 | HG01099.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.749-177T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23027930 | |||||||
chr8:23028080 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.748+251C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23028080 | |||||||
chr8:23028091 | T | A | 1 | a0003c0003t0003g0111 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.748+240A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23028091 | |||||||
chr8:23028156 | A | G | 3 | a0001c0001t0001g0221 a0002c0002t0004g0322 a0002c0002t0004g0350 |
3 | HG02109.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.748+175T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23028156 | |||||||
chr8:23028226 | G | A | 1 | a0001c0001t0009g0217 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.748+105C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23028226 | |||||||
chr8:23028248 | G | A | 4 | a0001c0001t0008g0037 a0001c0001t0008g0120 a0001c0001t0008g0125 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.748+83C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23028248 | |||||||
chr8:23028318 | A | T | 3 | a0001c0001t0001g0221 a0002c0002t0004g0322 a0002c0002t0004g0350 |
3 | HG02109.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.748+13T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23028318 | |||||||
chr8:23028617 | A | G | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(321): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.477-15T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028617 | |||||||
chr8:23028629 | G | T | 1 | a0001c0001t0009g0217 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.477-27C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028629 | |||||||
chr8:23028717 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(93): Show |
100 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.477-115G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028717 | |||||||
chr8:23028742 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0200 |
2 | HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.477-140G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028742 | |||||||
chr8:23028812 | C | A | 12 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0100 others(9): Show |
13 | HG01993.hp2 NA18747.hp2 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.477-210G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028812 | |||||||
chr8:23028872 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.477-270A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028872 | |||||||
chr8:23028877 | T | C | 1 | a0004c0004t0001g0135 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.477-275A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028877 | |||||||
chr8:23029034 | G | A | 3 | a0001c0001t0001g0221 a0002c0002t0004g0322 a0002c0002t0004g0350 |
3 | HG02109.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.477-432C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029034 | |||||||
chr8:23029072 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.477-470T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029072 | |||||||
chr8:23029124 | G | A | 1 | a0002c0002t0005g0313 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.476+486C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029124 | |||||||
chr8:23029305 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(94): Show |
101 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.476+305G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029305 | |||||||
chr8:23029319 | C | T | 1 | a0002c0002t0004g0372 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.476+291G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029319 | |||||||
chr8:23029321 | A | G | 1 | a0002c0002t0005g0335 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.476+289T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029321 | |||||||
chr8:23029339 | C | A | 1 | a0001c0001t0002g0301 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.476+271G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029339 | |||||||
chr8:23029420 | G | A | 5 | a0001c0001t0002g0193 a0001c0001t0002g0292 a0001c0001t0002g0310 others(2): Show |
5 | HG01074.hp2 HG03017.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.476+190C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029420 | |||||||
chr8:23029471 | C | T | 2 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.476+139G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029471 | |||||||
chr8:23029472 | G | C | 1 | a0001c0001t0001g0249 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.476+138C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029472 | |||||||
chr8:23029500 | C | G | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(313): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.476+110G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029500 | |||||||
chr8:23029595 | C | T | 1 | a0001c0001t0009g0217 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.476+15G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029595 | |||||||
chr8:23029726 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02717.hp2 | splice_region_variant&intron_variant | LOW | c.365-5G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23029726 | |||||||
chr8:23029741 | T | C | 14 | a0001c0001t0003g0043 a0001c0001t0008g0037 a0001c0001t0008g0120 others(11): Show |
14 | HG01192.hp1 HG02615.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.365-20A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23029741 | |||||||
chr8:23029968 | G | A | 1 | a0003c0003t0001g0264 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.365-247C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23029968 | |||||||
chr8:23029986 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.365-265C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23029986 | |||||||
chr8:23030095 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(97): Show |
104 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.365-374C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23030095 | |||||||
chr8:23030456 | G | A | 201 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0045 others(198): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.364+303C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23030456 | |||||||
chr8:23030594 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.364+165C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23030594 | |||||||
chr8:23030894 | G | A | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(321): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.251-22C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23030894 | |||||||
chr8:23030948 | C | T | 1 | a0006c0006t0001g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.251-76G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23030948 | |||||||
chr8:23031108 | C | T | 13 | a0001c0001t0008g0037 a0001c0001t0008g0120 a0001c0001t0008g0125 others(10): Show |
13 | HG01192.hp1 HG02723.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.251-236G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031108 | |||||||
chr8:23031258 | A | G | 1 | a0001c0001t0021g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.251-386T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031258 | |||||||
chr8:23031309 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.251-437G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031309 | |||||||
chr8:23031323 | G | T | 3 | a0001c0001t0010g0207 a0001c0001t0010g0208 a0002c0002t0029g0354 |
3 | HG02630.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.251-451C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031323 | |||||||
chr8:23031372 | G | A | 6 | a0001c0001t0001g0221 a0001c0001t0002g0186 a0001c0001t0002g0255 others(3): Show |
6 | HG02109.hp1 HG02965.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-500C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031372 | |||||||
chr8:23031375 | C | CTATT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0039 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.251-507_251-504dup others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031375 | |||||||
chr8:23031375 | C | CTATTTAT others(1): Show |
61 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0025 others(58): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.251-511_251-504dup others(8): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031375 | |||||||
chr8:23031375 | C | CTATTTAT others(5): Show |
17 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0159 others(14): Show |
17 | HG00438.hp1 HG02109.hp1 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.251-515_251-504dup others(12): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031375 | |||||||
chr8:23031375 | CTATT | C | 60 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0083 others(57): Show |
61 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.251-507_251-504del others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031375 | |||||||
chr8:23031504 | C | G | 5 | a0001c0001t0001g0219 a0001c0001t0004g0373 a0001c0001t0010g0207 others(2): Show |
5 | HG02630.hp2 HG02809.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-632G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031504 | |||||||
chr8:23031544 | C | T | 186 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0045 others(183): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.251-672G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031544 | |||||||
chr8:23031545 | A | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(312): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.251-673T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031545 | |||||||
chr8:23031547 | C | T | 1 | a0002c0002t0004g0359 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.251-675G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031547 | |||||||
chr8:23031561 | G | C | 1 | a0001c0001t0009g0217 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.251-689C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031561 | |||||||
chr8:23031584 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG02717.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.251-712C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031584 | |||||||
chr8:23031873 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.251-1001C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031873 | |||||||
chr8:23031911 | C | CAT | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(172): Show |
180 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.251-1041_251-1040d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031911 | |||||||
chr8:23031912 | A | ATAT | 6 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0001g0221 others(3): Show |
6 | HG00597.hp1 HG02109.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-1041_251-1040i others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031912 | |||||||
chr8:23031913 | T | TA | 142 | a0001c0001t0001g0216 a0001c0001t0001g0256 a0001c0001t0002g0007 others(139): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.251-1042_251-1041i others(3): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031913 | |||||||
chr8:23031915 | T | A | 1 | a0001c0001t0007g0081 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.251-1043A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031915 | |||||||
chr8:23032068 | G | A | 1 | a0004c0004t0001g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.251-1196C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032068 | |||||||
chr8:23032140 | C | T | 1 | a0004c0004t0001g0019 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.251-1268G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032140 | |||||||
chr8:23032270 | C | T | 18 | a0001c0001t0003g0044 a0001c0001t0003g0071 a0001c0001t0003g0153 others(15): Show |
20 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.251-1398G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032270 | |||||||
chr8:23032342 | C | G | 1 | a0001c0001t0026g0028 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.251-1470G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032342 | |||||||
chr8:23032368 | G | A | 1 | a0002c0002t0004g0345 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.251-1496C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032368 | |||||||
chr8:23032384 | G | A | 1 | a0002c0002t0004g0353 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.251-1512C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032384 | |||||||
chr8:23032449 | T | C | 13 | a0001c0001t0008g0037 a0001c0001t0008g0120 a0001c0001t0008g0125 others(10): Show |
13 | HG01192.hp1 HG02723.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.251-1577A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032449 | |||||||
chr8:23032527 | C | CGA | 73 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0032 others(70): Show |
74 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.251-1657_251-1656d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032527 | |||||||
chr8:23032584 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0218 |
3 | HG01884.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.251-1712C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032584 | |||||||
chr8:23032800 | G | A | 1 | a0001c0001t0012g0230 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.251-1928C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032800 | |||||||
chr8:23033113 | A | G | 1 | a0002c0002t0005g0369 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.251-2241T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033113 | |||||||
chr8:23033259 | T | C | 4 | a0004c0004t0001g0149 a0004c0004t0001g0150 a0004c0004t0001g0177 others(1): Show |
4 | NA18939.hp2 NA19002.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-2387A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033259 | |||||||
chr8:23033306 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0215 a0002c0002t0004g0331 others(3): Show |
6 | HG02055.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-2434G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033306 | |||||||
chr8:23033401 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(96): Show |
103 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.251-2529C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033401 | |||||||
chr8:23033412 | G | A | 216 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0032 others(213): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.251-2540C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033412 | |||||||
chr8:23033444 | G | A | 6 | a0004c0004t0001g0135 a0004c0004t0001g0141 a0004c0004t0001g0214 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-2572C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033444 | |||||||
chr8:23033529 | A | C | 1 | a0004c0004t0001g0131 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.251-2657T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033529 | |||||||
chr8:23033585 | C | CA | 6 | a0004c0004t0001g0026 a0004c0004t0001g0135 a0004c0004t0001g0177 others(3): Show |
6 | HG01099.hp2 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-2714dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CA | C | 12 | a0003c0003t0007g0113 a0004c0004t0001g0019 a0004c0004t0001g0033 others(9): Show |
12 | HG00621.hp2 HG00639.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.251-2714delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAA | C | 13 | a0001c0001t0002g0076 a0001c0001t0002g0152 a0001c0001t0002g0196 others(10): Show |
13 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.251-2717_251-2714d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAA | C | 36 | a0001c0001t0002g0007 a0001c0001t0002g0052 a0001c0001t0002g0055 others(33): Show |
39 | HG00621.hp1 HG01074.hp1 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.251-2718_251-2714d others(7): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAAA | C | 82 | a0001c0001t0001g0297 a0001c0001t0001g0299 a0001c0001t0002g0017 others(79): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.251-2719_251-2714d others(8): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAAAA | C | 6 | a0001c0001t0003g0071 a0001c0001t0003g0153 a0002c0002t0006g0351 others(3): Show |
6 | HG01891.hp1 HG03017.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-2720_251-2714d others(9): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAAAA others(1): Show |
C | 22 | a0001c0001t0001g0236 a0001c0001t0002g0056 a0001c0001t0003g0004 others(19): Show |
23 | HG00423.hp1 HG01106.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.251-2721_251-2714d others(10): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAAAA others(2): Show |
C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0127 others(11): Show |
14 | HG02055.hp1 HG02055.hp2 HG02273.hp2 others(11): Show |
intron_variant | MODIFIER | c.251-2722_251-2714d others(11): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAAAA others(3): Show |
C | 36 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0067 others(33): Show |
36 | HG00408.hp1 HG00609.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.251-2723_251-2714d others(12): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0278 a0002c0002t0004g0345 |
2 | HG02135.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.251-2724_251-2714d others(13): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0011g0210 a0001c0001t0011g0225 a0001c0001t0012g0142 others(1): Show |
4 | HG01243.hp2 HG02886.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-2725_251-2714d others(14): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0001g0169 a0001c0001t0001g0175 a0001c0001t0001g0231 others(3): Show |
6 | HG01978.hp2 HG02258.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-2726_251-2714d others(15): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAAAA others(7): Show |
C | 42 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0034 others(39): Show |
43 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.251-2727_251-2714d others(16): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAAAA others(8): Show |
C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(44): Show |
50 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.251-2728_251-2714d others(17): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251-2729_251-2714d others(18): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAAAA others(15): Show |
C | 2 | a0001c0001t0002g0158 a0001c0001t0002g0166 |
2 | HG02602.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.251-2735_251-2714d others(24): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033585 | CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0002g0060 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.251-2736_251-2714d others(25): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | |||||||
chr8:23033620 | A | AAAAAAAA others(3): Show |
2 | a0002c0002t0004g0322 a0002c0002t0004g0350 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.251-2749_251-2748i others(12): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033620 | |||||||
chr8:23033620 | A | G | 75 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0032 others(72): Show |
76 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.251-2748T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033620 | |||||||
chr8:23033666 | A | G | 1 | a0004c0004t0001g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.251-2794T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033666 | |||||||
chr8:23033685 | T | C | 2 | a0001c0001t0011g0210 a0001c0001t0011g0225 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.251-2813A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033685 | |||||||
chr8:23033776 | G | A | 7 | a0004c0004t0001g0040 a0004c0004t0001g0126 a0004c0004t0001g0132 others(4): Show |
7 | HG01099.hp2 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-2904C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033776 | |||||||
chr8:23033807 | G | A | 21 | a0001c0001t0003g0044 a0001c0001t0003g0071 a0001c0001t0003g0153 others(18): Show |
23 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.251-2935C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033807 | |||||||
chr8:23033836 | A | G | 1 | a0001c0001t0003g0234 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.251-2964T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033836 | |||||||
chr8:23033898 | C | G | 3 | a0001c0001t0001g0221 a0002c0002t0004g0322 a0002c0002t0004g0350 |
3 | HG02109.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.251-3026G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033898 | |||||||
chr8:23034004 | G | A | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(317): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.251-3132C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034004 | |||||||
chr8:23034160 | G | A | 9 | a0001c0001t0001g0016 a0001c0001t0001g0127 a0001c0001t0001g0215 others(6): Show |
9 | HG02055.hp1 HG02055.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-3288C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034160 | |||||||
chr8:23034243 | G | C | 1 | a0001c0001t0003g0243 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.251-3371C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034243 | |||||||
chr8:23034373 | G | T | 5 | a0001c0001t0009g0217 a0001c0001t0011g0210 a0001c0001t0011g0225 others(2): Show |
5 | HG01243.hp2 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-3501C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034373 | |||||||
chr8:23034437 | G | T | 1 | a0001c0001t0002g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.251-3565C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034437 | |||||||
chr8:23034572 | A | T | 5 | a0004c0004t0001g0121 a0004c0004t0001g0209 a0009c0009t0001g0206 others(2): Show |
5 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-3700T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034572 | |||||||
chr8:23034644 | C | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(316): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.251-3772G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034644 | |||||||
chr8:23034761 | T | C | 133 | a0001c0001t0001g0067 a0001c0001t0001g0151 a0001c0001t0001g0192 others(130): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.251-3889A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034761 | |||||||
chr8:23034937 | T | C | 80 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0032 others(77): Show |
81 | HG00423.hp1 HG00609.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.251-4065A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034937 | |||||||
chr8:23035058 | T | TTGGCAAG others(8): Show |
1 | a0003c0003t0003g0111 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.251-4201_251-4187d others(17): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035058 | |||||||
chr8:23035142 | TA | T | 9 | a0006c0006t0001g0031 a0006c0006t0001g0128 a0006c0006t0001g0129 others(6): Show |
9 | HG01192.hp1 HG02723.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.251-4271delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035142 | |||||||
chr8:23035402 | A | T | 4 | a0001c0001t0003g0004 a0001c0001t0003g0173 a0001c0001t0016g0013 others(1): Show |
5 | NA18939.hp1 NA18941.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.251-4530T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035402 | |||||||
chr8:23035521 | G | A | 130 | a0001c0001t0001g0067 a0001c0001t0001g0151 a0001c0001t0001g0192 others(127): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.251-4649C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035521 | |||||||
chr8:23035897 | A | T | 1 | a0002c0002t0006g0351 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.251-5025T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035897 | |||||||
chr8:23035924 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.251-5052C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035924 | |||||||
chr8:23035934 | T | A | 3 | a0001c0001t0001g0221 a0002c0002t0004g0322 a0002c0002t0004g0350 |
3 | HG02109.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.251-5062A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035934 | |||||||
chr8:23035953 | C | T | 2 | a0001c0001t0011g0210 a0001c0001t0011g0225 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.251-5081G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035953 | |||||||
chr8:23036078 | A | AGAT | 131 | a0001c0001t0001g0067 a0001c0001t0001g0151 a0001c0001t0001g0192 others(128): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.251-5207_251-5206i others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036078 | |||||||
chr8:23036079 | T | A | 131 | a0001c0001t0001g0067 a0001c0001t0001g0151 a0001c0001t0001g0192 others(128): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.251-5207A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036079 | |||||||
chr8:23036080 | C | A | 131 | a0001c0001t0001g0067 a0001c0001t0001g0151 a0001c0001t0001g0192 others(128): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.251-5208G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036080 | |||||||
chr8:23036150 | A | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0127 a0001c0001t0001g0215 others(6): Show |
9 | HG02055.hp1 HG02055.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-5278T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036150 | |||||||
chr8:23036301 | G | A | 3 | a0001c0001t0001g0221 a0002c0002t0004g0322 a0002c0002t0004g0350 |
3 | HG02109.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.251-5429C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036301 | |||||||
chr8:23036455 | C | G | 66 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0032 others(63): Show |
67 | HG00423.hp1 HG00609.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.251-5583G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036455 | |||||||
chr8:23036495 | G | A | 5 | a0001c0001t0003g0043 a0001c0001t0008g0037 a0001c0001t0008g0120 others(2): Show |
5 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.251-5623C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036495 | |||||||
chr8:23036611 | G | A | 127 | a0001c0001t0001g0067 a0001c0001t0001g0151 a0001c0001t0001g0192 others(124): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.251-5739C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036611 | |||||||
chr8:23036718 | C | T | 3 | a0001c0001t0001g0270 a0003c0003t0001g0098 a0016c0018t0001g0085 |
3 | HG01081.hp1 NA18992.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.251-5846G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036718 | |||||||
chr8:23037135 | A | T | 2 | a0001c0001t0011g0210 a0001c0001t0011g0225 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.250+6003T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037135 | |||||||
chr8:23037164 | A | G | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(322): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.250+5974T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037164 | |||||||
chr8:23037252 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(102): Show |
109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.250+5886A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037252 | |||||||
chr8:23037359 | T | C | 1 | a0001c0001t0003g0035 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.250+5779A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037359 | |||||||
chr8:23037500 | A | G | 1 | a0001c0001t0018g0170 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.250+5638T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037500 | |||||||
chr8:23037692 | A | T | 2 | a0004c0004t0001g0026 a0004c0004t0001g0059 |
2 | HG01981.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.250+5446T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037692 | |||||||
chr8:23037728 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(102): Show |
109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.250+5410A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037728 | |||||||
chr8:23037974 | G | T | 1 | a0002c0002t0004g0366 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.250+5164C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037974 | |||||||
chr8:23038005 | A | G | 1 | a0011c0017t0001g0106 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.250+5133T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038005 | |||||||
chr8:23038186 | T | C | 1 | a0003c0003t0002g0088 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.250+4952A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038186 | |||||||
chr8:23038267 | T | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(318): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.250+4871A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038267 | |||||||
chr8:23038475 | G | A | 1 | a0007c0008t0004g0338 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.250+4663C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038475 | |||||||
chr8:23038483 | G | A | 1 | a0017c0015t0001g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.250+4655C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038483 | |||||||
chr8:23038544 | A | G | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(318): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.250+4594T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038544 | |||||||
chr8:23038595 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(102): Show |
109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.250+4543T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038595 | |||||||
chr8:23038709 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0011g0210 a0001c0001t0011g0225 |
3 | HG01243.hp2 HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.250+4429A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038709 | |||||||
chr8:23038877 | G | A | 2 | a0004c0004t0001g0238 a0010c0014t0001g0211 |
2 | HG01099.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.250+4261C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038877 | |||||||
chr8:23038982 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0011g0210 a0001c0001t0011g0225 |
3 | HG01243.hp2 HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.250+4156T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038982 | |||||||
chr8:23039179 | C | T | 2 | a0002c0002t0004g0322 a0002c0002t0004g0350 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.250+3959G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039179 | |||||||
chr8:23039191 | G | A | 4 | a0001c0001t0002g0055 a0001c0001t0003g0035 a0002c0002t0015g0012 others(1): Show |
4 | HG02280.hp1 HG02965.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+3947C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039191 | |||||||
chr8:23039269 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250+3869G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039269 | |||||||
chr8:23039305 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.250+3833G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039305 | |||||||
chr8:23039382 | ACAGGATA others(3): Show |
A | 1 | a0001c0001t0001g0204 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.250+3746_250+3755d others(12): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039382 | |||||||
chr8:23039544 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.250+3594G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039544 | |||||||
chr8:23039720 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.250+3418C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039720 | |||||||
chr8:23039845 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0002g0172 |
2 | HG02040.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.250+3293G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039845 | |||||||
chr8:23039922 | G | A | 7 | a0004c0004t0001g0040 a0004c0004t0020g0041 a0005c0005t0004g0321 others(4): Show |
7 | HG01192.hp1 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+3216C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039922 | |||||||
chr8:23039998 | C | G | 1 | a0006c0006t0001g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.250+3140G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039998 | |||||||
chr8:23040039 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(191): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.250+3099T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040039 | |||||||
chr8:23040084 | G | C | 1 | a0001c0001t0003g0155 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.250+3054C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040084 | |||||||
chr8:23040106 | A | G | 8 | a0001c0001t0001g0039 a0001c0001t0001g0219 a0001c0001t0004g0373 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.250+3032T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040106 | |||||||
chr8:23040173 | C | T | 139 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0038 others(136): Show |
143 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.250+2965G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040173 | |||||||
chr8:23040255 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.250+2883A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040255 | |||||||
chr8:23040264 | TAA | T | 8 | a0001c0001t0003g0212 a0001c0001t0003g0213 a0001c0001t0003g0244 others(5): Show |
8 | HG01261.hp2 HG02148.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.250+2872_250+2873d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040264 | |||||||
chr8:23040266 | A | T | 104 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0061 others(101): Show |
108 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.250+2872T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040266 | |||||||
chr8:23040267 | A | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(173): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.250+2871T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040267 | |||||||
chr8:23040274 | TATAATAT others(45): Show |
T | 1 | a0001c0001t0001g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.250+2812_250+2863d others(54): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040274 | |||||||
chr8:23040276 | T | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(172): Show |
181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.250+2862A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040276 | |||||||
chr8:23040289 | T | A | 96 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0061 others(93): Show |
100 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.250+2849A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040289 | |||||||
chr8:23040290 | TAA | T | 42 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0083 others(39): Show |
42 | HG00438.hp1 HG00609.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.250+2846_250+2847d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040290 | |||||||
chr8:23040292 | A | T | 1 | a0003c0003t0001g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.250+2846T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040292 | |||||||
chr8:23040294 | TATATATA others(15): Show |
T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(166): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2822_250+2843d others(24): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040294 | |||||||
chr8:23040294 | TATATATA others(69): Show |
T | 6 | a0001c0001t0001g0204 a0001c0001t0001g0272 a0006c0006t0001g0128 others(3): Show |
6 | HG01192.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+2768_250+2843d others(78): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040294 | |||||||
chr8:23040298 | T | TAATATAT others(45): Show |
1 | a0003c0003t0001g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.250+2839_250+2840i others(54): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040298 | |||||||
chr8:23040300 | T | A | 1 | a0003c0003t0001g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.250+2838A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040300 | |||||||
chr8:23040313 | A | T | 1 | a0008c0007t0004g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+2825T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040313 | |||||||
chr8:23040313 | ATAAATAT others(75): Show |
A | 1 | a0005c0005t0004g0365 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.250+2743_250+2824d others(84): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040313 | |||||||
chr8:23040318 | TATATATA others(19): Show |
T | 1 | a0008c0007t0004g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+2794_250+2819d others(28): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040318 | |||||||
chr8:23040324 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.250+2814A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040324 | |||||||
chr8:23040326 | C | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0218 |
3 | HG01884.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.250+2812G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040326 | |||||||
chr8:23040341 | T | A | 1 | a0001c0001t0003g0020 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.250+2797A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040341 | |||||||
chr8:23040344 | A | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(166): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2794T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040344 | |||||||
chr8:23040344 | AATATATA others(21): Show |
A | 86 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0061 others(83): Show |
90 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.250+2766_250+2793d others(30): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040344 | |||||||
chr8:23040349 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(166): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2789T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040349 | |||||||
chr8:23040360 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(166): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2778T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040360 | |||||||
chr8:23040367 | A | T | 21 | a0001c0001t0001g0247 a0001c0001t0002g0017 a0001c0001t0002g0115 others(18): Show |
21 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.250+2771T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040367 | |||||||
chr8:23040367 | AT | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(166): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2770delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040367 | |||||||
chr8:23040367 | ATAAATAT others(21): Show |
T | 1 | a0001c0001t0001g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.250+2744_250+2771d others(30): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040367 | |||||||
chr8:23040370 | A | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(166): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2768T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040370 | |||||||
chr8:23040375 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(166): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2763T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040375 | |||||||
chr8:23040383 | AAT | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(166): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2753_250+2754d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040383 | |||||||
chr8:23040396 | TAA | T | 6 | a0001c0001t0001g0204 a0001c0001t0001g0272 a0006c0006t0001g0128 others(3): Show |
6 | HG01192.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+2740_250+2741d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040396 | |||||||
chr8:23040398 | A | AAT | 14 | a0001c0001t0001g0219 a0001c0001t0002g0115 a0001c0001t0002g0116 others(11): Show |
14 | HG02293.hp1 HG02572.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.250+2738_250+2739d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040398 | |||||||
chr8:23040398 | A | AATATATA others(23): Show |
35 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0083 others(32): Show |
35 | HG00438.hp1 HG00609.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.250+2710_250+2739d others(32): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040398 | |||||||
chr8:23040405 | A | G | 6 | a0001c0001t0001g0204 a0001c0001t0001g0272 a0006c0006t0001g0128 others(3): Show |
6 | HG01192.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+2733T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040405 | |||||||
chr8:23040406 | TACAAAAT others(53): Show |
T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(166): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2672_250+2731d others(62): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040406 | |||||||
chr8:23040416 | A | G | 6 | a0001c0001t0001g0204 a0001c0001t0001g0272 a0006c0006t0001g0128 others(3): Show |
6 | HG01192.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+2722T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040416 | |||||||
chr8:23040419 | TTTA | T | 6 | a0001c0001t0001g0204 a0001c0001t0001g0272 a0006c0006t0001g0128 others(3): Show |
6 | HG01192.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+2716_250+2718d others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040419 | |||||||
chr8:23040422 | A | ATTATATA others(16): Show |
5 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0220 others(2): Show |
5 | HG02293.hp1 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+2715_250+2716i others(25): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040422 | |||||||
chr8:23040423 | T | A | 2 | a0001c0001t0003g0285 a0001c0001t0003g0305 |
2 | HG00140.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.250+2715A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040423 | |||||||
chr8:23040433 | A | G | 11 | a0001c0001t0001g0204 a0001c0001t0001g0272 a0001c0001t0002g0115 others(8): Show |
11 | HG01192.hp1 HG02293.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.250+2705T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040433 | |||||||
chr8:23040436 | TACAAAAT others(23): Show |
T | 1 | a0002c0002t0005g0368 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.250+2672_250+2701d others(32): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040436 | |||||||
chr8:23040441 | AAT | A | 11 | a0001c0001t0001g0204 a0001c0001t0001g0272 a0001c0001t0002g0115 others(8): Show |
11 | HG01192.hp1 HG02293.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.250+2695_250+2696d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040441 | |||||||
chr8:23040464 | TAC | T | 11 | a0001c0001t0001g0204 a0001c0001t0001g0272 a0001c0001t0002g0115 others(8): Show |
11 | HG01192.hp1 HG02293.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.250+2672_250+2673d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040464 | |||||||
chr8:23040466 | C | T | 151 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0032 others(148): Show |
155 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.250+2672G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040466 | |||||||
chr8:23040499 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(175): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.250+2639A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040499 | |||||||
chr8:23040572 | C | T | 110 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0039 others(107): Show |
114 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.250+2566G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040572 | |||||||
chr8:23040616 | AAAAC | A | 8 | a0001c0001t0001g0219 a0001c0001t0004g0373 a0001c0001t0010g0207 others(5): Show |
8 | HG02630.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.250+2518_250+2521d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040616 | |||||||
chr8:23040620 | C | T | 77 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0104 others(74): Show |
78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.250+2518G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040620 | |||||||
chr8:23040646 | C | A | 32 | a0001c0001t0001g0032 a0001c0001t0001g0083 a0001c0001t0001g0101 others(29): Show |
32 | HG00438.hp1 HG00609.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.250+2492G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040646 | |||||||
chr8:23040709 | G | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(317): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.250+2429C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040709 | |||||||
chr8:23040732 | C | T | 4 | a0001c0001t0003g0035 a0001c0001t0008g0037 a0001c0001t0008g0120 others(1): Show |
4 | HG02280.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+2406G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040732 | |||||||
chr8:23040733 | G | A | 2 | a0001c0001t0001g0236 a0003c0003t0003g0111 |
2 | NA18975.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.250+2405C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040733 | |||||||
chr8:23040891 | C | T | 138 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0078 others(135): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.250+2247G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040891 | |||||||
chr8:23040910 | T | C | 3 | a0001c0001t0001g0159 a0001c0001t0001g0282 a0001c0001t0022g0289 |
3 | NA18954.hp2 NA18993.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.250+2228A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040910 | |||||||
chr8:23040922 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(89): Show |
95 | HG00597.hp1 HG00597.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.250+2216G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040922 | |||||||
chr8:23041058 | TTTG | T | 40 | a0001c0001t0001g0179 a0001c0001t0001g0181 a0001c0001t0001g0215 others(37): Show |
41 | HG01123.hp1 HG01243.hp2 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.250+2077_250+2079d others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041058 | |||||||
chr8:23041060 | TG | T | 21 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0218 others(18): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.250+2077delC | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041060 | |||||||
chr8:23041061 | G | T | 19 | a0001c0001t0001g0061 a0001c0001t0001g0067 a0001c0001t0001g0069 others(16): Show |
19 | HG02004.hp2 HG02027.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.250+2077C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041061 | |||||||
chr8:23041062 | TTG | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(271): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.250+2074_250+2075d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041062 | |||||||
chr8:23041063 | TG | T | 3 | a0001c0001t0001g0295 a0002c0002t0004g0372 a0004c0004t0001g0026 |
3 | HG02257.hp1 HG03195.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.250+2074delC | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041063 | |||||||
chr8:23041085 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.250+2053C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041085 | |||||||
chr8:23041097 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0165 a0001c0001t0026g0028 |
3 | HG03654.hp2 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.250+2041G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041097 | |||||||
chr8:23041119 | C | T | 2 | a0001c0001t0001g0240 a0003c0016t0001g0307 |
2 | NA18953.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.250+2019G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041119 | |||||||
chr8:23041191 | T | C | 1 | a0001c0001t0002g0060 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.250+1947A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041191 | |||||||
chr8:23041223 | A | C | 32 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0165 others(29): Show |
33 | HG00639.hp1 HG01891.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.250+1915T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041223 | |||||||
chr8:23041253 | C | T | 1 | a0004c0004t0009g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.250+1885G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041253 | |||||||
chr8:23041255 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.250+1883G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041255 | |||||||
chr8:23041265 | C | A | 4 | a0001c0001t0001g0151 a0004c0004t0001g0149 a0004c0004t0001g0150 others(1): Show |
4 | NA19002.hp2 NA19058.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+1873G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041265 | |||||||
chr8:23041317 | G | A | 2 | a0001c0001t0003g0222 a0001c0001t0003g0259 |
2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.250+1821C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041317 | |||||||
chr8:23041346 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0045 others(155): Show |
164 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.250+1792A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041346 | |||||||
chr8:23041352 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.250+1786G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041352 | |||||||
chr8:23041382 | T | C | 4 | a0001c0001t0001g0191 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | NA18983.hp2 NA18998.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+1756A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041382 | |||||||
chr8:23041393 | G | A | 1 | a0003c0003t0002g0189 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.250+1745C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041393 | |||||||
chr8:23041447 | G | A | 28 | a0001c0001t0001g0117 a0001c0001t0001g0179 a0001c0001t0001g0181 others(25): Show |
28 | HG01123.hp1 HG02523.hp2 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.250+1691C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041447 | |||||||
chr8:23041537 | G | GTCAA | 6 | a0001c0001t0001g0032 a0001c0001t0001g0165 a0001c0001t0026g0028 others(3): Show |
6 | HG00639.hp1 HG02257.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+1597_250+1600d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041537 | |||||||
chr8:23041568 | C | G | 2 | a0004c0004t0001g0019 a0004c0004t0001g0026 |
2 | HG00639.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.250+1570G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041568 | |||||||
chr8:23041603 | T | TA | 23 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0027 others(20): Show |
23 | HG00738.hp2 HG01081.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.250+1534dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041603 | |||||||
chr8:23041603 | TA | T | 60 | a0001c0001t0001g0034 a0001c0001t0001g0045 a0001c0001t0001g0101 others(57): Show |
60 | HG00639.hp1 HG00738.hp1 HG01123.hp1 others(57): Show |
intron_variant | MODIFIER | c.250+1534delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041603 | |||||||
chr8:23041603 | TAA | T | 37 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0001c0001t0001g0077 others(34): Show |
38 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.250+1533_250+1534d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041603 | |||||||
chr8:23041638 | A | C | 1 | a0001c0001t0002g0182 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.250+1500T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041638 | |||||||
chr8:23041663 | C | A | 9 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0002c0002t0004g0316 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.250+1475G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041663 | |||||||
chr8:23041792 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.250+1346T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041792 | |||||||
chr8:23041845 | T | C | 9 | a0001c0001t0001g0216 a0001c0001t0003g0261 a0001c0001t0009g0217 others(6): Show |
9 | HG00639.hp2 HG01123.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.250+1293A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041845 | |||||||
chr8:23041871 | G | A | 26 | a0001c0001t0001g0117 a0001c0001t0001g0179 a0001c0001t0001g0181 others(23): Show |
26 | HG01123.hp1 HG01433.hp2 HG02523.hp2 others(23): Show |
intron_variant | MODIFIER | c.250+1267C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041871 | |||||||
chr8:23041912 | C | G | 2 | a0001c0001t0001g0221 a0006c0006t0001g0031 |
2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.250+1226G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041912 | |||||||
chr8:23042086 | C | T | 3 | a0001c0001t0001g0231 a0001c0001t0011g0225 a0008c0007t0004g0317 |
3 | HG02258.hp2 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.250+1052G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042086 | |||||||
chr8:23042110 | T | C | 1 | a0006c0006t0001g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.250+1028A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042110 | |||||||
chr8:23042119 | T | C | 12 | a0001c0001t0001g0038 a0001c0001t0001g0218 a0001c0001t0001g0219 others(9): Show |
12 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.250+1019A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042119 | |||||||
chr8:23042120 | C | G | 47 | a0001c0001t0001g0045 a0001c0001t0001g0117 a0001c0001t0001g0179 others(44): Show |
48 | HG00099.hp2 HG00733.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.250+1018G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042120 | |||||||
chr8:23042125 | C | T | 9 | a0001c0001t0001g0039 a0001c0001t0003g0234 a0001c0001t0003g0261 others(6): Show |
9 | HG00639.hp2 HG02257.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.250+1013G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042125 | |||||||
chr8:23042161 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.250+977G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042161 | |||||||
chr8:23042249 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(134): Show |
141 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.250+889A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042249 | |||||||
chr8:23042250 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.250+888C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042250 | |||||||
chr8:23042252 | G | A | 1 | a0004c0004t0001g0065 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.250+886C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042252 | |||||||
chr8:23042265 | T | C | 9 | a0001c0001t0001g0215 a0002c0002t0004g0331 a0002c0002t0004g0352 others(6): Show |
9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.250+873A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042265 | |||||||
chr8:23042444 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.250+694G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042444 | |||||||
chr8:23042597 | C | G | 3 | a0006c0006t0001g0128 a0006c0006t0001g0129 a0006c0006t0001g0130 |
3 | HG01192.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.250+541G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042597 | |||||||
chr8:23042611 | G | T | 1 | a0004c0004t0001g0300 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.250+527C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042611 | |||||||
chr8:23042729 | C | G | 1 | a0001c0001t0001g0272 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.250+409G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042729 | |||||||
chr8:23042974 | G | A | 11 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0248 others(8): Show |
12 | HG02717.hp2 HG02886.hp2 HG03098.hp1 others(9): Show |
intron_variant | MODIFIER | c.250+164C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042974 | |||||||
chr8:23042984 | T | C | 5 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0002g0100 others(2): Show |
5 | HG00609.hp2 NA19004.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+154A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042984 | |||||||
chr8:23043060 | A | G | 2 | a0001c0001t0003g0212 a0001c0001t0003g0213 |
2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.250+78T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23043060 | |||||||
chr8:23043091 | A | C | 2 | a0001c0001t0003g0212 a0001c0001t0003g0213 |
2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.250+47T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23043091 | |||||||
chr8:23043381 | T | A | 1 | a0002c0002t0006g0339 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.145-138A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043381 | |||||||
chr8:23043436 | C | T | 157 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(154): Show |
159 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.145-193G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043436 | |||||||
chr8:23043483 | A | G | 1 | a0001c0001t0012g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.145-240T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043483 | |||||||
chr8:23043533 | T | C | 1 | a0001c0001t0003g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.145-290A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043533 | |||||||
chr8:23043660 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0026g0028 others(1): Show |
4 | HG02735.hp1 HG03669.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-417C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043660 | |||||||
chr8:23043689 | T | C | 162 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(159): Show |
164 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.145-446A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043689 | |||||||
chr8:23043724 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.145-481G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043724 | |||||||
chr8:23043738 | G | A | 1 | a0001c0001t0002g0283 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.145-495C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043738 | |||||||
chr8:23043821 | A | G | 1 | a0001c0001t0001g0269 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.145-578T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043821 | |||||||
chr8:23043858 | A | G | 161 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(158): Show |
163 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.145-615T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043858 | |||||||
chr8:23043959 | C | T | 1 | a0005c0005t0004g0364 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.145-716G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043959 | |||||||
chr8:23044042 | T | C | 1 | a0004c0004t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-799A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044042 | |||||||
chr8:23044055 | A | C | 269 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(266): Show |
274 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.145-812T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044055 | |||||||
chr8:23044096 | C | T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-853G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044096 | |||||||
chr8:23044139 | G | A | 1 | a0003c0003t0003g0123 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.145-896C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044139 | |||||||
chr8:23044209 | C | T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-966G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044209 | |||||||
chr8:23044234 | A | T | 1 | a0002c0002t0004g0349 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.145-991T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044234 | |||||||
chr8:23044358 | A | G | 161 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(158): Show |
163 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.145-1115T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044358 | |||||||
chr8:23044430 | T | C | 70 | a0001c0001t0001g0127 a0001c0001t0001g0145 a0001c0001t0001g0231 others(67): Show |
72 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.145-1187A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044430 | |||||||
chr8:23044436 | T | C | 1 | a0012c0011t0006g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.145-1193A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044436 | |||||||
chr8:23044477 | A | C | 70 | a0001c0001t0001g0127 a0001c0001t0001g0145 a0001c0001t0001g0231 others(67): Show |
72 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.145-1234T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044477 | |||||||
chr8:23044693 | A | C | 65 | a0001c0001t0001g0024 a0001c0001t0001g0104 a0001c0001t0001g0117 others(62): Show |
65 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.145-1450T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044693 | |||||||
chr8:23044698 | A | G | 2 | a0003c0003t0007g0072 a0003c0003t0025g0073 |
2 | HG02165.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.145-1455T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044698 | |||||||
chr8:23044860 | A | C | 1 | a0001c0001t0012g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.145-1617T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044860 | |||||||
chr8:23044950 | T | A | 11 | a0001c0001t0004g0373 a0001c0001t0008g0125 a0001c0001t0010g0207 others(8): Show |
11 | HG00733.hp2 HG01099.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.145-1707A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044950 | |||||||
chr8:23045008 | G | A | 1 | a0012c0011t0006g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.145-1765C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045008 | |||||||
chr8:23045013 | G | A | 68 | a0001c0001t0001g0127 a0001c0001t0001g0145 a0001c0001t0001g0231 others(65): Show |
70 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.145-1770C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045013 | |||||||
chr8:23045060 | C | CA | 123 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0045 others(120): Show |
126 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.145-1818dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045060 | |||||||
chr8:23045060 | C | CAA | 9 | a0001c0001t0001g0029 a0001c0001t0001g0119 a0001c0001t0026g0028 others(6): Show |
9 | HG01891.hp1 HG02135.hp1 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.145-1819_145-1818d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045060 | |||||||
chr8:23045060 | CA | C | 110 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.145-1818delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045060 | |||||||
chr8:23045060 | CAA | C | 27 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(24): Show |
28 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.145-1819_145-1818d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045060 | |||||||
chr8:23045100 | T | C | 69 | a0001c0001t0001g0127 a0001c0001t0001g0145 a0001c0001t0001g0231 others(66): Show |
71 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.145-1857A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045100 | |||||||
chr8:23045103 | A | G | 1 | a0001c0001t0002g0220 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.145-1860T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045103 | |||||||
chr8:23045131 | G | A | 1 | a0001c0001t0018g0170 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.145-1888C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045131 | |||||||
chr8:23045145 | A | G | 278 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(275): Show |
283 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.145-1902T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045145 | |||||||
chr8:23045159 | G | T | 1 | a0002c0002t0005g0340 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.145-1916C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045159 | |||||||
chr8:23045184 | T | C | 91 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(88): Show |
91 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.145-1941A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045184 | |||||||
chr8:23045213 | G | A | 10 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(7): Show |
10 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.145-1970C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045213 | |||||||
chr8:23045276 | G | A | 1 | a0003c0003t0002g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.145-2033C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045276 | |||||||
chr8:23045332 | C | T | 1 | a0004c0004t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-2089G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045332 | |||||||
chr8:23045355 | G | A | 2 | a0003c0003t0001g0098 a0003c0003t0003g0108 |
2 | HG01081.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.145-2112C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045355 | |||||||
chr8:23045377 | T | C | 69 | a0001c0001t0001g0127 a0001c0001t0001g0145 a0001c0001t0001g0231 others(66): Show |
71 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.145-2134A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045377 | |||||||
chr8:23045401 | C | T | 6 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(3): Show |
6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-2158G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045401 | |||||||
chr8:23045560 | G | C | 1 | a0001c0001t0002g0277 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.145-2317C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045560 | |||||||
chr8:23045575 | A | C | 1 | a0004c0004t0009g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.145-2332T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045575 | |||||||
chr8:23045696 | C | T | 2 | a0001c0001t0003g0212 a0001c0001t0003g0213 |
2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.145-2453G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045696 | |||||||
chr8:23045941 | C | CA | 89 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(86): Show |
89 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.145-2699dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045941 | |||||||
chr8:23046072 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.145-2829C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046072 | |||||||
chr8:23046119 | G | C | 10 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(7): Show |
10 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.145-2876C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046119 | |||||||
chr8:23046161 | C | T | 65 | a0001c0001t0001g0127 a0001c0001t0001g0145 a0001c0001t0001g0231 others(62): Show |
67 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.145-2918G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046161 | |||||||
chr8:23046164 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0002g0060 a0004c0004t0001g0059 |
3 | HG01192.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.145-2921A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046164 | |||||||
chr8:23046264 | A | T | 1 | a0001c0001t0002g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.145-3021T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046264 | |||||||
chr8:23046265 | T | C | 1 | a0001c0001t0003g0305 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.145-3022A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046265 | |||||||
chr8:23046387 | C | T | 79 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(76): Show |
79 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.145-3144G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046387 | |||||||
chr8:23046442 | C | T | 1 | a0002c0002t0004g0359 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.145-3199G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046442 | |||||||
chr8:23046495 | T | A | 1 | a0005c0005t0004g0364 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.145-3252A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046495 | |||||||
chr8:23046548 | C | T | 12 | a0001c0001t0001g0145 a0001c0001t0001g0248 a0001c0001t0001g0249 others(9): Show |
13 | HG01123.hp1 HG02717.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.145-3305G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046548 | |||||||
chr8:23046614 | A | T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-3371T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046614 | |||||||
chr8:23046615 | TA | T | 14 | a0001c0001t0001g0117 a0001c0001t0001g0269 a0001c0001t0001g0272 others(11): Show |
14 | HG00099.hp2 HG01515.hp1 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.145-3373delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046615 | |||||||
chr8:23046615 | TAAA | T | 223 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0027 others(220): Show |
228 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.145-3375_145-3373d others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046615 | |||||||
chr8:23046615 | TAAAA | T | 41 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0036 others(38): Show |
41 | HG00423.hp1 HG00733.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-3376_145-3373d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046615 | |||||||
chr8:23046631 | A | C | 1 | a0002c0002t0015g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-3388T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046631 | |||||||
chr8:23046633 | A | C | 187 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(184): Show |
192 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.145-3390T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046633 | |||||||
chr8:23046747 | T | C | 2 | a0001c0001t0002g0242 a0001c0001t0003g0241 |
2 | HG00423.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.145-3504A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046747 | |||||||
chr8:23046951 | A | C | 1 | a0003c0003t0001g0046 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.145-3708T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046951 | |||||||
chr8:23046955 | C | T | 2 | a0001c0001t0001g0027 a0004c0004t0001g0026 |
2 | HG02257.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.145-3712G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046955 | |||||||
chr8:23047013 | C | T | 1 | a0002c0002t0015g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-3770G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047013 | |||||||
chr8:23047080 | A | G | 1 | a0001c0001t0002g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.145-3837T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047080 | |||||||
chr8:23047097 | T | C | 1 | a0002c0002t0015g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-3854A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047097 | |||||||
chr8:23047107 | G | A | 1 | a0002c0002t0005g0346 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.145-3864C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047107 | |||||||
chr8:23047135 | G | A | 2 | a0001c0001t0001g0027 a0004c0004t0001g0026 |
2 | HG02257.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.145-3892C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047135 | |||||||
chr8:23047191 | C | G | 28 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(25): Show |
29 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.145-3948G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047191 | |||||||
chr8:23047232 | C | T | 1 | a0002c0002t0015g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-3989G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047232 | |||||||
chr8:23047234 | G | A | 86 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(83): Show |
86 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.145-3991C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047234 | |||||||
chr8:23047234 | G | ATAATCCC others(1072): Show |
1 | a0004c0004t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-3991_145-3990i others(1081): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047234 | |||||||
chr8:23047272 | A | G | 202 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(199): Show |
205 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.145-4029T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047272 | |||||||
chr8:23047294 | T | C | 1 | a0002c0002t0015g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-4051A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047294 | |||||||
chr8:23047309 | A | G | 114 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0061 others(111): Show |
117 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.145-4066T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047309 | |||||||
chr8:23047357 | C | CA | 74 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(71): Show |
74 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.145-4115dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047357 | |||||||
chr8:23047357 | C | CAAAAAAA others(1074): Show |
7 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(4): Show |
7 | HG02257.hp2 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.145-4115_145-4114i others(1083): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047357 | |||||||
chr8:23047357 | C | CAAAAAAA others(1075): Show |
1 | a0001c0001t0008g0037 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.145-4115_145-4114i others(1084): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047357 | |||||||
chr8:23047357 | CA | C | 155 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(152): Show |
159 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.145-4115delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047357 | |||||||
chr8:23047357 | CAA | C | 6 | a0001c0001t0003g0054 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG02602.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-4116_145-4115d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047357 | |||||||
chr8:23047404 | T | C | 4 | a0001c0001t0001g0127 a0006c0006t0001g0128 a0006c0006t0001g0129 others(1): Show |
4 | HG01192.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-4161A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047404 | |||||||
chr8:23047423 | C | T | 4 | a0001c0001t0008g0120 a0004c0004t0001g0121 a0005c0005t0004g0365 others(1): Show |
4 | HG02280.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.145-4180G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047423 | |||||||
chr8:23047699 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0003g0222 a0004c0004t0001g0223 |
3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.145-4456G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047699 | |||||||
chr8:23048162 | G | A | 9 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(6): Show |
9 | HG02257.hp2 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-4919C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048162 | |||||||
chr8:23048162 | G | GGTGGCTC others(1073): Show |
1 | a0004c0004t0020g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.145-4920_145-4919i others(1082): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048162 | |||||||
chr8:23048209 | G | T | 1 | a0003c0003t0002g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.145-4966C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048209 | |||||||
chr8:23048264 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.145-5021A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048264 | |||||||
chr8:23048337 | A | G | 9 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-5094T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048337 | |||||||
chr8:23048343 | G | A | 8 | a0001c0001t0010g0207 a0001c0001t0010g0208 a0001c0001t0011g0210 others(5): Show |
8 | HG00733.hp2 HG01099.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.145-5100C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048343 | |||||||
chr8:23048358 | C | G | 2 | a0001c0001t0004g0373 a0002c0002t0004g0372 |
2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.145-5115G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048358 | |||||||
chr8:23048435 | G | C | 91 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(88): Show |
91 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.145-5192C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048435 | |||||||
chr8:23048437 | C | CA | 46 | a0001c0001t0001g0195 a0001c0001t0001g0247 a0001c0001t0001g0248 others(43): Show |
47 | HG01123.hp1 HG01175.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.145-5195dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048437 | |||||||
chr8:23048437 | CA | C | 16 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(13): Show |
16 | HG01884.hp1 HG02004.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.145-5195delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048437 | |||||||
chr8:23048437 | CAA | C | 71 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(68): Show |
71 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.145-5196_145-5195d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048437 | |||||||
chr8:23048457 | C | T | 1 | a0001c0001t0002g0185 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.145-5214G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048457 | |||||||
chr8:23048667 | T | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0137 others(54): Show |
59 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.145-5424A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048667 | |||||||
chr8:23048793 | T | G | 9 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-5550A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048793 | |||||||
chr8:23048851 | C | T | 1 | a0003c0003t0003g0111 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.145-5608G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048851 | |||||||
chr8:23048856 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.145-5613G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048856 | |||||||
chr8:23048870 | G | C | 6 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(3): Show |
6 | HG02809.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-5627C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048870 | |||||||
chr8:23048937 | A | T | 33 | a0001c0001t0001g0127 a0001c0001t0001g0231 a0001c0001t0001g0232 others(30): Show |
34 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.145-5694T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048937 | |||||||
chr8:23048982 | A | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(3): Show |
6 | HG02809.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-5739T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048982 | |||||||
chr8:23049031 | G | A | 3 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0006c0006t0001g0031 |
3 | HG02572.hp2 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.145-5788C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049031 | |||||||
chr8:23049128 | A | G | 92 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-5885T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049128 | |||||||
chr8:23049295 | G | C | 1 | a0004c0004t0001g0135 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.145-6052C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049295 | |||||||
chr8:23049509 | A | C | 1 | a0002c0002t0015g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-6266T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049509 | |||||||
chr8:23049554 | C | A | 4 | a0001c0001t0001g0127 a0006c0006t0001g0128 a0006c0006t0001g0129 others(1): Show |
4 | HG01192.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-6311G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049554 | |||||||
chr8:23049577 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0002g0100 |
2 | NA19004.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.145-6334A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049577 | |||||||
chr8:23049614 | T | C | 1 | a0003c0003t0002g0102 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.145-6371A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049614 | |||||||
chr8:23049677 | G | T | 2 | a0001c0001t0003g0285 a0004c0004t0001g0286 |
2 | HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.145-6434C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049677 | |||||||
chr8:23049728 | T | G | 79 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(76): Show |
79 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.145-6485A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049728 | |||||||
chr8:23049772 | T | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(3): Show |
6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-6529A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049772 | |||||||
chr8:23049783 | C | T | 3 | a0001c0001t0002g0143 a0004c0004t0001g0124 a0004c0004t0001g0144 |
3 | HG01123.hp1 HG03942.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.145-6540G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049783 | |||||||
chr8:23049795 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.145-6552G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049795 | |||||||
chr8:23049817 | C | A | 80 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(77): Show |
80 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.145-6574G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049817 | |||||||
chr8:23049817 | C | CTTATTGG others(24): Show |
1 | a0003c0003t0002g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.145-6605_145-6575d others(33): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049817 | |||||||
chr8:23049873 | T | G | 8 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(5): Show |
8 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-6630A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049873 | |||||||
chr8:23049909 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.145-6666T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049909 | |||||||
chr8:23049944 | G | C | 19 | a0001c0001t0001g0151 a0001c0001t0001g0171 a0001c0001t0001g0175 others(16): Show |
19 | HG02040.hp2 NA18939.hp1 NA18955.hp1 others(16): Show |
intron_variant | MODIFIER | c.145-6701C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049944 | |||||||
chr8:23049949 | G | A | 5 | a0001c0001t0001g0253 a0001c0001t0001g0256 a0001c0001t0002g0254 others(2): Show |
5 | HG02015.hp2 NA18941.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-6706C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049949 | |||||||
chr8:23050012 | G | T | 2 | a0002c0002t0015g0012 a0012c0011t0006g0312 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.145-6769C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050012 | |||||||
chr8:23050208 | G | C | 10 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0003g0212 others(7): Show |
11 | HG02717.hp2 HG02886.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.145-6965C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050208 | |||||||
chr8:23050243 | G | T | 1 | a0001c0001t0009g0217 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.145-7000C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050243 | |||||||
chr8:23050293 | G | GT | 97 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0061 others(94): Show |
100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.145-7051dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050293 | |||||||
chr8:23050301 | G | A | 1 | a0004c0004t0001g0135 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.145-7058C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050301 | |||||||
chr8:23050412 | G | A | 91 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(88): Show |
91 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.145-7169C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050412 | |||||||
chr8:23050463 | T | C | 10 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0003g0212 others(7): Show |
11 | HG02717.hp2 HG02886.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.145-7220A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050463 | |||||||
chr8:23050472 | G | A | 1 | a0010c0014t0001g0211 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.145-7229C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050472 | |||||||
chr8:23050805 | G | A | 92 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-7562C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050805 | |||||||
chr8:23050823 | C | T | 92 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-7580G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050823 | |||||||
chr8:23050840 | G | A | 1 | a0004c0004t0001g0131 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.145-7597C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050840 | |||||||
chr8:23050863 | C | A | 2 | a0002c0002t0015g0012 a0012c0011t0006g0312 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.145-7620G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050863 | |||||||
chr8:23050868 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.145-7625C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050868 | |||||||
chr8:23050950 | T | C | 27 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(24): Show |
28 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.145-7707A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050950 | |||||||
chr8:23050953 | A | T | 1 | a0001c0001t0001g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.145-7710T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050953 | |||||||
chr8:23050968 | G | A | 92 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-7725C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050968 | |||||||
chr8:23050994 | T | A | 93 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(90): Show |
93 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.145-7751A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050994 | |||||||
chr8:23051000 | G | T | 1 | a0001c0001t0001g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.145-7757C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051000 | |||||||
chr8:23051025 | G | C | 92 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-7782C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051025 | |||||||
chr8:23051060 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.145-7817C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051060 | |||||||
chr8:23051083 | C | T | 84 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.145-7840G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051083 | |||||||
chr8:23051100 | C | T | 92 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-7857G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051100 | |||||||
chr8:23051105 | A | G | 79 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(76): Show |
79 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.145-7862T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051105 | |||||||
chr8:23051170 | CAA | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0026g0028 others(1): Show |
4 | HG02735.hp1 HG03669.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-7929_145-7928d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051170 | |||||||
chr8:23051200 | A | AAAAT | 92 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-7958_145-7957i others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051200 | |||||||
chr8:23051545 | CT | C | 10 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(7): Show |
10 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.145-8303delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051545 | |||||||
chr8:23051546 | T | C | 82 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(79): Show |
82 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.145-8303A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051546 | |||||||
chr8:23051547 | CT | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0058 others(154): Show |
162 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.145-8305delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051547 | |||||||
chr8:23051548 | T | C | 10 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(7): Show |
10 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.145-8305A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051548 | |||||||
chr8:23051550 | T | C | 1 | a0004c0004t0001g0131 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.145-8307A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051550 | |||||||
chr8:23051584 | G | A | 96 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0061 others(93): Show |
99 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.145-8341C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051584 | |||||||
chr8:23051607 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0026g0028 others(1): Show |
4 | HG02735.hp1 HG03669.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-8364G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051607 | |||||||
chr8:23051621 | T | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(3): Show |
6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-8378A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051621 | |||||||
chr8:23051638 | G | A | 1 | a0004c0004t0009g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.145-8395C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051638 | |||||||
chr8:23051694 | G | A | 84 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.145-8451C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051694 | |||||||
chr8:23051698 | C | G | 1 | a0001c0001t0012g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.145-8455G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051698 | |||||||
chr8:23051701 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.145-8458G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051701 | |||||||
chr8:23051765 | C | G | 1 | a0003c0003t0003g0003 | 2 | NA18970.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.145-8522G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051765 | |||||||
chr8:23051785 | C | T | 1 | a0002c0002t0006g0333 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.145-8542G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051785 | |||||||
chr8:23051878 | A | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(3): Show |
6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-8635T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051878 | |||||||
chr8:23052033 | G | A | 1 | a0004c0004t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-8790C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052033 | |||||||
chr8:23052150 | C | T | 1 | a0005c0005t0004g0364 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.145-8907G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052150 | |||||||
chr8:23052163 | G | C | 78 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(75): Show |
78 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.145-8920C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052163 | |||||||
chr8:23052239 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0137 others(48): Show |
53 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.145-8996C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052239 | |||||||
chr8:23052285 | C | CT | 113 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0045 others(110): Show |
116 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.145-9043dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052285 | |||||||
chr8:23052285 | C | CTTTT | 75 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(72): Show |
75 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.145-9046_145-9043d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052285 | |||||||
chr8:23052285 | C | CTTTTT | 12 | a0001c0001t0001g0151 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
12 | HG00597.hp1 HG00733.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.145-9047_145-9043d others(7): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052285 | |||||||
chr8:23052285 | CT | C | 6 | a0001c0001t0001g0287 a0001c0001t0002g0308 a0001c0001t0003g0285 others(3): Show |
6 | HG01934.hp1 HG02293.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-9043delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052285 | |||||||
chr8:23052398 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0137 others(49): Show |
54 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.145-9155C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052398 | |||||||
chr8:23052436 | C | A | 11 | a0001c0001t0008g0125 a0001c0001t0010g0207 a0001c0001t0010g0208 others(8): Show |
11 | HG00733.hp2 HG01099.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.145-9193G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052436 | |||||||
chr8:23052488 | G | A | 1 | a0006c0006t0001g0226 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.145-9245C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052488 | |||||||
chr8:23052529 | G | A | 2 | a0001c0001t0004g0373 a0002c0002t0004g0372 |
2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.145-9286C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052529 | |||||||
chr8:23052577 | C | A | 1 | a0001c0001t0002g0196 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.145-9334G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052577 | |||||||
chr8:23052602 | T | G | 2 | a0001c0001t0003g0212 a0001c0001t0003g0213 |
2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.145-9359A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052602 | |||||||
chr8:23052675 | C | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(247): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.145-9432G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052675 | |||||||
chr8:23052745 | G | A | 1 | a0001c0001t0008g0125 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.145-9502C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052745 | |||||||
chr8:23052865 | A | C | 6 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0218 others(3): Show |
6 | HG01884.hp1 HG02004.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-9622T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052865 | |||||||
chr8:23052958 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.145-9715G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052958 | |||||||
chr8:23053236 | G | C | 2 | a0001c0001t0001g0201 a0001c0001t0007g0205 |
2 | NA18991.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.145-9993C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053236 | |||||||
chr8:23053314 | C | T | 26 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(23): Show |
27 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.145-10071G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053314 | |||||||
chr8:23053349 | T | C | 2 | a0001c0001t0001g0288 a0001c0001t0002g0052 |
2 | HG03491.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.145-10106A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053349 | |||||||
chr8:23053368 | G | T | 34 | a0001c0001t0001g0127 a0001c0001t0001g0231 a0001c0001t0001g0232 others(31): Show |
35 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.145-10125C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053368 | |||||||
chr8:23053404 | A | G | 2 | a0001c0001t0008g0125 a0004c0004t0001g0126 |
2 | HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.145-10161T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053404 | |||||||
chr8:23053426 | A | G | 1 | a0002c0002t0005g0332 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.145-10183T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053426 | |||||||
chr8:23053444 | A | C | 1 | a0002c0002t0004g0366 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.145-10201T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053444 | |||||||
chr8:23053457 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0137 others(49): Show |
54 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.145-10214C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053457 | |||||||
chr8:23053481 | TAAAATA | T | 83 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(80): Show |
83 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.145-10244_145-1023 others(10): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053481 | |||||||
chr8:23053526 | A | C | 28 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(25): Show |
29 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.145-10283T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053526 | |||||||
chr8:23053534 | T | A | 1 | a0004c0004t0009g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.145-10291A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053534 | |||||||
chr8:23053536 | CTG | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(3): Show |
6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-10295_145-1029 others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053536 | |||||||
chr8:23053544 | A | G | 1 | a0004c0004t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-10301T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053544 | |||||||
chr8:23053560 | A | G | 83 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(80): Show |
83 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.145-10317T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053560 | |||||||
chr8:23053667 | TA | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0002c0002t0002g0015 |
3 | HG03704.hp1 NA18980.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.145-10425delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053667 | |||||||
chr8:23053670 | G | T | 1 | a0003c0003t0003g0123 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.145-10427C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053670 | |||||||
chr8:23053785 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0137 others(49): Show |
54 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.145-10542T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053785 | |||||||
chr8:23053815 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.145-10572C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053815 | |||||||
chr8:23054001 | C | T | 1 | a0004c0004t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-10758G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054001 | |||||||
chr8:23054012 | T | C | 8 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0004c0004t0001g0006 others(5): Show |
9 | HG02717.hp2 HG02886.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-10769A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054012 | |||||||
chr8:23054114 | G | A | 2 | a0001c0001t0002g0115 a0001c0001t0002g0116 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.145-10871C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054114 | |||||||
chr8:23054189 | A | G | 2 | a0001c0001t0012g0142 a0004c0004t0001g0140 |
2 | HG00738.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.145-10946T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054189 | |||||||
chr8:23054386 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.145-11143T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054386 | |||||||
chr8:23054453 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0026g0028 others(1): Show |
4 | HG02735.hp1 HG03669.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-11210C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054453 | |||||||
chr8:23054723 | G | C | 89 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(86): Show |
89 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.145-11480C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054723 | |||||||
chr8:23054774 | G | A | 1 | a0004c0004t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-11531C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054774 | |||||||
chr8:23054800 | G | A | 5 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 others(2): Show |
5 | HG02698.hp1 HG02738.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-11557C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054800 | |||||||
chr8:23054915 | G | C | 3 | a0002c0002t0004g0370 a0002c0002t0004g0371 a0002c0002t0005g0369 |
3 | HG02056.hp2 NA18961.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.145-11672C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054915 | |||||||
chr8:23054929 | A | G | 1 | a0001c0001t0002g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.145-11686T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054929 | |||||||
chr8:23054935 | A | T | 94 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(91): Show |
94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.145-11692T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054935 | |||||||
chr8:23055026 | T | C | 2 | a0001c0001t0002g0182 a0002c0002t0005g0368 |
2 | HG00099.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.145-11783A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055026 | |||||||
chr8:23055037 | G | A | 1 | a0005c0005t0004g0364 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.145-11794C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055037 | |||||||
chr8:23055154 | C | G | 1 | a0002c0002t0005g0313 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.145-11911G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055154 | |||||||
chr8:23055228 | G | C | 1 | a0001c0001t0001g0151 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.145-11985C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055228 | |||||||
chr8:23055445 | C | A | 1 | a0004c0004t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-12202G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055445 | |||||||
chr8:23055519 | C | CT | 77 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(74): Show |
77 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.145-12277dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055519 | |||||||
chr8:23055521 | T | TAA | 8 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(5): Show |
8 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-12280_145-1227 others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | |||||||
chr8:23055521 | T | TAAA | 6 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0026g0028 others(3): Show |
6 | HG02257.hp1 HG02735.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-12281_145-1227 others(7): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | |||||||
chr8:23055521 | T | TAAAAAAA others(2): Show |
34 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0137 others(31): Show |
36 | HG00280.hp1 HG01069.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.145-12287_145-1227 others(13): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | |||||||
chr8:23055521 | T | TAAAAAAA others(3): Show |
12 | a0001c0001t0001g0247 a0001c0001t0001g0290 a0001c0001t0001g0295 others(9): Show |
12 | HG00140.hp2 HG00639.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.145-12288_145-1227 others(14): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | |||||||
chr8:23055521 | T | TAAAAAAA others(4): Show |
3 | a0001c0001t0001g0299 a0001c0001t0002g0310 a0001c0001t0003g0298 |
3 | HG01074.hp2 HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.145-12289_145-1227 others(15): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | |||||||
chr8:23055521 | T | TAAAAAAA others(7): Show |
1 | a0001c0001t0004g0373 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.145-12292_145-1227 others(18): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | |||||||
chr8:23055521 | T | TAAAAAAA others(11): Show |
1 | a0004c0004t0009g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.145-12296_145-1227 others(22): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | |||||||
chr8:23055521 | T | TTAAAAAA others(3): Show |
1 | a0004c0004t0001g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.145-12279_145-1227 others(14): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | |||||||
chr8:23055521 | T | TTAAAAAA others(4): Show |
2 | a0001c0001t0012g0142 a0012c0011t0006g0312 |
2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.145-12279_145-1227 others(15): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | |||||||
chr8:23055521 | T | TTAAAAAA others(5): Show |
1 | a0002c0002t0015g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-12279_145-1227 others(16): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | |||||||
chr8:23055521 | TA | T | 84 | a0001c0001t0001g0058 a0001c0001t0001g0077 a0001c0001t0001g0078 others(81): Show |
87 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.145-12279delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | |||||||
chr8:23055521 | TAA | T | 38 | a0001c0001t0001g0045 a0001c0001t0001g0061 a0001c0001t0001g0067 others(35): Show |
39 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.145-12280_145-1227 others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | |||||||
chr8:23055522 | A | T | 13 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0218 others(10): Show |
13 | HG01167.hp1 HG01884.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.145-12279T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055522 | |||||||
chr8:23055596 | T | C | 2 | a0002c0002t0015g0012 a0012c0011t0006g0312 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.145-12353A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055596 | |||||||
chr8:23055615 | A | C | 2 | a0002c0002t0015g0012 a0012c0011t0006g0312 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.145-12372T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055615 | |||||||
chr8:23055647 | C | A | 3 | a0002c0002t0004g0326 a0002c0002t0004g0345 a0002c0002t0005g0344 |
3 | HG02135.hp2 NA18987.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.145-12404G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055647 | |||||||
chr8:23055818 | C | T | 1 | a0001c0001t0027g0268 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.145-12575G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055818 | |||||||
chr8:23055853 | T | C | 89 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(86): Show |
89 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.145-12610A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055853 | |||||||
chr8:23055878 | T | C | 1 | a0011c0017t0001g0106 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.145-12635A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055878 | |||||||
chr8:23055915 | A | T | 2 | a0004c0004t0001g0064 a0004c0004t0001g0065 |
2 | HG01175.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.145-12672T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055915 | |||||||
chr8:23055962 | G | C | 88 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0061 others(85): Show |
91 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.145-12719C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055962 | |||||||
chr8:23055968 | C | T | 1 | a0004c0004t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-12725G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055968 | |||||||
chr8:23056067 | G | C | 2 | a0002c0002t0015g0012 a0012c0011t0006g0312 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.144+12684C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056067 | |||||||
chr8:23056140 | C | G | 1 | a0004c0004t0001g0300 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.144+12611G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056140 | |||||||
chr8:23056216 | C | CATAT | 94 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(91): Show |
94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.144+12534_144+1253 others(8): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056216 | |||||||
chr8:23056259 | G | C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(4): Show |
7 | HG02257.hp1 HG02717.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.144+12492C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056259 | |||||||
chr8:23056300 | A | G | 9 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.144+12451T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056300 | |||||||
chr8:23056347 | T | G | 1 | a0004c0004t0001g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.144+12404A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056347 | |||||||
chr8:23056422 | C | T | 1 | a0001c0001t0002g0271 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.144+12329G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056422 | |||||||
chr8:23056540 | A | G | 89 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(86): Show |
89 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.144+12211T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056540 | |||||||
chr8:23056541 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0002g0060 a0004c0004t0001g0059 |
3 | HG01192.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.144+12210G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056541 | |||||||
chr8:23056544 | A | G | 94 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(91): Show |
94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.144+12207T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056544 | |||||||
chr8:23056600 | A | G | 94 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(91): Show |
94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.144+12151T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056600 | |||||||
chr8:23056650 | C | CA | 107 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0027 others(104): Show |
108 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.144+12100dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056650 | |||||||
chr8:23056735 | T | A | 94 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(91): Show |
94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.144+12016A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056735 | |||||||
chr8:23056822 | T | C | 2 | a0001c0001t0012g0142 a0004c0004t0001g0140 |
2 | HG00738.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.144+11929A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056822 | |||||||
chr8:23057003 | C | A | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+11748G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057003 | |||||||
chr8:23057036 | C | CT | 22 | a0001c0001t0017g0053 a0002c0002t0004g0316 a0002c0002t0004g0320 others(19): Show |
22 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.144+11714dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057036 | |||||||
chr8:23057036 | CT | C | 151 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0061 others(148): Show |
157 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.144+11714delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057036 | |||||||
chr8:23057036 | CTT | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0029 others(62): Show |
67 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.144+11713_144+1171 others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057036 | |||||||
chr8:23057036 | CTTT | C | 93 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(90): Show |
93 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.144+11712_144+1171 others(7): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057036 | |||||||
chr8:23057058 | CGGAGTCT others(390): Show |
C | 2 | a0002c0002t0015g0012 a0012c0011t0006g0312 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.144+11296_144+1169 others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057058 | |||||||
chr8:23057072 | G | A | 1 | a0002c0002t0006g0337 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.144+11679C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057072 | |||||||
chr8:23057122 | C | T | 2 | a0001c0001t0012g0142 a0004c0004t0001g0140 |
2 | HG00738.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.144+11629G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057122 | |||||||
chr8:23057292 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0012g0142 a0004c0004t0001g0026 others(1): Show |
4 | HG00738.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+11459C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057292 | |||||||
chr8:23057297 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(252): Show |
260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.144+11454T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057297 | |||||||
chr8:23057337 | G | A | 1 | a0001c0001t0003g0004 | 2 | NA18941.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.144+11414C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057337 | |||||||
chr8:23057378 | A | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(287): Show |
296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.144+11373T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057378 | |||||||
chr8:23057429 | A | AT | 19 | a0001c0001t0001g0187 a0001c0001t0001g0248 a0001c0001t0002g0183 others(16): Show |
19 | HG00733.hp2 HG01099.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.144+11321dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057429 | |||||||
chr8:23057429 | AT | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0117 others(64): Show |
69 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.144+11321delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057429 | |||||||
chr8:23057502 | G | A | 94 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(91): Show |
94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.144+11249C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057502 | |||||||
chr8:23057519 | G | A | 1 | a0001c0001t0003g0259 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.144+11232C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057519 | |||||||
chr8:23057589 | C | T | 2 | a0003c0003t0001g0062 a0003c0003t0001g0063 |
2 | HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.144+11162G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057589 | |||||||
chr8:23057622 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0137 others(49): Show |
54 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.144+11129T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057622 | |||||||
chr8:23057741 | G | A | 8 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0004c0004t0001g0006 others(5): Show |
9 | HG02717.hp2 HG02886.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.144+11010C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057741 | |||||||
chr8:23057885 | G | A | 1 | a0004c0004t0001g0124 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.144+10866C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057885 | |||||||
chr8:23057975 | A | C | 1 | a0001c0001t0003g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.144+10776T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057975 | |||||||
chr8:23058371 | C | G | 1 | a0001c0001t0001g0232 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.144+10380G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058371 | |||||||
chr8:23058483 | T | A | 1 | a0001c0001t0001g0138 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.144+10268A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058483 | |||||||
chr8:23058491 | C | CT | 163 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0029 others(160): Show |
168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.144+10259dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058491 | |||||||
chr8:23058542 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.144+10209T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058542 | |||||||
chr8:23058555 | G | T | 2 | a0001c0001t0001g0027 a0004c0004t0001g0026 |
2 | HG02257.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.144+10196C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058555 | |||||||
chr8:23058568 | C | T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(5): Show |
8 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.144+10183G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058568 | |||||||
chr8:23058636 | T | C | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+10115A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058636 | |||||||
chr8:23058685 | G | A | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+10066C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058685 | |||||||
chr8:23058775 | G | A | 35 | a0001c0001t0001g0127 a0001c0001t0001g0231 a0001c0001t0001g0232 others(32): Show |
36 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.144+9976C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058775 | |||||||
chr8:23058846 | A | T | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+9905T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058846 | |||||||
chr8:23058937 | G | T | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.144+9814C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058937 | |||||||
chr8:23058964 | C | T | 2 | a0002c0002t0005g0348 a0002c0002t0006g0347 |
2 | HG02148.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.144+9787G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058964 | |||||||
chr8:23059027 | C | T | 91 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0061 others(88): Show |
94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.144+9724G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059027 | |||||||
chr8:23059392 | C | T | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+9359G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059392 | |||||||
chr8:23059483 | T | C | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+9268A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059483 | |||||||
chr8:23059509 | G | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0029 others(172): Show |
181 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.144+9242C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059509 | |||||||
chr8:23059514 | T | TTTCG | 8 | a0001c0001t0001g0138 a0001c0001t0002g0301 a0001c0001t0002g0303 others(5): Show |
8 | HG00140.hp2 HG00280.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.144+9236_144+9237i others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059514 | |||||||
chr8:23059514 | T | TTTTG | 166 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0029 others(163): Show |
172 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.144+9233_144+9236d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059514 | |||||||
chr8:23059530 | A | C | 1 | a0001c0001t0012g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.144+9221T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059530 | |||||||
chr8:23059530 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0029 others(168): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.144+9221T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059530 | |||||||
chr8:23059539 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0029 others(172): Show |
181 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.144+9212A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059539 | |||||||
chr8:23059592 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0002g0060 a0004c0004t0001g0059 |
3 | HG01192.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.144+9159G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059592 | |||||||
chr8:23059651 | C | T | 8 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0004c0004t0001g0006 others(5): Show |
9 | HG02717.hp2 HG02886.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.144+9100G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059651 | |||||||
chr8:23059652 | G | A | 2 | a0002c0002t0015g0012 a0012c0011t0006g0312 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.144+9099C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059652 | |||||||
chr8:23059655 | T | C | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+9096A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059655 | |||||||
chr8:23059663 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.144+9088G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059663 | |||||||
chr8:23059680 | TG | T | 110 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(107): Show |
114 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.144+9070delC | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059680 | |||||||
chr8:23059683 | AT | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0029 others(205): Show |
215 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.144+9067delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059683 | |||||||
chr8:23059684 | T | A | 1 | a0001c0001t0004g0373 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.144+9067A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059684 | |||||||
chr8:23059702 | C | T | 2 | a0001c0001t0003g0043 a0001c0001t0003g0234 |
2 | HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.144+9049G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059702 | |||||||
chr8:23059754 | C | T | 1 | a0001c0001t0002g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.144+8997G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059754 | |||||||
chr8:23059792 | A | G | 300 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(297): Show |
307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.144+8959T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059792 | |||||||
chr8:23059802 | G | A | 2 | a0001c0001t0012g0142 a0004c0004t0001g0140 |
2 | HG00738.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.144+8949C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059802 | |||||||
chr8:23059833 | T | A | 2 | a0002c0002t0015g0012 a0012c0011t0006g0312 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.144+8918A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059833 | |||||||
chr8:23059921 | A | T | 1 | a0001c0001t0001g0233 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.144+8830T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059921 | |||||||
chr8:23060026 | T | G | 1 | a0002c0002t0005g0346 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.144+8725A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060026 | |||||||
chr8:23060110 | G | T | 3 | a0002c0002t0004g0370 a0002c0002t0004g0371 a0002c0002t0005g0369 |
3 | HG02056.hp2 NA18961.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.144+8641C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060110 | |||||||
chr8:23060118 | T | A | 1 | a0004c0004t0001g0026 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.144+8633A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060118 | |||||||
chr8:23060128 | G | A | 1 | a0001c0001t0002g0220 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.144+8623C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060128 | |||||||
chr8:23060130 | G | A | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+8621C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060130 | |||||||
chr8:23060151 | C | T | 1 | a0001c0001t0002g0308 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.144+8600G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060151 | |||||||
chr8:23060161 | AT | A | 35 | a0001c0001t0001g0127 a0001c0001t0001g0231 a0001c0001t0001g0232 others(32): Show |
36 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.144+8589delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060161 | |||||||
chr8:23060180 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0029 others(172): Show |
181 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.144+8571T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060180 | |||||||
chr8:23060197 | T | G | 1 | a0003c0016t0001g0307 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.144+8554A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060197 | |||||||
chr8:23060279 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.144+8472G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060279 | |||||||
chr8:23060286 | A | C | 2 | a0004c0004t0001g0214 a0006c0006t0001g0224 |
2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.144+8465T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060286 | |||||||
chr8:23060290 | T | C | 1 | a0001c0001t0002g0308 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.144+8461A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060290 | |||||||
chr8:23060334 | G | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0137 others(49): Show |
54 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.144+8417C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060334 | |||||||
chr8:23060378 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.144+8373G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060378 | |||||||
chr8:23060394 | C | T | 5 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(2): Show |
5 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+8357G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060394 | |||||||
chr8:23060403 | C | T | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+8348G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060403 | |||||||
chr8:23060573 | G | A | 1 | a0005c0005t0004g0364 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.144+8178C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060573 | |||||||
chr8:23060614 | G | A | 2 | a0001c0001t0002g0122 a0001c0001t0002g0184 |
2 | HG02074.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.144+8137C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060614 | |||||||
chr8:23060711 | T | G | 12 | a0001c0001t0001g0145 a0001c0001t0001g0248 a0001c0001t0001g0249 others(9): Show |
13 | HG01123.hp1 HG02717.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.144+8040A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060711 | |||||||
chr8:23060734 | T | C | 1 | a0001c0001t0003g0244 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.144+8017A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060734 | |||||||
chr8:23060751 | A | T | 1 | a0002c0002t0015g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.144+8000T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060751 | |||||||
chr8:23060835 | T | A | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+7916A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060835 | |||||||
chr8:23060910 | T | C | 1 | a0001c0001t0003g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.144+7841A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060910 | |||||||
chr8:23060952 | A | G | 3 | a0001c0001t0001g0058 a0001c0001t0002g0060 a0004c0004t0001g0059 |
3 | HG01192.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.144+7799T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060952 | |||||||
chr8:23060980 | C | T | 1 | a0004c0004t0001g0026 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.144+7771G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060980 | |||||||
chr8:23061138 | T | A | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+7613A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23061138 | |||||||
chr8:23061517 | C | T | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+7234G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23061517 | |||||||
chr8:23061718 | A | G | 1 | a0004c0004t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.144+7033T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23061718 | |||||||
chr8:23061809 | C | T | 101 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(98): Show |
104 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.144+6942G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23061809 | |||||||
chr8:23061844 | G | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(257): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.144+6907C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23061844 | |||||||
chr8:23061970 | G | A | 2 | a0001c0001t0012g0142 a0004c0004t0001g0140 |
2 | HG00738.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.144+6781C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23061970 | |||||||
chr8:23062097 | A | T | 2 | a0001c0001t0004g0373 a0002c0002t0004g0372 |
2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.144+6654T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062097 | |||||||
chr8:23062110 | G | A | 1 | a0005c0005t0004g0364 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.144+6641C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062110 | |||||||
chr8:23062128 | G | C | 3 | a0001c0001t0001g0145 a0001c0001t0002g0143 a0004c0004t0001g0144 |
3 | HG01123.hp1 HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.144+6623C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062128 | |||||||
chr8:23062312 | C | T | 1 | a0001c0001t0002g0220 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.144+6439G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062312 | |||||||
chr8:23062402 | G | A | 1 | a0012c0011t0006g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.144+6349C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062402 | |||||||
chr8:23062498 | G | A | 10 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(7): Show |
10 | HG00738.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.144+6253C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062498 | |||||||
chr8:23062636 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0029 others(72): Show |
77 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.144+6115G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062636 | |||||||
chr8:23062672 | C | A | 1 | a0001c0001t0002g0220 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.144+6079G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062672 | |||||||
chr8:23062743 | A | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(3): Show |
6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+6008T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062743 | |||||||
chr8:23062885 | A | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(3): Show |
6 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+5866T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062885 | |||||||
chr8:23062925 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.144+5826T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062925 | |||||||
chr8:23063035 | A | G | 1 | a0001c0001t0017g0053 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.144+5716T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063035 | |||||||
chr8:23063120 | G | A | 1 | a0002c0002t0005g0313 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.144+5631C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063120 | |||||||
chr8:23063137 | C | CAGG | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+5613_144+5614i others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063137 | |||||||
chr8:23063179 | C | A | 1 | a0001c0001t0001g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.144+5572G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063179 | |||||||
chr8:23063191 | T | C | 1 | a0006c0006t0001g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.144+5560A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063191 | |||||||
chr8:23063225 | G | A | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+5526C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063225 | |||||||
chr8:23063297 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0137 others(48): Show |
53 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.144+5454C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063297 | |||||||
chr8:23063304 | C | T | 1 | a0001c0001t0002g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.144+5447G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063304 | |||||||
chr8:23063323 | G | A | 2 | a0002c0002t0005g0348 a0002c0002t0006g0347 |
2 | HG02148.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.144+5428C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063323 | |||||||
chr8:23063346 | C | CA | 150 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0058 others(147): Show |
155 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.144+5404dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063346 | |||||||
chr8:23063346 | C | CAA | 12 | a0001c0001t0001g0045 a0001c0001t0001g0109 a0001c0001t0001g0110 others(9): Show |
12 | HG00621.hp2 HG02572.hp2 HG03688.hp1 others(9): Show |
intron_variant | MODIFIER | c.144+5403_144+5404d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063346 | |||||||
chr8:23063346 | C | CAAAAAAA others(3544): Show |
1 | a0003c0003t0003g0108 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.144+5404_144+5405i others(3553): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063346 | |||||||
chr8:23063346 | CA | C | 35 | a0001c0001t0001g0127 a0001c0001t0001g0231 a0001c0001t0001g0233 others(32): Show |
36 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.144+5404delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063346 | |||||||
chr8:23063411 | G | A | 1 | a0002c0002t0006g0361 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.144+5340C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063411 | |||||||
chr8:23063425 | GCAGGTCT others(7): Show |
G | 1 | a0001c0001t0001g0045 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.144+5312_144+5325d others(16): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063425 | |||||||
chr8:23063492 | G | A | 3 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 |
3 | HG01496.hp1 HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.144+5259C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063492 | |||||||
chr8:23063513 | TTTC | T | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+5235_144+5237d others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063513 | |||||||
chr8:23063699 | C | T | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0012g0230 |
3 | HG02258.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.144+5052G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063699 | |||||||
chr8:23063739 | G | T | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+5012C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063739 | |||||||
chr8:23063809 | C | T | 6 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(3): Show |
6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+4942G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063809 | |||||||
chr8:23063848 | T | C | 1 | a0001c0001t0002g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.144+4903A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063848 | |||||||
chr8:23063916 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.144+4835A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063916 | |||||||
chr8:23063921 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0029 others(205): Show |
214 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.144+4830G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063921 | |||||||
chr8:23063938 | G | A | 1 | a0002c0002t0004g0359 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.144+4813C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063938 | |||||||
chr8:23063941 | C | T | 1 | a0002c0002t0005g0324 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.144+4810G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063941 | |||||||
chr8:23063957 | C | T | 18 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(15): Show |
18 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.144+4794G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063957 | |||||||
chr8:23063959 | T | A | 1 | a0001c0001t0002g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.144+4792A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063959 | |||||||
chr8:23063990 | T | C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(4): Show |
7 | HG02257.hp1 HG02717.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.144+4761A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063990 | |||||||
chr8:23064075 | G | A | 1 | a0002c0002t0005g0358 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.144+4676C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064075 | |||||||
chr8:23064266 | A | T | 1 | a0001c0001t0003g0229 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.144+4485T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064266 | |||||||
chr8:23064418 | C | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(284): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.144+4333G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064418 | |||||||
chr8:23064437 | G | A | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+4314C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064437 | |||||||
chr8:23064871 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.144+3880G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064871 | |||||||
chr8:23064905 | T | C | 1 | a0002c0002t0004g0359 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.144+3846A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064905 | |||||||
chr8:23064923 | T | C | 1 | a0004c0004t0001g0141 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.144+3828A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064923 | |||||||
chr8:23064965 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.144+3786C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064965 | |||||||
chr8:23065172 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0137 others(49): Show |
54 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.144+3579C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065172 | |||||||
chr8:23065234 | C | T | 3 | a0001c0001t0001g0151 a0004c0004t0001g0149 a0004c0004t0001g0150 |
3 | NA19002.hp2 NA19058.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.144+3517G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065234 | |||||||
chr8:23065235 | G | A | 1 | a0001c0001t0003g0259 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.144+3516C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065235 | |||||||
chr8:23065504 | A | G | 1 | a0001c0001t0002g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.144+3247T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065504 | |||||||
chr8:23065648 | C | T | 9 | a0002c0002t0004g0316 a0002c0002t0004g0320 a0002c0002t0004g0322 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.144+3103G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065648 | |||||||
chr8:23065664 | T | C | 10 | a0001c0001t0008g0125 a0001c0001t0010g0207 a0001c0001t0010g0208 others(7): Show |
10 | HG00733.hp2 HG01099.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.144+3087A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065664 | |||||||
chr8:23065697 | A | G | 1 | a0001c0001t0003g0228 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.144+3054T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065697 | |||||||
chr8:23065705 | G | C | 1 | a0001c0001t0002g0310 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.144+3046C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065705 | |||||||
chr8:23065759 | G | A | 4 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(1): Show |
4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+2992C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065759 | |||||||
chr8:23065761 | G | A | 1 | a0001c0001t0003g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.144+2990C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065761 | |||||||
chr8:23065799 | A | C | 5 | a0001c0001t0004g0373 a0001c0001t0012g0142 a0002c0002t0015g0012 others(2): Show |
5 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+2952T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065799 | |||||||
chr8:23066011 | G | A | 1 | a0006c0006t0001g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.144+2740C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066011 | |||||||
chr8:23066058 | G | C | 1 | a0001c0001t0013g0246 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.144+2693C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066058 | |||||||
chr8:23066070 | C | T | 1 | a0002c0002t0004g0314 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.144+2681G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066070 | |||||||
chr8:23066383 | T | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0137 others(49): Show |
54 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.144+2368A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066383 | |||||||
chr8:23066518 | T | C | 102 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0061 others(99): Show |
105 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.144+2233A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066518 | |||||||
chr8:23066678 | C | T | 6 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(3): Show |
6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+2073G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066678 | |||||||
chr8:23066814 | G | A | 1 | a0004c0004t0001g0126 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.144+1937C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066814 | |||||||
chr8:23066845 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(294): Show |
304 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.144+1906A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066845 | |||||||
chr8:23066855 | C | A | 3 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0012c0011t0006g0312 |
3 | HG01891.hp1 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.144+1896G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066855 | |||||||
chr8:23066898 | AAAAC | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0137 others(52): Show |
57 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.144+1849_144+1852d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066898 | |||||||
chr8:23066898 | AAAACAAA others(1): Show |
A | 5 | a0001c0001t0012g0142 a0002c0002t0015g0012 a0004c0004t0001g0140 others(2): Show |
5 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+1845_144+1852d others(10): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066898 | |||||||
chr8:23066929 | A | T | 1 | a0006c0006t0001g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.144+1822T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066929 | |||||||
chr8:23067015 | G | T | 1 | a0006c0006t0001g0226 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.144+1736C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067015 | |||||||
chr8:23067112 | G | A | 1 | a0001c0001t0011g0225 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.144+1639C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067112 | |||||||
chr8:23067205 | T | C | 1 | a0003c0003t0002g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.144+1546A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067205 | |||||||
chr8:23067230 | G | A | 3 | a0001c0001t0001g0145 a0001c0001t0002g0143 a0004c0004t0001g0144 |
3 | HG01123.hp1 HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.144+1521C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067230 | |||||||
chr8:23067397 | A | G | 79 | a0001c0001t0001g0024 a0001c0001t0001g0151 a0001c0001t0001g0159 others(76): Show |
79 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.144+1354T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067397 | |||||||
chr8:23067445 | T | TA | 102 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.144+1305dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067445 | |||||||
chr8:23067455 | A | C | 1 | a0002c0002t0004g0372 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.144+1296T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067455 | |||||||
chr8:23067456 | C | A | 27 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(24): Show |
28 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.144+1295G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067456 | |||||||
chr8:23067480 | A | C | 108 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(105): Show |
111 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.144+1271T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067480 | |||||||
chr8:23067532 | A | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0026g0028 others(1): Show |
4 | HG02257.hp1 HG03654.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+1219T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067532 | |||||||
chr8:23067641 | A | C | 309 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(306): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.144+1110T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067641 | |||||||
chr8:23067694 | G | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.144+1057C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067694 | |||||||
chr8:23067804 | C | G | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.144+947G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067804 | |||||||
chr8:23067839 | AG | A | 9 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(6): Show |
9 | HG02015.hp2 HG03704.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.144+911delC | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067839 | |||||||
chr8:23067851 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.144+900C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067851 | |||||||
chr8:23067915 | T | C | 1 | a0001c0001t0003g0259 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.144+836A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067915 | |||||||
chr8:23067943 | G | A | 1 | a0003c0003t0001g0260 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.144+808C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067943 | |||||||
chr8:23067945 | T | C | 1 | a0002c0002t0004g0372 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.144+806A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067945 | |||||||
chr8:23067964 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.144+787G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067964 | |||||||
chr8:23068002 | G | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(307): Show |
317 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.144+749C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23068002 | |||||||
chr8:23068051 | A | G | 1 | a0001c0001t0003g0261 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.144+700T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23068051 | |||||||
chr8:23068239 | C | G | 1 | a0014c0012t0023g0018 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.144+512G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23068239 | |||||||
chr8:23068247 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.144+504G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23068247 | |||||||
chr8:23068373 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.144+378T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23068373 | |||||||
chr8:23068498 | T | C | 50 | a0001c0001t0001g0262 a0001c0001t0001g0266 a0001c0001t0001g0269 others(47): Show |
50 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.144+253A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23068498 |