Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 114897 |
| ensemblid | ENSG00000173918.15 |
| hgncid | 14324 |
| symbol | C1QTNF1 |
| name | C1q and TNF related 1 |
| refseq_nuc | NM_030968.5 |
| refseq_prot | NP_112230.1 |
| ensembl_nuc | ENST00000579760.6 |
| ensembl_prot | ENSP00000463922.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 79024169 |
| end | 79049788 |
| strand | + |
| ver | v1.2 |
| region | chr17:79024169-79049788 |
| region5000 | chr17:79019169-79054788 |
| regionname0 | C1QTNF1_chr17_79024169_79049788 |
| regionname5000 | C1QTNF1_chr17_79019169_79054788 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 281 | 383 | 98 | 60 | 175 | 9 | 39 | 133 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | MGSRG others(276): Show |
chr17 | 79019169 | 79054788 |
| a0002 | 0/0 | 281 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | MGSRG others(276): Show |
chr17 | 79019169 | 79054788 |
| a0003 | 0/0 | 281 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | MGSRG others(276): Show |
chr17 | 79019169 | 79054788 |
| a0004 | 0/0 | 281 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | MGSRG others(276): Show |
chr17 | 79019169 | 79054788 |
| a0005 | 0/0 | 281 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | MGSRG others(276): Show |
chr17 | 79019169 | 79054788 |
| a0006 | 0/0 | 281 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | MGSRG others(276): Show |
chr17 | 79019169 | 79054788 |
| a0007 | 0/0 | 281 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | MGSRG others(276): Show |
chr17 | 79019169 | 79054788 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 843 | 175 | 39 | 26 | 82 | 6 | 20 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0001c0002 | 0/0 | 843 | 132 | 17 | 20 | 81 | 1 | 13 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0001c0003 | 0/0 | 843 | 25 | 16 | 3 | 0 | 2 | 4 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0001c0004 | 0/0 | 843 | 20 | 7 | 1 | 11 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0001c0005 | 0/0 | 843 | 12 | 8 | 3 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0001c0006 | 0/0 | 843 | 9 | 7 | 2 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0001c0007 | 0/0 | 843 | 4 | 1 | 3 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0001c0008 | 0/0 | 843 | 4 | 2 | 2 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0001c0013 | 0/0 | 843 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0001c0015 | 0/0 | 843 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0002c0010 | 0/0 | 843 | 2 | 0 | 0 | 0 | 1 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0003c0009 | 0/0 | 843 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0004c0011 | 0/0 | 843 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0005c0014 | 0/0 | 843 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0006c0012 | 0/0 | 843 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 | ||
| a0007c0016 | 0/0 | 843 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ATGGG others(838): Show |
chr17 | 79019169 | 79054788 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2886 | 147 | 36 | 26 | 60 | 5 | 18 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0001t0004 | 0/0 | 2886 | 11 | 0 | 0 | 11 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0001t0005 | 0/0 | 2886 | 2 | 2 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0001t0010 | 0/0 | 2886 | 5 | 0 | 0 | 5 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0001t0012 | 0/0 | 2886 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0001t0013 | 0/0 | 2886 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0001t0015 | 0/0 | 2886 | 2 | 0 | 0 | 0 | 0 | 2 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0001t0019 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0001t0020 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0001t0022 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 1 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0001t0024 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0002t0002 | 0/0 | 2910 | 78 | 4 | 20 | 47 | 0 | 7 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0001c0002t0003 | 0/0 | 2910 | 49 | 12 | 0 | 31 | 0 | 6 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0001c0002t0025 | 0/0 | 2910 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0001c0002t0026 | 0/0 | 2910 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0001c0002t0029 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0002t0031 | 0/0 | 2910 | 1 | 0 | 0 | 0 | 1 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0001c0002t0032 | 0/0 | 2910 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0001c0003t0001 | 0/0 | 2886 | 4 | 3 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0003t0006 | 0/0 | 2886 | 9 | 7 | 0 | 0 | 0 | 2 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0003t0007 | 0/0 | 2886 | 8 | 3 | 2 | 0 | 2 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0003t0014 | 0/0 | 2875 | 2 | 2 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2870): Show |
chr17 | 79019169 | 79054788 |
| a0001c0003t0021 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0003t0033 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0004t0002 | 0/0 | 2910 | 6 | 1 | 0 | 4 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0001c0004t0003 | 0/0 | 2910 | 7 | 0 | 0 | 7 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0001c0004t0008 | 0/0 | 2886 | 6 | 6 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0004t0023 | 0/0 | 2886 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0005t0001 | 0/0 | 2886 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0005t0005 | 0/0 | 2886 | 7 | 5 | 2 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0005t0017 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0005t0027 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0005t0028 | 0/0 | 2875 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2870): Show |
chr17 | 79019169 | 79054788 |
| a0001c0005t0030 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0006t0009 | 0/0 | 2910 | 5 | 4 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0001c0006t0011 | 0/0 | 2910 | 3 | 2 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0001c0006t0018 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0007t0001 | 0/0 | 2886 | 4 | 1 | 3 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0008t0001 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0008t0009 | 0/0 | 2910 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0001c0008t0016 | 0/0 | 2886 | 2 | 1 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0013t0001 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0001c0015t0005 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0002c0010t0003 | 0/0 | 2910 | 2 | 0 | 0 | 0 | 1 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0003c0009t0002 | 0/0 | 2910 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0004c0011t0001 | 0/0 | 2886 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0005c0014t0001 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| a0006c0012t0003 | 0/0 | 2910 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2905): Show |
chr17 | 79019169 | 79054788 |
| a0007c0016t0001 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | ACATC others(2881): Show |
chr17 | 79019169 | 79054788 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 17 | 3 | 5 | 6 | 0 | 2 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0003 | 0/0 | 11 | 1 | 2 | 1 | 1 | 6 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0006 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0004g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0010g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0010g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0010g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0010g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0010g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0012g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0012g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0013g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0013g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0015g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0019g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0020g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0022g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0001t0024g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0002 | 0/0 | 10 | 0 | 6 | 3 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0004 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0025g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0026g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0029g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0031g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0002t0032g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0006g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0007g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0007g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0007g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0014g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0014g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0021g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0003t0033g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0003g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0008g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0008g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0008g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0004t0023g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0005t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0005t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0005t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0005t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0005t0005g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0005t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0005t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0005t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0005t0017g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0005t0027g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0005t0028g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0005t0030g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0006t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0006t0009g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0006t0009g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0006t0009g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0006t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0006t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0006t0011g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0006t0018g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0007t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0007t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0007t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0008t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0008t0009g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0008t0016g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0008t0016g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0013t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0001c0015t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0002c0010t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0002c0010t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0003c0009t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0004c0011t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0004c0011t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0005c0014t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0006c0012t0003g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| a0007c0016t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0010 | t0003 | g0206 | EUR | GBR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | GBR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00280 | hp1 | a0001 | c0003 | t0007 | g0025 | EUR | FIN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00280 | hp2 | a0001 | c0001 | t0022 | g0006 | EUR | FIN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0174 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0037 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00639 | hp2 | a0001 | c0005 | t0005 | g0152 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0168 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00673 | hp2 | a0001 | c0001 | t0010 | g0064 | EAS | CHS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0234 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0225 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0241 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01106 | hp1 | a0001 | c0008 | t0016 | g0069 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01167 | hp1 | a0001 | c0007 | t0001 | g0024 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01168 | hp1 | a0001 | c0007 | t0001 | g0024 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01243 | hp1 | a0001 | c0008 | t0009 | g0123 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01243 | hp2 | a0001 | c0006 | t0009 | g0049 | AMR | PUR | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01255 | hp1 | a0001 | c0005 | t0001 | g0155 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01256 | hp1 | a0001 | c0007 | t0001 | g0083 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01261 | hp1 | a0001 | c0003 | t0007 | g0084 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01261 | hp2 | a0001 | c0006 | t0011 | g0151 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0079 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0027 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0232 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01516 | hp2 | a0001 | c0002 | t0031 | g0181 | EUR | IBS | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0251 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0173 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0249 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0244 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0260 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0245 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02004 | hp1 | a0001 | c0003 | t0007 | g0089 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02027 | hp2 | a0001 | c0004 | t0002 | g0119 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02055 | hp1 | a0001 | c0003 | t0006 | g0028 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02055 | hp2 | a0001 | c0003 | t0007 | g0166 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0202 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02056 | hp2 | a0001 | c0001 | t0019 | g0125 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02074 | hp2 | a0001 | c0002 | t0003 | g0184 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02132 | hp2 | a0001 | c0002 | t0032 | g0198 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0243 | EAS | KHV | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02145 | hp1 | a0001 | c0002 | t0003 | g0020 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0027 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CDX | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02165 | hp1 | a0001 | c0002 | t0026 | g0255 | EAS | CDX | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0186 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02257 | hp2 | a0001 | c0003 | t0006 | g0086 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02258 | hp1 | a0001 | c0015 | t0005 | g0074 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02280 | hp1 | a0001 | c0005 | t0005 | g0159 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02300 | hp1 | a0001 | c0004 | t0023 | g0030 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0095 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02572 | hp1 | a0001 | c0004 | t0008 | g0023 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02572 | hp2 | a0001 | c0005 | t0005 | g0154 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0250 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02615 | hp1 | a0001 | c0001 | t0024 | g0226 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02622 | hp1 | a0001 | c0003 | t0014 | g0207 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02630 | hp2 | a0001 | c0006 | t0009 | g0048 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02647 | hp2 | a0001 | c0003 | t0006 | g0137 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02683 | hp1 | a0001 | c0003 | t0006 | g0171 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02683 | hp2 | a0005 | c0014 | t0001 | g0087 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02698 | hp2 | a0001 | c0013 | t0001 | g0043 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02717 | hp1 | a0001 | c0004 | t0002 | g0103 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0039 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02723 | hp1 | a0001 | c0005 | t0005 | g0153 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0256 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0014 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02809 | hp2 | a0001 | c0005 | t0017 | g0097 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02818 | hp2 | a0001 | c0003 | t0006 | g0133 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02886 | hp1 | a0001 | c0008 | t0016 | g0076 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02895 | hp2 | a0001 | c0004 | t0008 | g0023 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0014 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02922 | hp1 | a0001 | c0005 | t0005 | g0157 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02965 | hp1 | a0001 | c0006 | t0009 | g0049 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0210 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03017 | hp2 | a0006 | c0012 | t0003 | g0004 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03041 | hp2 | a0001 | c0006 | t0011 | g0150 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03098 | hp2 | a0001 | c0006 | t0011 | g0092 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03130 | hp1 | a0001 | c0003 | t0006 | g0028 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03130 | hp2 | a0001 | c0003 | t0006 | g0147 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03139 | hp1 | a0001 | c0002 | t0029 | g0014 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03195 | hp2 | a0001 | c0008 | t0001 | g0073 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03209 | hp2 | a0001 | c0003 | t0007 | g0160 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03225 | hp1 | a0001 | c0003 | t0007 | g0088 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0039 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0224 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03453 | hp1 | a0001 | c0004 | t0008 | g0022 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03453 | hp2 | a0001 | c0004 | t0008 | g0075 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03486 | hp1 | a0001 | c0002 | t0003 | g0038 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0205 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03516 | hp2 | a0001 | c0006 | t0018 | g0048 | AFR | ESN | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03540 | hp1 | a0001 | c0005 | t0028 | g0192 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0085 | AFR | GWD | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03579 | hp1 | a0001 | c0003 | t0033 | g0090 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0190 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03669 | hp1 | a0001 | c0001 | t0015 | g0031 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03669 | hp2 | a0001 | c0004 | t0002 | g0107 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03688 | hp1 | a0001 | c0003 | t0021 | g0080 | SAS | STU | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | STU | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0252 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03704 | hp2 | a0001 | c0003 | t0007 | g0082 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0183 | SAS | PJL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03834 | hp1 | a0001 | c0003 | t0006 | g0170 | SAS | BEB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0187 | SAS | BEB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03927 | hp2 | a0001 | c0001 | t0015 | g0031 | SAS | BEB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG04184 | hp1 | a0001 | c0002 | t0003 | g0188 | SAS | BEB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18522 | hp1 | a0001 | c0003 | t0014 | g0209 | AFR | YRI | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0020 | AFR | YRI | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | CHB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | CHB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0038 | AFR | YRI | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18939 | hp2 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18946 | hp1 | a0001 | c0004 | t0003 | g0178 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18946 | hp2 | a0001 | c0001 | t0010 | g0067 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0036 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18951 | hp1 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18952 | hp1 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18952 | hp2 | a0001 | c0002 | t0025 | g0229 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18960 | hp2 | a0001 | c0004 | t0003 | g0201 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0013 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18965 | hp2 | a0001 | c0004 | t0002 | g0148 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18966 | hp2 | a0001 | c0001 | t0013 | g0120 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0013 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18969 | hp1 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18970 | hp1 | a0001 | c0002 | t0003 | g0013 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18973 | hp2 | a0001 | c0004 | t0003 | g0019 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18977 | hp2 | a0001 | c0004 | t0003 | g0019 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18980 | hp2 | a0003 | c0009 | t0002 | g0002 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18981 | hp2 | a0001 | c0002 | t0003 | g0200 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18985 | hp1 | a0001 | c0002 | t0003 | g0203 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18987 | hp2 | a0001 | c0001 | t0013 | g0121 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18991 | hp1 | a0001 | c0001 | t0010 | g0053 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18993 | hp1 | a0001 | c0004 | t0003 | g0019 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18994 | hp1 | a0004 | c0011 | t0001 | g0140 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0189 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19002 | hp2 | a0001 | c0004 | t0002 | g0030 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19005 | hp2 | a0001 | c0001 | t0010 | g0063 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19011 | hp2 | a0001 | c0004 | t0003 | g0195 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19043 | hp1 | a0001 | c0003 | t0006 | g0169 | AFR | LWK | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | LWK | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19055 | hp2 | a0001 | c0004 | t0003 | g0179 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19057 | hp1 | a0001 | c0001 | t0012 | g0142 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19058 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19058 | hp2 | a0001 | c0001 | t0012 | g0141 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19063 | hp2 | a0001 | c0004 | t0002 | g0127 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19078 | hp1 | a0001 | c0002 | t0003 | g0175 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19079 | hp1 | a0001 | c0005 | t0030 | g0199 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19083 | hp2 | a0003 | c0009 | t0002 | g0002 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19084 | hp1 | a0001 | c0001 | t0010 | g0065 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19084 | hp2 | a0004 | c0011 | t0001 | g0001 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19087 | hp1 | a0007 | c0016 | t0001 | g0058 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0013 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0176 | EAS | JPT | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19240 | hp1 | a0001 | c0005 | t0005 | g0158 | AFR | YRI | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA19240 | hp2 | a0001 | c0006 | t0009 | g0258 | AFR | YRI | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ASW | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ASW | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA20805 | hp2 | a0001 | c0003 | t0007 | g0025 | EUR | TSI | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA20905 | hp1 | a0002 | c0010 | t0003 | g0204 | SAS | GIH | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0257 | SAS | GIH | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01123 | hp1 | a0001 | c0005 | t0005 | g0156 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02486 | hp1 | a0001 | c0005 | t0027 | g0193 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02486 | hp2 | a0001 | c0007 | t0001 | g0081 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0020 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0208 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG03471 | hp2 | a0001 | c0004 | t0008 | g0022 | AFR | MSL | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| HG06807 | hp2 | a0001 | c0006 | t0009 | g0259 | AFR | USA | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0172 | AFR | USA | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| NA21309 | hp2 | a0001 | c0004 | t0008 | g0077 | AFR | LWK | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0139 | REF | REF | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | C1QTNF1_chr17_79019169_79054788 | C1QTNF1 | chr17 | 79019169 | 79054788 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:79044108 | C | T | 1 | a0004 | 2 | NA18994.hp1 NA19084.hp2 |
missense_variant | MODERATE | c.140C>T | p.Pro47Leu | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/4 | 480/2886 | 140/846 | 47/281 | chr17 | 79044108 | |||
| chr17:79046637 | G | A | 1 | a0005 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.238G>A | p.Gly80Ser | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/4 | 578/2886 | 238/846 | 80/281 | chr17 | 79046637 | |||
| chr17:79047661 | G | A | 1 | a0006 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.419G>A | p.Arg140Gln | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 759/2886 | 419/846 | 140/281 | chr17 | 79047661 | |||
| chr17:79047688 | C | T | 1 | a0007 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.446C>T | p.Ser149Leu | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 786/2886 | 446/846 | 149/281 | chr17 | 79047688 | |||
| chr17:79047807 | G | A | 1 | a0003 | 2 | NA18980.hp2 NA19083.hp2 |
missense_variant | MODERATE | c.565G>A | p.Val189Met | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 905/2886 | 565/846 | 189/281 | chr17 | 79047807 | |||
| chr17:79047964 | G | A | 1 | a0002 | 2 | HG00140.hp1 NA20905.hp1 |
missense_variant | MODERATE | c.722G>A | p.Arg241Gln | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 1062/2886 | 722/846 | 241/281 | chr17 | 79047964 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:79044046 | T | C | 5 | a0001c0002 a0001c0005 a0002c0010 others(2): Show |
149 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
synonymous_variant | LOW | c.78T>C | p.Arg26Arg | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/4 | 418/2886 | 78/846 | 26/281 | chr17 | 79044046 | |||
| chr17:79044049 | G | A | 1 | a0001c0013 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.81G>A | p.Val27Val | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/4 | 421/2886 | 81/846 | 27/281 | chr17 | 79044049 | |||
| chr17:79044103 | G | C | 10 | a0001c0002 a0001c0003 a0001c0005 others(7): Show |
189 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(186): Show |
synonymous_variant | LOW | c.135G>C | p.Ser45Ser | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/4 | 475/2886 | 135/846 | 45/281 | chr17 | 79044103 | |||
| chr17:79046636 | C | T | 6 | a0001c0002 a0001c0004 a0001c0015 others(3): Show |
158 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
synonymous_variant | LOW | c.237C>T | p.Pro79Pro | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/4 | 577/2886 | 237/846 | 79/281 | chr17 | 79046636 | |||
| chr17:79047677 | C | T | 2 | a0001c0006 a0001c0008 |
13 | HG01106.hp1 HG01243.hp1 HG01243.hp2 others(10): Show |
synonymous_variant | LOW | c.435C>T | p.Tyr145Tyr | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 775/2886 | 435/846 | 145/281 | chr17 | 79047677 | |||
| chr17:79047812 | C | T | 1 | a0001c0007 | 4 | HG01167.hp1 HG01168.hp1 HG01256.hp1 others(1): Show |
synonymous_variant | LOW | c.570C>T | p.Pro190Pro | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 910/2886 | 570/846 | 190/281 | chr17 | 79047812 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:79024240 | C | T | 1 | a0001c0003t0033 | 1 | HG03579.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-269C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/4 | chr17 | 79024240 | |||||||
| chr17:79024305 | G | T | 10 | a0001c0002t0003 a0001c0002t0029 a0001c0002t0031 others(7): Show |
65 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(62): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-204G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/4 | chr17 | 79024305 | |||||||
| chr17:79024357 | C | T | 1 | a0001c0001t0010 | 5 | HG00673.hp2 NA18946.hp2 NA18991.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-152C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/4 | 19612 | chr17 | 79024357 | ||||||
| chr17:79048136 | T | TGCTGACC others(17): Show |
14 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0025 others(11): Show |
158 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*58_*59insGGGCTCAG others(16): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 59 | INFO_REALIGN_3_PRIME | chr17 | 79048136 | |||||
| chr17:79048163 | C | T | 1 | a0001c0008t0016 | 2 | HG01106.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*75C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 75 | chr17 | 79048163 | ||||||
| chr17:79048292 | G | A | 1 | a0001c0002t0031 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*204G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 204 | chr17 | 79048292 | ||||||
| chr17:79048303 | G | A | 11 | a0001c0001t0005 a0001c0004t0008 a0001c0005t0005 others(8): Show |
30 | HG00639.hp2 HG01106.hp1 HG01123.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*215G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 215 | chr17 | 79048303 | ||||||
| chr17:79048399 | G | A | 1 | a0001c0005t0017 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*311G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 311 | chr17 | 79048399 | ||||||
| chr17:79048399 | G | C | 1 | a0001c0002t0025 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*311G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 311 | chr17 | 79048399 | ||||||
| chr17:79048414 | G | A | 1 | a0001c0001t0012 | 2 | NA19057.hp1 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*326G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 326 | chr17 | 79048414 | ||||||
| chr17:79048490 | T | C | 1 | a0001c0001t0013 | 2 | NA18966.hp2 NA18987.hp2 |
3_prime_UTR_variant | MODIFIER | c.*402T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 402 | chr17 | 79048490 | ||||||
| chr17:79048518 | CTGGCTCC others(4): Show |
C | 2 | a0001c0003t0014 a0001c0005t0028 |
3 | HG02622.hp1 HG03540.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*431_*441delTGGCTC others(5): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 431 | chr17 | 79048518 | ||||||
| chr17:79048533 | G | C | 1 | a0001c0001t0015 | 2 | HG03669.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*445G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 445 | chr17 | 79048533 | ||||||
| chr17:79048765 | C | T | 1 | a0001c0001t0024 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*677C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 677 | chr17 | 79048765 | ||||||
| chr17:79049025 | G | A | 1 | a0001c0002t0026 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*937G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 937 | chr17 | 79049025 | ||||||
| chr17:79049319 | G | A | 16 | a0001c0001t0019 a0001c0002t0002 a0001c0002t0003 others(13): Show |
169 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1231G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 1231 | chr17 | 79049319 | ||||||
| chr17:79049332 | G | A | 2 | a0001c0001t0020 a0001c0004t0008 |
7 | HG02572.hp1 HG02895.hp2 HG03453.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1244G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 1244 | chr17 | 79049332 | ||||||
| chr17:79049340 | A | G | 1 | a0001c0003t0006 | 9 | HG02055.hp1 HG02257.hp2 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1252A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 1252 | chr17 | 79049340 | ||||||
| chr17:79049416 | C | T | 1 | a0001c0001t0004 | 11 | HG00558.hp2 HG00621.hp1 NA18612.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1328C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 1328 | chr17 | 79049416 | ||||||
| chr17:79049426 | A | G | 14 | a0001c0001t0019 a0001c0002t0002 a0001c0002t0003 others(11): Show |
152 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1338A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 1338 | chr17 | 79049426 | ||||||
| chr17:79049437 | G | A | 2 | a0001c0003t0014 a0001c0005t0028 |
3 | HG02622.hp1 HG03540.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1349G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 1349 | chr17 | 79049437 | ||||||
| chr17:79049469 | C | T | 1 | a0001c0001t0022 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1381C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 1381 | chr17 | 79049469 | ||||||
| chr17:79049542 | C | T | 1 | a0001c0002t0032 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1454C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 1454 | chr17 | 79049542 | ||||||
| chr17:79049581 | C | T | 3 | a0001c0006t0009 a0001c0006t0018 a0001c0008t0009 |
7 | HG01243.hp1 HG01243.hp2 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1493C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 1493 | chr17 | 79049581 | ||||||
| chr17:79049670 | G | A | 1 | a0001c0003t0021 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1582G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 4/4 | 1582 | chr17 | 79049670 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:79024580 | C | A | 1 | a0001c0002t0002g0051 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-15+86C>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79024580 | |||||||
| chr17:79024618 | C | CG | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+126dupG | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79024618 | ||||||
| chr17:79024633 | G | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+139G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79024633 | |||||||
| chr17:79024726 | A | G | 76 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0042 others(73): Show |
103 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-15+232A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79024726 | |||||||
| chr17:79024889 | AT | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+396delT | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79024889 | |||||||
| chr17:79024892 | C | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+398C>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79024892 | |||||||
| chr17:79024923 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+429C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79024923 | |||||||
| chr17:79024989 | G | C | 12 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(9): Show |
14 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+495G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79024989 | |||||||
| chr17:79025100 | C | T | 1 | a0001c0002t0002g0260 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-15+606C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79025100 | |||||||
| chr17:79025226 | T | C | 14 | a0001c0003t0001g0079 a0001c0003t0001g0085 a0001c0003t0006g0086 others(11): Show |
16 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15+732T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79025226 | |||||||
| chr17:79025321 | A | T | 13 | a0001c0003t0001g0085 a0001c0003t0006g0086 a0001c0003t0007g0025 others(10): Show |
15 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15+827A>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79025321 | |||||||
| chr17:79025365 | C | G | 14 | a0001c0003t0001g0079 a0001c0003t0001g0085 a0001c0003t0006g0086 others(11): Show |
16 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15+871C>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79025365 | |||||||
| chr17:79025439 | C | G | 14 | a0001c0003t0001g0079 a0001c0003t0001g0085 a0001c0003t0006g0086 others(11): Show |
16 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15+945C>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79025439 | |||||||
| chr17:79025468 | G | C | 5 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
6 | HG02145.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+974G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79025468 | |||||||
| chr17:79025493 | C | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+999C>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79025493 | |||||||
| chr17:79025549 | A | G | 183 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(180): Show |
237 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.-15+1055A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79025549 | |||||||
| chr17:79025578 | A | G | 1 | a0001c0002t0002g0050 | 2 | NA19003.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-15+1084A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79025578 | |||||||
| chr17:79025712 | G | A | 1 | a0001c0002t0002g0222 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-15+1218G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79025712 | |||||||
| chr17:79025763 | G | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+1269G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79025763 | |||||||
| chr17:79025785 | T | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+1291T>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79025785 | |||||||
| chr17:79025885 | CCATCATC others(5): Show |
C | 2 | a0001c0006t0011g0150 a0001c0006t0011g0151 |
2 | HG01261.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-15+1397_-15+1408d others(14): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79025885 | ||||||
| chr17:79025989 | T | C | 2 | a0001c0001t0005g0091 a0001c0001t0005g0095 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-15+1495T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79025989 | |||||||
| chr17:79026006 | G | A | 12 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(9): Show |
14 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+1512G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79026006 | |||||||
| chr17:79026128 | A | G | 12 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(9): Show |
14 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+1634A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79026128 | |||||||
| chr17:79026151 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0022g0006 |
6 | HG00280.hp2 HG00735.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+1657G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79026151 | |||||||
| chr17:79026161 | T | G | 1 | a0001c0008t0016g0069 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-15+1667T>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79026161 | |||||||
| chr17:79026162 | C | CT | 9 | a0001c0001t0001g0078 a0001c0004t0008g0022 a0001c0004t0008g0023 others(6): Show |
11 | HG01106.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15+1679dupT | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79026162 | ||||||
| chr17:79026242 | A | G | 12 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(9): Show |
14 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+1748A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79026242 | |||||||
| chr17:79026320 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-15+1826A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79026320 | |||||||
| chr17:79026401 | G | A | 9 | a0001c0005t0001g0155 a0001c0005t0005g0152 a0001c0005t0005g0153 others(6): Show |
9 | HG00639.hp2 HG01123.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+1907G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79026401 | |||||||
| chr17:79026453 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-15+1959C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79026453 | |||||||
| chr17:79026585 | C | T | 5 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 others(2): Show |
6 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+2091C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79026585 | |||||||
| chr17:79026587 | C | T | 1 | a0001c0004t0002g0148 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-15+2093C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79026587 | |||||||
| chr17:79026765 | G | A | 12 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0071 others(9): Show |
14 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+2271G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79026765 | |||||||
| chr17:79026779 | C | CAAGTAGG others(8): Show |
1 | a0001c0001t0001g0068 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-15+2289_-15+2303d others(17): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79026779 | ||||||
| chr17:79027010 | A | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+2516A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027010 | |||||||
| chr17:79027081 | C | CG | 53 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0235 others(50): Show |
74 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-15+2596dupG | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79027081 | ||||||
| chr17:79027081 | C | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+2587C>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027081 | |||||||
| chr17:79027081 | CG | C | 117 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(114): Show |
149 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.-15+2596delG | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79027081 | ||||||
| chr17:79027083 | G | A | 1 | a0001c0006t0011g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-15+2589G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027083 | |||||||
| chr17:79027085 | G | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+2591G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027085 | |||||||
| chr17:79027086 | G | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+2592G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027086 | |||||||
| chr17:79027089 | G | T | 1 | a0001c0003t0006g0147 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-15+2595G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027089 | |||||||
| chr17:79027101 | G | A | 1 | a0001c0001t0010g0053 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-15+2607G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027101 | |||||||
| chr17:79027188 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-15+2694C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027188 | |||||||
| chr17:79027239 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+2745C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027239 | |||||||
| chr17:79027294 | G | A | 1 | a0001c0008t0001g0073 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-15+2800G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027294 | |||||||
| chr17:79027422 | AG | A | 4 | a0001c0005t0001g0155 a0001c0005t0005g0152 a0001c0005t0005g0153 others(1): Show |
4 | HG00639.hp2 HG01255.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+2929delG | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027422 | |||||||
| chr17:79027586 | A | T | 1 | a0001c0001t0001g0052 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-15+3092A>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027586 | |||||||
| chr17:79027603 | C | T | 1 | a0001c0002t0002g0217 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-15+3109C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027603 | |||||||
| chr17:79027655 | T | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+3161T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027655 | |||||||
| chr17:79027660 | G | C | 1 | a0001c0003t0007g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-15+3166G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027660 | |||||||
| chr17:79027694 | C | T | 51 | a0001c0001t0001g0146 a0001c0001t0001g0235 a0001c0002t0002g0002 others(48): Show |
72 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-15+3200C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027694 | |||||||
| chr17:79027914 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(14): Show |
25 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.-15+3420G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027914 | |||||||
| chr17:79027964 | G | A | 1 | a0001c0002t0002g0211 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-15+3470G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79027964 | |||||||
| chr17:79028014 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
4 | HG01070.hp1 HG01071.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+3520C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79028014 | |||||||
| chr17:79028127 | C | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(6): Show |
11 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+3633C>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79028127 | |||||||
| chr17:79028238 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-15+3744G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79028238 | |||||||
| chr17:79028411 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(14): Show |
25 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.-15+3917C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79028411 | |||||||
| chr17:79028543 | G | C | 14 | a0001c0003t0001g0079 a0001c0003t0001g0085 a0001c0003t0006g0086 others(11): Show |
16 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15+4049G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79028543 | |||||||
| chr17:79028553 | G | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(14): Show |
25 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.-15+4059G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79028553 | |||||||
| chr17:79028883 | G | GGT | 45 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0143 others(42): Show |
75 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.-15+4417_-15+4418d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79028883 | ||||||
| chr17:79028883 | G | GGTGT | 6 | a0001c0002t0002g0047 a0001c0002t0002g0051 a0001c0002t0002g0211 others(3): Show |
7 | HG00544.hp2 HG00621.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+4415_-15+4418d others(6): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79028883 | ||||||
| chr17:79028883 | G | GGTGTGT | 3 | a0001c0002t0002g0041 a0001c0002t0002g0256 a0001c0002t0002g0257 |
4 | HG02080.hp1 HG02738.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+4413_-15+4418d others(8): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79028883 | ||||||
| chr17:79028883 | GGT | G | 85 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0161 others(82): Show |
108 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15+4417_-15+4418d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79028883 | ||||||
| chr17:79028883 | GGTGT | G | 24 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(21): Show |
26 | HG00639.hp2 HG01106.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-15+4415_-15+4418d others(6): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79028883 | ||||||
| chr17:79028883 | GGTGTGT | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp1 HG00673.hp2 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.-15+4413_-15+4418d others(8): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79028883 | ||||||
| chr17:79028883 | GGTGTGTG others(7): Show |
G | 1 | a0001c0002t0003g0167 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-15+4405_-15+4418d others(16): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79028883 | ||||||
| chr17:79028914 | A | G | 2 | a0001c0005t0005g0158 a0001c0005t0005g0159 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-15+4420A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79028914 | |||||||
| chr17:79029329 | G | A | 1 | a0001c0003t0006g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-15+4835G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79029329 | |||||||
| chr17:79029340 | G | C | 1 | a0001c0001t0001g0101 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-15+4846G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79029340 | |||||||
| chr17:79029371 | G | A | 1 | a0001c0002t0002g0233 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-15+4877G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79029371 | |||||||
| chr17:79029545 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+5051C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79029545 | |||||||
| chr17:79029546 | G | T | 1 | a0001c0002t0003g0203 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-15+5052G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79029546 | |||||||
| chr17:79029645 | G | A | 2 | a0001c0003t0001g0172 a0001c0003t0001g0173 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-15+5151G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79029645 | |||||||
| chr17:79029653 | G | A | 2 | a0001c0002t0002g0027 a0001c0002t0002g0098 |
3 | HG01433.hp1 HG02148.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-15+5159G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79029653 | |||||||
| chr17:79029731 | A | T | 1 | a0001c0002t0003g0202 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-15+5237A>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79029731 | |||||||
| chr17:79029832 | G | A | 1 | a0001c0003t0007g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-15+5338G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79029832 | |||||||
| chr17:79029927 | T | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+5433T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79029927 | |||||||
| chr17:79029981 | G | A | 5 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 others(2): Show |
6 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+5487G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79029981 | |||||||
| chr17:79030209 | G | C | 1 | a0001c0002t0003g0174 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-15+5715G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030209 | |||||||
| chr17:79030267 | G | A | 2 | a0001c0003t0014g0207 a0001c0003t0014g0209 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-15+5773G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030267 | |||||||
| chr17:79030279 | T | C | 4 | a0001c0002t0002g0227 a0001c0002t0003g0175 a0001c0002t0003g0176 others(1): Show |
4 | NA18973.hp1 NA19078.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5785T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030279 | |||||||
| chr17:79030317 | T | TTG | 18 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(15): Show |
26 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(23): Show |
intron_variant | MODIFIER | c.-15+5824_-15+5825i others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030317 | ||||||
| chr17:79030319 | T | G | 18 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(15): Show |
26 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(23): Show |
intron_variant | MODIFIER | c.-15+5825T>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030319 | |||||||
| chr17:79030319 | T | TTG | 21 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(18): Show |
23 | HG01123.hp1 HG01261.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15+5851_-15+5852d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030319 | ||||||
| chr17:79030319 | T | TTGTG | 14 | a0001c0002t0002g0254 a0001c0003t0014g0207 a0001c0003t0014g0209 others(11): Show |
15 | HG00639.hp2 HG01243.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15+5849_-15+5852d others(6): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030319 | ||||||
| chr17:79030319 | T | TTGTGTG | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0003t0007g0082 others(5): Show |
8 | HG01106.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+5847_-15+5852d others(8): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030319 | ||||||
| chr17:79030319 | T | TTGTGTGT others(1): Show |
15 | a0001c0001t0001g0072 a0001c0003t0001g0079 a0001c0003t0001g0085 others(12): Show |
19 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.-15+5845_-15+5852d others(10): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030319 | ||||||
| chr17:79030319 | T | TTGTGTGT others(5): Show |
1 | a0001c0003t0007g0089 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-15+5841_-15+5852d others(14): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030319 | ||||||
| chr17:79030319 | TTG | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0102 others(5): Show |
15 | HG00735.hp1 HG02451.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.-15+5851_-15+5852d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030319 | ||||||
| chr17:79030347 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-15+5853A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030347 | |||||||
| chr17:79030373 | G | A | 1 | a0001c0002t0002g0215 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-15+5879G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030373 | |||||||
| chr17:79030435 | TTCTC | T | 18 | a0001c0003t0001g0079 a0001c0003t0001g0085 a0001c0003t0006g0086 others(15): Show |
21 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-15+5947_-15+5950d others(6): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030435 | ||||||
| chr17:79030441 | C | T | 1 | a0001c0006t0009g0259 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+5947C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030441 | |||||||
| chr17:79030443 | CTTTCTTC others(26): Show |
C | 1 | a0001c0006t0009g0259 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+5952_-15+5984d others(35): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030443 | ||||||
| chr17:79030454 | CTTTCTTT others(23): Show |
C | 2 | a0001c0004t0008g0023 a0001c0004t0008g0075 |
3 | HG02572.hp1 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-15+5964_-15+5993d others(32): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030454 | ||||||
| chr17:79030455 | T | C | 1 | a0001c0002t0003g0205 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-15+5961T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030455 | |||||||
| chr17:79030455 | TTTCTTTT others(5): Show |
T | 2 | a0001c0004t0008g0022 a0001c0008t0001g0073 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-15+5964_-15+5975d others(14): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030455 | ||||||
| chr17:79030455 | TTTCTTTT others(9): Show |
T | 1 | a0001c0008t0016g0069 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-15+5964_-15+5979d others(18): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030455 | ||||||
| chr17:79030455 | TTTCTTTT others(13): Show |
T | 1 | a0001c0004t0008g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-15+5964_-15+5983d others(22): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030455 | ||||||
| chr17:79030456 | TTCTTTTC others(8): Show |
T | 1 | a0001c0006t0018g0048 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-15+5964_-15+5978d others(17): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030456 | ||||||
| chr17:79030456 | TTCTTTTC others(12): Show |
T | 3 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 |
4 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+5964_-15+5982d others(21): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030456 | ||||||
| chr17:79030457 | TCTTTTCT others(19): Show |
T | 2 | a0001c0004t0008g0022 a0001c0008t0016g0076 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-15+5964_-15+5989d others(28): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030457 | |||||||
| chr17:79030458 | CTTTTCTT others(19): Show |
C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0057 others(7): Show |
14 | HG00280.hp1 HG01167.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+5993_-15+6018d others(28): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030458 | ||||||
| chr17:79030459 | TTTTCTTT others(23): Show |
T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(17): Show |
21 | HG00673.hp2 HG01358.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.-15+5993_-15+6022d others(32): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030459 | ||||||
| chr17:79030459 | TTTTCTTT others(27): Show |
T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0062 |
2 | NA18982.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-15+5993_-15+6026d others(36): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030459 | ||||||
| chr17:79030459 | TTTTCTTT others(31): Show |
T | 1 | a0001c0003t0007g0166 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-15+5993_-15+6030d others(40): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030459 | ||||||
| chr17:79030463 | CTTTCTTT others(15): Show |
C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0060 a0001c0001t0001g0066 others(7): Show |
11 | HG00639.hp2 HG01256.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+5993_-15+6014d others(24): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030463 | ||||||
| chr17:79030467 | CTTTCTTT others(11): Show |
C | 9 | a0001c0001t0010g0067 a0001c0003t0001g0172 a0001c0003t0007g0089 others(6): Show |
9 | HG01168.hp1 HG02004.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+5993_-15+6010d others(20): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030467 | ||||||
| chr17:79030471 | C | CTTTCTTT others(3): Show |
1 | a0001c0001t0001g0003 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-15+5979_-15+5988d others(12): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030471 | ||||||
| chr17:79030471 | CTTTCTTT others(7): Show |
C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0002t0003g0205 others(3): Show |
6 | HG01255.hp1 HG02080.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+5993_-15+6006d others(16): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030471 | ||||||
| chr17:79030475 | CTTTCTTT others(3): Show |
C | 5 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
5 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+5993_-15+6002d others(12): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030475 | ||||||
| chr17:79030479 | CTTTCTT | C | 18 | a0001c0002t0002g0036 a0001c0002t0002g0037 a0001c0002t0002g0180 others(15): Show |
20 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15+5993_-15+5998d others(8): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030479 | ||||||
| chr17:79030481 | TTCTTTTT others(5): Show |
T | 4 | a0001c0002t0002g0252 a0001c0003t0006g0028 a0001c0003t0006g0133 others(1): Show |
5 | HG02055.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+5989_-15+6000d others(14): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030481 | ||||||
| chr17:79030481 | TTCTTTTT others(9): Show |
T | 2 | a0001c0002t0002g0243 a0001c0003t0006g0147 |
2 | HG02135.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-15+5989_-15+6004d others(18): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030481 | ||||||
| chr17:79030483 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-15+5989C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030483 | |||||||
| chr17:79030483 | CTT | C | 14 | a0001c0002t0003g0040 a0001c0002t0003g0191 a0001c0004t0003g0195 others(11): Show |
16 | HG00140.hp1 HG01106.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+5993_-15+5994d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030483 | ||||||
| chr17:79030485 | T | C | 4 | a0001c0001t0001g0135 a0001c0003t0006g0171 a0001c0004t0008g0022 others(1): Show |
4 | HG00741.hp1 HG02683.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+5991T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030485 | |||||||
| chr17:79030485 | T | TTC | 3 | a0001c0001t0001g0003 a0001c0003t0006g0169 a0001c0003t0006g0170 |
3 | HG03834.hp1 HG04115.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-15+5992_-15+5993i others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030485 | ||||||
| chr17:79030485 | T | TTCTTTCT others(7): Show |
1 | a0001c0001t0001g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-15+5992_-15+5993i others(16): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030485 | ||||||
| chr17:79030485 | T | TTCTTTTT others(5): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0143 |
2 | HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-15+5992_-15+5993i others(14): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030485 | ||||||
| chr17:79030485 | T | TTTTC | 17 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(14): Show |
21 | HG00423.hp2 HG00621.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.-15+6034_-15+6037d others(6): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030485 | ||||||
| chr17:79030485 | T | TTTTCTTT others(1): Show |
29 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(26): Show |
37 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15+6030_-15+6037d others(10): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030485 | ||||||
| chr17:79030485 | T | TTTTCTTT others(5): Show |
21 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(18): Show |
28 | HG00735.hp2 HG01081.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-15+6026_-15+6037d others(14): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030485 | ||||||
| chr17:79030485 | T | TTTTCTTT others(9): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
13 | HG00280.hp2 HG00544.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+6022_-15+6037d others(18): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030485 | ||||||
| chr17:79030485 | T | TTTTCTTT others(13): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0110 others(4): Show |
8 | HG02976.hp1 HG03098.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+6018_-15+6037d others(22): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030485 | ||||||
| chr17:79030485 | TTTTC | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(10): Show |
16 | HG00408.hp2 HG00423.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+6034_-15+6037d others(6): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030485 | ||||||
| chr17:79030485 | TTTTCTTT others(1): Show |
T | 17 | a0001c0001t0001g0113 a0001c0001t0001g0146 a0001c0002t0002g0002 others(14): Show |
22 | HG01891.hp1 HG01928.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.-15+6030_-15+6037d others(10): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030485 | ||||||
| chr17:79030485 | TTTTCTTT others(5): Show |
T | 67 | a0001c0001t0001g0138 a0001c0001t0001g0235 a0001c0002t0002g0002 others(64): Show |
89 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.-15+6026_-15+6037d others(14): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030485 | ||||||
| chr17:79030485 | TTTTCTTT others(9): Show |
T | 1 | a0001c0002t0002g0002 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-15+6022_-15+6037d others(18): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030485 | ||||||
| chr17:79030487 | T | C | 2 | a0001c0001t0001g0105 a0001c0002t0031g0181 |
2 | HG01516.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.-15+5993T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030487 | |||||||
| chr17:79030489 | C | T | 2 | a0001c0001t0001g0105 a0001c0002t0031g0181 |
2 | HG01516.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.-15+5995C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030489 | |||||||
| chr17:79030491 | TTC | T | 2 | a0001c0002t0003g0040 a0001c0004t0003g0201 |
3 | NA18951.hp1 NA18960.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-15+5999_-15+6000d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030491 | ||||||
| chr17:79030495 | TTC | T | 18 | a0001c0002t0002g0036 a0001c0002t0002g0037 a0001c0002t0002g0180 others(15): Show |
20 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15+6003_-15+6004d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030495 | ||||||
| chr17:79030581 | CT | C | 10 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(7): Show |
12 | HG01106.hp1 HG02109.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-15+6089delT | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79030581 | ||||||
| chr17:79030642 | C | T | 9 | a0001c0005t0001g0155 a0001c0005t0005g0152 a0001c0005t0005g0153 others(6): Show |
9 | HG00639.hp2 HG01123.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+6148C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030642 | |||||||
| chr17:79030661 | G | A | 14 | a0001c0003t0001g0079 a0001c0003t0001g0085 a0001c0003t0006g0086 others(11): Show |
16 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15+6167G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030661 | |||||||
| chr17:79030739 | T | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(26): Show |
39 | HG00673.hp2 HG01106.hp1 HG02080.hp2 others(36): Show |
intron_variant | MODIFIER | c.-15+6245T>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030739 | |||||||
| chr17:79030749 | G | A | 9 | a0001c0002t0002g0044 a0001c0002t0002g0050 a0001c0002t0002g0233 others(6): Show |
11 | HG00597.hp1 HG02074.hp1 NA18944.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15+6255G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030749 | |||||||
| chr17:79030789 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15+6295C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030789 | |||||||
| chr17:79030858 | C | T | 10 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(7): Show |
12 | HG01106.hp1 HG02109.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-15+6364C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030858 | |||||||
| chr17:79030971 | C | T | 2 | a0001c0002t0003g0200 a0001c0005t0030g0199 |
2 | NA18981.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-15+6477C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79030971 | |||||||
| chr17:79031008 | C | CT | 31 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0043 others(28): Show |
41 | HG00673.hp2 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.-15+6529dupT | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79031008 | ||||||
| chr17:79031008 | CT | C | 16 | a0001c0001t0001g0018 a0001c0001t0001g0102 a0001c0001t0001g0161 others(13): Show |
18 | HG01074.hp1 HG01256.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15+6529delT | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79031008 | ||||||
| chr17:79031013 | T | C | 1 | a0001c0003t0006g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-15+6519T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79031013 | |||||||
| chr17:79031167 | G | A | 7 | a0001c0001t0001g0054 a0001c0002t0002g0045 a0001c0002t0002g0228 others(4): Show |
8 | HG02135.hp2 NA18977.hp1 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+6673G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79031167 | |||||||
| chr17:79031206 | C | T | 1 | a0001c0002t0002g0211 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-15+6712C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79031206 | |||||||
| chr17:79031251 | T | C | 28 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(25): Show |
38 | HG00673.hp2 HG01106.hp1 HG02080.hp2 others(35): Show |
intron_variant | MODIFIER | c.-15+6757T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79031251 | |||||||
| chr17:79031338 | G | A | 1 | a0001c0002t0002g0230 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-15+6844G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79031338 | |||||||
| chr17:79031339 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-15+6845C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79031339 | |||||||
| chr17:79031587 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-15+7093C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79031587 | |||||||
| chr17:79031649 | G | A | 2 | a0001c0001t0005g0091 a0001c0001t0005g0095 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-15+7155G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79031649 | |||||||
| chr17:79031795 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0106 others(1): Show |
7 | HG00140.hp2 HG01123.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+7301G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79031795 | |||||||
| chr17:79031830 | A | G | 1 | a0001c0008t0001g0073 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-15+7336A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79031830 | |||||||
| chr17:79031856 | G | A | 2 | a0001c0002t0003g0013 a0001c0002t0003g0182 |
5 | NA18964.hp1 NA18968.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+7362G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79031856 | |||||||
| chr17:79031999 | C | T | 2 | a0001c0003t0006g0133 a0001c0003t0006g0137 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-15+7505C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79031999 | |||||||
| chr17:79032206 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-15+7712G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79032206 | |||||||
| chr17:79032223 | G | A | 1 | a0001c0002t0002g0100 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-15+7729G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79032223 | |||||||
| chr17:79032613 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0024g0226 |
2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-15+8119G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79032613 | |||||||
| chr17:79032668 | C | T | 1 | a0001c0002t0032g0198 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-15+8174C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79032668 | |||||||
| chr17:79032832 | C | T | 1 | a0001c0003t0006g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-15+8338C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79032832 | |||||||
| chr17:79032936 | T | C | 66 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(63): Show |
80 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.-15+8442T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79032936 | |||||||
| chr17:79033063 | T | C | 186 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(183): Show |
242 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.-15+8569T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79033063 | |||||||
| chr17:79033068 | C | CA | 23 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0001g0109 others(20): Show |
26 | HG00544.hp1 HG00741.hp2 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.-15+8594dupA | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79033068 | ||||||
| chr17:79033068 | CA | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0104 a0001c0001t0001g0132 others(7): Show |
12 | HG01167.hp2 HG02602.hp1 HG03041.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+8594delA | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79033068 | ||||||
| chr17:79033068 | CAAA | C | 49 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(46): Show |
61 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.-15+8592_-15+8594d others(5): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79033068 | ||||||
| chr17:79033068 | CAAAA | C | 13 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0071 others(10): Show |
15 | HG01106.hp1 HG01123.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15+8591_-15+8594d others(6): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79033068 | ||||||
| chr17:79033184 | G | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(61): Show |
78 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.-15+8690G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79033184 | |||||||
| chr17:79033313 | T | C | 6 | a0001c0003t0006g0169 a0001c0003t0006g0170 a0001c0003t0006g0171 others(3): Show |
6 | HG01261.hp2 HG02683.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+8819T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79033313 | |||||||
| chr17:79033463 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0003t0006g0137 |
3 | HG00741.hp1 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-15+8969C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79033463 | |||||||
| chr17:79033531 | TA | T | 66 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(63): Show |
80 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.-15+9049delA | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79033531 | ||||||
| chr17:79033543 | AT | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0110 others(3): Show |
7 | HG02965.hp2 NA18964.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+9060delT | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79033543 | ||||||
| chr17:79033573 | G | C | 7 | a0001c0004t0008g0022 a0001c0004t0008g0023 a0001c0004t0008g0075 others(4): Show |
9 | HG01106.hp1 HG02572.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+9079G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79033573 | |||||||
| chr17:79033698 | G | A | 2 | a0001c0001t0001g0043 a0001c0013t0001g0043 |
2 | HG01081.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-15+9204G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79033698 | |||||||
| chr17:79033769 | G | A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+9275G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79033769 | |||||||
| chr17:79033914 | T | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+9420T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79033914 | |||||||
| chr17:79033947 | A | C | 9 | a0001c0005t0001g0155 a0001c0005t0005g0152 a0001c0005t0005g0153 others(6): Show |
9 | HG00639.hp2 HG01123.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+9453A>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79033947 | |||||||
| chr17:79033956 | G | A | 5 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 others(2): Show |
6 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+9462G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79033956 | |||||||
| chr17:79033962 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-15+9468A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79033962 | |||||||
| chr17:79034143 | G | A | 7 | a0001c0004t0008g0022 a0001c0004t0008g0023 a0001c0004t0008g0075 others(4): Show |
9 | HG01106.hp1 HG02572.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+9649G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79034143 | |||||||
| chr17:79034212 | C | T | 1 | a0001c0002t0002g0252 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-15+9718C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79034212 | |||||||
| chr17:79034333 | G | T | 6 | a0001c0003t0006g0169 a0001c0003t0006g0170 a0001c0003t0006g0171 others(3): Show |
6 | HG01261.hp2 HG02683.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-9622G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79034333 | |||||||
| chr17:79034414 | G | A | 1 | a0001c0004t0008g0075 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-14-9541G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79034414 | |||||||
| chr17:79034495 | T | C | 37 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(34): Show |
41 | HG00280.hp1 HG00639.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.-14-9460T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79034495 | |||||||
| chr17:79034513 | G | A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-9442G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79034513 | |||||||
| chr17:79034671 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(11): Show |
22 | HG02080.hp2 HG02129.hp1 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-9284G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79034671 | |||||||
| chr17:79034694 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-14-9261C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79034694 | |||||||
| chr17:79034878 | C | T | 3 | a0001c0001t0010g0063 a0001c0001t0010g0064 a0001c0001t0010g0065 |
3 | HG00673.hp2 NA19005.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-14-9077C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79034878 | |||||||
| chr17:79034879 | G | A | 1 | a0001c0002t0003g0185 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-14-9076G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79034879 | |||||||
| chr17:79035075 | G | A | 2 | a0001c0003t0001g0172 a0001c0003t0001g0173 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-14-8880G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035075 | |||||||
| chr17:79035176 | C | A | 1 | a0001c0004t0008g0022 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-14-8779C>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035176 | |||||||
| chr17:79035270 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-8685C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035270 | |||||||
| chr17:79035279 | C | T | 1 | a0001c0002t0002g0222 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-14-8676C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035279 | |||||||
| chr17:79035353 | A | G | 71 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(68): Show |
86 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.-14-8602A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035353 | |||||||
| chr17:79035386 | G | A | 1 | a0001c0005t0017g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-14-8569G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035386 | |||||||
| chr17:79035411 | T | C | 16 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(13): Show |
19 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-8544T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035411 | |||||||
| chr17:79035412 | G | A | 1 | a0001c0006t0009g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-14-8543G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035412 | |||||||
| chr17:79035432 | C | T | 35 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(32): Show |
39 | HG00280.hp1 HG00639.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.-14-8523C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035432 | |||||||
| chr17:79035435 | AT | A | 129 | a0001c0001t0001g0066 a0001c0001t0001g0070 a0001c0001t0001g0071 others(126): Show |
172 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.-14-8505delT | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79035435 | ||||||
| chr17:79035435 | ATT | A | 45 | a0001c0001t0001g0018 a0001c0001t0001g0072 a0001c0001t0001g0161 others(42): Show |
50 | HG00280.hp1 HG00639.hp2 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.-14-8506_-14-8505d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79035435 | ||||||
| chr17:79035484 | G | A | 2 | a0001c0002t0003g0187 a0001c0002t0003g0188 |
2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-14-8471G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035484 | |||||||
| chr17:79035533 | C | T | 23 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(20): Show |
27 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14-8422C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035533 | |||||||
| chr17:79035534 | G | A | 7 | a0001c0004t0008g0022 a0001c0004t0008g0023 a0001c0004t0008g0075 others(4): Show |
9 | HG01106.hp1 HG02572.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-14-8421G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035534 | |||||||
| chr17:79035551 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-8404C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035551 | |||||||
| chr17:79035621 | G | A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-8334G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035621 | |||||||
| chr17:79035708 | G | C | 5 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 others(2): Show |
6 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-8247G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035708 | |||||||
| chr17:79035719 | C | T | 3 | a0001c0002t0003g0167 a0001c0002t0003g0184 a0001c0002t0003g0197 |
3 | HG02074.hp2 NA18939.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-14-8236C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035719 | |||||||
| chr17:79035735 | T | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14-8220T>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035735 | |||||||
| chr17:79035737 | C | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(16): Show |
27 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14-8218C>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035737 | |||||||
| chr17:79035759 | T | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0106 |
6 | HG00140.hp2 HG01123.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8196T>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035759 | |||||||
| chr17:79035820 | G | A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-8135G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79035820 | |||||||
| chr17:79036046 | TCA | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(6): Show |
11 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-7906_-14-7905d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79036046 | ||||||
| chr17:79036167 | C | CATGTGGC others(11): Show |
1 | a0001c0001t0001g0113 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-14-7783_-14-7766d others(20): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79036167 | ||||||
| chr17:79036174 | CTTTTTA | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-7773_-14-7768d others(8): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79036174 | ||||||
| chr17:79036227 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-7728C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79036227 | |||||||
| chr17:79036360 | A | G | 42 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(39): Show |
47 | HG00280.hp1 HG00639.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.-14-7595A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79036360 | |||||||
| chr17:79036427 | G | A | 2 | a0001c0004t0008g0023 a0001c0004t0008g0075 |
3 | HG02572.hp1 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-14-7528G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79036427 | |||||||
| chr17:79036476 | A | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG02109.hp1 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-14-7479A>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79036476 | |||||||
| chr17:79036493 | T | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-7462T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79036493 | |||||||
| chr17:79036585 | A | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-7370A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79036585 | |||||||
| chr17:79036873 | G | T | 3 | a0001c0003t0001g0172 a0001c0003t0001g0173 a0001c0003t0007g0160 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-14-7082G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79036873 | |||||||
| chr17:79036878 | T | A | 1 | a0001c0001t0004g0114 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-14-7077T>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79036878 | |||||||
| chr17:79036989 | A | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-6966A>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79036989 | |||||||
| chr17:79037010 | A | G | 71 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(68): Show |
86 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.-14-6945A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037010 | |||||||
| chr17:79037059 | G | A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-6896G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037059 | |||||||
| chr17:79037122 | T | A | 71 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(68): Show |
86 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.-14-6833T>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037122 | |||||||
| chr17:79037127 | TTG | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-6826_-14-6825d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79037127 | ||||||
| chr17:79037198 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-6757C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037198 | |||||||
| chr17:79037256 | A | G | 1 | a0001c0002t0002g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-14-6699A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037256 | |||||||
| chr17:79037351 | A | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-6604A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037351 | |||||||
| chr17:79037353 | T | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-6602T>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037353 | |||||||
| chr17:79037364 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-6591C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037364 | |||||||
| chr17:79037375 | C | G | 1 | a0001c0004t0003g0179 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-14-6580C>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037375 | |||||||
| chr17:79037376 | G | C | 1 | a0001c0004t0003g0179 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-14-6579G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037376 | |||||||
| chr17:79037382 | G | T | 3 | a0001c0002t0003g0196 a0001c0002t0003g0200 a0001c0005t0030g0199 |
3 | NA18953.hp2 NA18981.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-14-6573G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037382 | |||||||
| chr17:79037515 | C | T | 48 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0071 others(45): Show |
54 | HG00280.hp1 HG00639.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.-14-6440C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037515 | |||||||
| chr17:79037556 | G | A | 3 | a0001c0003t0007g0089 a0001c0003t0014g0207 a0001c0003t0014g0209 |
3 | HG02004.hp1 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-6399G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037556 | |||||||
| chr17:79037574 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-14-6381A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037574 | |||||||
| chr17:79037675 | A | G | 1 | a0001c0002t0002g0250 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-14-6280A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037675 | |||||||
| chr17:79037732 | G | A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-6223G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037732 | |||||||
| chr17:79037883 | G | T | 1 | a0001c0001t0004g0131 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-14-6072G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79037883 | |||||||
| chr17:79037996 | C | CT | 12 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(9): Show |
14 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-14-5948dupT | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79037996 | ||||||
| chr17:79038036 | C | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(21): Show |
34 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(31): Show |
intron_variant | MODIFIER | c.-14-5919C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038036 | |||||||
| chr17:79038075 | T | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(73): Show |
93 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.-14-5880T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038075 | |||||||
| chr17:79038241 | T | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-5714T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038241 | |||||||
| chr17:79038270 | G | A | 1 | a0001c0003t0006g0170 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-14-5685G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038270 | |||||||
| chr17:79038281 | C | T | 1 | a0001c0005t0005g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-14-5674C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038281 | |||||||
| chr17:79038359 | G | T | 34 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(31): Show |
38 | HG00280.hp1 HG00639.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.-14-5596G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038359 | |||||||
| chr17:79038362 | T | C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(15): Show |
20 | HG00639.hp2 HG01123.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14-5593T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038362 | |||||||
| chr17:79038458 | C | T | 1 | a0001c0001t0005g0091 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-14-5497C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038458 | |||||||
| chr17:79038468 | C | T | 7 | a0001c0002t0002g0021 a0001c0002t0002g0249 a0001c0006t0009g0048 others(4): Show |
10 | HG01243.hp2 HG01928.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-5487C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038468 | |||||||
| chr17:79038635 | T | C | 11 | a0001c0001t0001g0146 a0001c0003t0006g0028 a0001c0003t0006g0133 others(8): Show |
12 | HG01261.hp2 HG02055.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14-5320T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038635 | |||||||
| chr17:79038646 | A | G | 73 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(70): Show |
89 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.-14-5309A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038646 | |||||||
| chr17:79038658 | T | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-5297T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038658 | |||||||
| chr17:79038706 | A | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-5249A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038706 | |||||||
| chr17:79038742 | T | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(75): Show |
95 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.-14-5213T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038742 | |||||||
| chr17:79038831 | G | A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-5124G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79038831 | |||||||
| chr17:79039130 | A | G | 1 | a0001c0002t0003g0194 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-14-4825A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039130 | |||||||
| chr17:79039180 | A | T | 1 | a0001c0003t0007g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-14-4775A>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039180 | |||||||
| chr17:79039387 | C | T | 32 | a0001c0001t0001g0018 a0001c0001t0001g0115 a0001c0001t0001g0161 others(29): Show |
35 | HG00280.hp1 HG00639.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.-14-4568C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039387 | |||||||
| chr17:79039525 | C | T | 104 | a0001c0001t0001g0033 a0001c0001t0001g0144 a0001c0002t0002g0002 others(101): Show |
143 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.-14-4430C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039525 | |||||||
| chr17:79039526 | G | A | 3 | a0001c0003t0001g0172 a0001c0003t0001g0173 a0001c0003t0007g0160 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-14-4429G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039526 | |||||||
| chr17:79039662 | T | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-4293T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039662 | |||||||
| chr17:79039675 | C | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(75): Show |
95 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.-14-4280C>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039675 | |||||||
| chr17:79039686 | T | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-4269T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039686 | |||||||
| chr17:79039747 | G | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-4208G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039747 | |||||||
| chr17:79039783 | A | ATG | 15 | a0001c0002t0002g0036 a0001c0002t0002g0037 a0001c0002t0002g0180 others(12): Show |
16 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.-14-4158_-14-4157d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79039783 | ||||||
| chr17:79039783 | A | ATGTGTG | 9 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(6): Show |
11 | HG01106.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-14-4162_-14-4157d others(8): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79039783 | ||||||
| chr17:79039799 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(46): Show |
61 | HG00673.hp2 HG00741.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.-14-4156A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039799 | |||||||
| chr17:79039801 | A | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-4154A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039801 | |||||||
| chr17:79039803 | A | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-4152A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039803 | |||||||
| chr17:79039805 | A | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-4150A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039805 | |||||||
| chr17:79039807 | A | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-4148A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039807 | |||||||
| chr17:79039809 | A | G | 1 | a0001c0004t0008g0023 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-14-4146A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039809 | |||||||
| chr17:79039821 | GTATATAT others(3): Show |
G | 3 | a0001c0003t0001g0172 a0001c0003t0001g0173 a0001c0003t0007g0160 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-14-4123_-14-4114d others(12): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79039821 | ||||||
| chr17:79039849 | G | A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-4106G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039849 | |||||||
| chr17:79039954 | A | C | 1 | a0001c0004t0002g0127 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-14-4001A>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79039954 | |||||||
| chr17:79040001 | G | A | 49 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0071 others(46): Show |
55 | HG00280.hp1 HG00639.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.-14-3954G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79040001 | |||||||
| chr17:79040147 | G | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(21): Show |
34 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(31): Show |
intron_variant | MODIFIER | c.-14-3808G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79040147 | |||||||
| chr17:79040163 | T | G | 5 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 others(2): Show |
6 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-3792T>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79040163 | |||||||
| chr17:79040182 | T | C | 49 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0071 others(46): Show |
55 | HG00280.hp1 HG00639.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.-14-3773T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79040182 | |||||||
| chr17:79040212 | T | C | 49 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0071 others(46): Show |
55 | HG00280.hp1 HG00639.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.-14-3743T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79040212 | |||||||
| chr17:79040232 | G | A | 1 | a0001c0002t0002g0027 | 2 | HG01433.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-14-3723G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79040232 | |||||||
| chr17:79040240 | G | T | 5 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 others(2): Show |
6 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-3715G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79040240 | |||||||
| chr17:79040263 | G | C | 49 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0071 others(46): Show |
55 | HG00280.hp1 HG00639.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.-14-3692G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79040263 | |||||||
| chr17:79040286 | C | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(21): Show |
34 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(31): Show |
intron_variant | MODIFIER | c.-14-3669C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79040286 | |||||||
| chr17:79040312 | A | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(5): Show |
10 | HG02258.hp2 HG02559.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-3643A>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79040312 | |||||||
| chr17:79040581 | A | C | 38 | a0001c0001t0001g0018 a0001c0001t0001g0115 a0001c0001t0001g0161 others(35): Show |
42 | HG00280.hp1 HG00639.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.-14-3374A>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79040581 | |||||||
| chr17:79040730 | C | CA | 56 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(53): Show |
69 | HG00140.hp1 HG00280.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.-14-3201dupA | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79040730 | ||||||
| chr17:79040730 | C | CAA | 15 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0116 others(12): Show |
17 | HG01123.hp1 HG02055.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-3202_-14-3201d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79040730 | ||||||
| chr17:79040730 | C | CAAA | 6 | a0001c0001t0001g0057 a0001c0001t0001g0161 a0001c0005t0001g0155 others(3): Show |
6 | HG00639.hp2 HG01255.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-3203_-14-3201d others(5): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79040730 | ||||||
| chr17:79040730 | CA | C | 10 | a0001c0001t0001g0009 a0001c0001t0001g0102 a0001c0001t0004g0126 others(7): Show |
14 | HG00597.hp2 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-14-3201delA | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79040730 | ||||||
| chr17:79040730 | CAA | C | 17 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(14): Show |
19 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-3202_-14-3201d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79040730 | ||||||
| chr17:79040812 | G | A | 1 | a0001c0002t0003g0190 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-14-3143G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79040812 | |||||||
| chr17:79040870 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-3085C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79040870 | |||||||
| chr17:79040894 | C | CA | 12 | a0001c0002t0002g0256 a0001c0002t0002g0257 a0001c0003t0001g0172 others(9): Show |
13 | HG01243.hp2 HG01891.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-3050dupA | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79040894 | ||||||
| chr17:79040996 | G | GATTA | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(26): Show |
40 | HG00673.hp2 HG01243.hp2 HG02080.hp2 others(37): Show |
intron_variant | MODIFIER | c.-14-2956_-14-2955i others(6): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79040996 | ||||||
| chr17:79041012 | G | A | 1 | a0001c0008t0001g0073 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-14-2943G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041012 | |||||||
| chr17:79041024 | A | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(26): Show |
40 | HG00673.hp2 HG01243.hp2 HG02080.hp2 others(37): Show |
intron_variant | MODIFIER | c.-14-2931A>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041024 | |||||||
| chr17:79041041 | A | G | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(26): Show |
40 | HG00673.hp2 HG01243.hp2 HG02080.hp2 others(37): Show |
intron_variant | MODIFIER | c.-14-2914A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041041 | |||||||
| chr17:79041062 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0221 |
2 | HG00741.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-14-2893C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041062 | |||||||
| chr17:79041081 | C | T | 15 | a0001c0001t0001g0115 a0001c0003t0001g0079 a0001c0003t0001g0085 others(12): Show |
17 | HG00280.hp1 HG01081.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-14-2874C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041081 | |||||||
| chr17:79041185 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-14-2770C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041185 | |||||||
| chr17:79041303 | A | G | 78 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(75): Show |
95 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.-14-2652A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041303 | |||||||
| chr17:79041375 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0110 a0001c0001t0001g0128 |
4 | NA18964.hp2 NA18968.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-2580C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041375 | |||||||
| chr17:79041396 | C | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-2559C>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041396 | |||||||
| chr17:79041426 | C | T | 2 | a0001c0007t0001g0024 a0001c0007t0001g0081 |
3 | HG01167.hp1 HG01168.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-14-2529C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041426 | |||||||
| chr17:79041463 | G | A | 2 | a0001c0003t0014g0207 a0001c0003t0014g0209 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-2492G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041463 | |||||||
| chr17:79041501 | T | G | 74 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(71): Show |
91 | HG00280.hp1 HG00673.hp2 HG01081.hp2 others(88): Show |
intron_variant | MODIFIER | c.-14-2454T>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041501 | |||||||
| chr17:79041507 | G | A | 32 | a0001c0001t0001g0018 a0001c0001t0001g0115 a0001c0001t0001g0161 others(29): Show |
36 | HG00280.hp1 HG01081.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.-14-2448G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041507 | |||||||
| chr17:79041588 | G | A | 10 | a0001c0003t0006g0028 a0001c0003t0006g0133 a0001c0003t0006g0137 others(7): Show |
11 | HG01261.hp2 HG02055.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-2367G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041588 | |||||||
| chr17:79041715 | G | C | 10 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(7): Show |
12 | HG01106.hp1 HG02109.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-14-2240G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041715 | |||||||
| chr17:79041770 | C | CA | 52 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0001t0001g0102 others(49): Show |
56 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.-14-2168dupA | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79041770 | ||||||
| chr17:79041770 | C | CAA | 37 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(34): Show |
49 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(46): Show |
intron_variant | MODIFIER | c.-14-2169_-14-2168d others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79041770 | ||||||
| chr17:79041770 | C | CAAA | 11 | a0001c0001t0001g0059 a0001c0001t0001g0070 a0001c0001t0001g0071 others(8): Show |
13 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-2170_-14-2168d others(5): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79041770 | ||||||
| chr17:79041808 | G | A | 1 | a0001c0002t0002g0225 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-14-2147G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041808 | |||||||
| chr17:79041808 | G | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(75): Show |
95 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.-14-2147G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041808 | |||||||
| chr17:79041869 | T | G | 5 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 others(2): Show |
6 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-2086T>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041869 | |||||||
| chr17:79041925 | C | CTT | 190 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(187): Show |
246 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.-14-2030_-14-2029i others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79041925 | |||||||
| chr17:79042046 | C | T | 38 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(35): Show |
43 | HG00280.hp1 HG00639.hp2 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.-14-1909C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042046 | |||||||
| chr17:79042134 | C | T | 16 | a0001c0001t0001g0115 a0001c0001t0001g0163 a0001c0003t0001g0079 others(13): Show |
18 | HG00280.hp1 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14-1821C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042134 | |||||||
| chr17:79042212 | G | A | 1 | a0001c0002t0002g0245 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-14-1743G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042212 | |||||||
| chr17:79042218 | G | A | 35 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(32): Show |
39 | HG00280.hp1 HG00639.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.-14-1737G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042218 | |||||||
| chr17:79042249 | C | T | 38 | a0001c0001t0001g0018 a0001c0001t0001g0115 a0001c0001t0001g0161 others(35): Show |
42 | HG00280.hp1 HG00639.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.-14-1706C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042249 | |||||||
| chr17:79042337 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-14-1618C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042337 | |||||||
| chr17:79042452 | G | C | 2 | a0001c0005t0005g0158 a0001c0005t0005g0159 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-14-1503G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042452 | |||||||
| chr17:79042466 | C | CTGGAAGG others(15): Show |
1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-14-1488_-14-1467d others(24): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79042466 | ||||||
| chr17:79042472 | G | C | 2 | a0001c0003t0014g0207 a0001c0003t0014g0209 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-1483G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042472 | |||||||
| chr17:79042542 | C | T | 34 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(31): Show |
38 | HG00280.hp1 HG00639.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.-14-1413C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042542 | |||||||
| chr17:79042656 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG02109.hp1 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-14-1299G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042656 | |||||||
| chr17:79042665 | G | A | 2 | a0001c0003t0014g0207 a0001c0003t0014g0209 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-1290G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042665 | |||||||
| chr17:79042685 | A | G | 1 | a0001c0002t0003g0167 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-14-1270A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042685 | |||||||
| chr17:79042828 | C | T | 75 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(72): Show |
92 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.-14-1127C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042828 | |||||||
| chr17:79042909 | C | T | 16 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(13): Show |
19 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-1046C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042909 | |||||||
| chr17:79042914 | G | A | 2 | a0001c0003t0014g0207 a0001c0003t0014g0209 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-1041G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042914 | |||||||
| chr17:79042989 | T | C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(15): Show |
20 | HG00639.hp2 HG01123.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14-966T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79042989 | |||||||
| chr17:79043006 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-14-949C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043006 | |||||||
| chr17:79043050 | ATGTGTGG others(10): Show |
A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-884_-14-868del others(17): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79043050 | ||||||
| chr17:79043059 | T | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(5): Show |
10 | HG02258.hp2 HG02559.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-896T>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043059 | |||||||
| chr17:79043137 | G | A | 34 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(31): Show |
38 | HG00280.hp1 HG00639.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.-14-818G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043137 | |||||||
| chr17:79043138 | T | TG | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-817_-14-816ins others(1): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043138 | |||||||
| chr17:79043162 | A | C | 1 | a0001c0002t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-14-793A>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043162 | |||||||
| chr17:79043175 | G | A | 14 | a0001c0003t0001g0079 a0001c0003t0001g0085 a0001c0003t0006g0086 others(11): Show |
16 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-14-780G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043175 | |||||||
| chr17:79043227 | T | TGTGTGCA others(22): Show |
11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
13 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-716_-14-715ins others(29): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79043227 | ||||||
| chr17:79043360 | G | GTTT | 5 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 others(2): Show |
6 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-595_-14-594ins others(3): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043360 | |||||||
| chr17:79043378 | T | G | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-14-577T>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043378 | |||||||
| chr17:79043379 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-14-576G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043379 | |||||||
| chr17:79043408 | TGA | T | 14 | a0001c0003t0001g0079 a0001c0003t0001g0085 a0001c0003t0006g0086 others(11): Show |
16 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-14-545_-14-544del others(2): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79043408 | ||||||
| chr17:79043415 | ATG | A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(21): Show |
34 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(31): Show |
intron_variant | MODIFIER | c.-14-534_-14-533del others(2): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79043415 | ||||||
| chr17:79043426 | CTGTG | C | 2 | a0001c0002t0002g0210 a0001c0002t0003g0039 |
3 | HG02717.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-14-526_-14-523del others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79043426 | ||||||
| chr17:79043477 | G | A | 5 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 others(2): Show |
6 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-478G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043477 | |||||||
| chr17:79043520 | A | G | 5 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 others(2): Show |
6 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-435A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043520 | |||||||
| chr17:79043549 | CTG | C | 5 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 others(2): Show |
6 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-403_-14-402del others(2): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79043549 | ||||||
| chr17:79043561 | A | G | 5 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 others(2): Show |
6 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-394A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043561 | |||||||
| chr17:79043624 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-14-331T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043624 | |||||||
| chr17:79043636 | A | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0071 others(15): Show |
22 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-319A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043636 | |||||||
| chr17:79043652 | CTG | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(32): Show |
46 | HG00673.hp2 HG01106.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.-14-296_-14-295del others(2): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79043652 | ||||||
| chr17:79043659 | TGC | T | 4 | a0001c0004t0008g0022 a0001c0004t0008g0023 a0001c0004t0008g0075 others(1): Show |
6 | HG02572.hp1 HG02895.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-295_-14-294del others(2): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043659 | |||||||
| chr17:79043685 | AGT | A | 20 | a0001c0003t0006g0028 a0001c0003t0006g0133 a0001c0003t0006g0137 others(17): Show |
21 | HG00639.hp2 HG01123.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.-14-264_-14-263del others(2): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79043685 | ||||||
| chr17:79043734 | C | CGT | 36 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0071 others(33): Show |
42 | HG01106.hp1 HG01243.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.-14-215_-14-214dup others(2): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 79043734 | ||||||
| chr17:79043744 | C | T | 5 | a0001c0002t0002g0248 a0001c0005t0001g0155 a0001c0005t0005g0152 others(2): Show |
5 | HG00639.hp2 HG01255.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-211C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043744 | |||||||
| chr17:79043747 | G | A | 1 | a0001c0002t0002g0254 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-14-208G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043747 | |||||||
| chr17:79043753 | G | A | 189 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(186): Show |
245 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.-14-202G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043753 | |||||||
| chr17:79043763 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-14-192C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043763 | |||||||
| chr17:79043770 | G | A | 179 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(176): Show |
235 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-14-185G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043770 | |||||||
| chr17:79043779 | G | A | 1 | a0001c0001t0015g0031 | 2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-14-176G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043779 | |||||||
| chr17:79043794 | T | C | 13 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(10): Show |
16 | HG01243.hp2 HG02258.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.-14-161T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043794 | |||||||
| chr17:79043858 | C | T | 1 | a0001c0001t0019g0125 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-14-97C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043858 | |||||||
| chr17:79043906 | C | T | 2 | a0001c0002t0002g0046 a0001c0002t0002g0241 |
3 | HG01074.hp1 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-14-49C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043906 | |||||||
| chr17:79043911 | C | G | 3 | a0001c0003t0001g0172 a0001c0003t0001g0173 a0001c0003t0007g0160 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-14-44C>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 1/3 | chr17 | 79043911 | |||||||
| chr17:79044163 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.155+40C>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044163 | |||||||
| chr17:79044321 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.155+198G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044321 | |||||||
| chr17:79044351 | C | T | 1 | a0001c0004t0003g0195 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.155+228C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044351 | |||||||
| chr17:79044491 | T | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(21): Show |
34 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(31): Show |
intron_variant | MODIFIER | c.155+368T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044491 | |||||||
| chr17:79044554 | T | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(31): Show |
46 | HG00673.hp2 HG01106.hp1 HG02080.hp2 others(43): Show |
intron_variant | MODIFIER | c.155+431T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044554 | |||||||
| chr17:79044564 | G | A | 2 | a0001c0003t0001g0172 a0001c0003t0001g0173 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.155+441G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044564 | |||||||
| chr17:79044568 | T | C | 174 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(171): Show |
228 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.155+445T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044568 | |||||||
| chr17:79044597 | G | A | 1 | a0001c0002t0002g0239 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.155+474G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044597 | |||||||
| chr17:79044608 | G | A | 7 | a0001c0004t0008g0022 a0001c0004t0008g0023 a0001c0004t0008g0075 others(4): Show |
9 | HG01106.hp1 HG02572.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.155+485G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044608 | |||||||
| chr17:79044609 | G | T | 1 | a0001c0003t0007g0166 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.155+486G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044609 | |||||||
| chr17:79044705 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.155+582A>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044705 | |||||||
| chr17:79044712 | C | T | 1 | a0001c0001t0001g0017 | 3 | HG01070.hp2 HG01109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.155+589C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044712 | |||||||
| chr17:79044722 | C | T | 6 | a0001c0005t0005g0152 a0001c0005t0005g0153 a0001c0005t0005g0154 others(3): Show |
6 | HG00639.hp2 HG01123.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.155+599C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044722 | |||||||
| chr17:79044724 | A | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0162 others(6): Show |
11 | HG01255.hp1 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.155+601A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044724 | |||||||
| chr17:79044817 | G | A | 3 | a0001c0003t0014g0207 a0001c0003t0014g0209 a0001c0005t0028g0192 |
3 | HG02622.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.155+694G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044817 | |||||||
| chr17:79044909 | T | C | 134 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(131): Show |
184 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.155+786T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044909 | |||||||
| chr17:79044968 | A | T | 10 | a0001c0001t0001g0115 a0001c0003t0006g0086 a0001c0003t0007g0025 others(7): Show |
11 | HG00280.hp1 HG01081.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.155+845A>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79044968 | |||||||
| chr17:79045019 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.155+896G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045019 | |||||||
| chr17:79045039 | CAT | C | 20 | a0001c0003t0014g0207 a0001c0003t0014g0209 a0001c0005t0005g0152 others(17): Show |
21 | HG00639.hp2 HG01123.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.155+917_155+918del others(2): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045039 | |||||||
| chr17:79045103 | G | C | 1 | a0001c0003t0007g0166 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.155+980G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045103 | |||||||
| chr17:79045120 | C | G | 14 | a0001c0001t0001g0016 a0001c0001t0001g0055 a0001c0001t0001g0056 others(11): Show |
18 | HG02129.hp1 NA18939.hp1 NA18946.hp1 others(15): Show |
intron_variant | MODIFIER | c.155+997C>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045120 | |||||||
| chr17:79045240 | G | A | 1 | a0001c0015t0005g0074 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.155+1117G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045240 | |||||||
| chr17:79045254 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.155+1131G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045254 | |||||||
| chr17:79045256 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.155+1133C>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045256 | |||||||
| chr17:79045257 | T | A | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.155+1134T>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045257 | |||||||
| chr17:79045262 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.155+1139G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045262 | |||||||
| chr17:79045310 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.155+1187A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045310 | |||||||
| chr17:79045314 | T | C | 134 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(131): Show |
184 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.155+1191T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045314 | |||||||
| chr17:79045320 | A | T | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.155+1197A>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045320 | |||||||
| chr17:79045333 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.155+1210G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045333 | |||||||
| chr17:79045398 | T | C | 1 | a0001c0002t0002g0247 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.156-1157T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045398 | |||||||
| chr17:79045426 | C | T | 3 | a0001c0008t0001g0073 a0001c0008t0016g0069 a0001c0008t0016g0076 |
3 | HG01106.hp1 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.156-1129C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045426 | |||||||
| chr17:79045430 | A | C | 2 | a0001c0005t0005g0158 a0001c0005t0005g0159 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.156-1125A>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045430 | |||||||
| chr17:79045469 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0109 a0001c0001t0001g0117 others(3): Show |
10 | HG02056.hp2 NA18612.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.156-1086C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045469 | |||||||
| chr17:79045490 | T | C | 120 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0062 others(117): Show |
168 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.156-1065T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045490 | |||||||
| chr17:79045537 | G | A | 17 | a0001c0001t0001g0115 a0001c0003t0006g0028 a0001c0003t0006g0086 others(14): Show |
19 | HG00280.hp1 HG01081.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.156-1018G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045537 | |||||||
| chr17:79045586 | A | G | 43 | a0001c0001t0001g0115 a0001c0001t0005g0091 a0001c0001t0005g0095 others(40): Show |
46 | HG00280.hp1 HG00639.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.156-969A>G | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045586 | |||||||
| chr17:79045615 | C | T | 10 | a0001c0001t0005g0091 a0001c0001t0005g0095 a0001c0005t0005g0152 others(7): Show |
10 | HG00639.hp2 HG01123.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.156-940C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045615 | |||||||
| chr17:79045627 | C | T | 1 | a0001c0002t0002g0217 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.156-928C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045627 | |||||||
| chr17:79045663 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.156-892G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045663 | |||||||
| chr17:79045696 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.156-859C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045696 | |||||||
| chr17:79045820 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.156-735G>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045820 | |||||||
| chr17:79045855 | G | C | 2 | a0001c0003t0001g0172 a0001c0003t0001g0173 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.156-700G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79045855 | |||||||
| chr17:79046033 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.156-522G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79046033 | |||||||
| chr17:79046064 | C | T | 18 | a0001c0001t0001g0115 a0001c0003t0006g0028 a0001c0003t0006g0086 others(15): Show |
20 | HG00280.hp1 HG01081.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.156-491C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79046064 | |||||||
| chr17:79046065 | G | A | 1 | a0001c0001t0013g0120 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.156-490G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79046065 | |||||||
| chr17:79046080 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.156-475G>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79046080 | |||||||
| chr17:79046240 | G | A | 111 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0015 others(108): Show |
151 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.156-315G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79046240 | |||||||
| chr17:79046266 | T | C | 146 | a0001c0001t0001g0115 a0001c0001t0005g0091 a0001c0001t0005g0095 others(143): Show |
190 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.156-289T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79046266 | |||||||
| chr17:79046442 | G | A | 9 | a0001c0006t0009g0048 a0001c0006t0009g0049 a0001c0006t0009g0258 others(6): Show |
10 | HG01243.hp1 HG01243.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.156-113G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 2/3 | chr17 | 79046442 | |||||||
| chr17:79046729 | G | A | 2 | a0001c0003t0001g0172 a0001c0003t0001g0173 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.295+35G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | chr17 | 79046729 | |||||||
| chr17:79046923 | G | A | 1 | a0001c0015t0005g0074 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.295+229G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | chr17 | 79046923 | |||||||
| chr17:79046945 | G | A | 3 | a0001c0005t0005g0152 a0001c0005t0005g0153 a0001c0005t0005g0154 |
3 | HG00639.hp2 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.295+251G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | chr17 | 79046945 | |||||||
| chr17:79046946 | C | A | 1 | a0001c0002t0002g0244 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.295+252C>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | chr17 | 79046946 | |||||||
| chr17:79047054 | C | T | 3 | a0001c0008t0001g0073 a0001c0008t0016g0069 a0001c0008t0016g0076 |
3 | HG01106.hp1 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.295+360C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | chr17 | 79047054 | |||||||
| chr17:79047083 | C | T | 1 | a0001c0003t0006g0147 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.295+389C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | chr17 | 79047083 | |||||||
| chr17:79047195 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.296-343C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | chr17 | 79047195 | |||||||
| chr17:79047238 | C | CT | 11 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0013g0121 others(8): Show |
13 | HG01516.hp2 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.296-285dupT | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 79047238 | ||||||
| chr17:79047238 | C | CTTT | 8 | a0001c0003t0006g0028 a0001c0003t0006g0086 a0001c0003t0006g0133 others(5): Show |
9 | HG02055.hp1 HG02257.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.296-287_296-285dup others(3): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 79047238 | ||||||
| chr17:79047238 | C | CTTTT | 7 | a0001c0001t0001g0115 a0001c0003t0007g0025 a0001c0003t0007g0082 others(4): Show |
8 | HG00280.hp1 HG01081.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.296-288_296-285dup others(4): Show |
C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 79047238 | ||||||
| chr17:79047241 | T | C | 23 | a0001c0002t0002g0004 a0001c0002t0002g0027 a0001c0002t0002g0098 others(20): Show |
33 | HG00408.hp2 HG01433.hp1 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.296-297T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | chr17 | 79047241 | |||||||
| chr17:79047242 | T | C | 1 | a0001c0004t0002g0148 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.296-296T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | chr17 | 79047242 | |||||||
| chr17:79047254 | A | T | 1 | a0001c0015t0005g0074 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.296-284A>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | chr17 | 79047254 | |||||||
| chr17:79047272 | GA | G | 3 | a0001c0002t0003g0013 a0001c0002t0003g0182 a0001c0002t0003g0196 |
6 | NA18953.hp2 NA18964.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.296-257delA | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 79047272 | ||||||
| chr17:79047439 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.296-99C>T | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | chr17 | 79047439 | |||||||
| chr17:79047492 | T | C | 130 | a0001c0001t0005g0091 a0001c0001t0005g0095 a0001c0002t0002g0002 others(127): Show |
172 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.296-46T>C | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | chr17 | 79047492 | |||||||
| chr17:79047519 | G | A | 3 | a0001c0002t0002g0041 a0001c0002t0002g0215 a0001c0002t0002g0216 |
4 | HG00544.hp2 HG02080.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-19G>A | C1QTNF1 | ENSG00000173918.15 | transcript | ENST00000579760.6 | protein_coding | 3/3 | chr17 | 79047519 |