Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27242 |
| ensemblid | ENSG00000146072.6 |
| hgncid | 13469 |
| symbol | TNFRSF21 |
| name | TNF receptor superfamily member 21 |
| refseq_nuc | NM_014452.5 |
| refseq_prot | NP_055267.1 |
| ensembl_nuc | ENST00000296861.2 |
| ensembl_prot | ENSP00000296861.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 47231532 |
| end | 47309905 |
| strand | - |
| ver | v1.2 |
| region | chr6:47231532-47309905 |
| region5000 | chr6:47226532-47314905 |
| regionname0 | TNFRSF21_chr6_47231532_47309905 |
| regionname5000 | TNFRSF21_chr6_47226532_47314905 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 655 | 335 | 83 | 61 | 138 | 14 | 37 | 102 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | MGTSP others(650): Show |
chr6 | 47226532 | 47314905 |
| a0002 | 0/0 | 655 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | MGTSP others(650): Show |
chr6 | 47226532 | 47314905 |
| a0003 | 0/0 | 655 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | MGTSP others(650): Show |
chr6 | 47226532 | 47314905 |
| a0004 | 0/0 | 655 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | MGTSP others(650): Show |
chr6 | 47226532 | 47314905 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1965 | 328 | 79 | 60 | 137 | 14 | 36 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | ATGGG others(1960): Show |
chr6 | 47226532 | 47314905 | ||
| a0001c0003 | 0/0 | 1965 | 3 | 2 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | ATGGG others(1960): Show |
chr6 | 47226532 | 47314905 | ||
| a0001c0005 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | ATGGG others(1960): Show |
chr6 | 47226532 | 47314905 | ||
| a0001c0007 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | ATGGG others(1960): Show |
chr6 | 47226532 | 47314905 | ||
| a0001c0008 | 0/0 | 1965 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | ATGGG others(1960): Show |
chr6 | 47226532 | 47314905 | ||
| a0001c0009 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | ATGGG others(1960): Show |
chr6 | 47226532 | 47314905 | ||
| a0002c0002 | 0/0 | 1965 | 11 | 11 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | ATGGG others(1960): Show |
chr6 | 47226532 | 47314905 | ||
| a0003c0006 | 0/0 | 1965 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | ATGGG others(1960): Show |
chr6 | 47226532 | 47314905 | ||
| a0004c0004 | 0/0 | 1965 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | ATGGG others(1960): Show |
chr6 | 47226532 | 47314905 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3593 | 88 | 6 | 30 | 32 | 9 | 10 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3588): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0002 | 0/0 | 3593 | 85 | 14 | 7 | 55 | 2 | 7 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3588): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0003 | 1/0 | 3595 | 37 | 6 | 6 | 14 | 0 | 10 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0004 | 0/0 | 3595 | 25 | 10 | 1 | 12 | 0 | 2 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0005 | 0/0 | 3588 | 12 | 9 | 2 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3583): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0006 | 0/0 | 3609 | 10 | 0 | 3 | 6 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3604): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0007 | 0/0 | 3588 | 8 | 4 | 3 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3583): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0008 | 0/0 | 3609 | 6 | 1 | 2 | 1 | 0 | 2 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3604): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0009 | 0/0 | 3607 | 5 | 1 | 0 | 4 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3602): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0010 | 0/0 | 3601 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3596): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0011 | 0/0 | 3593 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3588): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0012 | 0/0 | 3601 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3596): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0013 | 0/0 | 3577 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3572): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0014 | 0/0 | 3605 | 3 | 2 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3600): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0015 | 0/0 | 3593 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3588): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0016 | 0/0 | 3591 | 3 | 0 | 0 | 2 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3586): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0017 | 0/0 | 3589 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3584): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0018 | 0/0 | 3611 | 2 | 0 | 0 | 0 | 1 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3606): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0019 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3592): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0020 | 0/0 | 3591 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3586): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0021 | 0/0 | 3603 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3598): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0022 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3592): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0023 | 0/0 | 3577 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3572): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0024 | 0/0 | 3607 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3602): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0025 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3598): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0027 | 0/0 | 3599 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3594): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0028 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3592): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0029 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3592): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0030 | 0/0 | 3595 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0031 | 0/0 | 3595 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0032 | 0/0 | 3595 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0033 | 0/0 | 3595 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0034 | 0/0 | 3591 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3586): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0035 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3592): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0037 | 0/0 | 3599 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3594): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0038 | 0/0 | 3595 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0039 | 0/0 | 3593 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3588): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0041 | 0/0 | 3593 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3588): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0042 | 0/0 | 3589 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3584): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0043 | 0/0 | 3607 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3602): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0045 | 0/0 | 3595 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0046 | 0/0 | 3595 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0047 | 0/0 | 3591 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3586): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0048 | 0/0 | 3593 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3588): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0049 | 0/0 | 3595 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0050 | 0/0 | 3593 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3588): Show |
chr6 | 47226532 | 47314905 |
| a0001c0001t0051 | 0/0 | 3588 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3583): Show |
chr6 | 47226532 | 47314905 |
| a0001c0003t0011 | 0/0 | 3593 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3588): Show |
chr6 | 47226532 | 47314905 |
| a0001c0003t0044 | 0/0 | 3595 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0001c0005t0011 | 0/0 | 3593 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3588): Show |
chr6 | 47226532 | 47314905 |
| a0001c0007t0019 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3592): Show |
chr6 | 47226532 | 47314905 |
| a0001c0008t0040 | 0/0 | 3588 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3583): Show |
chr6 | 47226532 | 47314905 |
| a0001c0009t0003 | 0/0 | 3595 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0002c0002t0002 | 0/0 | 3593 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3588): Show |
chr6 | 47226532 | 47314905 |
| a0002c0002t0004 | 0/0 | 3595 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0002c0002t0010 | 0/0 | 3601 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3596): Show |
chr6 | 47226532 | 47314905 |
| a0002c0002t0026 | 0/0 | 3601 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3596): Show |
chr6 | 47226532 | 47314905 |
| a0002c0002t0036 | 0/0 | 3595 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3590): Show |
chr6 | 47226532 | 47314905 |
| a0003c0006t0002 | 0/0 | 3593 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3588): Show |
chr6 | 47226532 | 47314905 |
| a0004c0004t0020 | 0/0 | 3591 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | AGTCC others(3586): Show |
chr6 | 47226532 | 47314905 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0034 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0007g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0007g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0008g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0008g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0008g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0008g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0008g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0009g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0009g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0009g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0009g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0009g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0010g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0011g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0012g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0012g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0012g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0013g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0013g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0013g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0014g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0014g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0014g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0015g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0015g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0015g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0016g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0016g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0016g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0017g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0017g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0018g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0018g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0019g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0020g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0021g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0021g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0022g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0023g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0024g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0025g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0027g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0028g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0029g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0030g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0031g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0032g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0033g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0034g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0035g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0037g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0038g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0039g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0041g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0042g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0043g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0045g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0046g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0047g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0048g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0049g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0050g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0001t0051g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0003t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0003t0011g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0003t0044g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0005t0011g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0007t0019g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0008t0040g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0001c0009t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0002c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0002c0002t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0002c0002t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0002c0002t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0002c0002t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0002c0002t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0002c0002t0010g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0002c0002t0010g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0002c0002t0010g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0002c0002t0026g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0002c0002t0036g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0003c0006t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| a0004c0004t0020g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0304 | EUR | FIN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | FIN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00621 | hp1 | a0001 | c0001 | t0031 | g0072 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00621 | hp2 | a0001 | c0001 | t0043 | g0223 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00639 | hp1 | a0001 | c0001 | t0037 | g0168 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00642 | hp2 | a0001 | c0001 | t0045 | g0330 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00735 | hp2 | a0001 | c0001 | t0048 | g0333 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0174 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0003 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0238 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0009 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0306 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01106 | hp2 | a0001 | c0003 | t0011 | g0305 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01169 | hp1 | a0001 | c0001 | t0039 | g0167 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0078 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01255 | hp2 | a0001 | c0001 | t0051 | g0334 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0074 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01358 | hp2 | a0003 | c0006 | t0002 | g0289 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0288 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01515 | hp1 | a0001 | c0001 | t0018 | g0103 | EUR | IBS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0251 | EUR | IBS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0243 | EUR | IBS | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01884 | hp1 | a0001 | c0001 | t0013 | g0285 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01891 | hp1 | a0002 | c0002 | t0036 | g0165 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0298 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0139 | AMR | PEL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01952 | hp2 | a0001 | c0001 | t0033 | g0050 | AMR | PEL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02055 | hp1 | a0001 | c0001 | t0038 | g0169 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02055 | hp2 | a0002 | c0002 | t0026 | g0049 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02129 | hp2 | a0001 | c0001 | t0030 | g0162 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02132 | hp2 | a0001 | c0001 | t0009 | g0246 | EAS | KHV | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02145 | hp2 | a0001 | c0001 | t0013 | g0326 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | PEL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | CDX | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | CDX | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02165 | hp1 | a0001 | c0001 | t0009 | g0270 | EAS | CDX | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0327 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0302 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02280 | hp2 | a0001 | c0001 | t0049 | g0336 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0325 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02572 | hp2 | a0001 | c0001 | t0042 | g0171 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02615 | hp1 | a0001 | c0001 | t0013 | g0322 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02622 | hp2 | a0001 | c0007 | t0019 | g0041 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0317 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02683 | hp1 | a0001 | c0008 | t0040 | g0166 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02717 | hp1 | a0001 | c0001 | t0035 | g0164 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0319 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02723 | hp1 | a0002 | c0002 | t0010 | g0294 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02723 | hp2 | a0001 | c0001 | t0050 | g0335 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0145 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0324 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02818 | hp2 | a0001 | c0003 | t0044 | g0290 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0316 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02886 | hp2 | a0002 | c0002 | t0004 | g0253 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0300 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02895 | hp2 | a0001 | c0001 | t0012 | g0038 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0310 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0296 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0173 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02970 | hp1 | a0001 | c0001 | t0017 | g0011 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02970 | hp2 | a0001 | c0001 | t0041 | g0170 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02976 | hp1 | a0001 | c0001 | t0017 | g0011 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0309 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03041 | hp1 | a0002 | c0002 | t0004 | g0297 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03041 | hp2 | a0001 | c0001 | t0027 | g0043 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0292 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03098 | hp2 | a0001 | c0001 | t0047 | g0328 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03130 | hp1 | a0001 | c0001 | t0014 | g0254 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0332 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03139 | hp2 | a0001 | c0001 | t0028 | g0048 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03209 | hp2 | a0001 | c0003 | t0011 | g0172 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03225 | hp1 | a0002 | c0002 | t0010 | g0313 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03225 | hp2 | a0001 | c0001 | t0019 | g0042 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0241 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03453 | hp1 | a0002 | c0002 | t0010 | g0312 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0315 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0308 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0329 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0299 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03516 | hp2 | a0001 | c0001 | t0012 | g0144 | AFR | ESN | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0208 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | GWD | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03579 | hp2 | a0001 | c0005 | t0011 | g0301 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0114 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03688 | hp2 | a0001 | c0001 | t0024 | g0058 | SAS | STU | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03710 | hp1 | a0001 | c0001 | t0018 | g0126 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0147 | SAS | PJL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0163 | SAS | BEB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0278 | SAS | BEB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | BEB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | BEB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | BEB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | BEB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | BEB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0099 | SAS | BEB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0247 | SAS | BEB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG04184 | hp2 | a0001 | c0001 | t0016 | g0272 | SAS | BEB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG04204 | hp1 | a0001 | c0001 | t0029 | g0088 | SAS | STU | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG04204 | hp2 | a0001 | c0001 | t0008 | g0009 | SAS | STU | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG04228 | hp1 | a0004 | c0004 | t0020 | g0029 | SAS | STU | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0117 | SAS | STU | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18522 | hp1 | a0002 | c0002 | t0004 | g0293 | AFR | YRI | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18522 | hp2 | a0001 | c0001 | t0021 | g0291 | AFR | YRI | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | CHB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | CHB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CHB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0314 | AFR | YRI | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0268 | AFR | YRI | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0152 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18950 | hp1 | a0001 | c0001 | t0015 | g0183 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18951 | hp1 | a0001 | c0001 | t0006 | g0092 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18951 | hp2 | a0001 | c0001 | t0032 | g0151 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18952 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18953 | hp1 | a0001 | c0001 | t0008 | g0214 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0105 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18971 | hp1 | a0001 | c0001 | t0016 | g0259 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18972 | hp2 | a0001 | c0009 | t0003 | g0086 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18973 | hp1 | a0001 | c0001 | t0015 | g0180 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0160 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18998 | hp1 | a0001 | c0001 | t0046 | g0196 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19004 | hp1 | a0001 | c0001 | t0016 | g0189 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19004 | hp2 | a0001 | c0001 | t0020 | g0123 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19010 | hp2 | a0001 | c0001 | t0014 | g0250 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0331 | AFR | LWK | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | LWK | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19043 | hp2 | a0001 | c0001 | t0021 | g0318 | AFR | LWK | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19057 | hp1 | a0001 | c0001 | t0009 | g0203 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19058 | hp1 | a0001 | c0001 | t0009 | g0175 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19078 | hp1 | a0001 | c0001 | t0015 | g0184 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19078 | hp2 | a0001 | c0001 | t0022 | g0015 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | YRI | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0023 | AFR | ASW | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | ASW | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA20805 | hp1 | a0001 | c0001 | t0007 | g0033 | EUR | TSI | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | GIH | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | GIH | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0242 | AMR | CLM | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02109 | hp1 | a0001 | c0001 | t0023 | g0017 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02486 | hp1 | a0001 | c0001 | t0034 | g0036 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0021 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG02559 | hp2 | a0002 | c0002 | t0004 | g0295 | AFR | ACB | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0283 | AFR | MSL | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0323 | AFR | USA | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| HG06807 | hp2 | a0001 | c0001 | t0025 | g0039 | AFR | USA | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | USA | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | USA | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0321 | AFR | LWK | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0284 | AFR | LWK | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0034 | REF | REF | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0133 | REF | REF | TNFRSF21_chr6_47226532_47314905 | TNFRSF21 | chr6 | 47226532 | 47314905 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:47253302 | T | G | 1 | a0003 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.1463A>C | p.Asn488Thr | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/6 | 1857/3595 | 1463/1968 | 488/655 | chr6 | 47253302 | |||
| chr6:47284022 | C | T | 1 | a0002 | 11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
missense_variant | MODERATE | c.1159G>A | p.Ala387Thr | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/6 | 1553/3595 | 1159/1968 | 387/655 | chr6 | 47284022 | |||
| chr6:47284319 | C | T | 1 | a0004 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.862G>A | p.Val288Met | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/6 | 1256/3595 | 862/1968 | 288/655 | chr6 | 47284319 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:47232972 | C | A | 1 | a0001c0003 | 3 | HG01106.hp2 HG02818.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.1761G>T | p.Arg587Arg | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 2155/3595 | 1761/1968 | 587/655 | chr6 | 47232972 | |||
| chr6:47234782 | T | C | 1 | a0001c0005 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1626A>G | p.Pro542Pro | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/6 | 2020/3595 | 1626/1968 | 542/655 | chr6 | 47234782 | |||
| chr6:47253340 | G | A | 1 | a0001c0007 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1425C>T | p.Leu475Leu | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/6 | 1819/3595 | 1425/1968 | 475/655 | chr6 | 47253340 | |||
| chr6:47284161 | T | C | 1 | a0001c0008 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.1020A>G | p.Leu340Leu | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/6 | 1414/3595 | 1020/1968 | 340/655 | chr6 | 47284161 | |||
| chr6:47284320 | G | A | 1 | a0001c0009 | 1 | NA18972.hp2 | synonymous_variant | LOW | c.861C>T | p.Asp287Asp | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/6 | 1255/3595 | 861/1968 | 287/655 | chr6 | 47284320 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:47231651 | T | C | 1 | a0001c0001t0031 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1114A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 1114 | chr6 | 47231651 | ||||||
| chr6:47231797 | C | G | 1 | a0001c0001t0030 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*968G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 968 | chr6 | 47231797 | ||||||
| chr6:47231884 | C | A | 1 | a0001c0001t0032 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*881G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 881 | chr6 | 47231884 | ||||||
| chr6:47232115 | G | A | 1 | a0001c0001t0015 | 3 | NA18950.hp1 NA18973.hp1 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*650C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 650 | chr6 | 47232115 | ||||||
| chr6:47232148 | T | G | 1 | a0001c0001t0033 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*617A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 617 | chr6 | 47232148 | ||||||
| chr6:47232316 | C | T | 1 | a0001c0001t0045 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*449G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 449 | chr6 | 47232316 | ||||||
| chr6:47232354 | GAAGTT | G | 4 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0051 others(1): Show |
22 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*406_*410delAACTT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 406 | chr6 | 47232354 | ||||||
| chr6:47232407 | G | C | 4 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0051 others(1): Show |
22 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*358C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 358 | chr6 | 47232407 | ||||||
| chr6:47232443 | T | C | 4 | a0001c0001t0010 a0001c0001t0028 a0002c0002t0010 others(1): Show |
6 | HG02055.hp2 HG02723.hp1 HG03139.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*322A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 322 | chr6 | 47232443 | ||||||
| chr6:47232502 | G | A | 1 | a0001c0001t0043 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 263 | chr6 | 47232502 | ||||||
| chr6:47232525 | G | A | 1 | a0001c0001t0046 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*240C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 240 | chr6 | 47232525 | ||||||
| chr6:47232564 | A | T | 1 | a0001c0001t0045 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*201T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 201 | chr6 | 47232564 | ||||||
| chr6:47232572 | AAG | A | 15 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0013 others(12): Show |
20 | HG01106.hp2 HG01884.hp1 HG02055.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*191_*192delCT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 191 | chr6 | 47232572 | ||||||
| chr6:47232624 | A | AAC | 3 | a0001c0001t0022 a0001c0001t0029 a0001c0003t0044 |
3 | HG02818.hp2 HG04204.hp1 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*139_*140dupGT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 140 | chr6 | 47232624 | ||||||
| chr6:47232624 | A | AACAC | 6 | a0001c0001t0019 a0001c0001t0027 a0001c0001t0028 others(3): Show |
6 | HG00639.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*137_*140dupGTGT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 140 | chr6 | 47232624 | ||||||
| chr6:47232624 | A | AACACAC | 1 | a0001c0001t0012 | 3 | HG02809.hp2 HG02895.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*135_*140dupGTGTGT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 140 | chr6 | 47232624 | ||||||
| chr6:47232624 | A | AACACACA others(1): Show |
5 | a0001c0001t0010 a0001c0001t0021 a0001c0001t0025 others(2): Show |
8 | HG02055.hp2 HG02723.hp1 HG03225.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*133_*140dupGTGTGT others(2): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 140 | chr6 | 47232624 | ||||||
| chr6:47232624 | A | AACACACA others(3): Show |
1 | a0001c0001t0014 | 3 | HG02818.hp1 HG03130.hp1 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*131_*140dupGTGTGT others(4): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 140 | chr6 | 47232624 | ||||||
| chr6:47232624 | A | AACACACA others(5): Show |
3 | a0001c0001t0009 a0001c0001t0024 a0001c0001t0043 |
7 | HG00621.hp2 HG02132.hp2 HG02165.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*129_*140dupGTGTGT others(6): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 140 | chr6 | 47232624 | ||||||
| chr6:47232624 | A | AACACACA others(7): Show |
2 | a0001c0001t0006 a0001c0001t0008 |
16 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*127_*140dupGTGTGT others(8): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 140 | chr6 | 47232624 | ||||||
| chr6:47232624 | A | AACACACA others(9): Show |
1 | a0001c0001t0018 | 2 | HG01515.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*125_*140dupGTGTGT others(10): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 140 | chr6 | 47232624 | ||||||
| chr6:47232624 | AAC | A | 15 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(12): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*139_*140delGT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 139 | chr6 | 47232624 | ||||||
| chr6:47232624 | AACAC | A | 3 | a0001c0001t0016 a0001c0001t0020 a0004c0004t0020 |
5 | HG04184.hp2 HG04228.hp1 NA18971.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*137_*140delGTGT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 137 | chr6 | 47232624 | ||||||
| chr6:47232624 | AACACAC | A | 2 | a0001c0001t0017 a0001c0001t0042 |
4 | HG02572.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*135_*140delGTGTGT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 135 | chr6 | 47232624 | ||||||
| chr6:47232644 | CACACACA others(9): Show |
C | 2 | a0001c0001t0013 a0001c0001t0023 |
4 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*105_*120delTTGTGT others(10): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 105 | chr6 | 47232644 | ||||||
| chr6:47232646 | CACACACA others(7): Show |
C | 1 | a0001c0001t0011 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*105_*118delTTGTGT others(8): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 105 | chr6 | 47232646 | ||||||
| chr6:47232706 | A | T | 1 | a0001c0001t0022 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*59T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 6/6 | 59 | chr6 | 47232706 | ||||||
| chr6:47309582 | A | T | 2 | a0001c0001t0041 a0001c0001t0042 |
2 | HG02572.hp2 HG02970.hp2 |
5_prime_UTR_variant | MODIFIER | c.-71T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/6 | 71 | chr6 | 47309582 | ||||||
| chr6:47309593 | C | G | 4 | a0001c0001t0037 a0001c0001t0038 a0001c0001t0039 others(1): Show |
4 | HG00639.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-82G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/6 | 82 | chr6 | 47309593 | ||||||
| chr6:47309718 | G | A | 1 | a0001c0001t0048 | 1 | HG00735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-207C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/6 | 207 | chr6 | 47309718 | ||||||
| chr6:47309736 | A | C | 2 | a0001c0001t0035 a0002c0002t0036 |
2 | HG01891.hp1 HG02717.hp1 |
5_prime_UTR_variant | MODIFIER | c.-225T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/6 | 225 | chr6 | 47309736 | ||||||
| chr6:47309788 | G | C | 3 | a0001c0001t0049 a0001c0001t0050 a0001c0001t0051 |
3 | HG01255.hp2 HG02280.hp2 HG02723.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-277C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/6 | chr6 | 47309788 | |||||||
| chr6:47309833 | G | A | 36 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(33): Show |
182 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(179): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-322C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/6 | chr6 | 47309833 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:47233064 | G | A | 1 | a0001c0005t0011g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1739-70C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47233064 | |||||||
| chr6:47233073 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1739-79A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47233073 | |||||||
| chr6:47233260 | G | A | 5 | a0001c0001t0010g0268 a0002c0002t0010g0294 a0002c0002t0010g0312 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1739-266C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47233260 | |||||||
| chr6:47233275 | A | G | 151 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(148): Show |
156 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.1739-281T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47233275 | |||||||
| chr6:47233304 | A | T | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1739-310T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47233304 | |||||||
| chr6:47233511 | T | C | 1 | a0001c0001t0004g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1739-517A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47233511 | |||||||
| chr6:47233589 | G | C | 1 | a0001c0001t0002g0209 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1739-595C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47233589 | |||||||
| chr6:47233676 | A | AT | 77 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(74): Show |
80 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1739-683dupA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47233676 | |||||||
| chr6:47233742 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1739-748T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47233742 | |||||||
| chr6:47234041 | G | C | 20 | a0001c0001t0010g0268 a0001c0001t0011g0302 a0001c0001t0013g0285 others(17): Show |
20 | HG01106.hp2 HG01884.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1738+629C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47234041 | |||||||
| chr6:47234068 | T | C | 2 | a0001c0001t0004g0241 a0001c0001t0004g0247 |
2 | HG03239.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1738+602A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47234068 | |||||||
| chr6:47234147 | C | CT | 6 | a0001c0001t0003g0035 a0001c0001t0004g0283 a0001c0001t0004g0287 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738+522dupA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47234147 | |||||||
| chr6:47234337 | C | G | 1 | a0001c0001t0003g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1738+333G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47234337 | |||||||
| chr6:47234405 | G | T | 5 | a0001c0001t0011g0302 a0001c0001t0013g0285 a0001c0001t0013g0322 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738+265C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47234405 | |||||||
| chr6:47234458 | G | A | 4 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0017g0011 others(1): Show |
5 | HG02257.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738+212C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47234458 | |||||||
| chr6:47234478 | G | A | 1 | a0001c0003t0044g0290 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1738+192C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47234478 | |||||||
| chr6:47234526 | G | A | 1 | a0001c0001t0004g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1738+144C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 5/5 | chr6 | 47234526 | |||||||
| chr6:47234922 | T | A | 4 | a0001c0001t0009g0317 a0001c0001t0012g0038 a0001c0001t0012g0144 others(1): Show |
4 | HG02647.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-24A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47234922 | |||||||
| chr6:47234930 | A | AT | 5 | a0001c0001t0005g0242 a0001c0001t0005g0304 a0001c0001t0007g0004 others(2): Show |
6 | HG00323.hp1 HG01123.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-33dupA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47234930 | |||||||
| chr6:47234933 | G | GA | 33 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0006g0012 others(30): Show |
35 | HG00621.hp2 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1510-36dupT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47234933 | |||||||
| chr6:47235084 | T | A | 25 | a0001c0001t0009g0317 a0001c0001t0010g0268 a0001c0001t0011g0302 others(22): Show |
25 | HG00642.hp2 HG01106.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1510-186A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235084 | |||||||
| chr6:47235169 | G | A | 19 | a0001c0001t0009g0317 a0001c0001t0010g0268 a0001c0001t0011g0302 others(16): Show |
19 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1510-271C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235169 | |||||||
| chr6:47235237 | G | A | 6 | a0001c0001t0003g0035 a0001c0001t0004g0283 a0001c0001t0004g0287 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-339C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235237 | |||||||
| chr6:47235291 | T | G | 3 | a0001c0001t0002g0286 a0001c0001t0002g0311 a0001c0001t0041g0170 |
3 | HG02970.hp2 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1510-393A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235291 | |||||||
| chr6:47235342 | G | GT | 3 | a0001c0001t0003g0027 a0001c0001t0003g0146 a0001c0001t0003g0147 |
3 | HG01123.hp1 HG01433.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1510-445dupA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235342 | |||||||
| chr6:47235405 | C | A | 53 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(50): Show |
56 | HG00621.hp1 HG00621.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1510-507G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235405 | |||||||
| chr6:47235444 | A | T | 1 | a0001c0001t0004g0323 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1510-546T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235444 | |||||||
| chr6:47235504 | G | A | 1 | a0001c0005t0011g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1510-606C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235504 | |||||||
| chr6:47235612 | G | C | 139 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(136): Show |
142 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1510-714C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235612 | |||||||
| chr6:47235636 | C | T | 1 | a0001c0001t0002g0220 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1510-738G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235636 | |||||||
| chr6:47235647 | G | A | 1 | a0001c0001t0013g0322 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1510-749C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235647 | |||||||
| chr6:47235657 | T | C | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1510-759A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235657 | |||||||
| chr6:47235676 | A | G | 167 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0016 others(164): Show |
173 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.1510-778T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235676 | |||||||
| chr6:47235884 | A | G | 69 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(66): Show |
70 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1510-986T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235884 | |||||||
| chr6:47235930 | C | T | 1 | a0001c0001t0002g0279 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1510-1032G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47235930 | |||||||
| chr6:47236021 | A | G | 167 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0016 others(164): Show |
173 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.1510-1123T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47236021 | |||||||
| chr6:47236107 | A | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(15): Show |
19 | HG00621.hp1 HG00735.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1510-1209T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47236107 | |||||||
| chr6:47236352 | C | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(16): Show |
20 | HG00621.hp1 HG00735.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1510-1454G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47236352 | |||||||
| chr6:47236425 | C | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(175): Show |
185 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.1510-1527G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47236425 | |||||||
| chr6:47236675 | T | A | 20 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(17): Show |
21 | HG00621.hp1 HG00735.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1510-1777A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47236675 | |||||||
| chr6:47236731 | A | G | 167 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0016 others(164): Show |
173 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.1510-1833T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47236731 | |||||||
| chr6:47236813 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1510-1915A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47236813 | |||||||
| chr6:47236822 | T | G | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1510-1924A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47236822 | |||||||
| chr6:47236912 | T | A | 1 | a0001c0001t0001g0157 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1510-2014A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47236912 | |||||||
| chr6:47236979 | C | T | 166 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0016 others(163): Show |
172 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.1510-2081G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47236979 | |||||||
| chr6:47237238 | G | A | 2 | a0001c0001t0043g0223 a0001c0005t0011g0301 |
2 | HG00621.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1510-2340C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47237238 | |||||||
| chr6:47237262 | T | C | 1 | a0001c0001t0042g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1510-2364A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47237262 | |||||||
| chr6:47237322 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0127 a0001c0001t0001g0131 |
3 | HG00642.hp1 HG00733.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1510-2424C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47237322 | |||||||
| chr6:47237630 | TATAAA | T | 29 | a0001c0001t0006g0012 a0001c0001t0006g0074 a0001c0001t0006g0078 others(26): Show |
30 | HG00621.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1510-2737_1510-273 others(9): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47237630 | |||||||
| chr6:47237668 | T | C | 167 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0016 others(164): Show |
173 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.1510-2770A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47237668 | |||||||
| chr6:47237836 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1510-2938C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47237836 | |||||||
| chr6:47238028 | C | G | 2 | a0001c0001t0034g0036 a0001c0001t0047g0328 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1510-3130G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47238028 | |||||||
| chr6:47238132 | G | A | 29 | a0001c0001t0006g0012 a0001c0001t0006g0074 a0001c0001t0006g0078 others(26): Show |
30 | HG00621.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1510-3234C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47238132 | |||||||
| chr6:47238176 | T | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(175): Show |
185 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.1510-3278A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47238176 | |||||||
| chr6:47238247 | C | G | 29 | a0001c0001t0006g0012 a0001c0001t0006g0074 a0001c0001t0006g0078 others(26): Show |
30 | HG00621.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1510-3349G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47238247 | |||||||
| chr6:47238250 | T | C | 10 | a0001c0001t0009g0317 a0001c0001t0010g0268 a0001c0001t0012g0038 others(7): Show |
10 | HG02055.hp2 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1510-3352A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47238250 | |||||||
| chr6:47238297 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(174): Show |
184 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1510-3399C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47238297 | |||||||
| chr6:47238819 | C | T | 5 | a0001c0001t0011g0302 a0001c0001t0013g0285 a0001c0001t0013g0322 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510-3921G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47238819 | |||||||
| chr6:47239281 | A | C | 1 | a0001c0001t0002g0331 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1510-4383T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239281 | |||||||
| chr6:47239285 | C | CA | 15 | a0001c0001t0001g0032 a0001c0001t0001g0098 a0001c0001t0001g0150 others(12): Show |
15 | HG00438.hp1 HG01074.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1510-4388dupT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239285 | |||||||
| chr6:47239285 | CA | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0134 a0001c0001t0001g0135 others(15): Show |
19 | HG00639.hp1 HG01081.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1510-4388delT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239285 | |||||||
| chr6:47239285 | CAA | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(81): Show |
85 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1510-4389_1510-438 others(6): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239285 | |||||||
| chr6:47239285 | CAAAAA | C | 50 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(47): Show |
53 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.1510-4392_1510-438 others(9): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239285 | |||||||
| chr6:47239285 | CAAAAAAA | C | 11 | a0001c0001t0003g0035 a0001c0001t0004g0283 a0001c0001t0004g0287 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1510-4394_1510-438 others(11): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239285 | |||||||
| chr6:47239285 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1510-4397_1510-438 others(14): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239285 | |||||||
| chr6:47239345 | A | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0067 others(11): Show |
14 | HG01975.hp1 NA18944.hp2 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.1510-4447T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239345 | |||||||
| chr6:47239365 | C | T | 20 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0242 others(17): Show |
22 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.1510-4467G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239365 | |||||||
| chr6:47239415 | G | A | 1 | a0001c0001t0023g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1510-4517C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239415 | |||||||
| chr6:47239566 | T | C | 1 | a0001c0001t0002g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1510-4668A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239566 | |||||||
| chr6:47239588 | C | A | 1 | a0001c0001t0006g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1510-4690G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239588 | |||||||
| chr6:47239810 | T | C | 33 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0006g0012 others(30): Show |
35 | HG00621.hp2 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1510-4912A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239810 | |||||||
| chr6:47239900 | C | T | 1 | a0001c0001t0005g0316 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1510-5002G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47239900 | |||||||
| chr6:47240684 | G | A | 4 | a0001c0001t0009g0317 a0001c0001t0012g0038 a0001c0001t0012g0144 others(1): Show |
4 | HG02647.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-5786C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47240684 | |||||||
| chr6:47240934 | C | T | 1 | a0001c0001t0042g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1510-6036G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47240934 | |||||||
| chr6:47241071 | A | G | 3 | a0001c0001t0003g0044 a0001c0001t0003g0064 a0001c0001t0003g0115 |
3 | HG02698.hp1 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1510-6173T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47241071 | |||||||
| chr6:47241181 | T | G | 4 | a0001c0001t0001g0134 a0001c0001t0001g0155 a0001c0001t0002g0288 others(1): Show |
4 | HG01081.hp1 HG01175.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-6283A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47241181 | |||||||
| chr6:47241253 | C | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(174): Show |
184 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1510-6355G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47241253 | |||||||
| chr6:47241353 | C | T | 5 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0155 others(2): Show |
5 | HG01081.hp1 HG01175.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510-6455G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47241353 | |||||||
| chr6:47241462 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(59): Show |
66 | HG00323.hp1 HG00621.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1510-6564G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47241462 | |||||||
| chr6:47241481 | A | AT | 18 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(15): Show |
19 | HG00621.hp1 HG00735.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1510-6584dupA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47241481 | |||||||
| chr6:47241481 | AT | A | 80 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(77): Show |
83 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1510-6584delA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47241481 | |||||||
| chr6:47241482 | T | A | 1 | a0001c0001t0017g0011 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1510-6584A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47241482 | |||||||
| chr6:47241693 | G | A | 1 | a0001c0001t0003g0019 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1510-6795C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47241693 | |||||||
| chr6:47241836 | CTT | C | 4 | a0001c0001t0009g0317 a0001c0001t0012g0038 a0001c0001t0012g0144 others(1): Show |
4 | HG02647.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-6940_1510-693 others(6): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47241836 | |||||||
| chr6:47242057 | CTGCTCAG others(10): Show |
C | 1 | a0001c0001t0046g0196 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1510-7176_1510-716 others(21): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47242057 | |||||||
| chr6:47242406 | C | T | 3 | a0001c0001t0019g0042 a0001c0001t0035g0164 a0001c0007t0019g0041 |
3 | HG02622.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1510-7508G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47242406 | |||||||
| chr6:47242481 | T | C | 6 | a0001c0001t0003g0035 a0001c0001t0004g0283 a0001c0001t0004g0287 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-7583A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47242481 | |||||||
| chr6:47242542 | T | G | 1 | a0001c0001t0042g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1510-7644A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47242542 | |||||||
| chr6:47242612 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1510-7714G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47242612 | |||||||
| chr6:47242652 | G | A | 1 | a0001c0005t0011g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1510-7754C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47242652 | |||||||
| chr6:47242693 | G | A | 3 | a0001c0001t0019g0042 a0001c0001t0035g0164 a0001c0007t0019g0041 |
3 | HG02622.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1510-7795C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47242693 | |||||||
| chr6:47242846 | G | C | 4 | a0001c0001t0001g0140 a0001c0001t0015g0180 a0001c0001t0015g0183 others(1): Show |
4 | NA18950.hp1 NA18973.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-7948C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47242846 | |||||||
| chr6:47242979 | G | A | 3 | a0001c0003t0011g0172 a0001c0003t0011g0305 a0001c0003t0044g0290 |
3 | HG01106.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1510-8081C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47242979 | |||||||
| chr6:47242984 | A | G | 1 | a0001c0001t0048g0333 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1510-8086T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47242984 | |||||||
| chr6:47243130 | T | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
12 | HG00639.hp1 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1510-8232A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47243130 | |||||||
| chr6:47243185 | C | T | 38 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(35): Show |
40 | HG00621.hp1 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1510-8287G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47243185 | |||||||
| chr6:47243247 | C | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(18): Show |
22 | HG00621.hp1 HG00735.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1510-8349G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47243247 | |||||||
| chr6:47243276 | G | C | 1 | a0001c0001t0002g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1510-8378C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47243276 | |||||||
| chr6:47243326 | C | T | 4 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0017g0011 others(1): Show |
5 | HG02257.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510-8428G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47243326 | |||||||
| chr6:47243377 | G | A | 1 | a0001c0001t0004g0323 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1510-8479C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47243377 | |||||||
| chr6:47243681 | G | A | 2 | a0001c0001t0016g0272 a0001c0007t0019g0041 |
2 | HG02622.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1510-8783C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47243681 | |||||||
| chr6:47243722 | A | G | 28 | a0001c0001t0003g0035 a0001c0001t0004g0283 a0001c0001t0004g0287 others(25): Show |
30 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1510-8824T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47243722 | |||||||
| chr6:47243879 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1510-8981G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47243879 | |||||||
| chr6:47244043 | T | C | 4 | a0001c0001t0009g0317 a0001c0001t0012g0038 a0001c0001t0012g0144 others(1): Show |
4 | HG02647.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-9145A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47244043 | |||||||
| chr6:47244097 | G | A | 3 | a0002c0002t0010g0312 a0002c0002t0010g0313 a0002c0002t0026g0049 |
3 | HG02055.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1509+9159C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47244097 | |||||||
| chr6:47244239 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(81): Show |
85 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1509+9017C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47244239 | |||||||
| chr6:47244255 | G | C | 106 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(103): Show |
108 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1509+9001C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47244255 | |||||||
| chr6:47244323 | C | CA | 7 | a0001c0001t0002g0217 a0001c0001t0002g0240 a0001c0001t0002g0286 others(4): Show |
7 | HG01261.hp1 HG01261.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.1509+8932dupT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47244323 | |||||||
| chr6:47244323 | C | CAAA | 87 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(84): Show |
89 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.1509+8930_1509+893 others(7): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47244323 | |||||||
| chr6:47244323 | C | CAAAA | 13 | a0001c0001t0001g0060 a0001c0001t0001g0069 a0001c0001t0001g0076 others(10): Show |
13 | HG00642.hp2 HG01109.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.1509+8929_1509+893 others(8): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47244323 | |||||||
| chr6:47244323 | CA | C | 77 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(74): Show |
81 | HG00140.hp1 HG00621.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1509+8932delT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47244323 | |||||||
| chr6:47244442 | C | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
12 | HG00639.hp1 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1509+8814G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47244442 | |||||||
| chr6:47244676 | C | G | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1509+8580G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47244676 | |||||||
| chr6:47244700 | G | A | 20 | a0001c0001t0005g0173 a0001c0001t0005g0242 a0001c0001t0005g0282 others(17): Show |
21 | HG00323.hp1 HG01069.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1509+8556C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47244700 | |||||||
| chr6:47244795 | C | T | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1509+8461G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47244795 | |||||||
| chr6:47244968 | T | A | 1 | a0001c0001t0042g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1509+8288A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47244968 | |||||||
| chr6:47245002 | C | T | 1 | a0001c0001t0042g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1509+8254G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245002 | |||||||
| chr6:47245141 | C | A | 1 | a0001c0007t0019g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1509+8115G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245141 | |||||||
| chr6:47245142 | C | G | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1509+8114G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245142 | |||||||
| chr6:47245184 | A | G | 2 | a0001c0001t0005g0300 a0001c0001t0007g0022 |
2 | HG02615.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1509+8072T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245184 | |||||||
| chr6:47245186 | C | A | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1509+8070G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245186 | |||||||
| chr6:47245427 | A | AGT | 15 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0055 others(12): Show |
15 | HG00642.hp1 HG00733.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1509+7827_1509+782 others(6): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245427 | |||||||
| chr6:47245427 | AGT | A | 28 | a0001c0001t0001g0096 a0001c0001t0002g0210 a0001c0001t0002g0213 others(25): Show |
29 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1509+7827_1509+782 others(6): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245427 | |||||||
| chr6:47245427 | AGTGT | A | 29 | a0001c0001t0001g0065 a0001c0001t0002g0269 a0001c0001t0006g0012 others(26): Show |
31 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1509+7825_1509+782 others(8): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245427 | |||||||
| chr6:47245427 | AGTGTGT | A | 10 | a0001c0001t0010g0268 a0001c0001t0014g0254 a0001c0001t0014g0324 others(7): Show |
10 | HG02055.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1509+7823_1509+782 others(10): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245427 | |||||||
| chr6:47245436 | GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0041g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1509+7798_1509+781 others(26): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245436 | |||||||
| chr6:47245437 | T | C | 1 | a0001c0005t0011g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1509+7819A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245437 | |||||||
| chr6:47245440 | GTGTGTGT others(11): Show |
G | 2 | a0001c0001t0002g0001 a0001c0001t0002g0307 |
4 | HG02109.hp2 HG02257.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+7798_1509+781 others(22): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245440 | |||||||
| chr6:47245444 | GTGTGTGT others(7): Show |
G | 1 | a0001c0007t0019g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1509+7798_1509+781 others(18): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245444 | |||||||
| chr6:47245446 | GTGTGTGT others(5): Show |
G | 17 | a0001c0001t0005g0173 a0001c0001t0005g0242 a0001c0001t0005g0282 others(14): Show |
18 | HG00323.hp1 HG01069.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.1509+7798_1509+780 others(16): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245446 | |||||||
| chr6:47245448 | GTGTGTGT others(3): Show |
G | 2 | a0001c0001t0007g0023 a0001c0001t0045g0330 |
2 | HG00642.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1509+7798_1509+780 others(14): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245448 | |||||||
| chr6:47245450 | G | T | 4 | a0001c0001t0009g0317 a0001c0001t0012g0038 a0001c0001t0012g0144 others(1): Show |
4 | HG02647.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1509+7806C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245450 | |||||||
| chr6:47245452 | G | T | 5 | a0001c0001t0011g0302 a0001c0001t0013g0285 a0001c0001t0013g0322 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1509+7804C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245452 | |||||||
| chr6:47245452 | GTGTGTT | G | 4 | a0001c0001t0009g0317 a0001c0001t0012g0038 a0001c0001t0012g0144 others(1): Show |
4 | HG02647.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1509+7798_1509+780 others(10): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245452 | |||||||
| chr6:47245454 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0002g0234 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1509+7801_1509+780 others(14): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245454 | |||||||
| chr6:47245454 | G | T | 4 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0017g0011 others(1): Show |
5 | HG02257.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1509+7802C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245454 | |||||||
| chr6:47245454 | GTGTT | G | 5 | a0001c0001t0011g0302 a0001c0001t0013g0285 a0001c0001t0013g0322 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1509+7798_1509+780 others(8): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245454 | |||||||
| chr6:47245456 | GT | G | 3 | a0001c0001t0001g0083 a0001c0001t0002g0216 a0001c0001t0003g0051 |
3 | NA18970.hp1 NA18970.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1509+7799delA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245456 | |||||||
| chr6:47245456 | GTT | G | 4 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0017g0011 others(1): Show |
5 | HG02257.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1509+7798_1509+779 others(6): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245456 | |||||||
| chr6:47245458 | T | G | 3 | a0001c0001t0001g0118 a0001c0001t0002g0234 a0001c0001t0016g0272 |
3 | HG01978.hp2 HG03195.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1509+7798A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245458 | |||||||
| chr6:47245458 | T | TTG | 7 | a0001c0001t0001g0006 a0001c0001t0001g0059 a0001c0001t0001g0079 others(4): Show |
8 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1509+7796_1509+779 others(6): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245458 | |||||||
| chr6:47245458 | T | TTGTG | 14 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0056 others(11): Show |
14 | HG00140.hp1 HG00621.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1509+7794_1509+779 others(8): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245458 | |||||||
| chr6:47245462 | G | T | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1509+7794C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245462 | |||||||
| chr6:47245475 | T | C | 18 | a0001c0001t0005g0173 a0001c0001t0005g0242 a0001c0001t0005g0282 others(15): Show |
19 | HG00323.hp1 HG01069.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1509+7781A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245475 | |||||||
| chr6:47245544 | G | C | 18 | a0001c0001t0005g0173 a0001c0001t0005g0242 a0001c0001t0005g0282 others(15): Show |
19 | HG00323.hp1 HG01069.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1509+7712C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245544 | |||||||
| chr6:47245659 | T | TTTTC | 43 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(40): Show |
45 | HG00140.hp1 HG00323.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1509+7593_1509+759 others(8): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245659 | |||||||
| chr6:47245692 | A | G | 20 | a0001c0001t0005g0173 a0001c0001t0005g0242 a0001c0001t0005g0282 others(17): Show |
21 | HG00323.hp1 HG01069.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1509+7564T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245692 | |||||||
| chr6:47245931 | T | C | 188 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0016 others(185): Show |
194 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1509+7325A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47245931 | |||||||
| chr6:47246084 | G | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(19): Show |
23 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1509+7172C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47246084 | |||||||
| chr6:47246123 | G | T | 42 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(39): Show |
44 | HG00140.hp1 HG00323.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1509+7133C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47246123 | |||||||
| chr6:47246255 | A | G | 5 | a0001c0001t0011g0302 a0001c0001t0013g0285 a0001c0001t0013g0322 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1509+7001T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47246255 | |||||||
| chr6:47246560 | T | G | 1 | a0001c0001t0004g0332 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1509+6696A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47246560 | |||||||
| chr6:47246677 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(81): Show |
85 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1509+6579T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47246677 | |||||||
| chr6:47246733 | AG | A | 14 | a0001c0001t0005g0173 a0001c0001t0005g0282 a0001c0001t0005g0284 others(11): Show |
15 | HG01069.hp1 HG01255.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1509+6522delC | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47246733 | |||||||
| chr6:47246964 | T | G | 1 | a0001c0005t0011g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1509+6292A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47246964 | |||||||
| chr6:47246981 | C | T | 43 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(40): Show |
45 | HG00140.hp1 HG00621.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1509+6275G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47246981 | |||||||
| chr6:47247004 | G | A | 15 | a0001c0001t0005g0173 a0001c0001t0005g0282 a0001c0001t0005g0284 others(12): Show |
16 | HG00642.hp2 HG01069.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1509+6252C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47247004 | |||||||
| chr6:47247140 | A | C | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1509+6116T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47247140 | |||||||
| chr6:47247144 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1509+6112G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47247144 | |||||||
| chr6:47247178 | G | A | 3 | a0001c0001t0034g0036 a0001c0001t0047g0328 a0001c0003t0044g0290 |
3 | HG02486.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1509+6078C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47247178 | |||||||
| chr6:47247488 | T | C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(26): Show |
30 | HG00140.hp1 HG00621.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1509+5768A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47247488 | |||||||
| chr6:47247868 | C | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(19): Show |
23 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1509+5388G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47247868 | |||||||
| chr6:47247906 | T | G | 1 | a0001c0001t0041g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1509+5350A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47247906 | |||||||
| chr6:47247965 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1509+5291C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47247965 | |||||||
| chr6:47248398 | C | T | 5 | a0001c0001t0010g0268 a0002c0002t0010g0294 a0002c0002t0010g0312 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1509+4858G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47248398 | |||||||
| chr6:47248503 | A | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(196): Show |
206 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.1509+4753T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47248503 | |||||||
| chr6:47248636 | C | T | 1 | a0001c0001t0042g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1509+4620G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47248636 | |||||||
| chr6:47248826 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(81): Show |
85 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1509+4430C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47248826 | |||||||
| chr6:47249044 | C | T | 4 | a0001c0001t0009g0317 a0001c0001t0012g0038 a0001c0001t0012g0144 others(1): Show |
4 | HG02647.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1509+4212G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47249044 | |||||||
| chr6:47249064 | C | T | 23 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(20): Show |
24 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1509+4192G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47249064 | |||||||
| chr6:47249113 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1509+4143G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47249113 | |||||||
| chr6:47249153 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0127 a0001c0001t0001g0131 |
3 | HG00642.hp1 HG00733.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1509+4103G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47249153 | |||||||
| chr6:47249546 | G | A | 12 | a0001c0001t0003g0035 a0001c0001t0004g0283 a0001c0001t0004g0287 others(9): Show |
12 | HG00642.hp2 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1509+3710C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47249546 | |||||||
| chr6:47249610 | G | A | 2 | a0001c0001t0002g0243 a0001c0001t0002g0251 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1509+3646C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47249610 | |||||||
| chr6:47249776 | A | G | 1 | a0001c0001t0004g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1509+3480T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47249776 | |||||||
| chr6:47249819 | A | G | 5 | a0001c0001t0010g0268 a0002c0002t0010g0294 a0002c0002t0010g0312 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1509+3437T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47249819 | |||||||
| chr6:47249964 | G | A | 1 | a0001c0001t0002g0279 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1509+3292C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47249964 | |||||||
| chr6:47249990 | T | G | 1 | a0001c0001t0002g0257 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1509+3266A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47249990 | |||||||
| chr6:47250385 | T | C | 1 | a0001c0001t0002g0200 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1509+2871A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47250385 | |||||||
| chr6:47250393 | A | G | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1509+2863T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47250393 | |||||||
| chr6:47250425 | C | A | 1 | a0001c0001t0016g0272 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1509+2831G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47250425 | |||||||
| chr6:47250658 | G | A | 1 | a0001c0001t0011g0302 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1509+2598C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47250658 | |||||||
| chr6:47250827 | A | G | 1 | a0001c0001t0028g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1509+2429T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47250827 | |||||||
| chr6:47250839 | C | T | 1 | a0001c0007t0019g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1509+2417G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47250839 | |||||||
| chr6:47251035 | T | C | 37 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(34): Show |
39 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1509+2221A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47251035 | |||||||
| chr6:47251110 | G | A | 3 | a0001c0001t0002g0001 a0001c0001t0002g0303 a0001c0001t0002g0307 |
5 | HG02109.hp2 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1509+2146C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47251110 | |||||||
| chr6:47251356 | A | G | 1 | a0001c0001t0016g0272 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1509+1900T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47251356 | |||||||
| chr6:47251371 | T | C | 1 | a0001c0001t0024g0058 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1509+1885A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47251371 | |||||||
| chr6:47251519 | T | C | 2 | a0001c0001t0008g0009 a0001c0001t0008g0238 |
3 | HG01070.hp1 HG01071.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1509+1737A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47251519 | |||||||
| chr6:47251648 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1509+1608C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47251648 | |||||||
| chr6:47251708 | T | G | 24 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(21): Show |
25 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1509+1548A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47251708 | |||||||
| chr6:47251761 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(81): Show |
85 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1509+1495C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47251761 | |||||||
| chr6:47251888 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(81): Show |
85 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1509+1368C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47251888 | |||||||
| chr6:47251919 | T | C | 1 | a0001c0009t0003g0086 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1509+1337A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47251919 | |||||||
| chr6:47252170 | C | G | 24 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(21): Show |
25 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1509+1086G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47252170 | |||||||
| chr6:47252280 | G | C | 1 | a0001c0001t0003g0115 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1509+976C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47252280 | |||||||
| chr6:47252286 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1509+970A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47252286 | |||||||
| chr6:47252488 | G | A | 17 | a0001c0001t0005g0173 a0001c0001t0005g0242 a0001c0001t0005g0282 others(14): Show |
18 | HG00323.hp1 HG01069.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.1509+768C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47252488 | |||||||
| chr6:47252672 | C | G | 1 | a0001c0001t0004g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1509+584G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47252672 | |||||||
| chr6:47252751 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1509+505G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47252751 | |||||||
| chr6:47252847 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0128 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1509+409A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47252847 | |||||||
| chr6:47252969 | C | T | 24 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(21): Show |
25 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1509+287G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47252969 | |||||||
| chr6:47252998 | G | A | 1 | a0001c0003t0044g0290 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1509+258C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47252998 | |||||||
| chr6:47253001 | G | GTGAC | 4 | a0001c0001t0005g0242 a0001c0001t0005g0304 a0001c0001t0007g0033 others(1): Show |
4 | HG00323.hp1 HG01123.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+251_1509+254d others(6): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47253001 | |||||||
| chr6:47253035 | A | AT | 20 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0056 others(17): Show |
21 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1509+220dupA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47253035 | |||||||
| chr6:47253067 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1509+189A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47253067 | |||||||
| chr6:47253088 | C | T | 4 | a0001c0001t0001g0055 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
4 | HG02027.hp1 NA18954.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+168G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47253088 | |||||||
| chr6:47253131 | C | CGT | 109 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0016 others(106): Show |
111 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1509+123_1509+124d others(4): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47253131 | |||||||
| chr6:47253132 | G | A | 4 | a0001c0001t0003g0007 a0001c0001t0003g0014 a0001c0001t0004g0187 others(1): Show |
5 | HG00609.hp1 HG00673.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.1509+124C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47253132 | |||||||
| chr6:47253167 | T | C | 6 | a0001c0001t0003g0035 a0001c0001t0004g0283 a0001c0001t0004g0287 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1509+89A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 4/5 | chr6 | 47253167 | |||||||
| chr6:47253661 | A | G | 17 | a0001c0001t0005g0173 a0001c0001t0005g0242 a0001c0001t0005g0282 others(14): Show |
18 | HG00323.hp1 HG01069.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.1244-140T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47253661 | |||||||
| chr6:47253667 | T | G | 1 | a0001c0001t0001g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1244-146A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47253667 | |||||||
| chr6:47253786 | G | A | 4 | a0001c0001t0001g0087 a0001c0001t0002g0182 a0001c0001t0002g0185 others(1): Show |
4 | NA18964.hp2 NA19057.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.1244-265C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47253786 | |||||||
| chr6:47253838 | T | C | 1 | a0002c0002t0002g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1244-317A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47253838 | |||||||
| chr6:47253933 | C | T | 1 | a0001c0001t0005g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1244-412G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47253933 | |||||||
| chr6:47253937 | G | C | 3 | a0001c0001t0003g0057 a0001c0001t0004g0241 a0001c0001t0004g0247 |
3 | HG03239.hp2 HG03492.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1244-416C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47253937 | |||||||
| chr6:47254040 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1244-519C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47254040 | |||||||
| chr6:47254048 | C | A | 1 | a0001c0001t0016g0272 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1244-527G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47254048 | |||||||
| chr6:47254087 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0002g0176 |
2 | NA18974.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1244-566T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47254087 | |||||||
| chr6:47254206 | C | T | 1 | a0001c0001t0004g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1244-685G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47254206 | |||||||
| chr6:47254498 | T | G | 1 | a0001c0001t0001g0055 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1244-977A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47254498 | |||||||
| chr6:47254509 | A | C | 1 | a0001c0001t0001g0055 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1244-988T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47254509 | |||||||
| chr6:47254817 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1244-1296C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47254817 | |||||||
| chr6:47254854 | T | A | 4 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0017g0011 others(1): Show |
5 | HG02257.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1244-1333A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47254854 | |||||||
| chr6:47255326 | G | A | 34 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0006g0012 others(31): Show |
36 | HG00621.hp2 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1244-1805C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47255326 | |||||||
| chr6:47255329 | T | G | 1 | a0001c0001t0002g0252 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1244-1808A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47255329 | |||||||
| chr6:47255341 | T | C | 12 | a0001c0001t0003g0035 a0001c0001t0004g0283 a0001c0001t0004g0287 others(9): Show |
12 | HG00642.hp2 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1244-1820A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47255341 | |||||||
| chr6:47255459 | G | GT | 36 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(33): Show |
38 | HG00140.hp1 HG00323.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1244-1939dupA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47255459 | |||||||
| chr6:47255459 | G | T | 3 | a0001c0001t0002g0001 a0001c0001t0002g0303 a0001c0001t0002g0307 |
5 | HG02109.hp2 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1244-1938C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47255459 | |||||||
| chr6:47255471 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1244-1950C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47255471 | |||||||
| chr6:47255484 | G | A | 1 | a0001c0001t0002g0252 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1244-1963C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47255484 | |||||||
| chr6:47255580 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0100 a0001c0001t0002g0239 |
3 | HG01243.hp2 HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1244-2059G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47255580 | |||||||
| chr6:47255681 | T | G | 2 | a0001c0001t0002g0217 a0001c0001t0004g0219 |
2 | HG02027.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1244-2160A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47255681 | |||||||
| chr6:47255790 | C | T | 1 | a0001c0005t0011g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1244-2269G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47255790 | |||||||
| chr6:47255988 | A | G | 1 | a0001c0001t0042g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1244-2467T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47255988 | |||||||
| chr6:47256022 | T | C | 1 | a0001c0001t0012g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1244-2501A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256022 | |||||||
| chr6:47256081 | C | T | 1 | a0001c0001t0002g0331 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1244-2560G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256081 | |||||||
| chr6:47256082 | G | A | 1 | a0001c0001t0042g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1244-2561C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256082 | |||||||
| chr6:47256100 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1244-2579C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256100 | |||||||
| chr6:47256204 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1244-2683T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256204 | |||||||
| chr6:47256234 | A | C | 17 | a0001c0001t0005g0173 a0001c0001t0005g0242 a0001c0001t0005g0282 others(14): Show |
18 | HG00323.hp1 HG01069.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.1244-2713T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256234 | |||||||
| chr6:47256265 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
12 | HG00639.hp1 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1244-2744G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256265 | |||||||
| chr6:47256277 | A | C | 1 | a0001c0001t0006g0139 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1244-2756T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256277 | |||||||
| chr6:47256318 | GT | G | 9 | a0001c0001t0001g0085 a0001c0001t0001g0089 a0001c0001t0001g0112 others(6): Show |
9 | HG00609.hp2 NA18747.hp1 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.1244-2798delA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256318 | |||||||
| chr6:47256323 | A | G | 9 | a0001c0001t0001g0085 a0001c0001t0001g0089 a0001c0001t0001g0112 others(6): Show |
9 | HG00609.hp2 NA18747.hp1 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.1244-2802T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256323 | |||||||
| chr6:47256326 | C | G | 1 | a0001c0001t0033g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1244-2805G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256326 | |||||||
| chr6:47256458 | G | C | 1 | a0001c0007t0019g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1244-2937C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256458 | |||||||
| chr6:47256471 | C | T | 1 | a0001c0007t0019g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1244-2950G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256471 | |||||||
| chr6:47256672 | T | C | 1 | a0001c0001t0002g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1244-3151A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256672 | |||||||
| chr6:47256708 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1244-3187T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256708 | |||||||
| chr6:47256975 | G | T | 11 | a0001c0001t0001g0052 a0001c0001t0001g0060 a0001c0001t0001g0073 others(8): Show |
11 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.1244-3454C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256975 | |||||||
| chr6:47256995 | C | T | 1 | a0001c0001t0003g0115 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1244-3474G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47256995 | |||||||
| chr6:47257167 | C | A | 24 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(21): Show |
25 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1244-3646G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47257167 | |||||||
| chr6:47257395 | A | T | 1 | a0001c0007t0019g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1244-3874T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47257395 | |||||||
| chr6:47257621 | T | G | 1 | a0001c0001t0006g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1244-4100A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47257621 | |||||||
| chr6:47257640 | G | C | 155 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0016 others(152): Show |
159 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.1244-4119C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47257640 | |||||||
| chr6:47257760 | T | C | 34 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0006g0012 others(31): Show |
36 | HG00621.hp2 HG00642.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1244-4239A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47257760 | |||||||
| chr6:47257890 | G | A | 23 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(20): Show |
24 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1244-4369C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47257890 | |||||||
| chr6:47257910 | A | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(193): Show |
202 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1244-4389T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47257910 | |||||||
| chr6:47257965 | G | A | 1 | a0001c0001t0028g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1244-4444C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47257965 | |||||||
| chr6:47257987 | A | G | 1 | a0001c0001t0042g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1244-4466T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47257987 | |||||||
| chr6:47257988 | T | C | 1 | a0001c0001t0016g0272 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1244-4467A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47257988 | |||||||
| chr6:47258018 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1244-4497T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258018 | |||||||
| chr6:47258048 | G | T | 1 | a0001c0001t0004g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1244-4527C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258048 | |||||||
| chr6:47258103 | G | A | 1 | a0001c0001t0016g0272 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1244-4582C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258103 | |||||||
| chr6:47258109 | C | T | 1 | a0001c0001t0016g0272 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1244-4588G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258109 | |||||||
| chr6:47258236 | G | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0016 others(168): Show |
176 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.1244-4715C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258236 | |||||||
| chr6:47258328 | C | G | 1 | a0001c0001t0004g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1244-4807G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258328 | |||||||
| chr6:47258332 | C | T | 24 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(21): Show |
25 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1244-4811G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258332 | |||||||
| chr6:47258396 | TG | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(19): Show |
23 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1244-4876delC | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258396 | |||||||
| chr6:47258397 | G | GT | 21 | a0001c0001t0001g0076 a0001c0001t0001g0154 a0001c0001t0002g0181 others(18): Show |
22 | HG00323.hp1 HG00597.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.1244-4877_1244-487 others(5): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258397 | |||||||
| chr6:47258398 | G | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0016 others(171): Show |
179 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.1244-4877C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258398 | |||||||
| chr6:47258674 | A | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(75): Show |
81 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1244-5153T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258674 | |||||||
| chr6:47258709 | G | A | 23 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(20): Show |
24 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1244-5188C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258709 | |||||||
| chr6:47258915 | A | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0104 |
2 | HG01496.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1244-5394T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258915 | |||||||
| chr6:47258931 | G | C | 1 | a0001c0001t0003g0031 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1244-5410C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258931 | |||||||
| chr6:47258996 | G | T | 1 | a0001c0001t0002g0273 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1244-5475C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47258996 | |||||||
| chr6:47259068 | T | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0016 others(170): Show |
178 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.1244-5547A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47259068 | |||||||
| chr6:47259206 | G | A | 1 | a0002c0002t0004g0253 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1244-5685C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47259206 | |||||||
| chr6:47259231 | T | C | 1 | a0001c0001t0016g0272 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1244-5710A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47259231 | |||||||
| chr6:47259370 | T | C | 1 | a0001c0001t0002g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1244-5849A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47259370 | |||||||
| chr6:47259374 | C | CT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(20): Show |
24 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1244-5854dupA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47259374 | |||||||
| chr6:47259374 | CT | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0016 others(153): Show |
160 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.1244-5854delA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47259374 | |||||||
| chr6:47259374 | CTT | C | 17 | a0001c0001t0005g0173 a0001c0001t0005g0242 a0001c0001t0005g0282 others(14): Show |
18 | HG00323.hp1 HG01069.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.1244-5855_1244-585 others(6): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47259374 | |||||||
| chr6:47259386 | T | C | 3 | a0001c0001t0004g0283 a0001c0001t0004g0309 a0001c0001t0004g0327 |
3 | HG02258.hp1 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1244-5865A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47259386 | |||||||
| chr6:47259481 | T | C | 1 | a0001c0001t0016g0272 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1244-5960A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47259481 | |||||||
| chr6:47259489 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0003g0111 |
2 | NA18941.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1244-5968G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47259489 | |||||||
| chr6:47259535 | C | T | 1 | a0001c0001t0016g0272 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1244-6014G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47259535 | |||||||
| chr6:47259579 | T | C | 85 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(82): Show |
86 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1244-6058A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47259579 | |||||||
| chr6:47259851 | T | C | 1 | a0001c0001t0016g0272 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1244-6330A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47259851 | |||||||
| chr6:47260010 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1244-6489T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260010 | |||||||
| chr6:47260093 | T | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(193): Show |
202 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1244-6572A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260093 | |||||||
| chr6:47260179 | T | C | 98 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(95): Show |
99 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.1244-6658A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260179 | |||||||
| chr6:47260204 | T | C | 12 | a0001c0001t0009g0317 a0001c0001t0011g0302 a0001c0001t0012g0038 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1244-6683A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260204 | |||||||
| chr6:47260208 | G | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0016 others(166): Show |
174 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1244-6687C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260208 | |||||||
| chr6:47260268 | CAGG | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(194): Show |
203 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1244-6750_1244-674 others(7): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260268 | |||||||
| chr6:47260306 | C | A | 1 | a0001c0001t0018g0103 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1244-6785G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260306 | |||||||
| chr6:47260307 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(194): Show |
203 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1244-6786C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260307 | |||||||
| chr6:47260400 | C | T | 1 | a0001c0001t0032g0151 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1244-6879G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260400 | |||||||
| chr6:47260506 | G | A | 1 | a0001c0001t0028g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1244-6985C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260506 | |||||||
| chr6:47260540 | A | G | 2 | a0001c0001t0034g0036 a0001c0001t0047g0328 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1244-7019T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260540 | |||||||
| chr6:47260589 | A | C | 5 | a0001c0001t0011g0302 a0001c0001t0013g0285 a0001c0001t0013g0322 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1244-7068T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260589 | |||||||
| chr6:47260827 | T | C | 4 | a0001c0001t0009g0317 a0001c0001t0012g0038 a0001c0001t0012g0144 others(1): Show |
4 | HG02647.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1244-7306A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260827 | |||||||
| chr6:47260832 | T | G | 1 | a0001c0001t0002g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1244-7311A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47260832 | |||||||
| chr6:47261057 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1244-7536G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261057 | |||||||
| chr6:47261058 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1244-7537C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261058 | |||||||
| chr6:47261094 | C | T | 1 | a0001c0001t0003g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1244-7573G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261094 | |||||||
| chr6:47261100 | C | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(126): Show |
137 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1244-7579G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261100 | |||||||
| chr6:47261176 | G | A | 316 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(313): Show |
326 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.1244-7655C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261176 | |||||||
| chr6:47261200 | A | G | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1244-7679T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261200 | |||||||
| chr6:47261374 | C | T | 1 | a0001c0001t0003g0057 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1244-7853G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261374 | |||||||
| chr6:47261401 | G | A | 1 | a0001c0001t0002g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1244-7880C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261401 | |||||||
| chr6:47261451 | G | A | 6 | a0001c0001t0002g0234 a0001c0001t0005g0282 a0001c0001t0005g0315 others(3): Show |
6 | HG02109.hp1 HG02145.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1244-7930C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261451 | |||||||
| chr6:47261493 | A | G | 170 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(167): Show |
178 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.1244-7972T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261493 | |||||||
| chr6:47261635 | T | C | 1 | a0001c0001t0047g0328 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1244-8114A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261635 | |||||||
| chr6:47261645 | G | T | 11 | a0001c0001t0004g0283 a0002c0002t0002g0208 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1244-8124C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261645 | |||||||
| chr6:47261788 | T | C | 1 | a0001c0001t0001g0013 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1244-8267A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261788 | |||||||
| chr6:47261890 | T | C | 153 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0024 others(150): Show |
159 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.1244-8369A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47261890 | |||||||
| chr6:47262053 | T | G | 1 | a0001c0001t0023g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1244-8532A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47262053 | |||||||
| chr6:47262154 | C | G | 145 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0024 others(142): Show |
151 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1244-8633G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47262154 | |||||||
| chr6:47262174 | T | A | 114 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0024 others(111): Show |
120 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1244-8653A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47262174 | |||||||
| chr6:47262362 | T | C | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1244-8841A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47262362 | |||||||
| chr6:47262370 | G | A | 146 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0024 others(143): Show |
152 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.1244-8849C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47262370 | |||||||
| chr6:47262460 | T | A | 145 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0024 others(142): Show |
151 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1244-8939A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47262460 | |||||||
| chr6:47262690 | A | G | 1 | a0001c0001t0002g0331 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1244-9169T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47262690 | |||||||
| chr6:47262769 | A | G | 2 | a0001c0001t0002g0243 a0001c0001t0002g0251 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1244-9248T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47262769 | |||||||
| chr6:47262879 | A | G | 38 | a0001c0001t0001g0024 a0001c0001t0001g0087 a0001c0001t0001g0124 others(35): Show |
38 | HG00423.hp2 HG00621.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1244-9358T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47262879 | |||||||
| chr6:47262953 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1244-9432G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47262953 | |||||||
| chr6:47263000 | G | A | 1 | a0001c0001t0005g0329 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1244-9479C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47263000 | |||||||
| chr6:47263288 | A | G | 8 | a0001c0001t0002g0331 a0001c0001t0005g0174 a0001c0001t0005g0314 others(5): Show |
8 | HG00642.hp2 HG00741.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244-9767T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47263288 | |||||||
| chr6:47263401 | G | C | 1 | a0001c0001t0001g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1244-9880C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47263401 | |||||||
| chr6:47263437 | G | C | 1 | a0001c0001t0005g0329 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1244-9916C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47263437 | |||||||
| chr6:47263444 | T | C | 3 | a0001c0001t0002g0001 a0001c0001t0002g0303 a0001c0001t0002g0307 |
5 | HG02109.hp2 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1244-9923A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47263444 | |||||||
| chr6:47263634 | A | C | 117 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0024 others(114): Show |
122 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1244-10113T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47263634 | |||||||
| chr6:47263787 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0003g0115 |
2 | HG01106.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1244-10266C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47263787 | |||||||
| chr6:47263820 | C | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(148): Show |
158 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1244-10299G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47263820 | |||||||
| chr6:47263850 | T | G | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1244-10329A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47263850 | |||||||
| chr6:47263895 | G | A | 1 | a0001c0001t0004g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1244-10374C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47263895 | |||||||
| chr6:47263944 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0002g0311 |
3 | HG02486.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1244-10423T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47263944 | |||||||
| chr6:47264005 | G | A | 150 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(147): Show |
157 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1244-10484C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264005 | |||||||
| chr6:47264110 | T | C | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1244-10589A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264110 | |||||||
| chr6:47264126 | G | C | 1 | a0002c0002t0004g0295 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1244-10605C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264126 | |||||||
| chr6:47264234 | A | G | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1244-10713T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264234 | |||||||
| chr6:47264250 | G | A | 10 | a0001c0001t0002g0298 a0001c0001t0004g0319 a0001c0001t0004g0323 others(7): Show |
10 | HG01255.hp2 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1244-10729C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264250 | |||||||
| chr6:47264412 | A | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(149): Show |
159 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.1244-10891T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264412 | |||||||
| chr6:47264444 | G | A | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1244-10923C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264444 | |||||||
| chr6:47264455 | C | T | 3 | a0001c0001t0011g0302 a0001c0001t0050g0335 a0001c0001t0051g0334 |
3 | HG01255.hp2 HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1244-10934G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264455 | |||||||
| chr6:47264470 | G | A | 6 | a0001c0001t0001g0040 a0001c0001t0005g0292 a0001c0001t0012g0144 others(3): Show |
6 | HG02809.hp2 HG02896.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1244-10949C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264470 | |||||||
| chr6:47264481 | C | CT | 104 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(101): Show |
111 | HG00140.hp2 HG00423.hp2 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.1244-10961dupA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264481 | |||||||
| chr6:47264610 | C | T | 43 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0045 others(40): Show |
45 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.1244-11089G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264610 | |||||||
| chr6:47264722 | A | G | 16 | a0001c0001t0002g0298 a0001c0001t0002g0331 a0001c0001t0004g0319 others(13): Show |
16 | HG00642.hp2 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1244-11201T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264722 | |||||||
| chr6:47264723 | A | G | 1 | a0001c0001t0004g0319 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1244-11202T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264723 | |||||||
| chr6:47264745 | A | G | 1 | a0001c0001t0043g0223 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1244-11224T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264745 | |||||||
| chr6:47264848 | A | T | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1244-11327T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264848 | |||||||
| chr6:47264876 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(104): Show |
114 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1244-11355T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264876 | |||||||
| chr6:47264888 | C | T | 6 | a0001c0001t0001g0089 a0001c0001t0001g0098 a0001c0001t0001g0112 others(3): Show |
6 | HG00438.hp1 HG00609.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1244-11367G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264888 | |||||||
| chr6:47264977 | A | G | 1 | a0001c0001t0002g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1244-11456T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47264977 | |||||||
| chr6:47265307 | C | T | 1 | a0001c0001t0005g0174 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1244-11786G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47265307 | |||||||
| chr6:47265397 | GT | G | 83 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0024 others(80): Show |
88 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1244-11877delA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47265397 | |||||||
| chr6:47265402 | T | G | 2 | a0001c0001t0003g0007 a0001c0001t0003g0014 |
3 | NA18966.hp1 NA18995.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1244-11881A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47265402 | |||||||
| chr6:47265587 | C | G | 19 | a0001c0001t0001g0040 a0001c0001t0001g0150 a0001c0001t0003g0037 others(16): Show |
19 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.1244-12066G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47265587 | |||||||
| chr6:47265824 | C | A | 1 | a0001c0001t0006g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1244-12303G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47265824 | |||||||
| chr6:47265870 | G | A | 4 | a0001c0001t0002g0331 a0001c0001t0013g0285 a0001c0001t0013g0322 others(1): Show |
4 | HG01884.hp1 HG02615.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1244-12349C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47265870 | |||||||
| chr6:47265885 | T | G | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1244-12364A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47265885 | |||||||
| chr6:47266190 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0006g0117 |
2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1244-12669C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47266190 | |||||||
| chr6:47266381 | T | C | 43 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0045 others(40): Show |
45 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.1244-12860A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47266381 | |||||||
| chr6:47266509 | T | A | 98 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0024 others(95): Show |
103 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1244-12988A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47266509 | |||||||
| chr6:47266598 | TTCAAACT others(6): Show |
T | 1 | a0001c0001t0002g0279 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1244-13090_1244-13 others(19): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47266598 | |||||||
| chr6:47266793 | T | C | 2 | a0001c0001t0002g0286 a0001c0001t0004g0308 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1244-13272A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47266793 | |||||||
| chr6:47266948 | T | C | 3 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0028g0048 |
3 | HG03139.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1244-13427A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47266948 | |||||||
| chr6:47267041 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0002g0311 others(1): Show |
4 | HG02486.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1244-13520G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47267041 | |||||||
| chr6:47267084 | T | C | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1244-13563A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47267084 | |||||||
| chr6:47267092 | CT | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(190): Show |
201 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.1244-13572delA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47267092 | |||||||
| chr6:47267092 | CTT | C | 32 | a0001c0001t0001g0161 a0001c0001t0002g0298 a0001c0001t0002g0331 others(29): Show |
32 | HG00642.hp2 HG01106.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.1244-13573_1244-13 others(8): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47267092 | |||||||
| chr6:47267094 | T | C | 1 | a0001c0001t0002g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1244-13573A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47267094 | |||||||
| chr6:47267319 | C | T | 81 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0055 others(78): Show |
81 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1244-13798G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47267319 | |||||||
| chr6:47267324 | T | A | 43 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0045 others(40): Show |
45 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.1244-13803A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47267324 | |||||||
| chr6:47267363 | G | C | 1 | a0001c0001t0002g0228 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1244-13842C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47267363 | |||||||
| chr6:47267627 | G | A | 2 | a0001c0001t0045g0330 a0001c0003t0011g0172 |
2 | HG00642.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1244-14106C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47267627 | |||||||
| chr6:47267750 | A | T | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1244-14229T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47267750 | |||||||
| chr6:47267920 | T | C | 1 | a0001c0001t0002g0191 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1244-14399A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47267920 | |||||||
| chr6:47268058 | C | T | 5 | a0001c0001t0002g0331 a0001c0001t0013g0285 a0001c0001t0013g0322 others(2): Show |
5 | HG01884.hp1 HG02615.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1244-14537G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47268058 | |||||||
| chr6:47268145 | A | G | 1 | a0001c0001t0005g0174 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1244-14624T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47268145 | |||||||
| chr6:47268334 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1244-14813A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47268334 | |||||||
| chr6:47268336 | C | T | 17 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0009g0317 others(14): Show |
17 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1244-14815G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47268336 | |||||||
| chr6:47268584 | C | T | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1244-15063G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47268584 | |||||||
| chr6:47268622 | G | GCCA | 93 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(90): Show |
98 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1244-15104_1244-15 others(9): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47268622 | |||||||
| chr6:47268658 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0002g0311 others(1): Show |
4 | HG02486.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1244-15137T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47268658 | |||||||
| chr6:47268671 | T | A | 1 | a0001c0001t0004g0332 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1244-15150A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47268671 | |||||||
| chr6:47268680 | G | C | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1244-15159C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47268680 | |||||||
| chr6:47268682 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0003g0053 |
2 | NA18941.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1244-15161A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47268682 | |||||||
| chr6:47268795 | C | G | 1 | a0001c0001t0002g0233 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1243+15143G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47268795 | |||||||
| chr6:47268809 | C | A | 76 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
81 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1243+15129G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47268809 | |||||||
| chr6:47268907 | G | A | 1 | a0001c0001t0007g0033 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1243+15031C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47268907 | |||||||
| chr6:47269098 | T | G | 1 | a0001c0001t0001g0040 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1243+14840A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269098 | |||||||
| chr6:47269099 | T | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(90): Show |
98 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1243+14839A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269099 | |||||||
| chr6:47269108 | C | T | 11 | a0001c0001t0002g0298 a0001c0001t0004g0319 a0001c0001t0004g0323 others(8): Show |
11 | HG01255.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+14830G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269108 | |||||||
| chr6:47269144 | A | G | 76 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
81 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1243+14794T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269144 | |||||||
| chr6:47269151 | G | A | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1243+14787C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269151 | |||||||
| chr6:47269181 | C | T | 5 | a0001c0001t0001g0155 a0001c0001t0002g0239 a0001c0001t0002g0240 others(2): Show |
5 | HG01081.hp1 HG01123.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243+14757G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269181 | |||||||
| chr6:47269200 | C | A | 1 | a0001c0001t0001g0018 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1243+14738G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269200 | |||||||
| chr6:47269215 | A | G | 4 | a0001c0001t0002g0331 a0001c0001t0013g0285 a0001c0001t0013g0322 others(1): Show |
4 | HG01884.hp1 HG02615.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1243+14723T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269215 | |||||||
| chr6:47269221 | A | G | 1 | a0001c0001t0002g0200 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1243+14717T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269221 | |||||||
| chr6:47269226 | AACAC | A | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+14708_1243+14 others(10): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269226 | |||||||
| chr6:47269234 | C | G | 1 | a0001c0001t0005g0300 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1243+14704G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269234 | |||||||
| chr6:47269240 | A | AAC | 5 | a0001c0001t0003g0019 a0001c0001t0004g0247 a0001c0001t0004g0299 others(2): Show |
5 | HG03139.hp2 HG03516.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243+14696_1243+14 others(8): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269240 | |||||||
| chr6:47269260 | C | T | 18 | a0001c0001t0001g0040 a0001c0001t0001g0150 a0001c0001t0003g0037 others(15): Show |
18 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1243+14678G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269260 | |||||||
| chr6:47269546 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1243+14392G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269546 | |||||||
| chr6:47269548 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0149 |
2 | HG00140.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1243+14390A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269548 | |||||||
| chr6:47269684 | T | G | 93 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(90): Show |
98 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1243+14254A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269684 | |||||||
| chr6:47269722 | T | A | 9 | a0001c0001t0002g0298 a0001c0001t0004g0319 a0001c0001t0004g0323 others(6): Show |
9 | HG01255.hp2 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1243+14216A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269722 | |||||||
| chr6:47269818 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1243+14120C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269818 | |||||||
| chr6:47269842 | G | C | 1 | a0001c0001t0001g0091 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1243+14096C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269842 | |||||||
| chr6:47269965 | G | A | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+13973C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269965 | |||||||
| chr6:47269968 | C | T | 1 | a0001c0001t0005g0314 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1243+13970G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47269968 | |||||||
| chr6:47270153 | G | A | 18 | a0001c0001t0001g0040 a0001c0001t0001g0150 a0001c0001t0003g0037 others(15): Show |
18 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1243+13785C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47270153 | |||||||
| chr6:47270256 | T | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(90): Show |
98 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1243+13682A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47270256 | |||||||
| chr6:47270275 | C | T | 1 | a0001c0001t0034g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1243+13663G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47270275 | |||||||
| chr6:47270366 | G | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(23): Show |
29 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1243+13572C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47270366 | |||||||
| chr6:47270377 | G | C | 2 | a0001c0001t0001g0112 a0001c0001t0003g0111 |
2 | NA18962.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1243+13561C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47270377 | |||||||
| chr6:47270385 | C | A | 87 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(84): Show |
92 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1243+13553G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47270385 | |||||||
| chr6:47270452 | A | G | 11 | a0001c0001t0002g0298 a0001c0001t0004g0319 a0001c0001t0004g0323 others(8): Show |
11 | HG01255.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+13486T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47270452 | |||||||
| chr6:47270602 | C | G | 6 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0009g0317 others(3): Show |
6 | HG02647.hp2 HG02683.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1243+13336G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47270602 | |||||||
| chr6:47270630 | G | C | 109 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0040 others(106): Show |
109 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1243+13308C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47270630 | |||||||
| chr6:47270948 | G | A | 9 | a0001c0001t0002g0298 a0001c0001t0004g0319 a0001c0001t0004g0323 others(6): Show |
9 | HG01255.hp2 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1243+12990C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47270948 | |||||||
| chr6:47271168 | A | G | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+12770T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271168 | |||||||
| chr6:47271169 | C | G | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+12769G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271169 | |||||||
| chr6:47271173 | G | A | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+12765C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271173 | |||||||
| chr6:47271177 | C | A | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+12761G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271177 | |||||||
| chr6:47271199 | A | G | 1 | a0001c0001t0002g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1243+12739T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271199 | |||||||
| chr6:47271252 | G | A | 2 | a0001c0001t0015g0183 a0001c0001t0015g0184 |
2 | NA18950.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1243+12686C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271252 | |||||||
| chr6:47271299 | G | T | 1 | a0001c0001t0003g0037 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1243+12639C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271299 | |||||||
| chr6:47271374 | A | G | 3 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0028g0048 |
3 | HG03139.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1243+12564T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271374 | |||||||
| chr6:47271412 | C | A | 1 | a0001c0005t0011g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1243+12526G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271412 | |||||||
| chr6:47271419 | TC | T | 37 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(34): Show |
40 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.1243+12518delG | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271419 | |||||||
| chr6:47271430 | G | A | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1243+12508C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271430 | |||||||
| chr6:47271592 | A | T | 1 | a0001c0001t0002g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1243+12346T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271592 | |||||||
| chr6:47271612 | G | T | 8 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0005g0282 others(5): Show |
10 | HG01069.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1243+12326C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271612 | |||||||
| chr6:47271683 | T | C | 3 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0028g0048 |
3 | HG03139.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1243+12255A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271683 | |||||||
| chr6:47271715 | C | G | 6 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0009g0317 others(3): Show |
6 | HG02647.hp2 HG02683.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1243+12223G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271715 | |||||||
| chr6:47271727 | AT | A | 5 | a0001c0001t0002g0331 a0001c0001t0013g0285 a0001c0001t0013g0322 others(2): Show |
5 | HG01884.hp1 HG02615.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243+12210delA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271727 | |||||||
| chr6:47271734 | G | A | 5 | a0001c0001t0002g0236 a0001c0001t0002g0320 a0001c0001t0002g0321 others(2): Show |
6 | HG02257.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1243+12204C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271734 | |||||||
| chr6:47271854 | G | A | 1 | a0001c0001t0005g0329 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1243+12084C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271854 | |||||||
| chr6:47271897 | C | A | 1 | a0001c0001t0001g0091 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1243+12041G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271897 | |||||||
| chr6:47271938 | A | C | 80 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0055 others(77): Show |
80 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1243+12000T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47271938 | |||||||
| chr6:47272026 | G | C | 2 | a0001c0001t0005g0173 a0001c0001t0047g0328 |
2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1243+11912C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47272026 | |||||||
| chr6:47272031 | A | C | 2 | a0001c0001t0005g0173 a0001c0001t0047g0328 |
2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1243+11907T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47272031 | |||||||
| chr6:47272080 | C | A | 1 | a0001c0001t0009g0270 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1243+11858G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47272080 | |||||||
| chr6:47272222 | GCAC | G | 37 | a0001c0001t0001g0024 a0001c0001t0001g0155 a0001c0001t0001g0161 others(34): Show |
39 | HG00423.hp2 HG00621.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.1243+11713_1243+11 others(9): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47272222 | |||||||
| chr6:47272485 | G | A | 3 | a0001c0001t0011g0302 a0001c0001t0050g0335 a0001c0001t0051g0334 |
3 | HG01255.hp2 HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1243+11453C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47272485 | |||||||
| chr6:47272549 | C | A | 1 | a0001c0001t0003g0075 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1243+11389G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47272549 | |||||||
| chr6:47272637 | C | T | 3 | a0001c0001t0011g0302 a0001c0001t0050g0335 a0001c0001t0051g0334 |
3 | HG01255.hp2 HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1243+11301G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47272637 | |||||||
| chr6:47272653 | A | G | 1 | a0001c0001t0004g0299 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1243+11285T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47272653 | |||||||
| chr6:47272740 | G | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(90): Show |
98 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1243+11198C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47272740 | |||||||
| chr6:47272788 | G | T | 39 | a0001c0001t0001g0024 a0001c0001t0001g0155 a0001c0001t0001g0161 others(36): Show |
41 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.1243+11150C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47272788 | |||||||
| chr6:47272821 | A | T | 2 | a0001c0001t0002g0288 a0003c0006t0002g0289 |
2 | HG01358.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1243+11117T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47272821 | |||||||
| chr6:47272909 | T | A | 1 | a0001c0001t0002g0237 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1243+11029A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47272909 | |||||||
| chr6:47273146 | C | A | 5 | a0001c0001t0002g0331 a0001c0001t0013g0285 a0001c0001t0013g0322 others(2): Show |
5 | HG01884.hp1 HG02615.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243+10792G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273146 | |||||||
| chr6:47273224 | T | C | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+10714A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273224 | |||||||
| chr6:47273379 | T | C | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1243+10559A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273379 | |||||||
| chr6:47273477 | A | C | 87 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(84): Show |
92 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1243+10461T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273477 | |||||||
| chr6:47273478 | A | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(226): Show |
237 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1243+10460T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273478 | |||||||
| chr6:47273555 | A | T | 1 | a0001c0001t0002g0245 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1243+10383T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273555 | |||||||
| chr6:47273566 | G | C | 1 | a0001c0001t0003g0035 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1243+10372C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273566 | |||||||
| chr6:47273595 | A | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(226): Show |
237 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1243+10343T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273595 | |||||||
| chr6:47273811 | G | A | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1243+10127C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273811 | |||||||
| chr6:47273889 | T | G | 2 | a0001c0001t0002g0256 a0001c0001t0004g0258 |
2 | HG00609.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1243+10049A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273889 | |||||||
| chr6:47273904 | T | C | 1 | a0001c0001t0002g0232 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1243+10034A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273904 | |||||||
| chr6:47273953 | G | A | 1 | a0001c0005t0011g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1243+9985C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273953 | |||||||
| chr6:47273976 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1243+9962G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273976 | |||||||
| chr6:47273999 | T | A | 1 | a0001c0001t0010g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1243+9939A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47273999 | |||||||
| chr6:47274016 | C | G | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+9922G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274016 | |||||||
| chr6:47274062 | A | G | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1243+9876T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274062 | |||||||
| chr6:47274071 | T | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(90): Show |
98 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1243+9867A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274071 | |||||||
| chr6:47274118 | G | A | 2 | a0001c0001t0009g0317 a0001c0003t0011g0172 |
2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1243+9820C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274118 | |||||||
| chr6:47274166 | C | T | 76 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
81 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1243+9772G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274166 | |||||||
| chr6:47274218 | G | A | 1 | a0001c0001t0002g0228 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1243+9720C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274218 | |||||||
| chr6:47274246 | G | A | 109 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0040 others(106): Show |
109 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1243+9692C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274246 | |||||||
| chr6:47274312 | C | T | 87 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(84): Show |
92 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1243+9626G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274312 | |||||||
| chr6:47274391 | G | C | 9 | a0001c0001t0002g0298 a0001c0001t0004g0319 a0001c0001t0004g0323 others(6): Show |
9 | HG01255.hp2 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1243+9547C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274391 | |||||||
| chr6:47274427 | G | A | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1243+9511C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274427 | |||||||
| chr6:47274478 | A | G | 37 | a0001c0001t0001g0024 a0001c0001t0001g0155 a0001c0001t0001g0161 others(34): Show |
39 | HG00423.hp2 HG00621.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.1243+9460T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274478 | |||||||
| chr6:47274483 | T | C | 1 | a0001c0001t0002g0228 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1243+9455A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274483 | |||||||
| chr6:47274666 | C | T | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+9272G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274666 | |||||||
| chr6:47274707 | C | T | 2 | a0001c0001t0002g0273 a0001c0001t0051g0334 |
2 | HG01255.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1243+9231G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274707 | |||||||
| chr6:47274816 | A | G | 6 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0213 others(3): Show |
6 | NA18940.hp1 NA18949.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.1243+9122T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274816 | |||||||
| chr6:47274997 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1243+8941A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47274997 | |||||||
| chr6:47275262 | C | G | 1 | a0001c0001t0002g0204 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1243+8676G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47275262 | |||||||
| chr6:47275454 | C | T | 1 | a0001c0001t0004g0258 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1243+8484G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47275454 | |||||||
| chr6:47275492 | C | T | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1243+8446G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47275492 | |||||||
| chr6:47275493 | G | A | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1243+8445C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47275493 | |||||||
| chr6:47275507 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1243+8431C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47275507 | |||||||
| chr6:47275513 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0045 others(2): Show |
5 | HG02486.hp2 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243+8425C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47275513 | |||||||
| chr6:47275580 | C | A | 2 | a0002c0002t0002g0310 a0002c0002t0004g0253 |
2 | HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1243+8358G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47275580 | |||||||
| chr6:47275664 | G | GA | 87 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(84): Show |
92 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1243+8273dupT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47275664 | |||||||
| chr6:47275683 | T | C | 1 | a0001c0001t0014g0324 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1243+8255A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47275683 | |||||||
| chr6:47275832 | C | A | 1 | a0001c0001t0018g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1243+8106G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47275832 | |||||||
| chr6:47275845 | G | C | 87 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(84): Show |
92 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1243+8093C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47275845 | |||||||
| chr6:47275849 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1243+8089A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47275849 | |||||||
| chr6:47276005 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1243+7933G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47276005 | |||||||
| chr6:47276062 | T | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(226): Show |
237 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1243+7876A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47276062 | |||||||
| chr6:47276246 | G | C | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1243+7692C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47276246 | |||||||
| chr6:47276263 | G | A | 45 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0055 others(42): Show |
45 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1243+7675C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47276263 | |||||||
| chr6:47276376 | C | A | 5 | a0001c0001t0002g0331 a0001c0001t0013g0285 a0001c0001t0013g0322 others(2): Show |
5 | HG01884.hp1 HG02615.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243+7562G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47276376 | |||||||
| chr6:47276791 | T | C | 1 | a0001c0001t0005g0329 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1243+7147A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47276791 | |||||||
| chr6:47277271 | C | T | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1243+6667G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47277271 | |||||||
| chr6:47277674 | T | C | 5 | a0001c0001t0002g0236 a0001c0001t0002g0320 a0001c0001t0002g0321 others(2): Show |
6 | HG02257.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1243+6264A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47277674 | |||||||
| chr6:47277717 | A | T | 3 | a0001c0001t0002g0209 a0001c0001t0004g0283 a0001c0001t0005g0284 |
3 | HG03195.hp1 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1243+6221T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47277717 | |||||||
| chr6:47277799 | C | G | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1243+6139G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47277799 | |||||||
| chr6:47278116 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0006g0158 |
2 | NA18952.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1243+5822T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47278116 | |||||||
| chr6:47278207 | A | G | 1 | a0001c0001t0004g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1243+5731T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47278207 | |||||||
| chr6:47278255 | C | G | 6 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0009g0317 others(3): Show |
6 | HG02647.hp2 HG02683.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1243+5683G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47278255 | |||||||
| chr6:47278436 | G | A | 1 | a0001c0001t0002g0273 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1243+5502C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47278436 | |||||||
| chr6:47278695 | C | T | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1243+5243G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47278695 | |||||||
| chr6:47278821 | G | A | 2 | a0001c0001t0008g0214 a0001c0001t0010g0268 |
2 | NA18906.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1243+5117C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47278821 | |||||||
| chr6:47278831 | T | A | 1 | a0001c0001t0005g0173 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1243+5107A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47278831 | |||||||
| chr6:47278957 | A | C | 1 | a0001c0001t0003g0031 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1243+4981T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47278957 | |||||||
| chr6:47279119 | C | A | 1 | a0001c0001t0003g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1243+4819G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279119 | |||||||
| chr6:47279372 | T | C | 17 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0009g0317 others(14): Show |
17 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1243+4566A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279372 | |||||||
| chr6:47279401 | G | A | 5 | a0001c0001t0002g0298 a0001c0001t0004g0319 a0001c0001t0004g0323 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1243+4537C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279401 | |||||||
| chr6:47279407 | T | C | 1 | a0001c0001t0007g0022 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1243+4531A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279407 | |||||||
| chr6:47279416 | C | A | 17 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0009g0317 others(14): Show |
17 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1243+4522G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279416 | |||||||
| chr6:47279435 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1243+4503C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279435 | |||||||
| chr6:47279453 | G | A | 18 | a0001c0001t0001g0040 a0001c0001t0001g0150 a0001c0001t0003g0037 others(15): Show |
18 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1243+4485C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279453 | |||||||
| chr6:47279509 | C | A | 1 | a0001c0001t0002g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1243+4429G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279509 | |||||||
| chr6:47279579 | T | A | 1 | a0001c0001t0001g0016 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1243+4359A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279579 | |||||||
| chr6:47279586 | C | A | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1243+4352G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279586 | |||||||
| chr6:47279596 | C | G | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+4342G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279596 | |||||||
| chr6:47279669 | C | A | 1 | a0001c0001t0033g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1243+4269G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279669 | |||||||
| chr6:47279955 | G | A | 4 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0028g0048 others(1): Show |
4 | HG02683.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1243+3983C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279955 | |||||||
| chr6:47279988 | T | C | 4 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0028g0048 others(1): Show |
4 | HG02683.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1243+3950A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47279988 | |||||||
| chr6:47280084 | T | G | 1 | a0001c0001t0003g0071 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1243+3854A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47280084 | |||||||
| chr6:47280091 | C | T | 1 | a0001c0003t0044g0290 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1243+3847G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47280091 | |||||||
| chr6:47280164 | G | T | 9 | a0001c0001t0002g0209 a0001c0001t0002g0331 a0001c0001t0004g0283 others(6): Show |
9 | HG01884.hp1 HG02615.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.1243+3774C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47280164 | |||||||
| chr6:47280310 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1243+3628G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47280310 | |||||||
| chr6:47280409 | C | T | 1 | a0001c0005t0011g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1243+3529G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47280409 | |||||||
| chr6:47280430 | A | T | 3 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0028g0048 |
3 | HG03139.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1243+3508T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47280430 | |||||||
| chr6:47280459 | T | C | 3 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0028g0048 |
3 | HG03139.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1243+3479A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47280459 | |||||||
| chr6:47280466 | A | G | 1 | a0001c0001t0004g0265 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1243+3472T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47280466 | |||||||
| chr6:47280490 | C | T | 80 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0055 others(77): Show |
80 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1243+3448G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47280490 | |||||||
| chr6:47280602 | T | A | 14 | a0001c0001t0009g0317 a0001c0003t0011g0172 a0001c0008t0040g0166 others(11): Show |
14 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1243+3336A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47280602 | |||||||
| chr6:47280681 | T | C | 3 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0028g0048 |
3 | HG03139.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1243+3257A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47280681 | |||||||
| chr6:47281096 | A | T | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1243+2842T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281096 | |||||||
| chr6:47281384 | A | AT | 6 | a0001c0001t0002g0210 a0001c0001t0003g0035 a0001c0001t0003g0071 others(3): Show |
6 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1243+2553dupA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281384 | |||||||
| chr6:47281439 | G | A | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1243+2499C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281439 | |||||||
| chr6:47281465 | C | T | 5 | a0001c0001t0002g0179 a0001c0001t0002g0193 a0001c0001t0002g0194 others(2): Show |
5 | NA18960.hp1 NA18973.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1243+2473G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281465 | |||||||
| chr6:47281537 | T | C | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1243+2401A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281537 | |||||||
| chr6:47281551 | C | T | 14 | a0001c0001t0009g0317 a0001c0003t0011g0172 a0001c0008t0040g0166 others(11): Show |
14 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1243+2387G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281551 | |||||||
| chr6:47281570 | G | A | 1 | a0001c0001t0005g0329 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1243+2368C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281570 | |||||||
| chr6:47281672 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1243+2266G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281672 | |||||||
| chr6:47281689 | G | A | 11 | a0001c0001t0002g0298 a0001c0001t0004g0319 a0001c0001t0004g0323 others(8): Show |
11 | HG01255.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+2249C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281689 | |||||||
| chr6:47281699 | C | T | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1243+2239G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281699 | |||||||
| chr6:47281700 | G | T | 1 | a0001c0001t0041g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1243+2238C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281700 | |||||||
| chr6:47281819 | A | AAATAATT others(10): Show |
11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+2118_1243+211 others(21): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281819 | |||||||
| chr6:47281820 | C | A | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+2118G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281820 | |||||||
| chr6:47281831 | A | AT | 27 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(24): Show |
30 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1243+2106dupA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281831 | |||||||
| chr6:47281904 | T | C | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1243+2034A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47281904 | |||||||
| chr6:47282044 | G | A | 1 | a0001c0001t0004g0287 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1243+1894C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282044 | |||||||
| chr6:47282105 | G | T | 2 | a0001c0001t0009g0317 a0001c0003t0011g0172 |
2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1243+1833C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282105 | |||||||
| chr6:47282282 | G | A | 9 | a0001c0001t0002g0298 a0001c0001t0004g0319 a0001c0001t0004g0323 others(6): Show |
9 | HG01255.hp2 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1243+1656C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282282 | |||||||
| chr6:47282316 | T | TG | 14 | a0001c0001t0009g0317 a0001c0003t0011g0172 a0001c0008t0040g0166 others(11): Show |
14 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1243+1621dupC | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282316 | |||||||
| chr6:47282358 | T | C | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+1580A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282358 | |||||||
| chr6:47282384 | C | CA | 42 | a0001c0001t0001g0045 a0001c0001t0001g0056 a0001c0001t0001g0073 others(39): Show |
42 | HG00621.hp1 HG00741.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.1243+1553dupT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282384 | |||||||
| chr6:47282384 | CAAAAAAA others(5): Show |
C | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+1542_1243+155 others(16): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282384 | |||||||
| chr6:47282385 | AAAAAAAA others(3): Show |
A | 19 | a0001c0001t0001g0040 a0001c0001t0001g0150 a0001c0001t0003g0037 others(16): Show |
19 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.1243+1543_1243+155 others(14): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282385 | |||||||
| chr6:47282394 | AT | A | 6 | a0001c0001t0002g0298 a0001c0001t0003g0019 a0001c0001t0005g0173 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1243+1543delA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282394 | |||||||
| chr6:47282395 | T | A | 180 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(177): Show |
185 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1243+1543A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282395 | |||||||
| chr6:47282408 | C | A | 1 | a0001c0001t0004g0332 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1243+1530G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282408 | |||||||
| chr6:47282430 | G | T | 8 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0005g0282 others(5): Show |
10 | HG01069.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1243+1508C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282430 | |||||||
| chr6:47282553 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1243+1385G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282553 | |||||||
| chr6:47282632 | C | T | 1 | a0001c0001t0008g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1243+1306G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282632 | |||||||
| chr6:47282711 | A | G | 1 | a0002c0002t0004g0293 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1243+1227T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47282711 | |||||||
| chr6:47283034 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0002g0298 others(11): Show |
16 | HG01069.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1243+904C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283034 | |||||||
| chr6:47283092 | G | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0134 a0001c0001t0003g0136 others(1): Show |
5 | HG01168.hp2 HG01169.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243+846C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283092 | |||||||
| chr6:47283229 | A | G | 4 | a0001c0001t0001g0095 a0001c0001t0001g0140 a0001c0001t0003g0094 others(1): Show |
4 | HG02071.hp2 NA18969.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1243+709T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283229 | |||||||
| chr6:47283230 | T | C | 19 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0002g0298 others(16): Show |
21 | HG01069.hp1 HG01255.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1243+708A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283230 | |||||||
| chr6:47283280 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1243+658G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283280 | |||||||
| chr6:47283317 | G | C | 14 | a0001c0001t0009g0317 a0001c0003t0011g0172 a0001c0008t0040g0166 others(11): Show |
14 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1243+621C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283317 | |||||||
| chr6:47283371 | T | G | 1 | a0001c0001t0005g0282 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1243+567A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283371 | |||||||
| chr6:47283430 | C | T | 18 | a0001c0001t0001g0040 a0001c0001t0001g0150 a0001c0001t0003g0037 others(15): Show |
18 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1243+508G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283430 | |||||||
| chr6:47283485 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1243+453G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283485 | |||||||
| chr6:47283601 | T | G | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1243+337A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283601 | |||||||
| chr6:47283781 | C | T | 1 | a0001c0001t0003g0115 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1243+157G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283781 | |||||||
| chr6:47283880 | G | C | 1 | a0001c0001t0014g0324 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1243+58C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283880 | |||||||
| chr6:47283921 | G | A | 13 | a0001c0001t0009g0317 a0001c0003t0011g0172 a0002c0002t0002g0208 others(10): Show |
13 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1243+17C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283921 | |||||||
| chr6:47283931 | G | C | 1 | a0001c0001t0003g0046 | 1 | HG01243.hp1 | splice_region_variant&intron_variant | LOW | c.1243+7C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 3/5 | chr6 | 47283931 | |||||||
| chr6:47284471 | T | C | 1 | a0001c0001t0005g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.749-39A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47284471 | |||||||
| chr6:47284991 | C | T | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.749-559G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47284991 | |||||||
| chr6:47285012 | T | C | 29 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0002g0298 others(26): Show |
31 | HG01069.hp1 HG01255.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.749-580A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47285012 | |||||||
| chr6:47285020 | T | A | 3 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0028g0048 |
3 | HG03139.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.749-588A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47285020 | |||||||
| chr6:47285026 | TAAG | T | 3 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0004g0231 |
3 | NA18952.hp1 NA19007.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.749-597_749-595del others(3): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47285026 | |||||||
| chr6:47285450 | T | G | 1 | a0001c0001t0004g0299 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.748+494A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47285450 | |||||||
| chr6:47285489 | C | T | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.748+455G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47285489 | |||||||
| chr6:47285598 | T | C | 3 | a0001c0001t0011g0302 a0001c0001t0050g0335 a0001c0001t0051g0334 |
3 | HG01255.hp2 HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.748+346A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47285598 | |||||||
| chr6:47285675 | G | A | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.748+269C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47285675 | |||||||
| chr6:47285765 | C | A | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.748+179G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47285765 | |||||||
| chr6:47285767 | T | C | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.748+177A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47285767 | |||||||
| chr6:47285775 | T | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0150 others(50): Show |
55 | HG00642.hp2 HG01069.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.748+169A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47285775 | |||||||
| chr6:47285782 | C | A | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.748+162G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47285782 | |||||||
| chr6:47285895 | A | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(33): Show |
39 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.748+49T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 2/5 | chr6 | 47285895 | |||||||
| chr6:47286910 | G | A | 1 | a0001c0001t0014g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.97-315C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47286910 | |||||||
| chr6:47286970 | G | A | 4 | a0001c0001t0004g0235 a0001c0001t0005g0300 a0001c0001t0005g0315 others(1): Show |
4 | HG02145.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-375C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47286970 | |||||||
| chr6:47286996 | C | CATTTGCA others(9): Show |
3 | a0001c0001t0002g0233 a0001c0001t0003g0047 a0001c0001t0003g0053 |
3 | NA19007.hp1 NA19007.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.97-417_97-402dupTG others(14): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47286996 | |||||||
| chr6:47287002 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.97-407G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287002 | |||||||
| chr6:47287145 | G | A | 19 | a0001c0001t0001g0040 a0001c0001t0001g0150 a0001c0001t0003g0037 others(16): Show |
19 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.97-550C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287145 | |||||||
| chr6:47287196 | A | G | 2 | a0001c0001t0009g0317 a0001c0003t0011g0172 |
2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.97-601T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287196 | |||||||
| chr6:47287222 | G | A | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-627C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287222 | |||||||
| chr6:47287307 | C | CA | 63 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0080 others(60): Show |
65 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.97-713dupT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287307 | |||||||
| chr6:47287307 | C | CAA | 7 | a0001c0001t0002g0215 a0001c0001t0002g0229 a0001c0001t0003g0019 others(4): Show |
7 | HG01074.hp2 HG02027.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-714_97-713dupTT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287307 | |||||||
| chr6:47287307 | CA | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0129 a0001c0001t0001g0131 others(18): Show |
23 | HG00642.hp2 HG01069.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.97-713delT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287307 | |||||||
| chr6:47287307 | CAAAA | C | 10 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(7): Show |
10 | HG01891.hp1 HG02559.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-716_97-713delTT others(2): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287307 | |||||||
| chr6:47287323 | A | AG | 79 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0055 others(76): Show |
79 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.97-729_97-728insC | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287323 | |||||||
| chr6:47287325 | A | G | 1 | a0001c0001t0002g0273 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.97-730T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287325 | |||||||
| chr6:47287326 | A | AAAAAAGA others(4): Show |
1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-732_97-731insCT others(9): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287326 | |||||||
| chr6:47287326 | A | AAAAAGAA others(3): Show |
1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97-732_97-731insCT others(8): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287326 | |||||||
| chr6:47287369 | T | C | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-774A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287369 | |||||||
| chr6:47287377 | G | GAAAATAA others(56): Show |
1 | a0001c0001t0004g0332 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.97-845_97-783dupAA others(61): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287377 | |||||||
| chr6:47287765 | T | C | 1 | a0001c0001t0002g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.97-1170A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287765 | |||||||
| chr6:47287826 | G | A | 4 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0004g0332 others(1): Show |
4 | HG03139.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-1231C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287826 | |||||||
| chr6:47287981 | G | A | 1 | a0001c0001t0006g0078 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.97-1386C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47287981 | |||||||
| chr6:47288105 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0002g0298 others(26): Show |
31 | HG01069.hp1 HG01255.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.97-1510G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288105 | |||||||
| chr6:47288106 | G | A | 1 | a0001c0001t0005g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.97-1511C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288106 | |||||||
| chr6:47288247 | T | C | 32 | a0001c0001t0001g0024 a0001c0001t0001g0155 a0001c0001t0001g0161 others(29): Show |
32 | HG00423.hp2 HG00621.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.97-1652A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288247 | |||||||
| chr6:47288340 | T | C | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-1745A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288340 | |||||||
| chr6:47288434 | C | T | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-1839G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288434 | |||||||
| chr6:47288487 | G | A | 15 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0002g0298 others(12): Show |
17 | HG01069.hp1 HG01255.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.97-1892C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288487 | |||||||
| chr6:47288573 | T | TA | 87 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0056 others(84): Show |
87 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.97-1979dupT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288573 | |||||||
| chr6:47288573 | TA | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0002g0234 others(14): Show |
19 | HG01069.hp1 HG01255.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.97-1979delT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288573 | |||||||
| chr6:47288582 | AAAAG | A | 19 | a0001c0001t0001g0040 a0001c0001t0001g0150 a0001c0001t0003g0037 others(16): Show |
19 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.97-1991_97-1988del others(4): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288582 | |||||||
| chr6:47288609 | T | G | 1 | a0001c0001t0002g0216 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.97-2014A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288609 | |||||||
| chr6:47288614 | C | T | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-2019G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288614 | |||||||
| chr6:47288767 | A | T | 2 | a0002c0002t0002g0310 a0002c0002t0004g0253 |
2 | HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.97-2172T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288767 | |||||||
| chr6:47288877 | A | T | 1 | a0001c0001t0008g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97-2282T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288877 | |||||||
| chr6:47288911 | C | T | 1 | a0001c0001t0005g0329 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.97-2316G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47288911 | |||||||
| chr6:47289036 | G | A | 1 | a0001c0001t0008g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97-2441C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47289036 | |||||||
| chr6:47289114 | C | T | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-2519G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47289114 | |||||||
| chr6:47289144 | T | C | 3 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0028g0048 |
3 | HG03139.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.97-2549A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47289144 | |||||||
| chr6:47289256 | C | T | 4 | a0001c0001t0008g0325 a0001c0001t0009g0317 a0001c0003t0011g0172 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-2661G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47289256 | |||||||
| chr6:47289317 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0002g0298 others(13): Show |
18 | HG01069.hp1 HG01255.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.97-2722G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47289317 | |||||||
| chr6:47289335 | A | C | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-2740T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47289335 | |||||||
| chr6:47289387 | T | C | 1 | a0001c0001t0008g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97-2792A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47289387 | |||||||
| chr6:47289424 | G | A | 10 | a0001c0001t0002g0209 a0001c0001t0002g0331 a0001c0001t0004g0283 others(7): Show |
10 | HG01884.hp1 HG02615.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-2829C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47289424 | |||||||
| chr6:47289646 | C | T | 1 | a0001c0001t0014g0324 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.97-3051G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47289646 | |||||||
| chr6:47289674 | C | T | 1 | a0001c0001t0013g0322 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.97-3079G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47289674 | |||||||
| chr6:47289715 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.97-3120G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47289715 | |||||||
| chr6:47289885 | T | C | 5 | a0001c0001t0002g0236 a0001c0001t0002g0320 a0001c0001t0002g0321 others(2): Show |
6 | HG02257.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-3290A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47289885 | |||||||
| chr6:47290054 | A | C | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-3459T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47290054 | |||||||
| chr6:47290101 | G | A | 29 | a0001c0001t0001g0040 a0001c0001t0001g0150 a0001c0001t0003g0037 others(26): Show |
29 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.97-3506C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47290101 | |||||||
| chr6:47290138 | A | G | 4 | a0001c0001t0008g0325 a0001c0001t0009g0317 a0001c0003t0011g0172 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-3543T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47290138 | |||||||
| chr6:47290191 | A | G | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-3596T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47290191 | |||||||
| chr6:47290261 | C | A | 1 | a0001c0001t0008g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97-3666G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47290261 | |||||||
| chr6:47290401 | T | C | 1 | a0001c0001t0002g0331 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97-3806A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47290401 | |||||||
| chr6:47290450 | C | T | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97-3855G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47290450 | |||||||
| chr6:47290621 | C | T | 1 | a0001c0001t0033g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.97-4026G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47290621 | |||||||
| chr6:47290625 | CCTGTTTA others(12): Show |
C | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-4049_97-4031del others(19): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47290625 | |||||||
| chr6:47290645 | C | A | 3 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0028g0048 |
3 | HG03139.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.97-4050G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47290645 | |||||||
| chr6:47290727 | G | A | 1 | a0001c0001t0008g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97-4132C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47290727 | |||||||
| chr6:47290880 | A | C | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-4285T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47290880 | |||||||
| chr6:47290987 | A | G | 18 | a0001c0001t0001g0040 a0001c0001t0001g0150 a0001c0001t0003g0037 others(15): Show |
18 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.97-4392T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47290987 | |||||||
| chr6:47291297 | A | C | 1 | a0001c0001t0002g0303 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.97-4702T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291297 | |||||||
| chr6:47291390 | C | T | 1 | a0001c0001t0002g0307 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.97-4795G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291390 | |||||||
| chr6:47291424 | GA | G | 20 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0002g0298 others(17): Show |
22 | HG01069.hp1 HG01255.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.97-4830delT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291424 | |||||||
| chr6:47291480 | G | T | 1 | a0001c0001t0004g0332 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.97-4885C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291480 | |||||||
| chr6:47291509 | G | A | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-4914C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291509 | |||||||
| chr6:47291550 | A | G | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-4955T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291550 | |||||||
| chr6:47291642 | G | A | 1 | a0001c0001t0018g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.97-5047C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291642 | |||||||
| chr6:47291741 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.97-5146A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291741 | |||||||
| chr6:47291764 | A | G | 1 | a0001c0001t0042g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.97-5169T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291764 | |||||||
| chr6:47291804 | T | G | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.97-5209A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291804 | |||||||
| chr6:47291866 | C | T | 6 | a0001c0001t0002g0001 a0001c0001t0002g0303 a0001c0001t0002g0307 others(3): Show |
8 | HG00323.hp1 HG01074.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-5271G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291866 | |||||||
| chr6:47291909 | C | G | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.97-5314G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291909 | |||||||
| chr6:47291947 | T | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(229): Show |
240 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.97-5352A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291947 | |||||||
| chr6:47291973 | A | G | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-5378T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47291973 | |||||||
| chr6:47292000 | C | T | 1 | a0001c0001t0003g0090 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.97-5405G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47292000 | |||||||
| chr6:47292087 | T | C | 1 | a0001c0005t0011g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.97-5492A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47292087 | |||||||
| chr6:47292104 | G | A | 2 | a0001c0001t0002g0288 a0003c0006t0002g0289 |
2 | HG01358.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.97-5509C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47292104 | |||||||
| chr6:47292278 | T | G | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-5683A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47292278 | |||||||
| chr6:47292319 | C | G | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97-5724G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47292319 | |||||||
| chr6:47292320 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.97-5725C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47292320 | |||||||
| chr6:47292323 | G | A | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-5728C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47292323 | |||||||
| chr6:47292377 | T | TA | 5 | a0001c0001t0001g0002 a0001c0001t0007g0003 a0001c0001t0007g0021 others(2): Show |
7 | HG01069.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-5783dupT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47292377 | |||||||
| chr6:47292755 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.97-6160G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47292755 | |||||||
| chr6:47292896 | C | T | 3 | a0001c0001t0003g0037 a0001c0001t0042g0171 a0001c0003t0044g0290 |
3 | HG02572.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.97-6301G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47292896 | |||||||
| chr6:47292920 | G | A | 2 | a0001c0001t0005g0173 a0001c0001t0047g0328 |
2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.97-6325C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47292920 | |||||||
| chr6:47293071 | A | G | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-6476T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47293071 | |||||||
| chr6:47293222 | C | T | 1 | a0001c0001t0016g0272 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.97-6627G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47293222 | |||||||
| chr6:47293225 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.97-6630C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47293225 | |||||||
| chr6:47293425 | C | T | 11 | a0002c0002t0002g0208 a0002c0002t0002g0310 a0002c0002t0004g0253 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-6830G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47293425 | |||||||
| chr6:47293588 | T | C | 1 | a0001c0001t0014g0250 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.97-6993A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47293588 | |||||||
| chr6:47293634 | A | T | 1 | a0001c0001t0005g0174 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.97-7039T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47293634 | |||||||
| chr6:47293795 | C | T | 1 | a0001c0001t0009g0203 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.97-7200G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47293795 | |||||||
| chr6:47294085 | C | T | 1 | a0001c0001t0014g0324 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.97-7490G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47294085 | |||||||
| chr6:47294183 | C | T | 2 | a0001c0001t0001g0154 a0001c0009t0003g0086 |
2 | NA18972.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.97-7588G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47294183 | |||||||
| chr6:47294224 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.97-7629T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47294224 | |||||||
| chr6:47294245 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.97-7650C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47294245 | |||||||
| chr6:47294422 | G | A | 3 | a0001c0001t0002g0298 a0001c0001t0004g0319 a0001c0001t0004g0323 |
3 | HG01891.hp2 HG02717.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.97-7827C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47294422 | |||||||
| chr6:47294505 | C | T | 3 | a0001c0001t0011g0302 a0001c0001t0050g0335 a0001c0001t0051g0334 |
3 | HG01255.hp2 HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.97-7910G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47294505 | |||||||
| chr6:47294673 | A | T | 85 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0045 others(82): Show |
85 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.97-8078T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47294673 | |||||||
| chr6:47294697 | CT | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(223): Show |
234 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.97-8103delA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47294697 | |||||||
| chr6:47294700 | T | C | 3 | a0001c0001t0002g0298 a0001c0001t0004g0319 a0001c0001t0004g0323 |
3 | HG01891.hp2 HG02717.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.97-8105A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47294700 | |||||||
| chr6:47294760 | G | A | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-8165C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47294760 | |||||||
| chr6:47295074 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.97-8479T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47295074 | |||||||
| chr6:47295210 | T | C | 1 | a0001c0001t0004g0265 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.97-8615A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47295210 | |||||||
| chr6:47295300 | G | A | 2 | a0001c0001t0003g0019 a0001c0001t0004g0299 |
2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.97-8705C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47295300 | |||||||
| chr6:47295345 | T | C | 1 | a0001c0001t0004g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.97-8750A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47295345 | |||||||
| chr6:47295462 | C | T | 1 | a0001c0001t0002g0256 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.97-8867G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47295462 | |||||||
| chr6:47295578 | C | G | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-8983G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47295578 | |||||||
| chr6:47295783 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0002g0311 others(1): Show |
4 | HG02486.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-9188A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47295783 | |||||||
| chr6:47295804 | T | TA | 321 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(318): Show |
333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.97-9210dupT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47295804 | |||||||
| chr6:47295804 | T | TAA | 9 | a0001c0001t0002g0209 a0001c0001t0002g0331 a0001c0001t0004g0283 others(6): Show |
9 | HG01884.hp1 HG02615.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-9211_97-9210dup others(2): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47295804 | |||||||
| chr6:47295821 | T | G | 1 | a0001c0001t0002g0266 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.97-9226A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47295821 | |||||||
| chr6:47295862 | T | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0150 others(36): Show |
41 | HG00642.hp2 HG01069.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.97-9267A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47295862 | |||||||
| chr6:47295878 | C | T | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-9283G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47295878 | |||||||
| chr6:47296006 | C | T | 4 | a0001c0001t0002g0205 a0001c0001t0003g0008 a0001c0001t0003g0163 others(1): Show |
5 | HG02015.hp1 HG02129.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-9411G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47296006 | |||||||
| chr6:47296053 | G | A | 1 | a0001c0001t0028g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.97-9458C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47296053 | |||||||
| chr6:47296142 | G | A | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-9547C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47296142 | |||||||
| chr6:47296232 | C | G | 1 | a0001c0001t0008g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97-9637G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47296232 | |||||||
| chr6:47296444 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.97-9849G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47296444 | |||||||
| chr6:47296477 | T | C | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-9882A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47296477 | |||||||
| chr6:47296603 | G | A | 1 | a0001c0001t0008g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97-10008C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47296603 | |||||||
| chr6:47296663 | A | G | 1 | a0001c0001t0003g0054 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.97-10068T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47296663 | |||||||
| chr6:47296713 | C | A | 2 | a0001c0001t0034g0036 a0001c0001t0035g0164 |
2 | HG02486.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.97-10118G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47296713 | |||||||
| chr6:47296824 | T | C | 14 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0004g0235 others(11): Show |
16 | HG01069.hp1 HG01255.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.97-10229A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47296824 | |||||||
| chr6:47296862 | C | T | 1 | a0001c0001t0002g0286 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.97-10267G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47296862 | |||||||
| chr6:47296891 | G | A | 1 | a0001c0001t0041g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.97-10296C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47296891 | |||||||
| chr6:47296992 | G | A | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-10397C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47296992 | |||||||
| chr6:47297014 | C | A | 1 | a0001c0001t0002g0237 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.97-10419G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297014 | |||||||
| chr6:47297185 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.97-10590C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297185 | |||||||
| chr6:47297208 | T | G | 1 | a0001c0001t0004g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.97-10613A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297208 | |||||||
| chr6:47297354 | C | CA | 4 | a0001c0001t0002g0205 a0001c0001t0003g0008 a0001c0001t0003g0163 others(1): Show |
5 | HG02015.hp1 HG02129.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-10760dupT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297354 | |||||||
| chr6:47297417 | C | T | 4 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0004g0241 others(1): Show |
4 | HG01123.hp2 HG01261.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-10822G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297417 | |||||||
| chr6:47297448 | T | C | 2 | a0001c0001t0001g0154 a0001c0009t0003g0086 |
2 | NA18972.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.97-10853A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297448 | |||||||
| chr6:47297510 | C | CT | 93 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0055 others(90): Show |
94 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.97-10916dupA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297510 | |||||||
| chr6:47297510 | CT | C | 48 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0028 others(45): Show |
50 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.97-10916delA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297510 | |||||||
| chr6:47297510 | CTTT | C | 10 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0004g0235 others(7): Show |
12 | HG01069.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.97-10918_97-10916d others(5): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297510 | |||||||
| chr6:47297514 | T | G | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-10919A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297514 | |||||||
| chr6:47297554 | G | A | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-10959C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297554 | |||||||
| chr6:47297625 | C | G | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97-11030G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297625 | |||||||
| chr6:47297765 | C | T | 1 | a0001c0001t0003g0053 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.97-11170G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297765 | |||||||
| chr6:47297842 | C | A | 1 | a0001c0001t0005g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.97-11247G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297842 | |||||||
| chr6:47297971 | C | G | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-11376G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297971 | |||||||
| chr6:47297988 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.97-11393T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47297988 | |||||||
| chr6:47298001 | C | T | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97-11406G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298001 | |||||||
| chr6:47298009 | T | A | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11407A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298009 | |||||||
| chr6:47298011 | T | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11405A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298011 | |||||||
| chr6:47298015 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11401T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298015 | |||||||
| chr6:47298016 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11400T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298016 | |||||||
| chr6:47298022 | T | G | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11394A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298022 | |||||||
| chr6:47298026 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11390T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298026 | |||||||
| chr6:47298027 | T | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11389A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298027 | |||||||
| chr6:47298028 | A | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11388T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298028 | |||||||
| chr6:47298029 | A | T | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11387T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298029 | |||||||
| chr6:47298030 | A | T | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11386T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298030 | |||||||
| chr6:47298035 | T | G | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11381A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298035 | |||||||
| chr6:47298036 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11380C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298036 | |||||||
| chr6:47298038 | T | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11378A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298038 | |||||||
| chr6:47298040 | T | G | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11376A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298040 | |||||||
| chr6:47298041 | A | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11375T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298041 | |||||||
| chr6:47298042 | T | G | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11374A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298042 | |||||||
| chr6:47298044 | G | T | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11372C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298044 | |||||||
| chr6:47298047 | A | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11369T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298047 | |||||||
| chr6:47298048 | A | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11368T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298048 | |||||||
| chr6:47298050 | G | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11366C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298050 | |||||||
| chr6:47298055 | A | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11361T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298055 | |||||||
| chr6:47298056 | A | T | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11360T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298056 | |||||||
| chr6:47298058 | A | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11358T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298058 | |||||||
| chr6:47298060 | A | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11356T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298060 | |||||||
| chr6:47298068 | A | T | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11348T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298068 | |||||||
| chr6:47298071 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11345T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298071 | |||||||
| chr6:47298072 | G | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11344C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298072 | |||||||
| chr6:47298075 | A | T | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11341T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298075 | |||||||
| chr6:47298076 | T | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11340A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298076 | |||||||
| chr6:47298077 | T | A | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11339A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298077 | |||||||
| chr6:47298078 | T | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11338A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298078 | |||||||
| chr6:47298085 | A | C | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+11331T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298085 | |||||||
| chr6:47298105 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0024 others(121): Show |
131 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.96+11311T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298105 | |||||||
| chr6:47298211 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0024 others(121): Show |
131 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.96+11205T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298211 | |||||||
| chr6:47298284 | T | TA | 9 | a0001c0001t0002g0267 a0001c0001t0002g0307 a0001c0001t0010g0268 others(6): Show |
9 | HG01255.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+11131dupT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298284 | |||||||
| chr6:47298284 | T | TAAA | 11 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0002g0298 others(8): Show |
13 | HG01069.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.96+11129_96+11131d others(5): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298284 | |||||||
| chr6:47298284 | TA | T | 16 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0087 others(13): Show |
16 | HG00639.hp2 HG01070.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.96+11131delT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298284 | |||||||
| chr6:47298516 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.96+10900A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298516 | |||||||
| chr6:47298522 | C | T | 10 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0004g0235 others(7): Show |
12 | HG01069.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.96+10894G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298522 | |||||||
| chr6:47298683 | G | A | 1 | a0001c0001t0008g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.96+10733C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298683 | |||||||
| chr6:47298960 | A | C | 326 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(323): Show |
337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.96+10456T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298960 | |||||||
| chr6:47298961 | C | T | 1 | a0001c0001t0003g0051 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.96+10455G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47298961 | |||||||
| chr6:47299005 | T | C | 2 | a0001c0001t0013g0285 a0001c0001t0013g0322 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.96+10411A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47299005 | |||||||
| chr6:47299159 | A | T | 2 | a0001c0001t0001g0154 a0001c0009t0003g0086 |
2 | NA18972.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.96+10257T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47299159 | |||||||
| chr6:47299190 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.96+10226C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47299190 | |||||||
| chr6:47299331 | C | G | 18 | a0001c0001t0001g0040 a0001c0001t0001g0150 a0001c0001t0003g0037 others(15): Show |
18 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.96+10085G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47299331 | |||||||
| chr6:47299409 | G | A | 1 | a0001c0001t0012g0145 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.96+10007C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47299409 | |||||||
| chr6:47299546 | A | G | 85 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(82): Show |
90 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.96+9870T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47299546 | |||||||
| chr6:47299741 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0004g0235 others(22): Show |
27 | HG01069.hp1 HG01255.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.96+9675A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47299741 | |||||||
| chr6:47299785 | T | C | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.96+9631A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47299785 | |||||||
| chr6:47299945 | G | A | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+9471C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47299945 | |||||||
| chr6:47299990 | A | G | 3 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0004g0219 |
3 | HG02027.hp2 NA18975.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.96+9426T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47299990 | |||||||
| chr6:47300088 | A | G | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+9328T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47300088 | |||||||
| chr6:47300111 | G | A | 17 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0004g0235 others(14): Show |
19 | HG00642.hp2 HG01069.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+9305C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47300111 | |||||||
| chr6:47300153 | G | T | 1 | a0001c0001t0002g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.96+9263C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47300153 | |||||||
| chr6:47300507 | G | T | 1 | a0001c0001t0004g0177 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.96+8909C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47300507 | |||||||
| chr6:47300706 | C | G | 3 | a0001c0001t0011g0302 a0001c0001t0050g0335 a0001c0001t0051g0334 |
3 | HG01255.hp2 HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.96+8710G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47300706 | |||||||
| chr6:47300804 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.96+8612G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47300804 | |||||||
| chr6:47300843 | T | C | 1 | a0001c0001t0028g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.96+8573A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47300843 | |||||||
| chr6:47301129 | C | T | 1 | a0001c0001t0005g0314 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.96+8287G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47301129 | |||||||
| chr6:47301162 | A | G | 1 | a0001c0001t0002g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.96+8254T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47301162 | |||||||
| chr6:47301247 | C | G | 219 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(216): Show |
226 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.96+8169G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47301247 | |||||||
| chr6:47301334 | C | T | 1 | a0001c0001t0002g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.96+8082G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47301334 | |||||||
| chr6:47301408 | G | A | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.96+8008C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47301408 | |||||||
| chr6:47301433 | T | G | 2 | a0001c0001t0004g0323 a0001c0001t0005g0173 |
2 | HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.96+7983A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47301433 | |||||||
| chr6:47301436 | T | C | 1 | a0001c0001t0002g0200 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.96+7980A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47301436 | |||||||
| chr6:47301576 | A | T | 1 | a0001c0001t0033g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.96+7840T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47301576 | |||||||
| chr6:47301634 | C | T | 80 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0055 others(77): Show |
80 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.96+7782G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47301634 | |||||||
| chr6:47301759 | T | C | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+7657A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47301759 | |||||||
| chr6:47301776 | C | T | 1 | a0001c0001t0002g0320 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+7640G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47301776 | |||||||
| chr6:47301850 | C | G | 42 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(39): Show |
44 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.96+7566G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47301850 | |||||||
| chr6:47301999 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.96+7417A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47301999 | |||||||
| chr6:47302033 | A | G | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+7383T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47302033 | |||||||
| chr6:47302210 | T | C | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.96+7206A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47302210 | |||||||
| chr6:47302214 | C | G | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+7202G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47302214 | |||||||
| chr6:47302344 | A | G | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.96+7072T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47302344 | |||||||
| chr6:47302412 | A | G | 1 | a0001c0001t0028g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.96+7004T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47302412 | |||||||
| chr6:47302502 | A | G | 1 | a0001c0001t0023g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.96+6914T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47302502 | |||||||
| chr6:47302545 | C | A | 1 | a0001c0001t0003g0044 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.96+6871G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47302545 | |||||||
| chr6:47302660 | C | G | 5 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0014g0324 others(2): Show |
6 | HG02257.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+6756G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47302660 | |||||||
| chr6:47302929 | A | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0024 others(121): Show |
131 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.96+6487T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47302929 | |||||||
| chr6:47303012 | T | C | 1 | a0001c0001t0047g0328 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+6404A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47303012 | |||||||
| chr6:47303119 | T | A | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+6297A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47303119 | |||||||
| chr6:47303280 | C | T | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+6136G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47303280 | |||||||
| chr6:47303457 | A | G | 1 | a0001c0001t0047g0328 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+5959T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47303457 | |||||||
| chr6:47303697 | A | C | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+5719T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47303697 | |||||||
| chr6:47303850 | G | A | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG01243.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.96+5566C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47303850 | |||||||
| chr6:47303863 | A | G | 7 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | NA18940.hp2 NA18951.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+5553T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47303863 | |||||||
| chr6:47303876 | A | G | 1 | a0001c0001t0002g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.96+5540T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47303876 | |||||||
| chr6:47303999 | C | T | 7 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0213 others(4): Show |
7 | HG02155.hp2 NA18940.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+5417G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47303999 | |||||||
| chr6:47304002 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.96+5414A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304002 | |||||||
| chr6:47304171 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.96+5245C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304171 | |||||||
| chr6:47304205 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.96+5211G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304205 | |||||||
| chr6:47304249 | T | C | 1 | a0001c0001t0047g0328 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+5167A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304249 | |||||||
| chr6:47304275 | C | A | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.96+5141G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304275 | |||||||
| chr6:47304292 | A | T | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+5124T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304292 | |||||||
| chr6:47304293 | C | A | 1 | a0001c0001t0002g0202 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96+5123G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304293 | |||||||
| chr6:47304294 | CA | C | 188 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(185): Show |
193 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.96+5121delT | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304294 | |||||||
| chr6:47304295 | A | C | 1 | a0001c0001t0002g0202 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96+5121T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304295 | |||||||
| chr6:47304309 | G | T | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.96+5107C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304309 | |||||||
| chr6:47304403 | G | A | 1 | a0001c0001t0004g0332 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.96+5013C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304403 | |||||||
| chr6:47304537 | T | C | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+4879A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304537 | |||||||
| chr6:47304614 | T | C | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+4802A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304614 | |||||||
| chr6:47304623 | C | T | 1 | a0001c0001t0004g0231 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.96+4793G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304623 | |||||||
| chr6:47304632 | CTT | C | 10 | a0001c0001t0002g0209 a0001c0001t0002g0331 a0001c0001t0004g0283 others(7): Show |
10 | HG01884.hp1 HG02615.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.96+4782_96+4783del others(2): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304632 | |||||||
| chr6:47304708 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.96+4708A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304708 | |||||||
| chr6:47304827 | T | C | 1 | a0001c0001t0002g0176 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.96+4589A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304827 | |||||||
| chr6:47304949 | A | T | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+4467T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304949 | |||||||
| chr6:47304953 | T | G | 80 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0055 others(77): Show |
80 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.96+4463A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47304953 | |||||||
| chr6:47305004 | C | T | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+4412G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305004 | |||||||
| chr6:47305030 | C | T | 217 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(214): Show |
224 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.96+4386G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305030 | |||||||
| chr6:47305124 | A | G | 2 | a0001c0001t0002g0236 a0001c0001t0003g0031 |
2 | HG02683.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.96+4292T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305124 | |||||||
| chr6:47305149 | C | T | 15 | a0001c0001t0001g0002 a0001c0001t0002g0234 a0001c0001t0004g0235 others(12): Show |
17 | HG01069.hp1 HG01255.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.96+4267G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305149 | |||||||
| chr6:47305257 | C | T | 4 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0004g0231 others(1): Show |
4 | HG00735.hp2 NA18952.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+4159G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305257 | |||||||
| chr6:47305291 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+4125C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305291 | |||||||
| chr6:47305302 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0007g0004 |
3 | HG01168.hp2 HG01169.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.96+4114T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305302 | |||||||
| chr6:47305353 | T | C | 1 | a0001c0001t0004g0332 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.96+4063A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305353 | |||||||
| chr6:47305452 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.96+3964C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305452 | |||||||
| chr6:47305604 | T | C | 2 | a0001c0001t0012g0144 a0001c0001t0012g0145 |
2 | HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.96+3812A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305604 | |||||||
| chr6:47305677 | A | G | 32 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(29): Show |
32 | HG00140.hp2 HG00423.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.96+3739T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305677 | |||||||
| chr6:47305708 | C | G | 1 | a0001c0001t0005g0173 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.96+3708G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305708 | |||||||
| chr6:47305779 | T | G | 1 | a0001c0001t0009g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.96+3637A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305779 | |||||||
| chr6:47305794 | T | C | 1 | a0001c0008t0040g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+3622A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305794 | |||||||
| chr6:47305799 | C | A | 1 | a0001c0001t0021g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.96+3617G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305799 | |||||||
| chr6:47305846 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0002g0209 a0001c0001t0004g0283 others(14): Show |
19 | HG01069.hp1 HG01255.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.96+3570G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305846 | |||||||
| chr6:47305916 | C | G | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3500G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305916 | |||||||
| chr6:47305942 | G | T | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3474C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305942 | |||||||
| chr6:47305947 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3469T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305947 | |||||||
| chr6:47305949 | C | G | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3467G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305949 | |||||||
| chr6:47305950 | C | A | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3466G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305950 | |||||||
| chr6:47305954 | A | T | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3462T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305954 | |||||||
| chr6:47305956 | C | A | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3460G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305956 | |||||||
| chr6:47305958 | C | A | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3458G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305958 | |||||||
| chr6:47305962 | T | G | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3454A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305962 | |||||||
| chr6:47305965 | A | T | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3451T>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305965 | |||||||
| chr6:47305966 | T | A | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3450A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305966 | |||||||
| chr6:47305967 | C | A | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3449G>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305967 | |||||||
| chr6:47305968 | T | G | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3448A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47305968 | |||||||
| chr6:47306012 | T | A | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3404A>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306012 | |||||||
| chr6:47306013 | C | G | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+3403G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306013 | |||||||
| chr6:47306029 | A | G | 5 | a0001c0001t0003g0019 a0001c0001t0004g0299 a0001c0001t0005g0300 others(2): Show |
5 | HG02572.hp1 HG02895.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+3387T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306029 | |||||||
| chr6:47306276 | G | A | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0003g0146 others(1): Show |
4 | HG00140.hp1 HG01123.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+3140C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306276 | |||||||
| chr6:47306315 | A | C | 2 | a0001c0001t0002g0298 a0002c0002t0004g0297 |
2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.96+3101T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306315 | |||||||
| chr6:47306600 | T | C | 1 | a0001c0001t0004g0319 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.96+2816A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306600 | |||||||
| chr6:47306601 | C | T | 1 | a0001c0001t0004g0319 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.96+2815G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306601 | |||||||
| chr6:47306612 | T | C | 2 | a0001c0001t0004g0323 a0001c0001t0013g0322 |
2 | HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.96+2804A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306612 | |||||||
| chr6:47306712 | G | A | 4 | a0001c0001t0037g0168 a0001c0001t0038g0169 a0001c0001t0039g0167 others(1): Show |
4 | HG00639.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+2704C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306712 | |||||||
| chr6:47306779 | A | C | 17 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0004g0283 others(14): Show |
17 | HG01358.hp2 HG01433.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.96+2637T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306779 | |||||||
| chr6:47306827 | T | C | 6 | a0001c0001t0001g0018 a0001c0001t0002g0281 a0001c0001t0004g0319 others(3): Show |
6 | HG02109.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+2589A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306827 | |||||||
| chr6:47306859 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0002g0281 a0001c0001t0023g0017 |
3 | HG02109.hp1 HG03579.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.96+2557G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306859 | |||||||
| chr6:47306943 | T | G | 8 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0004g0323 others(5): Show |
9 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+2473A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306943 | |||||||
| chr6:47306948 | T | C | 1 | a0001c0001t0014g0324 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.96+2468A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47306948 | |||||||
| chr6:47307036 | T | C | 2 | a0001c0001t0008g0325 a0001c0001t0013g0326 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.96+2380A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307036 | |||||||
| chr6:47307066 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.96+2350A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307066 | |||||||
| chr6:47307243 | T | C | 2 | a0001c0001t0008g0325 a0001c0001t0013g0326 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.96+2173A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307243 | |||||||
| chr6:47307295 | T | C | 1 | a0001c0001t0002g0206 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.96+2121A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307295 | |||||||
| chr6:47307358 | T | C | 1 | a0001c0001t0004g0327 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.96+2058A>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307358 | |||||||
| chr6:47307435 | G | A | 1 | a0001c0001t0002g0279 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.96+1981C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307435 | |||||||
| chr6:47307521 | G | A | 4 | a0001c0001t0037g0168 a0001c0001t0038g0169 a0001c0001t0039g0167 others(1): Show |
4 | HG00639.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1895C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307521 | |||||||
| chr6:47307523 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0022g0015 |
2 | NA18950.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.96+1893G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307523 | |||||||
| chr6:47307577 | T | G | 1 | a0001c0001t0002g0280 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.96+1839A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307577 | |||||||
| chr6:47307587 | A | G | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.96+1829T>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307587 | |||||||
| chr6:47307635 | A | C | 3 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0006g0012 |
3 | NA18945.hp1 NA18959.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.96+1781T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307635 | |||||||
| chr6:47307664 | G | GT | 4 | a0001c0001t0037g0168 a0001c0001t0038g0169 a0001c0001t0039g0167 others(1): Show |
4 | HG00639.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1751dupA | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307664 | |||||||
| chr6:47307803 | T | G | 1 | a0002c0002t0002g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.96+1613A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307803 | |||||||
| chr6:47307927 | G | T | 108 | a0001c0001t0001g0155 a0001c0001t0002g0010 a0001c0001t0002g0176 others(105): Show |
110 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.96+1489C>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47307927 | |||||||
| chr6:47308175 | A | C | 9 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0037g0168 others(6): Show |
9 | HG00639.hp1 HG00741.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+1241T>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47308175 | |||||||
| chr6:47308354 | G | A | 1 | a0001c0001t0032g0151 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.96+1062C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47308354 | |||||||
| chr6:47308374 | C | T | 8 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0037g0168 others(5): Show |
8 | HG00639.hp1 HG00741.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+1042G>A | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47308374 | |||||||
| chr6:47308388 | T | G | 2 | a0001c0001t0005g0329 a0001c0001t0047g0328 |
2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.96+1028A>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47308388 | |||||||
| chr6:47308620 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0006g0152 |
2 | HG01975.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.96+796C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47308620 | |||||||
| chr6:47308731 | CTGGCTGG others(12): Show |
C | 1 | a0001c0001t0045g0330 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.96+666_96+684delAA others(17): Show |
TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47308731 | |||||||
| chr6:47308768 | G | A | 4 | a0001c0001t0037g0168 a0001c0001t0038g0169 a0001c0001t0039g0167 others(1): Show |
4 | HG00639.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+648C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47308768 | |||||||
| chr6:47308821 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.96+595C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47308821 | |||||||
| chr6:47308998 | G | A | 1 | a0001c0001t0002g0331 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.96+418C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47308998 | |||||||
| chr6:47309002 | G | C | 187 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0159 others(184): Show |
194 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(191): Show |
intron_variant | MODIFIER | c.96+414C>G | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47309002 | |||||||
| chr6:47309074 | C | G | 32 | a0001c0001t0002g0176 a0001c0001t0002g0178 a0001c0001t0002g0179 others(29): Show |
32 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.96+342G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47309074 | |||||||
| chr6:47309108 | G | A | 1 | a0001c0001t0004g0332 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.96+308C>T | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47309108 | |||||||
| chr6:47309395 | C | G | 2 | a0001c0001t0005g0173 a0001c0001t0005g0174 |
2 | HG00741.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.96+21G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47309395 | |||||||
| chr6:47309403 | C | G | 1 | a0001c0003t0011g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.96+13G>C | TNFRSF21 | ENSG00000146072.6 | transcript | ENST00000296861.2 | protein_coding | 1/5 | chr6 | 47309403 |