Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1265 |
| ensemblid | ENSG00000064666.15 |
| hgncid | 2156 |
| symbol | CNN2 |
| name | calponin 2 |
| refseq_nuc | NM_004368.4 |
| refseq_prot | NP_004359.1 |
| ensembl_nuc | ENST00000263097.9 |
| ensembl_prot | ENSP00000263097.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 1026608 |
| end | 1039065 |
| strand | + |
| ver | v1.2 |
| region | chr19:1026608-1039065 |
| region5000 | chr19:1021608-1044065 |
| regionname0 | CNN2_chr19_1026608_1039065 |
| regionname5000 | CNN2_chr19_1021608_1044065 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 309 | 387 | 97 | 68 | 156 | 14 | 50 | 110 | CNN2_chr19_1021608_1044065 | CNN2 | MSSTQ others(304): Show |
chr19 | 1021608 | 1044065 |
| a0002 | 0/0 | 309 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | MSSTQ others(304): Show |
chr19 | 1021608 | 1044065 |
| a0003 | 0/0 | 309 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | MSSTQ others(304): Show |
chr19 | 1021608 | 1044065 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 927 | 233 | 68 | 25 | 108 | 10 | 22 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0002 | 0/0 | 927 | 46 | 5 | 22 | 5 | 2 | 12 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0003 | 1/1 | 927 | 30 | 16 | 3 | 7 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0004 | 0/0 | 927 | 29 | 0 | 3 | 22 | 1 | 3 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0005 | 0/0 | 927 | 20 | 0 | 4 | 11 | 0 | 5 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0006 | 0/0 | 927 | 10 | 0 | 7 | 0 | 1 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0007 | 0/0 | 927 | 5 | 0 | 3 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0008 | 0/0 | 927 | 4 | 4 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0009 | 0/0 | 927 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0011 | 0/0 | 927 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0013 | 0/0 | 927 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0014 | 0/0 | 927 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0015 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0016 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0017 | 0/0 | 927 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0001c0018 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0002c0010 | 0/0 | 927 | 2 | 0 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 | ||
| a0003c0012 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | ATGAG others(922): Show |
chr19 | 1021608 | 1044065 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2150 | 97 | 17 | 16 | 44 | 8 | 12 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0002 | 0/0 | 2150 | 55 | 1 | 0 | 50 | 0 | 4 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0003 | 0/0 | 2149 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0005 | 0/0 | 2149 | 27 | 18 | 4 | 1 | 2 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0006 | 0/0 | 2149 | 17 | 12 | 3 | 1 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0009 | 0/0 | 2151 | 10 | 8 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2146): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0010 | 0/0 | 2149 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0011 | 0/0 | 2150 | 7 | 7 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0014 | 0/0 | 2150 | 3 | 0 | 0 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0015 | 0/0 | 2149 | 3 | 1 | 0 | 1 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0017 | 0/0 | 2148 | 2 | 0 | 1 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2143): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0018 | 0/0 | 2150 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0022 | 0/0 | 2149 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0025 | 0/0 | 2150 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0026 | 0/0 | 2150 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0027 | 0/0 | 2150 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0028 | 0/0 | 2151 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2146): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0029 | 0/0 | 2151 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2146): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0030 | 0/0 | 2149 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0001t0034 | 0/0 | 2150 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0002t0004 | 0/0 | 2150 | 38 | 4 | 19 | 5 | 2 | 8 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0002t0012 | 0/0 | 2150 | 4 | 0 | 1 | 0 | 0 | 3 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0002t0013 | 0/0 | 2150 | 3 | 1 | 1 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0002t0023 | 0/0 | 2149 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0003t0003 | 1/1 | 2149 | 22 | 9 | 3 | 6 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0003t0010 | 0/0 | 2149 | 6 | 6 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0003t0031 | 0/0 | 2149 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0003t0033 | 0/0 | 2149 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0004t0003 | 0/0 | 2149 | 28 | 0 | 3 | 21 | 1 | 3 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0004t0032 | 0/0 | 2149 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0005t0007 | 0/0 | 2146 | 5 | 0 | 3 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2141): Show |
chr19 | 1021608 | 1044065 |
| a0001c0005t0008 | 0/0 | 2147 | 13 | 0 | 1 | 11 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2142): Show |
chr19 | 1021608 | 1044065 |
| a0001c0005t0016 | 0/0 | 2147 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2142): Show |
chr19 | 1021608 | 1044065 |
| a0001c0006t0007 | 0/0 | 2146 | 10 | 0 | 7 | 0 | 1 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2141): Show |
chr19 | 1021608 | 1044065 |
| a0001c0007t0001 | 0/0 | 2150 | 4 | 0 | 3 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0007t0002 | 0/0 | 2150 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0008t0019 | 0/0 | 2149 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0008t0020 | 0/0 | 2150 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0009t0010 | 0/0 | 2149 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0011t0004 | 0/0 | 2150 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0013t0001 | 0/0 | 2150 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0014t0005 | 0/0 | 2149 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| a0001c0015t0011 | 0/0 | 2150 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0016t0024 | 0/0 | 2150 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0001c0017t0021 | 0/0 | 2146 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2141): Show |
chr19 | 1021608 | 1044065 |
| a0001c0018t0008 | 0/0 | 2147 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2142): Show |
chr19 | 1021608 | 1044065 |
| a0002c0010t0001 | 0/0 | 2150 | 2 | 0 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2145): Show |
chr19 | 1021608 | 1044065 |
| a0003c0012t0005 | 0/0 | 2149 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | GGTCC others(2144): Show |
chr19 | 1021608 | 1044065 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 23 | 0 | 3 | 19 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0006 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0001 | 0/0 | 22 | 0 | 0 | 21 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0009 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0006g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0006g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0009g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0009g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0009g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0011g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0011g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0011g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0014g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0014g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0015g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0015g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0017g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0017g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0018g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0018g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0022g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0025g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0026g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0027g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0028g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0029g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0030g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0001t0034g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0001 | 0/0 | 10 | 2 | 5 | 2 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0004 | 0/0 | 5 | 0 | 0 | 1 | 0 | 4 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0007 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0012g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0012g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0012g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0012g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0013g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0013g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0002t0023g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0003g0008 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0003g0034 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0003g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0003g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0010g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0031g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0003t0033g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0004t0003g0003 | 0/0 | 15 | 0 | 0 | 14 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0004t0003g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0004t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0004t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0004t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0004t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0004t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0004t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0004t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0004t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0004t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0004t0032g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0005t0007g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0005t0007g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0005t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0005t0008g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0005t0008g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0005t0008g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0005t0008g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0005t0008g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0005t0008g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0005t0008g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0005t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0005t0016g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0006t0007g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0006t0007g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0006t0007g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0006t0007g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0006t0007g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0006t0007g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0007t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0007t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0007t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0007t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0008t0019g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0008t0019g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0008t0020g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0009t0010g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0009t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0011t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0011t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0013t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0014t0005g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0015t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0016t0024g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0017t0021g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0001c0018t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0002c0010t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0002c0010t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| a0003c0012t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00140 | hp1 | a0001 | c0006 | t0007 | g0141 | EUR | GBR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | FIN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0216 | EUR | FIN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00323 | hp2 | a0001 | c0002 | t0004 | g0217 | EUR | FIN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00438 | hp2 | a0001 | c0005 | t0008 | g0011 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00609 | hp1 | a0001 | c0005 | t0008 | g0024 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00609 | hp2 | a0001 | c0007 | t0001 | g0039 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00621 | hp1 | a0001 | c0001 | t0029 | g0002 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00639 | hp2 | a0001 | c0002 | t0004 | g0001 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00733 | hp1 | a0001 | c0002 | t0004 | g0009 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00733 | hp2 | a0001 | c0002 | t0004 | g0115 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00735 | hp1 | a0001 | c0006 | t0007 | g0010 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG00735 | hp2 | a0001 | c0002 | t0004 | g0191 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01070 | hp2 | a0001 | c0006 | t0007 | g0132 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01071 | hp1 | a0001 | c0002 | t0004 | g0112 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01071 | hp2 | a0001 | c0006 | t0007 | g0139 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01074 | hp1 | a0001 | c0007 | t0001 | g0113 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01074 | hp2 | a0001 | c0002 | t0004 | g0001 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01081 | hp1 | a0001 | c0002 | t0004 | g0001 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01099 | hp1 | a0001 | c0002 | t0004 | g0202 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01106 | hp1 | a0001 | c0006 | t0007 | g0010 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01106 | hp2 | a0001 | c0003 | t0003 | g0008 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0127 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01167 | hp1 | a0001 | c0001 | t0017 | g0009 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01168 | hp1 | a0001 | c0006 | t0007 | g0010 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01168 | hp2 | a0001 | c0005 | t0007 | g0099 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01169 | hp1 | a0001 | c0006 | t0007 | g0010 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01175 | hp1 | a0001 | c0003 | t0003 | g0036 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01175 | hp2 | a0001 | c0006 | t0007 | g0142 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01192 | hp2 | a0001 | c0003 | t0003 | g0008 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01243 | hp1 | a0001 | c0001 | t0030 | g0204 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01256 | hp1 | a0001 | c0004 | t0003 | g0017 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01257 | hp1 | a0001 | c0005 | t0007 | g0035 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01257 | hp2 | a0001 | c0002 | t0004 | g0183 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01258 | hp1 | a0001 | c0005 | t0007 | g0035 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01258 | hp2 | a0001 | c0004 | t0003 | g0017 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01261 | hp1 | a0001 | c0002 | t0004 | g0001 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01346 | hp1 | a0001 | c0002 | t0004 | g0007 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01433 | hp1 | a0001 | c0007 | t0001 | g0039 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01516 | hp1 | a0001 | c0002 | t0004 | g0001 | EUR | IBS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0001 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0123 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01934 | hp1 | a0001 | c0002 | t0004 | g0007 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01934 | hp2 | a0001 | c0005 | t0008 | g0200 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0054 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01943 | hp2 | a0001 | c0002 | t0013 | g0028 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01952 | hp1 | a0002 | c0010 | t0001 | g0006 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01975 | hp2 | a0001 | c0002 | t0004 | g0190 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0081 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01978 | hp2 | a0001 | c0007 | t0001 | g0143 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01981 | hp1 | a0001 | c0002 | t0004 | g0030 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01981 | hp2 | a0001 | c0002 | t0004 | g0001 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01993 | hp1 | a0001 | c0002 | t0023 | g0007 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0069 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02027 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02040 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02055 | hp2 | a0001 | c0008 | t0020 | g0020 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02071 | hp2 | a0001 | c0002 | t0004 | g0118 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02074 | hp1 | a0001 | c0003 | t0003 | g0193 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02083 | hp1 | a0001 | c0005 | t0008 | g0012 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02083 | hp2 | a0001 | c0001 | t0028 | g0114 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02129 | hp2 | a0001 | c0004 | t0003 | g0147 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02132 | hp1 | a0001 | c0005 | t0008 | g0050 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02132 | hp2 | a0001 | c0005 | t0008 | g0024 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02145 | hp1 | a0001 | c0003 | t0010 | g0160 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02148 | hp1 | a0001 | c0002 | t0004 | g0007 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02148 | hp2 | a0001 | c0017 | t0021 | g0137 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02155 | hp1 | a0001 | c0018 | t0008 | g0167 | EAS | CDX | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02155 | hp2 | a0001 | c0004 | t0032 | g0019 | EAS | CDX | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | CDX | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02165 | hp2 | a0001 | c0004 | t0003 | g0162 | EAS | CDX | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0117 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0001 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02293 | hp1 | a0001 | c0004 | t0003 | g0135 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02293 | hp2 | a0001 | c0002 | t0004 | g0007 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02300 | hp1 | a0002 | c0010 | t0001 | g0002 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02300 | hp2 | a0001 | c0002 | t0012 | g0186 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02451 | hp1 | a0001 | c0003 | t0010 | g0164 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02451 | hp2 | a0001 | c0001 | t0025 | g0061 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0154 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02572 | hp2 | a0001 | c0003 | t0010 | g0072 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02602 | hp2 | a0001 | c0002 | t0004 | g0004 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02615 | hp1 | a0001 | c0008 | t0019 | g0020 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0209 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0027 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0059 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02647 | hp2 | a0001 | c0003 | t0003 | g0151 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02683 | hp1 | a0001 | c0004 | t0003 | g0171 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02698 | hp1 | a0001 | c0004 | t0003 | g0003 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02698 | hp2 | a0001 | c0001 | t0027 | g0087 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02717 | hp1 | a0001 | c0008 | t0019 | g0125 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0068 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02723 | hp2 | a0001 | c0001 | t0015 | g0078 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02738 | hp2 | a0001 | c0002 | t0004 | g0004 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02809 | hp2 | a0001 | c0003 | t0010 | g0071 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0079 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02895 | hp1 | a0001 | c0009 | t0010 | g0158 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02895 | hp2 | a0001 | c0001 | t0022 | g0063 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02896 | hp2 | a0003 | c0012 | t0005 | g0067 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02897 | hp1 | a0001 | c0009 | t0010 | g0159 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02965 | hp1 | a0001 | c0003 | t0033 | g0155 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0065 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02970 | hp1 | a0001 | c0016 | t0024 | g0038 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02970 | hp2 | a0001 | c0003 | t0010 | g0163 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0124 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03017 | hp2 | a0001 | c0002 | t0004 | g0201 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03041 | hp1 | a0001 | c0003 | t0003 | g0008 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0001 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03098 | hp1 | a0001 | c0001 | t0010 | g0122 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0110 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03130 | hp2 | a0001 | c0003 | t0003 | g0008 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0070 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03209 | hp2 | a0001 | c0001 | t0011 | g0165 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03225 | hp1 | a0001 | c0008 | t0020 | g0020 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03225 | hp2 | a0001 | c0015 | t0011 | g0060 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03239 | hp1 | a0001 | c0004 | t0003 | g0169 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03239 | hp2 | a0001 | c0002 | t0012 | g0108 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0027 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03486 | hp1 | a0001 | c0003 | t0003 | g0008 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03486 | hp2 | a0001 | c0003 | t0003 | g0152 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03490 | hp1 | a0001 | c0006 | t0007 | g0040 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03491 | hp1 | a0001 | c0005 | t0007 | g0031 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03491 | hp2 | a0001 | c0001 | t0015 | g0083 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03492 | hp2 | a0001 | c0005 | t0007 | g0031 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03540 | hp1 | a0001 | c0003 | t0003 | g0153 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03579 | hp1 | a0001 | c0003 | t0003 | g0008 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03654 | hp1 | a0001 | c0002 | t0004 | g0025 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0080 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03669 | hp2 | a0001 | c0002 | t0004 | g0048 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03688 | hp1 | a0001 | c0011 | t0004 | g0140 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03688 | hp2 | a0001 | c0002 | t0012 | g0004 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03704 | hp1 | a0001 | c0002 | t0004 | g0025 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03704 | hp2 | a0001 | c0001 | t0017 | g0075 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03710 | hp1 | a0001 | c0003 | t0003 | g0036 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03710 | hp2 | a0001 | c0005 | t0016 | g0045 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03834 | hp1 | a0001 | c0006 | t0007 | g0040 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0038 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03927 | hp1 | a0001 | c0005 | t0008 | g0129 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03927 | hp2 | a0001 | c0003 | t0003 | g0034 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03942 | hp1 | a0001 | c0002 | t0004 | g0004 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03942 | hp2 | a0001 | c0011 | t0004 | g0149 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG04115 | hp2 | a0001 | c0013 | t0001 | g0056 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG04184 | hp2 | a0001 | c0002 | t0013 | g0004 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG04199 | hp2 | a0001 | c0005 | t0016 | g0045 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG04204 | hp1 | a0001 | c0002 | t0012 | g0195 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG04204 | hp2 | a0001 | c0002 | t0004 | g0004 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0009 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | YRI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | YRI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18612 | hp2 | a0001 | c0001 | t0014 | g0001 | EAS | CHB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18906 | hp1 | a0001 | c0003 | t0010 | g0157 | AFR | YRI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0128 | AFR | YRI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18944 | hp2 | a0001 | c0005 | t0008 | g0012 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18945 | hp2 | a0001 | c0004 | t0003 | g0134 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18950 | hp1 | a0001 | c0001 | t0009 | g0199 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18951 | hp1 | a0001 | c0005 | t0008 | g0011 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18954 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18954 | hp2 | a0001 | c0001 | t0006 | g0044 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18960 | hp2 | a0001 | c0004 | t0003 | g0136 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18964 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18966 | hp2 | a0001 | c0005 | t0008 | g0011 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18968 | hp2 | a0001 | c0003 | t0031 | g0013 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18969 | hp2 | a0001 | c0005 | t0008 | g0012 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18971 | hp2 | a0001 | c0005 | t0008 | g0210 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18972 | hp1 | a0001 | c0003 | t0003 | g0089 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18972 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18973 | hp1 | a0001 | c0007 | t0002 | g0138 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18975 | hp1 | a0001 | c0001 | t0018 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18979 | hp1 | a0001 | c0004 | t0003 | g0133 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18979 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18980 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18983 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18990 | hp2 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18995 | hp2 | a0001 | c0001 | t0014 | g0026 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19000 | hp1 | a0001 | c0004 | t0003 | g0019 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19004 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19005 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19005 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19009 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19011 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19012 | hp2 | a0001 | c0003 | t0003 | g0093 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | LWK | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0111 | AFR | LWK | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19055 | hp2 | a0001 | c0001 | t0026 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19056 | hp1 | a0001 | c0002 | t0004 | g0189 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19056 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19060 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19065 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19066 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19070 | hp2 | a0001 | c0001 | t0018 | g0016 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19079 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19080 | hp1 | a0001 | c0003 | t0003 | g0052 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19081 | hp1 | a0001 | c0004 | t0003 | g0019 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19085 | hp1 | a0001 | c0005 | t0008 | g0148 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19085 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19087 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | YRI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | YRI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA20129 | hp1 | a0001 | c0002 | t0004 | g0076 | AFR | ASW | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA20129 | hp2 | a0001 | c0002 | t0013 | g0028 | AFR | ASW | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA20805 | hp1 | a0001 | c0004 | t0003 | g0017 | EUR | TSI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0073 | EUR | TSI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA20905 | hp1 | a0001 | c0014 | t0005 | g0009 | SAS | GIH | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01123 | hp1 | a0001 | c0002 | t0004 | g0007 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG01123 | hp2 | a0001 | c0002 | t0004 | g0074 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0121 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0212 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02486 | hp2 | a0001 | c0003 | t0003 | g0008 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0049 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG02559 | hp2 | a0001 | c0001 | t0034 | g0131 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0058 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0126 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0166 | AFR | USA | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0001 | AFR | USA | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18955 | hp1 | a0001 | c0001 | t0014 | g0170 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | USA | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA20300 | hp2 | a0001 | c0002 | t0004 | g0007 | AFR | USA | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0003 | g0109 | REF | REF | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0003 | g0034 | REF | REF | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:1032624 | C | A | 1 | a0003 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.318C>A | p.Phe106Leu | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/7 | 372/2149 | 318/930 | 106/309 | chr19 | 1032624 | |||
| chr19:1037635 | C | T | 1 | a0002 | 2 | HG01952.hp1 HG02300.hp1 |
missense_variant | MODERATE | c.665C>T | p.Thr222Met | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 719/2149 | 665/930 | 222/309 | chr19 | 1037635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:1031115 | C | G | 1 | a0001c0018 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.108C>G | p.Thr36Thr | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/7 | 162/2149 | 108/930 | 36/309 | chr19 | 1031115 | |||
| chr19:1032690 | G | T | 5 | a0001c0004 a0001c0006 a0001c0007 others(2): Show |
47 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(44): Show |
synonymous_variant | LOW | c.384G>T | p.Ala128Ala | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/7 | 438/2149 | 384/930 | 128/309 | chr19 | 1032690 | |||
| chr19:1036153 | C | T | 1 | a0001c0016 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.414C>T | p.Ser138Ser | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 5/7 | 468/2149 | 414/930 | 138/309 | chr19 | 1036153 | |||
| chr19:1036204 | C | T | 1 | a0001c0015 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.465C>T | p.Asp155Asp | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 5/7 | 519/2149 | 465/930 | 155/309 | chr19 | 1036204 | |||
| chr19:1036445 | G | A | 3 | a0001c0002 a0001c0009 a0001c0011 |
50 | HG00323.hp2 HG00639.hp2 HG00733.hp1 others(47): Show |
synonymous_variant | LOW | c.537G>A | p.Ser179Ser | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/7 | 591/2149 | 537/930 | 179/309 | chr19 | 1036445 | |||
| chr19:1036457 | C | G | 4 | a0001c0005 a0001c0006 a0001c0017 others(1): Show |
32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
synonymous_variant | LOW | c.549C>G | p.Ala183Ala | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/7 | 603/2149 | 549/930 | 183/309 | chr19 | 1036457 | |||
| chr19:1036469 | A | G | 4 | a0001c0005 a0001c0006 a0001c0017 others(1): Show |
32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
synonymous_variant | LOW | c.561A>G | p.Arg187Arg | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/7 | 615/2149 | 561/930 | 187/309 | chr19 | 1036469 | |||
| chr19:1036544 | G | A | 1 | a0001c0013 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.636G>A | p.Thr212Thr | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/7 | 690/2149 | 636/930 | 212/309 | chr19 | 1036544 | |||
| chr19:1036553 | T | C | 14 | a0001c0001 a0001c0002 a0001c0005 others(11): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
synonymous_variant | LOW | c.645T>C | p.Cys215Cys | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/7 | 699/2149 | 645/930 | 215/309 | chr19 | 1036553 | |||
| chr19:1037762 | G | A | 1 | a0001c0014 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.792G>A | p.Leu264Leu | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 846/2149 | 792/930 | 264/309 | chr19 | 1037762 | |||
| chr19:1037810 | C | T | 1 | a0001c0017 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.840C>T | p.Ala280Ala | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 894/2149 | 840/930 | 280/309 | chr19 | 1037810 | |||
| chr19:1037858 | C | T | 1 | a0001c0008 | 4 | HG02055.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
synonymous_variant | LOW | c.888C>T | p.Val296Val | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 942/2149 | 888/930 | 296/309 | chr19 | 1037858 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:1026618 | C | G | 1 | a0001c0001t0034 | 1 | HG02559.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/7 | 44 | chr19 | 1026618 | ||||||
| chr19:1037933 | G | C | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(33): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*33G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 33 | chr19 | 1037933 | ||||||
| chr19:1037942 | G | T | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0014 others(2): Show |
72 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*42G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 42 | chr19 | 1037942 | ||||||
| chr19:1037965 | T | C | 1 | a0001c0001t0014 | 3 | NA18612.hp2 NA18955.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*65T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 65 | chr19 | 1037965 | ||||||
| chr19:1037969 | C | CT | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(20): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*83dupT | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 84 | INFO_REALIGN_3_PRIME | chr19 | 1037969 | |||||
| chr19:1037969 | C | CTT | 3 | a0001c0001t0009 a0001c0001t0028 a0001c0001t0029 |
12 | HG00621.hp1 HG02083.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*82_*83dupTT | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 84 | INFO_REALIGN_3_PRIME | chr19 | 1037969 | |||||
| chr19:1037969 | CTT | C | 3 | a0001c0005t0008 a0001c0005t0016 a0001c0018t0008 |
16 | HG00438.hp2 HG00609.hp1 HG01934.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*82_*83delTT | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 82 | INFO_REALIGN_3_PRIME | chr19 | 1037969 | |||||
| chr19:1037969 | CTTT | C | 3 | a0001c0005t0007 a0001c0006t0007 a0001c0017t0021 |
16 | HG00140.hp1 HG00735.hp1 HG01070.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*81_*83delTTT | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 81 | INFO_REALIGN_3_PRIME | chr19 | 1037969 | |||||
| chr19:1037987 | A | G | 5 | a0001c0002t0004 a0001c0002t0012 a0001c0002t0013 others(2): Show |
48 | HG00323.hp2 HG00639.hp2 HG00733.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*87A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 87 | chr19 | 1037987 | ||||||
| chr19:1038077 | T | G | 3 | a0001c0005t0008 a0001c0005t0016 a0001c0018t0008 |
16 | HG00438.hp2 HG00609.hp1 HG01934.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*177T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 177 | chr19 | 1038077 | ||||||
| chr19:1038125 | C | G | 1 | a0001c0001t0027 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*225C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 225 | chr19 | 1038125 | ||||||
| chr19:1038153 | C | T | 4 | a0001c0001t0010 a0001c0003t0010 a0001c0003t0033 others(1): Show |
10 | HG02145.hp1 HG02451.hp1 HG02572.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*253C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 253 | chr19 | 1038153 | ||||||
| chr19:1038154 | T | C | 1 | a0001c0016t0024 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 254 | chr19 | 1038154 | ||||||
| chr19:1038179 | G | T | 2 | a0001c0001t0018 a0001c0001t0026 |
3 | NA18975.hp1 NA19055.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*279G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 279 | chr19 | 1038179 | ||||||
| chr19:1038223 | C | G | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(33): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*323C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 323 | chr19 | 1038223 | ||||||
| chr19:1038290 | A | C | 4 | a0001c0001t0005 a0001c0001t0017 a0001c0014t0005 others(1): Show |
31 | HG00323.hp1 HG01109.hp1 HG01167.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*390A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 390 | chr19 | 1038290 | ||||||
| chr19:1038291 | AG | A | 4 | a0001c0001t0005 a0001c0001t0017 a0001c0014t0005 others(1): Show |
31 | HG00323.hp1 HG01109.hp1 HG01167.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*392delG | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 392 | chr19 | 1038291 | ||||||
| chr19:1038320 | C | T | 1 | a0001c0001t0028 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*420C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 420 | chr19 | 1038320 | ||||||
| chr19:1038371 | C | T | 1 | a0001c0004t0032 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*471C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 471 | chr19 | 1038371 | ||||||
| chr19:1038372 | T | G | 1 | a0001c0004t0032 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*472T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 472 | chr19 | 1038372 | ||||||
| chr19:1038378 | A | G | 1 | a0001c0003t0031 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 478 | chr19 | 1038378 | ||||||
| chr19:1038446 | C | T | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(33): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*546C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 546 | chr19 | 1038446 | ||||||
| chr19:1038572 | C | T | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(27): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*672C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 672 | chr19 | 1038572 | ||||||
| chr19:1038686 | G | C | 1 | a0001c0001t0028 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*786G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 786 | chr19 | 1038686 | ||||||
| chr19:1038687 | C | G | 1 | a0001c0001t0028 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*787C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 787 | chr19 | 1038687 | ||||||
| chr19:1038745 | T | G | 1 | a0001c0017t0021 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*845T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 845 | chr19 | 1038745 | ||||||
| chr19:1038845 | A | C | 1 | a0001c0002t0013 | 3 | HG01943.hp2 HG04184.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*945A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 945 | chr19 | 1038845 | ||||||
| chr19:1038850 | A | G | 1 | a0001c0005t0016 | 2 | HG03710.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*950A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 950 | chr19 | 1038850 | ||||||
| chr19:1038863 | C | G | 8 | a0001c0002t0012 a0001c0005t0007 a0001c0005t0008 others(5): Show |
38 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*963C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 963 | chr19 | 1038863 | ||||||
| chr19:1038872 | C | G | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(33): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*972C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 972 | chr19 | 1038872 | ||||||
| chr19:1038894 | C | T | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(33): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*994C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 994 | chr19 | 1038894 | ||||||
| chr19:1038896 | C | T | 1 | a0001c0001t0030 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*996C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 996 | chr19 | 1038896 | ||||||
| chr19:1038924 | C | T | 2 | a0001c0001t0011 a0001c0015t0011 |
8 | HG02630.hp2 HG02647.hp1 HG03209.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1024C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 1024 | chr19 | 1038924 | ||||||
| chr19:1038926 | G | A | 3 | a0001c0001t0010 a0001c0003t0010 a0001c0009t0010 |
9 | HG02145.hp1 HG02451.hp1 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1026G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 1026 | chr19 | 1038926 | ||||||
| chr19:1038948 | C | G | 1 | a0001c0001t0026 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1048C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 1048 | chr19 | 1038948 | ||||||
| chr19:1038950 | G | C | 1 | a0001c0001t0026 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1050G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 1050 | chr19 | 1038950 | ||||||
| chr19:1038996 | A | C | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(37): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
3_prime_UTR_variant | MODIFIER | c.*1096A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 1096 | chr19 | 1038996 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:1026845 | C | G | 11 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0214 others(8): Show |
11 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+121C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1026845 | |||||||
| chr19:1026849 | C | G | 7 | a0001c0001t0001g0023 a0001c0001t0001g0205 a0001c0001t0001g0206 others(4): Show |
9 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+125C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1026849 | |||||||
| chr19:1026928 | G | A | 9 | a0001c0001t0001g0051 a0001c0002t0004g0025 a0001c0003t0003g0013 others(6): Show |
16 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+204G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1026928 | |||||||
| chr19:1026958 | T | TC | 62 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0044 others(59): Show |
100 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.63+243dupC | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1026958 | ||||||
| chr19:1026962 | C | CA | 3 | a0001c0001t0001g0053 a0001c0001t0002g0026 a0001c0001t0014g0026 |
3 | HG00597.hp2 NA18949.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.63+238_63+239insA | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1026962 | |||||||
| chr19:1026965 | C | G | 1 | a0001c0001t0006g0022 | 3 | HG03579.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.63+241C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1026965 | |||||||
| chr19:1027064 | G | A | 1 | a0001c0005t0008g0024 | 2 | HG00609.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.63+340G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027064 | |||||||
| chr19:1027181 | G | A | 1 | a0001c0001t0006g0054 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.63+457G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027181 | |||||||
| chr19:1027287 | G | T | 20 | a0001c0001t0001g0051 a0001c0001t0001g0211 a0001c0001t0001g0213 others(17): Show |
27 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.63+563G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027287 | |||||||
| chr19:1027344 | G | T | 10 | a0001c0001t0001g0051 a0001c0002t0004g0025 a0001c0003t0003g0013 others(7): Show |
17 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.63+620G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027344 | |||||||
| chr19:1027372 | T | A | 1 | a0001c0018t0008g0167 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.63+648T>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027372 | |||||||
| chr19:1027416 | C | T | 1 | a0001c0001t0011g0166 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.63+692C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027416 | |||||||
| chr19:1027502 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0011g0165 a0001c0003t0010g0163 others(1): Show |
5 | HG02451.hp1 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+778C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027502 | |||||||
| chr19:1027611 | G | A | 10 | a0001c0001t0001g0051 a0001c0002t0004g0025 a0001c0003t0003g0013 others(7): Show |
17 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.63+887G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027611 | |||||||
| chr19:1027621 | C | A | 1 | a0001c0001t0030g0204 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.63+897C>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027621 | |||||||
| chr19:1027641 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0055 a0001c0001t0001g0168 |
5 | HG01516.hp2 HG02738.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+917G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027641 | |||||||
| chr19:1027741 | C | T | 1 | a0001c0004t0003g0162 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.63+1017C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027741 | |||||||
| chr19:1027798 | A | C | 70 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0161 others(67): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.63+1074A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027798 | |||||||
| chr19:1027873 | G | C | 1 | a0001c0001t0034g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.63+1149G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027873 | |||||||
| chr19:1027905 | T | C | 1 | a0001c0005t0008g0050 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.63+1181T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027905 | |||||||
| chr19:1028144 | G | C | 1 | a0001c0001t0001g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.63+1420G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1028144 | |||||||
| chr19:1028150 | G | A | 27 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0146 others(24): Show |
47 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.63+1426G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1028150 | |||||||
| chr19:1028298 | G | T | 1 | a0001c0006t0007g0040 | 2 | HG03490.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.63+1574G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1028298 | |||||||
| chr19:1028383 | C | T | 1 | a0001c0011t0004g0149 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.63+1659C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1028383 | |||||||
| chr19:1028404 | AG | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0055 a0001c0001t0001g0168 others(1): Show |
6 | HG01516.hp2 HG02559.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+1683delG | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1028404 | ||||||
| chr19:1028435 | C | G | 9 | a0001c0001t0001g0051 a0001c0002t0004g0025 a0001c0003t0003g0013 others(6): Show |
15 | HG00438.hp2 HG02083.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.63+1711C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1028435 | |||||||
| chr19:1028969 | G | GTCAGGGG others(33): Show |
1 | a0001c0013t0001g0056 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.64-2063_64-2062ins others(40): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1028969 | ||||||
| chr19:1028980 | C | G | 13 | a0001c0001t0001g0051 a0001c0001t0001g0130 a0001c0003t0003g0013 others(10): Show |
19 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-2091C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1028980 | |||||||
| chr19:1029023 | TCCCAAAT others(33): Show |
T | 1 | a0001c0018t0008g0167 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.64-2040_64-2001del others(40): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029023 | ||||||
| chr19:1029031 | A | C | 12 | a0001c0001t0001g0051 a0001c0001t0001g0130 a0001c0003t0003g0013 others(9): Show |
18 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-2040A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029031 | |||||||
| chr19:1029031 | AATCCCAG others(471): Show |
A | 4 | a0001c0002t0004g0007 a0001c0002t0004g0025 a0001c0002t0004g0112 others(1): Show |
10 | HG01071.hp1 HG01123.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-1982_64-1505del | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029031 | ||||||
| chr19:1029046 | CAGCTCAG others(152): Show |
C | 1 | a0001c0001t0009g0117 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.64-1902_64-1744del | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029046 | ||||||
| chr19:1029049 | C | G | 1 | a0001c0001t0011g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64-2022C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029049 | |||||||
| chr19:1029101 | T | C | 23 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(20): Show |
33 | HG01516.hp2 HG01891.hp2 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-1970T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029101 | |||||||
| chr19:1029129 | CTCAGGGG others(431): Show |
C | 24 | a0001c0001t0001g0042 a0001c0001t0005g0005 a0001c0001t0005g0009 others(21): Show |
34 | HG00733.hp1 HG01109.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.64-1920_64-1483del | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029129 | ||||||
| chr19:1029169 | CTCAGGGG others(391): Show |
C | 32 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(29): Show |
43 | HG01516.hp2 HG01891.hp2 HG01943.hp2 others(40): Show |
intron_variant | MODIFIER | c.64-1888_64-1491del | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029169 | ||||||
| chr19:1029176 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.64-1895G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029176 | |||||||
| chr19:1029275 | CAGGCAGG others(192): Show |
C | 10 | a0001c0001t0006g0018 a0001c0001t0006g0121 a0001c0001t0006g0123 others(7): Show |
12 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-1743_64-1545del | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029275 | ||||||
| chr19:1029331 | A | C | 1 | a0001c0001t0015g0083 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.64-1740A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029331 | |||||||
| chr19:1029340 | TACCCAAA others(73): Show |
T | 11 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0214 others(8): Show |
11 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-1707_64-1628del others(80): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029340 | ||||||
| chr19:1029364 | T | TAGCTCAG others(33): Show |
1 | a0001c0005t0008g0200 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-1637_64-1598dup others(40): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029364 | ||||||
| chr19:1029414 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.64-1657G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029414 | |||||||
| chr19:1029474 | T | C | 112 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0047 others(109): Show |
176 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.64-1597T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029474 | |||||||
| chr19:1029527 | C | A | 1 | a0001c0001t0027g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64-1544C>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029527 | |||||||
| chr19:1029567 | G | C | 10 | a0001c0001t0006g0018 a0001c0001t0006g0121 a0001c0001t0006g0123 others(7): Show |
12 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-1504G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029567 | |||||||
| chr19:1029637 | C | T | 1 | a0001c0001t0009g0199 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.64-1434C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029637 | |||||||
| chr19:1029708 | C | CT | 67 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(64): Show |
90 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(87): Show |
intron_variant | MODIFIER | c.64-1352dupT | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029708 | ||||||
| chr19:1029801 | G | A | 8 | a0001c0001t0005g0041 a0001c0001t0005g0156 a0001c0001t0005g0203 others(5): Show |
9 | HG02145.hp1 HG02486.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-1270G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029801 | |||||||
| chr19:1029831 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.64-1240C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029831 | |||||||
| chr19:1029989 | G | A | 1 | a0001c0001t0014g0170 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64-1082G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029989 | |||||||
| chr19:1029993 | C | T | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(54): Show |
79 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(76): Show |
intron_variant | MODIFIER | c.64-1078C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029993 | |||||||
| chr19:1030015 | C | T | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(54): Show |
79 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(76): Show |
intron_variant | MODIFIER | c.64-1056C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030015 | |||||||
| chr19:1030140 | G | A | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(54): Show |
79 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(76): Show |
intron_variant | MODIFIER | c.64-931G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030140 | |||||||
| chr19:1030163 | A | C | 47 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(44): Show |
67 | HG00733.hp1 HG01109.hp1 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.64-908A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030163 | |||||||
| chr19:1030169 | C | T | 47 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(44): Show |
67 | HG00733.hp1 HG01109.hp1 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.64-902C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030169 | |||||||
| chr19:1030170 | A | G | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(54): Show |
79 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(76): Show |
intron_variant | MODIFIER | c.64-901A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030170 | |||||||
| chr19:1030282 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | NA18973.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.64-789C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030282 | |||||||
| chr19:1030304 | C | T | 1 | a0001c0004t0003g0147 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.64-767C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030304 | |||||||
| chr19:1030305 | G | C | 47 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(44): Show |
67 | HG00733.hp1 HG01109.hp1 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.64-766G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030305 | |||||||
| chr19:1030321 | G | T | 61 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0047 others(58): Show |
99 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.64-750G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030321 | |||||||
| chr19:1030352 | C | T | 1 | a0001c0001t0011g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64-719C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030352 | |||||||
| chr19:1030365 | A | G | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(54): Show |
79 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(76): Show |
intron_variant | MODIFIER | c.64-706A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030365 | |||||||
| chr19:1030432 | T | C | 171 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0021 others(168): Show |
258 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.64-639T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030432 | |||||||
| chr19:1030478 | G | T | 49 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(46): Show |
69 | HG00733.hp1 HG01109.hp1 HG01123.hp2 others(66): Show |
intron_variant | MODIFIER | c.64-593G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030478 | |||||||
| chr19:1030482 | T | C | 2 | a0001c0001t0002g0049 a0001c0001t0009g0049 |
2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.64-589T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030482 | |||||||
| chr19:1030487 | C | G | 2 | a0001c0001t0002g0049 a0001c0001t0009g0049 |
2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.64-584C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030487 | |||||||
| chr19:1030495 | G | A | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | NA18980.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.64-576G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030495 | |||||||
| chr19:1030550 | G | C | 37 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(34): Show |
50 | HG01109.hp2 HG01516.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.64-521G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030550 | |||||||
| chr19:1030571 | A | G | 1 | a0001c0002t0004g0202 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.64-500A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030571 | |||||||
| chr19:1030593 | T | C | 1 | a0003c0012t0005g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.64-478T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030593 | |||||||
| chr19:1030594 | C | T | 1 | a0003c0012t0005g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.64-477C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030594 | |||||||
| chr19:1030612 | T | C | 1 | a0001c0011t0004g0149 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.64-459T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030612 | |||||||
| chr19:1030634 | T | G | 1 | a0001c0001t0002g0179 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.64-437T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030634 | |||||||
| chr19:1030651 | C | G | 178 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0021 others(175): Show |
266 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.64-420C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030651 | |||||||
| chr19:1030760 | G | C | 1 | a0001c0001t0001g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64-311G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030760 | |||||||
| chr19:1030767 | G | A | 21 | a0001c0001t0005g0005 a0001c0001t0005g0009 a0001c0001t0005g0068 others(18): Show |
30 | HG00733.hp1 HG00733.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.64-304G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030767 | |||||||
| chr19:1030788 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.64-283G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030788 | |||||||
| chr19:1030794 | C | T | 1 | a0001c0001t0028g0114 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.64-277C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030794 | |||||||
| chr19:1030903 | A | G | 6 | a0001c0001t0006g0018 a0001c0001t0006g0124 a0001c0001t0006g0127 others(3): Show |
8 | HG01109.hp2 HG01884.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-168A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030903 | |||||||
| chr19:1030957 | G | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(231): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.64-114G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030957 | |||||||
| chr19:1030997 | C | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0002g0196 |
3 | NA18955.hp2 NA18964.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.64-74C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030997 | |||||||
| chr19:1031051 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64-20C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1031051 | |||||||
| chr19:1031213 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(206): Show |
322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.185+21A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031213 | |||||||
| chr19:1031249 | A | C | 5 | a0001c0001t0006g0150 a0001c0003t0003g0008 a0001c0003t0003g0151 others(2): Show |
11 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.185+57A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031249 | |||||||
| chr19:1031286 | G | A | 1 | a0001c0001t0011g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.185+94G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031286 | |||||||
| chr19:1031330 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(97): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.185+138G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031330 | |||||||
| chr19:1031338 | T | TCGGGGG | 13 | a0001c0001t0001g0051 a0001c0001t0001g0130 a0001c0003t0003g0013 others(10): Show |
19 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.185+146_185+147ins others(6): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031338 | |||||||
| chr19:1031338 | T | TG | 5 | a0001c0001t0005g0041 a0001c0001t0005g0156 a0001c0003t0003g0036 others(2): Show |
7 | HG01175.hp1 HG02486.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+148dupG | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031338 | ||||||
| chr19:1031338 | T | TGG | 4 | a0001c0001t0001g0161 a0001c0001t0005g0203 a0001c0003t0010g0160 others(1): Show |
4 | HG02145.hp1 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+147_185+148dup others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031338 | ||||||
| chr19:1031338 | T | TGGGGGGG others(1): Show |
28 | a0001c0001t0001g0047 a0001c0001t0001g0194 a0001c0001t0001g0198 others(25): Show |
33 | HG00140.hp1 HG00423.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.185+148_185+149ins others(8): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031338 | ||||||
| chr19:1031339 | G | GGGGGGGA | 71 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0053 others(68): Show |
124 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.185+148_185+149ins others(7): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031339 | ||||||
| chr19:1031340 | G | A | 13 | a0001c0001t0001g0051 a0001c0001t0001g0130 a0001c0003t0003g0013 others(10): Show |
19 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.185+148G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031340 | |||||||
| chr19:1031340 | G | GGGGGGA | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(103): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.185+148_185+149ins others(6): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031340 | |||||||
| chr19:1031341 | C | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(246): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.185+149C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031341 | |||||||
| chr19:1031439 | C | T | 88 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0047 others(85): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.185+247C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031439 | |||||||
| chr19:1031444 | A | C | 1 | a0001c0001t0002g0146 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.185+252A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031444 | |||||||
| chr19:1031444 | A | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0175 |
2 | HG02071.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.185+252A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031444 | |||||||
| chr19:1031479 | T | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(231): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.185+287T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031479 | |||||||
| chr19:1031480 | G | A | 21 | a0001c0001t0005g0005 a0001c0001t0005g0009 a0001c0001t0005g0068 others(18): Show |
30 | HG00733.hp1 HG00733.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.185+288G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031480 | |||||||
| chr19:1031490 | G | A | 2 | a0001c0006t0007g0132 a0001c0006t0007g0139 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.185+298G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031490 | |||||||
| chr19:1031539 | G | A | 1 | a0001c0001t0006g0121 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.185+347G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031539 | |||||||
| chr19:1031551 | C | T | 88 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0047 others(85): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.185+359C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031551 | |||||||
| chr19:1031564 | C | CA | 27 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0082 others(24): Show |
42 | HG00408.hp1 HG00438.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.185+398dupA | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031564 | ||||||
| chr19:1031564 | C | CAA | 7 | a0001c0001t0005g0068 a0001c0001t0005g0069 a0001c0001t0005g0081 others(4): Show |
7 | HG00733.hp2 HG01978.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+397_185+398dup others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031564 | ||||||
| chr19:1031564 | CA | C | 26 | a0001c0001t0001g0051 a0001c0001t0001g0100 a0001c0001t0001g0101 others(23): Show |
38 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.185+398delA | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031564 | ||||||
| chr19:1031564 | CAAAAAAA | C | 37 | a0001c0001t0002g0181 a0001c0001t0002g0192 a0001c0001t0005g0041 others(34): Show |
60 | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.185+392_185+398del others(7): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031564 | ||||||
| chr19:1031564 | CAAAAAAA others(1): Show |
C | 59 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0047 others(56): Show |
97 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.185+391_185+398del others(8): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031564 | ||||||
| chr19:1031601 | C | T | 1 | a0001c0007t0002g0138 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.185+409C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031601 | |||||||
| chr19:1031622 | T | C | 1 | a0001c0004t0003g0134 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.185+430T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031622 | |||||||
| chr19:1031638 | G | A | 1 | a0001c0001t0005g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.185+446G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031638 | |||||||
| chr19:1031659 | A | G | 134 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0047 others(131): Show |
202 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.185+467A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031659 | |||||||
| chr19:1031670 | A | G | 1 | a0001c0001t0011g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.185+478A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031670 | |||||||
| chr19:1031683 | C | T | 1 | a0001c0005t0007g0035 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.185+491C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031683 | |||||||
| chr19:1031813 | G | T | 233 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(230): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.186-579G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031813 | |||||||
| chr19:1032004 | C | T | 2 | a0001c0008t0019g0020 a0001c0008t0020g0020 |
3 | HG02055.hp2 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.186-388C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032004 | |||||||
| chr19:1032010 | A | C | 1 | a0003c0012t0005g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.186-382A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032010 | |||||||
| chr19:1032030 | C | G | 1 | a0001c0005t0007g0035 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.186-362C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032030 | |||||||
| chr19:1032101 | A | G | 1 | a0001c0001t0011g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.186-291A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032101 | |||||||
| chr19:1032121 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0002g0116 a0001c0001t0002g0172 others(2): Show |
5 | NA18954.hp2 NA18967.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-271G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032121 | |||||||
| chr19:1032155 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.186-237A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032155 | |||||||
| chr19:1032159 | C | T | 1 | a0001c0001t0002g0001 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.186-233C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032159 | |||||||
| chr19:1032229 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(74): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.186-163C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032229 | |||||||
| chr19:1032234 | C | CA | 29 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0086 others(26): Show |
30 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.186-141dupA | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1032234 | ||||||
| chr19:1032234 | C | CAA | 22 | a0001c0001t0001g0042 a0001c0001t0005g0005 a0001c0001t0005g0009 others(19): Show |
32 | HG00733.hp1 HG00733.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.186-142_186-141dup others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1032234 | ||||||
| chr19:1032234 | CA | C | 13 | a0001c0001t0001g0064 a0001c0001t0001g0102 a0001c0001t0002g0180 others(10): Show |
15 | HG01109.hp2 HG01168.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.186-141delA | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1032234 | ||||||
| chr19:1032241 | A | C | 1 | a0001c0001t0011g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.186-151A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032241 | |||||||
| chr19:1032251 | A | AG | 22 | a0001c0004t0003g0003 a0001c0004t0003g0019 a0001c0004t0003g0133 others(19): Show |
42 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.186-140dupG | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1032251 | ||||||
| chr19:1032251 | A | G | 1 | a0001c0017t0021g0137 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.186-141A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032251 | |||||||
| chr19:1032324 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.186-68C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032324 | |||||||
| chr19:1032335 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.186-57G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032335 | |||||||
| chr19:1032336 | G | T | 1 | a0001c0001t0002g0180 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.186-56G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032336 | |||||||
| chr19:1032344 | C | A | 1 | a0003c0012t0005g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.186-48C>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032344 | |||||||
| chr19:1032370 | C | T | 202 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(199): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.186-22C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032370 | |||||||
| chr19:1032371 | G | A | 1 | a0001c0001t0011g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.186-21G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032371 | |||||||
| chr19:1032475 | G | T | 11 | a0001c0001t0005g0009 a0001c0001t0005g0069 a0001c0001t0005g0073 others(8): Show |
13 | HG00733.hp1 HG00733.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.252+17G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 3/6 | chr19 | 1032475 | |||||||
| chr19:1032703 | C | T | 65 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0047 others(62): Show |
103 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
splice_region_variant&intron_variant | LOW | c.390+7C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032703 | |||||||
| chr19:1032741 | G | C | 4 | a0001c0001t0001g0042 a0001c0001t0034g0131 a0001c0003t0010g0163 others(1): Show |
5 | HG02451.hp1 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+45G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032741 | |||||||
| chr19:1032757 | C | T | 70 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(67): Show |
109 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.390+61C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032757 | |||||||
| chr19:1032779 | TTC | T | 25 | a0001c0004t0003g0003 a0001c0004t0003g0017 a0001c0004t0003g0019 others(22): Show |
47 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.390+85_390+86delCT | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1032779 | ||||||
| chr19:1032863 | C | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0097 a0001c0001t0001g0173 |
3 | NA18947.hp1 NA18956.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.390+167C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032863 | |||||||
| chr19:1032872 | A | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(239): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.390+176A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032872 | |||||||
| chr19:1032875 | T | G | 1 | a0003c0012t0005g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.390+179T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032875 | |||||||
| chr19:1032882 | G | A | 1 | a0001c0001t0006g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.390+186G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032882 | |||||||
| chr19:1032941 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG00597.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.390+245G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032941 | |||||||
| chr19:1033191 | G | A | 12 | a0001c0001t0001g0051 a0001c0003t0003g0013 a0001c0003t0003g0052 others(9): Show |
18 | HG00438.hp2 HG00609.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.390+495G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033191 | |||||||
| chr19:1033244 | G | A | 1 | a0001c0001t0030g0204 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.390+548G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033244 | |||||||
| chr19:1033355 | T | C | 1 | a0001c0002t0004g0183 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.390+659T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033355 | |||||||
| chr19:1033361 | A | T | 87 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0047 others(84): Show |
128 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.390+665A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033361 | |||||||
| chr19:1033379 | G | T | 2 | a0001c0001t0011g0111 a0001c0001t0011g0165 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.390+683G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033379 | |||||||
| chr19:1033411 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(85): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.390+715G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033411 | |||||||
| chr19:1033463 | T | C | 2 | a0001c0001t0002g0184 a0001c0002t0004g0189 |
2 | HG03831.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.390+767T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033463 | |||||||
| chr19:1033560 | G | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(94): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.390+864G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033560 | |||||||
| chr19:1033586 | T | C | 1 | a0001c0003t0003g0151 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.390+890T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033586 | |||||||
| chr19:1033625 | A | T | 1 | a0001c0003t0003g0089 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.390+929A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033625 | |||||||
| chr19:1033638 | G | A | 1 | a0001c0002t0004g0201 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.390+942G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033638 | |||||||
| chr19:1033655 | A | ACG | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+959_390+960ins others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033655 | |||||||
| chr19:1033655 | AGTGTCTG others(29): Show |
A | 78 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(75): Show |
126 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.390+1011_390+1046d others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033655 | ||||||
| chr19:1033655 | AGTGTCTG others(379): Show |
A | 7 | a0001c0001t0006g0018 a0001c0001t0006g0121 a0001c0001t0006g0124 others(4): Show |
9 | HG01884.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+1029_390+1414d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033655 | ||||||
| chr19:1033655 | AGTGTCTG others(1223): Show |
A | 20 | a0001c0003t0003g0013 a0001c0003t0031g0013 a0001c0004t0003g0003 others(17): Show |
41 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+993_391-1212de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033655 | ||||||
| chr19:1033655 | AGTGTCTG others(1293): Show |
A | 1 | a0001c0007t0001g0143 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.390+993_391-1142de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033655 | ||||||
| chr19:1033657 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+961T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033657 | |||||||
| chr19:1033671 | CGGGAGCG others(1433): Show |
C | 1 | a0001c0001t0002g0185 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.390+1011_391-984de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033671 | ||||||
| chr19:1033672 | G | C | 9 | a0001c0001t0001g0051 a0001c0005t0008g0011 a0001c0005t0008g0012 others(6): Show |
14 | HG00438.hp2 HG00609.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.390+976G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033672 | |||||||
| chr19:1033674 | G | C | 3 | a0001c0001t0006g0022 a0001c0001t0022g0063 a0001c0001t0025g0061 |
5 | HG02451.hp2 HG02895.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+978G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033674 | |||||||
| chr19:1033678 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.390+982G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033678 | |||||||
| chr19:1033679 | TGGGTGGG others(1224): Show |
T | 1 | a0001c0003t0003g0052 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.390+986_391-1218de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033679 | ||||||
| chr19:1033686 | GAC | G | 4 | a0001c0004t0003g0133 a0001c0004t0003g0135 a0001c0004t0003g0136 others(1): Show |
4 | HG02293.hp1 HG03688.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+993_390+994del others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033686 | ||||||
| chr19:1033688 | CACGGTGT others(203): Show |
C | 3 | a0001c0001t0006g0054 a0001c0001t0022g0063 a0001c0001t0025g0061 |
3 | HG01943.hp1 HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.390+1084_390+1293d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033688 | ||||||
| chr19:1033691 | GGTGTCTG others(449): Show |
G | 1 | a0001c0001t0001g0051 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.390+996_390+1451de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033691 | |||||||
| chr19:1033692 | G | T | 9 | a0001c0001t0001g0188 a0001c0001t0002g0046 a0001c0001t0002g0048 others(6): Show |
9 | HG01099.hp2 HG01975.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+996G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033692 | |||||||
| chr19:1033693 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+997T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033693 | |||||||
| chr19:1033707 | C | G | 13 | a0001c0001t0001g0188 a0001c0001t0002g0046 a0001c0001t0002g0048 others(10): Show |
16 | HG01099.hp2 HG01123.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.390+1011C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033707 | |||||||
| chr19:1033707 | CGGGAGCG others(99): Show |
C | 4 | a0001c0001t0006g0123 a0001c0001t0006g0127 a0001c0001t0006g0128 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1029_390+1134d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033707 | ||||||
| chr19:1033710 | GAGCGTGG others(1151): Show |
G | 1 | a0001c0004t0003g0135 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.390+1047_391-1230d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033710 | ||||||
| chr19:1033716 | GGGTGGGA others(1220): Show |
G | 1 | a0001c0004t0003g0133 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.390+1023_391-1185d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033716 | ||||||
| chr19:1033722 | GAC | G | 11 | a0001c0001t0001g0188 a0001c0001t0002g0046 a0001c0001t0002g0048 others(8): Show |
11 | HG01099.hp2 HG01123.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.390+1029_390+1030d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033722 | ||||||
| chr19:1033724 | CACGGTGT others(237): Show |
C | 1 | a0001c0002t0013g0028 | 2 | HG01943.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.390+1047_390+1290d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033724 | ||||||
| chr19:1033728 | G | T | 50 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0053 others(47): Show |
88 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.390+1032G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033728 | |||||||
| chr19:1033729 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1033T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033729 | |||||||
| chr19:1033743 | G | C | 17 | a0001c0001t0001g0188 a0001c0001t0002g0046 a0001c0001t0002g0048 others(14): Show |
25 | HG01099.hp2 HG01106.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.390+1047G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033743 | |||||||
| chr19:1033743 | GGGGAGCG others(133): Show |
G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(61): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.390+1187_390+1326d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033743 | ||||||
| chr19:1033743 | GGGGAGCG others(377): Show |
G | 8 | a0001c0005t0008g0011 a0001c0005t0008g0012 a0001c0005t0008g0024 others(5): Show |
13 | HG00438.hp2 HG00609.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.390+1065_390+1448d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033743 | ||||||
| chr19:1033743 | GGGGAGCG others(447): Show |
G | 1 | a0001c0001t0002g0090 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.390+1065_390+1518d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033743 | ||||||
| chr19:1033746 | GAGCGTGG others(483): Show |
G | 2 | a0001c0001t0005g0073 a0001c0002t0004g0074 |
2 | HG01123.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.390+1065_390+1554d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033746 | ||||||
| chr19:1033758 | G | GAC | 7 | a0001c0001t0009g0046 a0001c0002t0004g0201 a0001c0002t0012g0195 others(4): Show |
13 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.390+1063_390+1064d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033758 | ||||||
| chr19:1033758 | G | GACACCGT others(65): Show |
6 | a0001c0001t0001g0188 a0001c0001t0002g0046 a0001c0001t0002g0048 others(3): Show |
6 | HG01099.hp2 HG01975.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+1064_390+1065i others(74): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033758 | ||||||
| chr19:1033758 | GACGGTGT others(555): Show |
G | 1 | a0001c0011t0004g0140 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.390+1117_390+1678d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033758 | ||||||
| chr19:1033761 | G | C | 3 | a0001c0001t0009g0046 a0001c0002t0004g0201 a0001c0002t0012g0195 |
3 | HG03017.hp2 HG03516.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.390+1065G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033761 | |||||||
| chr19:1033763 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1067T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033763 | |||||||
| chr19:1033774 | GACCGGGA others(1291): Show |
G | 2 | a0001c0001t0001g0062 a0001c0001t0005g0065 |
2 | HG02965.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.390+1135_391-1002d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033774 | ||||||
| chr19:1033777 | C | G | 3 | a0001c0001t0009g0046 a0001c0002t0004g0201 a0001c0002t0012g0195 |
3 | HG03017.hp2 HG03516.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.390+1081C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033777 | |||||||
| chr19:1033780 | G | C | 3 | a0001c0001t0001g0047 a0001c0001t0006g0022 a0001c0001t0006g0038 |
5 | HG03579.hp2 HG03834.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+1084G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033780 | |||||||
| chr19:1033780 | G | GAGCGTGG others(63): Show |
6 | a0001c0001t0001g0188 a0001c0001t0002g0046 a0001c0001t0002g0048 others(3): Show |
6 | HG01099.hp2 HG01975.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+1117_390+1186d others(72): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033780 | ||||||
| chr19:1033780 | GAGCGTGG others(203): Show |
G | 1 | a0001c0001t0001g0213 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.390+1154_390+1363d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033780 | ||||||
| chr19:1033780 | GAGCGTGG others(765): Show |
G | 1 | a0001c0003t0003g0089 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.390+1187_391-1476d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033780 | ||||||
| chr19:1033795 | ACG | A | 3 | a0001c0001t0009g0046 a0001c0002t0004g0201 a0001c0002t0012g0195 |
3 | HG03017.hp2 HG03516.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.390+1100_390+1101d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033795 | |||||||
| chr19:1033797 | G | C | 76 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(73): Show |
124 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.390+1101G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033797 | |||||||
| chr19:1033799 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1103T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033799 | |||||||
| chr19:1033813 | G | C | 9 | a0001c0001t0006g0022 a0001c0001t0009g0046 a0001c0002t0004g0201 others(6): Show |
17 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.390+1117G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033813 | |||||||
| chr19:1033813 | GGGGAGCG others(449): Show |
G | 8 | a0001c0001t0001g0053 a0001c0001t0005g0009 a0001c0001t0005g0069 others(5): Show |
10 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.390+1154_390+1609d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033813 | ||||||
| chr19:1033814 | G | A | 3 | a0001c0001t0009g0046 a0001c0002t0004g0201 a0001c0002t0012g0195 |
3 | HG03017.hp2 HG03516.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.390+1118G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033814 | |||||||
| chr19:1033828 | G | GAC | 7 | a0001c0001t0009g0046 a0001c0002t0004g0201 a0001c0002t0012g0195 others(4): Show |
13 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.390+1133_390+1134d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033828 | ||||||
| chr19:1033828 | GACGGTGT others(1117): Show |
G | 1 | a0001c0001t0006g0022 | 3 | HG03579.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.390+1154_391-1157d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033828 | ||||||
| chr19:1033831 | G | A | 69 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(66): Show |
114 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.390+1135G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033831 | |||||||
| chr19:1033833 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1137T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033833 | |||||||
| chr19:1033848 | G | A | 49 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0197 others(46): Show |
86 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.390+1152G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033848 | |||||||
| chr19:1033850 | C | G | 81 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(78): Show |
132 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.390+1154C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033850 | |||||||
| chr19:1033864 | CACGGTGT others(27): Show |
C | 65 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(62): Show |
110 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.390+1205_390+1238d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033864 | ||||||
| chr19:1033864 | CACGGTGT others(519): Show |
C | 2 | a0001c0002t0004g0009 a0001c0002t0004g0076 |
2 | HG00733.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.390+1205_391-1704d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033864 | ||||||
| chr19:1033864 | CACGGTGT others(1291): Show |
C | 1 | a0001c0004t0003g0136 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.390+1187_391-950de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033864 | ||||||
| chr19:1033868 | G | T | 4 | a0001c0001t0006g0123 a0001c0001t0006g0127 a0001c0001t0006g0128 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1172G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033868 | |||||||
| chr19:1033869 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1173T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033869 | |||||||
| chr19:1033883 | C | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0029 others(18): Show |
25 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.390+1187C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033883 | |||||||
| chr19:1033886 | G | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0029 others(7): Show |
14 | HG00597.hp1 HG00639.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.390+1190G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033886 | |||||||
| chr19:1033886 | G | T | 1 | a0001c0001t0001g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+1190G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033886 | |||||||
| chr19:1033887 | AGCGTGGG others(236): Show |
A | 1 | a0001c0001t0001g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+1192_390+1434d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033887 | |||||||
| chr19:1033898 | G | GAC | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
9 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+1203_390+1204d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033898 | ||||||
| chr19:1033898 | G | GACACGGC others(103): Show |
1 | a0001c0003t0003g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.390+1204_390+1205i others(112): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033898 | ||||||
| chr19:1033898 | GACGGTGT others(169): Show |
G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0130 a0001c0001t0001g0168 |
3 | HG00099.hp2 HG01516.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.390+1239_390+1414d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033898 | ||||||
| chr19:1033903 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1207T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033903 | |||||||
| chr19:1033908 | G | C | 1 | a0001c0001t0001g0206 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.390+1212G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033908 | |||||||
| chr19:1033917 | C | G | 5 | a0001c0001t0011g0111 a0001c0001t0011g0165 a0001c0001t0022g0063 others(2): Show |
5 | HG02451.hp2 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+1221C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033917 | |||||||
| chr19:1033920 | G | C | 24 | a0001c0001t0001g0047 a0001c0001t0001g0161 a0001c0001t0001g0188 others(21): Show |
26 | HG01099.hp2 HG01243.hp1 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.390+1224G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033920 | |||||||
| chr19:1033934 | CACGGTGT others(97): Show |
C | 1 | a0001c0001t0001g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.390+1257_390+1360d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033934 | ||||||
| chr19:1033937 | GGTGTCTG others(203): Show |
G | 2 | a0001c0001t0001g0002 a0001c0001t0002g0145 |
2 | HG02080.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.390+1242_390+1451d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033937 | |||||||
| chr19:1033938 | GTGTCTGG others(203): Show |
G | 4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0174 others(1): Show |
4 | HG00639.hp1 HG00642.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+1257_390+1466d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033938 | ||||||
| chr19:1033939 | T | C | 6 | a0001c0001t0001g0091 a0001c0003t0003g0008 a0001c0003t0003g0151 others(3): Show |
12 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.390+1243T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033939 | |||||||
| chr19:1033953 | G | C | 5 | a0001c0001t0001g0211 a0001c0001t0022g0063 a0001c0001t0025g0061 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+1257G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033953 | |||||||
| chr19:1033953 | GGGGAGCG others(167): Show |
G | 4 | a0001c0001t0006g0123 a0001c0001t0006g0127 a0001c0001t0006g0128 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1275_390+1448d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033953 | ||||||
| chr19:1033956 | GAGCGTGG others(273): Show |
G | 2 | a0001c0008t0019g0020 a0001c0008t0020g0020 |
3 | HG02055.hp2 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.390+1275_390+1554d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033956 | ||||||
| chr19:1033968 | G | GAC | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
9 | HG01106.hp2 HG01192.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+1273_390+1274d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033968 | ||||||
| chr19:1033968 | G | GACACGGC others(31): Show |
1 | a0001c0003t0003g0008 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.390+1274_390+1275i others(40): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033968 | ||||||
| chr19:1033970 | CGGTGTCT others(1009): Show |
C | 2 | a0001c0001t0001g0091 a0001c0005t0007g0099 |
2 | HG01168.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.390+1275_391-1144d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033970 | |||||||
| chr19:1033973 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1277T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033973 | |||||||
| chr19:1033982 | T | A | 1 | a0003c0012t0005g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.390+1286T>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033982 | |||||||
| chr19:1033987 | C | G | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1291C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033987 | |||||||
| chr19:1033990 | C | G | 22 | a0001c0001t0001g0042 a0001c0001t0001g0211 a0001c0001t0005g0005 others(19): Show |
36 | HG01106.hp2 HG01192.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.390+1294C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033990 | |||||||
| chr19:1033992 | G | A | 1 | a0001c0001t0030g0204 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.390+1296G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033992 | |||||||
| chr19:1034008 | G | T | 2 | a0001c0001t0001g0211 a0001c0005t0008g0210 |
2 | HG04199.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.390+1312G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034008 | |||||||
| chr19:1034009 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1313T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034009 | |||||||
| chr19:1034023 | G | C | 7 | a0001c0001t0001g0211 a0001c0001t0009g0046 a0001c0001t0022g0063 others(4): Show |
7 | HG02451.hp2 HG02895.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+1327G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034023 | |||||||
| chr19:1034026 | G | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(46): Show |
84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.390+1330G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034026 | |||||||
| chr19:1034038 | G | GAC | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1343_390+1344d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034038 | ||||||
| chr19:1034038 | GACGGTGT others(275): Show |
G | 12 | a0001c0001t0002g0001 a0001c0001t0009g0001 a0001c0001t0009g0117 others(9): Show |
19 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.390+1451_391-1702d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034038 | ||||||
| chr19:1034040 | C | T | 1 | a0001c0002t0012g0195 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.390+1344C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034040 | |||||||
| chr19:1034043 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1347T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034043 | |||||||
| chr19:1034057 | C | G | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1361C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034057 | |||||||
| chr19:1034060 | G | C | 62 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(59): Show |
97 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.390+1364G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034060 | |||||||
| chr19:1034064 | G | A | 10 | a0001c0001t0001g0161 a0001c0001t0005g0041 a0001c0001t0005g0156 others(7): Show |
11 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.390+1368G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034064 | |||||||
| chr19:1034074 | CACGGTGT others(27): Show |
C | 1 | a0001c0001t0011g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.390+1415_390+1448d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034074 | ||||||
| chr19:1034077 | G | A | 9 | a0001c0001t0001g0161 a0001c0001t0005g0041 a0001c0001t0005g0156 others(6): Show |
10 | HG02486.hp1 HG02572.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.390+1381G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034077 | |||||||
| chr19:1034079 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1383T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034079 | |||||||
| chr19:1034093 | C | G | 10 | a0001c0001t0001g0211 a0001c0001t0009g0046 a0001c0002t0004g0201 others(7): Show |
16 | HG01106.hp2 HG01192.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.390+1397C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034093 | |||||||
| chr19:1034093 | CGGGAGCG others(345): Show |
C | 3 | a0001c0001t0014g0026 a0001c0002t0004g0001 a0001c0002t0004g0004 |
6 | HG00639.hp2 HG01081.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+1434_391-1649d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034093 | ||||||
| chr19:1034095 | G | T | 2 | a0001c0001t0001g0211 a0001c0005t0008g0210 |
2 | HG04199.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.390+1399G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034095 | |||||||
| chr19:1034096 | G | A | 2 | a0001c0001t0001g0211 a0001c0005t0008g0210 |
2 | HG04199.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.390+1400G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034096 | |||||||
| chr19:1034096 | GAGCGTGG others(133): Show |
G | 2 | a0001c0001t0022g0063 a0001c0001t0025g0061 |
2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.390+1415_390+1554d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034096 | ||||||
| chr19:1034108 | G | GAC | 4 | a0001c0001t0011g0111 a0001c0003t0003g0008 a0001c0003t0003g0153 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1413_390+1414d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034108 | ||||||
| chr19:1034108 | GACGGTGT others(205): Show |
G | 14 | a0001c0001t0001g0042 a0001c0001t0002g0001 a0001c0001t0002g0026 others(11): Show |
16 | HG00597.hp2 HG02056.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.390+1451_390+1662d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034108 | ||||||
| chr19:1034110 | CGGTGTCT others(61): Show |
C | 3 | a0001c0001t0001g0211 a0001c0003t0003g0151 a0001c0003t0003g0152 |
3 | HG02647.hp2 HG03486.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.390+1415_390+1482d others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034110 | |||||||
| chr19:1034113 | T | C | 2 | a0001c0003t0003g0008 a0001c0003t0003g0153 |
8 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.390+1417T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034113 | |||||||
| chr19:1034127 | C | G | 3 | a0001c0001t0011g0111 a0001c0003t0003g0008 a0001c0003t0003g0153 |
9 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+1431C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034127 | |||||||
| chr19:1034128 | G | C | 3 | a0001c0001t0006g0123 a0001c0001t0006g0127 a0001c0001t0006g0128 |
3 | HG01109.hp2 HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.390+1432G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034128 | |||||||
| chr19:1034129 | G | T | 4 | a0001c0001t0006g0123 a0001c0001t0006g0127 a0001c0001t0006g0128 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1433G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034129 | |||||||
| chr19:1034130 | G | A | 4 | a0001c0001t0006g0123 a0001c0001t0006g0127 a0001c0001t0006g0128 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1434G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034130 | |||||||
| chr19:1034130 | G | C | 46 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(43): Show |
71 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.390+1434G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034130 | |||||||
| chr19:1034134 | G | A | 1 | a0001c0003t0010g0160 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.390+1438G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034134 | |||||||
| chr19:1034144 | CACATTGT others(27): Show |
C | 1 | a0001c0003t0003g0008 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.390+1451_390+1484d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034144 | ||||||
| chr19:1034147 | A | G | 161 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(158): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.390+1451A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034147 | |||||||
| chr19:1034148 | T | G | 58 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(55): Show |
87 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.390+1452T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034148 | |||||||
| chr19:1034149 | T | C | 2 | a0001c0003t0003g0008 a0001c0003t0003g0153 |
6 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+1453T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034149 | |||||||
| chr19:1034163 | C | G | 50 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(47): Show |
79 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.390+1467C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034163 | |||||||
| chr19:1034178 | G | GAC | 4 | a0001c0001t0011g0111 a0001c0003t0003g0008 a0001c0003t0003g0153 others(1): Show |
8 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.390+1483_390+1484d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034178 | ||||||
| chr19:1034183 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1487T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034183 | |||||||
| chr19:1034197 | C | G | 5 | a0001c0001t0011g0111 a0001c0003t0003g0008 a0001c0003t0003g0151 others(2): Show |
11 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.390+1501C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034197 | |||||||
| chr19:1034200 | G | C | 44 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(41): Show |
69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.390+1504G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034200 | |||||||
| chr19:1034200 | GAGCGTGG others(29): Show |
G | 2 | a0001c0001t0009g0046 a0001c0003t0010g0160 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.390+1537_390+1572d others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034200 | ||||||
| chr19:1034204 | G | A | 3 | a0001c0001t0006g0123 a0001c0001t0006g0127 a0001c0001t0006g0128 |
3 | HG01109.hp2 HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.390+1508G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034204 | |||||||
| chr19:1034204 | GTGGGTGG others(625): Show |
G | 1 | a0001c0002t0004g0025 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.390+1661_391-1142d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034204 | ||||||
| chr19:1034212 | GAC | G | 3 | a0001c0001t0001g0211 a0001c0001t0011g0111 a0001c0005t0008g0210 |
3 | HG04199.hp1 NA18971.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.390+1519_390+1520d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034212 | ||||||
| chr19:1034217 | G | C | 1 | a0001c0001t0001g0051 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.390+1521G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034217 | |||||||
| chr19:1034219 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1523T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034219 | |||||||
| chr19:1034233 | G | C | 3 | a0001c0001t0001g0211 a0001c0001t0011g0111 a0001c0005t0008g0210 |
3 | HG04199.hp1 NA18971.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.390+1537G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034233 | |||||||
| chr19:1034234 | G | C | 7 | a0001c0001t0006g0018 a0001c0001t0006g0121 a0001c0001t0006g0124 others(4): Show |
9 | HG01884.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+1538G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034234 | |||||||
| chr19:1034235 | T | G | 60 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(57): Show |
91 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.390+1539T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034235 | |||||||
| chr19:1034236 | A | AGCGTGGG others(26): Show |
2 | a0001c0002t0004g0201 a0001c0002t0012g0195 |
2 | HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.390+1540_390+1541i others(35): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034236 | |||||||
| chr19:1034236 | A | C | 1 | a0001c0001t0011g0111 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.390+1540A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034236 | |||||||
| chr19:1034236 | A | G | 57 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(54): Show |
88 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.390+1540A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034236 | |||||||
| chr19:1034240 | G | A | 2 | a0001c0001t0002g0046 a0001c0001t0002g0048 |
2 | NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.390+1544G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034240 | |||||||
| chr19:1034248 | GAC | G | 45 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(42): Show |
70 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.390+1555_390+1556d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034248 | ||||||
| chr19:1034253 | G | C | 2 | a0001c0001t0005g0073 a0001c0002t0004g0074 |
2 | HG01123.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.390+1557G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034253 | |||||||
| chr19:1034254 | G | T | 4 | a0001c0001t0009g0046 a0001c0002t0004g0201 a0001c0002t0012g0195 others(1): Show |
4 | HG02145.hp1 HG03017.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+1558G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034254 | |||||||
| chr19:1034255 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1559T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034255 | |||||||
| chr19:1034266 | GACCGGGA others(799): Show |
G | 1 | a0001c0001t0002g0092 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.390+1591_391-1038d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034266 | ||||||
| chr19:1034269 | C | CGGGAGCG others(27): Show |
1 | a0001c0007t0001g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.390+1606_390+1607i others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034269 | ||||||
| chr19:1034269 | C | G | 13 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0005g0073 others(10): Show |
19 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.390+1573C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034269 | |||||||
| chr19:1034269 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.390+1573C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034269 | |||||||
| chr19:1034272 | G | C | 1 | a0001c0001t0011g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.390+1576G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034272 | |||||||
| chr19:1034275 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0130 a0001c0001t0001g0168 |
3 | HG00099.hp2 HG01516.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.390+1579C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034275 | |||||||
| chr19:1034276 | G | A | 1 | a0001c0003t0010g0160 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.390+1580G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034276 | |||||||
| chr19:1034276 | GTGGGTGG others(553): Show |
G | 1 | a0001c0001t0002g0090 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.390+1591_391-1284d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034276 | ||||||
| chr19:1034284 | G | GAC | 51 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(48): Show |
82 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.390+1589_390+1590d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034284 | ||||||
| chr19:1034284 | GACGGTGT others(29): Show |
G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0213 |
2 | HG00099.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.390+1661_390+1696d others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034284 | ||||||
| chr19:1034284 | GACGGTGT others(801): Show |
G | 2 | a0001c0001t0001g0023 a0001c0001t0005g0207 |
4 | HG02258.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1607_391-1020d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034284 | ||||||
| chr19:1034286 | CGGTGTCT others(693): Show |
C | 1 | a0001c0001t0011g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.390+1591_391-1144d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034286 | |||||||
| chr19:1034287 | G | A | 10 | a0001c0001t0001g0053 a0001c0001t0005g0009 a0001c0001t0005g0069 others(7): Show |
12 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.390+1591G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034287 | |||||||
| chr19:1034289 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1593T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034289 | |||||||
| chr19:1034300 | GACCGGGA others(765): Show |
G | 16 | a0001c0001t0001g0098 a0001c0001t0002g0088 a0001c0001t0002g0096 others(13): Show |
23 | HG00438.hp2 HG00609.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.390+1643_391-1020d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034300 | ||||||
| chr19:1034303 | C | G | 12 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0005g0208 others(9): Show |
18 | HG01106.hp2 HG01109.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.390+1607C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034303 | |||||||
| chr19:1034303 | CGGGAGCG others(871): Show |
C | 1 | a0001c0001t0001g0029 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.390+1678_391-879de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034303 | ||||||
| chr19:1034304 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0009g0001 |
2 | HG02280.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.390+1608G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034304 | |||||||
| chr19:1034304 | G | GGGAGCGT others(97): Show |
2 | a0001c0001t0001g0188 a0001c0002t0004g0190 |
2 | HG01099.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.390+1624_390+1625i others(106): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034304 | ||||||
| chr19:1034306 | G | C | 3 | a0001c0001t0011g0111 a0001c0008t0019g0020 a0001c0008t0020g0020 |
4 | HG02055.hp2 HG02615.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1610G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034306 | |||||||
| chr19:1034310 | G | A | 7 | a0001c0001t0006g0018 a0001c0001t0006g0121 a0001c0001t0006g0124 others(4): Show |
9 | HG01884.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+1614G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034310 | |||||||
| chr19:1034318 | GAC | G | 47 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(44): Show |
72 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.390+1625_390+1626d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034318 | ||||||
| chr19:1034322 | C | T | 1 | a0001c0001t0018g0002 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.390+1626C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034322 | |||||||
| chr19:1034325 | T | C | 5 | a0001c0001t0005g0208 a0001c0003t0003g0008 a0001c0003t0003g0151 others(2): Show |
11 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.390+1629T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034325 | |||||||
| chr19:1034339 | C | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(88): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.390+1643C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034339 | |||||||
| chr19:1034341 | G | T | 4 | a0001c0001t0009g0046 a0001c0002t0004g0201 a0001c0002t0012g0195 others(1): Show |
4 | HG02145.hp1 HG03017.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+1645G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034341 | |||||||
| chr19:1034342 | G | A | 4 | a0001c0001t0009g0046 a0001c0002t0004g0201 a0001c0002t0012g0195 others(1): Show |
4 | HG02145.hp1 HG03017.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+1646G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034342 | |||||||
| chr19:1034342 | G | C | 24 | a0001c0001t0001g0042 a0001c0001t0002g0001 a0001c0001t0002g0026 others(21): Show |
36 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.390+1646G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034342 | |||||||
| chr19:1034342 | GAGCGTGG others(273): Show |
G | 1 | a0001c0001t0001g0043 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.390+1679_391-1476d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034342 | ||||||
| chr19:1034354 | GAC | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0055 a0001c0001t0001g0168 others(11): Show |
17 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.390+1661_390+1662d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034354 | ||||||
| chr19:1034356 | CACGGTGT others(799): Show |
C | 1 | a0001c0001t0005g0208 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.390+1679_391-950de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034356 | ||||||
| chr19:1034359 | G | CGTGTCTG others(99): Show |
1 | a0001c0002t0004g0048 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.390+1662_390+1663i others(108): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034359 | |||||||
| chr19:1034360 | G | T | 44 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(41): Show |
69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.390+1664G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034360 | |||||||
| chr19:1034361 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1665T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034361 | |||||||
| chr19:1034375 | C | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(110): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.390+1679C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034375 | |||||||
| chr19:1034378 | G | C | 1 | a0001c0001t0011g0111 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.390+1682G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034378 | |||||||
| chr19:1034390 | G | GAC | 18 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0002g0046 others(15): Show |
26 | HG01106.hp2 HG01109.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.390+1695_390+1696d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034390 | ||||||
| chr19:1034390 | GACGGTGT others(695): Show |
G | 1 | a0001c0001t0015g0083 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.390+1713_391-1020d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034390 | ||||||
| chr19:1034390 | GACGGTGT others(801): Show |
G | 44 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(41): Show |
76 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.391-1686_391-879de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034390 | ||||||
| chr19:1034392 | C | T | 2 | a0001c0002t0012g0004 a0001c0002t0012g0186 |
2 | HG02300.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.390+1696C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034392 | |||||||
| chr19:1034392 | CGGTGTCT others(131): Show |
C | 10 | a0001c0001t0001g0055 a0001c0001t0001g0168 a0001c0001t0001g0214 others(7): Show |
10 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1697_391-1600d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034392 | |||||||
| chr19:1034392 | CGGTGTCT others(587): Show |
C | 1 | a0001c0001t0001g0051 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.390+1697_391-1144d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034392 | |||||||
| chr19:1034392 | CGGTGTCT others(657): Show |
C | 1 | a0001c0001t0001g0016 | 2 | HG00099.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.390+1697_391-1074d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034392 | |||||||
| chr19:1034395 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1699T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034395 | |||||||
| chr19:1034406 | GACCGGGA others(659): Show |
G | 1 | a0001c0001t0001g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.391-1667_391-1002d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034406 | ||||||
| chr19:1034409 | C | G | 40 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0085 others(37): Show |
50 | HG01106.hp2 HG01109.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.390+1713C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034409 | |||||||
| chr19:1034412 | G | C | 29 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0188 others(26): Show |
42 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.390+1716G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034412 | |||||||
| chr19:1034426 | CACGGTGT others(167): Show |
C | 1 | a0001c0001t0001g0105 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.391-1685_391-1512d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034426 | ||||||
| chr19:1034431 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1699T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034431 | |||||||
| chr19:1034442 | GACGGGGA others(623): Show |
G | 1 | a0001c0001t0001g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.391-1685_391-1056d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034442 | ||||||
| chr19:1034443 | ACGGGGAG others(28): Show |
A | 1 | a0003c0012t0005g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.391-1683_391-1649d others(37): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034443 | ||||||
| chr19:1034445 | G | C | 4 | a0001c0001t0001g0130 a0001c0001t0011g0111 a0001c0003t0003g0008 others(1): Show |
5 | HG00099.hp2 HG01192.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-1685G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034445 | |||||||
| chr19:1034445 | GGGGAGCG others(27): Show |
G | 40 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0197 others(37): Show |
65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.391-1682_391-1649d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034445 | ||||||
| chr19:1034445 | GGGGAGCG others(167): Show |
G | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.391-1682_391-1509d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034445 | ||||||
| chr19:1034445 | GGGGAGCG others(483): Show |
G | 4 | a0001c0001t0006g0123 a0001c0001t0006g0127 a0001c0001t0006g0128 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-1667_391-1178d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034445 | ||||||
| chr19:1034447 | G | T | 2 | a0001c0001t0002g0180 a0001c0014t0005g0009 |
2 | NA18956.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.391-1683G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034447 | |||||||
| chr19:1034448 | G | A | 2 | a0001c0001t0002g0180 a0001c0014t0005g0009 |
2 | NA18956.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.391-1682G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034448 | |||||||
| chr19:1034448 | GAGCGTGG others(97): Show |
G | 1 | a0001c0001t0001g0213 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.391-1667_391-1564d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034448 | ||||||
| chr19:1034448 | GAGCGTGG others(167): Show |
G | 1 | a0001c0003t0010g0160 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.391-1667_391-1494d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034448 | ||||||
| chr19:1034448 | GAGCGTGG others(413): Show |
G | 3 | a0001c0001t0005g0041 a0001c0001t0009g0046 a0001c0003t0010g0072 |
3 | HG02572.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.391-1667_391-1248d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034448 | ||||||
| chr19:1034452 | GTGGGTGG others(377): Show |
G | 5 | a0001c0001t0006g0018 a0001c0001t0006g0121 a0001c0001t0006g0124 others(2): Show |
7 | HG01884.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.391-1667_391-1284d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034452 | ||||||
| chr19:1034460 | G | GAC | 17 | a0001c0001t0001g0211 a0001c0001t0002g0046 a0001c0001t0002g0048 others(14): Show |
23 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.391-1669_391-1668d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034460 | ||||||
| chr19:1034462 | C | T | 1 | a0001c0008t0019g0020 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.391-1668C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034462 | |||||||
| chr19:1034462 | CGGTGTCT others(341): Show |
C | 5 | a0001c0001t0001g0161 a0001c0001t0005g0041 a0001c0001t0005g0156 others(2): Show |
5 | HG02486.hp1 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-1667_391-1320d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034462 | |||||||
| chr19:1034462 | CGGTGTCT others(517): Show |
C | 5 | a0001c0001t0001g0047 a0001c0001t0006g0038 a0001c0001t0022g0063 others(2): Show |
5 | HG01243.hp1 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-1667_391-1144d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034462 | |||||||
| chr19:1034465 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1665T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034465 | |||||||
| chr19:1034476 | GACCGGCA others(589): Show |
G | 3 | a0001c0008t0019g0020 a0001c0008t0020g0020 a0001c0011t0004g0140 |
4 | HG02055.hp2 HG02615.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-1648_391-1053d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034476 | ||||||
| chr19:1034479 | C | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0211 a0001c0001t0002g0046 others(11): Show |
18 | HG02895.hp1 HG02897.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.391-1651C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034479 | |||||||
| chr19:1034479 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0034g0131 a0001c0003t0010g0163 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-1651C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034479 | |||||||
| chr19:1034481 | G | T | 40 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0197 others(37): Show |
65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.391-1649G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034481 | |||||||
| chr19:1034482 | C | A | 40 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0197 others(37): Show |
65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.391-1648C>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034482 | |||||||
| chr19:1034482 | C | G | 36 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0130 others(33): Show |
46 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.391-1648C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034482 | |||||||
| chr19:1034482 | C | T | 1 | a0003c0012t0005g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.391-1648C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034482 | |||||||
| chr19:1034494 | GAC | G | 3 | a0001c0001t0002g0180 a0001c0001t0011g0111 a0001c0014t0005g0009 |
3 | NA18956.hp2 NA19043.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.391-1633_391-1632d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034494 | ||||||
| chr19:1034495 | A | T | 1 | a0001c0002t0004g0183 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.391-1635A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034495 | |||||||
| chr19:1034501 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1629T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034501 | |||||||
| chr19:1034515 | C | G | 30 | a0001c0001t0001g0014 a0001c0001t0001g0130 a0001c0001t0001g0211 others(27): Show |
44 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.391-1615C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034515 | |||||||
| chr19:1034518 | GAGCGTGG others(27): Show |
G | 1 | a0001c0001t0001g0130 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.391-1597_391-1564d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034518 | ||||||
| chr19:1034530 | G | GAC | 16 | a0001c0001t0001g0014 a0001c0001t0002g0046 a0001c0001t0002g0048 others(13): Show |
24 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.391-1599_391-1598d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034530 | ||||||
| chr19:1034534 | G | T | 1 | a0001c0001t0011g0111 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.391-1596G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034534 | |||||||
| chr19:1034535 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1595T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034535 | |||||||
| chr19:1034549 | C | G | 23 | a0001c0001t0001g0014 a0001c0001t0001g0055 a0001c0001t0001g0168 others(20): Show |
25 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.391-1581C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034549 | |||||||
| chr19:1034550 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.391-1580G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034550 | |||||||
| chr19:1034552 | C | G | 91 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0042 others(88): Show |
138 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.391-1578C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034552 | |||||||
| chr19:1034570 | G | T | 15 | a0001c0001t0001g0042 a0001c0001t0002g0001 a0001c0001t0002g0026 others(12): Show |
17 | HG00597.hp2 HG02056.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.391-1560G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034570 | |||||||
| chr19:1034571 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1559T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034571 | |||||||
| chr19:1034585 | G | C | 28 | a0001c0001t0001g0042 a0001c0001t0002g0001 a0001c0001t0002g0026 others(25): Show |
46 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.391-1545G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034585 | |||||||
| chr19:1034588 | GAGCGTGG others(27): Show |
G | 3 | a0001c0001t0001g0057 a0001c0001t0001g0211 a0001c0008t0019g0125 |
3 | HG02717.hp1 HG04199.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.391-1527_391-1494d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034588 | ||||||
| chr19:1034600 | G | GAC | 52 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0197 others(49): Show |
83 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.391-1529_391-1528d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034600 | ||||||
| chr19:1034600 | G | GACACGGT others(31): Show |
2 | a0001c0001t0002g0046 a0001c0001t0002g0048 |
2 | NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.391-1528_391-1527i others(40): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034600 | ||||||
| chr19:1034602 | CGGTGTCT others(307): Show |
C | 2 | a0001c0009t0010g0158 a0001c0009t0010g0159 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.391-1527_391-1214d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034602 | |||||||
| chr19:1034603 | G | C | 1 | a0001c0001t0002g0180 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.391-1527G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034603 | |||||||
| chr19:1034605 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1525T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034605 | |||||||
| chr19:1034615 | A | G | 1 | a0001c0005t0016g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1515A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034615 | |||||||
| chr19:1034619 | C | G | 63 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0044 others(60): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.391-1511C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034619 | |||||||
| chr19:1034619 | C | T | 3 | a0001c0002t0004g0009 a0001c0002t0004g0074 a0001c0002t0004g0076 |
3 | HG00733.hp1 HG01123.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-1511C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034619 | |||||||
| chr19:1034620 | G | A | 1 | a0001c0002t0004g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.391-1510G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034620 | |||||||
| chr19:1034621 | G | T | 2 | a0001c0001t0001g0042 a0001c0001t0011g0111 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.391-1509G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034621 | |||||||
| chr19:1034622 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0011g0111 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.391-1508C>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034622 | |||||||
| chr19:1034622 | C | G | 91 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0042 others(88): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.391-1508C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034622 | |||||||
| chr19:1034634 | GAC | G | 3 | a0001c0001t0009g0110 a0001c0002t0012g0195 a0001c0003t0010g0157 |
3 | HG03130.hp1 HG04204.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.391-1493_391-1492d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034634 | ||||||
| chr19:1034640 | G | T | 12 | a0001c0001t0002g0001 a0001c0001t0009g0001 a0001c0001t0009g0117 others(9): Show |
19 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.391-1490G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034640 | |||||||
| chr19:1034641 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1489T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034641 | |||||||
| chr19:1034651 | A | G | 1 | a0001c0005t0016g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1479A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034651 | |||||||
| chr19:1034655 | G | C | 25 | a0001c0001t0001g0042 a0001c0001t0001g0057 a0001c0001t0002g0001 others(22): Show |
41 | HG00639.hp2 HG00735.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.391-1475G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034655 | |||||||
| chr19:1034655 | GGGGAGCG others(27): Show |
G | 8 | a0001c0001t0001g0042 a0001c0001t0002g0184 a0001c0001t0009g0049 others(5): Show |
9 | HG02451.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-1457_391-1424d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034655 | ||||||
| chr19:1034657 | G | T | 7 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0037 others(4): Show |
8 | HG00597.hp2 HG02056.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-1473G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034657 | |||||||
| chr19:1034658 | G | A | 7 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0037 others(4): Show |
8 | HG00597.hp2 HG02056.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-1472G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034658 | |||||||
| chr19:1034658 | G | C | 2 | a0001c0001t0001g0105 a0001c0003t0003g0089 |
2 | NA18972.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.391-1472G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034658 | |||||||
| chr19:1034670 | G | GAC | 57 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0044 others(54): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.391-1459_391-1458d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034670 | ||||||
| chr19:1034672 | CGGTGTCT others(61): Show |
C | 1 | a0001c0001t0001g0055 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.391-1457_391-1390d others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034672 | |||||||
| chr19:1034672 | CGGTGTCT others(131): Show |
C | 13 | a0001c0001t0002g0001 a0001c0001t0002g0021 a0001c0001t0002g0049 others(10): Show |
22 | HG00423.hp1 HG00621.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.391-1457_391-1320d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034672 | |||||||
| chr19:1034675 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1455T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034675 | |||||||
| chr19:1034685 | A | G | 1 | a0001c0005t0016g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1445A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034685 | |||||||
| chr19:1034689 | C | G | 49 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0044 others(46): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.391-1441C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034689 | |||||||
| chr19:1034691 | G | T | 8 | a0001c0001t0001g0042 a0001c0001t0002g0184 a0001c0001t0009g0049 others(5): Show |
9 | HG02451.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-1439G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034691 | |||||||
| chr19:1034692 | G | A | 8 | a0001c0001t0001g0042 a0001c0001t0002g0184 a0001c0001t0009g0049 others(5): Show |
9 | HG02451.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-1438G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034692 | |||||||
| chr19:1034692 | G | C | 2 | a0001c0001t0001g0057 a0001c0008t0019g0125 |
2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.391-1438G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034692 | |||||||
| chr19:1034704 | GAC | G | 7 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0037 others(4): Show |
8 | HG00597.hp2 HG02056.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-1423_391-1422d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034704 | ||||||
| chr19:1034706 | C | CGGTGTCT others(61): Show |
1 | a0001c0001t0009g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1424_391-1423i others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034706 | |||||||
| chr19:1034709 | GGTGTCTG others(63): Show |
G | 1 | a0001c0001t0001g0043 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.391-1420_391-1351d others(72): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034709 | |||||||
| chr19:1034710 | G | T | 4 | a0001c0001t0009g0126 a0001c0001t0014g0026 a0001c0002t0004g0001 others(1): Show |
7 | HG00639.hp2 HG01081.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.391-1420G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034710 | |||||||
| chr19:1034711 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1419T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034711 | |||||||
| chr19:1034721 | A | G | 1 | a0001c0005t0016g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1409A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034721 | |||||||
| chr19:1034723 | AC | A | 12 | a0001c0001t0002g0001 a0001c0001t0009g0001 a0001c0001t0009g0117 others(9): Show |
18 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.391-1405delC | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034723 | ||||||
| chr19:1034725 | C | G | 57 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0042 others(54): Show |
74 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.391-1405C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034725 | |||||||
| chr19:1034727 | G | T | 1 | a0001c0002t0004g0004 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.391-1403G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034727 | |||||||
| chr19:1034728 | G | A | 1 | a0001c0002t0004g0004 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.391-1402G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034728 | |||||||
| chr19:1034728 | G | C | 1 | a0001c0001t0009g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1402G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034728 | |||||||
| chr19:1034728 | G | T | 12 | a0001c0001t0002g0001 a0001c0001t0009g0001 a0001c0001t0009g0117 others(9): Show |
18 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.391-1402G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034728 | |||||||
| chr19:1034729 | AGCGTGGG others(26): Show |
A | 12 | a0001c0001t0002g0001 a0001c0001t0009g0001 a0001c0001t0009g0117 others(9): Show |
18 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.391-1400_391-1368d others(35): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034729 | |||||||
| chr19:1034732 | GTGGGTGG others(97): Show |
G | 16 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0197 others(13): Show |
18 | HG00408.hp2 HG00544.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.391-1387_391-1284d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034732 | ||||||
| chr19:1034740 | G | GAC | 24 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0211 others(21): Show |
35 | HG00544.hp2 HG00597.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.391-1389_391-1388d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034740 | ||||||
| chr19:1034740 | G | GACACGGT others(65): Show |
2 | a0001c0001t0002g0046 a0001c0001t0002g0048 |
2 | NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.391-1388_391-1387i others(74): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034740 | ||||||
| chr19:1034740 | GACGGTGT others(205): Show |
G | 2 | a0001c0001t0001g0057 a0001c0008t0019g0125 |
2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.391-1353_391-1142d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034740 | ||||||
| chr19:1034742 | CGGTGTCT others(61): Show |
C | 13 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0037 others(10): Show |
19 | HG00423.hp2 HG01243.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.391-1387_391-1320d others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034742 | |||||||
| chr19:1034742 | CGGTGTCT others(167): Show |
C | 2 | a0001c0001t0002g0037 a0001c0014t0005g0009 |
2 | HG02056.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.391-1387_391-1214d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034742 | |||||||
| chr19:1034744 | GTGTCTGG others(29): Show |
G | 1 | a0001c0001t0001g0211 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.391-1353_391-1318d others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034744 | ||||||
| chr19:1034745 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1385T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034745 | |||||||
| chr19:1034759 | C | G | 35 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0055 others(32): Show |
45 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.391-1371C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034759 | |||||||
| chr19:1034761 | G | T | 1 | a0001c0002t0004g0201 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.391-1369G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034761 | |||||||
| chr19:1034762 | G | A | 1 | a0001c0002t0004g0201 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.391-1368G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034762 | |||||||
| chr19:1034762 | G | GAGCGTGG others(29): Show |
1 | a0001c0001t0009g0126 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.391-1352_391-1351i others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034762 | ||||||
| chr19:1034766 | GTGGGTGG others(63): Show |
G | 5 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0219 others(2): Show |
5 | HG00280.hp2 HG00323.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-1351_391-1282d others(72): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034766 | ||||||
| chr19:1034775 | A | T | 2 | a0001c0002t0004g0001 a0001c0002t0004g0004 |
4 | HG01074.hp2 HG01516.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-1355A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034775 | |||||||
| chr19:1034776 | CACATTGT others(27): Show |
C | 9 | a0001c0001t0001g0130 a0001c0001t0001g0168 a0001c0001t0001g0214 others(6): Show |
9 | HG00099.hp2 HG01192.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-1351_391-1318d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034776 | ||||||
| chr19:1034779 | A | G | 61 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0053 others(58): Show |
90 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.391-1351A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034779 | |||||||
| chr19:1034780 | T | G | 45 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0055 others(42): Show |
71 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.391-1350T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034780 | |||||||
| chr19:1034781 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
9 | HG01106.hp2 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-1349T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034781 | |||||||
| chr19:1034795 | C | G | 30 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0055 others(27): Show |
45 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.391-1335C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034795 | |||||||
| chr19:1034797 | G | T | 3 | a0001c0001t0014g0026 a0001c0002t0004g0001 a0001c0002t0004g0004 |
6 | HG00639.hp2 HG01081.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-1333G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034797 | |||||||
| chr19:1034798 | G | A | 3 | a0001c0001t0014g0026 a0001c0002t0004g0001 a0001c0002t0004g0004 |
6 | HG00639.hp2 HG01081.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-1332G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034798 | |||||||
| chr19:1034810 | G | GAC | 26 | a0001c0001t0001g0042 a0001c0001t0002g0001 a0001c0001t0002g0026 others(23): Show |
41 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.391-1319_391-1318d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034810 | ||||||
| chr19:1034810 | G | GACGGTGT others(29): Show |
1 | a0001c0001t0002g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.391-1302_391-1301i others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034810 | ||||||
| chr19:1034812 | CGGTGTCT others(97): Show |
C | 1 | a0001c0001t0005g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.391-1317_391-1214d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034812 | |||||||
| chr19:1034815 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1315T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034815 | |||||||
| chr19:1034829 | C | G | 60 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0130 others(57): Show |
90 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.391-1301C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034829 | |||||||
| chr19:1034836 | A | G | 106 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0043 others(103): Show |
165 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.391-1294A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034836 | |||||||
| chr19:1034844 | GAC | G | 4 | a0001c0001t0014g0026 a0001c0002t0004g0001 a0001c0002t0004g0004 others(1): Show |
7 | HG00639.hp2 HG01081.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.391-1283_391-1282d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034844 | ||||||
| chr19:1034851 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1279T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034851 | |||||||
| chr19:1034861 | A | G | 1 | a0001c0005t0016g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1269A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034861 | |||||||
| chr19:1034865 | G | C | 6 | a0001c0001t0001g0211 a0001c0001t0002g0048 a0001c0001t0014g0026 others(3): Show |
9 | HG00639.hp2 HG01081.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.391-1265G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034865 | |||||||
| chr19:1034865 | G | GGGGAGCG others(27): Show |
1 | a0001c0001t0009g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1264_391-1263i others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034865 | ||||||
| chr19:1034865 | GGTAAGCG others(63): Show |
G | 1 | a0001c0001t0001g0014 | 3 | HG03490.hp2 HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.391-1263_391-1194d others(72): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034865 | ||||||
| chr19:1034867 | T | G | 100 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(97): Show |
151 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.391-1263T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034867 | |||||||
| chr19:1034868 | A | C | 1 | a0001c0001t0009g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1262A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034868 | |||||||
| chr19:1034868 | A | G | 99 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(96): Show |
151 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.391-1262A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034868 | |||||||
| chr19:1034882 | CACGGTGT others(27): Show |
C | 1 | a0001c0001t0001g0055 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.391-1211_391-1178d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034882 | ||||||
| chr19:1034887 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1243T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034887 | |||||||
| chr19:1034897 | A | G | 1 | a0001c0005t0016g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1233A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034897 | |||||||
| chr19:1034901 | C | G | 100 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(97): Show |
153 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.391-1229C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034901 | |||||||
| chr19:1034904 | G | C | 1 | a0001c0001t0009g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1226G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034904 | |||||||
| chr19:1034916 | G | GAC | 89 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(86): Show |
142 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.391-1213_391-1212d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034916 | ||||||
| chr19:1034916 | G | GACACGGC others(103): Show |
1 | a0001c0003t0003g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.391-1212_391-1211i others(112): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034916 | ||||||
| chr19:1034916 | G | GACACGGT others(65): Show |
1 | a0001c0001t0002g0048 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.391-1212_391-1211i others(74): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034916 | ||||||
| chr19:1034917 | A | C | 1 | a0001c0003t0003g0052 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.391-1213A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034917 | |||||||
| chr19:1034918 | CGGTGTCT others(61): Show |
C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0168 a0001c0001t0001g0218 others(1): Show |
4 | HG00099.hp2 HG02135.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-1211_391-1144d others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034918 | |||||||
| chr19:1034918 | CGGTGTCT others(131): Show |
C | 1 | a0001c0001t0001g0043 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.391-1211_391-1074d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034918 | |||||||
| chr19:1034921 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1209T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034921 | |||||||
| chr19:1034931 | A | G | 1 | a0001c0005t0016g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1199A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034931 | |||||||
| chr19:1034932 | GACCGGGA others(133): Show |
G | 1 | a0001c0001t0001g0105 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.391-1159_391-1020d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034932 | ||||||
| chr19:1034935 | C | G | 98 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(95): Show |
152 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.391-1195C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034935 | |||||||
| chr19:1034950 | GAC | G | 3 | a0001c0002t0012g0195 a0001c0003t0003g0193 a0001c0005t0016g0045 |
3 | HG02074.hp1 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.391-1177_391-1176d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034950 | ||||||
| chr19:1034952 | CACGGTGT others(27): Show |
C | 6 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0219 others(3): Show |
6 | HG00280.hp2 HG00323.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-1141_391-1108d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034952 | ||||||
| chr19:1034957 | T | C | 4 | a0001c0003t0003g0008 a0001c0003t0003g0151 a0001c0003t0003g0152 others(1): Show |
10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1173T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034957 | |||||||
| chr19:1034971 | C | G | 114 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0042 others(111): Show |
172 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.391-1159C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034971 | |||||||
| chr19:1034986 | G | GAC | 82 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0044 others(79): Show |
123 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.391-1143_391-1142d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034986 | ||||||
| chr19:1034986 | G | GACACGGT others(67): Show |
1 | a0001c0001t0001g0188 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.391-1142_391-1141i others(76): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034986 | ||||||
| chr19:1034986 | G | GACACGGT others(103): Show |
2 | a0001c0002t0004g0048 a0001c0002t0004g0190 |
2 | HG01975.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.391-1142_391-1141i others(112): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034986 | ||||||
| chr19:1034986 | G | GACACGGT others(65): Show |
1 | a0001c0001t0002g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.391-1142_391-1141i others(74): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034986 | ||||||
| chr19:1034986 | G | GACGGTGT others(29): Show |
1 | a0001c0001t0002g0048 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.391-1126_391-1125i others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034986 | ||||||
| chr19:1034988 | CGGTGTCT others(61): Show |
C | 1 | a0001c0001t0001g0053 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.391-1141_391-1074d others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034988 | |||||||
| chr19:1034988 | CGGTGTCT others(167): Show |
C | 2 | a0001c0001t0002g0090 a0001c0003t0003g0089 |
2 | HG02129.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.391-1141_391-968de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034988 | |||||||
| chr19:1034991 | T | C | 6 | a0001c0001t0001g0091 a0001c0003t0003g0008 a0001c0003t0003g0151 others(3): Show |
12 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.391-1139T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034991 | |||||||
| chr19:1035002 | GACCGGGA others(63): Show |
G | 29 | a0001c0001t0001g0042 a0001c0001t0001g0161 a0001c0001t0002g0001 others(26): Show |
38 | HG00423.hp2 HG00544.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.391-1089_391-1020d others(72): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035002 | ||||||
| chr19:1035005 | C | G | 110 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0042 others(107): Show |
153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.391-1125C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035005 | |||||||
| chr19:1035026 | G | T | 1 | a0001c0001t0009g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1104G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035026 | |||||||
| chr19:1035027 | T | C | 6 | a0001c0001t0001g0091 a0001c0003t0003g0008 a0001c0003t0003g0151 others(3): Show |
12 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.391-1103T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035027 | |||||||
| chr19:1035038 | GACCGGGA others(27): Show |
G | 6 | a0001c0001t0005g0009 a0001c0001t0005g0069 a0001c0001t0017g0075 others(3): Show |
6 | HG00733.hp1 HG00733.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-1071_391-1038d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035038 | ||||||
| chr19:1035041 | C | G | 104 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0042 others(101): Show |
146 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.391-1089C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035041 | |||||||
| chr19:1035056 | G | GAC | 21 | a0001c0001t0001g0091 a0001c0001t0002g0001 a0001c0001t0002g0187 others(18): Show |
30 | HG00423.hp1 HG01081.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.391-1073_391-1072d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035056 | ||||||
| chr19:1035058 | C | T | 1 | a0001c0008t0019g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391-1072C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035058 | |||||||
| chr19:1035058 | CGGTGTCT others(97): Show |
C | 1 | a0001c0001t0005g0079 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.391-1071_391-968de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035058 | |||||||
| chr19:1035061 | T | C | 6 | a0001c0001t0001g0091 a0001c0003t0003g0008 a0001c0003t0003g0151 others(3): Show |
12 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.391-1069T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035061 | |||||||
| chr19:1035072 | T | G | 135 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0021 others(132): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.391-1058T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035072 | |||||||
| chr19:1035075 | C | G | 30 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0053 others(27): Show |
41 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-1055C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035075 | |||||||
| chr19:1035090 | GAC | G | 4 | a0001c0001t0001g0043 a0001c0002t0004g0001 a0001c0002t0004g0004 others(1): Show |
6 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-1037_391-1036d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035090 | ||||||
| chr19:1035092 | C | CACGGTGT others(27): Show |
1 | a0001c0002t0004g0074 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.391-1035_391-1002d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035092 | ||||||
| chr19:1035097 | T | C | 6 | a0001c0001t0001g0091 a0001c0003t0003g0008 a0001c0003t0003g0151 others(3): Show |
12 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.391-1033T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035097 | |||||||
| chr19:1035111 | G | C | 1 | a0001c0005t0008g0210 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.391-1019G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035111 | |||||||
| chr19:1035113 | G | T | 1 | a0001c0001t0009g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1017G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035113 | |||||||
| chr19:1035114 | G | A | 1 | a0001c0001t0009g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1016G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035114 | |||||||
| chr19:1035118 | G | A | 1 | a0001c0001t0006g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.391-1012G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035118 | |||||||
| chr19:1035126 | GACACGGT others(65): Show |
G | 1 | a0001c0005t0016g0045 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.391-1001_391-930de others(73): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035126 | ||||||
| chr19:1035132 | G | T | 1 | a0001c0001t0002g0185 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.391-998G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035132 | |||||||
| chr19:1035133 | T | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0091 a0001c0001t0005g0207 others(5): Show |
16 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.391-997T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035133 | |||||||
| chr19:1035147 | G | C | 2 | a0001c0001t0009g0110 a0001c0002t0004g0074 |
2 | HG01123.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.391-983G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035147 | |||||||
| chr19:1035162 | G | GAC | 11 | a0001c0001t0001g0023 a0001c0001t0001g0053 a0001c0001t0001g0091 others(8): Show |
19 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.391-967_391-966dup others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035162 | ||||||
| chr19:1035164 | C | T | 1 | a0001c0004t0003g0135 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.391-966C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035164 | |||||||
| chr19:1035167 | T | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0091 a0001c0001t0005g0207 others(6): Show |
17 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.391-963T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035167 | |||||||
| chr19:1035181 | G | A | 1 | a0001c0002t0012g0186 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.391-949G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035181 | |||||||
| chr19:1035181 | G | C | 3 | a0001c0001t0002g0185 a0001c0001t0009g0110 a0001c0003t0010g0157 |
3 | HG02135.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.391-949G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035181 | |||||||
| chr19:1035181 | GGGGAGCG others(29): Show |
G | 4 | a0001c0002t0004g0201 a0001c0006t0007g0132 a0001c0006t0007g0139 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-914_391-879del others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035181 | ||||||
| chr19:1035196 | GAC | G | 6 | a0001c0001t0001g0053 a0001c0001t0002g0088 a0001c0001t0002g0090 others(3): Show |
6 | HG01123.hp2 HG02129.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-931_391-930del others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035196 | ||||||
| chr19:1035198 | C | CACGGTGT others(63): Show |
2 | a0001c0001t0009g0110 a0001c0003t0010g0157 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.391-914_391-913ins others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035198 | ||||||
| chr19:1035203 | T | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0091 a0001c0001t0005g0207 others(6): Show |
17 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.391-927T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035203 | |||||||
| chr19:1035216 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.391-914C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035216 | |||||||
| chr19:1035217 | C | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(44): Show |
80 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.391-913C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035217 | |||||||
| chr19:1035251 | A | G | 1 | a0003c0012t0005g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.391-879A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035251 | |||||||
| chr19:1035253 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(117): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.391-877T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035253 | |||||||
| chr19:1035451 | C | T | 32 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0098 others(29): Show |
39 | HG00423.hp1 HG00544.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.391-679C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035451 | |||||||
| chr19:1035456 | A | C | 39 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0062 others(36): Show |
57 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.391-674A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035456 | |||||||
| chr19:1035493 | G | A | 1 | a0001c0006t0007g0141 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.391-637G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035493 | |||||||
| chr19:1035500 | G | C | 1 | a0001c0001t0001g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.391-630G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035500 | |||||||
| chr19:1035540 | G | A | 1 | a0001c0003t0003g0089 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.391-590G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035540 | |||||||
| chr19:1035541 | A | G | 1 | a0001c0003t0003g0089 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.391-589A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035541 | |||||||
| chr19:1035610 | A | T | 1 | a0001c0001t0002g0146 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.391-520A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035610 | |||||||
| chr19:1035651 | G | A | 7 | a0001c0003t0010g0072 a0001c0003t0010g0157 a0001c0003t0010g0163 others(4): Show |
7 | HG02451.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.391-479G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035651 | |||||||
| chr19:1035709 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.391-421G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035709 | |||||||
| chr19:1035711 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.391-419C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035711 | |||||||
| chr19:1035796 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.391-334C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035796 | |||||||
| chr19:1035806 | T | C | 3 | a0001c0008t0019g0020 a0001c0008t0019g0125 a0001c0008t0020g0020 |
4 | HG02055.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-324T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035806 | |||||||
| chr19:1035814 | T | C | 1 | a0001c0002t0004g0189 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.391-316T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035814 | |||||||
| chr19:1035846 | T | A | 1 | a0001c0003t0003g0089 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.391-284T>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035846 | |||||||
| chr19:1035887 | A | T | 1 | a0001c0001t0001g0032 | 2 | NA18990.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.391-243A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035887 | |||||||
| chr19:1035960 | G | A | 18 | a0001c0003t0003g0013 a0001c0003t0003g0052 a0001c0003t0003g0070 others(15): Show |
34 | HG02027.hp2 HG02040.hp1 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.391-170G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035960 | |||||||
| chr19:1036018 | C | T | 1 | a0001c0002t0004g0118 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.391-112C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1036018 | |||||||
| chr19:1036019 | G | A | 105 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0161 others(102): Show |
161 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.391-111G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1036019 | |||||||
| chr19:1036032 | G | T | 1 | a0001c0015t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.391-98G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1036032 | |||||||
| chr19:1036315 | A | G | 20 | a0001c0005t0007g0031 a0001c0005t0007g0035 a0001c0005t0007g0099 others(17): Show |
32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.507+69A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 5/6 | chr19 | 1036315 | |||||||
| chr19:1036575 | C | T | 18 | a0001c0003t0003g0013 a0001c0003t0003g0052 a0001c0003t0003g0070 others(15): Show |
34 | HG02027.hp2 HG02040.hp1 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.654+13C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036575 | |||||||
| chr19:1036576 | G | A | 20 | a0001c0005t0007g0031 a0001c0005t0007g0035 a0001c0005t0007g0099 others(17): Show |
32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+14G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036576 | |||||||
| chr19:1036621 | C | T | 1 | a0001c0001t0030g0204 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.654+59C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036621 | |||||||
| chr19:1036632 | T | C | 20 | a0001c0005t0007g0031 a0001c0005t0007g0035 a0001c0005t0007g0099 others(17): Show |
32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+70T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036632 | |||||||
| chr19:1036651 | T | C | 1 | a0001c0001t0011g0027 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.654+89T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036651 | |||||||
| chr19:1036664 | AGTCTCAG others(41): Show |
A | 1 | a0001c0001t0011g0027 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.654+108_654+155del others(48): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 1036664 | ||||||
| chr19:1036692 | C | T | 10 | a0001c0005t0007g0031 a0001c0005t0007g0035 a0001c0005t0007g0099 others(7): Show |
16 | HG00140.hp1 HG00735.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.654+130C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036692 | |||||||
| chr19:1036705 | C | T | 10 | a0001c0005t0007g0031 a0001c0005t0007g0035 a0001c0005t0007g0099 others(7): Show |
16 | HG00140.hp1 HG00735.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.654+143C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036705 | |||||||
| chr19:1036719 | G | A | 20 | a0001c0005t0007g0031 a0001c0005t0007g0035 a0001c0005t0007g0099 others(17): Show |
32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+157G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036719 | |||||||
| chr19:1036736 | CTG | C | 9 | a0001c0001t0006g0018 a0001c0001t0006g0022 a0001c0001t0006g0121 others(6): Show |
13 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.654+176_654+177del others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 1036736 | ||||||
| chr19:1036794 | T | A | 20 | a0001c0005t0007g0031 a0001c0005t0007g0035 a0001c0005t0007g0099 others(17): Show |
32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+232T>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036794 | |||||||
| chr19:1036838 | T | A | 1 | a0001c0001t0002g0094 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.654+276T>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036838 | |||||||
| chr19:1036914 | C | T | 20 | a0001c0005t0007g0031 a0001c0005t0007g0035 a0001c0005t0007g0099 others(17): Show |
32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+352C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036914 | |||||||
| chr19:1037070 | C | T | 1 | a0001c0001t0006g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.654+508C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037070 | |||||||
| chr19:1037089 | C | T | 18 | a0001c0003t0003g0013 a0001c0003t0003g0052 a0001c0003t0003g0070 others(15): Show |
34 | HG02027.hp2 HG02040.hp1 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.654+527C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037089 | |||||||
| chr19:1037109 | T | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(210): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.655-516T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037109 | |||||||
| chr19:1037171 | T | A | 20 | a0001c0005t0007g0031 a0001c0005t0007g0035 a0001c0005t0007g0099 others(17): Show |
32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-454T>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037171 | |||||||
| chr19:1037552 | G | A | 20 | a0001c0005t0007g0031 a0001c0005t0007g0035 a0001c0005t0007g0099 others(17): Show |
32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-73G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037552 | |||||||
| chr19:1037564 | A | G | 20 | a0001c0005t0007g0031 a0001c0005t0007g0035 a0001c0005t0007g0099 others(17): Show |
32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-61A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037564 | |||||||
| chr19:1037585 | C | T | 20 | a0001c0005t0007g0031 a0001c0005t0007g0035 a0001c0005t0007g0099 others(17): Show |
32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-40C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037585 |