Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25816 |
| ensemblid | ENSG00000145779.8 |
| hgncid | 17260 |
| symbol | TNFAIP8 |
| name | TNF alpha induced protein 8 |
| refseq_nuc | NM_014350.4 |
| refseq_prot | NP_055165.2 |
| ensembl_nuc | ENST00000504771.3 |
| ensembl_prot | ENSP00000422245.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 119356019 |
| end | 119399688 |
| strand | + |
| ver | v1.2 |
| region | chr5:119356019-119399688 |
| region5000 | chr5:119351019-119404688 |
| regionname0 | TNFAIP8_chr5_119356019_119399688 |
| regionname5000 | TNFAIP8_chr5_119351019_119404688 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 198 | 382 | 92 | 76 | 164 | 12 | 36 | 124 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | MHSEA others(193): Show |
chr5 | 119351019 | 119404688 |
| a0002 | 0/0 | 198 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | MHSEA others(193): Show |
chr5 | 119351019 | 119404688 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 594 | 279 | 46 | 53 | 140 | 10 | 28 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | ATGCA others(589): Show |
chr5 | 119351019 | 119404688 | ||
| a0001c0002 | 0/0 | 594 | 103 | 46 | 23 | 24 | 2 | 8 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | ATGCA others(589): Show |
chr5 | 119351019 | 119404688 | ||
| a0002c0003 | 0/0 | 594 | 2 | 0 | 0 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | ATGCA others(589): Show |
chr5 | 119351019 | 119404688 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6976 | 61 | 1 | 7 | 44 | 3 | 4 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0002 | 0/0 | 6976 | 56 | 0 | 0 | 55 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0003 | 0/0 | 6973 | 45 | 8 | 13 | 13 | 2 | 9 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0005 | 0/0 | 6973 | 13 | 1 | 7 | 0 | 3 | 2 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0008 | 0/0 | 6976 | 5 | 1 | 2 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0009 | 0/0 | 6974 | 5 | 4 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6969): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0010 | 0/0 | 6975 | 4 | 2 | 2 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6970): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0011 | 0/0 | 6977 | 3 | 0 | 0 | 1 | 0 | 2 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0012 | 0/0 | 6976 | 4 | 0 | 0 | 4 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0013 | 0/0 | 6977 | 4 | 0 | 0 | 4 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0014 | 0/0 | 6976 | 4 | 0 | 4 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0016 | 0/0 | 6976 | 4 | 0 | 4 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0017 | 0/0 | 6973 | 3 | 3 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0021 | 0/0 | 6972 | 3 | 0 | 1 | 0 | 0 | 2 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6967): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0022 | 0/0 | 6977 | 3 | 0 | 0 | 3 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0025 | 0/0 | 6974 | 2 | 2 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6969): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0026 | 0/0 | 6996 | 2 | 0 | 2 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6991): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0027 | 0/0 | 6973 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0028 | 0/0 | 6979 | 2 | 0 | 2 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6974): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0029 | 0/0 | 6978 | 2 | 2 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6973): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0030 | 0/0 | 6977 | 2 | 2 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0031 | 0/0 | 6991 | 2 | 1 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6986): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0037 | 0/0 | 6977 | 2 | 0 | 0 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0038 | 0/0 | 6973 | 2 | 2 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0041 | 0/0 | 6995 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6990): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0042 | 0/0 | 6979 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6974): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0043 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0044 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0045 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0046 | 0/0 | 6972 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6967): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0047 | 0/0 | 6976 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0048 | 0/0 | 6993 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6988): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0049 | 0/0 | 6992 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6987): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0050 | 0/0 | 7002 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6997): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0067 | 0/0 | 6974 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6969): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0068 | 0/0 | 6973 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0069 | 0/0 | 6972 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6967): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0070 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0071 | 0/0 | 6974 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6969): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0072 | 0/0 | 6979 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6974): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0073 | 0/0 | 6976 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0074 | 0/0 | 6976 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0075 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6973): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0076 | 0/0 | 6975 | 1 | 0 | 0 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6970): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0077 | 0/0 | 6970 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6965): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0078 | 0/0 | 6976 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0079 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0080 | 0/0 | 6976 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0081 | 0/0 | 6976 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0082 | 0/0 | 6975 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6970): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0083 | 0/0 | 6974 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6969): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0084 | 0/0 | 6974 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6969): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0085 | 0/0 | 6973 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0086 | 0/0 | 6978 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6973): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0087 | 0/0 | 6977 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0088 | 0/0 | 6974 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6969): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0089 | 0/0 | 7320 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7315): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0090 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6973): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0091 | 0/0 | 6976 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0092 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0093 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0094 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0102 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0103 | 0/0 | 6974 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6969): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0104 | 0/0 | 6971 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6966): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0105 | 0/0 | 6976 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0106 | 0/0 | 6975 | 1 | 0 | 0 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6970): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0107 | 0/0 | 6976 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0001t0108 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0004 | 0/0 | 6975 | 18 | 2 | 6 | 9 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6970): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0006 | 0/0 | 6975 | 11 | 1 | 5 | 5 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6970): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0007 | 0/0 | 7008 | 5 | 5 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7003): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0015 | 0/0 | 7007 | 4 | 4 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7002): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0018 | 0/0 | 7000 | 3 | 1 | 0 | 1 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6995): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0019 | 0/0 | 7005 | 3 | 3 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7000): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0020 | 0/0 | 7007 | 3 | 3 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7002): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0023 | 0/0 | 6976 | 3 | 0 | 0 | 3 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0024 | 0/0 | 6976 | 3 | 0 | 2 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0027 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0032 | 0/0 | 6977 | 2 | 1 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0033 | 0/0 | 7001 | 2 | 1 | 0 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6996): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0034 | 0/0 | 7003 | 2 | 0 | 2 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6998): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0035 | 0/0 | 7007 | 2 | 2 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7002): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0036 | 0/0 | 7003 | 2 | 2 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6998): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0039 | 0/0 | 6972 | 2 | 1 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6967): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0040 | 0/0 | 6977 | 2 | 0 | 0 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0051 | 0/0 | 6974 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6969): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0052 | 0/0 | 7002 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6997): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0053 | 0/0 | 6989 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6984): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0054 | 0/0 | 7002 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6997): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0055 | 0/0 | 7001 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6996): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0056 | 0/0 | 7003 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6998): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0057 | 0/0 | 7006 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7001): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0058 | 0/0 | 7007 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7002): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0059 | 0/0 | 7008 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7003): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0060 | 0/0 | 7010 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7005): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0061 | 0/0 | 7009 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7004): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0062 | 0/0 | 7008 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7003): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0063 | 0/0 | 7002 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6997): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0064 | 0/0 | 7004 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6999): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0065 | 0/0 | 7009 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7004): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0066 | 0/0 | 6976 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0095 | 0/0 | 6979 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6974): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0096 | 0/0 | 7003 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6998): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0097 | 0/0 | 7014 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(7009): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0098 | 0/0 | 6974 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6969): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0099 | 0/0 | 6975 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6970): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0100 | 0/0 | 6977 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0101 | 0/0 | 6976 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0109 | 0/0 | 6975 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6970): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0110 | 0/0 | 6962 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6957): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0111 | 0/0 | 6971 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6966): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0112 | 0/0 | 6975 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6970): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0113 | 0/0 | 6974 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6969): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0114 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6968): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0115 | 0/0 | 6975 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6970): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0116 | 0/0 | 6979 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6974): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0117 | 0/0 | 6972 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6967): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0118 | 0/0 | 6976 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0119 | 0/0 | 6977 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| a0001c0002t0120 | 0/0 | 6975 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6970): Show |
chr5 | 119351019 | 119404688 |
| a0002c0003t0001 | 0/0 | 6976 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6971): Show |
chr5 | 119351019 | 119404688 |
| a0002c0003t0011 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | GCAGA others(6972): Show |
chr5 | 119351019 | 119404688 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 11 | 0 | 3 | 6 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0005g0002 | 0/0 | 7 | 0 | 5 | 0 | 0 | 2 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0008g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0008g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0008g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0008g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0008g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0009g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0010g0008 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0011g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0011g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0011g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0012g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0012g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0012g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0012g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0013g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0013g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0013g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0013g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0014g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0014g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0014g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0016g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0016g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0017g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0017g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0021g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0021g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0021g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0022g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0022g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0022g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0025g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0025g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0026g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0027g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0028g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0028g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0029g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0029g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0030g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0031g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0031g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0037g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0037g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0038g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0041g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0042g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0043g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0044g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0045g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0046g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0047g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0048g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0049g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0050g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0067g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0068g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0069g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0070g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0071g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0072g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0073g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0074g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0075g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0076g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0077g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0078g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0079g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0080g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0081g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0082g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0083g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0084g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0085g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0086g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0087g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0088g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0089g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0090g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0091g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0092g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0093g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0094g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0102g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0103g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0104g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0105g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0106g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0107g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0001t0108g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0010 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0004g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0006g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0015g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0015g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0018g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0018g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0018g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0019g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0019g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0020g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0020g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0020g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0023g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0023g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0024g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0024g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0024g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0027g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0032g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0032g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0033g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0033g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0034g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0034g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0035g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0035g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0036g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0036g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0039g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0039g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0040g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0040g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0051g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0052g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0053g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0054g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0055g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0056g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0057g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0058g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0059g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0060g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0061g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0062g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0063g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0064g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0065g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0066g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0095g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0096g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0097g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0098g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0099g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0100g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0101g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0109g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0110g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0111g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0112g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0113g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0114g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0115g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0116g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0117g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0118g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0119g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0001c0002t0120g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0002c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| a0002c0003t0011g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0088 | EUR | GBR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0095 | EUR | GBR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00280 | hp1 | a0001 | c0002 | t0033 | g0235 | EUR | FIN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00280 | hp2 | a0001 | c0001 | t0076 | g0152 | EUR | FIN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00408 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00408 | hp2 | a0001 | c0002 | t0040 | g0252 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00558 | hp2 | a0001 | c0001 | t0022 | g0208 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00639 | hp1 | a0001 | c0001 | t0083 | g0081 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00639 | hp2 | a0001 | c0002 | t0032 | g0247 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00642 | hp1 | a0001 | c0001 | t0010 | g0008 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00642 | hp2 | a0001 | c0002 | t0004 | g0284 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0280 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00738 | hp1 | a0001 | c0001 | t0008 | g0041 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG00741 | hp2 | a0001 | c0002 | t0096 | g0144 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01069 | hp1 | a0001 | c0001 | t0026 | g0036 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0265 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01070 | hp2 | a0001 | c0002 | t0117 | g0268 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01071 | hp1 | a0001 | c0001 | t0026 | g0036 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01074 | hp2 | a0001 | c0001 | t0010 | g0008 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01106 | hp1 | a0001 | c0002 | t0039 | g0289 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01109 | hp1 | a0001 | c0002 | t0024 | g0272 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01109 | hp2 | a0001 | c0001 | t0028 | g0230 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01167 | hp1 | a0001 | c0002 | t0006 | g0019 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01168 | hp2 | a0001 | c0001 | t0021 | g0022 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01169 | hp1 | a0001 | c0001 | t0085 | g0022 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01169 | hp2 | a0001 | c0002 | t0098 | g0019 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01175 | hp2 | a0001 | c0002 | t0024 | g0010 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01243 | hp2 | a0001 | c0001 | t0031 | g0231 | AMR | PUR | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01255 | hp1 | a0001 | c0002 | t0006 | g0162 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01255 | hp2 | a0001 | c0001 | t0077 | g0102 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01257 | hp1 | a0001 | c0001 | t0027 | g0232 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01258 | hp1 | a0001 | c0002 | t0006 | g0187 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01346 | hp1 | a0001 | c0002 | t0004 | g0274 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01346 | hp2 | a0001 | c0002 | t0006 | g0167 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01361 | hp2 | a0001 | c0001 | t0028 | g0229 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01496 | hp1 | a0001 | c0001 | t0042 | g0246 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01496 | hp2 | a0001 | c0002 | t0055 | g0236 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0091 | EUR | IBS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01515 | hp2 | a0001 | c0002 | t0004 | g0259 | EUR | IBS | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01884 | hp1 | a0001 | c0001 | t0070 | g0049 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01884 | hp2 | a0001 | c0001 | t0031 | g0213 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01891 | hp1 | a0001 | c0002 | t0111 | g0043 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01891 | hp2 | a0001 | c0001 | t0104 | g0285 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01934 | hp1 | a0001 | c0002 | t0056 | g0017 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01934 | hp2 | a0001 | c0001 | t0014 | g0205 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01952 | hp1 | a0001 | c0001 | t0087 | g0001 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01952 | hp2 | a0001 | c0002 | t0006 | g0161 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01975 | hp1 | a0001 | c0002 | t0004 | g0261 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01975 | hp2 | a0001 | c0001 | t0014 | g0027 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01978 | hp1 | a0001 | c0002 | t0004 | g0277 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01978 | hp2 | a0001 | c0001 | t0016 | g0016 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01981 | hp1 | a0001 | c0001 | t0016 | g0016 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0062 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01993 | hp2 | a0001 | c0001 | t0050 | g0044 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02004 | hp1 | a0001 | c0002 | t0054 | g0045 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02004 | hp2 | a0001 | c0001 | t0014 | g0027 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02055 | hp1 | a0001 | c0002 | t0058 | g0037 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02055 | hp2 | a0001 | c0002 | t0060 | g0226 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02056 | hp1 | a0001 | c0002 | t0112 | g0254 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02071 | hp2 | a0001 | c0002 | t0040 | g0255 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02129 | hp1 | a0001 | c0001 | t0102 | g0174 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02145 | hp1 | a0001 | c0002 | t0100 | g0070 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02145 | hp2 | a0001 | c0001 | t0025 | g0293 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02148 | hp1 | a0001 | c0001 | t0016 | g0279 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02148 | hp2 | a0001 | c0002 | t0034 | g0017 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CDX | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CDX | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02257 | hp1 | a0001 | c0002 | t0015 | g0018 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02273 | hp2 | a0001 | c0001 | t0016 | g0016 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02280 | hp1 | a0001 | c0002 | t0007 | g0215 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02280 | hp2 | a0001 | c0002 | t0027 | g0249 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02300 | hp1 | a0001 | c0002 | t0034 | g0046 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02300 | hp2 | a0001 | c0001 | t0014 | g0184 | AMR | PEL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02451 | hp1 | a0001 | c0002 | t0035 | g0227 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02451 | hp2 | a0001 | c0001 | t0069 | g0103 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02523 | hp2 | a0001 | c0001 | t0078 | g0047 | EAS | KHV | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02572 | hp1 | a0001 | c0002 | t0053 | g0225 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02572 | hp2 | a0001 | c0002 | t0036 | g0241 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02602 | hp1 | a0001 | c0001 | t0011 | g0034 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02602 | hp2 | a0001 | c0002 | t0119 | g0010 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02615 | hp2 | a0001 | c0002 | t0007 | g0220 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02622 | hp1 | a0001 | c0001 | t0017 | g0035 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02622 | hp2 | a0001 | c0002 | t0018 | g0294 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02630 | hp1 | a0001 | c0001 | t0030 | g0039 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02630 | hp2 | a0001 | c0002 | t0019 | g0038 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02647 | hp1 | a0001 | c0002 | t0064 | g0239 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02647 | hp2 | a0001 | c0002 | t0057 | g0242 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0100 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02723 | hp1 | a0001 | c0001 | t0029 | g0243 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02723 | hp2 | a0001 | c0001 | t0029 | g0245 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02735 | hp1 | a0001 | c0001 | t0084 | g0060 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02735 | hp2 | a0001 | c0001 | t0105 | g0282 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0008 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02886 | hp1 | a0001 | c0002 | t0020 | g0015 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0278 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02895 | hp2 | a0001 | c0001 | t0038 | g0042 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0005 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02896 | hp2 | a0001 | c0001 | t0046 | g0216 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02897 | hp1 | a0001 | c0001 | t0038 | g0042 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0286 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02922 | hp1 | a0001 | c0002 | t0019 | g0238 | AFR | ESN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02922 | hp2 | a0001 | c0001 | t0094 | g0059 | AFR | ESN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02970 | hp1 | a0001 | c0001 | t0047 | g0251 | AFR | ESN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | ESN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02976 | hp1 | a0001 | c0001 | t0041 | g0218 | AFR | ESN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02976 | hp2 | a0001 | c0002 | t0020 | g0224 | AFR | ESN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03017 | hp1 | a0001 | c0002 | t0120 | g0275 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03041 | hp1 | a0001 | c0001 | t0045 | g0094 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03041 | hp2 | a0001 | c0002 | t0114 | g0288 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03098 | hp1 | a0001 | c0002 | t0061 | g0257 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03098 | hp2 | a0001 | c0001 | t0107 | g0005 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03130 | hp1 | a0001 | c0002 | t0019 | g0038 | AFR | ESN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03130 | hp2 | a0001 | c0001 | t0017 | g0217 | AFR | ESN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03195 | hp1 | a0001 | c0001 | t0030 | g0039 | AFR | ESN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03195 | hp2 | a0001 | c0001 | t0067 | g0006 | AFR | ESN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03209 | hp1 | a0001 | c0002 | t0109 | g0290 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03209 | hp2 | a0001 | c0002 | t0035 | g0037 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03225 | hp1 | a0001 | c0002 | t0015 | g0050 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03225 | hp2 | a0001 | c0001 | t0044 | g0258 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03239 | hp1 | a0001 | c0001 | t0021 | g0082 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03239 | hp2 | a0001 | c0001 | t0021 | g0101 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03453 | hp1 | a0001 | c0002 | t0063 | g0240 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03453 | hp2 | a0001 | c0002 | t0033 | g0212 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03486 | hp1 | a0001 | c0002 | t0015 | g0051 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03486 | hp2 | a0001 | c0002 | t0020 | g0222 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | ESN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03516 | hp2 | a0001 | c0002 | t0036 | g0015 | AFR | ESN | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03540 | hp1 | a0001 | c0002 | t0007 | g0250 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03540 | hp2 | a0001 | c0002 | t0039 | g0043 | AFR | GWD | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03579 | hp1 | a0001 | c0002 | t0115 | g0295 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03579 | hp2 | a0001 | c0001 | t0073 | g0206 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | STU | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03704 | hp1 | a0001 | c0001 | t0011 | g0013 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03704 | hp2 | a0001 | c0002 | t0099 | g0096 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03710 | hp2 | a0001 | c0002 | t0097 | g0071 | SAS | PJL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03831 | hp1 | a0001 | c0001 | t0071 | g0052 | SAS | BEB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | BEB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03834 | hp2 | a0001 | c0002 | t0018 | g0233 | SAS | BEB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03927 | hp1 | a0001 | c0001 | t0086 | g0201 | SAS | BEB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0072 | SAS | BEB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03942 | hp1 | a0001 | c0002 | t0118 | g0281 | SAS | BEB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | BEB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG04115 | hp1 | a0001 | c0001 | t0074 | g0164 | SAS | STU | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG04115 | hp2 | a0001 | c0002 | t0052 | g0237 | SAS | STU | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG04204 | hp1 | a0001 | c0002 | t0095 | g0048 | SAS | STU | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG04204 | hp2 | a0001 | c0001 | t0088 | g0077 | SAS | STU | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | STU | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG04228 | hp2 | a0001 | c0001 | t0068 | g0080 | SAS | STU | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18522 | hp1 | a0001 | c0002 | t0015 | g0018 | AFR | YRI | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18522 | hp2 | a0001 | c0002 | t0113 | g0291 | AFR | YRI | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18612 | hp2 | a0001 | c0001 | t0108 | g0270 | EAS | CHB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18906 | hp1 | a0001 | c0001 | t0049 | g0214 | AFR | YRI | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18906 | hp2 | a0001 | c0001 | t0082 | g0006 | AFR | YRI | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18939 | hp2 | a0001 | c0002 | t0004 | g0267 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18942 | hp1 | a0001 | c0001 | t0090 | g0110 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18943 | hp1 | a0001 | c0001 | t0091 | g0194 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18943 | hp2 | a0001 | c0001 | t0008 | g0271 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18944 | hp2 | a0001 | c0002 | t0004 | g0009 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18947 | hp1 | a0001 | c0002 | t0018 | g0234 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18947 | hp2 | a0002 | c0003 | t0001 | g0029 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18949 | hp2 | a0002 | c0003 | t0011 | g0029 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18952 | hp2 | a0001 | c0002 | t0004 | g0009 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18962 | hp1 | a0001 | c0002 | t0004 | g0009 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18963 | hp1 | a0001 | c0002 | t0004 | g0266 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18965 | hp2 | a0001 | c0002 | t0004 | g0260 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18968 | hp1 | a0001 | c0001 | t0012 | g0122 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18970 | hp1 | a0001 | c0001 | t0037 | g0003 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18975 | hp1 | a0001 | c0001 | t0012 | g0138 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18977 | hp2 | a0001 | c0001 | t0075 | g0191 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18980 | hp1 | a0001 | c0002 | t0101 | g0032 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18980 | hp2 | a0001 | c0001 | t0022 | g0150 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18983 | hp1 | a0001 | c0001 | t0081 | g0117 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18989 | hp1 | a0001 | c0001 | t0079 | g0189 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18990 | hp2 | a0001 | c0002 | t0023 | g0040 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18993 | hp1 | a0001 | c0002 | t0006 | g0032 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18993 | hp2 | a0001 | c0001 | t0012 | g0121 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18994 | hp1 | a0001 | c0002 | t0004 | g0262 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18999 | hp1 | a0001 | c0001 | t0013 | g0025 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA18999 | hp2 | a0001 | c0002 | t0006 | g0079 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19007 | hp2 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19010 | hp1 | a0001 | c0001 | t0080 | g0014 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19010 | hp2 | a0001 | c0002 | t0024 | g0009 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0264 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19011 | hp2 | a0001 | c0002 | t0006 | g0074 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19030 | hp1 | a0001 | c0002 | t0110 | g0287 | AFR | LWK | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19030 | hp2 | a0001 | c0002 | t0066 | g0248 | AFR | LWK | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19043 | hp1 | a0001 | c0002 | t0032 | g0256 | AFR | LWK | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19043 | hp2 | a0001 | c0002 | t0007 | g0211 | AFR | LWK | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19054 | hp1 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19055 | hp2 | a0001 | c0002 | t0006 | g0078 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19057 | hp1 | a0001 | c0002 | t0023 | g0273 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19060 | hp2 | a0001 | c0001 | t0089 | g0093 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19062 | hp2 | a0001 | c0001 | t0022 | g0203 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19064 | hp1 | a0001 | c0001 | t0037 | g0118 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19067 | hp1 | a0001 | c0001 | t0013 | g0113 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19074 | hp1 | a0001 | c0001 | t0012 | g0111 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19075 | hp2 | a0001 | c0001 | t0103 | g0276 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19077 | hp2 | a0001 | c0002 | t0116 | g0253 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19079 | hp1 | a0001 | c0001 | t0092 | g0200 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19083 | hp1 | a0001 | c0002 | t0023 | g0040 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19086 | hp1 | a0001 | c0002 | t0004 | g0263 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19086 | hp2 | a0001 | c0001 | t0013 | g0134 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19087 | hp1 | a0001 | c0002 | t0006 | g0182 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19240 | hp1 | a0001 | c0001 | t0043 | g0210 | AFR | YRI | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | YRI | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA20129 | hp1 | a0001 | c0002 | t0062 | g0228 | AFR | ASW | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | ASW | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0089 | EUR | TSI | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0011 | EUR | TSI | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA20805 | hp1 | a0001 | c0001 | t0106 | g0041 | EUR | TSI | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | GIH | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA20905 | hp2 | a0001 | c0001 | t0072 | g0034 | SAS | GIH | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG01123 | hp2 | a0001 | c0002 | t0004 | g0283 | AMR | CLM | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02109 | hp2 | a0001 | c0002 | t0004 | g0010 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02486 | hp1 | a0001 | c0002 | t0059 | g0221 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02486 | hp2 | a0001 | c0001 | t0048 | g0219 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02559 | hp1 | a0001 | c0001 | t0017 | g0035 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG02559 | hp2 | a0001 | c0002 | t0065 | g0015 | AFR | ACB | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03471 | hp1 | a0001 | c0002 | t0007 | g0223 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | MSL | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG06807 | hp1 | a0001 | c0001 | t0093 | g0055 | AFR | USA | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0269 | AFR | USA | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA20300 | hp1 | a0001 | c0002 | t0006 | g0163 | AFR | USA | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA20300 | hp2 | a0001 | c0001 | t0025 | g0292 | AFR | USA | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0008 | AFR | LWK | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| NA21309 | hp2 | a0001 | c0002 | t0051 | g0244 | AFR | LWK | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0190 | REF | REF | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | TNFAIP8_chr5_119351019_119404688 | TNFAIP8 | chr5 | 119351019 | 119404688 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:119393079 | A | T | 1 | a0002 | 2 | NA18947.hp2 NA18949.hp2 |
missense_variant | MODERATE | c.295A>T | p.Met99Leu | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 367/6976 | 295/597 | 99/198 | chr5 | 119393079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:119393258 | G | C | 1 | a0001c0002 | 103 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
synonymous_variant | LOW | c.474G>C | p.Val158Val | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 546/6976 | 474/597 | 158/198 | chr5 | 119393258 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:119356042 | C | G | 27 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0016 others(24): Show |
62 | HG00408.hp1 HG00408.hp2 HG00642.hp2 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-49C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/2 | 49 | chr5 | 119356042 | ||||||
| chr5:119356050 | T | C | 1 | a0001c0001t0025 | 2 | HG02145.hp2 NA20300.hp2 |
5_prime_UTR_variant | MODIFIER | c.-41T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/2 | 41 | chr5 | 119356050 | ||||||
| chr5:119356066 | C | T | 1 | a0001c0001t0102 | 1 | HG02129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/2 | 25 | chr5 | 119356066 | ||||||
| chr5:119356089 | T | C | 72 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0010 others(69): Show |
133 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
5_prime_UTR_variant | MODIFIER | c.-2T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/2 | 2 | chr5 | 119356089 | ||||||
| chr5:119393591 | C | T | 49 | a0001c0002t0004 a0001c0002t0006 a0001c0002t0007 others(46): Show |
99 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*210C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 210 | chr5 | 119393591 | ||||||
| chr5:119393632 | A | G | 52 | a0001c0001t0050 a0001c0002t0004 a0001c0002t0006 others(49): Show |
103 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*251A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 251 | chr5 | 119393632 | ||||||
| chr5:119393693 | A | G | 39 | a0001c0001t0050 a0001c0002t0004 a0001c0002t0006 others(36): Show |
87 | HG00280.hp1 HG00408.hp1 HG00642.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*312A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 312 | chr5 | 119393693 | ||||||
| chr5:119393775 | A | G | 1 | a0001c0001t0094 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*394A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 394 | chr5 | 119393775 | ||||||
| chr5:119393995 | G | A | 1 | a0001c0002t0032 | 2 | HG00639.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*614G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 614 | chr5 | 119393995 | ||||||
| chr5:119394142 | A | T | 1 | a0001c0001t0093 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*761A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 761 | chr5 | 119394142 | ||||||
| chr5:119394179 | G | A | 26 | a0001c0001t0050 a0001c0002t0007 a0001c0002t0015 others(23): Show |
43 | HG00280.hp1 HG00741.hp2 HG01496.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*798G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 798 | chr5 | 119394179 | ||||||
| chr5:119394233 | TAAC | T | 4 | a0001c0002t0036 a0001c0002t0063 a0001c0002t0064 others(1): Show |
5 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*855_*857delCAA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 855 | INFO_REALIGN_3_PRIME | chr5 | 119394233 | |||||
| chr5:119394386 | T | C | 2 | a0001c0001t0026 a0001c0001t0041 |
3 | HG01069.hp1 HG01071.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1005T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1005 | chr5 | 119394386 | ||||||
| chr5:119394452 | T | G | 3 | a0001c0001t0042 a0001c0001t0043 a0001c0001t0044 |
3 | HG01496.hp1 HG03225.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1071T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1071 | chr5 | 119394452 | ||||||
| chr5:119394471 | A | T | 2 | a0001c0001t0043 a0001c0001t0044 |
2 | HG03225.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1090A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1090 | chr5 | 119394471 | ||||||
| chr5:119394475 | T | C | 1 | a0001c0001t0103 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1094T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1094 | chr5 | 119394475 | ||||||
| chr5:119394609 | T | C | 1 | a0001c0002t0052 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1228T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1228 | chr5 | 119394609 | ||||||
| chr5:119394611 | A | AT | 24 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0013 others(21): Show |
95 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1249dupT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATT | 6 | a0001c0001t0030 a0001c0001t0037 a0001c0001t0042 others(3): Show |
9 | HG00639.hp2 HG01496.hp1 HG02630.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1248_*1249dupTT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTT | 11 | a0001c0002t0004 a0001c0002t0006 a0001c0002t0023 others(8): Show |
41 | HG00408.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1246_*1249dupTTTT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTT | 4 | a0001c0002t0024 a0001c0002t0066 a0001c0002t0100 others(1): Show |
6 | HG01109.hp1 HG01175.hp2 HG02145.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1245_*1249dupTTTT others(1): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(6): Show |
1 | a0001c0002t0053 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1237_*1249dupTTTT others(9): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(12): Show |
1 | a0001c0001t0031 | 2 | HG01243.hp2 HG01884.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1231_*1249dupTTTT others(15): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(13): Show |
2 | a0001c0001t0048 a0001c0001t0049 |
2 | HG02486.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(16): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(17): Show |
4 | a0001c0001t0041 a0001c0001t0050 a0001c0002t0018 others(1): Show |
6 | HG01993.hp2 HG02004.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(20): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(18): Show |
4 | a0001c0001t0026 a0001c0002t0033 a0001c0002t0034 others(1): Show |
7 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(21): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(19): Show |
2 | a0001c0002t0052 a0001c0002t0056 |
2 | HG01934.hp1 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(22): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(20): Show |
1 | a0001c0002t0096 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(23): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(21): Show |
1 | a0001c0002t0057 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(24): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(22): Show |
3 | a0001c0002t0019 a0001c0002t0063 a0001c0002t0064 |
5 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(25): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(23): Show |
1 | a0001c0002t0036 | 2 | HG02572.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(26): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(24): Show |
3 | a0001c0002t0015 a0001c0002t0020 a0001c0002t0035 |
9 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(27): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(25): Show |
2 | a0001c0002t0007 a0001c0002t0058 |
6 | HG02055.hp1 HG02280.hp1 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(28): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(26): Show |
1 | a0001c0002t0059 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(29): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(27): Show |
2 | a0001c0002t0060 a0001c0002t0061 |
2 | HG02055.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(30): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(29): Show |
2 | a0001c0002t0062 a0001c0002t0065 |
2 | HG02559.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(32): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394611 | A | ATTTTTTT others(31): Show |
1 | a0001c0002t0097 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1249_*1250insTTTT others(34): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1250 | INFO_REALIGN_3_PRIME | chr5 | 119394611 | |||||
| chr5:119394689 | C | T | 4 | a0001c0002t0040 a0001c0002t0095 a0001c0002t0112 others(1): Show |
5 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1308C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1308 | chr5 | 119394689 | ||||||
| chr5:119394756 | A | G | 26 | a0001c0001t0050 a0001c0002t0007 a0001c0002t0015 others(23): Show |
43 | HG00280.hp1 HG00741.hp2 HG01496.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1375A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1375 | chr5 | 119394756 | ||||||
| chr5:119394900 | C | T | 17 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0012 others(14): Show |
92 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*1519C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1519 | chr5 | 119394900 | ||||||
| chr5:119394909 | T | C | 1 | a0001c0001t0012 | 4 | NA18968.hp1 NA18975.hp1 NA18993.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1528T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1528 | chr5 | 119394909 | ||||||
| chr5:119394916 | C | T | 1 | a0001c0001t0088 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1535C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1535 | chr5 | 119394916 | ||||||
| chr5:119395072 | C | G | 2 | a0001c0002t0035 a0001c0002t0058 |
3 | HG02055.hp1 HG02451.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1691C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1691 | chr5 | 119395072 | ||||||
| chr5:119395172 | G | A | 72 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0021 others(69): Show |
182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*1791G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1791 | chr5 | 119395172 | ||||||
| chr5:119395214 | C | G | 1 | a0001c0001t0071 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1833C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1833 | chr5 | 119395214 | ||||||
| chr5:119395302 | C | T | 1 | a0001c0002t0055 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1921C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1921 | chr5 | 119395302 | ||||||
| chr5:119395372 | A | C | 77 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0016 others(74): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*1991A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 1991 | chr5 | 119395372 | ||||||
| chr5:119395425 | C | G | 4 | a0001c0002t0040 a0001c0002t0095 a0001c0002t0112 others(1): Show |
5 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2044C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 2044 | chr5 | 119395425 | ||||||
| chr5:119395498 | C | T | 1 | a0001c0001t0070 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2117C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 2117 | chr5 | 119395498 | ||||||
| chr5:119395552 | T | G | 77 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0016 others(74): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*2171T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 2171 | chr5 | 119395552 | ||||||
| chr5:119395578 | A | C | 19 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0016 others(16): Show |
80 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*2197A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 2197 | chr5 | 119395578 | ||||||
| chr5:119396078 | G | C | 1 | a0001c0001t0071 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2697G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 2697 | chr5 | 119396078 | ||||||
| chr5:119396156 | A | G | 1 | a0001c0001t0042 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2775A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 2775 | chr5 | 119396156 | ||||||
| chr5:119396243 | T | C | 36 | a0001c0001t0031 a0001c0001t0048 a0001c0001t0049 others(33): Show |
56 | HG00280.hp1 HG00408.hp2 HG00741.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2862T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 2862 | chr5 | 119396243 | ||||||
| chr5:119396294 | C | T | 2 | a0001c0001t0079 a0001c0001t0080 |
2 | NA18989.hp1 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2913C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 2913 | chr5 | 119396294 | ||||||
| chr5:119396398 | C | G | 1 | a0001c0002t0109 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3017C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3017 | chr5 | 119396398 | ||||||
| chr5:119396414 | C | T | 2 | a0001c0002t0099 a0001c0002t0120 |
2 | HG03017.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3033C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3033 | chr5 | 119396414 | ||||||
| chr5:119396416 | A | G | 1 | a0001c0001t0092 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3035A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3035 | chr5 | 119396416 | ||||||
| chr5:119396492 | C | G | 56 | a0001c0001t0026 a0001c0001t0038 a0001c0001t0041 others(53): Show |
108 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3111C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3111 | chr5 | 119396492 | ||||||
| chr5:119396633 | GT | G | 33 | a0001c0001t0050 a0001c0002t0007 a0001c0002t0015 others(30): Show |
52 | HG00280.hp1 HG00408.hp2 HG00741.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*3254delT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3254 | INFO_REALIGN_3_PRIME | chr5 | 119396633 | |||||
| chr5:119396657 | C | G | 1 | a0001c0001t0042 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3276C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3276 | chr5 | 119396657 | ||||||
| chr5:119396678 | T | C | 29 | a0001c0001t0050 a0001c0002t0007 a0001c0002t0015 others(26): Show |
47 | HG00280.hp1 HG00741.hp2 HG01106.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3297T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3297 | chr5 | 119396678 | ||||||
| chr5:119396689 | A | G | 15 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0012 others(12): Show |
87 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*3308A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3308 | chr5 | 119396689 | ||||||
| chr5:119396908 | C | T | 1 | a0001c0001t0078 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3527C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3527 | chr5 | 119396908 | ||||||
| chr5:119396956 | T | C | 1 | a0001c0002t0032 | 2 | HG00639.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3575T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3575 | chr5 | 119396956 | ||||||
| chr5:119396981 | C | T | 1 | a0001c0001t0091 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3600C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3600 | chr5 | 119396981 | ||||||
| chr5:119396994 | C | CA | 28 | a0001c0001t0011 a0001c0001t0050 a0001c0001t0072 others(25): Show |
47 | HG00280.hp1 HG00741.hp2 HG01496.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3636dupA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3637 | INFO_REALIGN_3_PRIME | chr5 | 119396994 | |||||
| chr5:119396994 | CA | C | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(46): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*3636delA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3636 | INFO_REALIGN_3_PRIME | chr5 | 119396994 | |||||
| chr5:119396994 | CAA | C | 14 | a0001c0001t0009 a0001c0001t0021 a0001c0001t0031 others(11): Show |
24 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3635_*3636delAA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3635 | INFO_REALIGN_3_PRIME | chr5 | 119396994 | |||||
| chr5:119397036 | G | A | 2 | a0001c0001t0045 a0001c0001t0093 |
2 | HG03041.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3655G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3655 | chr5 | 119397036 | ||||||
| chr5:119397082 | C | A | 15 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0012 others(12): Show |
88 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*3701C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3701 | chr5 | 119397082 | ||||||
| chr5:119397126 | T | TAC | 13 | a0001c0001t0028 a0001c0001t0029 a0001c0001t0042 others(10): Show |
16 | HG01109.hp2 HG01361.hp2 HG01496.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3771_*3772dupCA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3773 | INFO_REALIGN_3_PRIME | chr5 | 119397126 | |||||
| chr5:119397126 | TAC | T | 34 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(31): Show |
99 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*3771_*3772delCA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3771 | INFO_REALIGN_3_PRIME | chr5 | 119397126 | |||||
| chr5:119397126 | TACAC | T | 16 | a0001c0001t0026 a0001c0001t0041 a0001c0001t0077 others(13): Show |
46 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*3769_*3772delCACA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3769 | INFO_REALIGN_3_PRIME | chr5 | 119397126 | |||||
| chr5:119397126 | TACACACA others(3): Show |
T | 1 | a0001c0002t0110 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3763_*3772delCACA others(6): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3763 | INFO_REALIGN_3_PRIME | chr5 | 119397126 | |||||
| chr5:119397198 | G | C | 1 | a0001c0001t0043 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3817G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3817 | chr5 | 119397198 | ||||||
| chr5:119397223 | A | C | 1 | a0001c0002t0100 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3842A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 3842 | chr5 | 119397223 | ||||||
| chr5:119397769 | G | A | 2 | a0001c0001t0005 a0001c0001t0069 |
14 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4388G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 4388 | chr5 | 119397769 | ||||||
| chr5:119397895 | A | T | 1 | a0001c0001t0074 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4514A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 4514 | chr5 | 119397895 | ||||||
| chr5:119397911 | C | T | 2 | a0001c0002t0113 a0001c0002t0114 |
2 | HG03041.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4530C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 4530 | chr5 | 119397911 | ||||||
| chr5:119397968 | C | T | 3 | a0001c0002t0039 a0001c0002t0110 a0001c0002t0111 |
4 | HG01106.hp1 HG01891.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4587C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 4587 | chr5 | 119397968 | ||||||
| chr5:119398110 | G | C | 7 | a0001c0002t0039 a0001c0002t0040 a0001c0002t0095 others(4): Show |
9 | HG00408.hp2 HG01106.hp1 HG01891.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4729G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 4729 | chr5 | 119398110 | ||||||
| chr5:119398128 | A | G | 1 | a0001c0001t0042 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4747A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 4747 | chr5 | 119398128 | ||||||
| chr5:119398470 | C | G | 1 | a0001c0001t0068 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5089C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 5089 | chr5 | 119398470 | ||||||
| chr5:119398615 | G | A | 2 | a0001c0002t0035 a0001c0002t0058 |
3 | HG02055.hp1 HG02451.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5234G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 5234 | chr5 | 119398615 | ||||||
| chr5:119398712 | A | AAATAAAT others(337): Show |
1 | a0001c0001t0089 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5346_*5347insTTTT others(340): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 5347 | INFO_REALIGN_3_PRIME | chr5 | 119398712 | |||||
| chr5:119398765 | G | A | 4 | a0001c0001t0026 a0001c0001t0038 a0001c0001t0041 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5384G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 5384 | chr5 | 119398765 | ||||||
| chr5:119398863 | A | T | 1 | a0001c0001t0084 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5482A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 5482 | chr5 | 119398863 | ||||||
| chr5:119398867 | T | C | 2 | a0001c0001t0073 a0001c0001t0105 |
2 | HG02735.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5486T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 5486 | chr5 | 119398867 | ||||||
| chr5:119399006 | TCTC | T | 3 | a0001c0002t0039 a0001c0002t0110 a0001c0002t0111 |
4 | HG01106.hp1 HG01891.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5628_*5630delCCT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 5628 | INFO_REALIGN_3_PRIME | chr5 | 119399006 | |||||
| chr5:119399036 | A | G | 34 | a0001c0001t0050 a0001c0001t0107 a0001c0002t0007 others(31): Show |
53 | HG00280.hp1 HG00408.hp2 HG00741.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*5655A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 5655 | chr5 | 119399036 | ||||||
| chr5:119399186 | C | T | 4 | a0001c0002t0040 a0001c0002t0095 a0001c0002t0112 others(1): Show |
5 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5805C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 5805 | chr5 | 119399186 | ||||||
| chr5:119399360 | C | T | 4 | a0001c0001t0026 a0001c0001t0038 a0001c0001t0041 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5979C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 5979 | chr5 | 119399360 | ||||||
| chr5:119399412 | A | G | 102 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(99): Show |
293 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*6031A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 2/2 | 6031 | chr5 | 119399412 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:119356137 | C | T | 53 | a0001c0001t0008g0041 a0001c0001t0008g0264 a0001c0001t0008g0265 others(50): Show |
63 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.31+16C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356137 | |||||||
| chr5:119356193 | A | C | 110 | a0001c0001t0008g0041 a0001c0001t0008g0264 a0001c0001t0008g0265 others(107): Show |
127 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.31+72A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356193 | |||||||
| chr5:119356297 | T | C | 2 | a0001c0001t0044g0258 a0001c0002t0061g0257 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+176T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356297 | |||||||
| chr5:119356309 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.31+188C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356309 | |||||||
| chr5:119356523 | G | C | 244 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(241): Show |
287 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.31+402G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356523 | |||||||
| chr5:119356567 | G | A | 1 | a0001c0001t0043g0210 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.31+446G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356567 | |||||||
| chr5:119356606 | T | G | 2 | a0001c0002t0007g0211 a0001c0002t0033g0212 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.31+485T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356606 | |||||||
| chr5:119356672 | A | G | 1 | a0001c0001t0002g0026 | 2 | NA19007.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.31+551A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356672 | |||||||
| chr5:119356675 | T | C | 2 | a0001c0001t0031g0213 a0001c0001t0049g0214 |
2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.31+554T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356675 | |||||||
| chr5:119356760 | A | T | 129 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(126): Show |
155 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.31+639A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356760 | |||||||
| chr5:119356770 | A | G | 245 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(242): Show |
288 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.31+649A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356770 | |||||||
| chr5:119356777 | AG | A | 35 | a0001c0001t0008g0041 a0001c0001t0008g0264 a0001c0001t0008g0265 others(32): Show |
41 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.31+659delG | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119356777 | ||||||
| chr5:119356806 | A | G | 2 | a0001c0002t0032g0256 a0001c0002t0115g0295 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.31+685A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356806 | |||||||
| chr5:119356901 | A | G | 4 | a0001c0002t0040g0252 a0001c0002t0040g0255 a0001c0002t0112g0254 others(1): Show |
4 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+780A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356901 | |||||||
| chr5:119356917 | A | G | 117 | a0001c0001t0003g0207 a0001c0001t0008g0041 a0001c0001t0008g0264 others(114): Show |
134 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.31+796A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119356917 | |||||||
| chr5:119357007 | G | A | 1 | a0001c0001t0076g0152 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.31+886G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119357007 | |||||||
| chr5:119357361 | T | C | 58 | a0001c0001t0010g0008 a0001c0001t0017g0035 a0001c0001t0017g0217 others(55): Show |
65 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.31+1240T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119357361 | |||||||
| chr5:119357504 | T | C | 111 | a0001c0001t0008g0041 a0001c0001t0008g0264 a0001c0001t0008g0265 others(108): Show |
128 | HG00280.hp1 HG00408.hp1 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.31+1383T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119357504 | |||||||
| chr5:119357592 | A | C | 111 | a0001c0001t0008g0041 a0001c0001t0008g0264 a0001c0001t0008g0265 others(108): Show |
128 | HG00280.hp1 HG00408.hp1 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.31+1471A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119357592 | |||||||
| chr5:119357840 | A | G | 1 | a0001c0002t0018g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+1719A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119357840 | |||||||
| chr5:119358094 | C | T | 2 | a0001c0001t0025g0292 a0001c0001t0025g0293 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.31+1973C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358094 | |||||||
| chr5:119358099 | C | CT | 57 | a0001c0001t0010g0008 a0001c0001t0014g0205 a0001c0001t0027g0232 others(54): Show |
62 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.31+1993dupT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119358099 | ||||||
| chr5:119358099 | CT | C | 133 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(130): Show |
159 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.31+1993delT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119358099 | ||||||
| chr5:119358116 | A | G | 6 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0026g0036 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.31+1995A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358116 | |||||||
| chr5:119358139 | A | G | 1 | a0001c0001t0047g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31+2018A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358139 | |||||||
| chr5:119358185 | A | G | 2 | a0001c0001t0044g0258 a0001c0002t0061g0257 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+2064A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358185 | |||||||
| chr5:119358194 | C | G | 6 | a0001c0002t0004g0009 a0001c0002t0004g0260 a0001c0002t0004g0261 others(3): Show |
8 | HG01975.hp1 NA18944.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.31+2073C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358194 | |||||||
| chr5:119358219 | G | A | 2 | a0001c0001t0044g0258 a0001c0002t0061g0257 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+2098G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358219 | |||||||
| chr5:119358263 | G | T | 1 | a0001c0002t0113g0291 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.31+2142G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358263 | |||||||
| chr5:119358391 | C | T | 2 | a0001c0001t0025g0292 a0001c0001t0025g0293 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.31+2270C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358391 | |||||||
| chr5:119358409 | A | G | 1 | a0001c0001t0002g0148 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.31+2288A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358409 | |||||||
| chr5:119358504 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.31+2383G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358504 | |||||||
| chr5:119358547 | T | A | 4 | a0001c0002t0040g0252 a0001c0002t0040g0255 a0001c0002t0112g0254 others(1): Show |
4 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+2426T>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358547 | |||||||
| chr5:119358559 | A | G | 2 | a0001c0001t0044g0258 a0001c0002t0061g0257 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+2438A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358559 | |||||||
| chr5:119358682 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.31+2561T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358682 | |||||||
| chr5:119358893 | C | T | 6 | a0001c0001t0042g0246 a0001c0002t0007g0250 a0001c0002t0027g0249 others(3): Show |
6 | HG00639.hp2 HG01496.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.31+2772C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358893 | |||||||
| chr5:119358921 | A | T | 4 | a0001c0002t0040g0252 a0001c0002t0040g0255 a0001c0002t0112g0254 others(1): Show |
4 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+2800A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358921 | |||||||
| chr5:119358934 | C | T | 2 | a0001c0001t0031g0213 a0001c0001t0049g0214 |
2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.31+2813C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358934 | |||||||
| chr5:119358975 | T | C | 59 | a0001c0001t0010g0008 a0001c0001t0017g0035 a0001c0001t0017g0217 others(56): Show |
66 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.31+2854T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119358975 | |||||||
| chr5:119359019 | C | T | 2 | a0001c0001t0044g0258 a0001c0002t0061g0257 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+2898C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119359019 | |||||||
| chr5:119359215 | A | G | 1 | a0001c0001t0047g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31+3094A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119359215 | |||||||
| chr5:119359292 | A | G | 1 | a0001c0002t0018g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+3171A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119359292 | |||||||
| chr5:119359356 | G | A | 54 | a0001c0001t0008g0041 a0001c0001t0008g0264 a0001c0001t0008g0265 others(51): Show |
64 | HG00408.hp1 HG00408.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.31+3235G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119359356 | |||||||
| chr5:119359465 | C | T | 1 | a0001c0002t0007g0250 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31+3344C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119359465 | |||||||
| chr5:119359556 | C | CA | 54 | a0001c0001t0001g0156 a0001c0001t0008g0041 a0001c0001t0008g0264 others(51): Show |
64 | HG00408.hp1 HG00408.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.31+3447dupA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119359556 | ||||||
| chr5:119359668 | T | A | 13 | a0001c0001t0048g0219 a0001c0002t0007g0215 a0001c0002t0007g0220 others(10): Show |
13 | HG02055.hp1 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.31+3547T>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119359668 | |||||||
| chr5:119359884 | G | A | 56 | a0001c0001t0008g0041 a0001c0001t0008g0264 a0001c0001t0008g0265 others(53): Show |
66 | HG00408.hp1 HG00408.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.31+3763G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119359884 | |||||||
| chr5:119359947 | A | G | 1 | a0001c0001t0003g0147 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.31+3826A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119359947 | |||||||
| chr5:119359979 | A | G | 6 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0026g0036 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.31+3858A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119359979 | |||||||
| chr5:119360002 | A | C | 1 | a0001c0001t0003g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.31+3881A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119360002 | |||||||
| chr5:119360102 | A | G | 53 | a0001c0001t0001g0130 a0001c0001t0001g0135 a0001c0001t0002g0003 others(50): Show |
64 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.31+3981A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119360102 | |||||||
| chr5:119360141 | C | G | 1 | a0001c0002t0062g0228 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.31+4020C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119360141 | |||||||
| chr5:119360141 | C | T | 130 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(127): Show |
156 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.31+4020C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119360141 | |||||||
| chr5:119360544 | T | A | 44 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0026g0036 others(41): Show |
47 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.31+4423T>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119360544 | |||||||
| chr5:119360599 | A | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0202 a0001c0001t0001g0204 others(2): Show |
8 | NA18942.hp2 NA18961.hp1 NA19006.hp2 others(5): Show |
intron_variant | MODIFIER | c.31+4478A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119360599 | |||||||
| chr5:119360654 | C | T | 8 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0100 others(5): Show |
12 | HG00738.hp2 HG00741.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.31+4533C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119360654 | |||||||
| chr5:119360696 | A | G | 2 | a0001c0001t0005g0104 a0001c0001t0069g0103 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.31+4575A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119360696 | |||||||
| chr5:119360736 | A | AGTAGGAC others(193): Show |
1 | a0001c0002t0004g0284 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.31+4620_31+4819dup others(200): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119360736 | ||||||
| chr5:119360800 | C | T | 53 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0026g0036 others(50): Show |
56 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.31+4679C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119360800 | |||||||
| chr5:119361123 | A | G | 1 | a0001c0002t0057g0242 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.31+5002A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119361123 | |||||||
| chr5:119361181 | C | G | 1 | a0001c0001t0002g0145 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.31+5060C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119361181 | |||||||
| chr5:119361211 | A | G | 5 | a0001c0001t0003g0023 a0001c0001t0003g0097 a0001c0001t0003g0098 others(2): Show |
6 | HG00423.hp2 HG00673.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.31+5090A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119361211 | |||||||
| chr5:119361216 | C | T | 116 | a0001c0001t0008g0041 a0001c0001t0008g0265 a0001c0001t0008g0271 others(113): Show |
133 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.31+5095C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119361216 | |||||||
| chr5:119361223 | G | T | 1 | a0001c0001t0005g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.31+5102G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119361223 | |||||||
| chr5:119361230 | A | C | 1 | a0001c0001t0002g0143 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.31+5109A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119361230 | |||||||
| chr5:119361233 | G | GC | 55 | a0001c0001t0008g0041 a0001c0001t0008g0271 a0001c0001t0008g0278 others(52): Show |
65 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.31+5119dupC | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119361233 | ||||||
| chr5:119361582 | A | G | 3 | a0001c0001t0011g0034 a0001c0001t0072g0034 a0001c0001t0086g0201 |
3 | HG02602.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.31+5461A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119361582 | |||||||
| chr5:119361628 | G | T | 1 | a0001c0001t0089g0093 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.31+5507G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119361628 | |||||||
| chr5:119361632 | C | G | 1 | a0001c0001t0086g0201 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.31+5511C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119361632 | |||||||
| chr5:119361658 | T | C | 1 | a0001c0001t0002g0105 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.31+5537T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119361658 | |||||||
| chr5:119361733 | C | T | 2 | a0001c0002t0027g0249 a0001c0002t0066g0248 |
2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.31+5612C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119361733 | |||||||
| chr5:119362018 | G | A | 1 | a0001c0002t0007g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31+5897G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362018 | |||||||
| chr5:119362022 | C | G | 1 | a0001c0002t0109g0290 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.31+5901C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362022 | |||||||
| chr5:119362151 | C | T | 1 | a0001c0002t0007g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31+6030C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362151 | |||||||
| chr5:119362154 | A | G | 242 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(239): Show |
285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.31+6033A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362154 | |||||||
| chr5:119362336 | A | G | 1 | a0001c0001t0021g0101 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.31+6215A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362336 | |||||||
| chr5:119362402 | C | A | 2 | a0001c0001t0025g0292 a0001c0001t0025g0293 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.31+6281C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362402 | |||||||
| chr5:119362456 | C | T | 2 | a0001c0001t0043g0210 a0001c0001t0044g0258 |
2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.31+6335C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362456 | |||||||
| chr5:119362470 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.31+6349T>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362470 | |||||||
| chr5:119362514 | G | A | 5 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0100 others(2): Show |
9 | HG00738.hp2 HG00741.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+6393G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362514 | |||||||
| chr5:119362620 | A | ACC | 47 | a0001c0001t0008g0041 a0001c0001t0008g0265 a0001c0001t0008g0271 others(44): Show |
57 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.31+6504_31+6505dup others(2): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119362620 | ||||||
| chr5:119362746 | C | T | 59 | a0001c0001t0003g0092 a0001c0001t0010g0008 a0001c0001t0017g0035 others(56): Show |
66 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.31+6625C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362746 | |||||||
| chr5:119362757 | A | G | 2 | a0001c0002t0039g0043 a0001c0002t0111g0043 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.31+6636A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362757 | |||||||
| chr5:119362791 | C | CA | 14 | a0001c0001t0002g0024 a0001c0001t0002g0106 a0001c0001t0002g0107 others(11): Show |
16 | HG00408.hp2 HG00621.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.31+6683dupA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119362791 | ||||||
| chr5:119362791 | CA | C | 36 | a0001c0001t0003g0092 a0001c0001t0027g0232 a0001c0001t0031g0231 others(33): Show |
37 | HG00280.hp1 HG00741.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.31+6683delA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119362791 | ||||||
| chr5:119362888 | C | A | 60 | a0001c0001t0003g0092 a0001c0001t0010g0008 a0001c0001t0017g0035 others(57): Show |
68 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.31+6767C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362888 | |||||||
| chr5:119362914 | T | A | 45 | a0001c0001t0003g0092 a0001c0001t0017g0035 a0001c0001t0017g0217 others(42): Show |
49 | HG00280.hp1 HG00741.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+6793T>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362914 | |||||||
| chr5:119362933 | C | A | 1 | a0001c0002t0004g0267 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.31+6812C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119362933 | |||||||
| chr5:119363303 | T | C | 116 | a0001c0001t0003g0092 a0001c0001t0008g0041 a0001c0001t0008g0265 others(113): Show |
133 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.31+7182T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119363303 | |||||||
| chr5:119363413 | A | C | 129 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(126): Show |
155 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.31+7292A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119363413 | |||||||
| chr5:119363513 | G | A | 2 | a0001c0001t0025g0292 a0001c0001t0025g0293 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.31+7392G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119363513 | |||||||
| chr5:119363561 | G | A | 1 | a0001c0001t0002g0148 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.31+7440G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119363561 | |||||||
| chr5:119363586 | T | C | 1 | a0001c0001t0002g0109 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.31+7465T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119363586 | |||||||
| chr5:119363651 | C | T | 5 | a0001c0002t0040g0252 a0001c0002t0040g0255 a0001c0002t0095g0048 others(2): Show |
5 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+7530C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119363651 | |||||||
| chr5:119363811 | C | T | 2 | a0001c0001t0048g0219 a0001c0002t0051g0244 |
2 | HG02486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.31+7690C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119363811 | |||||||
| chr5:119363842 | A | G | 5 | a0001c0001t0003g0089 a0001c0001t0003g0090 a0001c0001t0005g0091 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+7721A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119363842 | |||||||
| chr5:119363853 | T | A | 1 | a0001c0001t0071g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.31+7732T>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119363853 | |||||||
| chr5:119363865 | G | A | 1 | a0001c0001t0047g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31+7744G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119363865 | |||||||
| chr5:119363918 | C | G | 1 | a0001c0002t0018g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+7797C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119363918 | |||||||
| chr5:119363960 | A | G | 8 | a0001c0002t0019g0038 a0001c0002t0019g0238 a0001c0002t0020g0015 others(5): Show |
9 | HG02559.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.31+7839A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119363960 | |||||||
| chr5:119364094 | G | A | 2 | a0001c0001t0025g0292 a0001c0001t0025g0293 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.31+7973G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364094 | |||||||
| chr5:119364104 | C | G | 1 | a0001c0001t0005g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.31+7983C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364104 | |||||||
| chr5:119364256 | A | G | 240 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(237): Show |
283 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.31+8135A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364256 | |||||||
| chr5:119364316 | A | G | 2 | a0001c0001t0001g0197 a0001c0001t0001g0209 |
2 | HG01081.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.31+8195A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364316 | |||||||
| chr5:119364478 | G | C | 2 | a0001c0002t0027g0249 a0001c0002t0066g0248 |
2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.31+8357G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364478 | |||||||
| chr5:119364483 | G | T | 5 | a0001c0002t0040g0252 a0001c0002t0040g0255 a0001c0002t0095g0048 others(2): Show |
5 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+8362G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364483 | |||||||
| chr5:119364537 | A | G | 63 | a0001c0001t0003g0092 a0001c0001t0010g0008 a0001c0001t0017g0035 others(60): Show |
71 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.31+8416A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364537 | |||||||
| chr5:119364587 | G | T | 2 | a0001c0002t0007g0211 a0001c0002t0018g0294 |
2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.31+8466G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364587 | |||||||
| chr5:119364778 | G | A | 7 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0026g0036 others(4): Show |
10 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.31+8657G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364778 | |||||||
| chr5:119364841 | G | GT | 26 | a0001c0001t0001g0014 a0001c0001t0001g0185 a0001c0001t0001g0186 others(23): Show |
28 | HG00423.hp1 HG00544.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.31+8748dupT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119364841 | ||||||
| chr5:119364841 | GT | G | 184 | a0001c0001t0001g0013 a0001c0001t0001g0075 a0001c0001t0001g0130 others(181): Show |
221 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.31+8748delT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119364841 | ||||||
| chr5:119364841 | GTT | G | 7 | a0001c0001t0009g0286 a0001c0001t0012g0111 a0001c0001t0031g0231 others(4): Show |
7 | HG01070.hp2 HG01243.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+8747_31+8748del others(2): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119364841 | ||||||
| chr5:119364841 | GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0005g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.31+8735_31+8748del others(14): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119364841 | ||||||
| chr5:119364854 | T | G | 5 | a0001c0001t0002g0108 a0001c0001t0002g0142 a0001c0001t0003g0021 others(2): Show |
5 | HG01192.hp1 HG02273.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+8733T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364854 | |||||||
| chr5:119364855 | T | G | 117 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(114): Show |
143 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.31+8734T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364855 | |||||||
| chr5:119364856 | T | G | 1 | a0001c0001t0012g0111 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.31+8735T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364856 | |||||||
| chr5:119364895 | A | G | 37 | a0001c0001t0003g0092 a0001c0001t0027g0232 a0001c0001t0031g0231 others(34): Show |
38 | HG00280.hp1 HG00741.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.31+8774A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364895 | |||||||
| chr5:119364960 | C | G | 1 | a0001c0001t0002g0183 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.31+8839C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364960 | |||||||
| chr5:119364996 | C | T | 1 | a0001c0002t0006g0182 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.31+8875C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119364996 | |||||||
| chr5:119365002 | C | G | 1 | a0001c0002t0007g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31+8881C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365002 | |||||||
| chr5:119365032 | A | T | 1 | a0001c0002t0004g0266 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.31+8911A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365032 | |||||||
| chr5:119365141 | C | T | 22 | a0001c0001t0031g0231 a0001c0002t0007g0215 a0001c0002t0007g0220 others(19): Show |
23 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.31+9020C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365141 | |||||||
| chr5:119365232 | C | T | 5 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0086 others(2): Show |
5 | HG02027.hp2 HG02056.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+9111C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365232 | |||||||
| chr5:119365267 | G | C | 63 | a0001c0001t0003g0092 a0001c0001t0010g0008 a0001c0001t0017g0035 others(60): Show |
71 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.31+9146G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365267 | |||||||
| chr5:119365378 | C | T | 116 | a0001c0001t0003g0092 a0001c0001t0008g0041 a0001c0001t0008g0265 others(113): Show |
133 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.31+9257C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365378 | |||||||
| chr5:119365445 | C | G | 5 | a0001c0002t0040g0252 a0001c0002t0040g0255 a0001c0002t0095g0048 others(2): Show |
5 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+9324C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365445 | |||||||
| chr5:119365454 | T | G | 2 | a0001c0001t0025g0292 a0001c0001t0025g0293 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.31+9333T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365454 | |||||||
| chr5:119365480 | A | T | 61 | a0001c0001t0003g0092 a0001c0001t0010g0008 a0001c0001t0017g0035 others(58): Show |
69 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.31+9359A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365480 | |||||||
| chr5:119365531 | C | G | 35 | a0001c0001t0008g0041 a0001c0001t0008g0265 a0001c0001t0008g0271 others(32): Show |
41 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.31+9410C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365531 | |||||||
| chr5:119365639 | C | T | 9 | a0001c0001t0031g0231 a0001c0002t0019g0038 a0001c0002t0019g0238 others(6): Show |
10 | HG01243.hp2 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.31+9518C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365639 | |||||||
| chr5:119365661 | G | A | 6 | a0001c0002t0039g0043 a0001c0002t0039g0289 a0001c0002t0110g0287 others(3): Show |
6 | HG01106.hp1 HG01891.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.31+9540G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365661 | |||||||
| chr5:119365701 | T | C | 1 | a0001c0002t0007g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.31+9580T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365701 | |||||||
| chr5:119365735 | T | C | 1 | a0001c0002t0055g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.31+9614T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365735 | |||||||
| chr5:119365738 | G | T | 53 | a0001c0001t0008g0041 a0001c0001t0008g0265 a0001c0001t0008g0271 others(50): Show |
62 | HG00408.hp1 HG00408.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.31+9617G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365738 | |||||||
| chr5:119365782 | C | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0202 a0001c0001t0001g0204 others(4): Show |
10 | HG02523.hp2 NA18942.hp2 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+9661C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365782 | |||||||
| chr5:119365795 | A | G | 2 | a0001c0001t0025g0292 a0001c0001t0025g0293 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.31+9674A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365795 | |||||||
| chr5:119365816 | A | G | 2 | a0001c0001t0002g0141 a0001c0001t0002g0145 |
2 | NA18963.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.31+9695A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365816 | |||||||
| chr5:119365855 | A | G | 116 | a0001c0001t0003g0092 a0001c0001t0008g0041 a0001c0001t0008g0265 others(113): Show |
133 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.31+9734A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119365855 | |||||||
| chr5:119366148 | G | GA | 6 | a0001c0001t0002g0112 a0001c0001t0003g0097 a0001c0001t0008g0265 others(3): Show |
6 | HG01069.hp2 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.31+10040dupA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119366148 | ||||||
| chr5:119366180 | A | G | 70 | a0001c0001t0003g0092 a0001c0001t0010g0008 a0001c0001t0017g0035 others(67): Show |
78 | HG00280.hp1 HG00408.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.31+10059A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119366180 | |||||||
| chr5:119366204 | G | T | 46 | a0001c0001t0008g0041 a0001c0001t0008g0265 a0001c0001t0008g0271 others(43): Show |
55 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.31+10083G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119366204 | |||||||
| chr5:119366378 | G | T | 1 | a0001c0002t0007g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31+10257G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119366378 | |||||||
| chr5:119366379 | A | T | 1 | a0001c0001t0003g0140 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.31+10258A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119366379 | |||||||
| chr5:119366645 | G | A | 1 | a0001c0002t0007g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31+10524G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119366645 | |||||||
| chr5:119366781 | A | C | 1 | a0001c0001t0002g0139 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.31+10660A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119366781 | |||||||
| chr5:119366818 | C | T | 1 | a0001c0002t0020g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.31+10697C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119366818 | |||||||
| chr5:119366871 | A | G | 1 | a0001c0001t0073g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.31+10750A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119366871 | |||||||
| chr5:119366903 | C | T | 5 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0086 others(2): Show |
5 | HG02027.hp2 HG02056.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+10782C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119366903 | |||||||
| chr5:119367301 | T | C | 1 | a0001c0002t0033g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.31+11180T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119367301 | |||||||
| chr5:119367311 | TGTTTA | T | 130 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(127): Show |
159 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.31+11194_31+11198d others(7): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119367311 | ||||||
| chr5:119367389 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.31+11268C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119367389 | |||||||
| chr5:119367498 | A | G | 3 | a0001c0002t0035g0037 a0001c0002t0035g0227 a0001c0002t0058g0037 |
3 | HG02055.hp1 HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.31+11377A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119367498 | |||||||
| chr5:119367918 | C | T | 1 | a0001c0002t0018g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+11797C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119367918 | |||||||
| chr5:119367967 | G | T | 126 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(123): Show |
154 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.31+11846G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119367967 | |||||||
| chr5:119367994 | T | C | 1 | a0001c0002t0018g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+11873T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119367994 | |||||||
| chr5:119368117 | A | G | 1 | a0001c0001t0002g0180 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.31+11996A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119368117 | |||||||
| chr5:119368166 | C | T | 133 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(130): Show |
162 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.31+12045C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119368166 | |||||||
| chr5:119368366 | CCTGT | C | 13 | a0001c0001t0010g0008 a0001c0001t0029g0243 a0001c0001t0042g0246 others(10): Show |
16 | HG00639.hp2 HG00642.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.31+12250_31+12253d others(6): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368366 | ||||||
| chr5:119368375 | T | TA | 47 | a0001c0001t0003g0092 a0001c0001t0013g0113 a0001c0001t0017g0035 others(44): Show |
51 | HG00280.hp1 HG00741.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.31+12265dupA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368375 | ||||||
| chr5:119368412 | C | G | 1 | a0001c0002t0007g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31+12291C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119368412 | |||||||
| chr5:119368430 | C | CGT | 38 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0179 others(35): Show |
41 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.31+12337_31+12338d others(4): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368430 | ||||||
| chr5:119368430 | C | CGTGT | 90 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0007 others(87): Show |
118 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.31+12335_31+12338d others(6): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368430 | ||||||
| chr5:119368430 | C | CGTGTGT | 24 | a0001c0001t0001g0075 a0001c0001t0001g0135 a0001c0001t0002g0025 others(21): Show |
27 | HG00544.hp1 HG00621.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.31+12333_31+12338d others(8): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368430 | ||||||
| chr5:119368430 | C | CGTGTGTG others(1): Show |
10 | a0001c0001t0002g0086 a0001c0001t0003g0085 a0001c0001t0003g0146 others(7): Show |
10 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+12331_31+12338d others(10): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368430 | ||||||
| chr5:119368430 | C | CGTGTGTG others(3): Show |
1 | a0001c0002t0095g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.31+12329_31+12338d others(12): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368430 | ||||||
| chr5:119368430 | C | CGTGTGTG others(7): Show |
1 | a0001c0002t0040g0255 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.31+12325_31+12338d others(16): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368430 | ||||||
| chr5:119368430 | C | CGTGTGTG others(9): Show |
1 | a0001c0002t0040g0252 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.31+12323_31+12338d others(18): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368430 | ||||||
| chr5:119368450 | TGTGTGTG others(3): Show |
T | 3 | a0001c0002t0035g0037 a0001c0002t0035g0227 a0001c0002t0058g0037 |
3 | HG02055.hp1 HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.31+12339_31+12348d others(12): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368450 | ||||||
| chr5:119368452 | TGTGTGTG others(1): Show |
T | 40 | a0001c0001t0008g0041 a0001c0001t0008g0265 a0001c0001t0008g0271 others(37): Show |
45 | HG00408.hp1 HG00735.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.31+12339_31+12346d others(10): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368452 | ||||||
| chr5:119368454 | TGTGTGC | T | 8 | a0001c0001t0009g0005 a0001c0001t0009g0286 a0001c0001t0107g0005 others(5): Show |
9 | HG00642.hp2 HG01515.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+12339_31+12344d others(8): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368454 | ||||||
| chr5:119368456 | TGTGC | T | 5 | a0001c0001t0009g0005 a0001c0001t0038g0042 a0001c0001t0104g0285 others(2): Show |
6 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.31+12339_31+12342d others(6): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368456 | ||||||
| chr5:119368458 | TGC | T | 14 | a0001c0001t0025g0292 a0001c0001t0025g0293 a0001c0001t0043g0210 others(11): Show |
15 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.31+12339_31+12340d others(4): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368458 | ||||||
| chr5:119368460 | C | G | 1 | a0001c0001t0002g0116 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.31+12339C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119368460 | |||||||
| chr5:119368460 | C | T | 178 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(175): Show |
212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.31+12339C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119368460 | |||||||
| chr5:119368470 | T | TGTGTG | 3 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0003g0053 |
3 | HG02074.hp1 HG02074.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.31+12349_31+12350i others(7): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119368470 | |||||||
| chr5:119368558 | C | A | 2 | a0001c0001t0001g0185 a0001c0001t0074g0164 |
2 | HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.31+12437C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119368558 | |||||||
| chr5:119368651 | G | A | 132 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(129): Show |
161 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.31+12530G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119368651 | |||||||
| chr5:119368713 | A | G | 1 | a0001c0001t0046g0216 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.31+12592A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119368713 | |||||||
| chr5:119368839 | A | C | 3 | a0001c0001t0009g0005 a0001c0001t0009g0286 a0001c0001t0107g0005 |
6 | HG01243.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.31+12718A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119368839 | |||||||
| chr5:119368859 | TCCTTGAC others(19): Show |
T | 1 | a0001c0001t0003g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31+12740_31+12765d others(28): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119368859 | ||||||
| chr5:119368876 | A | C | 1 | a0001c0001t0003g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.31+12755A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119368876 | |||||||
| chr5:119368915 | C | G | 240 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(237): Show |
283 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.31+12794C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119368915 | |||||||
| chr5:119368948 | A | T | 133 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(130): Show |
162 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.31+12827A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119368948 | |||||||
| chr5:119369004 | G | A | 2 | a0001c0002t0006g0019 a0001c0002t0098g0019 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.31+12883G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369004 | |||||||
| chr5:119369053 | TTC | T | 15 | a0001c0001t0010g0008 a0001c0001t0029g0243 a0001c0001t0038g0042 others(12): Show |
19 | HG00639.hp2 HG00642.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.31+12934_31+12935d others(4): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119369053 | ||||||
| chr5:119369054 | TC | T | 41 | a0001c0001t0003g0092 a0001c0001t0017g0035 a0001c0001t0017g0217 others(38): Show |
44 | HG00280.hp1 HG00741.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.31+12934delC | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369054 | |||||||
| chr5:119369055 | C | CT | 9 | a0001c0001t0001g0176 a0001c0001t0003g0087 a0001c0001t0016g0279 others(6): Show |
9 | HG01884.hp2 HG02145.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+12950dupT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119369055 | ||||||
| chr5:119369055 | C | T | 1 | a0001c0002t0007g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.31+12934C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369055 | |||||||
| chr5:119369060 | T | C | 2 | a0001c0001t0048g0219 a0001c0002t0051g0244 |
2 | HG02486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.31+12939T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369060 | |||||||
| chr5:119369099 | G | C | 37 | a0001c0001t0003g0092 a0001c0001t0027g0232 a0001c0001t0031g0231 others(34): Show |
38 | HG00280.hp1 HG00741.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.31+12978G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369099 | |||||||
| chr5:119369225 | T | C | 2 | a0001c0001t0038g0042 a0001c0001t0104g0285 |
3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.31+13104T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369225 | |||||||
| chr5:119369280 | A | T | 12 | a0001c0001t0003g0092 a0001c0001t0027g0232 a0001c0001t0050g0044 others(9): Show |
12 | HG00280.hp1 HG01257.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.31+13159A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369280 | |||||||
| chr5:119369451 | C | T | 1 | a0001c0002t0034g0046 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.31+13330C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369451 | |||||||
| chr5:119369452 | G | A | 1 | a0001c0001t0002g0119 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.31+13331G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369452 | |||||||
| chr5:119369503 | T | C | 1 | a0001c0002t0115g0295 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.31+13382T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369503 | |||||||
| chr5:119369607 | C | G | 1 | a0001c0001t0025g0293 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.31+13486C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369607 | |||||||
| chr5:119369719 | C | G | 1 | a0001c0001t0002g0177 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.31+13598C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369719 | |||||||
| chr5:119369739 | G | T | 7 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0026g0036 others(4): Show |
10 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.31+13618G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369739 | |||||||
| chr5:119369791 | C | T | 1 | a0001c0001t0013g0134 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.31+13670C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369791 | |||||||
| chr5:119369805 | G | A | 2 | a0001c0001t0031g0213 a0001c0001t0049g0214 |
2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.31+13684G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369805 | |||||||
| chr5:119369850 | T | G | 247 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(244): Show |
291 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.31+13729T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369850 | |||||||
| chr5:119369881 | A | G | 2 | a0001c0001t0068g0080 a0001c0002t0097g0071 |
2 | HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.31+13760A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369881 | |||||||
| chr5:119369913 | G | A | 2 | a0001c0001t0003g0064 a0001c0001t0003g0072 |
2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.31+13792G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119369913 | |||||||
| chr5:119370083 | GC | G | 3 | a0001c0001t0010g0008 a0001c0001t0029g0243 a0001c0001t0047g0251 |
6 | HG00642.hp1 HG01074.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.31+13964delC | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119370083 | ||||||
| chr5:119370132 | T | G | 1 | a0001c0002t0007g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31+14011T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119370132 | |||||||
| chr5:119370335 | TC | T | 5 | a0001c0002t0040g0252 a0001c0002t0040g0255 a0001c0002t0095g0048 others(2): Show |
5 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+14216delC | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119370335 | ||||||
| chr5:119370377 | A | C | 2 | a0001c0001t0031g0213 a0001c0001t0049g0214 |
2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.31+14256A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119370377 | |||||||
| chr5:119370413 | C | G | 5 | a0001c0002t0040g0252 a0001c0002t0040g0255 a0001c0002t0095g0048 others(2): Show |
5 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+14292C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119370413 | |||||||
| chr5:119370457 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.31+14336G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119370457 | |||||||
| chr5:119370528 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.31+14407G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119370528 | |||||||
| chr5:119370585 | T | C | 1 | a0001c0002t0109g0290 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.31+14464T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119370585 | |||||||
| chr5:119370750 | C | A | 1 | a0001c0002t0032g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.31+14629C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119370750 | |||||||
| chr5:119370914 | A | G | 2 | a0001c0001t0038g0042 a0001c0001t0104g0285 |
3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.31+14793A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119370914 | |||||||
| chr5:119371310 | C | T | 14 | a0001c0001t0010g0008 a0001c0001t0029g0243 a0001c0001t0029g0245 others(11): Show |
18 | HG00639.hp2 HG00642.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.31+15189C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119371310 | |||||||
| chr5:119371403 | A | G | 1 | a0001c0002t0018g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+15282A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119371403 | |||||||
| chr5:119371410 | A | G | 1 | a0001c0002t0006g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.31+15289A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119371410 | |||||||
| chr5:119371618 | GA | G | 234 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0001g0135 others(231): Show |
277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.31+15499delA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119371618 | ||||||
| chr5:119371638 | G | A | 7 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0026g0036 others(4): Show |
10 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.31+15517G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119371638 | |||||||
| chr5:119371673 | G | T | 24 | a0001c0001t0010g0008 a0001c0001t0017g0035 a0001c0001t0017g0217 others(21): Show |
31 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.31+15552G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119371673 | |||||||
| chr5:119371718 | T | C | 6 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0100 others(3): Show |
10 | HG00738.hp2 HG00741.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+15597T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119371718 | |||||||
| chr5:119371761 | C | T | 1 | a0001c0002t0015g0051 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.31+15640C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119371761 | |||||||
| chr5:119371855 | C | T | 2 | a0001c0002t0006g0032 a0001c0002t0101g0032 |
2 | NA18980.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.31+15734C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119371855 | |||||||
| chr5:119371917 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.31+15796C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119371917 | |||||||
| chr5:119371981 | C | T | 1 | a0001c0002t0007g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31+15860C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119371981 | |||||||
| chr5:119372012 | C | T | 19 | a0001c0001t0010g0008 a0001c0001t0017g0035 a0001c0001t0017g0217 others(16): Show |
25 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.31+15891C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372012 | |||||||
| chr5:119372061 | C | T | 1 | a0001c0002t0033g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.31+15940C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372061 | |||||||
| chr5:119372092 | G | A | 1 | a0001c0001t0003g0085 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.31+15971G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372092 | |||||||
| chr5:119372136 | C | CA | 8 | a0001c0001t0001g0158 a0001c0001t0001g0202 a0001c0001t0003g0054 others(5): Show |
8 | HG03098.hp1 HG03942.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.31+16029dupA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119372136 | ||||||
| chr5:119372231 | G | A | 7 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0026g0036 others(4): Show |
10 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.31+16110G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372231 | |||||||
| chr5:119372258 | A | T | 46 | a0001c0001t0008g0041 a0001c0001t0008g0265 a0001c0001t0008g0271 others(43): Show |
54 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.31+16137A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372258 | |||||||
| chr5:119372322 | C | CA | 62 | a0001c0001t0001g0130 a0001c0001t0001g0135 a0001c0001t0001g0165 others(59): Show |
73 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.31+16218dupA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119372322 | ||||||
| chr5:119372322 | C | CAA | 68 | a0001c0001t0001g0075 a0001c0001t0002g0069 a0001c0001t0002g0084 others(65): Show |
85 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.31+16217_31+16218d others(4): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119372322 | ||||||
| chr5:119372322 | CA | C | 46 | a0001c0001t0008g0041 a0001c0001t0008g0265 a0001c0001t0008g0271 others(43): Show |
56 | HG00408.hp1 HG00642.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.31+16218delA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119372322 | ||||||
| chr5:119372478 | A | G | 1 | a0001c0002t0018g0234 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.31+16357A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372478 | |||||||
| chr5:119372505 | G | C | 1 | a0001c0002t0109g0290 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.31+16384G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372505 | |||||||
| chr5:119372551 | G | T | 1 | a0001c0001t0076g0152 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.31+16430G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372551 | |||||||
| chr5:119372608 | A | G | 6 | a0001c0001t0025g0292 a0001c0001t0025g0293 a0001c0001t0031g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.31+16487A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372608 | |||||||
| chr5:119372661 | T | A | 2 | a0001c0001t0003g0065 a0001c0001t0003g0066 |
2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.31+16540T>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372661 | |||||||
| chr5:119372676 | G | A | 1 | a0001c0002t0066g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.31+16555G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372676 | |||||||
| chr5:119372723 | G | A | 7 | a0001c0001t0010g0008 a0001c0001t0029g0243 a0001c0001t0029g0245 others(4): Show |
11 | HG00642.hp1 HG01074.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.31+16602G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372723 | |||||||
| chr5:119372853 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.31+16732C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372853 | |||||||
| chr5:119372854 | G | A | 4 | a0001c0001t0025g0292 a0001c0001t0025g0293 a0001c0001t0031g0213 others(1): Show |
4 | HG01884.hp2 HG02145.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+16733G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119372854 | |||||||
| chr5:119373098 | C | A | 2 | a0001c0002t0057g0242 a0001c0002t0096g0144 |
2 | HG00741.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.31+16977C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373098 | |||||||
| chr5:119373158 | C | G | 1 | a0001c0002t0066g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.31+17037C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373158 | |||||||
| chr5:119373185 | A | C | 18 | a0001c0001t0009g0005 a0001c0001t0009g0286 a0001c0001t0042g0246 others(15): Show |
21 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.31+17064A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373185 | |||||||
| chr5:119373238 | G | A | 37 | a0001c0001t0003g0092 a0001c0001t0027g0232 a0001c0001t0031g0231 others(34): Show |
38 | HG00280.hp1 HG00741.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.31+17117G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373238 | |||||||
| chr5:119373336 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.31+17215A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373336 | |||||||
| chr5:119373360 | T | G | 9 | a0001c0001t0010g0008 a0001c0001t0029g0243 a0001c0001t0029g0245 others(6): Show |
13 | HG00642.hp1 HG01074.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.31+17239T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373360 | |||||||
| chr5:119373436 | C | T | 1 | a0001c0001t0045g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.31+17315C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373436 | |||||||
| chr5:119373467 | C | G | 3 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 |
3 | NA18945.hp2 NA18948.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.31+17346C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373467 | |||||||
| chr5:119373483 | A | T | 9 | a0001c0001t0010g0008 a0001c0001t0029g0243 a0001c0001t0029g0245 others(6): Show |
13 | HG00642.hp1 HG01074.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.31+17362A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373483 | |||||||
| chr5:119373549 | C | A | 1 | a0001c0001t0003g0147 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.31+17428C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373549 | |||||||
| chr5:119373642 | G | T | 4 | a0001c0001t0009g0005 a0001c0001t0009g0286 a0001c0001t0107g0005 others(1): Show |
7 | HG01243.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+17521G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373642 | |||||||
| chr5:119373760 | C | A | 7 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0026g0036 others(4): Show |
10 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.31+17639C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373760 | |||||||
| chr5:119373912 | T | C | 1 | a0001c0002t0018g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+17791T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373912 | |||||||
| chr5:119373964 | G | A | 1 | a0001c0002t0018g0234 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.31+17843G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373964 | |||||||
| chr5:119373995 | G | T | 1 | a0001c0002t0018g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+17874G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119373995 | |||||||
| chr5:119374011 | A | G | 1 | a0001c0002t0004g0267 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.31+17890A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119374011 | |||||||
| chr5:119374031 | T | G | 1 | a0001c0001t0002g0145 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.31+17910T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119374031 | |||||||
| chr5:119374217 | A | G | 2 | a0001c0001t0008g0265 a0001c0001t0008g0278 |
2 | HG01069.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.31+18096A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119374217 | |||||||
| chr5:119374223 | A | G | 2 | a0001c0002t0113g0291 a0001c0002t0114g0288 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.31+18102A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119374223 | |||||||
| chr5:119374267 | C | G | 2 | a0001c0002t0007g0220 a0001c0002t0062g0228 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.31+18146C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119374267 | |||||||
| chr5:119374378 | C | T | 1 | a0001c0002t0066g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.31+18257C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119374378 | |||||||
| chr5:119374385 | G | A | 5 | a0001c0002t0040g0252 a0001c0002t0040g0255 a0001c0002t0095g0048 others(2): Show |
5 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+18264G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119374385 | |||||||
| chr5:119374471 | A | G | 2 | a0001c0001t0010g0008 a0001c0001t0029g0243 |
5 | HG00642.hp1 HG01074.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-18345A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119374471 | |||||||
| chr5:119374802 | A | C | 40 | a0001c0001t0008g0041 a0001c0001t0008g0265 a0001c0001t0008g0271 others(37): Show |
44 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.32-18014A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119374802 | |||||||
| chr5:119374836 | G | A | 1 | a0001c0002t0066g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.32-17980G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119374836 | |||||||
| chr5:119374857 | C | A | 1 | a0001c0002t0109g0290 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.32-17959C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119374857 | |||||||
| chr5:119374963 | A | T | 1 | a0001c0002t0109g0290 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.32-17853A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119374963 | |||||||
| chr5:119375230 | G | C | 2 | a0001c0001t0038g0042 a0001c0001t0104g0285 |
3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.32-17586G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119375230 | |||||||
| chr5:119375277 | G | A | 2 | a0001c0001t0038g0042 a0001c0001t0104g0285 |
3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.32-17539G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119375277 | |||||||
| chr5:119375284 | C | T | 1 | a0001c0002t0004g0261 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.32-17532C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119375284 | |||||||
| chr5:119375363 | G | A | 1 | a0001c0001t0001g0033 | 2 | NA18968.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.32-17453G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119375363 | |||||||
| chr5:119375443 | A | G | 2 | a0001c0002t0004g0277 a0001c0002t0004g0283 |
2 | HG01123.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.32-17373A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119375443 | |||||||
| chr5:119375533 | A | C | 3 | a0001c0001t0011g0034 a0001c0001t0072g0034 a0001c0001t0086g0201 |
3 | HG02602.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.32-17283A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119375533 | |||||||
| chr5:119375536 | A | G | 1 | a0001c0002t0052g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.32-17280A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119375536 | |||||||
| chr5:119376025 | T | C | 1 | a0001c0001t0003g0065 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.32-16791T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119376025 | |||||||
| chr5:119376040 | G | A | 2 | a0001c0001t0031g0213 a0001c0001t0049g0214 |
2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.32-16776G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119376040 | |||||||
| chr5:119376121 | G | GT | 8 | a0001c0001t0002g0115 a0001c0001t0008g0265 a0001c0001t0008g0278 others(5): Show |
8 | HG00639.hp2 HG01069.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.32-16684dupT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119376121 | ||||||
| chr5:119376139 | A | G | 110 | a0001c0001t0003g0092 a0001c0001t0008g0041 a0001c0001t0009g0005 others(107): Show |
122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.32-16677A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119376139 | |||||||
| chr5:119376179 | A | G | 1 | a0001c0001t0003g0099 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.32-16637A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119376179 | |||||||
| chr5:119376358 | T | TGATC | 63 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0158 others(60): Show |
67 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.32-16457_32-16454d others(6): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119376358 | ||||||
| chr5:119376380 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.32-16436C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119376380 | |||||||
| chr5:119376527 | G | A | 1 | a0001c0001t0094g0059 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.32-16289G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119376527 | |||||||
| chr5:119376562 | A | AC | 21 | a0001c0001t0003g0020 a0001c0001t0003g0067 a0001c0001t0003g0073 others(18): Show |
23 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.32-16246dupC | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119376562 | ||||||
| chr5:119376562 | A | C | 3 | a0001c0002t0006g0161 a0001c0002t0006g0162 a0001c0002t0006g0163 |
3 | HG01255.hp1 HG01952.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.32-16254A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119376562 | |||||||
| chr5:119376566 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.32-16250C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119376566 | |||||||
| chr5:119376655 | G | C | 2 | a0001c0001t0026g0036 a0001c0001t0041g0218 |
3 | HG01069.hp1 HG01071.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.32-16161G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119376655 | |||||||
| chr5:119376961 | C | T | 1 | a0001c0001t0003g0140 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.32-15855C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119376961 | |||||||
| chr5:119377000 | G | A | 1 | a0001c0001t0003g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.32-15816G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119377000 | |||||||
| chr5:119377051 | G | C | 4 | a0001c0001t0031g0213 a0001c0001t0031g0231 a0001c0001t0048g0219 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-15765G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119377051 | |||||||
| chr5:119377360 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.32-15456G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119377360 | |||||||
| chr5:119377394 | T | A | 2 | a0001c0002t0113g0291 a0001c0002t0114g0288 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.32-15422T>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119377394 | |||||||
| chr5:119377406 | T | TA | 50 | a0001c0001t0002g0120 a0001c0001t0008g0278 a0001c0001t0012g0121 others(47): Show |
55 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.32-15400dupA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119377406 | ||||||
| chr5:119377562 | A | G | 42 | a0001c0001t0003g0092 a0001c0001t0050g0044 a0001c0002t0007g0211 others(39): Show |
44 | HG00280.hp1 HG00741.hp2 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.32-15254A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119377562 | |||||||
| chr5:119377572 | C | T | 1 | a0001c0001t0002g0026 | 2 | NA19007.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.32-15244C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119377572 | |||||||
| chr5:119377573 | G | A | 4 | a0001c0001t0031g0213 a0001c0001t0031g0231 a0001c0001t0048g0219 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-15243G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119377573 | |||||||
| chr5:119377660 | T | C | 2 | a0001c0001t0038g0042 a0001c0001t0104g0285 |
3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.32-15156T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119377660 | |||||||
| chr5:119377761 | A | AT | 108 | a0001c0001t0003g0092 a0001c0001t0026g0036 a0001c0001t0029g0245 others(105): Show |
117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.32-15055_32-15054i others(3): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119377761 | |||||||
| chr5:119377830 | C | G | 1 | a0001c0002t0007g0223 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.32-14986C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119377830 | |||||||
| chr5:119377839 | A | G | 1 | a0001c0002t0060g0226 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.32-14977A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119377839 | |||||||
| chr5:119377926 | C | T | 3 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0046g0216 |
4 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-14890C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119377926 | |||||||
| chr5:119378098 | C | T | 42 | a0001c0001t0003g0092 a0001c0001t0050g0044 a0001c0002t0007g0211 others(39): Show |
44 | HG00280.hp1 HG00741.hp2 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.32-14718C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378098 | |||||||
| chr5:119378185 | G | A | 1 | a0001c0002t0064g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.32-14631G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378185 | |||||||
| chr5:119378187 | A | G | 4 | a0001c0001t0026g0036 a0001c0001t0038g0042 a0001c0001t0041g0218 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-14629A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378187 | |||||||
| chr5:119378341 | G | A | 3 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0046g0216 |
4 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-14475G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378341 | |||||||
| chr5:119378374 | G | A | 1 | a0001c0002t0023g0040 | 2 | NA18990.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.32-14442G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378374 | |||||||
| chr5:119378417 | C | T | 1 | a0001c0001t0002g0128 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.32-14399C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378417 | |||||||
| chr5:119378449 | A | G | 2 | a0001c0001t0031g0213 a0001c0001t0049g0214 |
2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.32-14367A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378449 | |||||||
| chr5:119378584 | A | T | 1 | a0001c0001t0002g0143 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.32-14232A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378584 | |||||||
| chr5:119378608 | T | C | 1 | a0001c0002t0054g0045 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.32-14208T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378608 | |||||||
| chr5:119378623 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.32-14193C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378623 | |||||||
| chr5:119378637 | G | A | 4 | a0001c0001t0026g0036 a0001c0001t0038g0042 a0001c0001t0041g0218 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-14179G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378637 | |||||||
| chr5:119378709 | A | G | 1 | a0001c0001t0002g0148 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.32-14107A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378709 | |||||||
| chr5:119378830 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.32-13986T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378830 | |||||||
| chr5:119378957 | A | G | 1 | a0001c0001t0003g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.32-13859A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119378957 | |||||||
| chr5:119379124 | G | A | 4 | a0001c0001t0026g0036 a0001c0001t0038g0042 a0001c0001t0041g0218 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-13692G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379124 | |||||||
| chr5:119379145 | A | G | 1 | a0001c0001t0068g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.32-13671A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379145 | |||||||
| chr5:119379297 | C | G | 252 | a0001c0001t0001g0130 a0001c0001t0001g0173 a0001c0001t0002g0003 others(249): Show |
296 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.32-13519C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379297 | |||||||
| chr5:119379385 | A | G | 1 | a0001c0001t0003g0100 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.32-13431A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379385 | |||||||
| chr5:119379418 | A | G | 1 | a0001c0001t0042g0246 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.32-13398A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379418 | |||||||
| chr5:119379517 | G | A | 46 | a0001c0001t0003g0092 a0001c0002t0007g0211 a0001c0002t0007g0215 others(43): Show |
48 | HG00280.hp1 HG00408.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.32-13299G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379517 | |||||||
| chr5:119379525 | A | G | 1 | a0001c0002t0117g0268 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.32-13291A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379525 | |||||||
| chr5:119379580 | G | T | 249 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0007 others(246): Show |
293 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.32-13236G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379580 | |||||||
| chr5:119379618 | G | T | 2 | a0001c0001t0031g0231 a0001c0001t0048g0219 |
2 | HG01243.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.32-13198G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379618 | |||||||
| chr5:119379649 | G | A | 3 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0046g0216 |
4 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-13167G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379649 | |||||||
| chr5:119379651 | C | T | 1 | a0001c0002t0027g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.32-13165C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379651 | |||||||
| chr5:119379733 | A | G | 4 | a0001c0001t0026g0036 a0001c0001t0038g0042 a0001c0001t0041g0218 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-13083A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379733 | |||||||
| chr5:119379754 | G | A | 4 | a0001c0001t0026g0036 a0001c0001t0038g0042 a0001c0001t0041g0218 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-13062G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379754 | |||||||
| chr5:119379887 | C | G | 4 | a0001c0001t0026g0036 a0001c0001t0038g0042 a0001c0001t0041g0218 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-12929C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379887 | |||||||
| chr5:119379913 | C | T | 11 | a0001c0001t0003g0092 a0001c0002t0018g0233 a0001c0002t0018g0234 others(8): Show |
11 | HG00280.hp1 HG01496.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.32-12903C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119379913 | |||||||
| chr5:119380093 | G | A | 12 | a0001c0001t0026g0036 a0001c0001t0038g0042 a0001c0001t0041g0218 others(9): Show |
15 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.32-12723G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119380093 | |||||||
| chr5:119380152 | C | A | 3 | a0001c0002t0035g0037 a0001c0002t0035g0227 a0001c0002t0058g0037 |
3 | HG02055.hp1 HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.32-12664C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119380152 | |||||||
| chr5:119380172 | A | G | 1 | a0001c0001t0002g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.32-12644A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119380172 | |||||||
| chr5:119380223 | C | G | 1 | a0001c0002t0057g0242 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.32-12593C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119380223 | |||||||
| chr5:119380312 | T | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0165 |
3 | HG00621.hp2 HG03834.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.32-12504T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119380312 | |||||||
| chr5:119380433 | C | G | 4 | a0001c0001t0031g0213 a0001c0001t0031g0231 a0001c0001t0048g0219 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-12383C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119380433 | |||||||
| chr5:119380479 | G | A | 41 | a0001c0001t0003g0092 a0001c0002t0007g0211 a0001c0002t0007g0215 others(38): Show |
43 | HG00280.hp1 HG00741.hp2 HG01496.hp2 others(40): Show |
intron_variant | MODIFIER | c.32-12337G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119380479 | |||||||
| chr5:119380588 | G | T | 1 | a0001c0001t0038g0042 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.32-12228G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119380588 | |||||||
| chr5:119380631 | A | G | 19 | a0001c0002t0007g0211 a0001c0002t0007g0215 a0001c0002t0007g0220 others(16): Show |
20 | HG02055.hp1 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.32-12185A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119380631 | |||||||
| chr5:119380765 | C | T | 4 | a0001c0001t0026g0036 a0001c0001t0038g0042 a0001c0001t0041g0218 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-12051C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119380765 | |||||||
| chr5:119380825 | T | C | 2 | a0001c0001t0026g0036 a0001c0001t0041g0218 |
3 | HG01069.hp1 HG01071.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.32-11991T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119380825 | |||||||
| chr5:119381125 | G | A | 1 | a0001c0002t0032g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.32-11691G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119381125 | |||||||
| chr5:119381231 | A | C | 1 | a0001c0002t0027g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.32-11585A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119381231 | |||||||
| chr5:119381238 | C | A | 1 | a0001c0002t0024g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.32-11578C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119381238 | |||||||
| chr5:119381339 | A | G | 5 | a0001c0002t0040g0252 a0001c0002t0040g0255 a0001c0002t0095g0048 others(2): Show |
5 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.32-11477A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119381339 | |||||||
| chr5:119381399 | G | A | 1 | a0001c0001t0025g0293 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.32-11417G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119381399 | |||||||
| chr5:119381615 | C | CT | 4 | a0001c0001t0026g0036 a0001c0001t0038g0042 a0001c0001t0041g0218 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-11196dupT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119381615 | ||||||
| chr5:119381671 | G | T | 1 | a0001c0001t0003g0053 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.32-11145G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119381671 | |||||||
| chr5:119381714 | G | A | 12 | a0001c0001t0003g0020 a0001c0001t0003g0056 a0001c0001t0003g0057 others(9): Show |
13 | HG00639.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.32-11102G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119381714 | |||||||
| chr5:119381888 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.32-10928C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119381888 | |||||||
| chr5:119381939 | A | C | 1 | a0001c0001t0047g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.32-10877A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119381939 | |||||||
| chr5:119381993 | A | G | 2 | a0001c0001t0025g0292 a0001c0001t0025g0293 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.32-10823A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119381993 | |||||||
| chr5:119382008 | A | G | 2 | a0001c0001t0029g0245 a0001c0001t0030g0039 |
3 | HG02630.hp1 HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.32-10808A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119382008 | |||||||
| chr5:119382058 | A | G | 39 | a0001c0001t0001g0181 a0001c0002t0004g0009 a0001c0002t0004g0010 others(36): Show |
43 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.32-10758A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119382058 | |||||||
| chr5:119382231 | T | C | 10 | a0001c0002t0027g0249 a0001c0002t0032g0247 a0001c0002t0032g0256 others(7): Show |
10 | HG00639.hp2 HG01106.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.32-10585T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119382231 | |||||||
| chr5:119382503 | C | G | 1 | a0001c0002t0109g0290 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.32-10313C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119382503 | |||||||
| chr5:119382616 | C | G | 1 | a0001c0002t0097g0071 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.32-10200C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119382616 | |||||||
| chr5:119382743 | G | A | 4 | a0001c0001t0026g0036 a0001c0001t0038g0042 a0001c0001t0041g0218 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-10073G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119382743 | |||||||
| chr5:119382876 | A | G | 1 | a0001c0002t0115g0295 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.32-9940A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119382876 | |||||||
| chr5:119383072 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.32-9744T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383072 | |||||||
| chr5:119383120 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.32-9696T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383120 | |||||||
| chr5:119383149 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.32-9667T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383149 | |||||||
| chr5:119383193 | G | A | 2 | a0001c0001t0025g0292 a0001c0001t0025g0293 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.32-9623G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383193 | |||||||
| chr5:119383220 | A | C | 1 | a0001c0002t0007g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32-9596A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383220 | |||||||
| chr5:119383232 | AATCCTTA others(1): Show |
A | 4 | a0001c0001t0031g0213 a0001c0001t0031g0231 a0001c0001t0048g0219 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-9583_32-9576del others(8): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383232 | |||||||
| chr5:119383271 | G | T | 1 | a0001c0001t0003g0054 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.32-9545G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383271 | |||||||
| chr5:119383342 | A | G | 1 | a0001c0001t0002g0127 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.32-9474A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383342 | |||||||
| chr5:119383474 | T | C | 46 | a0001c0001t0003g0072 a0001c0001t0003g0092 a0001c0001t0026g0036 others(43): Show |
50 | HG00280.hp1 HG00741.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.32-9342T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383474 | |||||||
| chr5:119383475 | G | A | 3 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0046g0216 |
4 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-9341G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383475 | |||||||
| chr5:119383479 | G | C | 1 | a0001c0001t0002g0116 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.32-9337G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383479 | |||||||
| chr5:119383497 | T | C | 1 | a0001c0002t0051g0244 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.32-9319T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383497 | |||||||
| chr5:119383503 | G | A | 5 | a0001c0002t0040g0252 a0001c0002t0040g0255 a0001c0002t0095g0048 others(2): Show |
5 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.32-9313G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383503 | |||||||
| chr5:119383648 | A | G | 1 | a0001c0002t0066g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.32-9168A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383648 | |||||||
| chr5:119383813 | G | A | 2 | a0001c0001t0025g0292 a0001c0001t0025g0293 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.32-9003G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383813 | |||||||
| chr5:119383827 | T | G | 1 | a0001c0001t0001g0135 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.32-8989T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119383827 | |||||||
| chr5:119384205 | C | T | 40 | a0001c0002t0007g0211 a0001c0002t0007g0215 a0001c0002t0007g0220 others(37): Show |
42 | HG00280.hp1 HG00741.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.32-8611C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119384205 | |||||||
| chr5:119384223 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0179 |
2 | HG00673.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.32-8593G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119384223 | |||||||
| chr5:119384284 | A | G | 1 | a0001c0001t0003g0098 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.32-8532A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119384284 | |||||||
| chr5:119384410 | G | C | 1 | a0001c0002t0096g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.32-8406G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119384410 | |||||||
| chr5:119384551 | A | T | 1 | a0001c0001t0001g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.32-8265A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119384551 | |||||||
| chr5:119384865 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.32-7951A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119384865 | |||||||
| chr5:119384984 | A | G | 3 | a0001c0002t0027g0249 a0001c0002t0032g0247 a0001c0002t0032g0256 |
3 | HG00639.hp2 HG02280.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.32-7832A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119384984 | |||||||
| chr5:119384984 | A | T | 1 | a0001c0001t0028g0230 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.32-7832A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119384984 | |||||||
| chr5:119385061 | C | T | 1 | a0001c0001t0002g0133 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.32-7755C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119385061 | |||||||
| chr5:119385100 | A | G | 1 | a0001c0002t0109g0290 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.32-7716A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119385100 | |||||||
| chr5:119385186 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.32-7630T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119385186 | |||||||
| chr5:119385466 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.32-7350G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119385466 | |||||||
| chr5:119385486 | G | A | 1 | a0001c0001t0012g0122 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.32-7330G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119385486 | |||||||
| chr5:119385566 | A | G | 6 | a0001c0001t0001g0159 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | NA18942.hp2 NA18943.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-7250A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119385566 | |||||||
| chr5:119385895 | T | C | 4 | a0001c0001t0009g0005 a0001c0001t0009g0286 a0001c0001t0077g0102 others(1): Show |
7 | HG01243.hp1 HG01255.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-6921T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119385895 | |||||||
| chr5:119385952 | T | C | 253 | a0001c0001t0001g0198 a0001c0001t0002g0003 a0001c0001t0002g0007 others(250): Show |
297 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.32-6864T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119385952 | |||||||
| chr5:119385997 | G | C | 7 | a0001c0002t0004g0009 a0001c0002t0004g0260 a0001c0002t0004g0261 others(4): Show |
9 | HG01975.hp1 NA18944.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.32-6819G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119385997 | |||||||
| chr5:119385999 | G | A | 95 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0259 others(92): Show |
101 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.32-6817G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119385999 | |||||||
| chr5:119386135 | T | A | 1 | a0001c0001t0076g0152 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.32-6681T>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119386135 | |||||||
| chr5:119386151 | G | A | 2 | a0001c0001t0031g0213 a0001c0001t0049g0214 |
2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.32-6665G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119386151 | |||||||
| chr5:119386196 | G | A | 1 | a0001c0001t0003g0089 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.32-6620G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119386196 | |||||||
| chr5:119386515 | G | GTGTTT | 180 | a0001c0001t0001g0198 a0001c0001t0002g0003 a0001c0001t0002g0007 others(177): Show |
217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.32-6278_32-6274dup others(5): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119386515 | ||||||
| chr5:119386515 | G | GTGTTTTG others(3): Show |
1 | a0001c0001t0021g0101 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.32-6283_32-6274dup others(10): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119386515 | ||||||
| chr5:119386695 | C | G | 1 | a0001c0001t0093g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.32-6121C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119386695 | |||||||
| chr5:119386724 | A | T | 6 | a0001c0002t0039g0043 a0001c0002t0039g0289 a0001c0002t0110g0287 others(3): Show |
6 | HG01106.hp1 HG01891.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-6092A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119386724 | |||||||
| chr5:119386734 | C | T | 1 | a0001c0001t0012g0121 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.32-6082C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119386734 | |||||||
| chr5:119386735 | G | A | 43 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0259 others(40): Show |
47 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.32-6081G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119386735 | |||||||
| chr5:119386819 | A | G | 3 | a0001c0001t0042g0246 a0001c0001t0043g0210 a0001c0001t0044g0258 |
3 | HG01496.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.32-5997A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119386819 | |||||||
| chr5:119386958 | T | TCTCCCTC others(1): Show |
82 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0259 others(79): Show |
88 | HG00280.hp1 HG00408.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.32-5842_32-5835dup others(8): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119386958 | ||||||
| chr5:119386974 | C | CCTCCCTC others(1): Show |
6 | a0001c0002t0039g0043 a0001c0002t0039g0289 a0001c0002t0110g0287 others(3): Show |
6 | HG01106.hp1 HG01891.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-5839_32-5832dup others(8): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119386974 | ||||||
| chr5:119386978 | C | CCTCCCTC others(9): Show |
13 | a0001c0001t0002g0123 a0001c0001t0002g0129 a0001c0001t0002g0133 others(10): Show |
13 | HG01168.hp2 HG01169.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.32-5835_32-5834ins others(16): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119386978 | ||||||
| chr5:119386978 | C | CCTCCCTC others(5): Show |
126 | a0001c0001t0001g0198 a0001c0001t0002g0003 a0001c0001t0002g0007 others(123): Show |
161 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.32-5835_32-5834ins others(12): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119386978 | ||||||
| chr5:119387037 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0188 |
2 | HG00544.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.32-5779A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119387037 | |||||||
| chr5:119387175 | C | G | 1 | a0001c0001t0045g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.32-5641C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119387175 | |||||||
| chr5:119387179 | C | T | 1 | a0001c0001t0003g0058 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.32-5637C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119387179 | |||||||
| chr5:119387296 | T | C | 1 | a0001c0002t0051g0244 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.32-5520T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119387296 | |||||||
| chr5:119387339 | G | A | 53 | a0001c0002t0007g0211 a0001c0002t0007g0215 a0001c0002t0007g0220 others(50): Show |
55 | HG00280.hp1 HG00408.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.32-5477G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119387339 | |||||||
| chr5:119387355 | T | C | 1 | a0001c0001t0042g0246 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.32-5461T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119387355 | |||||||
| chr5:119387423 | G | C | 1 | a0001c0001t0012g0138 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.32-5393G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119387423 | |||||||
| chr5:119387480 | A | C | 6 | a0001c0002t0020g0015 a0001c0002t0036g0015 a0001c0002t0036g0241 others(3): Show |
6 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-5336A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119387480 | |||||||
| chr5:119387483 | T | C | 3 | a0001c0001t0017g0035 a0001c0001t0017g0217 a0001c0001t0046g0216 |
4 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-5333T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119387483 | |||||||
| chr5:119387486 | T | C | 1 | a0001c0001t0002g0124 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.32-5330T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119387486 | |||||||
| chr5:119387666 | A | C | 40 | a0001c0002t0007g0211 a0001c0002t0007g0215 a0001c0002t0007g0220 others(37): Show |
42 | HG00280.hp1 HG00741.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.32-5150A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119387666 | |||||||
| chr5:119387903 | C | A | 3 | a0001c0002t0035g0037 a0001c0002t0035g0227 a0001c0002t0058g0037 |
3 | HG02055.hp1 HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.32-4913C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119387903 | |||||||
| chr5:119387914 | A | G | 96 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0259 others(93): Show |
102 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.32-4902A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119387914 | |||||||
| chr5:119388034 | C | T | 2 | a0001c0001t0005g0104 a0001c0001t0069g0103 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.32-4782C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388034 | |||||||
| chr5:119388079 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0198 |
2 | NA19005.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.32-4737A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388079 | |||||||
| chr5:119388084 | G | A | 2 | a0002c0003t0001g0029 a0002c0003t0011g0029 |
2 | NA18947.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.32-4732G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388084 | |||||||
| chr5:119388245 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.32-4571G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388245 | |||||||
| chr5:119388387 | A | T | 4 | a0001c0001t0010g0008 a0001c0001t0029g0243 a0001c0001t0029g0245 others(1): Show |
8 | HG00642.hp1 HG01074.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-4429A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388387 | |||||||
| chr5:119388403 | G | T | 2 | a0001c0002t0004g0274 a0001c0002t0118g0281 |
2 | HG01346.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.32-4413G>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388403 | |||||||
| chr5:119388430 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.32-4386G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388430 | |||||||
| chr5:119388516 | CAG | C | 2 | a0001c0002t0023g0040 a0001c0002t0023g0273 |
3 | NA18990.hp2 NA19057.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.32-4297_32-4296del others(2): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119388516 | ||||||
| chr5:119388546 | A | C | 4 | a0001c0001t0014g0027 a0001c0001t0014g0184 a0001c0001t0014g0205 others(1): Show |
5 | HG01934.hp2 HG01975.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.32-4270A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388546 | |||||||
| chr5:119388623 | A | ATCTTT | 5 | a0001c0002t0004g0009 a0001c0002t0004g0261 a0001c0002t0004g0262 others(2): Show |
7 | HG01975.hp1 NA18944.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.32-4191_32-4187dup others(5): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119388623 | ||||||
| chr5:119388623 | ATCTTTTT others(3): Show |
A | 1 | a0001c0002t0004g0260 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.32-4186_32-4177del others(10): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119388623 | ||||||
| chr5:119388630 | T | C | 5 | a0001c0002t0004g0009 a0001c0002t0004g0261 a0001c0002t0004g0262 others(2): Show |
7 | HG01975.hp1 NA18944.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.32-4186T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388630 | |||||||
| chr5:119388630 | T | TTTTTC | 43 | a0001c0002t0004g0010 a0001c0002t0004g0259 a0001c0002t0004g0266 others(40): Show |
45 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.32-4164_32-4160dup others(5): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119388630 | ||||||
| chr5:119388698 | G | A | 4 | a0001c0002t0039g0043 a0001c0002t0039g0289 a0001c0002t0110g0287 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-4118G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388698 | |||||||
| chr5:119388723 | T | C | 2 | a0001c0002t0032g0247 a0001c0002t0032g0256 |
2 | HG00639.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.32-4093T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388723 | |||||||
| chr5:119388798 | A | AT | 60 | a0001c0001t0001g0176 a0001c0001t0001g0181 a0001c0001t0002g0116 others(57): Show |
74 | HG00140.hp1 HG00408.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.32-4003dupT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119388798 | ||||||
| chr5:119388798 | A | ATT | 6 | a0001c0001t0077g0102 a0001c0001t0104g0285 a0001c0002t0051g0244 others(3): Show |
6 | HG01255.hp2 HG01891.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-4004_32-4003dup others(2): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119388798 | ||||||
| chr5:119388798 | AT | A | 51 | a0001c0001t0001g0188 a0001c0001t0002g0131 a0001c0001t0003g0021 others(48): Show |
53 | HG00280.hp1 HG00544.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.32-4003delT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119388798 | ||||||
| chr5:119388814 | G | A | 231 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0024 others(228): Show |
271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.32-4002G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388814 | |||||||
| chr5:119388867 | G | C | 231 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0024 others(228): Show |
271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.32-3949G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388867 | |||||||
| chr5:119388934 | G | A | 2 | a0001c0002t0036g0241 a0001c0002t0063g0240 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.32-3882G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388934 | |||||||
| chr5:119388939 | C | T | 2 | a0001c0002t0032g0247 a0001c0002t0032g0256 |
2 | HG00639.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.32-3877C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388939 | |||||||
| chr5:119388940 | G | A | 40 | a0001c0002t0007g0211 a0001c0002t0007g0215 a0001c0002t0007g0220 others(37): Show |
42 | HG00280.hp1 HG00741.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.32-3876G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388940 | |||||||
| chr5:119388984 | T | C | 4 | a0001c0002t0039g0043 a0001c0002t0039g0289 a0001c0002t0110g0287 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-3832T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119388984 | |||||||
| chr5:119389018 | C | T | 3 | a0001c0002t0035g0037 a0001c0002t0035g0227 a0001c0002t0058g0037 |
3 | HG02055.hp1 HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.32-3798C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119389018 | |||||||
| chr5:119389039 | A | G | 1 | a0001c0002t0032g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.32-3777A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119389039 | |||||||
| chr5:119389092 | T | C | 5 | a0001c0002t0040g0252 a0001c0002t0040g0255 a0001c0002t0095g0048 others(2): Show |
5 | HG00408.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.32-3724T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119389092 | |||||||
| chr5:119389169 | G | A | 1 | a0001c0002t0052g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.32-3647G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119389169 | |||||||
| chr5:119389251 | A | G | 7 | a0001c0001t0003g0020 a0001c0001t0003g0067 a0001c0001t0003g0073 others(4): Show |
8 | HG00639.hp1 HG00735.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-3565A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119389251 | |||||||
| chr5:119389287 | G | GA | 231 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0024 others(228): Show |
271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.32-3526dupA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119389287 | ||||||
| chr5:119389298 | C | A | 1 | a0001c0001t0031g0213 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.32-3518C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119389298 | |||||||
| chr5:119389410 | CAG | C | 133 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0024 others(130): Show |
167 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.32-3405_32-3404del others(2): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119389410 | |||||||
| chr5:119389443 | G | C | 41 | a0001c0001t0050g0044 a0001c0002t0007g0211 a0001c0002t0007g0215 others(38): Show |
43 | HG00280.hp1 HG00741.hp2 HG01496.hp2 others(40): Show |
intron_variant | MODIFIER | c.32-3373G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119389443 | |||||||
| chr5:119389532 | A | C | 1 | a0001c0002t0006g0079 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.32-3284A>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119389532 | |||||||
| chr5:119389621 | T | G | 1 | a0001c0001t0003g0087 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.32-3195T>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119389621 | |||||||
| chr5:119389627 | T | C | 230 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0024 others(227): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.32-3189T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119389627 | |||||||
| chr5:119389663 | A | G | 1 | a0001c0001t0075g0191 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.32-3153A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119389663 | |||||||
| chr5:119389813 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.32-3003G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119389813 | |||||||
| chr5:119390012 | T | A | 2 | a0001c0002t0007g0215 a0001c0002t0059g0221 |
2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.32-2804T>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119390012 | |||||||
| chr5:119390184 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.32-2632G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119390184 | |||||||
| chr5:119390348 | T | C | 7 | a0001c0002t0004g0009 a0001c0002t0004g0260 a0001c0002t0004g0261 others(4): Show |
9 | HG01975.hp1 NA18944.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.32-2468T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119390348 | |||||||
| chr5:119390524 | C | G | 2 | a0001c0001t0038g0042 a0001c0001t0104g0285 |
3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.32-2292C>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119390524 | |||||||
| chr5:119390533 | A | T | 1 | a0001c0001t0045g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.32-2283A>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119390533 | |||||||
| chr5:119390744 | G | C | 1 | a0001c0002t0095g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.32-2072G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119390744 | |||||||
| chr5:119390942 | C | A | 39 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0259 others(36): Show |
43 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.32-1874C>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119390942 | |||||||
| chr5:119390967 | T | C | 96 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0259 others(93): Show |
102 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.32-1849T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119390967 | |||||||
| chr5:119390968 | G | A | 4 | a0001c0002t0039g0043 a0001c0002t0039g0289 a0001c0002t0110g0287 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-1848G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119390968 | |||||||
| chr5:119390985 | A | AT | 129 | a0001c0001t0001g0031 a0001c0001t0001g0158 a0001c0001t0001g0166 others(126): Show |
160 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.32-1815dupT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119390985 | ||||||
| chr5:119390985 | A | ATT | 33 | a0001c0001t0002g0112 a0001c0001t0002g0126 a0001c0001t0003g0020 others(30): Show |
37 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.32-1816_32-1815dup others(2): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119390985 | ||||||
| chr5:119390985 | A | ATTT | 37 | a0001c0001t0003g0073 a0001c0002t0004g0009 a0001c0002t0004g0010 others(34): Show |
41 | HG00408.hp1 HG00735.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.32-1817_32-1815dup others(3): Show |
TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119390985 | ||||||
| chr5:119391089 | C | T | 1 | a0001c0001t0045g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.32-1727C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119391089 | |||||||
| chr5:119391220 | G | A | 2 | a0001c0002t0007g0215 a0001c0002t0059g0221 |
2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.32-1596G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119391220 | |||||||
| chr5:119391466 | G | A | 40 | a0001c0002t0007g0211 a0001c0002t0007g0215 a0001c0002t0007g0220 others(37): Show |
42 | HG00280.hp1 HG00741.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.32-1350G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119391466 | |||||||
| chr5:119391529 | A | G | 232 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0024 others(229): Show |
272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.32-1287A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119391529 | |||||||
| chr5:119391710 | G | C | 2 | a0001c0002t0039g0043 a0001c0002t0111g0043 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.32-1106G>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119391710 | |||||||
| chr5:119391759 | C | CA | 20 | a0001c0001t0002g0007 a0001c0001t0002g0105 a0001c0001t0002g0109 others(17): Show |
23 | HG00544.hp1 HG00558.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.32-1038dupA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119391759 | ||||||
| chr5:119391759 | CA | C | 59 | a0001c0001t0002g0025 a0001c0001t0002g0125 a0001c0001t0013g0025 others(56): Show |
63 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.32-1038delA | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119391759 | ||||||
| chr5:119391790 | G | A | 2 | a0001c0001t0005g0104 a0001c0001t0069g0103 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.32-1026G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119391790 | |||||||
| chr5:119391897 | T | C | 40 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0259 others(37): Show |
44 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.32-919T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119391897 | |||||||
| chr5:119392195 | A | G | 1 | a0001c0001t0021g0101 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.32-621A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119392195 | |||||||
| chr5:119392197 | G | A | 40 | a0001c0002t0007g0211 a0001c0002t0007g0215 a0001c0002t0007g0220 others(37): Show |
42 | HG00280.hp1 HG00741.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.32-619G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119392197 | |||||||
| chr5:119392392 | AT | A | 246 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0024 others(243): Show |
289 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.32-413delT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119392392 | ||||||
| chr5:119392433 | C | T | 1 | a0001c0001t0003g0023 | 2 | HG00423.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.32-383C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119392433 | |||||||
| chr5:119392434 | A | G | 64 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0011 others(61): Show |
80 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.32-382A>G | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119392434 | |||||||
| chr5:119392510 | C | T | 1 | a0001c0002t0036g0241 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.32-306C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119392510 | |||||||
| chr5:119392538 | C | T | 4 | a0001c0002t0039g0043 a0001c0002t0039g0289 a0001c0002t0110g0287 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-278C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119392538 | |||||||
| chr5:119392548 | G | A | 2 | a0001c0001t0005g0104 a0001c0001t0069g0103 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.32-268G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119392548 | |||||||
| chr5:119392561 | G | A | 96 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0259 others(93): Show |
102 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.32-255G>A | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119392561 | |||||||
| chr5:119392575 | C | T | 2 | a0001c0001t0026g0036 a0001c0001t0041g0218 |
3 | HG01069.hp1 HG01071.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.32-241C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119392575 | |||||||
| chr5:119392592 | T | C | 1 | a0001c0002t0006g0187 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.32-224T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119392592 | |||||||
| chr5:119392703 | C | T | 3 | a0001c0001t0042g0246 a0001c0001t0043g0210 a0001c0001t0044g0258 |
3 | HG01496.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.32-113C>T | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119392703 | |||||||
| chr5:119392800 | C | CT | 40 | a0001c0002t0007g0211 a0001c0002t0007g0215 a0001c0002t0007g0220 others(37): Show |
42 | HG00280.hp1 HG00741.hp2 HG01496.hp2 others(39): Show |
splice_acceptor_variant&intron_variant | HIGH | c.32-3dupT | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 119392800 | ||||||
| chr5:119392802 | T | C | 1 | a0001c0001t0003g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.32-14T>C | TNFAIP8 | ENSG00000145779.8 | transcript | ENST00000504771.3 | protein_coding | 1/1 | chr5 | 119392802 |