Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8840 |
| ensemblid | ENSG00000104415.14 |
| hgncid | 12769 |
| symbol | CCN4 |
| name | cellular communication network factor 4 |
| refseq_nuc | NM_003882.4 |
| refseq_prot | NP_003873.1 |
| ensembl_nuc | ENST00000250160.11 |
| ensembl_prot | ENSP00000250160.5 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 133191039 |
| end | 133231690 |
| strand | + |
| ver | v1.2 |
| region | chr8:133191039-133231690 |
| region5000 | chr8:133186039-133236690 |
| regionname0 | CCN4_chr8_133191039_133231690 |
| regionname5000 | CCN4_chr8_133186039_133236690 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 367 | 373 | 86 | 64 | 165 | 16 | 40 | 128 | CCN4_chr8_133186039_133236690 | CCN4 | MRWFL others(362): Show |
chr8 | 133186039 | 133236690 |
| a0002 | 0/0 | 367 | 8 | 5 | 1 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | MRWFL others(362): Show |
chr8 | 133186039 | 133236690 |
| a0003 | 0/0 | 367 | 7 | 0 | 6 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | MRWFL others(362): Show |
chr8 | 133186039 | 133236690 |
| a0004 | 0/0 | 367 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | MRWFL others(362): Show |
chr8 | 133186039 | 133236690 |
| a0005 | 0/0 | 367 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CCN4_chr8_133186039_133236690 | CCN4 | MRWFL others(362): Show |
chr8 | 133186039 | 133236690 |
| a0006 | 0/0 | 367 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | MRWFL others(362): Show |
chr8 | 133186039 | 133236690 |
| a0007 | 0/0 | 367 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | MRWFL others(362): Show |
chr8 | 133186039 | 133236690 |
| a0008 | 0/0 | 367 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | MRWFL others(362): Show |
chr8 | 133186039 | 133236690 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1101 | 274 | 51 | 42 | 141 | 9 | 30 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0001c0002 | 0/1 | 1101 | 71 | 19 | 21 | 13 | 7 | 10 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0001c0003 | 0/0 | 1101 | 9 | 9 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0001c0005 | 0/0 | 1101 | 8 | 0 | 0 | 8 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0001c0009 | 0/0 | 1101 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0001c0010 | 0/0 | 1101 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0001c0012 | 0/0 | 1101 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0001c0014 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0001c0015 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0001c0016 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0001c0018 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0001c0020 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0002c0004 | 0/0 | 1101 | 8 | 5 | 1 | 0 | 2 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0003c0006 | 0/0 | 1101 | 5 | 0 | 4 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0003c0007 | 0/0 | 1101 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0004c0008 | 0/0 | 1101 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0004c0019 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0005c0011 | 0/0 | 1101 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0006c0017 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0007c0021 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 | ||
| a0008c0013 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | ATGAG others(1096): Show |
chr8 | 133186039 | 133236690 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5190 | 168 | 15 | 20 | 101 | 7 | 25 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0002 | 0/0 | 5190 | 67 | 5 | 18 | 39 | 1 | 4 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0005 | 0/0 | 5190 | 7 | 6 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0006 | 0/0 | 5190 | 7 | 7 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0007 | 1/0 | 5190 | 5 | 3 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0008 | 0/0 | 5190 | 4 | 4 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0009 | 0/0 | 5190 | 4 | 4 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0013 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0016 | 0/0 | 5190 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0019 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0020 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0022 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0023 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0024 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5169): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0026 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0035 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0036 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0001t0038 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0002t0003 | 0/1 | 5190 | 47 | 2 | 16 | 12 | 6 | 10 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0002t0004 | 0/0 | 5190 | 5 | 3 | 1 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0002t0010 | 0/0 | 5190 | 4 | 3 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0002t0011 | 0/0 | 5190 | 4 | 4 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0002t0012 | 0/0 | 5190 | 3 | 2 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0002t0018 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0002t0021 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0002t0028 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0002t0030 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0002t0032 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0002t0033 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0002t0034 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0003t0001 | 0/0 | 5190 | 4 | 4 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0003t0005 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0003t0014 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0003t0015 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0005t0001 | 0/0 | 5190 | 8 | 0 | 0 | 8 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0009t0004 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0009t0025 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0010t0027 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0010t0031 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0012t0001 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0014t0001 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0015t0002 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0016t0013 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0018t0002 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0001c0020t0001 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0002c0004t0004 | 0/0 | 5190 | 8 | 5 | 1 | 0 | 2 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0003c0006t0001 | 0/0 | 5190 | 5 | 0 | 4 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0003c0007t0017 | 0/0 | 5190 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0004c0008t0029 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0004c0008t0037 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0004c0019t0001 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0005c0011t0002 | 0/0 | 5190 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0006c0017t0001 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0007c0021t0001 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| a0008c0013t0001 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | ATATC others(5185): Show |
chr8 | 133186039 | 133236690 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0005g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0007g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0008g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0008g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0013g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0016g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0016g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0019g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0020g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0022g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0023g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0024g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0026g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0035g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0036g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0001t0038g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0029 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0003g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0010g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0010g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0011g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0011g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0012g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0012g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0018g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0018g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0021g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0028g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0030g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0032g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0033g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0002t0034g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0003t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0003t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0003t0014g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0003t0014g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0003t0015g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0003t0015g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0005t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0005t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0005t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0005t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0005t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0009t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0009t0025g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0010t0027g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0010t0031g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0012t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0012t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0014t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0015t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0016t0013g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0018t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0001c0020t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0002c0004t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0002c0004t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0002c0004t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0002c0004t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0002c0004t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0002c0004t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0002c0004t0004g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0003c0006t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0003c0006t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0003c0006t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0003c0006t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0003c0006t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0003c0007t0017g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0003c0007t0017g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0004c0008t0029g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0004c0008t0037g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0004c0019t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0005c0011t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0006c0017t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0007c0021t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| a0008c0013t0001g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | GBR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0185 | EUR | GBR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00140 | hp2 | a0002 | c0004 | t0004 | g0222 | EUR | GBR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00280 | hp1 | a0002 | c0004 | t0004 | g0089 | EUR | FIN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0057 | EUR | FIN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0085 | EUR | FIN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0150 | EUR | FIN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0355 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0034 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00438 | hp2 | a0001 | c0005 | t0001 | g0180 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0336 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0126 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00642 | hp2 | a0003 | c0006 | t0001 | g0047 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00733 | hp2 | a0001 | c0002 | t0003 | g0369 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00735 | hp1 | a0001 | c0001 | t0016 | g0061 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00735 | hp2 | a0001 | c0002 | t0032 | g0201 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0366 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0194 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01069 | hp1 | a0006 | c0017 | t0001 | g0060 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01070 | hp1 | a0003 | c0007 | t0017 | g0124 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0152 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0049 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01106 | hp1 | a0001 | c0001 | t0020 | g0044 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01109 | hp2 | a0001 | c0002 | t0010 | g0266 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01167 | hp2 | a0001 | c0002 | t0012 | g0362 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01168 | hp1 | a0003 | c0006 | t0001 | g0071 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0145 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01169 | hp2 | a0003 | c0006 | t0001 | g0067 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01175 | hp1 | a0001 | c0001 | t0016 | g0123 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01175 | hp2 | a0001 | c0002 | t0003 | g0190 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01192 | hp1 | a0003 | c0006 | t0001 | g0213 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0147 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01358 | hp1 | a0001 | c0002 | t0004 | g0083 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0050 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0084 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0076 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0118 | EUR | IBS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0009 | EUR | IBS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0009 | EUR | IBS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0093 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0347 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01891 | hp2 | a0001 | c0001 | t0022 | g0280 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01981 | hp1 | a0001 | c0014 | t0001 | g0324 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02004 | hp1 | a0001 | c0002 | t0033 | g0325 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02004 | hp2 | a0003 | c0007 | t0017 | g0241 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02040 | hp1 | a0001 | c0015 | t0002 | g0292 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02040 | hp2 | a0007 | c0021 | t0001 | g0132 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0244 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02055 | hp2 | a0001 | c0010 | t0031 | g0365 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0053 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02145 | hp2 | a0001 | c0002 | t0004 | g0109 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | CDX | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | CDX | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | CDX | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02257 | hp1 | a0001 | c0002 | t0018 | g0231 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0100 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02258 | hp1 | a0001 | c0001 | t0009 | g0110 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02258 | hp2 | a0001 | c0001 | t0035 | g0345 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0242 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0338 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02280 | hp1 | a0001 | c0002 | t0010 | g0259 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0344 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02293 | hp1 | a0001 | c0002 | t0003 | g0011 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02293 | hp2 | a0001 | c0002 | t0003 | g0127 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02300 | hp2 | a0002 | c0004 | t0004 | g0075 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02451 | hp1 | a0001 | c0001 | t0023 | g0268 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02451 | hp2 | a0002 | c0004 | t0004 | g0005 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02523 | hp1 | a0001 | c0002 | t0034 | g0302 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02572 | hp1 | a0004 | c0008 | t0029 | g0108 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0274 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0193 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02615 | hp1 | a0001 | c0001 | t0026 | g0233 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0277 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0103 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02622 | hp2 | a0001 | c0002 | t0021 | g0045 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0234 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0111 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02647 | hp2 | a0001 | c0002 | t0011 | g0263 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0078 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02717 | hp1 | a0001 | c0002 | t0011 | g0247 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02717 | hp2 | a0001 | c0012 | t0001 | g0068 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0082 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02738 | hp1 | a0001 | c0002 | t0003 | g0368 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02738 | hp2 | a0001 | c0001 | t0036 | g0125 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0153 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02809 | hp2 | a0001 | c0002 | t0011 | g0236 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0371 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0159 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02886 | hp2 | a0001 | c0009 | t0004 | g0237 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02896 | hp1 | a0001 | c0002 | t0011 | g0262 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0079 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02897 | hp2 | a0001 | c0002 | t0003 | g0248 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02922 | hp1 | a0001 | c0012 | t0001 | g0363 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0255 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02965 | hp1 | a0001 | c0010 | t0027 | g0272 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02965 | hp2 | a0001 | c0001 | t0024 | g0252 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0278 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02970 | hp2 | a0001 | c0001 | t0019 | g0098 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0246 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02976 | hp2 | a0001 | c0003 | t0015 | g0256 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03017 | hp1 | a0003 | c0006 | t0001 | g0031 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03041 | hp1 | a0001 | c0002 | t0012 | g0106 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03130 | hp1 | a0001 | c0002 | t0010 | g0258 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0370 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0271 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03139 | hp2 | a0002 | c0004 | t0004 | g0081 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03195 | hp1 | a0004 | c0008 | t0037 | g0107 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03195 | hp2 | a0001 | c0002 | t0018 | g0043 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03209 | hp1 | a0001 | c0003 | t0014 | g0077 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03225 | hp1 | a0001 | c0002 | t0012 | g0094 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0122 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03239 | hp2 | a0001 | c0002 | t0003 | g0196 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0097 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0250 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0352 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0128 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0033 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0353 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03516 | hp1 | a0001 | c0002 | t0004 | g0273 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03540 | hp2 | a0001 | c0003 | t0014 | g0343 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03579 | hp1 | a0001 | c0016 | t0013 | g0267 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0361 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0176 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03688 | hp1 | a0001 | c0002 | t0003 | g0070 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0195 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03710 | hp2 | a0008 | c0013 | t0001 | g0372 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0199 | SAS | BEB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0359 | SAS | BEB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0261 | AFR | YRI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18522 | hp2 | a0002 | c0004 | t0004 | g0005 | AFR | YRI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18906 | hp1 | a0001 | c0003 | t0015 | g0257 | AFR | YRI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18906 | hp2 | a0002 | c0004 | t0004 | g0358 | AFR | YRI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18946 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18947 | hp1 | a0001 | c0002 | t0003 | g0205 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18950 | hp1 | a0001 | c0018 | t0002 | g0165 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18956 | hp2 | a0001 | c0005 | t0001 | g0179 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18957 | hp1 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18961 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18978 | hp1 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0321 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18982 | hp1 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18983 | hp1 | a0001 | c0005 | t0001 | g0178 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18983 | hp2 | a0001 | c0005 | t0001 | g0136 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18985 | hp1 | a0005 | c0011 | t0002 | g0007 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18993 | hp1 | a0001 | c0005 | t0001 | g0181 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0206 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0373 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0192 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19003 | hp1 | a0005 | c0011 | t0002 | g0007 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0161 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19030 | hp1 | a0001 | c0003 | t0005 | g0232 | AFR | LWK | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19030 | hp2 | a0001 | c0009 | t0025 | g0245 | AFR | LWK | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0346 | AFR | LWK | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19043 | hp2 | a0001 | c0002 | t0030 | g0087 | AFR | LWK | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19067 | hp2 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19070 | hp2 | a0001 | c0020 | t0001 | g0360 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0041 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19077 | hp2 | a0001 | c0001 | t0038 | g0207 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19084 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19240 | hp1 | a0001 | c0002 | t0010 | g0279 | AFR | YRI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0158 | AFR | YRI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0367 | AFR | ASW | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ASW | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA20752 | hp1 | a0001 | c0002 | t0004 | g0091 | EUR | TSI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | TSI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA20805 | hp2 | a0001 | c0002 | t0003 | g0088 | EUR | TSI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01123 | hp1 | a0001 | c0002 | t0003 | g0059 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02486 | hp1 | a0002 | c0004 | t0004 | g0048 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02486 | hp2 | a0001 | c0002 | t0028 | g0235 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0251 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03471 | hp1 | a0004 | c0019 | t0001 | g0270 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | USA | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | LWK | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0003 | g0029 | REF | REF | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0189 | REF | REF | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:133191212 | C | T | 1 | a0007 | 1 | HG02040.hp2 | missense_variant&splice_region_variant | MODERATE | c.68C>T | p.Thr23Met | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/5 | 174/5190 | 68/1104 | 23/367 | chr8 | 133191212 | |||
| chr8:133220665 | C | T | 1 | a0006 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.434C>T | p.Thr145Met | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 540/5190 | 434/1104 | 145/367 | chr8 | 133220665 | |||
| chr8:133220680 | C | T | 1 | a0005 | 2 | NA18985.hp1 NA19003.hp1 |
missense_variant | MODERATE | c.449C>T | p.Ala150Val | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 555/5190 | 449/1104 | 150/367 | chr8 | 133220680 | |||
| chr8:133220707 | G | A | 1 | a0008 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.476G>A | p.Arg159Gln | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 582/5190 | 476/1104 | 159/367 | chr8 | 133220707 | |||
| chr8:133220781 | G | A | 1 | a0003 | 7 | HG00642.hp2 HG01070.hp1 HG01168.hp1 others(4): Show |
missense_variant | MODERATE | c.550G>A | p.Val184Ile | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 656/5190 | 550/1104 | 184/367 | chr8 | 133220781 | |||
| chr8:133220796 | G | A | 1 | a0004 | 3 | HG02572.hp1 HG03195.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.565G>A | p.Ala189Thr | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 671/5190 | 565/1104 | 189/367 | chr8 | 133220796 | |||
| chr8:133225392 | G | T | 1 | a0002 | 8 | HG00140.hp2 HG00280.hp1 HG02300.hp2 others(5): Show |
missense_variant&splice_region_variant | MODERATE | c.613G>T | p.Ala205Ser | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/5 | 719/5190 | 613/1104 | 205/367 | chr8 | 133225392 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:133212878 | C | T | 1 | a0001c0020 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.84C>T | p.Ala28Ala | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/5 | 190/5190 | 84/1104 | 28/367 | chr8 | 133212878 | |||
| chr8:133212917 | C | T | 1 | a0004c0019 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.123C>T | p.Asp41Asp | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/5 | 229/5190 | 123/1104 | 41/367 | chr8 | 133212917 | |||
| chr8:133212935 | A | G | 1 | a0001c0018 | 1 | NA18950.hp1 | synonymous_variant | LOW | c.141A>G | p.Gln47Gln | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/5 | 247/5190 | 141/1104 | 47/367 | chr8 | 133212935 | |||
| chr8:133212980 | C | T | 1 | a0001c0005 | 8 | HG00438.hp2 NA18946.hp2 NA18956.hp2 others(5): Show |
synonymous_variant | LOW | c.186C>T | p.Cys62Cys | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/5 | 292/5190 | 186/1104 | 62/367 | chr8 | 133212980 | |||
| chr8:133213085 | G | A | 1 | a0001c0003 | 9 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(6): Show |
synonymous_variant | LOW | c.291G>A | p.Arg97Arg | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/5 | 397/5190 | 291/1104 | 97/367 | chr8 | 133213085 | |||
| chr8:133213091 | C | T | 1 | a0001c0012 | 2 | HG02717.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.297C>T | p.Leu99Leu | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/5 | 403/5190 | 297/1104 | 99/367 | chr8 | 133213091 | |||
| chr8:133220789 | G | A | 1 | a0001c0014 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.558G>A | p.Glu186Glu | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 664/5190 | 558/1104 | 186/367 | chr8 | 133220789 | |||
| chr8:133220795 | C | T | 1 | a0001c0016 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.564C>T | p.Asp188Asp | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 670/5190 | 564/1104 | 188/367 | chr8 | 133220795 | |||
| chr8:133227461 | C | T | 1 | a0001c0010 | 2 | HG02055.hp2 HG02965.hp1 |
synonymous_variant | LOW | c.855C>T | p.Phe285Phe | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 961/5190 | 855/1104 | 285/367 | chr8 | 133227461 | |||
| chr8:133227470 | G | A | 1 | a0001c0009 | 2 | HG02886.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.864G>A | p.Ala288Ala | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 970/5190 | 864/1104 | 288/367 | chr8 | 133227470 | |||
| chr8:133227503 | G | A | 1 | a0001c0015 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.897G>A | p.Lys299Lys | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1003/5190 | 897/1104 | 299/367 | chr8 | 133227503 | |||
| chr8:133227527 | T | C | 6 | a0001c0002 a0001c0009 a0001c0010 others(3): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
synonymous_variant | LOW | c.921T>C | p.Asn307Asn | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1027/5190 | 921/1104 | 307/367 | chr8 | 133227527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:133191061 | C | T | 1 | a0001c0001t0038 | 1 | NA19077.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-84C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/5 | chr8 | 133191061 | |||||||
| chr8:133191093 | G | C | 1 | a0001c0001t0019 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-52G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/5 | 52 | chr8 | 133191093 | ||||||
| chr8:133191098 | G | A | 2 | a0001c0001t0020 a0001c0002t0021 |
2 | HG01106.hp1 HG02622.hp2 |
5_prime_UTR_variant | MODIFIER | c.-47G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/5 | 47 | chr8 | 133191098 | ||||||
| chr8:133227971 | C | T | 1 | a0004c0008t0037 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*261C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 261 | chr8 | 133227971 | ||||||
| chr8:133228161 | C | T | 2 | a0001c0002t0010 a0001c0002t0011 |
8 | HG01109.hp2 HG02280.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*451C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 451 | chr8 | 133228161 | ||||||
| chr8:133228351 | G | A | 2 | a0001c0001t0013 a0001c0016t0013 |
2 | HG03579.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*641G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 641 | chr8 | 133228351 | ||||||
| chr8:133228454 | G | A | 47 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(44): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*744G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 744 | chr8 | 133228454 | ||||||
| chr8:133228680 | C | T | 4 | a0001c0002t0003 a0001c0002t0032 a0001c0002t0033 others(1): Show |
49 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*970C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 970 | chr8 | 133228680 | ||||||
| chr8:133228695 | G | C | 1 | a0001c0002t0010 | 4 | HG01109.hp2 HG02280.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*985G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 985 | chr8 | 133228695 | ||||||
| chr8:133228843 | C | G | 12 | a0001c0002t0010 a0001c0002t0011 a0001c0002t0012 others(9): Show |
22 | HG01070.hp1 HG01109.hp2 HG01167.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1133C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1133 | chr8 | 133228843 | ||||||
| chr8:133228894 | G | A | 28 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(25): Show |
231 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*1184G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1184 | chr8 | 133228894 | ||||||
| chr8:133228968 | T | C | 1 | a0003c0007t0017 | 2 | HG01070.hp1 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1258T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1258 | chr8 | 133228968 | ||||||
| chr8:133228991 | T | C | 1 | a0001c0001t0035 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1281T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1281 | chr8 | 133228991 | ||||||
| chr8:133229173 | A | G | 2 | a0001c0010t0027 a0001c0010t0031 |
2 | HG02055.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1463A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1463 | chr8 | 133229173 | ||||||
| chr8:133229227 | C | A | 1 | a0001c0001t0022 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1517C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1517 | chr8 | 133229227 | ||||||
| chr8:133229757 | A | G | 1 | a0003c0007t0017 | 2 | HG01070.hp1 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2047A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2047 | chr8 | 133229757 | ||||||
| chr8:133229790 | C | T | 29 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(26): Show |
232 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*2080C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2080 | chr8 | 133229790 | ||||||
| chr8:133230093 | G | T | 2 | a0001c0002t0010 a0001c0002t0011 |
8 | HG01109.hp2 HG02280.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2383G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2383 | chr8 | 133230093 | ||||||
| chr8:133230095 | T | G | 1 | a0001c0002t0028 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2385T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2385 | chr8 | 133230095 | ||||||
| chr8:133230108 | G | A | 1 | a0001c0001t0023 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2398G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2398 | chr8 | 133230108 | ||||||
| chr8:133230129 | C | G | 46 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(43): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*2419C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2419 | chr8 | 133230129 | ||||||
| chr8:133230160 | T | C | 1 | a0001c0009t0025 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2450T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2450 | chr8 | 133230160 | ||||||
| chr8:133230212 | G | A | 29 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(26): Show |
232 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*2502G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2502 | chr8 | 133230212 | ||||||
| chr8:133230265 | G | T | 48 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(45): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*2555G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2555 | chr8 | 133230265 | ||||||
| chr8:133230437 | T | G | 1 | a0001c0001t0006 | 7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2727T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2727 | chr8 | 133230437 | ||||||
| chr8:133230557 | T | C | 1 | a0001c0001t0036 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2847T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2847 | chr8 | 133230557 | ||||||
| chr8:133230566 | T | C | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(50): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
3_prime_UTR_variant | MODIFIER | c.*2856T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2856 | chr8 | 133230566 | ||||||
| chr8:133230681 | A | G | 1 | a0001c0001t0016 | 2 | HG00735.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2971A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2971 | chr8 | 133230681 | ||||||
| chr8:133230713 | C | G | 1 | a0001c0001t0008 | 4 | HG02257.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3003C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3003 | chr8 | 133230713 | ||||||
| chr8:133231005 | C | T | 5 | a0001c0002t0012 a0001c0002t0018 a0001c0002t0021 others(2): Show |
8 | HG01167.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3295C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3295 | chr8 | 133231005 | ||||||
| chr8:133231024 | C | T | 1 | a0001c0002t0033 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3314C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3314 | chr8 | 133231024 | ||||||
| chr8:133231113 | T | G | 1 | a0001c0002t0018 | 2 | HG02257.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3403T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3403 | chr8 | 133231113 | ||||||
| chr8:133231123 | G | C | 8 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0020 others(5): Show |
15 | HG01074.hp1 HG01106.hp1 HG01891.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3413G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3413 | chr8 | 133231123 | ||||||
| chr8:133231127 | GACATGAT others(9): Show |
G | 1 | a0001c0001t0024 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3418_*3433delACAT others(12): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3418 | chr8 | 133231127 | ||||||
| chr8:133231179 | A | T | 1 | a0001c0003t0015 | 2 | HG02976.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3469A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3469 | chr8 | 133231179 | ||||||
| chr8:133231186 | A | G | 5 | a0001c0002t0012 a0001c0002t0018 a0001c0002t0021 others(2): Show |
8 | HG01167.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3476A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3476 | chr8 | 133231186 | ||||||
| chr8:133231225 | T | G | 1 | a0001c0003t0014 | 2 | HG03209.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3515T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3515 | chr8 | 133231225 | ||||||
| chr8:133231242 | T | C | 1 | a0001c0002t0032 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3532T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3532 | chr8 | 133231242 | ||||||
| chr8:133231288 | C | G | 1 | a0001c0001t0020 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3578C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3578 | chr8 | 133231288 | ||||||
| chr8:133231307 | C | T | 31 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(28): Show |
235 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*3597C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3597 | chr8 | 133231307 | ||||||
| chr8:133231596 | A | G | 4 | a0001c0002t0012 a0001c0002t0018 a0001c0002t0021 others(1): Show |
7 | HG01167.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3886A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3886 | chr8 | 133231596 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:133191340 | C | T | 1 | a0001c0001t0002g0373 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.69+127C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133191340 | |||||||
| chr8:133191601 | C | T | 1 | a0008c0013t0001g0372 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.69+388C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133191601 | |||||||
| chr8:133191778 | A | T | 2 | a0001c0001t0001g0370 a0001c0001t0001g0371 |
2 | HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.69+565A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133191778 | |||||||
| chr8:133191793 | G | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(73): Show |
80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.69+580G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133191793 | |||||||
| chr8:133191819 | AG | A | 6 | a0001c0001t0001g0092 a0001c0001t0001g0095 a0001c0001t0001g0370 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+607delG | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133191819 | |||||||
| chr8:133191982 | C | T | 1 | a0001c0002t0003g0369 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.69+769C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133191982 | |||||||
| chr8:133192215 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(79): Show |
86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.69+1002A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192215 | |||||||
| chr8:133192328 | C | A | 2 | a0001c0001t0005g0096 a0001c0001t0005g0097 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.69+1115C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192328 | |||||||
| chr8:133192357 | G | T | 6 | a0001c0001t0001g0092 a0001c0001t0001g0095 a0001c0001t0001g0370 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+1144G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192357 | |||||||
| chr8:133192359 | C | T | 1 | a0001c0002t0003g0368 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.69+1146C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192359 | |||||||
| chr8:133192396 | C | T | 1 | a0001c0001t0002g0367 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.69+1183C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192396 | |||||||
| chr8:133192549 | A | T | 1 | a0001c0002t0003g0366 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.69+1336A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192549 | |||||||
| chr8:133192581 | T | G | 1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.69+1368T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192581 | |||||||
| chr8:133192620 | G | A | 1 | a0001c0001t0019g0098 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.69+1407G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192620 | |||||||
| chr8:133192660 | C | T | 1 | a0001c0010t0031g0365 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.69+1447C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192660 | |||||||
| chr8:133192685 | A | G | 1 | a0001c0002t0004g0091 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.69+1472A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192685 | |||||||
| chr8:133192733 | G | T | 1 | a0001c0001t0001g0364 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.69+1520G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192733 | |||||||
| chr8:133192739 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.69+1526G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192739 | |||||||
| chr8:133192798 | T | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(70): Show |
77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.69+1585T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192798 | |||||||
| chr8:133192805 | C | A | 1 | a0001c0001t0008g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.69+1592C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192805 | |||||||
| chr8:133192838 | G | T | 1 | a0001c0001t0008g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.69+1625G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192838 | |||||||
| chr8:133192858 | G | C | 6 | a0001c0001t0001g0092 a0001c0001t0001g0095 a0001c0001t0001g0370 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+1645G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192858 | |||||||
| chr8:133192936 | C | A | 6 | a0001c0001t0001g0092 a0001c0001t0001g0095 a0001c0001t0001g0370 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+1723C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192936 | |||||||
| chr8:133192936 | C | T | 1 | a0001c0001t0002g0367 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.69+1723C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192936 | |||||||
| chr8:133192999 | C | A | 1 | a0001c0010t0031g0365 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.69+1786C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192999 | |||||||
| chr8:133193080 | C | T | 2 | a0001c0002t0012g0362 a0001c0012t0001g0363 |
2 | HG01167.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.69+1867C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193080 | |||||||
| chr8:133193130 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.69+1917G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193130 | |||||||
| chr8:133193375 | A | G | 2 | a0001c0001t0005g0096 a0001c0001t0005g0097 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.69+2162A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193375 | |||||||
| chr8:133193438 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.69+2225G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193438 | |||||||
| chr8:133193470 | G | A | 66 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0102 others(63): Show |
69 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.69+2257G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193470 | |||||||
| chr8:133193564 | A | G | 2 | a0001c0001t0005g0361 a0001c0010t0031g0365 |
2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.69+2351A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193564 | |||||||
| chr8:133193665 | A | G | 1 | a0001c0020t0001g0360 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.69+2452A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193665 | |||||||
| chr8:133193727 | T | G | 1 | a0001c0001t0005g0361 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69+2514T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193727 | |||||||
| chr8:133193781 | C | T | 1 | a0001c0001t0002g0359 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.69+2568C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193781 | |||||||
| chr8:133193896 | G | T | 1 | a0002c0004t0004g0358 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2683G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193896 | |||||||
| chr8:133194004 | G | A | 7 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0163 others(4): Show |
7 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+2791G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194004 | |||||||
| chr8:133194036 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(80): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.69+2823C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194036 | |||||||
| chr8:133194085 | TTCAG | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(79): Show |
86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.69+2873_69+2876del others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194085 | |||||||
| chr8:133194181 | C | T | 1 | a0001c0001t0001g0357 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.69+2968C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194181 | |||||||
| chr8:133194293 | G | GGT | 70 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0101 others(67): Show |
73 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.69+3092_69+3093dup others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194293 | ||||||
| chr8:133194307 | G | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(206): Show |
218 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.69+3094G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194307 | |||||||
| chr8:133194308 | T | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(206): Show |
218 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.69+3095T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194308 | |||||||
| chr8:133194361 | T | G | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0027 others(5): Show |
8 | HG02970.hp2 NA18945.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+3148T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194361 | |||||||
| chr8:133194367 | T | G | 1 | a0001c0001t0005g0244 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.69+3154T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194367 | |||||||
| chr8:133194429 | GGTATGTG others(10): Show |
G | 1 | a0001c0003t0001g0347 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.69+3219_69+3235del others(17): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194429 | ||||||
| chr8:133194442 | GGTGT | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(205): Show |
217 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.69+3237_69+3240del others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194442 | ||||||
| chr8:133194466 | GGT | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(204): Show |
216 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.69+3267_69+3268del others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194466 | ||||||
| chr8:133194468 | T | A | 2 | a0001c0001t0013g0346 a0001c0001t0035g0345 |
2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.69+3255T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194468 | |||||||
| chr8:133194470 | T | G | 2 | a0001c0001t0005g0246 a0001c0009t0025g0245 |
2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.69+3257T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194470 | |||||||
| chr8:133194510 | AGTGTGGT others(14): Show |
A | 4 | a0001c0001t0001g0032 a0001c0001t0002g0030 a0001c0002t0003g0033 others(1): Show |
4 | HG01106.hp2 HG02683.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+3309_69+3329del others(21): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194510 | ||||||
| chr8:133194550 | G | A | 2 | a0001c0001t0002g0035 a0001c0002t0003g0034 |
2 | HG00423.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.69+3337G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194550 | |||||||
| chr8:133194561 | G | C | 1 | a0001c0002t0004g0091 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.69+3348G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194561 | |||||||
| chr8:133194647 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0009g0093 |
2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.69+3434G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194647 | |||||||
| chr8:133194689 | G | GTGTGGGG others(1): Show |
38 | a0001c0001t0001g0016 a0001c0001t0001g0249 a0001c0001t0001g0253 others(35): Show |
39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3480_69+3481ins others(8): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194689 | ||||||
| chr8:133194695 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.69+3482G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194695 | |||||||
| chr8:133194696 | G | T | 38 | a0001c0001t0001g0016 a0001c0001t0001g0249 a0001c0001t0001g0253 others(35): Show |
39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3483G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194696 | |||||||
| chr8:133194699 | G | T | 38 | a0001c0001t0001g0016 a0001c0001t0001g0249 a0001c0001t0001g0253 others(35): Show |
39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3486G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194699 | |||||||
| chr8:133194717 | G | GTGGTGTG others(3): Show |
38 | a0001c0001t0001g0016 a0001c0001t0001g0249 a0001c0001t0001g0253 others(35): Show |
39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3504_69+3505ins others(10): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194717 | |||||||
| chr8:133194721 | A | G | 38 | a0001c0001t0001g0016 a0001c0001t0001g0249 a0001c0001t0001g0253 others(35): Show |
39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3508A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194721 | |||||||
| chr8:133194722 | T | G | 38 | a0001c0001t0001g0016 a0001c0001t0001g0249 a0001c0001t0001g0253 others(35): Show |
39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3509T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194722 | |||||||
| chr8:133194729 | A | G | 38 | a0001c0001t0001g0016 a0001c0001t0001g0249 a0001c0001t0001g0253 others(35): Show |
39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3516A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194729 | |||||||
| chr8:133194730 | G | C | 38 | a0001c0001t0001g0016 a0001c0001t0001g0249 a0001c0001t0001g0253 others(35): Show |
39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3517G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194730 | |||||||
| chr8:133194730 | G | GTGTGTGG others(31): Show |
74 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0090 others(71): Show |
78 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.69+3523_69+3524ins others(38): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194730 | ||||||
| chr8:133194730 | G | GTGTGTGT others(35): Show |
97 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(94): Show |
101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.69+3533_69+3534ins others(42): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194730 | ||||||
| chr8:133194774 | G | T | 1 | a0001c0001t0005g0361 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69+3561G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194774 | |||||||
| chr8:133194828 | C | T | 4 | a0001c0001t0007g0344 a0001c0001t0008g0100 a0001c0003t0014g0343 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+3615C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194828 | |||||||
| chr8:133194837 | G | A | 1 | a0001c0001t0005g0361 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69+3624G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194837 | |||||||
| chr8:133194928 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.69+3715T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194928 | |||||||
| chr8:133194985 | T | G | 1 | a0001c0001t0001g0281 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.69+3772T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194985 | |||||||
| chr8:133194995 | TTG | T | 6 | a0001c0001t0002g0001 a0001c0001t0002g0239 a0001c0001t0002g0240 others(3): Show |
9 | HG01074.hp2 HG01258.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+3792_69+3793del others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194995 | ||||||
| chr8:133195006 | T | G | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
6 | HG02129.hp2 NA18978.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+3793T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195006 | |||||||
| chr8:133195017 | G | T | 1 | a0001c0002t0003g0033 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.69+3804G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195017 | |||||||
| chr8:133195082 | T | G | 66 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0102 others(63): Show |
69 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.69+3869T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195082 | |||||||
| chr8:133195101 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0002t0003g0034 |
3 | HG00423.hp2 HG01934.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.69+3888G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195101 | |||||||
| chr8:133195123 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0370 a0001c0001t0001g0371 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+3910G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195123 | |||||||
| chr8:133195160 | GTGTGTAT others(10): Show |
G | 1 | a0001c0001t0001g0036 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+3964_69+3980del others(17): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133195160 | ||||||
| chr8:133195164 | GTATGTGG others(36): Show |
G | 1 | a0001c0001t0001g0042 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.69+3953_69+3995del others(43): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133195164 | ||||||
| chr8:133195173 | G | A | 1 | a0001c0001t0019g0098 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.69+3960G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195173 | |||||||
| chr8:133195207 | A | G | 79 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(76): Show |
81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.69+3994A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195207 | |||||||
| chr8:133195319 | G | GGTGT | 10 | a0001c0001t0002g0238 a0001c0001t0006g0234 a0001c0001t0026g0233 others(7): Show |
10 | HG01167.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+4118_69+4121dup others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133195319 | ||||||
| chr8:133195325 | T | C | 1 | a0001c0001t0002g0367 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.69+4112T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195325 | |||||||
| chr8:133195588 | C | A | 1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.69+4375C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195588 | |||||||
| chr8:133195590 | C | T | 1 | a0001c0001t0013g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+4377C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195590 | |||||||
| chr8:133195601 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.69+4388C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195601 | |||||||
| chr8:133195626 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | NA18950.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.69+4413C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195626 | |||||||
| chr8:133195720 | A | G | 27 | a0001c0001t0001g0095 a0001c0001t0001g0276 a0001c0001t0001g0341 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.69+4507A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195720 | |||||||
| chr8:133195802 | C | A | 2 | a0001c0002t0012g0362 a0001c0012t0001g0363 |
2 | HG01167.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.69+4589C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195802 | |||||||
| chr8:133195869 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0174 a0001c0001t0001g0175 |
4 | HG01123.hp2 HG03654.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+4656G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195869 | |||||||
| chr8:133195955 | C | T | 3 | a0001c0002t0004g0273 a0001c0003t0001g0271 a0001c0010t0027g0272 |
3 | HG02965.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.69+4742C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195955 | |||||||
| chr8:133195963 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.69+4750C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195963 | |||||||
| chr8:133196197 | C | G | 5 | a0001c0002t0004g0273 a0001c0003t0001g0271 a0001c0003t0001g0347 others(2): Show |
5 | HG01891.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+4984C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196197 | |||||||
| chr8:133196246 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0002g0150 a0001c0002t0003g0152 |
3 | HG00323.hp2 HG01070.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.69+5033C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196246 | |||||||
| chr8:133196356 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.69+5143G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196356 | |||||||
| chr8:133196438 | T | G | 2 | a0001c0001t0001g0095 a0001c0002t0012g0094 |
2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.69+5225T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196438 | |||||||
| chr8:133196512 | G | T | 1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+5299G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196512 | |||||||
| chr8:133196596 | A | T | 141 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(138): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.69+5383A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196596 | |||||||
| chr8:133196601 | AAGGGTTC others(7): Show |
A | 2 | a0001c0002t0003g0084 a0001c0002t0004g0083 |
2 | HG01358.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.69+5391_69+5404del others(14): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133196601 | ||||||
| chr8:133196643 | CTCAGGTA others(35): Show |
C | 1 | a0001c0001t0002g0348 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.69+5432_69+5473del others(42): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133196643 | ||||||
| chr8:133196682 | T | C | 4 | a0001c0002t0004g0273 a0001c0003t0001g0271 a0001c0003t0001g0347 others(1): Show |
4 | HG01891.hp1 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+5469T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196682 | |||||||
| chr8:133196732 | T | G | 1 | a0001c0001t0005g0244 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.69+5519T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196732 | |||||||
| chr8:133196882 | T | C | 3 | a0001c0002t0030g0087 a0001c0009t0025g0245 a0002c0004t0004g0358 |
3 | NA18906.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.69+5669T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196882 | |||||||
| chr8:133196906 | T | G | 5 | a0001c0001t0002g0149 a0001c0001t0005g0246 a0001c0001t0013g0346 others(2): Show |
5 | HG02976.hp1 HG04199.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+5693T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196906 | |||||||
| chr8:133196917 | G | A | 2 | a0001c0001t0008g0111 a0001c0001t0009g0110 |
2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.69+5704G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196917 | |||||||
| chr8:133197013 | C | T | 4 | a0001c0002t0004g0273 a0001c0003t0001g0271 a0001c0003t0001g0347 others(1): Show |
4 | HG01891.hp1 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+5800C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197013 | |||||||
| chr8:133197210 | C | G | 72 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(69): Show |
77 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.69+5997C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197210 | |||||||
| chr8:133197273 | C | A | 1 | a0001c0002t0028g0235 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.69+6060C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197273 | |||||||
| chr8:133197366 | G | A | 1 | a0001c0003t0001g0271 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.69+6153G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197366 | |||||||
| chr8:133197528 | C | G | 36 | a0001c0001t0001g0092 a0001c0001t0001g0253 a0001c0001t0001g0254 others(33): Show |
36 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.69+6315C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197528 | |||||||
| chr8:133197657 | C | A | 1 | a0001c0002t0011g0247 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.69+6444C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197657 | |||||||
| chr8:133197676 | C | T | 1 | a0002c0004t0004g0222 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.69+6463C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197676 | |||||||
| chr8:133197711 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+6498G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197711 | |||||||
| chr8:133197914 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.69+6701C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197914 | |||||||
| chr8:133197952 | T | C | 1 | a0001c0009t0025g0245 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.69+6739T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197952 | |||||||
| chr8:133197970 | A | G | 71 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(68): Show |
75 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.69+6757A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197970 | |||||||
| chr8:133197988 | C | A | 4 | a0001c0001t0001g0036 a0001c0001t0005g0049 a0002c0004t0004g0005 others(1): Show |
5 | HG01074.hp1 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+6775C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197988 | |||||||
| chr8:133198010 | G | A | 1 | a0001c0002t0003g0050 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.69+6797G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198010 | |||||||
| chr8:133198229 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.69+7016C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198229 | |||||||
| chr8:133198294 | T | G | 1 | a0001c0002t0003g0176 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.69+7081T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198294 | |||||||
| chr8:133198331 | T | G | 3 | a0001c0001t0013g0346 a0001c0001t0026g0233 a0002c0004t0004g0358 |
3 | HG02615.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.69+7118T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198331 | |||||||
| chr8:133198839 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0005g0049 a0002c0004t0004g0005 others(1): Show |
5 | HG01074.hp1 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+7626C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198839 | |||||||
| chr8:133198844 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.69+7631C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198844 | |||||||
| chr8:133198906 | C | T | 4 | a0001c0002t0004g0273 a0001c0003t0001g0271 a0001c0003t0001g0347 others(1): Show |
4 | HG01891.hp1 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+7693C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198906 | |||||||
| chr8:133198993 | C | A | 6 | a0001c0001t0019g0098 a0001c0002t0004g0273 a0001c0002t0018g0231 others(3): Show |
6 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+7780C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198993 | |||||||
| chr8:133198998 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(155): Show |
168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.69+7785C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198998 | |||||||
| chr8:133199167 | G | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(155): Show |
168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.69+7954G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199167 | |||||||
| chr8:133199283 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(156): Show |
169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.69+8070C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199283 | |||||||
| chr8:133199321 | G | A | 1 | a0001c0002t0012g0362 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.69+8108G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199321 | |||||||
| chr8:133199624 | C | T | 70 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(67): Show |
74 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.69+8411C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199624 | |||||||
| chr8:133199665 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0009g0093 a0001c0003t0005g0232 |
3 | HG01884.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.69+8452C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199665 | |||||||
| chr8:133199704 | A | G | 1 | a0001c0001t0002g0335 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.69+8491A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199704 | |||||||
| chr8:133199711 | C | T | 45 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0032 others(42): Show |
48 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.69+8498C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199711 | |||||||
| chr8:133199722 | G | A | 61 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(58): Show |
65 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.69+8509G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199722 | |||||||
| chr8:133199749 | G | C | 1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+8536G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199749 | |||||||
| chr8:133199887 | T | C | 74 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(71): Show |
78 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.69+8674T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199887 | |||||||
| chr8:133199919 | T | C | 8 | a0001c0001t0001g0177 a0001c0001t0001g0182 a0001c0001t0001g0183 others(5): Show |
10 | HG00438.hp2 NA18946.hp2 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+8706T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199919 | |||||||
| chr8:133200133 | C | T | 9 | a0001c0001t0001g0095 a0001c0001t0001g0223 a0001c0001t0002g0339 others(6): Show |
9 | HG02630.hp2 HG02886.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+8920C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200133 | |||||||
| chr8:133200143 | G | A | 45 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0032 others(42): Show |
48 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.69+8930G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200143 | |||||||
| chr8:133200220 | C | T | 1 | a0002c0004t0004g0075 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.69+9007C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200220 | |||||||
| chr8:133200222 | C | T | 4 | a0001c0001t0001g0370 a0001c0001t0002g0154 a0001c0001t0002g0367 others(1): Show |
4 | HG01891.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+9009C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200222 | |||||||
| chr8:133200245 | G | A | 2 | a0001c0001t0013g0346 a0002c0004t0004g0358 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.69+9032G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200245 | |||||||
| chr8:133200363 | C | T | 1 | a0001c0002t0003g0176 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.69+9150C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200363 | |||||||
| chr8:133200409 | C | T | 63 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(60): Show |
67 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.69+9196C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200409 | |||||||
| chr8:133200412 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.69+9199G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200412 | |||||||
| chr8:133200486 | G | A | 228 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(225): Show |
242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.69+9273G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200486 | |||||||
| chr8:133200505 | C | T | 1 | a0001c0001t0001g0354 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.69+9292C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200505 | |||||||
| chr8:133200506 | G | A | 1 | a0001c0002t0003g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.69+9293G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200506 | |||||||
| chr8:133200686 | A | G | 2 | a0001c0001t0001g0352 a0001c0001t0001g0353 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.69+9473A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200686 | |||||||
| chr8:133200851 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.69+9638C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200851 | |||||||
| chr8:133201008 | C | T | 62 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(59): Show |
66 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.69+9795C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201008 | |||||||
| chr8:133201056 | T | C | 1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+9843T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201056 | |||||||
| chr8:133201060 | C | T | 2 | a0001c0001t0001g0113 a0008c0013t0001g0372 |
2 | HG01346.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.69+9847C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201060 | |||||||
| chr8:133201128 | C | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(202): Show |
218 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.69+9915C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201128 | |||||||
| chr8:133201167 | C | T | 22 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(19): Show |
22 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.69+9954C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201167 | |||||||
| chr8:133201233 | C | T | 8 | a0001c0001t0005g0244 a0001c0001t0019g0098 a0001c0002t0004g0273 others(5): Show |
8 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+10020C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201233 | |||||||
| chr8:133201356 | T | C | 36 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(33): Show |
36 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.69+10143T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201356 | |||||||
| chr8:133201427 | A | G | 6 | a0001c0001t0019g0098 a0001c0002t0004g0273 a0001c0002t0018g0231 others(3): Show |
6 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+10214A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201427 | |||||||
| chr8:133201442 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(125): Show |
137 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.69+10229G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201442 | |||||||
| chr8:133201447 | G | A | 7 | a0001c0001t0001g0342 a0001c0001t0005g0246 a0001c0001t0006g0251 others(4): Show |
7 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+10234G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201447 | |||||||
| chr8:133201531 | G | A | 1 | a0001c0002t0003g0368 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.69+10318G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201531 | |||||||
| chr8:133201736 | G | A | 6 | a0001c0001t0019g0098 a0001c0002t0004g0273 a0001c0002t0018g0231 others(3): Show |
6 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+10523G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201736 | |||||||
| chr8:133201742 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.69+10529C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201742 | |||||||
| chr8:133201798 | A | G | 8 | a0001c0001t0001g0342 a0001c0001t0002g0149 a0001c0001t0005g0246 others(5): Show |
8 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+10585A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201798 | |||||||
| chr8:133201803 | A | C | 1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+10590A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201803 | |||||||
| chr8:133201844 | A | AAAAAG | 11 | a0001c0001t0001g0095 a0001c0001t0001g0173 a0001c0001t0005g0157 others(8): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+10656_69+10660d others(7): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133201844 | ||||||
| chr8:133201844 | AAAAAG | A | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(216): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.69+10656_69+10660d others(7): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133201844 | ||||||
| chr8:133201844 | AAAAAGAA others(3): Show |
A | 5 | a0001c0001t0002g0367 a0001c0002t0004g0273 a0001c0003t0001g0271 others(2): Show |
5 | HG01891.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+10651_69+10660d others(12): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133201844 | ||||||
| chr8:133201864 | G | GAAAAGAA others(1): Show |
32 | a0001c0001t0001g0092 a0001c0001t0001g0253 a0001c0001t0001g0254 others(29): Show |
32 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.69+10656_69+10663d others(10): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133201864 | ||||||
| chr8:133201864 | GAAAAGA | G | 7 | a0001c0001t0001g0342 a0001c0001t0005g0246 a0001c0001t0006g0251 others(4): Show |
7 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+10656_69+10661d others(8): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133201864 | ||||||
| chr8:133201878 | C | T | 8 | a0001c0001t0001g0177 a0001c0001t0001g0182 a0001c0001t0001g0183 others(5): Show |
10 | HG00438.hp2 NA18946.hp2 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+10665C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201878 | |||||||
| chr8:133201948 | C | A | 45 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0036 others(42): Show |
47 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.69+10735C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201948 | |||||||
| chr8:133201961 | C | T | 68 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(65): Show |
72 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.69+10748C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201961 | |||||||
| chr8:133201962 | G | A | 1 | a0001c0002t0012g0362 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.69+10749G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201962 | |||||||
| chr8:133201966 | T | C | 2 | a0001c0001t0019g0098 a0001c0002t0018g0231 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.69+10753T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201966 | |||||||
| chr8:133201981 | G | T | 75 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(72): Show |
79 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.69+10768G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201981 | |||||||
| chr8:133202336 | T | C | 2 | a0001c0001t0002g0348 a0001c0001t0002g0355 |
2 | HG00408.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.70-10528T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202336 | |||||||
| chr8:133202341 | C | T | 1 | a0001c0002t0003g0147 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.70-10523C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202341 | |||||||
| chr8:133202411 | C | A | 1 | a0001c0001t0002g0239 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.70-10453C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202411 | |||||||
| chr8:133202434 | A | T | 2 | a0001c0001t0005g0244 a0001c0002t0012g0094 |
2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70-10430A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202434 | |||||||
| chr8:133202663 | T | A | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(271): Show |
287 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.70-10201T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202663 | |||||||
| chr8:133202684 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.70-10180G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202684 | |||||||
| chr8:133202800 | A | G | 2 | a0001c0001t0019g0098 a0001c0002t0018g0231 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.70-10064A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202800 | |||||||
| chr8:133202869 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(141): Show |
153 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.70-9995G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202869 | |||||||
| chr8:133202939 | G | C | 2 | a0001c0001t0005g0244 a0001c0002t0012g0094 |
2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70-9925G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202939 | |||||||
| chr8:133203011 | C | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(4): Show |
9 | NA18612.hp1 NA18955.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-9853C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203011 | |||||||
| chr8:133203241 | C | T | 3 | a0001c0001t0001g0370 a0001c0001t0002g0154 a0001c0001t0022g0280 |
3 | HG01891.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.70-9623C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203241 | |||||||
| chr8:133203268 | C | T | 3 | a0001c0001t0008g0111 a0001c0001t0009g0110 a0001c0012t0001g0363 |
3 | HG02258.hp1 HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.70-9596C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203268 | |||||||
| chr8:133203388 | A | G | 326 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(323): Show |
344 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.70-9476A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203388 | |||||||
| chr8:133203703 | G | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(115): Show |
127 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.70-9161G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203703 | |||||||
| chr8:133203713 | T | A | 21 | a0001c0001t0001g0092 a0001c0001t0001g0253 a0001c0001t0001g0254 others(18): Show |
21 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.70-9151T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203713 | |||||||
| chr8:133203757 | G | C | 162 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(159): Show |
170 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.70-9107G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203757 | |||||||
| chr8:133203841 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70-9023G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203841 | |||||||
| chr8:133203844 | C | T | 4 | a0001c0002t0004g0273 a0001c0003t0001g0271 a0001c0003t0001g0347 others(1): Show |
4 | HG01891.hp1 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-9020C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203844 | |||||||
| chr8:133203953 | A | G | 1 | a0001c0020t0001g0360 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.70-8911A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203953 | |||||||
| chr8:133204111 | C | T | 2 | a0001c0001t0019g0098 a0001c0002t0018g0231 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.70-8753C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204111 | |||||||
| chr8:133204285 | T | C | 1 | a0001c0002t0003g0192 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.70-8579T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204285 | |||||||
| chr8:133204312 | A | C | 46 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0032 others(43): Show |
49 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.70-8552A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204312 | |||||||
| chr8:133204354 | G | A | 2 | a0001c0001t0019g0098 a0001c0002t0018g0231 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.70-8510G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204354 | |||||||
| chr8:133204491 | AG | A | 7 | a0001c0001t0001g0016 a0001c0001t0005g0096 a0001c0001t0005g0097 others(4): Show |
8 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-8370delG | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133204491 | ||||||
| chr8:133204519 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.70-8345C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204519 | |||||||
| chr8:133204528 | A | G | 1 | a0001c0002t0003g0050 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.70-8336A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204528 | |||||||
| chr8:133204606 | A | G | 327 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(324): Show |
345 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.70-8258A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204606 | |||||||
| chr8:133204635 | G | A | 1 | a0001c0002t0011g0247 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70-8229G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204635 | |||||||
| chr8:133204676 | T | A | 2 | a0001c0001t0001g0058 a0002c0004t0004g0075 |
2 | HG00099.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.70-8188T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204676 | |||||||
| chr8:133204955 | G | C | 24 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(21): Show |
24 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.70-7909G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204955 | |||||||
| chr8:133204956 | G | A | 1 | a0002c0004t0004g0089 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.70-7908G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204956 | |||||||
| chr8:133205002 | G | A | 2 | a0001c0001t0005g0244 a0001c0002t0012g0094 |
2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70-7862G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205002 | |||||||
| chr8:133205057 | C | T | 1 | a0001c0009t0025g0245 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.70-7807C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205057 | |||||||
| chr8:133205107 | G | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
8 | NA18945.hp2 NA18964.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-7757G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205107 | |||||||
| chr8:133205144 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.70-7720G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205144 | |||||||
| chr8:133205380 | T | G | 4 | a0001c0001t0001g0370 a0001c0001t0002g0154 a0001c0001t0002g0367 others(1): Show |
4 | HG01891.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-7484T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205380 | |||||||
| chr8:133205462 | T | G | 265 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(262): Show |
281 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.70-7402T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205462 | |||||||
| chr8:133205909 | G | A | 5 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0220 others(2): Show |
5 | HG00323.hp2 HG01070.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-6955G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205909 | |||||||
| chr8:133206180 | G | A | 1 | a0001c0002t0003g0085 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.70-6684G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206180 | |||||||
| chr8:133206257 | G | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(151): Show |
165 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.70-6607G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206257 | |||||||
| chr8:133206291 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.70-6573T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206291 | |||||||
| chr8:133206292 | G | A | 7 | a0001c0001t0001g0016 a0001c0001t0005g0096 a0001c0001t0005g0097 others(4): Show |
8 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-6572G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206292 | |||||||
| chr8:133206297 | A | G | 300 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(297): Show |
317 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.70-6567A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206297 | |||||||
| chr8:133206299 | C | T | 6 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0002g0117 others(3): Show |
7 | HG01168.hp2 HG01255.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-6565C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206299 | |||||||
| chr8:133206342 | G | A | 1 | a0001c0001t0007g0118 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.70-6522G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206342 | |||||||
| chr8:133206357 | G | T | 1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.70-6507G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206357 | |||||||
| chr8:133206373 | G | C | 3 | a0001c0001t0008g0111 a0001c0001t0009g0110 a0001c0012t0001g0363 |
3 | HG02258.hp1 HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.70-6491G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206373 | |||||||
| chr8:133206573 | G | C | 9 | a0001c0001t0001g0342 a0001c0001t0002g0238 a0001c0001t0002g0367 others(6): Show |
9 | HG01243.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-6291G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206573 | |||||||
| chr8:133206576 | T | C | 1 | a0001c0001t0001g0370 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.70-6288T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206576 | |||||||
| chr8:133206583 | G | A | 1 | a0001c0002t0004g0091 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.70-6281G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206583 | |||||||
| chr8:133206687 | G | C | 8 | a0001c0001t0001g0342 a0001c0001t0005g0246 a0001c0001t0006g0251 others(5): Show |
8 | HG01243.hp2 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-6177G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206687 | |||||||
| chr8:133206790 | A | G | 13 | a0001c0001t0001g0095 a0001c0001t0005g0157 a0001c0001t0005g0361 others(10): Show |
13 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-6074A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206790 | |||||||
| chr8:133206799 | G | A | 20 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(17): Show |
20 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.70-6065G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206799 | |||||||
| chr8:133206821 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.70-6043G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206821 | |||||||
| chr8:133206995 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(87): Show |
97 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.70-5869G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206995 | |||||||
| chr8:133207034 | G | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(156): Show |
170 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.70-5830G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207034 | |||||||
| chr8:133207059 | C | T | 2 | a0001c0001t0001g0342 a0001c0002t0004g0103 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.70-5805C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207059 | |||||||
| chr8:133207185 | C | G | 1 | a0001c0001t0002g0216 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.70-5679C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207185 | |||||||
| chr8:133207537 | G | C | 1 | a0001c0001t0001g0253 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.70-5327G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207537 | |||||||
| chr8:133207561 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.70-5303C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207561 | |||||||
| chr8:133207575 | C | T | 67 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(64): Show |
71 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.70-5289C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207575 | |||||||
| chr8:133207631 | A | C | 6 | a0001c0001t0002g0238 a0001c0001t0002g0367 a0001c0001t0013g0346 others(3): Show |
6 | HG02615.hp1 HG03041.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-5233A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207631 | |||||||
| chr8:133207648 | C | T | 1 | a0001c0001t0019g0098 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.70-5216C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207648 | |||||||
| chr8:133207697 | TCTC | T | 7 | a0001c0001t0001g0016 a0001c0001t0005g0096 a0001c0001t0005g0097 others(4): Show |
8 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-5165_70-5163del others(3): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133207697 | ||||||
| chr8:133207820 | G | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(92): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.70-5044G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207820 | |||||||
| chr8:133207994 | G | GT | 6 | a0001c0001t0002g0001 a0001c0001t0002g0243 a0001c0002t0003g0242 others(3): Show |
9 | HG00733.hp2 HG01074.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.70-4856dupT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133207994 | ||||||
| chr8:133207994 | G | GTTTTTTT | 23 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0027 others(20): Show |
25 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.70-4862_70-4856dup others(7): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133207994 | ||||||
| chr8:133207994 | G | GTTTTTTT others(1): Show |
57 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0040 others(54): Show |
62 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.70-4863_70-4856dup others(8): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133207994 | ||||||
| chr8:133207994 | G | GTTTTTTT others(2): Show |
10 | a0001c0001t0001g0215 a0001c0001t0001g0320 a0001c0001t0001g0323 others(7): Show |
10 | HG00621.hp2 HG01981.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-4864_70-4856dup others(9): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133207994 | ||||||
| chr8:133207994 | GT | G | 174 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(171): Show |
185 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.70-4856delT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133207994 | ||||||
| chr8:133208205 | C | G | 7 | a0001c0001t0001g0342 a0001c0001t0005g0246 a0001c0001t0006g0251 others(4): Show |
7 | HG01243.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-4659C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208205 | |||||||
| chr8:133208448 | A | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(278): Show |
297 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.70-4416A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208448 | |||||||
| chr8:133208503 | AGGCATTC others(15): Show |
A | 1 | a0001c0001t0002g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.70-4359_70-4338del others(22): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133208503 | ||||||
| chr8:133208568 | G | A | 1 | a0001c0002t0003g0088 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.70-4296G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208568 | |||||||
| chr8:133208598 | A | T | 233 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(230): Show |
248 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.70-4266A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208598 | |||||||
| chr8:133208652 | C | T | 1 | a0001c0002t0003g0078 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.70-4212C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208652 | |||||||
| chr8:133208669 | G | A | 2 | a0001c0001t0005g0244 a0001c0002t0012g0094 |
2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70-4195G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208669 | |||||||
| chr8:133208736 | T | G | 118 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0019 others(115): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.70-4128T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208736 | |||||||
| chr8:133208832 | T | C | 4 | a0001c0001t0013g0346 a0001c0001t0019g0098 a0001c0002t0018g0231 others(1): Show |
4 | HG02257.hp1 HG02970.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-4032T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208832 | |||||||
| chr8:133208886 | T | C | 1 | a0001c0001t0023g0268 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.70-3978T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208886 | |||||||
| chr8:133209086 | C | T | 2 | a0001c0003t0001g0271 a0001c0003t0001g0347 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.70-3778C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209086 | |||||||
| chr8:133209210 | T | C | 13 | a0001c0001t0001g0016 a0001c0001t0005g0096 a0001c0001t0005g0097 others(10): Show |
14 | HG01167.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-3654T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209210 | |||||||
| chr8:133209230 | A | T | 229 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0012 others(226): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.70-3634A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209230 | |||||||
| chr8:133209259 | T | C | 241 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0012 others(238): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.70-3605T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209259 | |||||||
| chr8:133209498 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.70-3366G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209498 | |||||||
| chr8:133209516 | T | C | 4 | a0001c0001t0001g0289 a0001c0001t0001g0291 a0001c0001t0001g0320 others(1): Show |
4 | NA18977.hp1 NA18988.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-3348T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209516 | |||||||
| chr8:133209605 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0102 others(6): Show |
10 | HG01123.hp2 HG01192.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-3259C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209605 | |||||||
| chr8:133209680 | T | C | 6 | a0001c0001t0001g0036 a0001c0001t0001g0371 a0001c0001t0008g0111 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-3184T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209680 | |||||||
| chr8:133209743 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0092 a0001c0001t0005g0096 others(1): Show |
5 | HG02109.hp2 HG03209.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-3121G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209743 | |||||||
| chr8:133209926 | A | T | 1 | a0001c0002t0028g0235 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.70-2938A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209926 | |||||||
| chr8:133209976 | T | C | 24 | a0001c0001t0001g0095 a0001c0001t0001g0112 a0001c0001t0001g0249 others(21): Show |
28 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.70-2888T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209976 | |||||||
| chr8:133210005 | T | A | 2 | a0001c0001t0002g0150 a0001c0002t0004g0083 |
2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.70-2859T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210005 | |||||||
| chr8:133210043 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0225 a0001c0001t0002g0224 |
4 | NA18975.hp1 NA18988.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-2821T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210043 | |||||||
| chr8:133210054 | T | C | 29 | a0001c0001t0001g0221 a0001c0001t0001g0260 a0001c0001t0001g0269 others(26): Show |
29 | HG00735.hp1 HG01069.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.70-2810T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210054 | |||||||
| chr8:133210144 | T | C | 65 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(62): Show |
72 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.70-2720T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210144 | |||||||
| chr8:133210144 | T | G | 1 | a0001c0001t0002g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.70-2720T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210144 | |||||||
| chr8:133210386 | G | GGT | 19 | a0001c0001t0001g0102 a0001c0001t0005g0049 a0001c0001t0005g0157 others(16): Show |
19 | HG00280.hp1 HG00741.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.70-2443_70-2442dup others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210386 | ||||||
| chr8:133210386 | G | GGTGTGT | 9 | a0001c0001t0001g0016 a0001c0001t0001g0092 a0001c0001t0002g0142 others(6): Show |
10 | HG02109.hp2 HG03209.hp1 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-2447_70-2442dup others(6): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210386 | ||||||
| chr8:133210386 | G | GGTGTGTG others(3): Show |
4 | a0001c0003t0001g0153 a0001c0003t0001g0271 a0001c0003t0001g0274 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-2451_70-2442dup others(10): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210386 | ||||||
| chr8:133210386 | GGT | G | 123 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(120): Show |
130 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.70-2443_70-2442del others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210386 | ||||||
| chr8:133210386 | GGTGT | G | 25 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0177 others(22): Show |
29 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.70-2445_70-2442del others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210386 | ||||||
| chr8:133210407 | G | T | 4 | a0001c0002t0004g0109 a0001c0002t0012g0094 a0001c0002t0012g0362 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-2457G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210407 | |||||||
| chr8:133210420 | TG | T | 6 | a0001c0001t0001g0072 a0001c0001t0001g0101 a0001c0001t0001g0144 others(3): Show |
6 | HG00738.hp1 HG01515.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-2443delG | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210420 | |||||||
| chr8:133210421 | G | GT | 49 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(46): Show |
55 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.70-2440dupT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210421 | ||||||
| chr8:133210421 | G | GTGT | 5 | a0001c0001t0001g0032 a0001c0001t0001g0058 a0001c0001t0001g0341 others(2): Show |
5 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-2442_70-2441ins others(3): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210421 | ||||||
| chr8:133210549 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.70-2315T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210549 | |||||||
| chr8:133210622 | A | AT | 6 | a0001c0001t0002g0117 a0001c0001t0016g0123 a0001c0002t0003g0009 others(3): Show |
7 | HG00639.hp2 HG01168.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-2234dupT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210622 | ||||||
| chr8:133210629 | T | C | 2 | a0001c0002t0018g0231 a0001c0002t0028g0235 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.70-2235T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210629 | |||||||
| chr8:133210677 | T | A | 1 | a0001c0001t0001g0326 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.70-2187T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210677 | |||||||
| chr8:133210756 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0038 |
4 | NA18955.hp1 NA18981.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-2108G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210756 | |||||||
| chr8:133210830 | C | T | 3 | a0001c0001t0001g0102 a0001c0012t0001g0068 a0001c0012t0001g0363 |
3 | HG02717.hp2 HG02922.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.70-2034C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210830 | |||||||
| chr8:133210915 | T | C | 5 | a0001c0001t0006g0082 a0001c0001t0006g0234 a0001c0001t0006g0277 others(2): Show |
5 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-1949T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210915 | |||||||
| chr8:133210921 | G | A | 9 | a0001c0001t0006g0082 a0001c0001t0006g0143 a0001c0001t0006g0234 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-1943G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210921 | |||||||
| chr8:133210925 | C | T | 7 | a0001c0003t0001g0153 a0001c0003t0001g0271 a0001c0003t0001g0274 others(4): Show |
7 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-1939C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210925 | |||||||
| chr8:133211065 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.70-1799G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211065 | |||||||
| chr8:133211195 | A | T | 1 | a0001c0001t0001g0254 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.70-1669A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211195 | |||||||
| chr8:133211296 | C | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0269 |
2 | HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.70-1568C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211296 | |||||||
| chr8:133211502 | G | A | 1 | a0004c0019t0001g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.70-1362G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211502 | |||||||
| chr8:133211521 | C | T | 240 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(237): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.70-1343C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211521 | |||||||
| chr8:133211555 | G | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0184 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.70-1309G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211555 | |||||||
| chr8:133211712 | C | T | 6 | a0001c0001t0005g0157 a0001c0001t0008g0111 a0001c0001t0008g0122 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-1152C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211712 | |||||||
| chr8:133211724 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.70-1140G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211724 | |||||||
| chr8:133211819 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.70-1045C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211819 | |||||||
| chr8:133211835 | C | G | 1 | a0001c0001t0008g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.70-1029C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211835 | |||||||
| chr8:133211923 | C | G | 24 | a0001c0001t0001g0112 a0001c0001t0001g0156 a0001c0001t0001g0220 others(21): Show |
28 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.70-941C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211923 | |||||||
| chr8:133212104 | G | A | 3 | a0001c0001t0005g0049 a0001c0001t0005g0244 a0004c0019t0001g0270 |
3 | HG01074.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.70-760G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212104 | |||||||
| chr8:133212128 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.70-736C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212128 | |||||||
| chr8:133212182 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.70-682C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212182 | |||||||
| chr8:133212205 | A | C | 2 | a0004c0008t0029g0108 a0004c0008t0037g0107 |
2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.70-659A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212205 | |||||||
| chr8:133212291 | T | A | 25 | a0001c0001t0001g0112 a0001c0001t0001g0156 a0001c0001t0001g0220 others(22): Show |
29 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.70-573T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212291 | |||||||
| chr8:133212298 | C | T | 2 | a0001c0001t0005g0049 a0001c0001t0005g0244 |
2 | HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.70-566C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212298 | |||||||
| chr8:133212326 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(115): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.70-538G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212326 | |||||||
| chr8:133212335 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.70-529G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212335 | |||||||
| chr8:133212359 | G | A | 6 | a0001c0001t0005g0157 a0001c0001t0008g0111 a0001c0001t0008g0122 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-505G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212359 | |||||||
| chr8:133212395 | C | T | 1 | a0001c0002t0018g0043 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.70-469C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212395 | |||||||
| chr8:133212474 | C | T | 91 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(88): Show |
99 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.70-390C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212474 | |||||||
| chr8:133212557 | C | T | 3 | a0001c0001t0002g0275 a0001c0001t0035g0345 a0001c0010t0027g0272 |
3 | HG02258.hp2 HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.70-307C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212557 | |||||||
| chr8:133212621 | C | A | 55 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0112 others(52): Show |
59 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.70-243C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212621 | |||||||
| chr8:133212635 | A | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(139): Show |
153 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.70-229A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212635 | |||||||
| chr8:133212681 | T | G | 2 | a0001c0001t0005g0361 a0001c0001t0022g0280 |
2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.70-183T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212681 | |||||||
| chr8:133212687 | G | T | 1 | a0001c0001t0001g0249 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.70-177G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212687 | |||||||
| chr8:133212692 | A | G | 1 | a0001c0002t0004g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.70-172A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212692 | |||||||
| chr8:133212736 | G | A | 241 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(238): Show |
260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.70-128G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212736 | |||||||
| chr8:133212825 | T | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(177): Show |
194 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.70-39T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212825 | |||||||
| chr8:133212834 | C | G | 1 | a0001c0002t0003g0041 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.70-30C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212834 | |||||||
| chr8:133212856 | C | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0253 a0001c0001t0001g0260 others(16): Show |
19 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.70-8C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212856 | |||||||
| chr8:133213249 | C | A | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0002t0003g0192 |
3 | NA18986.hp2 NA18999.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.349+106C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213249 | |||||||
| chr8:133213250 | C | T | 9 | a0001c0003t0001g0153 a0001c0003t0001g0271 a0001c0003t0001g0274 others(6): Show |
9 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+107C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213250 | |||||||
| chr8:133213320 | A | T | 5 | a0001c0001t0005g0246 a0001c0001t0005g0361 a0001c0001t0022g0280 others(2): Show |
5 | HG01891.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+177A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213320 | |||||||
| chr8:133213368 | C | T | 17 | a0001c0001t0001g0102 a0001c0001t0005g0157 a0001c0001t0006g0082 others(14): Show |
17 | HG02055.hp2 HG02559.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.349+225C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213368 | |||||||
| chr8:133213409 | G | C | 29 | a0001c0001t0001g0095 a0001c0001t0001g0253 a0001c0001t0001g0260 others(26): Show |
29 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.349+266G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213409 | |||||||
| chr8:133213415 | C | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0370 |
2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.349+272C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213415 | |||||||
| chr8:133213566 | C | G | 9 | a0001c0003t0001g0153 a0001c0003t0001g0271 a0001c0003t0001g0274 others(6): Show |
9 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+423C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213566 | |||||||
| chr8:133213621 | C | G | 6 | a0001c0002t0004g0103 a0001c0002t0004g0109 a0001c0002t0012g0094 others(3): Show |
6 | HG01167.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+478C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213621 | |||||||
| chr8:133213636 | T | A | 241 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(238): Show |
260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.349+493T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213636 | |||||||
| chr8:133213644 | T | G | 5 | a0001c0001t0005g0246 a0001c0001t0005g0361 a0001c0001t0022g0280 others(2): Show |
5 | HG01891.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+501T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213644 | |||||||
| chr8:133213701 | A | T | 1 | a0001c0001t0001g0364 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.349+558A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213701 | |||||||
| chr8:133213749 | T | C | 1 | a0001c0002t0018g0043 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.349+606T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213749 | |||||||
| chr8:133213784 | G | A | 7 | a0001c0001t0006g0082 a0001c0001t0006g0143 a0001c0001t0006g0234 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+641G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213784 | |||||||
| chr8:133213832 | A | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0221 a0001c0001t0016g0061 others(6): Show |
10 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+689A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213832 | |||||||
| chr8:133213834 | T | C | 9 | a0001c0001t0001g0036 a0001c0001t0001g0221 a0001c0001t0016g0061 others(6): Show |
10 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+691T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213834 | |||||||
| chr8:133213842 | A | ATATACAC others(22): Show |
46 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0014 others(43): Show |
50 | HG00408.hp1 HG00558.hp2 HG01261.hp2 others(47): Show |
intron_variant | MODIFIER | c.349+751_349+779dup others(29): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213842 | ||||||
| chr8:133213865 | A | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0221 a0001c0001t0016g0061 others(6): Show |
10 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+722A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213865 | |||||||
| chr8:133213867 | T | C | 9 | a0001c0001t0001g0036 a0001c0001t0001g0221 a0001c0001t0016g0061 others(6): Show |
10 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+724T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213867 | |||||||
| chr8:133213871 | C | CACTATAT others(19): Show |
1 | a0001c0001t0001g0036 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349+728_349+729ins others(26): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213871 | |||||||
| chr8:133213871 | C | CTATA | 8 | a0001c0001t0001g0221 a0001c0001t0016g0061 a0002c0004t0004g0005 others(5): Show |
9 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+729_349+732dup others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213871 | ||||||
| chr8:133213894 | A | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0221 a0001c0001t0016g0061 others(6): Show |
10 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+751A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213894 | |||||||
| chr8:133213896 | T | C | 8 | a0001c0001t0001g0221 a0001c0001t0016g0061 a0002c0004t0004g0005 others(5): Show |
9 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+753T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213896 | |||||||
| chr8:133213900 | C | CACTATAT others(19): Show |
8 | a0001c0001t0001g0221 a0001c0001t0016g0061 a0002c0004t0004g0005 others(5): Show |
9 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+757_349+758ins others(26): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213900 | |||||||
| chr8:133213900 | C | CTATA | 3 | a0001c0001t0001g0036 a0001c0001t0002g0025 a0001c0001t0002g0039 |
3 | HG02109.hp1 NA18969.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.349+758_349+761dup others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213900 | ||||||
| chr8:133213900 | C | CTATACAC others(323): Show |
1 | a0001c0014t0001g0324 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.349+779_349+780ins others(330): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213900 | ||||||
| chr8:133213900 | C | CTATACAC others(356): Show |
2 | a0001c0001t0001g0349 a0001c0001t0001g0350 |
2 | NA18966.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.349+779_349+780ins others(363): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213900 | ||||||
| chr8:133213920 | T | TTAAATAT others(165): Show |
1 | a0001c0001t0001g0332 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.349+779_349+780ins others(172): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213920 | ||||||
| chr8:133213920 | T | TTAAATAT others(136): Show |
31 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0092 others(28): Show |
34 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.349+779_349+780ins others(143): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213920 | ||||||
| chr8:133213923 | T | A | 4 | a0001c0001t0005g0246 a0001c0001t0024g0252 a0001c0002t0004g0273 others(1): Show |
4 | HG02965.hp2 HG02976.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+780T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213923 | |||||||
| chr8:133213929 | C | CTATATAT others(108): Show |
1 | a0001c0001t0002g0187 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.349+814_349+815ins others(115): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | ||||||
| chr8:133213929 | C | CTATATAT others(106): Show |
3 | a0001c0001t0001g0156 a0001c0001t0001g0220 a0001c0001t0019g0098 |
3 | HG02735.hp2 HG02970.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.349+814_349+815ins others(113): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | ||||||
| chr8:133213929 | C | CTATATAT others(107): Show |
18 | a0001c0001t0001g0112 a0001c0001t0002g0001 a0001c0001t0002g0055 others(15): Show |
22 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.349+814_349+815ins others(114): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | ||||||
| chr8:133213929 | C | CTATATAT others(107): Show |
41 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0014 others(38): Show |
45 | HG00408.hp1 HG00558.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.349+841_349+842ins others(114): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | ||||||
| chr8:133213929 | C | CTATATAT others(127): Show |
2 | a0001c0001t0001g0130 a0001c0020t0001g0360 |
2 | NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.349+841_349+842ins others(134): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | ||||||
| chr8:133213929 | C | CTATATAT others(109): Show |
6 | a0001c0001t0006g0082 a0001c0001t0006g0143 a0001c0001t0006g0234 others(3): Show |
6 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(116): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | ||||||
| chr8:133213929 | C | CTATATAT others(107): Show |
1 | a0001c0002t0011g0247 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.349+840_349+841ins others(114): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | ||||||
| chr8:133213929 | C | CTATATAT others(88): Show |
1 | a0001c0001t0002g0238 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.349+840_349+841ins others(95): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | ||||||
| chr8:133213929 | C | CTATATAT others(74): Show |
1 | a0001c0001t0001g0177 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.349+808_349+809ins others(81): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | ||||||
| chr8:133213929 | C | G | 32 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0092 others(29): Show |
35 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.349+786C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213929 | |||||||
| chr8:133213951 | A | T | 1 | a0001c0001t0001g0254 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+808A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213951 | |||||||
| chr8:133213952 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+809G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213952 | |||||||
| chr8:133213953 | T | TATATACT others(219): Show |
1 | a0001c0001t0001g0254 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+810_349+811ins others(226): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213953 | |||||||
| chr8:133213953 | T | TTATATAT others(74): Show |
1 | a0001c0002t0018g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349+840_349+841ins others(81): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213953 | ||||||
| chr8:133213958 | T | TATACTAT others(195): Show |
1 | a0001c0002t0004g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349+840_349+841ins others(202): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213958 | ||||||
| chr8:133213958 | T | TATACTAT others(107): Show |
2 | a0001c0001t0002g0025 a0001c0001t0002g0039 |
2 | NA18969.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.349+840_349+841ins others(114): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213958 | ||||||
| chr8:133213962 | C | CTATATAT others(251): Show |
2 | a0001c0001t0005g0049 a0001c0001t0005g0244 |
2 | HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.349+880_349+881ins others(258): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(247): Show |
2 | a0001c0001t0005g0361 a0001c0001t0022g0280 |
2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.349+873_349+874ins others(254): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(225): Show |
2 | a0001c0001t0001g0062 a0001c0001t0001g0115 |
2 | HG00741.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.349+873_349+874ins others(232): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(217): Show |
1 | a0004c0019t0001g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.349+873_349+874ins others(224): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(76): Show |
7 | a0001c0001t0001g0212 a0001c0001t0006g0251 a0001c0002t0004g0109 others(4): Show |
7 | HG01167.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(83): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(74): Show |
1 | a0001c0012t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.349+840_349+841ins others(81): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(74): Show |
2 | a0001c0001t0001g0102 a0001c0012t0001g0363 |
2 | HG02922.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.349+840_349+841ins others(81): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(191): Show |
1 | a0001c0001t0001g0371 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.349+840_349+841ins others(198): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(109): Show |
8 | a0001c0003t0001g0153 a0001c0003t0001g0271 a0001c0003t0001g0274 others(5): Show |
8 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(116): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(163): Show |
2 | a0001c0001t0001g0174 a0001c0001t0001g0182 |
2 | HG04204.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.349+840_349+841ins others(170): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(192): Show |
50 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(47): Show |
56 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(199): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(221): Show |
1 | a0008c0013t0001g0372 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.349+840_349+841ins others(228): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(194): Show |
2 | a0001c0001t0001g0073 a0001c0002t0003g0248 |
2 | HG02897.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.349+840_349+841ins others(201): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(191): Show |
1 | a0001c0001t0001g0113 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.349+840_349+841ins others(198): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(139): Show |
1 | a0001c0003t0005g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.349+840_349+841ins others(146): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(190): Show |
3 | a0001c0001t0001g0017 a0001c0001t0001g0320 a0001c0001t0001g0357 |
4 | NA18948.hp2 NA18968.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(197): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(74): Show |
6 | a0001c0001t0005g0157 a0001c0001t0008g0111 a0001c0001t0008g0122 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(81): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | CTATATAT others(79): Show |
1 | a0001c0002t0018g0043 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.349+840_349+841ins others(86): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | ||||||
| chr8:133213962 | C | G | 1 | a0001c0001t0001g0254 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+819C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213962 | |||||||
| chr8:133213965 | T | TATATACA others(269): Show |
2 | a0004c0008t0029g0108 a0004c0008t0037g0107 |
2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.349+840_349+841ins others(276): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213965 | ||||||
| chr8:133213975 | A | ATATATAG others(281): Show |
1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349+840_349+841ins others(288): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213975 | ||||||
| chr8:133213977 | A | ATATAGTT others(188): Show |
1 | a0001c0001t0001g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.349+840_349+841ins others(195): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213977 | ||||||
| chr8:133213982 | G | GTTATATA others(161): Show |
6 | a0001c0001t0001g0253 a0001c0001t0001g0269 a0001c0001t0001g0342 others(3): Show |
6 | HG01243.hp2 HG01884.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(168): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213982 | ||||||
| chr8:133213991 | T | C | 25 | a0001c0001t0001g0112 a0001c0001t0001g0156 a0001c0001t0001g0220 others(22): Show |
29 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.349+848T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213991 | |||||||
| chr8:133213991 | T | TATACTAT others(142): Show |
1 | a0001c0001t0002g0024 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.349+860_349+861ins others(149): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | ||||||
| chr8:133213991 | T | TATACTAT others(173): Show |
5 | a0001c0001t0001g0283 a0001c0002t0003g0168 a0001c0002t0003g0193 others(2): Show |
5 | HG00741.hp1 HG01358.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+880_349+881ins others(180): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | ||||||
| chr8:133213991 | T | TATACTAT others(136): Show |
1 | a0001c0001t0002g0069 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.349+873_349+874ins others(143): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | ||||||
| chr8:133213991 | T | TATACTAT others(107): Show |
14 | a0001c0001t0001g0028 a0001c0001t0001g0218 a0001c0001t0001g0297 others(11): Show |
14 | HG00621.hp1 HG00639.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.349+873_349+874ins others(114): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | ||||||
| chr8:133213991 | T | TATACTAT others(140): Show |
98 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0090 others(95): Show |
102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.349+873_349+874ins others(147): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | ||||||
| chr8:133213991 | T | TATACTAT others(173): Show |
6 | a0001c0001t0002g0335 a0001c0002t0003g0034 a0001c0002t0003g0050 others(3): Show |
6 | HG00423.hp2 HG00735.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+873_349+874ins others(180): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | ||||||
| chr8:133213991 | T | TATACTAT others(138): Show |
1 | a0001c0001t0001g0202 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.349+873_349+874ins others(145): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | ||||||
| chr8:133213991 | T | TATACTAT others(130): Show |
1 | a0001c0001t0002g0348 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.349+873_349+874ins others(137): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | ||||||
| chr8:133213991 | T | TATACTAT others(107): Show |
1 | a0001c0015t0002g0292 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.349+873_349+874ins others(114): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | ||||||
| chr8:133213998 | T | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0253 a0001c0001t0001g0269 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.349+855T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213998 | |||||||
| chr8:133213998 | T | TATATACA others(163): Show |
2 | a0001c0001t0005g0096 a0001c0001t0005g0097 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.349+873_349+874ins others(170): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213998 | ||||||
| chr8:133213998 | T | TATATACA others(194): Show |
10 | a0001c0001t0001g0095 a0001c0001t0001g0260 a0001c0001t0001g0276 others(7): Show |
10 | HG01109.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+873_349+874ins others(201): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213998 | ||||||
| chr8:133214016 | TAG | T | 5 | a0001c0001t0001g0036 a0001c0001t0001g0221 a0001c0001t0016g0061 others(2): Show |
5 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+874_349+875del others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214016 | |||||||
| chr8:133214024 | C | T | 38 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0095 others(35): Show |
39 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.349+881C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214024 | |||||||
| chr8:133214037 | C | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0221 a0001c0001t0016g0061 others(2): Show |
5 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+894C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214037 | |||||||
| chr8:133214049 | TAG | T | 4 | a0002c0004t0004g0005 a0002c0004t0004g0048 a0002c0004t0004g0081 others(1): Show |
5 | HG02451.hp2 HG02486.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.349+907_349+908del others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214049 | |||||||
| chr8:133214057 | C | T | 38 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0095 others(35): Show |
39 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.349+914C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214057 | |||||||
| chr8:133214063 | A | ACTATATA others(285): Show |
5 | a0001c0001t0001g0036 a0001c0001t0001g0221 a0001c0001t0016g0061 others(2): Show |
5 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+920_349+921ins others(292): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214063 | |||||||
| chr8:133214063 | A | ATATATAA others(318): Show |
4 | a0002c0004t0004g0005 a0002c0004t0004g0048 a0002c0004t0004g0081 others(1): Show |
5 | HG02451.hp2 HG02486.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.349+926_349+927ins others(325): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214063 | ||||||
| chr8:133214070 | C | CACTATAT others(558): Show |
1 | a0001c0001t0001g0218 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.349+944_349+945ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(525): Show |
1 | a0001c0001t0001g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(532): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(501): Show |
1 | a0001c0001t0002g0238 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(508): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(592): Show |
2 | a0001c0001t0001g0289 a0001c0001t0002g0290 |
2 | NA18988.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(599): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(629): Show |
2 | a0001c0001t0001g0027 a0001c0001t0002g0026 |
2 | NA18964.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(636): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(596): Show |
1 | a0001c0001t0001g0208 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(603): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(596): Show |
1 | a0001c0001t0001g0295 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(603): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(596): Show |
60 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(57): Show |
67 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(603): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(629): Show |
1 | a0001c0001t0001g0333 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(636): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(568): Show |
1 | a0001c0002t0004g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(575): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(558): Show |
1 | a0001c0002t0003g0127 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(558): Show |
8 | a0001c0001t0001g0129 a0001c0002t0003g0033 a0001c0002t0003g0078 others(5): Show |
8 | HG01433.hp1 HG02698.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(558): Show |
2 | a0001c0001t0002g0301 a0001c0001t0002g0339 |
2 | NA19009.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.349+946_349+947ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(596): Show |
2 | a0001c0001t0001g0173 a0001c0001t0001g0184 |
2 | HG03669.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(603): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(565): Show |
1 | a0001c0001t0001g0086 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(572): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(596): Show |
1 | a0001c0001t0001g0249 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(603): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(524): Show |
1 | a0001c0001t0002g0018 | 2 | NA19002.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(531): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(563): Show |
2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG02071.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.349+946_349+947ins others(570): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(525): Show |
43 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0202 others(40): Show |
45 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(532): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(558): Show |
1 | a0001c0001t0002g0335 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(525): Show |
51 | a0001c0001t0001g0028 a0001c0001t0001g0090 a0001c0001t0001g0148 others(48): Show |
52 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(532): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(558): Show |
1 | a0001c0001t0002g0312 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(525): Show |
2 | a0001c0001t0001g0300 a0001c0001t0002g0200 |
2 | HG00621.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.349+946_349+947ins others(532): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(525): Show |
1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(532): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(491): Show |
1 | a0003c0006t0001g0047 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(498): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(523): Show |
1 | a0003c0007t0017g0124 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(530): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(492): Show |
11 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0007g0118 others(8): Show |
11 | HG00639.hp2 HG01123.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(499): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(492): Show |
1 | a0001c0001t0002g0348 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(499): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(525): Show |
1 | a0001c0015t0002g0292 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(532): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(629): Show |
1 | a0001c0001t0001g0212 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(636): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(601): Show |
1 | a0001c0002t0012g0362 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(608): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(601): Show |
4 | a0001c0002t0004g0109 a0001c0002t0012g0094 a0001c0002t0028g0235 others(1): Show |
4 | HG02145.hp2 HG02486.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(608): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(596): Show |
1 | a0001c0001t0001g0265 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(603): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(602): Show |
2 | a0001c0001t0002g0275 a0001c0010t0027g0272 |
2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.349+946_349+947ins others(609): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(569): Show |
1 | a0001c0001t0002g0240 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(576): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(600): Show |
2 | a0001c0001t0002g0055 a0001c0002t0003g0242 |
2 | HG00733.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(607): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(569): Show |
16 | a0001c0001t0001g0112 a0001c0001t0001g0156 a0001c0001t0001g0220 others(13): Show |
20 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(576): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(568): Show |
1 | a0001c0001t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(575): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(492): Show |
1 | a0001c0003t0015g0256 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.349+948_349+949ins others(499): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(501): Show |
4 | a0001c0003t0005g0232 a0001c0003t0014g0077 a0001c0003t0014g0343 others(1): Show |
4 | HG03209.hp1 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+948_349+949ins others(508): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(468): Show |
4 | a0001c0003t0001g0153 a0001c0003t0001g0271 a0001c0003t0001g0274 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+948_349+949ins others(475): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(531): Show |
1 | a0004c0019t0001g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.349+948_349+949ins others(538): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(436): Show |
1 | a0001c0001t0001g0254 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+948_349+949ins others(443): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(427): Show |
14 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0062 others(11): Show |
16 | HG00642.hp1 HG00741.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.349+948_349+949ins others(434): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(436): Show |
1 | a0001c0001t0001g0371 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.349+948_349+949ins others(443): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(438): Show |
2 | a0001c0001t0005g0361 a0001c0001t0022g0280 |
2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.349+948_349+949ins others(445): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(373): Show |
2 | a0001c0001t0001g0191 a0001c0001t0002g0186 |
2 | HG01928.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.349+948_349+949ins others(380): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(427): Show |
1 | a0001c0001t0001g0341 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.349+948_349+949ins others(434): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(436): Show |
40 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(37): Show |
45 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.349+948_349+949ins others(443): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(465): Show |
2 | a0001c0001t0001g0320 a0001c0001t0001g0357 |
2 | NA18968.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.349+948_349+949ins others(472): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(438): Show |
2 | a0001c0001t0005g0049 a0001c0001t0005g0244 |
2 | HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.349+948_349+949ins others(445): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(427): Show |
1 | a0001c0005t0001g0181 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.349+948_349+949ins others(434): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(434): Show |
1 | a0001c0001t0001g0217 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.349+948_349+949ins others(441): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(793): Show |
3 | a0001c0001t0005g0246 a0001c0001t0024g0252 a0001c0002t0004g0273 |
3 | HG02965.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.349+948_349+949ins others(800): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(512): Show |
2 | a0001c0001t0008g0100 a0001c0001t0020g0044 |
2 | HG01106.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.349+940_349+941ins others(519): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(376): Show |
1 | a0001c0014t0001g0324 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.349+939_349+940ins others(383): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(315): Show |
1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349+939_349+940ins others(322): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(369): Show |
12 | a0001c0001t0001g0253 a0001c0001t0001g0260 a0001c0001t0001g0269 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+939_349+940ins others(376): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(338): Show |
6 | a0001c0001t0001g0095 a0001c0001t0001g0276 a0001c0001t0001g0370 others(3): Show |
6 | HG02622.hp2 HG02723.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+939_349+940ins others(345): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | CACTATAT others(380): Show |
2 | a0004c0008t0029g0108 a0004c0008t0037g0107 |
2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.349+939_349+940ins others(387): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | ||||||
| chr8:133214070 | C | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0221 a0001c0001t0016g0061 others(6): Show |
10 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+927C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214070 | |||||||
| chr8:133214072 | C | CTATATAT others(535): Show |
6 | a0001c0001t0006g0082 a0001c0001t0006g0143 a0001c0001t0006g0234 others(3): Show |
6 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(542): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | ||||||
| chr8:133214072 | C | CTATATAT others(635): Show |
1 | a0001c0002t0018g0043 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(642): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | ||||||
| chr8:133214072 | C | CTATATAT others(568): Show |
1 | a0001c0001t0006g0251 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(575): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | ||||||
| chr8:133214072 | C | CTATATAT others(401): Show |
1 | a0001c0012t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(408): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | ||||||
| chr8:133214072 | C | CTATATAT others(646): Show |
1 | a0001c0001t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(653): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | ||||||
| chr8:133214072 | C | CTATATAT others(622): Show |
1 | a0001c0012t0001g0363 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(629): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | ||||||
| chr8:133214072 | C | CTATATAT others(558): Show |
6 | a0001c0001t0005g0157 a0001c0001t0008g0111 a0001c0001t0008g0122 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | ||||||
| chr8:133214072 | C | CTATATAT others(613): Show |
1 | a0001c0002t0011g0247 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(620): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | ||||||
| chr8:133214072 | C | CTATATAT others(613): Show |
1 | a0001c0002t0018g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(620): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | ||||||
| chr8:133214072 | C | CTATATAT others(376): Show |
2 | a0001c0001t0001g0349 a0001c0001t0001g0350 |
2 | NA18966.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.349+939_349+940ins others(383): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | ||||||
| chr8:133214084 | G | GTTATATA others(405): Show |
1 | a0001c0001t0001g0072 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.349+948_349+949ins others(412): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214084 | ||||||
| chr8:133214085 | T | TTATACAT others(656): Show |
2 | a0001c0001t0001g0314 a0001c0001t0001g0323 |
2 | NA18993.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(663): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214085 | ||||||
| chr8:133214085 | T | TTATACAT others(494): Show |
2 | a0001c0001t0009g0079 a0001c0001t0009g0080 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(501): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214085 | ||||||
| chr8:133214092 | A | T | 3 | a0001c0001t0001g0072 a0001c0001t0009g0079 a0001c0001t0009g0080 |
3 | HG00738.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.349+949A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214092 | |||||||
| chr8:133214103 | G | C | 18 | a0001c0001t0001g0072 a0001c0001t0001g0253 a0001c0001t0001g0260 others(15): Show |
18 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.349+960G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214103 | |||||||
| chr8:133214110 | T | TAGTAGTT others(20): Show |
5 | a0001c0001t0001g0130 a0001c0001t0001g0352 a0001c0001t0001g0353 others(2): Show |
5 | HG01515.hp1 HG02738.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+993_349+1019du others(28): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214110 | ||||||
| chr8:133214122 | AT | A | 3 | a0001c0001t0001g0072 a0001c0001t0009g0079 a0001c0001t0009g0080 |
3 | HG00738.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.349+980delT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214122 | |||||||
| chr8:133214124 | AACT | A | 9 | a0001c0003t0001g0153 a0001c0003t0001g0271 a0001c0003t0001g0274 others(6): Show |
9 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+986_349+988del others(3): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214124 | ||||||
| chr8:133214128 | AC | A | 3 | a0001c0001t0001g0072 a0001c0001t0009g0079 a0001c0001t0009g0080 |
3 | HG00738.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.349+986delC | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214128 | |||||||
| chr8:133214137 | C | T | 2 | a0001c0001t0009g0079 a0001c0001t0009g0080 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.349+994C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214137 | |||||||
| chr8:133214156 | CTA | C | 37 | a0001c0001t0001g0095 a0001c0001t0001g0253 a0001c0001t0001g0260 others(34): Show |
37 | HG01106.hp1 HG01109.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.349+1024_349+1025d others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214156 | ||||||
| chr8:133214300 | C | T | 1 | a0001c0001t0038g0207 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.349+1157C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214300 | |||||||
| chr8:133214364 | G | C | 6 | a0001c0002t0004g0103 a0001c0002t0004g0109 a0001c0002t0012g0094 others(3): Show |
6 | HG01167.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+1221G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214364 | |||||||
| chr8:133214471 | T | A | 1 | a0001c0001t0002g0339 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.349+1328T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214471 | |||||||
| chr8:133214474 | T | A | 1 | a0001c0002t0003g0152 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.349+1331T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214474 | |||||||
| chr8:133214507 | G | GGTT | 4 | a0001c0001t0001g0319 a0001c0001t0001g0331 a0001c0001t0002g0275 others(1): Show |
4 | HG02055.hp1 HG03471.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+1386_349+1388d others(5): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214507 | ||||||
| chr8:133214507 | G | GGTTGTTG others(2): Show |
6 | a0001c0001t0001g0095 a0001c0001t0001g0276 a0001c0001t0001g0370 others(3): Show |
6 | HG02257.hp2 HG02723.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+1380_349+1388d others(11): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214507 | ||||||
| chr8:133214507 | G | GGTTGTTG others(5): Show |
14 | a0001c0001t0001g0253 a0001c0001t0001g0260 a0001c0001t0001g0269 others(11): Show |
14 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.349+1377_349+1388d others(14): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214507 | ||||||
| chr8:133214510 | T | G | 1 | a0001c0001t0002g0282 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.349+1367T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214510 | |||||||
| chr8:133214569 | G | A | 1 | a0001c0001t0007g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.349+1426G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214569 | |||||||
| chr8:133214636 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(86): Show |
96 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.349+1493C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214636 | |||||||
| chr8:133214740 | A | C | 1 | a0001c0002t0003g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.349+1597A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214740 | |||||||
| chr8:133214832 | G | A | 2 | a0004c0008t0029g0108 a0004c0008t0037g0107 |
2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.349+1689G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214832 | |||||||
| chr8:133214954 | A | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(93): Show |
103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.349+1811A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214954 | |||||||
| chr8:133214982 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.349+1839C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214982 | |||||||
| chr8:133215076 | T | C | 2 | a0001c0002t0011g0247 a0001c0002t0018g0231 |
2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.349+1933T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215076 | |||||||
| chr8:133215197 | C | A | 1 | a0001c0001t0001g0281 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.349+2054C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215197 | |||||||
| chr8:133215253 | C | T | 60 | a0001c0001t0001g0028 a0001c0001t0001g0090 a0001c0001t0001g0148 others(57): Show |
62 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.349+2110C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215253 | |||||||
| chr8:133215457 | T | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(130): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.349+2314T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215457 | |||||||
| chr8:133215545 | T | A | 18 | a0001c0001t0001g0095 a0001c0001t0001g0253 a0001c0001t0001g0260 others(15): Show |
18 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.349+2402T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215545 | |||||||
| chr8:133215733 | A | G | 2 | a0001c0001t0005g0096 a0001c0001t0005g0097 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.349+2590A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215733 | |||||||
| chr8:133215736 | C | A | 13 | a0001c0001t0001g0253 a0001c0001t0001g0260 a0001c0001t0001g0269 others(10): Show |
13 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.349+2593C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215736 | |||||||
| chr8:133215761 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.349+2618G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215761 | |||||||
| chr8:133215775 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(105): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.349+2632G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215775 | |||||||
| chr8:133215917 | T | C | 1 | a0001c0002t0004g0083 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.349+2774T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215917 | |||||||
| chr8:133215953 | A | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(63): Show |
73 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.349+2810A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215953 | |||||||
| chr8:133215965 | C | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(111): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.349+2822C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215965 | |||||||
| chr8:133215984 | T | TAC | 21 | a0001c0001t0001g0102 a0001c0001t0001g0328 a0001c0001t0001g0329 others(18): Show |
21 | HG00609.hp2 HG01167.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.349+2863_349+2864d others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133215984 | ||||||
| chr8:133215984 | TAC | T | 47 | a0001c0001t0001g0095 a0001c0001t0001g0112 a0001c0001t0001g0156 others(44): Show |
51 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.349+2863_349+2864d others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133215984 | ||||||
| chr8:133216042 | A | T | 1 | a0004c0019t0001g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.349+2899A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216042 | |||||||
| chr8:133216054 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(111): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.349+2911A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216054 | |||||||
| chr8:133216279 | T | C | 11 | a0001c0001t0002g0001 a0001c0001t0002g0187 a0001c0001t0002g0188 others(8): Show |
15 | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.349+3136T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216279 | |||||||
| chr8:133216563 | AC | A | 8 | a0001c0001t0006g0082 a0001c0001t0006g0143 a0001c0001t0006g0234 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+3422delC | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133216563 | ||||||
| chr8:133216627 | G | A | 2 | a0004c0008t0029g0108 a0004c0008t0037g0107 |
2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.349+3484G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216627 | |||||||
| chr8:133216663 | A | C | 5 | a0001c0001t0005g0246 a0001c0001t0005g0361 a0001c0001t0022g0280 others(2): Show |
5 | HG01891.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+3520A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216663 | |||||||
| chr8:133216687 | T | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(189): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.349+3544T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216687 | |||||||
| chr8:133216739 | T | C | 8 | a0001c0001t0006g0082 a0001c0001t0006g0143 a0001c0001t0006g0234 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+3596T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216739 | |||||||
| chr8:133216756 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.349+3613G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216756 | |||||||
| chr8:133216786 | A | C | 1 | a0001c0001t0002g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.349+3643A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216786 | |||||||
| chr8:133216875 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.350-3706C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216875 | |||||||
| chr8:133216909 | C | G | 12 | a0001c0001t0001g0036 a0001c0001t0001g0095 a0001c0001t0001g0221 others(9): Show |
13 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.350-3672C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216909 | |||||||
| chr8:133217060 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.350-3521C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217060 | |||||||
| chr8:133217102 | T | C | 4 | a0001c0001t0002g0238 a0004c0008t0029g0108 a0004c0008t0037g0107 others(1): Show |
4 | HG02572.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-3479T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217102 | |||||||
| chr8:133217198 | G | T | 1 | a0001c0001t0001g0173 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.350-3383G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217198 | |||||||
| chr8:133217265 | C | A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(68): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.350-3316C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217265 | |||||||
| chr8:133217292 | A | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(190): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.350-3289A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217292 | |||||||
| chr8:133217547 | G | A | 2 | a0001c0001t0005g0361 a0001c0001t0022g0280 |
2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.350-3034G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217547 | |||||||
| chr8:133217640 | C | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(185): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.350-2941C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217640 | |||||||
| chr8:133217643 | G | A | 2 | a0001c0001t0020g0044 a0004c0008t0029g0108 |
2 | HG01106.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.350-2938G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217643 | |||||||
| chr8:133217813 | G | T | 1 | a0001c0002t0004g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.350-2768G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217813 | |||||||
| chr8:133217860 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.350-2721G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217860 | |||||||
| chr8:133217936 | C | CCACA | 4 | a0001c0001t0005g0246 a0001c0001t0006g0261 a0001c0001t0024g0252 others(1): Show |
4 | HG02965.hp2 HG02976.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-2623_350-2620d others(6): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133217936 | C | CCACACAC others(5): Show |
2 | a0001c0001t0002g0238 a0001c0012t0001g0068 |
2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.350-2631_350-2620d others(14): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133217936 | C | CCACACAC others(7): Show |
12 | a0001c0001t0005g0157 a0001c0001t0008g0111 a0001c0001t0008g0122 others(9): Show |
12 | HG01167.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.350-2633_350-2620d others(16): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133217936 | C | CCACACAC others(9): Show |
7 | a0001c0001t0001g0086 a0001c0001t0001g0209 a0001c0001t0001g0260 others(4): Show |
7 | HG01074.hp1 HG02055.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-2635_350-2620d others(18): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133217936 | C | CCACACAC others(11): Show |
29 | a0001c0001t0001g0027 a0001c0001t0001g0095 a0001c0001t0001g0105 others(26): Show |
29 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.350-2637_350-2620d others(20): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133217936 | C | CCACACAC others(13): Show |
79 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0014 others(76): Show |
86 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.350-2639_350-2620d others(22): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133217936 | C | CCACACAC others(15): Show |
80 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0022 others(77): Show |
87 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.350-2641_350-2620d others(24): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133217936 | C | CCACACAC others(17): Show |
23 | a0001c0001t0001g0028 a0001c0001t0001g0090 a0001c0001t0001g0131 others(20): Show |
23 | HG00597.hp1 HG01891.hp2 HG02135.hp1 others(20): Show |
intron_variant | MODIFIER | c.350-2643_350-2620d others(26): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133217936 | C | CCACACAC others(19): Show |
1 | a0001c0001t0001g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.350-2620_350-2619i others(28): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133217936 | C | CCACACAC others(23): Show |
1 | a0001c0001t0001g0036 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.350-2620_350-2619i others(32): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133217936 | C | CCACACAC others(13): Show |
2 | a0001c0001t0001g0254 a0001c0001t0002g0186 |
2 | HG01928.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.350-2632_350-2631i others(22): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133217936 | C | CCACACAC others(15): Show |
62 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(59): Show |
69 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.350-2632_350-2631i others(24): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133217936 | C | CCACACAC others(17): Show |
4 | a0001c0001t0001g0037 a0001c0001t0001g0101 a0001c0001t0001g0116 others(1): Show |
4 | HG00642.hp1 HG01934.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-2632_350-2631i others(26): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133217936 | C | CCACACAC others(19): Show |
2 | a0001c0001t0001g0062 a0001c0001t0001g0115 |
2 | HG00741.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.350-2632_350-2631i others(28): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | ||||||
| chr8:133218074 | C | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(144): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.350-2507C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218074 | |||||||
| chr8:133218212 | G | C | 1 | a0001c0001t0002g0304 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.350-2369G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218212 | |||||||
| chr8:133218225 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0038g0207 |
2 | NA19010.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.350-2356C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218225 | |||||||
| chr8:133218401 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(64): Show |
74 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.350-2180C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218401 | |||||||
| chr8:133218539 | C | A | 80 | a0001c0001t0001g0028 a0001c0001t0001g0090 a0001c0001t0001g0148 others(77): Show |
86 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.350-2042C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218539 | |||||||
| chr8:133218548 | A | G | 1 | a0001c0001t0007g0118 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.350-2033A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218548 | |||||||
| chr8:133218568 | G | A | 1 | a0001c0001t0001g0313 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.350-2013G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218568 | |||||||
| chr8:133218576 | T | A | 1 | a0001c0001t0002g0104 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.350-2005T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218576 | |||||||
| chr8:133218773 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.350-1808T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218773 | |||||||
| chr8:133218996 | TC | T | 3 | a0001c0001t0007g0158 a0001c0001t0007g0255 a0001c0001t0007g0344 |
3 | HG02280.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.350-1584delC | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218996 | |||||||
| chr8:133219009 | C | T | 1 | a0001c0001t0008g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-1572C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219009 | |||||||
| chr8:133219025 | T | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0177 others(5): Show |
10 | HG00408.hp1 NA18973.hp2 NA18978.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-1556T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219025 | |||||||
| chr8:133219069 | C | T | 6 | a0001c0002t0004g0103 a0001c0002t0004g0109 a0001c0002t0012g0094 others(3): Show |
6 | HG01167.hp2 HG02145.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1512C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219069 | |||||||
| chr8:133219353 | T | A | 1 | a0001c0002t0028g0235 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.350-1228T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219353 | |||||||
| chr8:133219425 | C | T | 1 | a0004c0019t0001g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.350-1156C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219425 | |||||||
| chr8:133219564 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(72): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.350-1017C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219564 | |||||||
| chr8:133219589 | C | A | 91 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(88): Show |
98 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.350-992C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219589 | |||||||
| chr8:133219620 | T | G | 1 | a0001c0001t0001g0022 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.350-961T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219620 | |||||||
| chr8:133219691 | G | A | 7 | a0001c0002t0004g0103 a0001c0002t0004g0109 a0001c0002t0012g0094 others(4): Show |
7 | HG01167.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-890G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219691 | |||||||
| chr8:133219791 | G | C | 2 | a0001c0001t0002g0309 a0001c0002t0003g0053 |
2 | HG02132.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.350-790G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219791 | |||||||
| chr8:133219969 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.350-612G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219969 | |||||||
| chr8:133220060 | T | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(83): Show |
93 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.350-521T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220060 | |||||||
| chr8:133220164 | G | T | 1 | a0003c0007t0017g0241 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.350-417G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220164 | |||||||
| chr8:133220181 | C | T | 1 | a0001c0002t0010g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.350-400C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220181 | |||||||
| chr8:133220194 | C | CT | 86 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(83): Show |
93 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.350-378dupT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133220194 | ||||||
| chr8:133220212 | G | A | 1 | a0001c0002t0003g0250 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.350-369G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220212 | |||||||
| chr8:133220315 | G | A | 1 | a0001c0001t0001g0314 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.350-266G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220315 | |||||||
| chr8:133220375 | C | T | 3 | a0004c0008t0029g0108 a0004c0008t0037g0107 a0004c0019t0001g0270 |
3 | HG02572.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.350-206C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220375 | |||||||
| chr8:133220533 | C | T | 1 | a0001c0001t0001g0017 | 2 | NA18948.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.350-48C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220533 | |||||||
| chr8:133220967 | G | T | 2 | a0001c0001t0002g0216 a0001c0001t0002g0334 |
2 | HG00621.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.610+126G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133220967 | |||||||
| chr8:133220982 | C | T | 6 | a0001c0001t0005g0157 a0001c0001t0008g0111 a0001c0001t0008g0122 others(3): Show |
6 | HG02055.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.610+141C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133220982 | |||||||
| chr8:133221159 | G | A | 3 | a0004c0008t0029g0108 a0004c0008t0037g0107 a0004c0019t0001g0270 |
3 | HG02572.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.610+318G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133221159 | |||||||
| chr8:133221187 | C | A | 1 | a0001c0001t0001g0226 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.610+346C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133221187 | |||||||
| chr8:133221532 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.610+691C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133221532 | |||||||
| chr8:133221661 | G | T | 12 | a0001c0001t0001g0253 a0001c0001t0001g0260 a0001c0001t0001g0269 others(9): Show |
12 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.610+820G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133221661 | |||||||
| chr8:133221724 | A | AATGGATG others(1): Show |
103 | a0001c0001t0001g0028 a0001c0001t0001g0090 a0001c0001t0001g0095 others(100): Show |
109 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.610+894_610+901dup others(8): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133221724 | ||||||
| chr8:133221852 | G | A | 1 | a0001c0002t0028g0235 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.610+1011G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133221852 | |||||||
| chr8:133221908 | T | C | 83 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(80): Show |
90 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.610+1067T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133221908 | |||||||
| chr8:133221919 | A | AGGAT | 3 | a0001c0001t0001g0023 a0001c0001t0001g0354 a0001c0002t0018g0043 |
3 | HG03195.hp2 NA18991.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.610+1099_610+1102d others(6): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133221919 | ||||||
| chr8:133221919 | AGGAT | A | 7 | a0001c0001t0005g0246 a0001c0001t0005g0361 a0001c0001t0022g0280 others(4): Show |
7 | HG01891.hp2 HG02572.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.610+1099_610+1102d others(6): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133221919 | ||||||
| chr8:133222083 | C | T | 8 | a0001c0001t0006g0082 a0001c0001t0006g0143 a0001c0001t0006g0234 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.610+1242C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222083 | |||||||
| chr8:133222095 | T | C | 1 | a0001c0005t0001g0178 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.610+1254T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222095 | |||||||
| chr8:133222115 | TAATG | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0229 a0001c0001t0001g0303 |
3 | NA18950.hp2 NA18977.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.610+1275_610+1278d others(6): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222115 | |||||||
| chr8:133222507 | T | C | 3 | a0001c0001t0001g0095 a0001c0001t0001g0276 a0001c0001t0001g0370 |
3 | HG02723.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.610+1666T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222507 | |||||||
| chr8:133222585 | A | G | 7 | a0001c0002t0004g0103 a0001c0002t0004g0109 a0001c0002t0012g0094 others(4): Show |
7 | HG01167.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.610+1744A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222585 | |||||||
| chr8:133222679 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.610+1838G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222679 | |||||||
| chr8:133222737 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.610+1896G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222737 | |||||||
| chr8:133222807 | T | TA | 17 | a0001c0001t0001g0036 a0001c0001t0002g0025 a0001c0003t0001g0271 others(14): Show |
17 | HG00642.hp2 HG01070.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.610+1974dupA | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133222807 | ||||||
| chr8:133222808 | A | T | 11 | a0001c0001t0005g0096 a0001c0001t0005g0097 a0001c0001t0026g0233 others(8): Show |
11 | HG01109.hp2 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.610+1967A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222808 | |||||||
| chr8:133223014 | C | T | 1 | a0001c0002t0003g0199 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.610+2173C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223014 | |||||||
| chr8:133223112 | T | C | 10 | a0001c0002t0018g0043 a0001c0002t0018g0231 a0003c0006t0001g0031 others(7): Show |
10 | HG00642.hp2 HG01070.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.610+2271T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223112 | |||||||
| chr8:133223132 | A | G | 1 | a0001c0001t0002g0290 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.611-2258A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223132 | |||||||
| chr8:133223133 | G | C | 1 | a0001c0001t0002g0290 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.611-2257G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223133 | |||||||
| chr8:133223150 | C | T | 1 | a0001c0001t0035g0345 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.611-2240C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223150 | |||||||
| chr8:133223157 | C | A | 14 | a0001c0003t0001g0153 a0001c0003t0001g0271 a0001c0003t0001g0274 others(11): Show |
14 | HG00642.hp2 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.611-2233C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223157 | |||||||
| chr8:133223212 | G | A | 1 | a0001c0001t0002g0304 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.611-2178G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223212 | |||||||
| chr8:133223228 | A | G | 7 | a0001c0002t0004g0109 a0003c0006t0001g0031 a0003c0006t0001g0047 others(4): Show |
7 | HG00642.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.611-2162A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223228 | |||||||
| chr8:133223430 | T | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0184 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.611-1960T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223430 | |||||||
| chr8:133223573 | T | C | 233 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(230): Show |
244 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.611-1817T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223573 | |||||||
| chr8:133223575 | C | T | 1 | a0001c0001t0020g0044 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.611-1815C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223575 | |||||||
| chr8:133223641 | T | A | 3 | a0001c0001t0001g0328 a0001c0010t0027g0272 a0001c0010t0031g0365 |
3 | HG02055.hp2 HG02965.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.611-1749T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223641 | |||||||
| chr8:133223641 | T | TCA | 116 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(113): Show |
125 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.611-1737_611-1736d others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133223641 | ||||||
| chr8:133223654 | C | T | 1 | a0001c0002t0003g0078 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.611-1736C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223654 | |||||||
| chr8:133223707 | A | G | 5 | a0001c0002t0012g0094 a0001c0002t0012g0106 a0001c0002t0012g0362 others(2): Show |
5 | HG01167.hp2 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-1683A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223707 | |||||||
| chr8:133223764 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.611-1626G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223764 | |||||||
| chr8:133223805 | C | T | 1 | a0001c0002t0004g0083 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.611-1585C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223805 | |||||||
| chr8:133223814 | T | C | 1 | a0001c0001t0005g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.611-1576T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223814 | |||||||
| chr8:133223856 | T | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0204 |
3 | HG03017.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.611-1534T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223856 | |||||||
| chr8:133223987 | C | G | 5 | a0001c0002t0012g0094 a0001c0002t0012g0106 a0001c0002t0012g0362 others(2): Show |
5 | HG01167.hp2 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-1403C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223987 | |||||||
| chr8:133224044 | GC | G | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(216): Show |
233 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.611-1345delC | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224044 | |||||||
| chr8:133224229 | C | CT | 14 | a0001c0001t0002g0006 a0001c0001t0002g0030 a0001c0001t0002g0054 others(11): Show |
15 | HG00621.hp2 HG00639.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.611-1132dupT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | ||||||
| chr8:133224229 | C | CTT | 8 | a0001c0001t0002g0001 a0001c0001t0002g0069 a0001c0001t0002g0154 others(5): Show |
11 | HG01074.hp2 HG01258.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.611-1133_611-1132d others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | ||||||
| chr8:133224229 | CT | C | 25 | a0001c0001t0001g0032 a0001c0001t0002g0200 a0001c0001t0005g0097 others(22): Show |
25 | HG00735.hp2 HG01106.hp2 HG02004.hp1 others(22): Show |
intron_variant | MODIFIER | c.611-1132delT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | ||||||
| chr8:133224229 | CTT | C | 66 | a0001c0001t0001g0056 a0001c0001t0001g0092 a0001c0001t0001g0160 others(63): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.611-1133_611-1132d others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | ||||||
| chr8:133224229 | CTTT | C | 105 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(102): Show |
112 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.611-1134_611-1132d others(5): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | ||||||
| chr8:133224229 | CTTTT | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0019 others(74): Show |
82 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.611-1135_611-1132d others(6): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | ||||||
| chr8:133224229 | CTTTTT | C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0352 a0001c0001t0005g0246 others(4): Show |
7 | HG01169.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.611-1136_611-1132d others(7): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | ||||||
| chr8:133224229 | CTTTTTT | C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0063 others(15): Show |
20 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.611-1137_611-1132d others(8): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | ||||||
| chr8:133224493 | G | A | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(198): Show |
215 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.611-897G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224493 | |||||||
| chr8:133224532 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.611-858C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224532 | |||||||
| chr8:133224536 | C | A | 2 | a0001c0001t0005g0049 a0001c0001t0005g0244 |
2 | HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.611-854C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224536 | |||||||
| chr8:133224650 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(215): Show |
232 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.611-740C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224650 | |||||||
| chr8:133224660 | C | T | 2 | a0001c0003t0014g0077 a0001c0003t0014g0343 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.611-730C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224660 | |||||||
| chr8:133224674 | C | A | 4 | a0001c0001t0008g0100 a0001c0001t0008g0111 a0001c0001t0008g0122 others(1): Show |
4 | HG02257.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.611-716C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224674 | |||||||
| chr8:133224682 | C | T | 2 | a0004c0008t0029g0108 a0004c0008t0037g0107 |
2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.611-708C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224682 | |||||||
| chr8:133224703 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.611-687G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224703 | |||||||
| chr8:133224705 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0140 a0001c0005t0001g0136 |
3 | HG00558.hp2 NA18964.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.611-685C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224705 | |||||||
| chr8:133224753 | G | A | 4 | a0001c0001t0008g0100 a0001c0001t0008g0111 a0001c0001t0008g0122 others(1): Show |
4 | HG02257.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.611-637G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224753 | |||||||
| chr8:133224849 | A | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(217): Show |
234 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.611-541A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224849 | |||||||
| chr8:133224935 | CA | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
216 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.611-439delA | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224935 | ||||||
| chr8:133225029 | G | A | 1 | a0001c0005t0001g0179 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.611-361G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133225029 | |||||||
| chr8:133225335 | G | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(218): Show |
235 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.611-55G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133225335 | |||||||
| chr8:133225378 | C | A | 1 | a0001c0002t0004g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.611-12C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133225378 | |||||||
| chr8:133225673 | T | C | 2 | a0001c0002t0018g0043 a0001c0002t0018g0231 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.804+90T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133225673 | |||||||
| chr8:133225931 | C | T | 1 | a0001c0002t0011g0247 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.804+348C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133225931 | |||||||
| chr8:133226009 | C | A | 3 | a0001c0002t0003g0192 a0001c0002t0003g0205 a0001c0002t0003g0206 |
3 | NA18947.hp1 NA18995.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.804+426C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226009 | |||||||
| chr8:133226150 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.804+567G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226150 | |||||||
| chr8:133226451 | T | C | 2 | a0004c0008t0029g0108 a0004c0008t0037g0107 |
2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.804+868T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226451 | |||||||
| chr8:133226528 | G | A | 279 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(276): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.805-883G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226528 | |||||||
| chr8:133226573 | C | T | 1 | a0001c0001t0002g0275 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.805-838C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226573 | |||||||
| chr8:133226778 | A | G | 22 | a0001c0002t0010g0258 a0001c0002t0010g0259 a0001c0002t0010g0266 others(19): Show |
22 | HG01070.hp1 HG01109.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.805-633A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226778 | |||||||
| chr8:133226916 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(47): Show |
55 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.805-495G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226916 | |||||||
| chr8:133226934 | C | A | 8 | a0001c0002t0012g0094 a0001c0002t0012g0106 a0001c0002t0012g0362 others(5): Show |
8 | HG01167.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-477C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226934 | |||||||
| chr8:133226977 | G | A | 18 | a0001c0002t0010g0258 a0001c0002t0010g0259 a0001c0002t0010g0266 others(15): Show |
18 | HG01109.hp2 HG01167.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.805-434G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226977 | |||||||
| chr8:133227035 | C | T | 5 | a0001c0002t0003g0041 a0001c0002t0003g0121 a0001c0002t0003g0161 others(2): Show |
5 | NA18957.hp1 NA18982.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-376C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133227035 | |||||||
| chr8:133227049 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.805-362C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133227049 |