Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7292 |
| ensemblid | ENSG00000117586.11 |
| hgncid | 11934 |
| symbol | TNFSF4 |
| name | TNF superfamily member 4 |
| refseq_nuc | NM_003326.5 |
| refseq_prot | NP_003317.1 |
| ensembl_nuc | ENST00000281834.4 |
| ensembl_prot | ENSP00000281834.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 173183731 |
| end | 173207331 |
| strand | - |
| ver | v1.2 |
| region | chr1:173183731-173207331 |
| region5000 | chr1:173178731-173212331 |
| regionname0 | TNFSF4_chr1_173183731_173207331 |
| regionname5000 | TNFSF4_chr1_173178731_173212331 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 549 | 287 | 85 | 64 | 94 | 16 | 26 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | ATGGA others(544): Show |
chr1 | 173178731 | 173212331 | ||
| a0001c0002 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | ATGGA others(544): Show |
chr1 | 173178731 | 173212331 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3492 | 146 | 16 | 35 | 63 | 12 | 18 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3487): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0002 | 0/0 | 3490 | 30 | 9 | 4 | 16 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3485): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0003 | 0/0 | 3490 | 21 | 3 | 8 | 3 | 3 | 4 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3485): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0004 | 0/0 | 3490 | 18 | 17 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3485): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0005 | 0/0 | 3491 | 12 | 12 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3486): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0006 | 0/0 | 3492 | 10 | 6 | 3 | 0 | 1 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3487): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0007 | 0/0 | 3492 | 7 | 5 | 2 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3487): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0008 | 0/0 | 3492 | 6 | 6 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3487): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0009 | 0/0 | 3490 | 5 | 0 | 5 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3485): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0010 | 0/0 | 3492 | 5 | 3 | 2 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3487): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0011 | 0/0 | 3490 | 5 | 4 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3485): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0012 | 0/0 | 3492 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3487): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0013 | 0/0 | 3491 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3486): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0014 | 0/0 | 3491 | 2 | 0 | 0 | 0 | 0 | 2 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3486): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0015 | 0/0 | 3490 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3485): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0016 | 0/0 | 3492 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3487): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0017 | 0/0 | 3492 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3487): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0018 | 0/0 | 3491 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3486): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0019 | 0/0 | 3490 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3485): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0020 | 0/0 | 3490 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3485): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0021 | 0/0 | 3492 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3487): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0022 | 0/0 | 3492 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3487): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0023 | 0/0 | 3493 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3488): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0024 | 0/0 | 3492 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3487): Show |
chr1 | 173178731 | 173212331 |
| a0001c0001t0025 | 0/0 | 3492 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3487): Show |
chr1 | 173178731 | 173212331 |
| a0001c0002t0004 | 0/0 | 3490 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | CAATC others(3485): Show |
chr1 | 173178731 | 173212331 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 39 | 10 | 5 | 16 | 0 | 7 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0002 | 0/0 | 24 | 0 | 5 | 12 | 5 | 2 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 5 | 4 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0008 | 0/0 | 6 | 1 | 3 | 0 | 1 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0003g0009 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0003g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0003g0024 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0004g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0004g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0004g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0005g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0005g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0006g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0006g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0007g0004 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0008g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0008g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0009g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0009g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0010g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0011g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0011g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0011g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0012g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0013g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0013g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0013g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0014g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0015g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0015g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0016g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0017g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0018g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0019g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0020g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0021g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0022g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0023g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0024g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0001t0025g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| a0001c0002t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | GBR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0061 | EUR | GBR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | FIN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00544 | hp1 | a0001 | c0001 | t0013 | g0099 | EAS | CHS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00597 | hp2 | a0001 | c0001 | t0013 | g0100 | EAS | CHS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | CHS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00738 | hp2 | a0001 | c0001 | t0011 | g0040 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01069 | hp2 | a0001 | c0001 | t0010 | g0027 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0032 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0033 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01192 | hp2 | a0001 | c0001 | t0009 | g0126 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0027 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01358 | hp2 | a0001 | c0001 | t0025 | g0058 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0015 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0024 | EUR | IBS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0024 | EUR | IBS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01884 | hp1 | a0001 | c0001 | t0018 | g0136 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01934 | hp2 | a0001 | c0001 | t0009 | g0015 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01943 | hp1 | a0001 | c0001 | t0009 | g0015 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0065 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01981 | hp1 | a0001 | c0001 | t0019 | g0042 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02004 | hp2 | a0001 | c0001 | t0023 | g0062 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02148 | hp2 | a0001 | c0001 | t0009 | g0015 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02258 | hp1 | a0001 | c0001 | t0010 | g0059 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0091 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0090 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0079 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0031 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0077 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02735 | hp1 | a0001 | c0001 | t0021 | g0063 | SAS | PJL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02965 | hp1 | a0001 | c0001 | t0011 | g0031 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0081 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0083 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0020 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0089 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0078 | AFR | MSL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0068 | AFR | MSL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0088 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0087 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03139 | hp1 | a0001 | c0001 | t0022 | g0080 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0004 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | MSL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03239 | hp1 | a0001 | c0001 | t0014 | g0034 | SAS | PJL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03453 | hp1 | a0001 | c0001 | t0015 | g0082 | AFR | MSL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0072 | AFR | GWD | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0004 | AFR | MSL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | MSL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0048 | SAS | BEB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | BEB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | YRI | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18946 | hp1 | a0001 | c0001 | t0024 | g0131 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18971 | hp2 | a0001 | c0001 | t0020 | g0045 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18983 | hp2 | a0001 | c0001 | t0012 | g0011 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19003 | hp1 | a0001 | c0001 | t0012 | g0011 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19004 | hp2 | a0001 | c0001 | t0017 | g0107 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | LWK | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0085 | AFR | LWK | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | LWK | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | LWK | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19060 | hp1 | a0001 | c0001 | t0016 | g0039 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19062 | hp2 | a0001 | c0001 | t0012 | g0011 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19067 | hp1 | a0001 | c0001 | t0013 | g0098 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19074 | hp1 | a0001 | c0001 | t0016 | g0039 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19074 | hp2 | a0001 | c0001 | t0012 | g0011 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0060 | EUR | TSI | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA20905 | hp1 | a0001 | c0001 | t0014 | g0034 | SAS | GIH | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0066 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | ACB | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | MSL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | USA | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | USA | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0108 | REF | REF | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | TNFSF4_chr1_173178731_173212331 | TNFSF4 | chr1 | 173178731 | 173212331 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:173188537 | G | A | 1 | a0001c0002 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.186C>T | p.Ile62Ile | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/3 | 341/3492 | 186/552 | 62/183 | chr1 | 173188537 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:173184001 | T | C | 1 | a0001c0001t0014 | 2 | HG03239.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2515A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 2515 | chr1 | 173184001 | ||||||
| chr1:173184047 | G | A | 2 | a0001c0001t0005 a0001c0001t0018 |
13 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2469C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 2469 | chr1 | 173184047 | ||||||
| chr1:173184089 | A | T | 4 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0011 others(1): Show |
41 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2427T>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 2427 | chr1 | 173184089 | ||||||
| chr1:173184303 | C | A | 9 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(6): Show |
58 | HG00544.hp1 HG00597.hp2 HG01069.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2213G>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 2213 | chr1 | 173184303 | ||||||
| chr1:173184329 | A | G | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0011 others(2): Show |
42 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2187T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 2187 | chr1 | 173184329 | ||||||
| chr1:173184342 | G | A | 1 | a0001c0001t0009 | 5 | HG01192.hp2 HG01433.hp2 HG01934.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2174C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 2174 | chr1 | 173184342 | ||||||
| chr1:173184526 | CT | C | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0018 |
34 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1989delA | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 1989 | chr1 | 173184526 | ||||||
| chr1:173184642 | G | A | 1 | a0001c0001t0021 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1874C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 1874 | chr1 | 173184642 | ||||||
| chr1:173184702 | TAC | T | 1 | a0001c0001t0003 | 21 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1812_*1813delGT | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 1812 | chr1 | 173184702 | ||||||
| chr1:173184864 | CTG | C | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0011 others(2): Show |
42 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1650_*1651delCA | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 1650 | chr1 | 173184864 | ||||||
| chr1:173184885 | C | T | 2 | a0001c0001t0013 a0001c0001t0014 |
5 | HG00544.hp1 HG00597.hp2 HG03239.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1631G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 1631 | chr1 | 173184885 | ||||||
| chr1:173185098 | A | G | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0011 others(2): Show |
42 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1418T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 1418 | chr1 | 173185098 | ||||||
| chr1:173185165 | G | T | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(15): Show |
127 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1351C>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 1351 | chr1 | 173185165 | ||||||
| chr1:173185215 | A | C | 2 | a0001c0001t0003 a0001c0001t0023 |
22 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1301T>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 1301 | chr1 | 173185215 | ||||||
| chr1:173185296 | G | A | 1 | a0001c0001t0022 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1220C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 1220 | chr1 | 173185296 | ||||||
| chr1:173185400 | T | C | 2 | a0001c0001t0003 a0001c0001t0023 |
22 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1116A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 1116 | chr1 | 173185400 | ||||||
| chr1:173185595 | T | C | 1 | a0001c0001t0011 | 5 | HG00738.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*921A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 921 | chr1 | 173185595 | ||||||
| chr1:173185748 | C | T | 1 | a0001c0001t0019 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*768G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 768 | chr1 | 173185748 | ||||||
| chr1:173185883 | G | GA | 2 | a0001c0001t0003 a0001c0001t0023 |
22 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*632dupT | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 632 | chr1 | 173185883 | ||||||
| chr1:173185929 | AT | A | 2 | a0001c0001t0013 a0001c0001t0014 |
5 | HG00544.hp1 HG00597.hp2 HG03239.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*586delA | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 586 | chr1 | 173185929 | ||||||
| chr1:173186007 | C | T | 1 | a0001c0001t0018 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*509G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 509 | chr1 | 173186007 | ||||||
| chr1:173186044 | G | C | 1 | a0001c0001t0008 | 6 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*472C>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 472 | chr1 | 173186044 | ||||||
| chr1:173186124 | CAT | C | 3 | a0001c0001t0004 a0001c0001t0015 a0001c0002t0004 |
21 | HG01192.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*390_*391delAT | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 390 | chr1 | 173186124 | ||||||
| chr1:173186146 | G | A | 1 | a0001c0001t0024 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*370C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 370 | chr1 | 173186146 | ||||||
| chr1:173186183 | T | A | 1 | a0001c0001t0012 | 4 | NA18983.hp2 NA19003.hp1 NA19062.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*333A>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 333 | chr1 | 173186183 | ||||||
| chr1:173186408 | G | A | 1 | a0001c0001t0025 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*108C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 108 | chr1 | 173186408 | ||||||
| chr1:173186449 | C | T | 1 | a0001c0001t0017 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*67G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 3/3 | 67 | chr1 | 173186449 | ||||||
| chr1:173207195 | G | C | 1 | a0001c0001t0016 | 2 | NA19060.hp1 NA19074.hp1 |
5_prime_UTR_variant | MODIFIER | c.-19C>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/3 | 19 | chr1 | 173207195 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:173186953 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.203-88C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173186953 | |||||||
| chr1:173187008 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.203-143C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173187008 | |||||||
| chr1:173187059 | A | G | 2 | a0001c0001t0002g0026 a0001c0001t0002g0037 |
4 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-194T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173187059 | |||||||
| chr1:173187085 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.203-220T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173187085 | |||||||
| chr1:173187153 | T | C | 79 | a0001c0001t0001g0030 a0001c0001t0001g0073 a0001c0001t0001g0074 others(76): Show |
136 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.203-288A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173187153 | |||||||
| chr1:173187191 | G | A | 1 | a0001c0001t0013g0099 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.203-326C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173187191 | |||||||
| chr1:173187266 | A | G | 11 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0001c0001t0006g0060 others(8): Show |
22 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.203-401T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173187266 | |||||||
| chr1:173187280 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.203-415C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173187280 | |||||||
| chr1:173187355 | C | T | 27 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(24): Show |
42 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.203-490G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173187355 | |||||||
| chr1:173187403 | C | G | 1 | a0001c0001t0002g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.203-538G>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173187403 | |||||||
| chr1:173187438 | C | T | 1 | a0001c0001t0006g0028 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.203-573G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173187438 | |||||||
| chr1:173187535 | G | A | 1 | a0001c0001t0009g0126 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.203-670C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173187535 | |||||||
| chr1:173187820 | C | G | 4 | a0001c0001t0013g0098 a0001c0001t0013g0099 a0001c0001t0013g0100 others(1): Show |
5 | HG00544.hp1 HG00597.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.202+701G>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173187820 | |||||||
| chr1:173187890 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.202+631G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173187890 | |||||||
| chr1:173188024 | T | A | 13 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(10): Show |
22 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.202+497A>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173188024 | |||||||
| chr1:173188062 | C | T | 11 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0001c0001t0006g0060 others(8): Show |
22 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.202+459G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173188062 | |||||||
| chr1:173188239 | A | T | 13 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(10): Show |
22 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.202+282T>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173188239 | |||||||
| chr1:173188402 | T | C | 13 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(10): Show |
22 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.202+119A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173188402 | |||||||
| chr1:173188496 | C | A | 1 | a0001c0001t0001g0012 | 4 | HG01496.hp2 HG02273.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+25G>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 2/2 | chr1 | 173188496 | |||||||
| chr1:173188625 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0111 others(1): Show |
9 | HG00323.hp1 HG00738.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.154-56C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173188625 | |||||||
| chr1:173188708 | G | T | 1 | a0001c0001t0001g0035 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.154-139C>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173188708 | |||||||
| chr1:173189066 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.154-497G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173189066 | |||||||
| chr1:173189129 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.154-560C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173189129 | |||||||
| chr1:173189227 | T | C | 11 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0001c0001t0006g0060 others(8): Show |
22 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.154-658A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173189227 | |||||||
| chr1:173189246 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.154-677T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173189246 | |||||||
| chr1:173189862 | T | C | 1 | a0001c0001t0002g0054 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.154-1293A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173189862 | |||||||
| chr1:173190048 | T | TA | 13 | a0001c0001t0002g0053 a0001c0001t0006g0028 a0001c0001t0006g0032 others(10): Show |
25 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.154-1480dupT | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173190048 | |||||||
| chr1:173190048 | TA | T | 35 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0001g0120 others(32): Show |
55 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.154-1480delT | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173190048 | |||||||
| chr1:173190105 | T | A | 27 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(24): Show |
42 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.154-1536A>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173190105 | |||||||
| chr1:173190271 | G | A | 3 | a0001c0001t0006g0032 a0001c0001t0006g0060 a0001c0001t0006g0065 |
4 | HG01074.hp2 HG01978.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-1702C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173190271 | |||||||
| chr1:173190377 | T | C | 79 | a0001c0001t0001g0030 a0001c0001t0001g0073 a0001c0001t0001g0074 others(76): Show |
136 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.154-1808A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173190377 | |||||||
| chr1:173190398 | G | A | 1 | a0001c0001t0006g0028 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.154-1829C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173190398 | |||||||
| chr1:173190481 | C | T | 13 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(10): Show |
22 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.154-1912G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173190481 | |||||||
| chr1:173190816 | G | T | 6 | a0001c0001t0005g0007 a0001c0001t0005g0018 a0001c0001t0005g0079 others(3): Show |
13 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.154-2247C>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173190816 | |||||||
| chr1:173190924 | T | A | 11 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0001c0001t0006g0060 others(8): Show |
22 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.154-2355A>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173190924 | |||||||
| chr1:173191144 | G | A | 27 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(24): Show |
42 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.154-2575C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173191144 | |||||||
| chr1:173191662 | G | A | 4 | a0001c0001t0013g0098 a0001c0001t0013g0099 a0001c0001t0013g0100 others(1): Show |
5 | HG00544.hp1 HG00597.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-3093C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173191662 | |||||||
| chr1:173191663 | C | G | 4 | a0001c0001t0013g0098 a0001c0001t0013g0099 a0001c0001t0013g0100 others(1): Show |
5 | HG00544.hp1 HG00597.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-3094G>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173191663 | |||||||
| chr1:173191709 | T | G | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.154-3140A>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173191709 | |||||||
| chr1:173191751 | G | A | 1 | a0001c0001t0013g0100 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.154-3182C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173191751 | |||||||
| chr1:173191996 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.154-3427C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173191996 | |||||||
| chr1:173192318 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.154-3749G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173192318 | |||||||
| chr1:173192377 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154-3808G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173192377 | |||||||
| chr1:173192519 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.154-3950T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173192519 | |||||||
| chr1:173192561 | G | T | 19 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(16): Show |
35 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.154-3992C>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173192561 | |||||||
| chr1:173192703 | C | T | 1 | a0001c0001t0006g0088 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.154-4134G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173192703 | |||||||
| chr1:173192879 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.154-4310A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173192879 | |||||||
| chr1:173192905 | T | A | 1 | a0001c0001t0016g0039 | 2 | NA19060.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.154-4336A>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173192905 | |||||||
| chr1:173193079 | T | C | 13 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(10): Show |
22 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.154-4510A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173193079 | |||||||
| chr1:173193088 | TC | T | 4 | a0001c0001t0013g0098 a0001c0001t0013g0099 a0001c0001t0013g0100 others(1): Show |
5 | HG00544.hp1 HG00597.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-4520delG | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173193088 | |||||||
| chr1:173193163 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.154-4594T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173193163 | |||||||
| chr1:173193300 | C | A | 41 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(38): Show |
80 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.154-4731G>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173193300 | |||||||
| chr1:173193579 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0128 |
2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.154-5010G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173193579 | |||||||
| chr1:173193581 | C | T | 1 | a0001c0001t0006g0028 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.154-5012G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173193581 | |||||||
| chr1:173193768 | C | CA | 47 | a0001c0001t0001g0103 a0001c0001t0001g0116 a0001c0001t0001g0117 others(44): Show |
87 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.154-5200dupT | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173193768 | |||||||
| chr1:173193768 | CA | C | 27 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(24): Show |
42 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.154-5200delT | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173193768 | |||||||
| chr1:173194143 | A | T | 3 | a0001c0001t0004g0083 a0001c0001t0015g0082 a0001c0001t0015g0091 |
3 | HG02451.hp1 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.154-5574T>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173194143 | |||||||
| chr1:173194218 | G | A | 41 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(38): Show |
80 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.154-5649C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173194218 | |||||||
| chr1:173194218 | G | C | 1 | a0001c0001t0010g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154-5649C>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173194218 | |||||||
| chr1:173194373 | A | G | 27 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(24): Show |
42 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.154-5804T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173194373 | |||||||
| chr1:173194429 | A | G | 78 | a0001c0001t0001g0030 a0001c0001t0001g0073 a0001c0001t0001g0074 others(75): Show |
134 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.154-5860T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173194429 | |||||||
| chr1:173194647 | T | A | 1 | a0001c0001t0001g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.154-6078A>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173194647 | |||||||
| chr1:173194648 | C | G | 3 | a0001c0001t0008g0020 a0001c0001t0008g0036 a0001c0001t0008g0085 |
6 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.154-6079G>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173194648 | |||||||
| chr1:173194658 | C | T | 1 | a0001c0001t0019g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.154-6089G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173194658 | |||||||
| chr1:173194728 | A | T | 1 | a0001c0001t0001g0111 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.154-6159T>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173194728 | |||||||
| chr1:173194738 | T | C | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.154-6169A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173194738 | |||||||
| chr1:173194880 | C | CA | 27 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0073 others(24): Show |
51 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.154-6312dupT | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173194880 | |||||||
| chr1:173194880 | CA | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0104 a0001c0001t0001g0111 others(15): Show |
27 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.154-6312delT | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173194880 | |||||||
| chr1:173194922 | A | C | 1 | a0001c0001t0016g0039 | 2 | NA19060.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.154-6353T>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173194922 | |||||||
| chr1:173195008 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.154-6439T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173195008 | |||||||
| chr1:173195318 | A | G | 45 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(42): Show |
85 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.154-6749T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173195318 | |||||||
| chr1:173195426 | C | T | 41 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(38): Show |
80 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.154-6857G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173195426 | |||||||
| chr1:173195648 | T | C | 72 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(69): Show |
127 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.154-7079A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173195648 | |||||||
| chr1:173195659 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.154-7090G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173195659 | |||||||
| chr1:173195672 | A | C | 27 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(24): Show |
42 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.154-7103T>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173195672 | |||||||
| chr1:173195783 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.154-7214C>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173195783 | |||||||
| chr1:173195902 | G | T | 1 | a0001c0001t0001g0023 | 3 | HG00099.hp2 HG00741.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.154-7333C>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173195902 | |||||||
| chr1:173195944 | G | A | 10 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0001c0001t0006g0060 others(7): Show |
21 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-7375C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173195944 | |||||||
| chr1:173195961 | C | T | 2 | a0001c0001t0004g0022 a0001c0001t0004g0090 |
4 | HG02451.hp2 HG02615.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-7392G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173195961 | |||||||
| chr1:173196320 | C | T | 22 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0022 others(19): Show |
45 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.154-7751G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173196320 | |||||||
| chr1:173196344 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.154-7775T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173196344 | |||||||
| chr1:173196433 | ATC | A | 27 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(24): Show |
42 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.154-7866_154-7865d others(4): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173196433 | |||||||
| chr1:173196539 | G | A | 1 | a0001c0001t0013g0100 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.154-7970C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173196539 | |||||||
| chr1:173197108 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0041 others(93): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.154-8539T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173197108 | |||||||
| chr1:173197395 | T | C | 1 | a0001c0001t0002g0044 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.154-8826A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173197395 | |||||||
| chr1:173197469 | A | G | 1 | a0001c0001t0006g0088 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.154-8900T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173197469 | |||||||
| chr1:173197501 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.154-8932A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173197501 | |||||||
| chr1:173197602 | C | A | 4 | a0001c0001t0013g0098 a0001c0001t0013g0099 a0001c0001t0013g0100 others(1): Show |
5 | HG00544.hp1 HG00597.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-9033G>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173197602 | |||||||
| chr1:173198592 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.153+8432G>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173198592 | |||||||
| chr1:173198777 | C | T | 1 | a0001c0001t0006g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.153+8247G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173198777 | |||||||
| chr1:173198783 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.153+8241A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173198783 | |||||||
| chr1:173199091 | T | C | 44 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(41): Show |
84 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.153+7933A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173199091 | |||||||
| chr1:173199120 | T | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG00423.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.153+7904A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173199120 | |||||||
| chr1:173199182 | A | G | 44 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(41): Show |
84 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.153+7842T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173199182 | |||||||
| chr1:173199198 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.153+7826G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173199198 | |||||||
| chr1:173199232 | G | A | 1 | a0001c0001t0004g0086 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.153+7792C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173199232 | |||||||
| chr1:173199258 | G | A | 44 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(41): Show |
72 | HG00140.hp2 HG00558.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.153+7766C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173199258 | |||||||
| chr1:173199354 | T | C | 5 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0102 others(2): Show |
5 | HG01981.hp1 HG02071.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+7670A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173199354 | |||||||
| chr1:173199783 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.153+7241A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173199783 | |||||||
| chr1:173199847 | T | TA | 13 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(10): Show |
22 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.153+7176dupT | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173199847 | |||||||
| chr1:173199847 | TA | T | 26 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(23): Show |
38 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.153+7176delT | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173199847 | |||||||
| chr1:173199849 | A | T | 5 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0102 others(2): Show |
5 | HG01981.hp1 HG02071.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+7175T>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173199849 | |||||||
| chr1:173200051 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.153+6973A>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173200051 | |||||||
| chr1:173200152 | A | C | 1 | a0001c0001t0006g0088 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.153+6872T>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173200152 | |||||||
| chr1:173200435 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.153+6589G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173200435 | |||||||
| chr1:173200749 | T | C | 1 | a0001c0001t0006g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.153+6275A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173200749 | |||||||
| chr1:173200883 | G | T | 4 | a0001c0001t0013g0098 a0001c0001t0013g0099 a0001c0001t0013g0100 others(1): Show |
5 | HG00544.hp1 HG00597.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+6141C>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173200883 | |||||||
| chr1:173201013 | G | T | 25 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(22): Show |
37 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.153+6011C>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173201013 | |||||||
| chr1:173201067 | T | C | 1 | a0001c0001t0008g0036 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.153+5957A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173201067 | |||||||
| chr1:173201195 | G | GCAAA | 25 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(22): Show |
37 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.153+5828_153+5829i others(6): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173201195 | |||||||
| chr1:173201311 | T | G | 1 | a0001c0001t0001g0014 | 4 | HG02071.hp2 HG04228.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+5713A>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173201311 | |||||||
| chr1:173201479 | C | T | 65 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(62): Show |
116 | HG00140.hp2 HG00558.hp1 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.153+5545G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173201479 | |||||||
| chr1:173201528 | G | A | 5 | a0001c0001t0005g0007 a0001c0001t0005g0018 a0001c0001t0005g0079 others(2): Show |
12 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.153+5496C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173201528 | |||||||
| chr1:173201898 | C | A | 5 | a0001c0001t0005g0007 a0001c0001t0005g0018 a0001c0001t0005g0079 others(2): Show |
12 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.153+5126G>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173201898 | |||||||
| chr1:173201987 | T | C | 1 | a0001c0001t0003g0048 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.153+5037A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173201987 | |||||||
| chr1:173202058 | C | CAT | 4 | a0001c0001t0013g0098 a0001c0001t0013g0099 a0001c0001t0013g0100 others(1): Show |
5 | HG00544.hp1 HG00597.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+4964_153+4965d others(4): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202058 | |||||||
| chr1:173202058 | C | T | 25 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(22): Show |
37 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.153+4966G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202058 | |||||||
| chr1:173202070 | T | TATATATA others(4): Show |
4 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0011g0077 others(1): Show |
4 | HG01981.hp1 HG02071.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+4953_153+4954i others(13): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202070 | |||||||
| chr1:173202070 | T | TATATATA others(6): Show |
8 | a0001c0001t0002g0021 a0001c0001t0002g0049 a0001c0001t0002g0075 others(5): Show |
10 | HG00738.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+4953_153+4954i others(15): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202070 | |||||||
| chr1:173202070 | T | TATATATA others(8): Show |
2 | a0001c0001t0002g0071 a0001c0001t0002g0093 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.153+4953_153+4954i others(17): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202070 | |||||||
| chr1:173202070 | T | TATATATA others(12): Show |
3 | a0001c0001t0002g0019 a0001c0001t0002g0052 a0001c0001t0002g0053 |
5 | HG00558.hp1 NA18983.hp1 NA19067.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+4953_153+4954i others(21): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202070 | |||||||
| chr1:173202070 | T | TATATATA others(12): Show |
3 | a0001c0001t0002g0026 a0001c0001t0002g0037 a0001c0001t0011g0031 |
6 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+4953_153+4954i others(21): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202070 | |||||||
| chr1:173202070 | T | TATATATA others(14): Show |
3 | a0001c0001t0002g0006 a0001c0001t0002g0054 a0001c0001t0002g0055 |
8 | HG02080.hp2 NA18612.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+4953_153+4954i others(23): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202070 | |||||||
| chr1:173202070 | T | TATATATA others(18): Show |
1 | a0001c0001t0002g0056 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.153+4953_153+4954i others(27): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202070 | |||||||
| chr1:173202070 | T | TATATATA others(18): Show |
1 | a0001c0001t0011g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.153+4953_153+4954i others(27): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202070 | |||||||
| chr1:173202096 | A | AAAG | 25 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(22): Show |
37 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.153+4925_153+4927d others(5): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202096 | |||||||
| chr1:173202534 | C | G | 43 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(40): Show |
71 | HG00140.hp2 HG00558.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.153+4490G>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202534 | |||||||
| chr1:173202702 | A | T | 25 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0021 others(22): Show |
37 | HG00558.hp1 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.153+4322T>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202702 | |||||||
| chr1:173202717 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0074 a0001c0001t0010g0027 others(2): Show |
7 | HG00642.hp1 HG01069.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+4307G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202717 | |||||||
| chr1:173202767 | C | T | 2 | a0001c0001t0006g0032 a0001c0001t0006g0065 |
3 | HG01074.hp2 HG01978.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.153+4257G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202767 | |||||||
| chr1:173202810 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.153+4214C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202810 | |||||||
| chr1:173202956 | CCCTCCCT | C | 13 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(10): Show |
22 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.153+4061_153+4067d others(9): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173202956 | |||||||
| chr1:173203019 | C | A | 13 | a0001c0001t0003g0009 a0001c0001t0003g0017 a0001c0001t0003g0024 others(10): Show |
22 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.153+4005G>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173203019 | |||||||
| chr1:173203045 | T | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
8 | HG00642.hp1 HG01069.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+3979A>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173203045 | |||||||
| chr1:173203271 | A | G | 8 | a0001c0001t0002g0021 a0001c0001t0002g0049 a0001c0001t0002g0071 others(5): Show |
10 | HG01884.hp1 HG02615.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+3753T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173203271 | |||||||
| chr1:173203284 | GC | G | 27 | a0001c0001t0001g0016 a0001c0001t0001g0070 a0001c0001t0002g0006 others(24): Show |
41 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.153+3739delG | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173203284 | |||||||
| chr1:173203491 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.153+3533T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173203491 | |||||||
| chr1:173203577 | T | G | 2 | a0001c0001t0009g0015 a0001c0001t0009g0126 |
5 | HG01192.hp2 HG01433.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+3447A>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173203577 | |||||||
| chr1:173203774 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.153+3250C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173203774 | |||||||
| chr1:173203806 | G | C | 1 | a0001c0001t0016g0039 | 2 | NA19060.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.153+3218C>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173203806 | |||||||
| chr1:173203819 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.153+3205G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173203819 | |||||||
| chr1:173203841 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.153+3183A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173203841 | |||||||
| chr1:173203864 | T | G | 1 | a0001c0001t0001g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.153+3160A>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173203864 | |||||||
| chr1:173204315 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0129 a0001c0001t0001g0130 |
5 | HG01981.hp2 HG02273.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+2709C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204315 | |||||||
| chr1:173204477 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.153+2547G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204477 | |||||||
| chr1:173204478 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0134 others(5): Show |
18 | HG00597.hp1 HG00741.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.153+2546C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204478 | |||||||
| chr1:173204680 | A | T | 13 | a0001c0001t0001g0051 a0001c0001t0003g0009 a0001c0001t0003g0017 others(10): Show |
20 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.153+2344T>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204680 | |||||||
| chr1:173204681 | T | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(40): Show |
79 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.153+2343A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204681 | |||||||
| chr1:173204723 | C | A | 4 | a0001c0001t0006g0028 a0001c0001t0010g0027 a0001c0001t0010g0068 others(1): Show |
6 | HG01069.hp2 HG01243.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+2301G>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204723 | |||||||
| chr1:173204731 | T | TACCAAC | 3 | a0001c0001t0010g0027 a0001c0001t0010g0068 a0001c0001t0010g0087 |
4 | HG01069.hp2 HG01243.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+2287_153+2292d others(8): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204731 | |||||||
| chr1:173204736 | A | C | 1 | a0001c0001t0006g0028 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.153+2288T>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204736 | |||||||
| chr1:173204791 | T | C | 4 | a0001c0001t0001g0030 a0001c0001t0001g0074 a0001c0001t0006g0066 others(1): Show |
5 | HG00642.hp1 HG01943.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+2233A>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204791 | |||||||
| chr1:173204918 | C | CAA | 3 | a0001c0001t0001g0030 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | HG00642.hp1 HG01943.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+2105_153+2106i others(4): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204918 | |||||||
| chr1:173204918 | C | CACAA | 2 | a0001c0001t0004g0010 a0001c0002t0004g0072 |
5 | HG02109.hp1 HG02486.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+2105_153+2106i others(6): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204918 | |||||||
| chr1:173204918 | C | CACACACA others(1): Show |
1 | a0001c0001t0008g0020 | 3 | HG02559.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.153+2105_153+2106i others(10): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204918 | |||||||
| chr1:173204920 | C | A | 2 | a0001c0001t0002g0092 a0001c0001t0002g0093 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.153+2104G>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204920 | |||||||
| chr1:173204920 | C | CAA | 22 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0057 others(19): Show |
45 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.153+2103_153+2104i others(4): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204920 | |||||||
| chr1:173204920 | C | CACACACA others(3): Show |
2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.153+2103_153+2104i others(12): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204920 | |||||||
| chr1:173204922 | C | A | 13 | a0001c0001t0001g0050 a0001c0001t0001g0070 a0001c0001t0002g0049 others(10): Show |
19 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.153+2102G>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204922 | |||||||
| chr1:173204924 | A | AACAC | 24 | a0001c0001t0001g0051 a0001c0001t0002g0021 a0001c0001t0004g0083 others(21): Show |
36 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.153+2096_153+2099d others(6): Show |
TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204924 | |||||||
| chr1:173204924 | A | C | 46 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0041 others(43): Show |
81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.153+2100T>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204924 | |||||||
| chr1:173204936 | C | T | 13 | a0001c0001t0001g0050 a0001c0001t0001g0070 a0001c0001t0002g0049 others(10): Show |
19 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.153+2088G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173204936 | |||||||
| chr1:173205250 | G | A | 2 | a0001c0001t0003g0061 a0001c0001t0023g0062 |
2 | HG00140.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.153+1774C>T | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173205250 | |||||||
| chr1:173205574 | A | G | 2 | a0001c0001t0010g0027 a0001c0001t0010g0068 |
3 | HG01069.hp2 HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.153+1450T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173205574 | |||||||
| chr1:173205611 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.153+1413G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173205611 | |||||||
| chr1:173205721 | C | T | 1 | a0001c0001t0006g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.153+1303G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173205721 | |||||||
| chr1:173206131 | C | T | 1 | a0001c0001t0006g0065 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.153+893G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173206131 | |||||||
| chr1:173206202 | G | C | 1 | a0001c0001t0018g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.153+822C>G | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173206202 | |||||||
| chr1:173206287 | A | T | 1 | a0001c0001t0003g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.153+737T>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173206287 | |||||||
| chr1:173206360 | A | G | 1 | a0001c0001t0021g0063 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.153+664T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173206360 | |||||||
| chr1:173206693 | A | G | 29 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0050 others(26): Show |
43 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.153+331T>C | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173206693 | |||||||
| chr1:173206808 | C | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0002g0043 others(4): Show |
9 | HG00423.hp1 HG00735.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+216G>A | TNFSF4 | ENSG00000117586.11 | transcript | ENST00000281834.4 | protein_coding | 1/2 | chr1 | 173206808 |