Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7186 |
| ensemblid | ENSG00000127191.18 |
| hgncid | 12032 |
| symbol | TRAF2 |
| name | TNF receptor associated factor 2 |
| refseq_nuc | NM_021138.4 |
| refseq_prot | NP_066961.2 |
| ensembl_nuc | ENST00000247668.7 |
| ensembl_prot | ENSP00000247668.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 136886516 |
| end | 136926607 |
| strand | + |
| ver | v1.2 |
| region | chr9:136886516-136926607 |
| region5000 | chr9:136881516-136931607 |
| regionname0 | TRAF2_chr9_136886516_136926607 |
| regionname5000 | TRAF2_chr9_136881516_136931607 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 501 | 306 | 87 | 79 | 94 | 12 | 32 | 68 | TRAF2_chr9_136881516_136931607 | TRAF2 | MAAAS others(496): Show |
chr9 | 136881516 | 136931607 |
| a0002 | 0/0 | 501 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | MAAAS others(496): Show |
chr9 | 136881516 | 136931607 |
| a0003 | 0/0 | 501 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | MAAAS others(496): Show |
chr9 | 136881516 | 136931607 |
| a0004 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | MAAAS others(496): Show |
chr9 | 136881516 | 136931607 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1503 | 288 | 74 | 77 | 92 | 11 | 32 | TRAF2_chr9_136881516_136931607 | TRAF2 | ATGGC others(1498): Show |
chr9 | 136881516 | 136931607 | ||
| a0001c0002 | 0/0 | 1503 | 5 | 5 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | ATGGC others(1498): Show |
chr9 | 136881516 | 136931607 | ||
| a0001c0003 | 0/0 | 1503 | 3 | 3 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | ATGGC others(1498): Show |
chr9 | 136881516 | 136931607 | ||
| a0001c0005 | 0/0 | 1503 | 2 | 0 | 1 | 0 | 1 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | ATGGC others(1498): Show |
chr9 | 136881516 | 136931607 | ||
| a0001c0006 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | ATGGC others(1498): Show |
chr9 | 136881516 | 136931607 | ||
| a0001c0007 | 0/0 | 1503 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | ATGGC others(1498): Show |
chr9 | 136881516 | 136931607 | ||
| a0001c0008 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | ATGGC others(1498): Show |
chr9 | 136881516 | 136931607 | ||
| a0001c0010 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | ATGGC others(1498): Show |
chr9 | 136881516 | 136931607 | ||
| a0001c0011 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | ATGGC others(1498): Show |
chr9 | 136881516 | 136931607 | ||
| a0001c0013 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | ATGGC others(1498): Show |
chr9 | 136881516 | 136931607 | ||
| a0002c0004 | 0/0 | 1503 | 2 | 0 | 1 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | ATGGC others(1498): Show |
chr9 | 136881516 | 136931607 | ||
| a0003c0009 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | ATGGC others(1498): Show |
chr9 | 136881516 | 136931607 | ||
| a0004c0012 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | ATGGC others(1498): Show |
chr9 | 136881516 | 136931607 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2266 | 154 | 48 | 35 | 52 | 2 | 16 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0001t0002 | 1/0 | 2266 | 70 | 3 | 33 | 18 | 5 | 10 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0001t0003 | 0/0 | 2265 | 20 | 7 | 6 | 3 | 3 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2260): Show |
chr9 | 136881516 | 136931607 |
| a0001c0001t0004 | 0/0 | 2264 | 22 | 4 | 1 | 16 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2259): Show |
chr9 | 136881516 | 136931607 |
| a0001c0001t0005 | 0/0 | 2266 | 8 | 6 | 0 | 0 | 1 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0001t0006 | 0/0 | 2266 | 3 | 1 | 0 | 2 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0001t0008 | 0/0 | 2263 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2258): Show |
chr9 | 136881516 | 136931607 |
| a0001c0001t0009 | 0/0 | 2266 | 2 | 0 | 0 | 0 | 0 | 2 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0001t0010 | 0/0 | 2264 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2259): Show |
chr9 | 136881516 | 136931607 |
| a0001c0001t0011 | 0/0 | 2266 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0001t0012 | 0/0 | 2266 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0001t0013 | 0/0 | 2277 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2272): Show |
chr9 | 136881516 | 136931607 |
| a0001c0001t0014 | 0/0 | 2266 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0001t0015 | 0/0 | 2266 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0002t0003 | 0/0 | 2265 | 5 | 5 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2260): Show |
chr9 | 136881516 | 136931607 |
| a0001c0003t0001 | 0/0 | 2266 | 3 | 3 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0005t0001 | 0/0 | 2266 | 2 | 0 | 1 | 0 | 1 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0006t0001 | 0/0 | 2266 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0007t0003 | 0/0 | 2265 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2260): Show |
chr9 | 136881516 | 136931607 |
| a0001c0008t0007 | 0/0 | 2266 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0010t0001 | 0/0 | 2266 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0001c0011t0004 | 0/0 | 2264 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2259): Show |
chr9 | 136881516 | 136931607 |
| a0001c0013t0007 | 0/0 | 2266 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0002c0004t0001 | 0/0 | 2266 | 2 | 0 | 1 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0003c0009t0001 | 0/0 | 2266 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| a0004c0012t0002 | 0/0 | 2266 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | AGTTC others(2261): Show |
chr9 | 136881516 | 136931607 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0005g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0008g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0010g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0010g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0011g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0012g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0013g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0014g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0001t0015g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0002t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0002t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0002t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0005t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0005t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0006t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0007t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0007t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0008t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0010t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0011t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0001c0013t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0002c0004t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0002c0004t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0003c0009t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| a0004c0012t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0108 | EUR | GBR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0099 | EUR | FIN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0084 | EUR | FIN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | CHS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00609 | hp2 | a0001 | c0001 | t0011 | g0095 | EAS | CHS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00735 | hp2 | a0001 | c0001 | t0014 | g0092 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01106 | hp2 | a0001 | c0005 | t0001 | g0187 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01358 | hp1 | a0001 | c0001 | t0015 | g0188 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0009 | EUR | IBS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0090 | EUR | IBS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0009 | EUR | IBS | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0139 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01975 | hp2 | a0001 | c0010 | t0001 | g0288 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0138 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | KHV | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | KHV | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | KHV | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CDX | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CDX | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CDX | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02258 | hp2 | a0001 | c0011 | t0004 | g0089 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0230 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0133 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0290 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02735 | hp1 | a0001 | c0001 | t0012 | g0228 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02738 | hp1 | a0003 | c0009 | t0001 | g0244 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02886 | hp2 | a0001 | c0013 | t0007 | g0295 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0140 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0011 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0033 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03130 | hp2 | a0001 | c0002 | t0003 | g0126 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0297 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0128 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0117 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03453 | hp1 | a0004 | c0012 | t0002 | g0052 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03516 | hp2 | a0001 | c0007 | t0003 | g0118 | AFR | ESN | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0011 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03654 | hp1 | a0002 | c0004 | t0001 | g0174 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0091 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0125 | SAS | BEB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | BEB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | STU | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | BEB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG04199 | hp1 | a0001 | c0001 | t0009 | g0072 | SAS | STU | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG04204 | hp1 | a0001 | c0001 | t0009 | g0067 | SAS | STU | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | YRI | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CHB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | CHB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18906 | hp1 | a0001 | c0002 | t0003 | g0129 | AFR | YRI | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | YRI | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18975 | hp1 | a0001 | c0006 | t0001 | g0236 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18979 | hp1 | a0001 | c0006 | t0001 | g0279 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18989 | hp2 | a0001 | c0001 | t0006 | g0258 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | LWK | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | YRI | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | YRI | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | TSI | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA20805 | hp2 | a0001 | c0005 | t0001 | g0186 | EUR | TSI | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | GIH | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | GIH | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01123 | hp1 | a0002 | c0004 | t0001 | g0219 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0291 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0127 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0296 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG03471 | hp2 | a0001 | c0008 | t0007 | g0294 | AFR | MSL | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG06807 | hp1 | a0001 | c0001 | t0013 | g0134 | AFR | USA | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | USA | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | USA | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | USA | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA21309 | hp1 | a0001 | c0007 | t0003 | g0119 | AFR | LWK | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0054 | AFR | LWK | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0109 | REF | REF | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0057 | REF | REF | TRAF2_chr9_136881516_136931607 | TRAF2 | chr9 | 136881516 | 136931607 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:136908115 | G | A | 1 | a0002 | 2 | HG01123.hp1 HG03654.hp1 |
missense_variant | MODERATE | c.412G>A | p.Ala138Thr | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/11 | 466/2266 | 412/1506 | 138/501 | chr9 | 136908115 | |||
| chr9:136916595 | G | A | 1 | a0003 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.658G>A | p.Ala220Thr | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/11 | 712/2266 | 658/1506 | 220/501 | chr9 | 136916595 | |||
| chr9:136920346 | C | T | 1 | a0004 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.791C>T | p.Ala264Val | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 8/11 | 845/2266 | 791/1506 | 264/501 | chr9 | 136920346 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:136908093 | G | A | 1 | a0001c0008 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.390G>A | p.Pro130Pro | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/11 | 444/2266 | 390/1506 | 130/501 | chr9 | 136908093 | |||
| chr9:136909961 | C | T | 1 | a0001c0003 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.570C>T | p.Asp190Asp | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/11 | 624/2266 | 570/1506 | 190/501 | chr9 | 136909961 | |||
| chr9:136916594 | C | T | 2 | a0001c0008 a0001c0013 |
2 | HG02886.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.657C>T | p.His219His | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/11 | 711/2266 | 657/1506 | 219/501 | chr9 | 136916594 | |||
| chr9:136920347 | G | A | 1 | a0001c0005 | 2 | HG01106.hp2 NA20805.hp2 |
synonymous_variant | LOW | c.792G>A | p.Ala264Ala | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 8/11 | 846/2266 | 792/1506 | 264/501 | chr9 | 136920347 | |||
| chr9:136920479 | G | T | 1 | a0001c0007 | 2 | HG03516.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.924G>T | p.Arg308Arg | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 8/11 | 978/2266 | 924/1506 | 308/501 | chr9 | 136920479 | |||
| chr9:136921160 | C | T | 1 | a0001c0002 | 5 | HG02486.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
synonymous_variant | LOW | c.1083C>T | p.Phe361Phe | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/11 | 1137/2266 | 1083/1506 | 361/501 | chr9 | 136921160 | |||
| chr9:136921202 | C | T | 1 | a0001c0011 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.1125C>T | p.Ala375Ala | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/11 | 1179/2266 | 1125/1506 | 375/501 | chr9 | 136921202 | |||
| chr9:136923964 | G | A | 1 | a0001c0010 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.1251G>A | p.Pro417Pro | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/11 | 1305/2266 | 1251/1506 | 417/501 | chr9 | 136923964 | |||
| chr9:136925856 | C | T | 1 | a0001c0006 | 2 | NA18975.hp1 NA18979.hp1 |
synonymous_variant | LOW | c.1461C>T | p.Asp487Asp | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 1515/2266 | 1461/1506 | 487/501 | chr9 | 136925856 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:136886526 | G | T | 1 | a0001c0001t0010 | 2 | HG02559.hp1 HG03139.hp1 |
5_prime_UTR_variant | MODIFIER | c.-44G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/11 | 12215 | chr9 | 136886526 | ||||||
| chr9:136925911 | A | G | 3 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0015 |
10 | HG00735.hp2 HG01358.hp1 HG01516.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*10A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 10 | chr9 | 136925911 | ||||||
| chr9:136925969 | G | A | 9 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(6): Show |
166 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*68G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 68 | chr9 | 136925969 | ||||||
| chr9:136926017 | G | A | 1 | a0001c0001t0014 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*116G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 116 | chr9 | 136926017 | ||||||
| chr9:136926148 | C | T | 1 | a0001c0001t0012 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 247 | chr9 | 136926148 | ||||||
| chr9:136926192 | C | G | 1 | a0001c0001t0009 | 2 | HG04199.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*291C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 291 | chr9 | 136926192 | ||||||
| chr9:136926401 | A | AGG | 10 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0012 others(7): Show |
169 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*502_*503dupGG | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 504 | INFO_REALIGN_3_PRIME | chr9 | 136926401 | |||||
| chr9:136926477 | GGA | G | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(14): Show |
223 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*580_*581delAG | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 580 | INFO_REALIGN_3_PRIME | chr9 | 136926477 | |||||
| chr9:136926481 | A | G | 1 | a0001c0001t0013 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*580A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 580 | chr9 | 136926481 | ||||||
| chr9:136926484 | G | GTCCCACG others(5): Show |
1 | a0001c0001t0013 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*585_*586insCCACGC others(6): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 586 | INFO_REALIGN_3_PRIME | chr9 | 136926484 | |||||
| chr9:136926489 | G | C | 1 | a0001c0001t0013 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*588G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 588 | chr9 | 136926489 | ||||||
| chr9:136926496 | G | A | 2 | a0001c0008t0007 a0001c0013t0007 |
2 | HG02886.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*595G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 595 | chr9 | 136926496 | ||||||
| chr9:136926531 | CA | C | 2 | a0001c0001t0008 a0001c0001t0013 |
3 | HG02970.hp1 HG03579.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*631delA | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 631 | chr9 | 136926531 | ||||||
| chr9:136926599 | T | TA | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0007t0003 |
27 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*698_*699insA | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 11/11 | 699 | chr9 | 136926599 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:136886547 | GCGAGCGC others(5): Show |
G | 2 | a0001c0001t0010g0296 a0001c0001t0010g0297 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-29+9_-29+20delAGC others(9): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136886547 | ||||||
| chr9:136886594 | T | C | 1 | a0001c0001t0002g0012 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-29+53T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136886594 | |||||||
| chr9:136886665 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0002g0013 a0001c0001t0002g0014 others(4): Show |
7 | HG02735.hp2 HG03017.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+124G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136886665 | |||||||
| chr9:136886723 | C | T | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-29+182C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136886723 | |||||||
| chr9:136886737 | C | T | 1 | a0001c0013t0007g0295 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-29+196C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136886737 | |||||||
| chr9:136886741 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG01993.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-29+200G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136886741 | |||||||
| chr9:136886793 | G | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-29+252G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136886793 | |||||||
| chr9:136887099 | G | A | 18 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0041 others(15): Show |
18 | HG00438.hp1 HG02071.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29+558G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136887099 | |||||||
| chr9:136887650 | C | T | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-29+1109C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136887650 | |||||||
| chr9:136887689 | T | G | 1 | a0001c0001t0001g0042 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-29+1148T>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136887689 | |||||||
| chr9:136887829 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+1288T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136887829 | |||||||
| chr9:136887892 | A | G | 1 | a0001c0001t0002g0293 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-29+1351A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136887892 | |||||||
| chr9:136888323 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-29+1782C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136888323 | |||||||
| chr9:136888347 | C | G | 228 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(225): Show |
229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.-29+1806C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136888347 | |||||||
| chr9:136888447 | C | T | 2 | a0001c0001t0003g0290 a0001c0001t0003g0291 |
2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-29+1906C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136888447 | |||||||
| chr9:136888590 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0289 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-29+2049C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136888590 | |||||||
| chr9:136888639 | A | G | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-29+2098A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136888639 | |||||||
| chr9:136888810 | G | A | 8 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(5): Show |
8 | HG01346.hp2 HG01928.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+2269G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136888810 | |||||||
| chr9:136888840 | C | T | 178 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(175): Show |
179 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.-29+2299C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136888840 | |||||||
| chr9:136888901 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-29+2360C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136888901 | |||||||
| chr9:136888946 | A | G | 2 | a0001c0001t0003g0135 a0001c0001t0003g0136 |
2 | NA18979.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-29+2405A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136888946 | |||||||
| chr9:136888967 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-29+2426G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136888967 | |||||||
| chr9:136889103 | C | T | 1 | a0001c0010t0001g0288 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-29+2562C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136889103 | |||||||
| chr9:136889219 | G | GT | 23 | a0001c0001t0001g0019 a0001c0001t0001g0277 a0001c0001t0001g0278 others(20): Show |
23 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-29+2694dupT | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136889219 | ||||||
| chr9:136889219 | GT | G | 6 | a0001c0001t0001g0137 a0001c0001t0008g0011 a0001c0001t0010g0296 others(3): Show |
7 | HG02559.hp1 HG02886.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+2694delT | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136889219 | ||||||
| chr9:136889241 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0002g0045 a0001c0001t0002g0046 |
3 | HG00609.hp1 NA18998.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-29+2700G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136889241 | |||||||
| chr9:136889289 | T | C | 3 | a0001c0003t0001g0138 a0001c0003t0001g0139 a0001c0003t0001g0140 |
3 | HG01884.hp1 HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-29+2748T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136889289 | |||||||
| chr9:136889305 | C | G | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-29+2764C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136889305 | |||||||
| chr9:136889406 | C | G | 3 | a0001c0001t0004g0130 a0001c0001t0004g0131 a0001c0001t0004g0132 |
3 | HG02818.hp1 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-29+2865C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136889406 | |||||||
| chr9:136889682 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-29+3141C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136889682 | |||||||
| chr9:136889932 | CGTCACCG others(37): Show |
C | 3 | a0001c0001t0001g0275 a0001c0001t0001g0286 a0001c0001t0001g0287 |
3 | HG00558.hp2 NA18612.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-29+3453_-29+3496d others(46): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136889932 | ||||||
| chr9:136889959 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-29+3418C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136889959 | |||||||
| chr9:136889990 | TGA | T | 231 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(228): Show |
233 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.-29+3453_-29+3454d others(4): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136889990 | ||||||
| chr9:136890028 | CGTGT | C | 4 | a0001c0001t0002g0003 a0001c0001t0002g0048 a0001c0001t0002g0049 others(1): Show |
5 | HG00639.hp2 HG01081.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+3491_-29+3494d others(6): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136890028 | ||||||
| chr9:136890040 | C | G | 1 | a0001c0001t0002g0007 | 2 | HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-29+3499C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136890040 | |||||||
| chr9:136890045 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-29+3504C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136890045 | |||||||
| chr9:136890084 | C | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-29+3543C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136890084 | |||||||
| chr9:136890095 | T | C | 235 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(232): Show |
238 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.-29+3554T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136890095 | |||||||
| chr9:136890125 | A | T | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-29+3584A>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136890125 | |||||||
| chr9:136890217 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-29+3676C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136890217 | |||||||
| chr9:136890227 | C | T | 4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | NA18939.hp2 NA18944.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29+3686C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136890227 | |||||||
| chr9:136890231 | T | C | 236 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(233): Show |
239 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-29+3690T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136890231 | |||||||
| chr9:136890772 | C | G | 1 | a0001c0001t0013g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-29+4231C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136890772 | |||||||
| chr9:136891019 | G | A | 233 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(230): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-29+4478G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136891019 | |||||||
| chr9:136891030 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-29+4489A>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136891030 | |||||||
| chr9:136891161 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-29+4620T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136891161 | |||||||
| chr9:136891244 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-29+4703G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136891244 | |||||||
| chr9:136891449 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-29+4908C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136891449 | |||||||
| chr9:136891539 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-29+4998T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136891539 | |||||||
| chr9:136891620 | C | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-29+5079C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136891620 | |||||||
| chr9:136891638 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-29+5097C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136891638 | |||||||
| chr9:136891724 | C | CT | 45 | a0001c0001t0001g0047 a0001c0001t0002g0001 a0001c0001t0002g0002 others(42): Show |
52 | HG00140.hp2 HG00323.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.-29+5197dupT | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136891724 | ||||||
| chr9:136891962 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0289 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-29+5421C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136891962 | |||||||
| chr9:136891990 | T | C | 2 | a0001c0001t0005g0090 a0001c0001t0005g0091 |
2 | HG01516.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-29+5449T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136891990 | |||||||
| chr9:136892013 | C | T | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-29+5472C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136892013 | |||||||
| chr9:136892189 | C | T | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01074.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.-29+5648C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136892189 | |||||||
| chr9:136892236 | G | GGCAGATC others(9): Show |
1 | a0001c0001t0004g0024 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-29+5697_-29+5712d others(18): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136892236 | ||||||
| chr9:136892259 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-29+5718C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136892259 | |||||||
| chr9:136892300 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-29+5759A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136892300 | |||||||
| chr9:136892319 | C | G | 1 | a0001c0001t0001g0266 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-29+5778C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136892319 | |||||||
| chr9:136892380 | C | T | 3 | a0001c0001t0010g0296 a0001c0001t0010g0297 a0001c0001t0013g0134 |
3 | HG02559.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-29+5839C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136892380 | |||||||
| chr9:136892711 | C | G | 1 | a0001c0001t0001g0271 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-28-6002C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136892711 | |||||||
| chr9:136892752 | C | T | 3 | a0001c0001t0010g0296 a0001c0001t0010g0297 a0001c0001t0013g0134 |
3 | HG02559.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-28-5961C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136892752 | |||||||
| chr9:136892772 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-28-5941C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136892772 | |||||||
| chr9:136892878 | A | G | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-28-5835A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136892878 | |||||||
| chr9:136892988 | G | T | 2 | a0001c0001t0003g0290 a0001c0001t0003g0291 |
2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-28-5725G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136892988 | |||||||
| chr9:136893001 | C | T | 233 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(230): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-28-5712C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136893001 | |||||||
| chr9:136893085 | A | C | 233 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(230): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-28-5628A>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136893085 | |||||||
| chr9:136893203 | G | C | 233 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(230): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-28-5510G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136893203 | |||||||
| chr9:136893326 | T | C | 236 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(233): Show |
239 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-28-5387T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136893326 | |||||||
| chr9:136893576 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-28-5137G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136893576 | |||||||
| chr9:136893618 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-28-5095C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136893618 | |||||||
| chr9:136893646 | G | T | 1 | a0001c0001t0001g0261 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-28-5067G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136893646 | |||||||
| chr9:136893650 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-28-5063A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136893650 | |||||||
| chr9:136893910 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-28-4803C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136893910 | |||||||
| chr9:136893911 | G | A | 25 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(22): Show |
25 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.-28-4802G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136893911 | |||||||
| chr9:136894047 | C | CT | 220 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(217): Show |
222 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.-28-4649dupT | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136894047 | ||||||
| chr9:136894047 | C | CTT | 6 | a0001c0001t0001g0261 a0001c0001t0001g0284 a0001c0001t0004g0040 others(3): Show |
6 | HG02559.hp1 HG03139.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-4650_-28-4649d others(4): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136894047 | ||||||
| chr9:136894402 | T | G | 1 | a0001c0001t0002g0061 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-28-4311T>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136894402 | |||||||
| chr9:136894441 | G | T | 3 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0013t0007g0295 |
4 | HG02886.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-4272G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136894441 | |||||||
| chr9:136894480 | A | G | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-28-4233A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136894480 | |||||||
| chr9:136894519 | G | A | 1 | a0004c0012t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-28-4194G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136894519 | |||||||
| chr9:136894582 | G | A | 1 | a0001c0008t0007g0294 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-28-4131G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136894582 | |||||||
| chr9:136894605 | A | T | 236 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(233): Show |
239 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-28-4108A>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136894605 | |||||||
| chr9:136894641 | C | T | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.-28-4072C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136894641 | |||||||
| chr9:136894734 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-28-3979G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136894734 | |||||||
| chr9:136894883 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28-3830C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136894883 | |||||||
| chr9:136894915 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-28-3798C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136894915 | |||||||
| chr9:136895073 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-28-3640G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895073 | |||||||
| chr9:136895104 | A | C | 4 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(1): Show |
4 | HG02071.hp2 HG02080.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-3609A>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895104 | |||||||
| chr9:136895152 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-28-3561G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895152 | |||||||
| chr9:136895247 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-28-3466C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895247 | |||||||
| chr9:136895284 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0004g0040 |
3 | NA19078.hp1 NA19083.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-28-3429C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895284 | |||||||
| chr9:136895361 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-28-3352A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895361 | |||||||
| chr9:136895365 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | NA18965.hp2 NA18966.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-3348G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895365 | |||||||
| chr9:136895388 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-28-3325A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895388 | |||||||
| chr9:136895406 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | NA18963.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-28-3307C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895406 | |||||||
| chr9:136895464 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-28-3249C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895464 | |||||||
| chr9:136895628 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-28-3085G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895628 | |||||||
| chr9:136895633 | C | T | 3 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0013t0007g0295 |
4 | HG02886.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-3080C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895633 | |||||||
| chr9:136895752 | A | G | 236 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(233): Show |
239 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-28-2961A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895752 | |||||||
| chr9:136895809 | G | A | 1 | a0001c0001t0003g0108 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-28-2904G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895809 | |||||||
| chr9:136895850 | GAA | G | 7 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0266 others(4): Show |
8 | HG00140.hp1 HG01255.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-2844_-28-2843d others(4): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136895850 | ||||||
| chr9:136895850 | GAAA | G | 222 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(219): Show |
224 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.-28-2845_-28-2843d others(5): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136895850 | ||||||
| chr9:136895850 | GAAAAAAA | G | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0083 others(3): Show |
8 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-2849_-28-2843d others(9): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136895850 | ||||||
| chr9:136895877 | G | T | 1 | a0001c0001t0002g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-28-2836G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895877 | |||||||
| chr9:136895935 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-28-2778G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895935 | |||||||
| chr9:136895950 | C | T | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-28-2763C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136895950 | |||||||
| chr9:136896019 | G | A | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.-28-2694G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896019 | |||||||
| chr9:136896070 | C | G | 236 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(233): Show |
239 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-28-2643C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896070 | |||||||
| chr9:136896099 | A | G | 1 | a0004c0012t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-28-2614A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896099 | |||||||
| chr9:136896174 | C | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-28-2539C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896174 | |||||||
| chr9:136896196 | A | G | 236 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(233): Show |
239 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-28-2517A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896196 | |||||||
| chr9:136896342 | C | G | 1 | a0001c0001t0014g0092 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-28-2371C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896342 | |||||||
| chr9:136896406 | C | T | 233 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(230): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-28-2307C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896406 | |||||||
| chr9:136896511 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-28-2202G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896511 | |||||||
| chr9:136896522 | T | A | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.-28-2191T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896522 | |||||||
| chr9:136896537 | C | T | 1 | a0001c0001t0005g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-28-2176C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896537 | |||||||
| chr9:136896613 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0002g0045 a0001c0001t0002g0046 |
3 | HG00609.hp1 NA18998.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-28-2100T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896613 | |||||||
| chr9:136896629 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-28-2084C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896629 | |||||||
| chr9:136896666 | A | C | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01074.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.-28-2047A>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896666 | |||||||
| chr9:136896703 | C | T | 233 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(230): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-28-2010C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896703 | |||||||
| chr9:136896744 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-28-1969G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896744 | |||||||
| chr9:136896745 | A | C | 1 | a0001c0001t0001g0261 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-28-1968A>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896745 | |||||||
| chr9:136896799 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02165.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-28-1914G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896799 | |||||||
| chr9:136896809 | C | T | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-28-1904C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896809 | |||||||
| chr9:136896886 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-28-1827G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896886 | |||||||
| chr9:136896921 | C | A | 1 | a0001c0001t0001g0261 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-28-1792C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896921 | |||||||
| chr9:136896960 | C | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-28-1753C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136896960 | |||||||
| chr9:136897164 | C | G | 1 | a0001c0001t0001g0261 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-28-1549C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897164 | |||||||
| chr9:136897172 | TGAGG | T | 233 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(230): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-28-1536_-28-1533d others(6): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136897172 | ||||||
| chr9:136897247 | C | T | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-28-1466C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897247 | |||||||
| chr9:136897304 | T | TAGAG | 236 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(233): Show |
239 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-28-1407_-28-1406i others(6): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136897304 | ||||||
| chr9:136897334 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-28-1379G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897334 | |||||||
| chr9:136897439 | C | A | 233 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(230): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-28-1274C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897439 | |||||||
| chr9:136897444 | G | A | 231 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(228): Show |
233 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.-28-1269G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897444 | |||||||
| chr9:136897459 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-28-1254C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897459 | |||||||
| chr9:136897461 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-28-1252T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897461 | |||||||
| chr9:136897588 | C | T | 1 | a0001c0001t0005g0058 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-28-1125C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897588 | |||||||
| chr9:136897593 | C | G | 1 | a0001c0001t0001g0261 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-28-1120C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897593 | |||||||
| chr9:136897594 | T | C | 1 | a0001c0001t0001g0261 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-28-1119T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897594 | |||||||
| chr9:136897595 | G | T | 1 | a0001c0001t0001g0261 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-28-1118G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897595 | |||||||
| chr9:136897660 | C | G | 1 | a0001c0001t0001g0270 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-28-1053C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897660 | |||||||
| chr9:136897663 | G | A | 1 | a0002c0004t0001g0174 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-28-1050G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897663 | |||||||
| chr9:136897710 | C | T | 5 | a0001c0002t0003g0126 a0001c0002t0003g0127 a0001c0002t0003g0128 others(2): Show |
5 | HG02486.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-1003C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897710 | |||||||
| chr9:136897711 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0257 a0001c0001t0001g0263 others(1): Show |
4 | HG02155.hp2 NA18939.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-1002C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897711 | |||||||
| chr9:136897737 | A | G | 4 | a0001c0001t0001g0173 a0001c0001t0010g0296 a0001c0001t0010g0297 others(1): Show |
4 | HG02559.hp1 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-976A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897737 | |||||||
| chr9:136897801 | T | TCCGCTCT others(67): Show |
3 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0013t0007g0295 |
4 | HG02886.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-876_-28-875ins others(74): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136897801 | ||||||
| chr9:136897801 | T | TCCGCTCT others(67): Show |
1 | a0001c0001t0001g0175 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-28-876_-28-875ins others(74): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136897801 | ||||||
| chr9:136897801 | T | TCCGCTCT others(140): Show |
216 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0021 others(213): Show |
218 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-28-876_-28-875ins others(147): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136897801 | ||||||
| chr9:136897801 | T | TCCGCTCT others(214): Show |
1 | a0001c0001t0010g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-28-876_-28-875ins others(221): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136897801 | ||||||
| chr9:136897801 | T | TCCGCTCT others(288): Show |
1 | a0001c0001t0004g0036 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-28-876_-28-875ins others(295): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136897801 | ||||||
| chr9:136897801 | T | TCCGCTCT others(213): Show |
1 | a0001c0001t0001g0284 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-28-876_-28-875ins others(220): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136897801 | ||||||
| chr9:136897801 | T | TCCGCTCT others(139): Show |
1 | a0001c0001t0001g0261 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-28-887_-28-886ins others(146): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136897801 | ||||||
| chr9:136897804 | G | GCTCTCGG others(69): Show |
1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-28-876_-28-875ins others(76): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136897804 | ||||||
| chr9:136897817 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-28-896G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897817 | |||||||
| chr9:136897828 | G | GTGGTAGC others(140): Show |
2 | a0001c0001t0002g0012 a0001c0001t0002g0289 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-28-876_-28-875ins others(147): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136897828 | ||||||
| chr9:136897838 | T | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0176 a0001c0001t0001g0177 others(6): Show |
9 | HG02735.hp2 HG03017.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28-875T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897838 | |||||||
| chr9:136897858 | C | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0176 a0001c0001t0001g0177 others(6): Show |
9 | HG02735.hp2 HG03017.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28-855C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897858 | |||||||
| chr9:136897859 | T | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0176 a0001c0001t0001g0177 others(6): Show |
9 | HG02735.hp2 HG03017.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28-854T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897859 | |||||||
| chr9:136897863 | G | A | 1 | a0001c0001t0004g0036 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-28-850G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897863 | |||||||
| chr9:136897872 | G | GTTCCGCT others(140): Show |
7 | a0001c0001t0001g0019 a0001c0001t0002g0013 a0001c0001t0002g0014 others(4): Show |
7 | HG02735.hp2 HG03017.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28-837_-28-836ins others(147): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136897872 | ||||||
| chr9:136897874 | TC | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0008g0011 |
4 | HG02970.hp1 HG03579.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-836delC | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 136897874 | ||||||
| chr9:136897883 | C | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-28-830C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897883 | |||||||
| chr9:136897884 | G | A | 1 | a0001c0001t0004g0036 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-28-829G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897884 | |||||||
| chr9:136897932 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-28-781C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897932 | |||||||
| chr9:136897933 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-28-780T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897933 | |||||||
| chr9:136897946 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-28-767G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897946 | |||||||
| chr9:136897951 | C | T | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-28-762C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897951 | |||||||
| chr9:136897973 | T | C | 236 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(233): Show |
239 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-28-740T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136897973 | |||||||
| chr9:136898011 | A | C | 1 | a0001c0001t0001g0284 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-28-702A>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898011 | |||||||
| chr9:136898026 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-28-687G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898026 | |||||||
| chr9:136898040 | A | G | 3 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 |
3 | HG02723.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-28-673A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898040 | |||||||
| chr9:136898080 | T | C | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-28-633T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898080 | |||||||
| chr9:136898134 | A | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-28-579A>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898134 | |||||||
| chr9:136898274 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-28-439T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898274 | |||||||
| chr9:136898431 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-28-282C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898431 | |||||||
| chr9:136898435 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-28-278C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898435 | |||||||
| chr9:136898474 | T | C | 233 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(230): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-28-239T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898474 | |||||||
| chr9:136898498 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-215C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898498 | |||||||
| chr9:136898578 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0251 others(1): Show |
4 | HG01346.hp1 HG01993.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-135C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898578 | |||||||
| chr9:136898614 | G | A | 1 | a0001c0013t0007g0295 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-28-99G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898614 | |||||||
| chr9:136898685 | G | A | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-28-28G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898685 | |||||||
| chr9:136898691 | C | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG01257.hp1 HG02056.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-22C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 1/10 | chr9 | 136898691 | |||||||
| chr9:136898966 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.188+38G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 2/10 | chr9 | 136898966 | |||||||
| chr9:136899122 | C | T | 3 | a0001c0001t0004g0130 a0001c0001t0004g0131 a0001c0001t0004g0132 |
3 | HG02818.hp1 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.188+194C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 2/10 | chr9 | 136899122 | |||||||
| chr9:136899153 | C | T | 1 | a0004c0012t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.188+225C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 2/10 | chr9 | 136899153 | |||||||
| chr9:136899154 | G | A | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.188+226G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 2/10 | chr9 | 136899154 | |||||||
| chr9:136899276 | G | A | 7 | a0001c0001t0005g0004 a0001c0001t0005g0053 a0001c0001t0005g0054 others(4): Show |
8 | HG00735.hp2 HG01516.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.189-318G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 2/10 | chr9 | 136899276 | |||||||
| chr9:136899295 | G | A | 1 | a0001c0008t0007g0294 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.189-299G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 2/10 | chr9 | 136899295 | |||||||
| chr9:136899319 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.189-275G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 2/10 | chr9 | 136899319 | |||||||
| chr9:136899319 | G | T | 1 | a0001c0001t0010g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.189-275G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 2/10 | chr9 | 136899319 | |||||||
| chr9:136899393 | C | A | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.189-201C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 2/10 | chr9 | 136899393 | |||||||
| chr9:136899397 | C | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.189-197C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 2/10 | chr9 | 136899397 | |||||||
| chr9:136899501 | G | T | 3 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0013t0007g0295 |
4 | HG02886.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-93G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 2/10 | chr9 | 136899501 | |||||||
| chr9:136899733 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.267+61A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 3/10 | chr9 | 136899733 | |||||||
| chr9:136899772 | C | G | 1 | a0001c0001t0001g0248 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.267+100C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 3/10 | chr9 | 136899772 | |||||||
| chr9:136899879 | C | T | 234 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(231): Show |
237 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.267+207C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 3/10 | chr9 | 136899879 | |||||||
| chr9:136899963 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.267+291C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 3/10 | chr9 | 136899963 | |||||||
| chr9:136900113 | G | A | 6 | a0001c0001t0003g0108 a0001c0001t0003g0110 a0001c0001t0003g0111 others(3): Show |
6 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.268-309G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 3/10 | chr9 | 136900113 | |||||||
| chr9:136900127 | C | T | 1 | a0001c0001t0004g0033 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.268-295C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 3/10 | chr9 | 136900127 | |||||||
| chr9:136900169 | T | TA | 6 | a0001c0001t0001g0143 a0001c0001t0001g0163 a0001c0001t0001g0183 others(3): Show |
6 | HG01123.hp2 HG01433.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-240dupA | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 136900169 | ||||||
| chr9:136900181 | AAG | A | 10 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0254 others(7): Show |
10 | HG01109.hp1 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.268-239_268-238del others(2): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 136900181 | ||||||
| chr9:136900182 | AG | A | 120 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0042 others(117): Show |
121 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.268-239delG | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 3/10 | chr9 | 136900182 | |||||||
| chr9:136900183 | G | A | 103 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0021 others(100): Show |
103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.268-239G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 3/10 | chr9 | 136900183 | |||||||
| chr9:136900186 | T | A | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.268-236T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 3/10 | chr9 | 136900186 | |||||||
| chr9:136900189 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.268-233A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 3/10 | chr9 | 136900189 | |||||||
| chr9:136900319 | G | A | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.268-103G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 3/10 | chr9 | 136900319 | |||||||
| chr9:136900561 | C | T | 3 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0013t0007g0295 |
4 | HG02886.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+41C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136900561 | |||||||
| chr9:136900565 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.366+45C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136900565 | |||||||
| chr9:136901052 | A | G | 233 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(230): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.366+532A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136901052 | |||||||
| chr9:136901099 | T | TGTGTGCT others(8): Show |
1 | a0001c0001t0003g0135 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.366+588_366+589ins others(15): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 136901099 | ||||||
| chr9:136901099 | T | TGTGTGCT others(9): Show |
51 | a0001c0001t0001g0164 a0001c0001t0001g0292 a0001c0001t0002g0012 others(48): Show |
53 | HG00140.hp1 HG00438.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.366+583_366+598dup others(16): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 136901099 | ||||||
| chr9:136901111 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.366+591G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136901111 | |||||||
| chr9:136901620 | G | C | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.366+1100G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136901620 | |||||||
| chr9:136901667 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0281 |
2 | HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.366+1147C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136901667 | |||||||
| chr9:136901770 | G | A | 1 | a0001c0001t0002g0013 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.366+1250G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136901770 | |||||||
| chr9:136901967 | T | C | 223 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(220): Show |
224 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.366+1447T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136901967 | |||||||
| chr9:136902027 | C | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366+1507C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136902027 | |||||||
| chr9:136902036 | C | T | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.366+1516C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136902036 | |||||||
| chr9:136902129 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.366+1609C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136902129 | |||||||
| chr9:136902178 | G | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0116 others(8): Show |
11 | HG00642.hp2 HG01074.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.366+1658G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136902178 | |||||||
| chr9:136902187 | G | A | 225 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(222): Show |
226 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.366+1667G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136902187 | |||||||
| chr9:136902220 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.366+1700G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136902220 | |||||||
| chr9:136902309 | A | G | 1 | a0003c0009t0001g0244 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.366+1789A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136902309 | |||||||
| chr9:136902437 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.366+1917C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136902437 | |||||||
| chr9:136902644 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.366+2124G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136902644 | |||||||
| chr9:136902878 | G | C | 4 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0011t0004g0089 others(1): Show |
5 | HG02258.hp2 HG02886.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.366+2358G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136902878 | |||||||
| chr9:136902969 | A | C | 1 | a0001c0001t0001g0253 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.366+2449A>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136902969 | |||||||
| chr9:136902991 | C | CAG | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.366+2471_366+2472i others(4): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136902991 | |||||||
| chr9:136903192 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.366+2672C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903192 | |||||||
| chr9:136903223 | T | C | 19 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(16): Show |
19 | HG01123.hp2 HG01192.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.366+2703T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903223 | |||||||
| chr9:136903347 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.366+2827C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903347 | |||||||
| chr9:136903363 | T | A | 1 | a0001c0013t0007g0295 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.366+2843T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903363 | |||||||
| chr9:136903379 | G | A | 1 | a0001c0001t0004g0025 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.366+2859G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903379 | |||||||
| chr9:136903449 | C | T | 1 | a0001c0001t0002g0289 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.366+2929C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903449 | |||||||
| chr9:136903454 | T | C | 228 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(225): Show |
229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.366+2934T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903454 | |||||||
| chr9:136903530 | A | G | 3 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0013t0007g0295 |
4 | HG02886.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+3010A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903530 | |||||||
| chr9:136903536 | A | AT | 218 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(215): Show |
219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.366+3029dupT | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 136903536 | ||||||
| chr9:136903550 | A | T | 228 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(225): Show |
229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.366+3030A>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903550 | |||||||
| chr9:136903624 | C | A | 1 | a0001c0001t0001g0163 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.366+3104C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903624 | |||||||
| chr9:136903690 | G | T | 231 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(228): Show |
233 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.366+3170G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903690 | |||||||
| chr9:136903712 | C | G | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.366+3192C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903712 | |||||||
| chr9:136903884 | A | G | 1 | a0001c0001t0002g0049 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.366+3364A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903884 | |||||||
| chr9:136903961 | C | T | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.366+3441C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136903961 | |||||||
| chr9:136904054 | C | CGCTGCCC others(13): Show |
2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.366+3543_366+3562d others(22): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 136904054 | ||||||
| chr9:136904083 | G | A | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366+3563G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904083 | |||||||
| chr9:136904096 | G | A | 2 | a0001c0001t0002g0012 a0001c0001t0002g0289 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.366+3576G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904096 | |||||||
| chr9:136904109 | T | C | 3 | a0001c0001t0010g0296 a0001c0001t0010g0297 a0001c0001t0013g0134 |
3 | HG02559.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.366+3589T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904109 | |||||||
| chr9:136904128 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.366+3608C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904128 | |||||||
| chr9:136904206 | A | G | 1 | a0001c0001t0002g0013 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.366+3686A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904206 | |||||||
| chr9:136904207 | TTAC | T | 3 | a0001c0008t0007g0294 a0001c0010t0001g0288 a0001c0013t0007g0295 |
3 | HG01975.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.366+3690_366+3692d others(5): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 136904207 | ||||||
| chr9:136904210 | C | T | 228 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(225): Show |
230 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.366+3690C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904210 | |||||||
| chr9:136904234 | C | T | 228 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(225): Show |
229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.366+3714C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904234 | |||||||
| chr9:136904365 | C | T | 228 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(225): Show |
229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.367-3705C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904365 | |||||||
| chr9:136904445 | G | A | 1 | a0001c0001t0004g0130 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.367-3625G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904445 | |||||||
| chr9:136904496 | C | T | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.367-3574C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904496 | |||||||
| chr9:136904500 | C | T | 228 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(225): Show |
229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.367-3570C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904500 | |||||||
| chr9:136904627 | T | C | 2 | a0001c0001t0010g0296 a0001c0001t0010g0297 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.367-3443T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904627 | |||||||
| chr9:136904631 | T | A | 2 | a0001c0001t0003g0120 a0001c0001t0003g0121 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.367-3439T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904631 | |||||||
| chr9:136904699 | C | T | 2 | a0001c0001t0003g0290 a0001c0001t0003g0291 |
2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.367-3371C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904699 | |||||||
| chr9:136904771 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.367-3299C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904771 | |||||||
| chr9:136904780 | G | GAATAGTT others(16): Show |
232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.367-3280_367-3279i others(25): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 136904780 | ||||||
| chr9:136904830 | A | G | 3 | a0001c0001t0001g0268 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | NA18939.hp2 NA18944.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.367-3240A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904830 | |||||||
| chr9:136904836 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.367-3234G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904836 | |||||||
| chr9:136904863 | G | A | 225 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(222): Show |
226 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.367-3207G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136904863 | |||||||
| chr9:136905098 | G | A | 1 | a0001c0001t0003g0122 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.367-2972G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136905098 | |||||||
| chr9:136905202 | G | A | 2 | a0001c0001t0003g0123 a0001c0001t0003g0124 |
2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.367-2868G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136905202 | |||||||
| chr9:136905309 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0283 |
2 | HG00408.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.367-2761C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136905309 | |||||||
| chr9:136905492 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.367-2578T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136905492 | |||||||
| chr9:136905823 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.367-2247C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136905823 | |||||||
| chr9:136905830 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.367-2240C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136905830 | |||||||
| chr9:136905898 | A | G | 1 | a0001c0001t0004g0032 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.367-2172A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136905898 | |||||||
| chr9:136905920 | C | T | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.367-2150C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136905920 | |||||||
| chr9:136905958 | A | T | 3 | a0001c0001t0004g0130 a0001c0001t0004g0131 a0001c0001t0004g0132 |
3 | HG02818.hp1 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.367-2112A>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136905958 | |||||||
| chr9:136905972 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.367-2098G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136905972 | |||||||
| chr9:136905982 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.367-2088G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136905982 | |||||||
| chr9:136906021 | C | T | 223 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(220): Show |
224 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.367-2049C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136906021 | |||||||
| chr9:136906060 | C | T | 7 | a0001c0001t0002g0051 a0001c0001t0002g0062 a0001c0001t0002g0076 others(4): Show |
7 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-2010C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136906060 | |||||||
| chr9:136906061 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.367-2009G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136906061 | |||||||
| chr9:136906080 | A | G | 1 | a0001c0001t0006g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.367-1990A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136906080 | |||||||
| chr9:136906300 | G | A | 1 | a0001c0001t0005g0058 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.367-1770G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136906300 | |||||||
| chr9:136906794 | C | T | 1 | a0001c0008t0007g0294 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.367-1276C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136906794 | |||||||
| chr9:136906797 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.367-1273C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136906797 | |||||||
| chr9:136906798 | C | T | 228 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(225): Show |
229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.367-1272C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136906798 | |||||||
| chr9:136906810 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01496.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.367-1260G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136906810 | |||||||
| chr9:136906903 | C | T | 1 | a0004c0012t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.367-1167C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136906903 | |||||||
| chr9:136906968 | C | T | 2 | a0001c0001t0010g0296 a0001c0001t0010g0297 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.367-1102C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136906968 | |||||||
| chr9:136907029 | G | A | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.367-1041G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907029 | |||||||
| chr9:136907170 | G | C | 1 | a0001c0001t0002g0055 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.367-900G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907170 | |||||||
| chr9:136907278 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.367-792C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907278 | |||||||
| chr9:136907315 | C | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0107 |
2 | HG01346.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.367-755C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907315 | |||||||
| chr9:136907331 | G | C | 2 | a0001c0001t0004g0037 a0001c0001t0004g0038 |
2 | HG02080.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.367-739G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907331 | |||||||
| chr9:136907404 | C | G | 1 | a0001c0001t0002g0048 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.367-666C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907404 | |||||||
| chr9:136907431 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.367-639C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907431 | |||||||
| chr9:136907471 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.367-599C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907471 | |||||||
| chr9:136907480 | T | C | 228 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(225): Show |
229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.367-590T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907480 | |||||||
| chr9:136907665 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.367-405C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907665 | |||||||
| chr9:136907666 | G | A | 1 | a0004c0012t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.367-404G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907666 | |||||||
| chr9:136907693 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.367-377G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907693 | |||||||
| chr9:136907745 | G | A | 7 | a0001c0001t0001g0165 a0001c0001t0001g0257 a0001c0001t0001g0263 others(4): Show |
8 | HG02155.hp2 HG02886.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.367-325G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907745 | |||||||
| chr9:136907787 | C | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.367-283C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907787 | |||||||
| chr9:136907820 | G | A | 1 | a0001c0001t0002g0293 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.367-250G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907820 | |||||||
| chr9:136907939 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.367-131C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907939 | |||||||
| chr9:136907982 | G | T | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.367-88G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136907982 | |||||||
| chr9:136908034 | G | C | 2 | a0001c0001t0003g0135 a0001c0001t0003g0136 |
2 | NA18979.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.367-36G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136908034 | |||||||
| chr9:136908062 | G | A | 1 | a0001c0001t0005g0091 | 1 | HG03710.hp1 | splice_region_variant&intron_variant | LOW | c.367-8G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 4/10 | chr9 | 136908062 | |||||||
| chr9:136908279 | T | A | 1 | a0001c0001t0005g0058 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.528+48T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136908279 | |||||||
| chr9:136908365 | C | G | 1 | a0001c0001t0002g0062 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.528+134C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136908365 | |||||||
| chr9:136908445 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.528+214G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136908445 | |||||||
| chr9:136908497 | C | T | 5 | a0001c0001t0003g0108 a0001c0001t0003g0111 a0001c0001t0003g0112 others(2): Show |
5 | HG00140.hp1 HG00733.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+266C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136908497 | |||||||
| chr9:136908594 | C | T | 1 | a0001c0001t0002g0013 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.528+363C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136908594 | |||||||
| chr9:136908755 | A | G | 2 | a0001c0001t0002g0012 a0001c0001t0002g0289 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.528+524A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136908755 | |||||||
| chr9:136908818 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.528+587C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136908818 | |||||||
| chr9:136908845 | A | G | 3 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0013t0007g0295 |
4 | HG02886.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+614A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136908845 | |||||||
| chr9:136908857 | G | A | 2 | a0001c0001t0002g0063 a0001c0001t0002g0064 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.528+626G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136908857 | |||||||
| chr9:136908871 | G | GA | 208 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(205): Show |
209 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.528+660dupA | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 136908871 | ||||||
| chr9:136908871 | G | GAA | 27 | a0001c0001t0001g0104 a0001c0001t0001g0145 a0001c0001t0001g0146 others(24): Show |
27 | HG00438.hp1 HG00438.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.528+659_528+660dup others(2): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 136908871 | ||||||
| chr9:136908906 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.528+675C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136908906 | |||||||
| chr9:136909024 | G | C | 228 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(225): Show |
229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.528+793G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909024 | |||||||
| chr9:136909037 | CA | C | 19 | a0001c0001t0002g0003 a0001c0001t0002g0048 a0001c0001t0002g0049 others(16): Show |
21 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.528+820delA | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 136909037 | ||||||
| chr9:136909037 | CAA | C | 10 | a0001c0001t0001g0165 a0001c0001t0001g0257 a0001c0001t0001g0261 others(7): Show |
12 | HG01515.hp1 HG01517.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.528+819_528+820del others(2): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 136909037 | ||||||
| chr9:136909037 | CAAA | C | 221 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(218): Show |
221 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.528+818_528+820del others(3): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 136909037 | ||||||
| chr9:136909066 | A | T | 6 | a0001c0001t0002g0003 a0001c0001t0002g0048 a0001c0001t0002g0049 others(3): Show |
7 | HG00639.hp2 HG01081.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.528+835A>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909066 | |||||||
| chr9:136909162 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.529-758C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909162 | |||||||
| chr9:136909166 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.529-754A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909166 | |||||||
| chr9:136909181 | T | C | 231 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(228): Show |
233 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.529-739T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909181 | |||||||
| chr9:136909234 | A | ATGCATTT others(23): Show |
231 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(228): Show |
233 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.529-685_529-684ins others(30): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 136909234 | ||||||
| chr9:136909390 | G | A | 3 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0013t0007g0295 |
4 | HG02886.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-530G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909390 | |||||||
| chr9:136909506 | G | A | 223 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(220): Show |
224 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.529-414G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909506 | |||||||
| chr9:136909581 | C | G | 1 | a0001c0001t0001g0240 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.529-339C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909581 | |||||||
| chr9:136909590 | C | G | 1 | a0004c0012t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.529-330C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909590 | |||||||
| chr9:136909667 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.529-253A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909667 | |||||||
| chr9:136909780 | A | G | 2 | a0001c0001t0002g0012 a0001c0001t0002g0289 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.529-140A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909780 | |||||||
| chr9:136909811 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.529-109C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909811 | |||||||
| chr9:136909822 | G | A | 225 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(222): Show |
226 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.529-98G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909822 | |||||||
| chr9:136909835 | T | C | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.529-85T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909835 | |||||||
| chr9:136909869 | C | T | 2 | a0001c0001t0001g0253 a0001c0001t0003g0114 |
2 | HG01433.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.529-51C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909869 | |||||||
| chr9:136909870 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.529-50G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909870 | |||||||
| chr9:136909872 | G | A | 2 | a0001c0001t0002g0012 a0001c0001t0002g0289 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.529-48G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909872 | |||||||
| chr9:136909894 | C | T | 225 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(222): Show |
226 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.529-26C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 5/10 | chr9 | 136909894 | |||||||
| chr9:136910024 | G | A | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.603+30G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136910024 | |||||||
| chr9:136910059 | C | T | 3 | a0001c0001t0004g0130 a0001c0001t0004g0131 a0001c0001t0004g0132 |
3 | HG02818.hp1 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.603+65C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136910059 | |||||||
| chr9:136910176 | G | A | 1 | a0001c0001t0003g0122 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.603+182G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136910176 | |||||||
| chr9:136910227 | T | C | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.603+233T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136910227 | |||||||
| chr9:136910264 | C | T | 1 | a0001c0001t0013g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.603+270C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136910264 | |||||||
| chr9:136910319 | T | C | 1 | a0001c0001t0002g0013 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.603+325T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136910319 | |||||||
| chr9:136910437 | T | C | 1 | a0001c0001t0002g0289 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.603+443T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136910437 | |||||||
| chr9:136910649 | A | G | 1 | a0001c0001t0003g0238 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.603+655A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136910649 | |||||||
| chr9:136910692 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.603+698A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136910692 | |||||||
| chr9:136910716 | T | C | 233 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(230): Show |
235 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.603+722T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136910716 | |||||||
| chr9:136910999 | G | A | 1 | a0001c0002t0003g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.603+1005G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136910999 | |||||||
| chr9:136911077 | G | C | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.603+1083G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136911077 | |||||||
| chr9:136911098 | G | A | 1 | a0001c0001t0004g0033 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.603+1104G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136911098 | |||||||
| chr9:136911136 | A | T | 1 | a0001c0001t0003g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.603+1142A>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136911136 | |||||||
| chr9:136911185 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03490.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.603+1191T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136911185 | |||||||
| chr9:136911264 | CTTT | C | 211 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(208): Show |
212 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.603+1288_603+1290d others(5): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136911264 | ||||||
| chr9:136911264 | CTTTT | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0104 a0001c0001t0001g0169 others(7): Show |
10 | HG02523.hp2 HG03491.hp1 HG06807.hp1 others(7): Show |
intron_variant | MODIFIER | c.603+1287_603+1290d others(6): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136911264 | ||||||
| chr9:136911320 | A | G | 1 | a0004c0012t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.603+1326A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136911320 | |||||||
| chr9:136911513 | C | T | 3 | a0001c0001t0001g0181 a0001c0006t0001g0236 a0001c0006t0001g0279 |
3 | NA18975.hp1 NA18979.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.603+1519C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136911513 | |||||||
| chr9:136911683 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.603+1689A>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136911683 | |||||||
| chr9:136911751 | C | T | 3 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0013t0007g0295 |
4 | HG02886.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.603+1757C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136911751 | |||||||
| chr9:136911846 | C | CTTTTT | 22 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0148 others(19): Show |
23 | HG01069.hp1 HG01243.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.603+1869_603+1873d others(7): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136911846 | ||||||
| chr9:136911846 | C | CTTTTTT | 61 | a0001c0001t0001g0010 a0001c0001t0001g0104 a0001c0001t0001g0142 others(58): Show |
62 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.603+1868_603+1873d others(8): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136911846 | ||||||
| chr9:136911846 | C | CTTTTTTT | 102 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0042 others(99): Show |
102 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.603+1867_603+1873d others(9): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136911846 | ||||||
| chr9:136911846 | C | CTTTTTTT others(1): Show |
28 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0106 others(25): Show |
28 | HG00642.hp2 HG00733.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.603+1866_603+1873d others(10): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136911846 | ||||||
| chr9:136911846 | C | CTTTTTTT others(2): Show |
13 | a0001c0001t0001g0019 a0001c0001t0001g0193 a0001c0001t0001g0203 others(10): Show |
13 | HG01168.hp1 HG01255.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.603+1865_603+1873d others(11): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136911846 | ||||||
| chr9:136911846 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0018 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.603+1864_603+1873d others(12): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136911846 | ||||||
| chr9:136911846 | C | T | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.603+1852C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136911846 | |||||||
| chr9:136911868 | G | T | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.603+1874G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136911868 | |||||||
| chr9:136911975 | G | A | 2 | a0001c0001t0002g0012 a0001c0001t0002g0289 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.603+1981G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136911975 | |||||||
| chr9:136911980 | G | C | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.603+1986G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136911980 | |||||||
| chr9:136912081 | C | T | 25 | a0001c0001t0001g0042 a0001c0001t0001g0167 a0001c0001t0001g0171 others(22): Show |
25 | HG01074.hp1 HG01099.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.603+2087C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136912081 | |||||||
| chr9:136912131 | C | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.603+2137C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136912131 | |||||||
| chr9:136912150 | CCCTTTTT others(8): Show |
C | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.603+2157_603+2171d others(17): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136912150 | |||||||
| chr9:136912152 | C | CT | 18 | a0001c0001t0002g0006 a0001c0001t0002g0059 a0001c0001t0002g0068 others(15): Show |
19 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.603+2185dupT | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136912152 | ||||||
| chr9:136912152 | C | CTTTTTTT others(3): Show |
1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.603+2176_603+2185d others(12): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136912152 | ||||||
| chr9:136912152 | C | CTTTTTTT others(44): Show |
1 | a0001c0001t0002g0012 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.603+2185_603+2186i others(53): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136912152 | ||||||
| chr9:136912152 | CTTTTTT | C | 19 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0177 others(16): Show |
19 | HG00408.hp1 HG00558.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.603+2180_603+2185d others(8): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136912152 | ||||||
| chr9:136912152 | CTTTTTTT | C | 141 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 others(138): Show |
142 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.603+2179_603+2185d others(9): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136912152 | ||||||
| chr9:136912152 | CTTTTTTT others(1): Show |
C | 61 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0043 others(58): Show |
61 | HG00140.hp1 HG00438.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.603+2178_603+2185d others(10): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136912152 | ||||||
| chr9:136912154 | T | C | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.603+2160T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136912154 | |||||||
| chr9:136912167 | T | C | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.603+2173T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136912167 | |||||||
| chr9:136912282 | C | T | 1 | a0001c0001t0014g0092 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.603+2288C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136912282 | |||||||
| chr9:136912559 | A | G | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.603+2565A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136912559 | |||||||
| chr9:136912751 | TG | T | 228 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(225): Show |
229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.603+2758delG | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136912751 | |||||||
| chr9:136912791 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.603+2797C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136912791 | |||||||
| chr9:136912793 | C | T | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.603+2799C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136912793 | |||||||
| chr9:136912826 | G | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.603+2832G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136912826 | |||||||
| chr9:136912939 | C | G | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.603+2945C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136912939 | |||||||
| chr9:136913097 | C | T | 1 | a0001c0008t0007g0294 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.603+3103C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136913097 | |||||||
| chr9:136913171 | A | C | 223 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(220): Show |
224 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.603+3177A>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136913171 | |||||||
| chr9:136913202 | T | C | 3 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0013t0007g0295 |
4 | HG02886.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.603+3208T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136913202 | |||||||
| chr9:136913262 | G | A | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.603+3268G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136913262 | |||||||
| chr9:136913295 | A | ATTT | 33 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0100 others(30): Show |
34 | HG00140.hp1 HG01070.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.604-3226_604-3224d others(5): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136913295 | ||||||
| chr9:136913295 | A | ATTTT | 161 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0034 others(158): Show |
162 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.604-3227_604-3224d others(6): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136913295 | ||||||
| chr9:136913295 | A | ATTTTT | 26 | a0001c0001t0001g0020 a0001c0001t0001g0107 a0001c0001t0001g0143 others(23): Show |
26 | HG01074.hp2 HG01106.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.604-3228_604-3224d others(7): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136913295 | ||||||
| chr9:136913295 | A | ATTTTTT | 8 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0153 others(5): Show |
8 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.604-3229_604-3224d others(8): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136913295 | ||||||
| chr9:136913295 | A | ATTTTTTT others(4): Show |
1 | a0001c0013t0007g0295 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.604-3234_604-3224d others(13): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136913295 | ||||||
| chr9:136913295 | A | ATTTTTTT others(5): Show |
1 | a0001c0008t0007g0294 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.604-3235_604-3224d others(14): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136913295 | ||||||
| chr9:136913295 | AT | A | 5 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0065 others(2): Show |
6 | HG01256.hp1 HG01516.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.604-3224delT | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 136913295 | ||||||
| chr9:136913380 | C | T | 1 | a0001c0001t0012g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.604-3161C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136913380 | |||||||
| chr9:136913417 | C | T | 1 | a0001c0001t0005g0090 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.604-3124C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136913417 | |||||||
| chr9:136913724 | C | A | 2 | a0001c0006t0001g0236 a0001c0006t0001g0279 |
2 | NA18975.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.604-2817C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136913724 | |||||||
| chr9:136913816 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.604-2725A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136913816 | |||||||
| chr9:136913845 | C | T | 3 | a0001c0001t0010g0296 a0001c0001t0010g0297 a0001c0001t0013g0134 |
3 | HG02559.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.604-2696C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136913845 | |||||||
| chr9:136913924 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.604-2617G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136913924 | |||||||
| chr9:136914008 | C | T | 1 | a0001c0002t0003g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.604-2533C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914008 | |||||||
| chr9:136914086 | C | T | 3 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0013t0007g0295 |
4 | HG02886.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.604-2455C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914086 | |||||||
| chr9:136914112 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.604-2429C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914112 | |||||||
| chr9:136914167 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.604-2374A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914167 | |||||||
| chr9:136914187 | T | C | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.604-2354T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914187 | |||||||
| chr9:136914206 | C | A | 1 | a0001c0001t0001g0163 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.604-2335C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914206 | |||||||
| chr9:136914229 | C | T | 1 | a0001c0008t0007g0294 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.604-2312C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914229 | |||||||
| chr9:136914617 | A | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.604-1924A>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914617 | |||||||
| chr9:136914670 | G | T | 1 | a0001c0001t0003g0136 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.604-1871G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914670 | |||||||
| chr9:136914796 | C | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.604-1745C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914796 | |||||||
| chr9:136914805 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.604-1736G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914805 | |||||||
| chr9:136914842 | G | A | 1 | a0001c0001t0004g0028 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.604-1699G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914842 | |||||||
| chr9:136914854 | C | A | 6 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(3): Show |
6 | HG02735.hp2 HG03017.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.604-1687C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914854 | |||||||
| chr9:136914901 | C | T | 1 | a0001c0001t0004g0031 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.604-1640C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914901 | |||||||
| chr9:136914943 | G | A | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.604-1598G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136914943 | |||||||
| chr9:136915036 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.604-1505G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915036 | |||||||
| chr9:136915120 | G | A | 9 | a0001c0001t0003g0122 a0001c0001t0008g0011 a0001c0002t0003g0126 others(6): Show |
10 | HG02486.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.604-1421G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915120 | |||||||
| chr9:136915175 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.604-1366G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915175 | |||||||
| chr9:136915235 | C | T | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.604-1306C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915235 | |||||||
| chr9:136915256 | C | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.604-1285C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915256 | |||||||
| chr9:136915257 | G | A | 1 | a0001c0001t0013g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.604-1284G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915257 | |||||||
| chr9:136915283 | C | T | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.604-1258C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915283 | |||||||
| chr9:136915429 | G | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.604-1112G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915429 | |||||||
| chr9:136915662 | T | A | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.604-879T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915662 | |||||||
| chr9:136915684 | C | T | 1 | a0001c0001t0013g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.604-857C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915684 | |||||||
| chr9:136915692 | C | G | 1 | a0001c0001t0001g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.604-849C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915692 | |||||||
| chr9:136915816 | T | C | 1 | a0001c0001t0015g0188 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.604-725T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915816 | |||||||
| chr9:136915847 | A | G | 1 | a0001c0013t0007g0295 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.604-694A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915847 | |||||||
| chr9:136915942 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0289 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.604-599C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915942 | |||||||
| chr9:136915981 | A | G | 229 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(226): Show |
230 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.604-560A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915981 | |||||||
| chr9:136915985 | T | C | 3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0272 |
3 | HG01081.hp2 HG01255.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.604-556T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136915985 | |||||||
| chr9:136916040 | C | T | 1 | a0001c0001t0006g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.604-501C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136916040 | |||||||
| chr9:136916143 | C | T | 229 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(226): Show |
230 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.604-398C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136916143 | |||||||
| chr9:136916200 | G | A | 228 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(225): Show |
229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.604-341G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136916200 | |||||||
| chr9:136916227 | CAGCACCG others(3): Show |
C | 6 | a0001c0001t0001g0035 a0001c0001t0001g0165 a0001c0001t0001g0257 others(3): Show |
6 | HG02155.hp2 NA18939.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.604-313_604-304del others(10): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136916227 | |||||||
| chr9:136916272 | A | C | 1 | a0001c0001t0001g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.604-269A>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136916272 | |||||||
| chr9:136916318 | C | G | 1 | a0001c0001t0003g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.604-223C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136916318 | |||||||
| chr9:136916437 | G | A | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.604-104G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136916437 | |||||||
| chr9:136916450 | T | G | 1 | a0001c0001t0001g0281 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.604-91T>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 6/10 | chr9 | 136916450 | |||||||
| chr9:136916670 | ACTGCCTC others(113): Show |
A | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.678+59_678+178del | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136916670 | ||||||
| chr9:136916923 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.678+308G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136916923 | |||||||
| chr9:136917030 | G | A | 225 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(222): Show |
226 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.678+415G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136917030 | |||||||
| chr9:136917133 | A | G | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.678+518A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136917133 | |||||||
| chr9:136917177 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.678+562G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136917177 | |||||||
| chr9:136917178 | A | C | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.678+563A>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136917178 | |||||||
| chr9:136917193 | C | T | 1 | a0001c0001t0005g0058 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.678+578C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136917193 | |||||||
| chr9:136917309 | G | A | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.678+694G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136917309 | |||||||
| chr9:136917437 | C | G | 1 | a0001c0001t0006g0258 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.678+822C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136917437 | |||||||
| chr9:136917493 | G | A | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.678+878G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136917493 | |||||||
| chr9:136917539 | T | C | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.678+924T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136917539 | |||||||
| chr9:136917563 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.678+948T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136917563 | |||||||
| chr9:136917718 | T | G | 1 | a0001c0001t0006g0258 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.678+1103T>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136917718 | |||||||
| chr9:136917849 | C | G | 1 | a0001c0001t0002g0008 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.678+1234C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136917849 | |||||||
| chr9:136917902 | C | T | 3 | a0001c0001t0010g0296 a0001c0001t0010g0297 a0001c0001t0013g0134 |
3 | HG02559.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.678+1287C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136917902 | |||||||
| chr9:136918005 | C | T | 16 | a0001c0001t0003g0009 a0001c0001t0003g0108 a0001c0001t0003g0110 others(13): Show |
17 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.678+1390C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918005 | |||||||
| chr9:136918145 | T | G | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.678+1530T>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918145 | |||||||
| chr9:136918227 | T | A | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.678+1612T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918227 | |||||||
| chr9:136918227 | T | TTA | 20 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0022 others(17): Show |
22 | HG00609.hp1 HG00738.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.678+1642_678+1643d others(4): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136918227 | ||||||
| chr9:136918227 | T | TTATA | 5 | a0001c0001t0002g0002 a0001c0001t0002g0071 a0001c0001t0002g0073 others(2): Show |
5 | HG00642.hp1 HG00735.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.678+1640_678+1643d others(6): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136918227 | ||||||
| chr9:136918227 | T | TTATATA | 4 | a0001c0001t0002g0087 a0001c0001t0002g0094 a0001c0001t0010g0296 others(1): Show |
4 | HG00735.hp2 HG02071.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.678+1638_678+1643d others(8): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136918227 | ||||||
| chr9:136918227 | T | TTATATAT others(3): Show |
1 | a0001c0001t0005g0004 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.678+1634_678+1643d others(12): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136918227 | ||||||
| chr9:136918227 | T | TTATATAT others(5): Show |
1 | a0001c0001t0005g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.678+1632_678+1643d others(14): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136918227 | ||||||
| chr9:136918227 | T | TTATATAT others(9): Show |
1 | a0001c0001t0013g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.678+1628_678+1643d others(18): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136918227 | ||||||
| chr9:136918227 | TTA | T | 13 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0051 others(10): Show |
15 | HG00140.hp2 HG00741.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.678+1642_678+1643d others(4): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136918227 | ||||||
| chr9:136918248 | TATATATA others(11): Show |
T | 2 | a0001c0001t0001g0257 a0001c0011t0004g0089 |
2 | HG02258.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.678+1634_678+1651d others(20): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918248 | |||||||
| chr9:136918250 | TATATATA others(9): Show |
T | 7 | a0001c0001t0003g0108 a0001c0001t0003g0110 a0001c0001t0003g0111 others(4): Show |
7 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.678+1636_678+1651d others(18): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918250 | |||||||
| chr9:136918251 | A | T | 2 | a0001c0001t0008g0011 a0001c0013t0007g0295 |
3 | HG02886.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.678+1636A>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918251 | |||||||
| chr9:136918252 | T | TATATATA others(5): Show |
1 | a0001c0001t0005g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.678+1643_678+1644i others(14): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136918252 | ||||||
| chr9:136918252 | TATATATT others(7): Show |
T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0212 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.678+1638_678+1651d others(16): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918252 | |||||||
| chr9:136918254 | TATATTTA others(5): Show |
T | 138 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0041 others(135): Show |
138 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.678+1640_678+1651d others(14): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918254 | |||||||
| chr9:136918255 | A | T | 3 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0013t0007g0295 |
4 | HG02886.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+1640A>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918255 | |||||||
| chr9:136918256 | TATTTATT others(3): Show |
T | 43 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0035 others(40): Show |
44 | HG00408.hp1 HG00438.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.678+1642_678+1651d others(12): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918256 | |||||||
| chr9:136918257 | ATTTATT | A | 9 | a0001c0001t0001g0152 a0001c0001t0001g0203 a0001c0001t0001g0232 others(6): Show |
9 | HG01168.hp1 HG01255.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.678+1644_678+1649d others(8): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136918257 | ||||||
| chr9:136918258 | TTTATTTA others(1): Show |
T | 14 | a0001c0001t0001g0021 a0001c0001t0001g0166 a0001c0001t0001g0204 others(11): Show |
14 | HG00738.hp1 HG02055.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.678+1647_678+1654d others(10): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136918258 | ||||||
| chr9:136918259 | T | A | 8 | a0001c0001t0001g0202 a0001c0001t0001g0223 a0001c0001t0001g0225 others(5): Show |
8 | HG00733.hp2 HG02559.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.678+1644T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918259 | |||||||
| chr9:136918262 | TTTAA | T | 6 | a0001c0001t0001g0202 a0001c0001t0001g0223 a0001c0001t0001g0225 others(3): Show |
6 | HG00733.hp2 HG02735.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.678+1658_678+1661d others(6): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136918262 | ||||||
| chr9:136918263 | T | A | 2 | a0001c0001t0010g0296 a0001c0001t0013g0134 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.678+1648T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918263 | |||||||
| chr9:136918266 | A | T | 14 | a0001c0001t0001g0152 a0001c0001t0001g0203 a0001c0001t0001g0232 others(11): Show |
15 | HG01168.hp1 HG01255.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.678+1651A>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918266 | |||||||
| chr9:136918273 | A | T | 2 | a0001c0001t0008g0011 a0001c0011t0004g0089 |
3 | HG02258.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.678+1658A>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918273 | |||||||
| chr9:136918362 | C | T | 1 | a0001c0001t0008g0011 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.678+1747C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918362 | |||||||
| chr9:136918450 | C | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.679-1784C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918450 | |||||||
| chr9:136918679 | G | C | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.679-1555G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918679 | |||||||
| chr9:136918733 | G | A | 3 | a0001c0001t0005g0004 a0001c0001t0005g0053 a0001c0001t0005g0054 |
4 | HG02886.hp1 HG03098.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.679-1501G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136918733 | |||||||
| chr9:136919042 | A | ATATATAT others(9): Show |
3 | a0001c0001t0010g0296 a0001c0001t0010g0297 a0001c0001t0013g0134 |
3 | HG02559.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.679-1189_679-1188i others(18): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136919042 | ||||||
| chr9:136919042 | A | ATATTTAT others(1): Show |
6 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0184 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.679-1166_679-1159d others(10): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136919042 | ||||||
| chr9:136919042 | A | ATATTTAT others(5): Show |
52 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0042 others(49): Show |
52 | HG00438.hp1 HG00738.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.679-1170_679-1159d others(14): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136919042 | ||||||
| chr9:136919042 | A | ATATTTAT others(9): Show |
142 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0034 others(139): Show |
142 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.679-1174_679-1159d others(18): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136919042 | ||||||
| chr9:136919042 | A | ATATTTAT others(13): Show |
24 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0116 others(21): Show |
24 | HG00642.hp2 HG01255.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.679-1178_679-1159d others(22): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136919042 | ||||||
| chr9:136919042 | A | ATATTTAT others(17): Show |
1 | a0001c0001t0003g0009 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.679-1182_679-1159d others(26): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136919042 | ||||||
| chr9:136919090 | C | T | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.679-1144C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136919090 | |||||||
| chr9:136919091 | G | A | 1 | a0001c0001t0004g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.679-1143G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136919091 | |||||||
| chr9:136919242 | C | G | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.679-992C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136919242 | |||||||
| chr9:136919274 | T | A | 1 | a0001c0001t0004g0190 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.679-960T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136919274 | |||||||
| chr9:136919280 | G | A | 1 | a0001c0001t0004g0190 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.679-954G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136919280 | |||||||
| chr9:136919295 | C | CT | 17 | a0001c0001t0001g0021 a0001c0001t0001g0198 a0001c0001t0001g0204 others(14): Show |
18 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.679-919dupT | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136919295 | ||||||
| chr9:136919295 | C | CTT | 182 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0034 others(179): Show |
184 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.679-920_679-919dup others(2): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136919295 | ||||||
| chr9:136919295 | C | CTTT | 35 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0100 others(32): Show |
35 | HG01074.hp1 HG01168.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.679-921_679-919dup others(3): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136919295 | ||||||
| chr9:136919355 | G | A | 229 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(226): Show |
230 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.679-879G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136919355 | |||||||
| chr9:136919360 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.679-874G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136919360 | |||||||
| chr9:136919403 | G | A | 232 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(229): Show |
234 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.679-831G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136919403 | |||||||
| chr9:136919529 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.679-705A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136919529 | |||||||
| chr9:136919680 | T | TTCTTCCC others(9): Show |
231 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(228): Show |
233 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.679-544_679-543ins others(16): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136919680 | ||||||
| chr9:136919680 | T | TTCTTCCC others(9): Show |
1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.679-545_679-544ins others(16): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 136919680 | ||||||
| chr9:136920105 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.679-129C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136920105 | |||||||
| chr9:136920160 | C | T | 2 | a0001c0001t0002g0098 a0001c0001t0002g0099 |
2 | HG00323.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.679-74C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136920160 | |||||||
| chr9:136920186 | A | G | 2 | a0001c0005t0001g0186 a0001c0005t0001g0187 |
2 | HG01106.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.679-48A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136920186 | |||||||
| chr9:136920204 | G | T | 2 | a0001c0001t0003g0290 a0001c0001t0003g0291 |
2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.679-30G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 7/10 | chr9 | 136920204 | |||||||
| chr9:136920601 | G | A | 176 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(173): Show |
176 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.960+86G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 8/10 | chr9 | 136920601 | |||||||
| chr9:136920707 | G | A | 7 | a0001c0001t0005g0004 a0001c0001t0005g0053 a0001c0001t0005g0054 others(4): Show |
8 | HG00735.hp2 HG01516.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.960+192G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 8/10 | chr9 | 136920707 | |||||||
| chr9:136920964 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.961-74C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 8/10 | chr9 | 136920964 | |||||||
| chr9:136920965 | G | A | 7 | a0001c0001t0005g0004 a0001c0001t0005g0053 a0001c0001t0005g0054 others(4): Show |
8 | HG00735.hp2 HG01516.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.961-73G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 8/10 | chr9 | 136920965 | |||||||
| chr9:136920968 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.961-70G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 8/10 | chr9 | 136920968 | |||||||
| chr9:136921235 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1138+20A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136921235 | |||||||
| chr9:136921437 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1138+222C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136921437 | |||||||
| chr9:136921475 | C | A | 1 | a0001c0001t0010g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1138+260C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136921475 | |||||||
| chr9:136921508 | A | G | 250 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(247): Show |
256 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.1138+293A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136921508 | |||||||
| chr9:136921511 | C | T | 7 | a0001c0001t0005g0004 a0001c0001t0005g0053 a0001c0001t0005g0054 others(4): Show |
8 | HG00735.hp2 HG01516.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1138+296C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136921511 | |||||||
| chr9:136921572 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1138+357G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136921572 | |||||||
| chr9:136921696 | C | CT | 104 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0021 others(101): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1138+493dupT | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136921696 | ||||||
| chr9:136921708 | T | TA | 7 | a0001c0001t0005g0004 a0001c0001t0005g0053 a0001c0001t0005g0054 others(4): Show |
8 | HG00735.hp2 HG01516.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1138+496dupA | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136921708 | ||||||
| chr9:136921744 | G | A | 2 | a0001c0001t0003g0123 a0001c0001t0003g0124 |
2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1138+529G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136921744 | |||||||
| chr9:136921782 | G | A | 2 | a0001c0001t0010g0296 a0001c0001t0010g0297 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1138+567G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136921782 | |||||||
| chr9:136921867 | C | T | 4 | a0001c0001t0008g0011 a0001c0008t0007g0294 a0001c0011t0004g0089 others(1): Show |
5 | HG02258.hp2 HG02886.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138+652C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136921867 | |||||||
| chr9:136922044 | T | C | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1138+829T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922044 | |||||||
| chr9:136922059 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1138+844T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922059 | |||||||
| chr9:136922133 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1138+918C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922133 | |||||||
| chr9:136922199 | G | T | 7 | a0001c0001t0005g0004 a0001c0001t0005g0053 a0001c0001t0005g0054 others(4): Show |
8 | HG00735.hp2 HG01516.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1138+984G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922199 | |||||||
| chr9:136922281 | A | G | 1 | a0001c0002t0003g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1138+1066A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922281 | |||||||
| chr9:136922420 | A | AC | 12 | a0001c0001t0001g0019 a0001c0001t0001g0203 a0001c0001t0001g0232 others(9): Show |
12 | HG01168.hp1 HG01255.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1138+1206dupC | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136922420 | ||||||
| chr9:136922428 | T | C | 99 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0021 others(96): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.1138+1213T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922428 | |||||||
| chr9:136922445 | A | G | 1 | a0001c0001t0014g0092 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1138+1230A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922445 | |||||||
| chr9:136922485 | T | C | 1 | a0001c0001t0002g0093 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1138+1270T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922485 | |||||||
| chr9:136922493 | G | GGCAAGAG others(5): Show |
1 | a0001c0001t0001g0148 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1138+1280_1138+129 others(16): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136922493 | ||||||
| chr9:136922558 | G | A | 134 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0042 others(131): Show |
138 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1139-1294G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922558 | |||||||
| chr9:136922586 | AATGGGCC others(32): Show |
A | 1 | a0001c0001t0002g0075 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1139-1212_1139-117 others(43): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136922586 | ||||||
| chr9:136922642 | G | A | 3 | a0001c0001t0004g0130 a0001c0001t0004g0131 a0001c0001t0004g0132 |
3 | HG02818.hp1 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1139-1210G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922642 | |||||||
| chr9:136922677 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1139-1175G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922677 | |||||||
| chr9:136922690 | A | G | 134 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0042 others(131): Show |
138 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1139-1162A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922690 | |||||||
| chr9:136922717 | G | C | 2 | a0001c0008t0007g0294 a0001c0013t0007g0295 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1139-1135G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922717 | |||||||
| chr9:136922807 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1139-1045C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922807 | |||||||
| chr9:136922840 | G | A | 2 | a0002c0004t0001g0174 a0002c0004t0001g0219 |
2 | HG01123.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1139-1012G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922840 | |||||||
| chr9:136922879 | A | C | 249 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(246): Show |
255 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1139-973A>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922879 | |||||||
| chr9:136922901 | G | A | 134 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0042 others(131): Show |
138 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1139-951G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922901 | |||||||
| chr9:136922979 | C | T | 1 | a0001c0008t0007g0294 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1139-873C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922979 | |||||||
| chr9:136922984 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1139-868G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922984 | |||||||
| chr9:136922988 | G | C | 1 | a0001c0001t0001g0237 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1139-864G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136922988 | |||||||
| chr9:136923075 | G | A | 238 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(235): Show |
242 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.1139-777G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136923075 | |||||||
| chr9:136923093 | C | A | 2 | a0001c0001t0010g0296 a0001c0001t0010g0297 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1139-759C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136923093 | |||||||
| chr9:136923121 | G | C | 237 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(234): Show |
241 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1139-731G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136923121 | |||||||
| chr9:136923259 | C | T | 2 | a0001c0001t0008g0011 a0001c0001t0013g0134 |
3 | HG02970.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1139-593C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136923259 | |||||||
| chr9:136923439 | C | T | 4 | a0001c0001t0008g0011 a0001c0001t0013g0134 a0001c0008t0007g0294 others(1): Show |
5 | HG02886.hp2 HG02970.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1139-413C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136923439 | |||||||
| chr9:136923594 | G | C | 1 | a0001c0001t0001g0246 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1139-258G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136923594 | |||||||
| chr9:136923610 | C | CA | 16 | a0001c0001t0002g0046 a0001c0001t0002g0051 a0001c0001t0002g0055 others(13): Show |
17 | HG01167.hp2 HG01928.hp1 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.1139-217dupA | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136923610 | ||||||
| chr9:136923610 | CA | C | 47 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0101 others(44): Show |
48 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1139-217delA | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136923610 | ||||||
| chr9:136923610 | CAA | C | 175 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(172): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.1139-218_1139-217d others(4): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136923610 | ||||||
| chr9:136923610 | CAAA | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0044 a0001c0001t0001g0137 others(10): Show |
13 | HG01257.hp1 HG02056.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1139-219_1139-217d others(5): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136923610 | ||||||
| chr9:136923717 | CTT | C | 226 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(223): Show |
227 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1139-132_1139-131d others(4): Show |
TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136923717 | ||||||
| chr9:136923718 | T | A | 1 | a0001c0001t0003g0135 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1139-134T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136923718 | |||||||
| chr9:136923719 | T | C | 1 | a0001c0001t0003g0135 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1139-133T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136923719 | |||||||
| chr9:136923825 | C | T | 1 | a0001c0001t0003g0122 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1139-27C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136923825 | |||||||
| chr9:136923837 | C | T | 1 | a0001c0001t0003g0122 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1139-15C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 9/10 | chr9 | 136923837 | |||||||
| chr9:136924009 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1287+9G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924009 | |||||||
| chr9:136924105 | G | A | 4 | a0001c0001t0001g0145 a0001c0001t0001g0151 a0001c0001t0001g0155 others(1): Show |
4 | HG02630.hp1 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1287+105G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924105 | |||||||
| chr9:136924318 | G | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01496.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1287+318G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924318 | |||||||
| chr9:136924396 | C | CA | 130 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0042 others(127): Show |
131 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1287+404dupA | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 136924396 | ||||||
| chr9:136924514 | A | G | 1 | a0001c0010t0001g0288 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1287+514A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924514 | |||||||
| chr9:136924666 | A | G | 1 | a0004c0012t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1287+666A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924666 | |||||||
| chr9:136924686 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1287+686G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924686 | |||||||
| chr9:136924687 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+687A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924687 | |||||||
| chr9:136924689 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+689T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924689 | |||||||
| chr9:136924690 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+690G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924690 | |||||||
| chr9:136924691 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+691C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924691 | |||||||
| chr9:136924693 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+693G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924693 | |||||||
| chr9:136924696 | G | T | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+696G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924696 | |||||||
| chr9:136924697 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+697A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924697 | |||||||
| chr9:136924698 | A | G | 4 | a0001c0001t0001g0267 a0001c0001t0002g0012 a0001c0001t0002g0289 others(1): Show |
4 | HG01109.hp1 HG02273.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1287+698A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924698 | |||||||
| chr9:136924700 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+700G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924700 | |||||||
| chr9:136924704 | A | C | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+704A>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924704 | |||||||
| chr9:136924705 | C | A | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+705C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924705 | |||||||
| chr9:136924707 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+707G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924707 | |||||||
| chr9:136924711 | C | T | 1 | a0001c0001t0002g0046 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1287+711C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924711 | |||||||
| chr9:136924717 | C | A | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+717C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924717 | |||||||
| chr9:136924718 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+718C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924718 | |||||||
| chr9:136924720 | C | A | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+720C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924720 | |||||||
| chr9:136924723 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+723C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924723 | |||||||
| chr9:136924724 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+724G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924724 | |||||||
| chr9:136924726 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+726C>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924726 | |||||||
| chr9:136924727 | G | T | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+727G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924727 | |||||||
| chr9:136924729 | A | C | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+729A>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924729 | |||||||
| chr9:136924730 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+730G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924730 | |||||||
| chr9:136924731 | G | T | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1287+731G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924731 | |||||||
| chr9:136924779 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1287+779G>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924779 | |||||||
| chr9:136924835 | T | A | 1 | a0001c0001t0003g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1287+835T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924835 | |||||||
| chr9:136924863 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1288-820T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924863 | |||||||
| chr9:136924870 | C | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG01261.hp2 HG02257.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288-813C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924870 | |||||||
| chr9:136924876 | C | T | 1 | a0001c0001t0004g0024 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1288-807C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924876 | |||||||
| chr9:136924884 | A | G | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1288-799A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924884 | |||||||
| chr9:136924885 | T | C | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1288-798T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924885 | |||||||
| chr9:136924886 | G | C | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1288-797G>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924886 | |||||||
| chr9:136924888 | A | G | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1288-795A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924888 | |||||||
| chr9:136924892 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1288-791C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924892 | |||||||
| chr9:136924895 | C | T | 65 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0044 others(62): Show |
69 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1288-788C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924895 | |||||||
| chr9:136924927 | T | C | 3 | a0001c0001t0001g0116 a0001c0001t0003g0112 a0001c0013t0007g0295 |
3 | HG00642.hp2 HG01952.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1288-756T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924927 | |||||||
| chr9:136924936 | T | A | 3 | a0001c0001t0002g0075 a0001c0001t0004g0025 a0001c0001t0004g0031 |
3 | HG00438.hp1 NA18747.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1288-747T>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924936 | |||||||
| chr9:136924946 | C | T | 244 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(241): Show |
251 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.1288-737C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924946 | |||||||
| chr9:136924948 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1288-735A>G | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924948 | |||||||
| chr9:136924965 | C | T | 1 | a0001c0001t0003g0135 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1288-718C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924965 | |||||||
| chr9:136924972 | T | C | 43 | a0001c0001t0001g0042 a0001c0001t0001g0105 a0001c0001t0001g0141 others(40): Show |
43 | HG00438.hp1 HG01069.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1288-711T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924972 | |||||||
| chr9:136924980 | G | A | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1288-703G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924980 | |||||||
| chr9:136924981 | C | A | 1 | a0001c0011t0004g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1288-702C>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136924981 | |||||||
| chr9:136925017 | G | A | 1 | a0004c0012t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1288-666G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136925017 | |||||||
| chr9:136925026 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1288-657T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136925026 | |||||||
| chr9:136925028 | T | C | 1 | a0001c0013t0007g0295 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1288-655T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136925028 | |||||||
| chr9:136925032 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1288-651T>C | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136925032 | |||||||
| chr9:136925198 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1288-485G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136925198 | |||||||
| chr9:136925513 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1288-170G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136925513 | |||||||
| chr9:136925532 | C | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0034 others(81): Show |
86 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1288-151C>T | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136925532 | |||||||
| chr9:136925596 | G | A | 69 | a0001c0001t0001g0167 a0001c0001t0001g0257 a0001c0001t0001g0263 others(66): Show |
76 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1288-87G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136925596 | |||||||
| chr9:136925640 | G | A | 1 | a0004c0012t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1288-43G>A | TRAF2 | ENSG00000127191.18 | transcript | ENST00000247668.7 | protein_coding | 10/10 | chr9 | 136925640 |