Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57333 |
| ensemblid | ENSG00000142552.8 |
| hgncid | 21145 |
| symbol | RCN3 |
| name | reticulocalbin 3 |
| refseq_nuc | NM_020650.3 |
| refseq_prot | NP_065701.2 |
| ensembl_nuc | ENST00000270645.8 |
| ensembl_prot | ENSP00000270645.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 49528003 |
| end | 49543633 |
| strand | + |
| ver | v1.2 |
| region | chr19:49528003-49543633 |
| region5000 | chr19:49523003-49548633 |
| regionname0 | RCN3_chr19_49528003_49543633 |
| regionname5000 | RCN3_chr19_49523003_49548633 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 328 | 343 | 77 | 66 | 141 | 16 | 41 | 98 | RCN3_chr19_49523003_49548633 | RCN3 | MMWRP others(323): Show |
chr19 | 49523003 | 49548633 |
| a0002 | 0/0 | 328 | 25 | 9 | 5 | 9 | 0 | 2 | 6 | RCN3_chr19_49523003_49548633 | RCN3 | MMWRP others(323): Show |
chr19 | 49523003 | 49548633 |
| a0003 | 0/0 | 328 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | MMWRP others(323): Show |
chr19 | 49523003 | 49548633 |
| a0004 | 0/0 | 328 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | MMWRP others(323): Show |
chr19 | 49523003 | 49548633 |
| a0005 | 0/0 | 328 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | MMWRP others(323): Show |
chr19 | 49523003 | 49548633 |
| a0006 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | MMWRP others(323): Show |
chr19 | 49523003 | 49548633 |
| a0007 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | MMWRP others(323): Show |
chr19 | 49523003 | 49548633 |
| a0008 | 0/0 | 328 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | MMWRP others(323): Show |
chr19 | 49523003 | 49548633 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 984 | 328 | 67 | 64 | 141 | 15 | 39 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 | ||
| a0001c0003 | 0/0 | 984 | 8 | 7 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 | ||
| a0001c0005 | 0/0 | 984 | 4 | 0 | 1 | 0 | 1 | 2 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 | ||
| a0001c0008 | 0/0 | 984 | 3 | 3 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 | ||
| a0002c0002 | 0/0 | 984 | 18 | 6 | 1 | 9 | 0 | 2 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 | ||
| a0002c0004 | 0/0 | 984 | 6 | 3 | 3 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 | ||
| a0002c0013 | 0/0 | 984 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 | ||
| a0003c0006 | 0/0 | 984 | 3 | 1 | 2 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 | ||
| a0003c0007 | 0/0 | 984 | 3 | 3 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 | ||
| a0004c0009 | 0/0 | 984 | 2 | 2 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 | ||
| a0005c0012 | 0/0 | 984 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 | ||
| a0006c0014 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 | ||
| a0007c0011 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 | ||
| a0008c0010 | 0/0 | 984 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | ATGAT others(979): Show |
chr19 | 49523003 | 49548633 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1469 | 315 | 65 | 64 | 131 | 15 | 38 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0001c0001t0003 | 0/0 | 1469 | 4 | 0 | 0 | 4 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0001c0001t0004 | 0/0 | 1469 | 2 | 0 | 0 | 2 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0001c0001t0005 | 0/0 | 1469 | 2 | 0 | 0 | 2 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0001c0001t0006 | 0/0 | 1469 | 2 | 2 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0001c0001t0007 | 0/0 | 1469 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0001c0001t0008 | 0/0 | 1469 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0001c0001t0009 | 0/0 | 1469 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0001c0003t0001 | 0/0 | 1469 | 8 | 7 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0001c0005t0001 | 0/0 | 1469 | 4 | 0 | 1 | 0 | 1 | 2 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0001c0008t0001 | 0/0 | 1469 | 3 | 3 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0002c0002t0002 | 0/0 | 1469 | 18 | 6 | 1 | 9 | 0 | 2 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0002c0004t0002 | 0/0 | 1469 | 6 | 3 | 3 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0002c0013t0002 | 0/0 | 1469 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0003c0006t0002 | 0/0 | 1469 | 3 | 1 | 2 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0003c0007t0002 | 0/0 | 1469 | 3 | 3 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0004c0009t0001 | 0/0 | 1469 | 2 | 2 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0005c0012t0001 | 0/0 | 1469 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0006c0014t0010 | 0/0 | 1469 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0007c0011t0001 | 0/0 | 1469 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| a0008c0010t0001 | 0/0 | 1469 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | ACATT others(1464): Show |
chr19 | 49523003 | 49548633 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 60 | 4 | 12 | 37 | 1 | 6 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 3 | 9 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0003 | 0/0 | 8 | 1 | 4 | 1 | 2 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0004 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 1 | 2 | 0 | 4 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 0 | 0 | 7 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0008 | 1/0 | 6 | 0 | 0 | 5 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0014 | 0/1 | 4 | 0 | 0 | 0 | 2 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0001t0009g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0003t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0003t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0005t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0005t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0008t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0008t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0001c0008t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0002t0002g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0002t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0004t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0004t0002g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0004t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0004t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0002c0013t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0003c0006t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0003c0006t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0003c0006t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0003c0007t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0003c0007t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0004c0009t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0004c0009t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0005c0012t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0006c0014t0010g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0007c0011t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| a0008c0010t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | GBR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00738 | hp2 | a0005 | c0012 | t0001 | g0128 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01070 | hp1 | a0003 | c0006 | t0002 | g0075 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01070 | hp2 | a0002 | c0004 | t0002 | g0029 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01071 | hp2 | a0003 | c0006 | t0002 | g0076 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01074 | hp2 | a0001 | c0005 | t0001 | g0003 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0025 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01109 | hp1 | a0002 | c0004 | t0002 | g0066 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01255 | hp2 | a0002 | c0004 | t0002 | g0027 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0028 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01515 | hp1 | a0001 | c0005 | t0001 | g0003 | EUR | IBS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | IBS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | IBS | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01884 | hp2 | a0001 | c0008 | t0001 | g0195 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01891 | hp1 | a0004 | c0009 | t0001 | g0169 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01943 | hp2 | a0002 | c0013 | t0002 | g0024 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0046 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02257 | hp2 | a0006 | c0014 | t0010 | g0067 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02258 | hp1 | a0003 | c0007 | t0002 | g0045 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02280 | hp1 | a0002 | c0004 | t0002 | g0027 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0026 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0028 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0134 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0063 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0068 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0064 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0181 | AFR | MSL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03130 | hp1 | a0003 | c0007 | t0002 | g0069 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03195 | hp1 | a0003 | c0006 | t0002 | g0077 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03225 | hp1 | a0003 | c0007 | t0002 | g0045 | AFR | MSL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03453 | hp2 | a0001 | c0008 | t0001 | g0199 | AFR | MSL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03490 | hp2 | a0001 | c0005 | t0001 | g0017 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03492 | hp1 | a0001 | c0005 | t0001 | g0003 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03516 | hp1 | a0007 | c0011 | t0001 | g0089 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0025 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG04115 | hp2 | a0008 | c0010 | t0001 | g0005 | SAS | STU | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0024 | SAS | STU | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0182 | AFR | YRI | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19002 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19083 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19084 | hp1 | a0001 | c0001 | t0009 | g0116 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0026 | AFR | YRI | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | ASW | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ASW | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA20905 | hp2 | a0001 | c0001 | t0008 | g0079 | SAS | GIH | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02109 | hp1 | a0001 | c0008 | t0001 | g0194 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02559 | hp1 | a0002 | c0004 | t0002 | g0029 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03471 | hp1 | a0004 | c0009 | t0001 | g0183 | AFR | MSL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG06807 | hp1 | a0002 | c0004 | t0002 | g0065 | AFR | USA | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | USA | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | USA | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0014 | REF | REF | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0008 | REF | REF | RCN3_chr19_49523003_49548633 | RCN3 | chr19 | 49523003 | 49548633 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49534233 | G | A | 1 | a0008 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.283G>A | p.Gly95Ser | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/7 | 345/1469 | 283/987 | 95/328 | chr19 | 49534233 | |||
| chr19:49537050 | G | A | 1 | a0003 | 6 | HG01070.hp1 HG01071.hp2 HG02258.hp1 others(3): Show |
missense_variant | MODERATE | c.463G>A | p.Val155Met | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/7 | 525/1469 | 463/987 | 155/328 | chr19 | 49537050 | |||
| chr19:49537096 | G | A | 1 | a0004 | 2 | HG01891.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.509G>A | p.Arg170Gln | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/7 | 571/1469 | 509/987 | 170/328 | chr19 | 49537096 | |||
| chr19:49537197 | G | A | 1 | a0007 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.610G>A | p.Val204Met | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/7 | 672/1469 | 610/987 | 204/328 | chr19 | 49537197 | |||
| chr19:49542621 | C | T | 3 | a0002 a0003 a0006 |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
missense_variant | MODERATE | c.748C>T | p.Arg250Trp | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/7 | 810/1469 | 748/987 | 250/328 | chr19 | 49542621 | |||
| chr19:49542684 | C | G | 1 | a0006 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.811C>G | p.Leu271Val | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/7 | 873/1469 | 811/987 | 271/328 | chr19 | 49542684 | |||
| chr19:49542722 | C | A | 1 | a0005 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.849C>A | p.Asn283Lys | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/7 | 911/1469 | 849/987 | 283/328 | chr19 | 49542722 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49537091 | C | T | 1 | a0001c0005 | 4 | HG01074.hp2 HG01515.hp1 HG03490.hp2 others(1): Show |
synonymous_variant | LOW | c.504C>T | p.Asp168Asp | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/7 | 566/1469 | 504/987 | 168/328 | chr19 | 49537091 | |||
| chr19:49537130 | G | A | 2 | a0001c0003 a0004c0009 |
10 | HG01433.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
synonymous_variant | LOW | c.543G>A | p.Ser181Ser | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/7 | 605/1469 | 543/987 | 181/328 | chr19 | 49537130 | |||
| chr19:49537169 | C | T | 2 | a0003c0006 a0003c0007 |
6 | HG01070.hp1 HG01071.hp2 HG02258.hp1 others(3): Show |
synonymous_variant | LOW | c.582C>T | p.Pro194Pro | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/7 | 644/1469 | 582/987 | 194/328 | chr19 | 49537169 | |||
| chr19:49542593 | G | A | 2 | a0003c0006 a0003c0007 |
6 | HG01070.hp1 HG01071.hp2 HG02258.hp1 others(3): Show |
synonymous_variant | LOW | c.720G>A | p.Ala240Ala | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/7 | 782/1469 | 720/987 | 240/328 | chr19 | 49542593 | |||
| chr19:49542659 | T | C | 7 | a0001c0003 a0001c0008 a0002c0002 others(4): Show |
36 | HG00438.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
synonymous_variant | LOW | c.786T>C | p.Asp262Asp | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/7 | 848/1469 | 786/987 | 262/328 | chr19 | 49542659 | |||
| chr19:49543108 | T | C | 5 | a0002c0002 a0002c0004 a0003c0006 others(2): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
splice_region_variant&synonymous_variant | LOW | c.882T>C | p.Asp294Asp | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 7/7 | 944/1469 | 882/987 | 294/328 | chr19 | 49543108 | |||
| chr19:49543180 | C | T | 6 | a0002c0002 a0002c0004 a0002c0013 others(3): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
synonymous_variant | LOW | c.954C>T | p.Gly318Gly | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 7/7 | 1016/1469 | 954/987 | 318/328 | chr19 | 49543180 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49528029 | G | A | 2 | a0001c0001t0004 a0001c0001t0007 |
3 | NA18964.hp1 NA19002.hp2 NA19079.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-36G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 1/7 | chr19 | 49528029 | |||||||
| chr19:49543216 | A | C | 6 | a0002c0002t0002 a0002c0004t0002 a0002c0013t0002 others(3): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3A>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 7/7 | 3 | chr19 | 49543216 | ||||||
| chr19:49543219 | G | A | 1 | a0001c0001t0005 | 2 | NA18998.hp2 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 7/7 | 6 | chr19 | 49543219 | ||||||
| chr19:49543249 | C | T | 2 | a0001c0001t0003 a0001c0001t0004 |
6 | HG02040.hp1 HG02132.hp2 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*36C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 7/7 | 36 | chr19 | 49543249 | ||||||
| chr19:49543302 | G | A | 1 | a0001c0001t0008 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 7/7 | 89 | chr19 | 49543302 | ||||||
| chr19:49543451 | C | T | 1 | a0001c0001t0006 | 2 | HG01891.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*238C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 7/7 | 238 | chr19 | 49543451 | ||||||
| chr19:49543461 | A | C | 1 | a0006c0014t0010 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*248A>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 7/7 | 248 | chr19 | 49543461 | ||||||
| chr19:49543472 | CT | C | 6 | a0002c0002t0002 a0002c0004t0002 a0002c0013t0002 others(3): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*261delT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 7/7 | 261 | INFO_REALIGN_3_PRIME | chr19 | 49543472 | |||||
| chr19:49543502 | C | CA | 6 | a0002c0002t0002 a0002c0004t0002 a0002c0013t0002 others(3): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*289_*290insA | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 7/7 | 290 | chr19 | 49543502 | ||||||
| chr19:49543515 | G | C | 1 | a0001c0001t0009 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*302G>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 7/7 | 302 | chr19 | 49543515 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49528093 | A | AGGGCGGC others(3): Show |
36 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
65 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-7+38_-7+47dupGCGG others(6): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 49528093 | ||||||
| chr19:49528200 | G | A | 1 | a0003c0007t0002g0069 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-7+142G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 1/6 | chr19 | 49528200 | |||||||
| chr19:49528743 | C | T | 2 | a0003c0007t0002g0045 a0003c0007t0002g0069 |
3 | HG02258.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.242+29C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49528743 | |||||||
| chr19:49528770 | C | CG | 6 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.242+61dupG | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49528770 | ||||||
| chr19:49528903 | C | T | 18 | a0001c0003t0001g0028 a0001c0003t0001g0046 a0002c0002t0002g0007 others(15): Show |
28 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.242+189C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49528903 | |||||||
| chr19:49528998 | A | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0197 others(3): Show |
11 | HG00733.hp1 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.242+284A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49528998 | |||||||
| chr19:49529183 | A | AAAC | 16 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
35 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.242+481_242+483dup others(3): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49529183 | ||||||
| chr19:49529183 | A | AAACAAC | 18 | a0001c0003t0001g0028 a0001c0003t0001g0046 a0002c0002t0002g0007 others(15): Show |
28 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.242+478_242+483dup others(6): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49529183 | ||||||
| chr19:49529248 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.242+534C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49529248 | |||||||
| chr19:49529455 | G | C | 3 | a0003c0006t0002g0075 a0003c0006t0002g0076 a0003c0006t0002g0077 |
3 | HG01070.hp1 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.242+741G>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49529455 | |||||||
| chr19:49529608 | G | A | 6 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(3): Show |
12 | HG00438.hp2 HG01106.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.242+894G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49529608 | |||||||
| chr19:49529659 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.242+945G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49529659 | |||||||
| chr19:49529672 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.242+958A>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49529672 | |||||||
| chr19:49529723 | T | TG | 37 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(34): Show |
66 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.242+1016dupG | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49529723 | ||||||
| chr19:49529740 | T | TTTTA | 18 | a0001c0003t0001g0028 a0001c0003t0001g0046 a0002c0002t0002g0007 others(15): Show |
28 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.242+1051_242+1054d others(6): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49529740 | ||||||
| chr19:49529740 | TTTTA | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
36 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.242+1051_242+1054d others(6): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49529740 | ||||||
| chr19:49529826 | G | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0058 a0001c0001t0001g0080 others(5): Show |
14 | HG00140.hp1 HG01175.hp2 HG02735.hp2 others(11): Show |
intron_variant | MODIFIER | c.242+1112G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49529826 | |||||||
| chr19:49529871 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.242+1157C>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49529871 | |||||||
| chr19:49529902 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.242+1188G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49529902 | |||||||
| chr19:49529928 | GTATTTTT others(6): Show |
G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.242+1228_242+1240d others(15): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49529928 | ||||||
| chr19:49529982 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.242+1268C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49529982 | |||||||
| chr19:49530034 | C | G | 1 | a0002c0002t0002g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.242+1320C>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530034 | |||||||
| chr19:49530037 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | NA18968.hp2 NA18983.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.242+1323C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530037 | |||||||
| chr19:49530068 | C | T | 2 | a0001c0008t0001g0194 a0001c0008t0001g0195 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.242+1354C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530068 | |||||||
| chr19:49530261 | G | GCAATTCT others(9): Show |
1 | a0001c0001t0001g0047 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.242+1548_242+1563d others(18): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49530261 | ||||||
| chr19:49530284 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG00639.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.242+1570C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530284 | |||||||
| chr19:49530326 | A | AT | 15 | a0001c0001t0001g0176 a0001c0001t0001g0179 a0001c0001t0001g0180 others(12): Show |
17 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.242+1629dupT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49530326 | ||||||
| chr19:49530450 | G | A | 18 | a0001c0003t0001g0028 a0001c0003t0001g0046 a0002c0002t0002g0007 others(15): Show |
28 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.242+1736G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530450 | |||||||
| chr19:49530468 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0185 |
2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.242+1754C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530468 | |||||||
| chr19:49530479 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.242+1765G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530479 | |||||||
| chr19:49530488 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.242+1774C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530488 | |||||||
| chr19:49530497 | C | CTT | 19 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(16): Show |
38 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.242+1798_242+1799d others(4): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49530497 | ||||||
| chr19:49530501 | T | TC | 18 | a0001c0003t0001g0028 a0001c0003t0001g0046 a0002c0002t0002g0007 others(15): Show |
28 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.242+1787_242+1788i others(3): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530501 | |||||||
| chr19:49530581 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0173 |
4 | HG00280.hp2 HG03239.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.242+1867C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530581 | |||||||
| chr19:49530657 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0172 |
2 | HG02145.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.242+1943C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530657 | |||||||
| chr19:49530782 | C | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.242+2068C>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530782 | |||||||
| chr19:49530788 | A | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(34): Show |
66 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.242+2074A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530788 | |||||||
| chr19:49530844 | G | A | 18 | a0001c0003t0001g0028 a0001c0003t0001g0046 a0002c0002t0002g0007 others(15): Show |
28 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.242+2130G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530844 | |||||||
| chr19:49530993 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.242+2279A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49530993 | |||||||
| chr19:49531225 | G | A | 1 | a0002c0002t0002g0026 | 2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.242+2511G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49531225 | |||||||
| chr19:49531260 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.242+2546A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49531260 | |||||||
| chr19:49531278 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
36 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.242+2564C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49531278 | |||||||
| chr19:49531378 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.242+2664C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49531378 | |||||||
| chr19:49531574 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.243-2619G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49531574 | |||||||
| chr19:49531958 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0172 |
2 | HG02145.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.243-2235G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49531958 | |||||||
| chr19:49532036 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
36 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.243-2157C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532036 | |||||||
| chr19:49532037 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.243-2156G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532037 | |||||||
| chr19:49532081 | G | A | 1 | a0002c0002t0002g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.243-2112G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532081 | |||||||
| chr19:49532100 | C | CT | 28 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0072 others(25): Show |
35 | HG00140.hp2 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.243-2070dupT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49532100 | ||||||
| chr19:49532100 | CTTTT | C | 19 | a0001c0001t0001g0056 a0001c0003t0001g0028 a0001c0003t0001g0046 others(16): Show |
29 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.243-2073_243-2070d others(6): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49532100 | ||||||
| chr19:49532100 | CTTTTT | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
35 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.243-2074_243-2070d others(7): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49532100 | ||||||
| chr19:49532134 | C | T | 1 | a0002c0004t0002g0029 | 2 | HG01070.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.243-2059C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532134 | |||||||
| chr19:49532206 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | NA18612.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.243-1987C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532206 | |||||||
| chr19:49532207 | G | A | 1 | a0002c0002t0002g0026 | 2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.243-1986G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532207 | |||||||
| chr19:49532295 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.243-1898C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532295 | |||||||
| chr19:49532438 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.243-1755C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532438 | |||||||
| chr19:49532500 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.243-1693C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532500 | |||||||
| chr19:49532523 | C | G | 1 | a0001c0001t0001g0043 | 2 | HG00597.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.243-1670C>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532523 | |||||||
| chr19:49532564 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.243-1629C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532564 | |||||||
| chr19:49532572 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.243-1621C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532572 | |||||||
| chr19:49532663 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.243-1530C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532663 | |||||||
| chr19:49532716 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.243-1477C>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532716 | |||||||
| chr19:49532866 | A | G | 5 | a0001c0003t0001g0020 a0001c0003t0001g0181 a0001c0003t0001g0182 others(2): Show |
7 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.243-1327A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49532866 | |||||||
| chr19:49533049 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.243-1144C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49533049 | |||||||
| chr19:49533066 | A | G | 17 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
36 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.243-1127A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49533066 | |||||||
| chr19:49533187 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
35 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.243-1006A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49533187 | |||||||
| chr19:49533205 | T | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0001g0088 |
4 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.243-988T>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49533205 | |||||||
| chr19:49533313 | G | C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(32): Show |
61 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.243-880G>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49533313 | |||||||
| chr19:49533340 | C | T | 16 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(13): Show |
25 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.243-853C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49533340 | |||||||
| chr19:49533377 | G | T | 18 | a0001c0001t0001g0042 a0001c0001t0001g0141 a0002c0002t0002g0007 others(15): Show |
28 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.243-816G>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49533377 | |||||||
| chr19:49533382 | T | G | 1 | a0007c0011t0001g0089 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.243-811T>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49533382 | |||||||
| chr19:49533668 | G | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0090 others(2): Show |
7 | HG00673.hp1 HG02129.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.243-525G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49533668 | |||||||
| chr19:49533714 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0054 |
5 | HG00423.hp1 HG02155.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.243-479C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49533714 | |||||||
| chr19:49533940 | G | A | 1 | a0001c0001t0001g0033 | 2 | NA18986.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.243-253G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49533940 | |||||||
| chr19:49534127 | G | GC | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.243-63dupC | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 49534127 | ||||||
| chr19:49534146 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.243-47C>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49534146 | |||||||
| chr19:49534165 | C | T | 16 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(13): Show |
25 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.243-28C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49534165 | |||||||
| chr19:49534189 | C | G | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
splice_region_variant&intron_variant | LOW | c.243-4C>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 2/6 | chr19 | 49534189 | |||||||
| chr19:49534509 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.445+114G>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49534509 | |||||||
| chr19:49534613 | A | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.445+218A>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49534613 | |||||||
| chr19:49534639 | C | T | 2 | a0003c0007t0002g0045 a0003c0007t0002g0069 |
3 | HG02258.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.445+244C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49534639 | |||||||
| chr19:49534673 | A | G | 5 | a0003c0006t0002g0075 a0003c0006t0002g0076 a0003c0006t0002g0077 others(2): Show |
6 | HG01070.hp1 HG01071.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.445+278A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49534673 | |||||||
| chr19:49534704 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.445+309C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49534704 | |||||||
| chr19:49534760 | C | T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(107): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.445+365C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49534760 | |||||||
| chr19:49534815 | C | T | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.445+420C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49534815 | |||||||
| chr19:49534957 | C | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
10 | HG02071.hp1 HG02165.hp1 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.445+562C>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49534957 | |||||||
| chr19:49534963 | A | C | 28 | a0001c0003t0001g0020 a0001c0003t0001g0028 a0001c0003t0001g0046 others(25): Show |
41 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.445+568A>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49534963 | |||||||
| chr19:49535024 | C | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0071 a0001c0001t0001g0133 others(5): Show |
10 | HG00140.hp2 HG01081.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.445+629C>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49535024 | |||||||
| chr19:49535058 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.445+663G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49535058 | |||||||
| chr19:49535059 | G | A | 1 | a0001c0001t0004g0150 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.445+664G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49535059 | |||||||
| chr19:49535351 | AC | A | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0090 others(4): Show |
9 | HG00673.hp1 HG02129.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.445+957delC | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49535351 | |||||||
| chr19:49535486 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.445+1091A>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49535486 | |||||||
| chr19:49535599 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.445+1204C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49535599 | |||||||
| chr19:49535602 | A | G | 17 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
36 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.445+1207A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49535602 | |||||||
| chr19:49535859 | AAAAT | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(13): Show |
33 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.446-1172_446-1169d others(6): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 49535859 | ||||||
| chr19:49535861 | A | AT | 7 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0137 others(4): Show |
10 | HG00735.hp1 HG00735.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.446-1172_446-1171i others(3): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49535861 | |||||||
| chr19:49535861 | A | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(39): Show |
58 | HG00140.hp1 HG00438.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.446-1172A>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49535861 | |||||||
| chr19:49535863 | T | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(28): Show |
46 | HG00099.hp1 HG00544.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.446-1170T>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49535863 | |||||||
| chr19:49535865 | T | TAGATAGA others(3): Show |
1 | a0003c0007t0002g0045 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.446-1167_446-1166i others(12): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 49535865 | ||||||
| chr19:49535869 | T | G | 2 | a0003c0007t0002g0045 a0003c0007t0002g0069 |
3 | HG02258.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.446-1164T>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49535869 | |||||||
| chr19:49535873 | T | G | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0151 others(9): Show |
18 | HG00408.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.446-1160T>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49535873 | |||||||
| chr19:49535873 | T | TAG | 9 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(6): Show |
17 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.446-1159_446-1158i others(4): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 49535873 | ||||||
| chr19:49535873 | T | TATAG | 5 | a0001c0001t0001g0094 a0001c0003t0001g0028 a0001c0003t0001g0046 others(2): Show |
6 | HG01433.hp2 HG02055.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.446-1136_446-1133d others(6): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 49535873 | ||||||
| chr19:49535873 | TATAG | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
8 | HG00423.hp2 HG00738.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-1136_446-1133d others(6): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 49535873 | ||||||
| chr19:49535877 | G | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(18): Show |
44 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.446-1156G>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49535877 | |||||||
| chr19:49535950 | TTAAA | T | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.446-1080_446-1077d others(6): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 49535950 | ||||||
| chr19:49535991 | C | CT | 6 | a0001c0001t0001g0054 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG01361.hp2 HG02074.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.446-1030dupT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 49535991 | ||||||
| chr19:49535991 | CT | C | 18 | a0001c0001t0001g0047 a0001c0001t0001g0052 a0002c0002t0002g0007 others(15): Show |
27 | HG00438.hp2 HG00544.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.446-1030delT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 49535991 | ||||||
| chr19:49536048 | G | A | 2 | a0001c0001t0001g0094 a0002c0002t0002g0062 |
2 | HG02055.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.446-985G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536048 | |||||||
| chr19:49536288 | C | CT | 12 | a0001c0001t0001g0023 a0001c0001t0001g0057 a0001c0001t0001g0074 others(9): Show |
14 | HG01070.hp1 HG01070.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.446-721dupT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 49536288 | ||||||
| chr19:49536288 | C | CTT | 15 | a0001c0001t0001g0138 a0002c0002t0002g0007 a0002c0002t0002g0025 others(12): Show |
24 | HG00438.hp2 HG01071.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.446-722_446-721dup others(2): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 49536288 | ||||||
| chr19:49536288 | CT | C | 21 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0055 others(18): Show |
22 | HG01069.hp1 HG01168.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.446-721delT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 49536288 | ||||||
| chr19:49536337 | G | C | 4 | a0002c0004t0002g0027 a0002c0004t0002g0029 a0002c0004t0002g0065 others(1): Show |
6 | HG01070.hp2 HG01109.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.446-696G>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536337 | |||||||
| chr19:49536362 | A | T | 1 | a0002c0002t0002g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.446-671A>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536362 | |||||||
| chr19:49536369 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.446-664C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536369 | |||||||
| chr19:49536374 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.446-659T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536374 | |||||||
| chr19:49536564 | G | T | 2 | a0001c0008t0001g0194 a0001c0008t0001g0195 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.446-469G>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536564 | |||||||
| chr19:49536607 | A | AT | 20 | a0001c0001t0001g0038 a0001c0001t0001g0053 a0001c0001t0001g0115 others(17): Show |
21 | HG00735.hp1 HG00735.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.446-407dupT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 49536607 | ||||||
| chr19:49536647 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.446-386C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536647 | |||||||
| chr19:49536769 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.446-264C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536769 | |||||||
| chr19:49536794 | TG | T | 7 | a0001c0003t0001g0020 a0001c0003t0001g0028 a0001c0003t0001g0046 others(4): Show |
10 | HG01433.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-235delG | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 49536794 | ||||||
| chr19:49536803 | G | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
36 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.446-230G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536803 | |||||||
| chr19:49536807 | TG | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0001g0088 |
4 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-225delG | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536807 | |||||||
| chr19:49536813 | C | T | 3 | a0003c0006t0002g0075 a0003c0006t0002g0076 a0003c0006t0002g0077 |
3 | HG01070.hp1 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.446-220C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536813 | |||||||
| chr19:49536895 | T | C | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.446-138T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536895 | |||||||
| chr19:49536954 | G | T | 7 | a0001c0003t0001g0020 a0001c0003t0001g0028 a0001c0003t0001g0046 others(4): Show |
10 | HG01433.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-79G>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536954 | |||||||
| chr19:49536964 | G | T | 7 | a0001c0003t0001g0020 a0001c0003t0001g0028 a0001c0003t0001g0046 others(4): Show |
10 | HG01433.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-69G>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49536964 | |||||||
| chr19:49537014 | GA | G | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.446-18delA | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 3/6 | chr19 | 49537014 | |||||||
| chr19:49537249 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0156 |
3 | HG01516.hp1 HG02738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.618+44G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49537249 | |||||||
| chr19:49537261 | C | T | 3 | a0002c0002t0002g0007 a0002c0002t0002g0060 a0002c0002t0002g0061 |
8 | HG00438.hp2 HG02083.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.618+56C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49537261 | |||||||
| chr19:49537286 | C | T | 16 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(13): Show |
25 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.618+81C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49537286 | |||||||
| chr19:49537369 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.618+164C>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49537369 | |||||||
| chr19:49537390 | T | C | 1 | a0001c0008t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.618+185T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49537390 | |||||||
| chr19:49537397 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.618+192G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49537397 | |||||||
| chr19:49537414 | G | A | 1 | a0002c0002t0002g0061 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.618+209G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49537414 | |||||||
| chr19:49537439 | G | A | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.618+234G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49537439 | |||||||
| chr19:49537512 | C | CT | 17 | a0001c0001t0001g0084 a0002c0002t0002g0007 a0002c0002t0002g0024 others(14): Show |
26 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.618+319dupT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 49537512 | ||||||
| chr19:49537726 | T | C | 5 | a0003c0006t0002g0075 a0003c0006t0002g0076 a0003c0006t0002g0077 others(2): Show |
6 | HG01070.hp1 HG01071.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.618+521T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49537726 | |||||||
| chr19:49537729 | C | T | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.618+524C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49537729 | |||||||
| chr19:49537788 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0120 a0001c0001t0001g0149 |
3 | NA18950.hp2 NA18954.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.618+583C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49537788 | |||||||
| chr19:49537789 | G | A | 1 | a0002c0004t0002g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.618+584G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49537789 | |||||||
| chr19:49537807 | AT | A | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.618+611delT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 49537807 | ||||||
| chr19:49537919 | A | G | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.618+714A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49537919 | |||||||
| chr19:49537969 | CT | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
78 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.618+773delT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 49537969 | ||||||
| chr19:49537990 | C | CT | 20 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(17): Show |
30 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.618+797dupT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 49537990 | ||||||
| chr19:49538022 | A | C | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.618+817A>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538022 | |||||||
| chr19:49538024 | C | T | 8 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0090 others(5): Show |
10 | HG00673.hp1 HG02129.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.618+819C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538024 | |||||||
| chr19:49538110 | G | A | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.618+905G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538110 | |||||||
| chr19:49538161 | G | GT | 14 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0043 others(11): Show |
17 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.619-939dupT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 49538161 | ||||||
| chr19:49538161 | GT | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0041 others(3): Show |
14 | HG00733.hp1 HG02486.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.619-939delT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 49538161 | ||||||
| chr19:49538161 | GTT | G | 18 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(15): Show |
27 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.619-940_619-939del others(2): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 49538161 | ||||||
| chr19:49538188 | A | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.619-931A>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538188 | |||||||
| chr19:49538193 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0142 |
4 | HG02723.hp2 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-926C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538193 | |||||||
| chr19:49538292 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.619-827G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538292 | |||||||
| chr19:49538298 | G | T | 1 | a0001c0001t0001g0100 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.619-821G>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538298 | |||||||
| chr19:49538314 | C | T | 17 | a0001c0001t0001g0166 a0002c0002t0002g0007 a0002c0002t0002g0024 others(14): Show |
26 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.619-805C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538314 | |||||||
| chr19:49538324 | G | A | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.619-795G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538324 | |||||||
| chr19:49538329 | AT | A | 6 | a0001c0001t0001g0035 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
7 | HG00099.hp1 HG00140.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.619-771delT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 49538329 | ||||||
| chr19:49538329 | ATT | A | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.619-772_619-771del others(2): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 49538329 | ||||||
| chr19:49538558 | C | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0042 others(11): Show |
25 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.619-561C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538558 | |||||||
| chr19:49538634 | T | C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0115 a0001c0001t0001g0117 others(2): Show |
6 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-485T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538634 | |||||||
| chr19:49538694 | G | A | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.619-425G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538694 | |||||||
| chr19:49538725 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.619-394A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538725 | |||||||
| chr19:49538759 | G | C | 16 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(13): Show |
25 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.619-360G>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538759 | |||||||
| chr19:49538777 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.619-342C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538777 | |||||||
| chr19:49538848 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.619-271C>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538848 | |||||||
| chr19:49538894 | T | C | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.619-225T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538894 | |||||||
| chr19:49538902 | G | T | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.619-217G>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538902 | |||||||
| chr19:49538973 | C | G | 2 | a0001c0008t0001g0194 a0001c0008t0001g0195 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.619-146C>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49538973 | |||||||
| chr19:49539018 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.619-101C>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49539018 | |||||||
| chr19:49539059 | C | T | 2 | a0001c0008t0001g0194 a0001c0008t0001g0195 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.619-60C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49539059 | |||||||
| chr19:49539114 | T | C | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
splice_region_variant&intron_variant | LOW | c.619-5T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 4/6 | chr19 | 49539114 | |||||||
| chr19:49539264 | CCCATCAT others(12): Show |
C | 1 | a0001c0001t0001g0047 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.679+86_679+104delC others(18): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539264 | |||||||
| chr19:49539278 | A | G | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.679+99A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539278 | |||||||
| chr19:49539309 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.679+130C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539309 | |||||||
| chr19:49539337 | A | AACATTTA others(69): Show |
4 | a0002c0004t0002g0027 a0002c0004t0002g0029 a0002c0004t0002g0065 others(1): Show |
6 | HG01070.hp2 HG01109.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.679+162_679+237dup others(76): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 49539337 | ||||||
| chr19:49539405 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.679+226G>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539405 | |||||||
| chr19:49539572 | C | T | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.679+393C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539572 | |||||||
| chr19:49539610 | T | TG | 107 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(104): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.679+436dupG | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 49539610 | ||||||
| chr19:49539658 | C | A | 2 | a0001c0008t0001g0194 a0001c0008t0001g0195 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.679+479C>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539658 | |||||||
| chr19:49539659 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.679+480T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539659 | |||||||
| chr19:49539715 | G | T | 1 | a0002c0002t0002g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.679+536G>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539715 | |||||||
| chr19:49539718 | A | AT | 21 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0038 others(18): Show |
27 | HG00733.hp1 HG01175.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.679+563dupT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 49539718 | ||||||
| chr19:49539718 | AT | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(53): Show |
97 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.679+563delT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 49539718 | ||||||
| chr19:49539718 | ATTTTT | A | 15 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(12): Show |
24 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.679+559_679+563del others(5): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 49539718 | ||||||
| chr19:49539718 | ATTTTTT | A | 6 | a0003c0006t0002g0075 a0003c0006t0002g0076 a0003c0006t0002g0077 others(3): Show |
7 | HG01070.hp1 HG01071.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.679+558_679+563del others(6): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 49539718 | ||||||
| chr19:49539722 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.679+543T>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539722 | |||||||
| chr19:49539747 | C | CAG | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.679+569_679+570dup others(2): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 49539747 | ||||||
| chr19:49539784 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.679+605G>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539784 | |||||||
| chr19:49539796 | C | G | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.679+617C>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539796 | |||||||
| chr19:49539815 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.679+636C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539815 | |||||||
| chr19:49539910 | A | G | 5 | a0003c0006t0002g0075 a0003c0006t0002g0076 a0003c0006t0002g0077 others(2): Show |
6 | HG01070.hp1 HG01071.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.679+731A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539910 | |||||||
| chr19:49539913 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.679+734G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539913 | |||||||
| chr19:49539952 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0159 |
2 | NA18988.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.679+773A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49539952 | |||||||
| chr19:49540018 | C | T | 23 | a0001c0001t0001g0105 a0002c0002t0002g0007 a0002c0002t0002g0024 others(20): Show |
33 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.679+839C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49540018 | |||||||
| chr19:49540161 | C | CTG | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.679+996_679+997dup others(2): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 49540161 | ||||||
| chr19:49540266 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.679+1087C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49540266 | |||||||
| chr19:49540429 | C | T | 4 | a0001c0003t0001g0028 a0001c0003t0001g0046 a0001c0003t0001g0181 others(1): Show |
5 | HG01433.hp2 HG02055.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.679+1250C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49540429 | |||||||
| chr19:49540476 | C | T | 1 | a0002c0002t0002g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.679+1297C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49540476 | |||||||
| chr19:49540570 | T | C | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.679+1391T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49540570 | |||||||
| chr19:49540581 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.679+1402T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49540581 | |||||||
| chr19:49540620 | T | TA | 24 | a0001c0001t0001g0047 a0001c0001t0001g0095 a0002c0002t0002g0007 others(21): Show |
34 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.679+1457dupA | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 49540620 | ||||||
| chr19:49540682 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.679+1503T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49540682 | |||||||
| chr19:49540850 | T | G | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.679+1671T>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49540850 | |||||||
| chr19:49540932 | CT | C | 8 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0090 others(5): Show |
10 | HG00673.hp1 HG01256.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.680-1606delT | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 49540932 | ||||||
| chr19:49540966 | T | C | 1 | a0001c0001t0009g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.680-1587T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49540966 | |||||||
| chr19:49541007 | T | A | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.680-1546T>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541007 | |||||||
| chr19:49541066 | G | T | 1 | a0002c0002t0002g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.680-1487G>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541066 | |||||||
| chr19:49541071 | T | C | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.680-1482T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541071 | |||||||
| chr19:49541082 | T | C | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.680-1471T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541082 | |||||||
| chr19:49541430 | C | T | 2 | a0004c0009t0001g0169 a0004c0009t0001g0183 |
2 | HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.680-1123C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541430 | |||||||
| chr19:49541474 | T | C | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.680-1079T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541474 | |||||||
| chr19:49541484 | C | G | 30 | a0001c0001t0001g0006 a0001c0001t0001g0058 a0001c0001t0001g0080 others(27): Show |
46 | HG00140.hp1 HG00438.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.680-1069C>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541484 | |||||||
| chr19:49541519 | T | C | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.680-1034T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541519 | |||||||
| chr19:49541594 | G | C | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.680-959G>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541594 | |||||||
| chr19:49541610 | G | A | 5 | a0001c0003t0001g0020 a0001c0003t0001g0028 a0001c0003t0001g0046 others(2): Show |
8 | HG01433.hp2 HG02055.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-943G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541610 | |||||||
| chr19:49541618 | G | A | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.680-935G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541618 | |||||||
| chr19:49541679 | G | T | 1 | a0004c0009t0001g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.680-874G>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541679 | |||||||
| chr19:49541697 | T | C | 7 | a0001c0003t0001g0020 a0001c0003t0001g0028 a0001c0003t0001g0046 others(4): Show |
10 | HG01433.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.680-856T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541697 | |||||||
| chr19:49541723 | T | A | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.680-830T>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541723 | |||||||
| chr19:49541825 | T | C | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.680-728T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541825 | |||||||
| chr19:49541840 | T | C | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.680-713T>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541840 | |||||||
| chr19:49541866 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.680-687G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541866 | |||||||
| chr19:49541948 | A | C | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.680-605A>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541948 | |||||||
| chr19:49541960 | A | T | 3 | a0002c0004t0002g0027 a0002c0004t0002g0029 a0002c0004t0002g0065 |
5 | HG01070.hp2 HG01255.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-593A>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49541960 | |||||||
| chr19:49542059 | C | CA | 17 | a0001c0001t0001g0057 a0001c0001t0001g0145 a0002c0002t0002g0007 others(14): Show |
26 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.680-477dupA | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 49542059 | ||||||
| chr19:49542059 | CA | C | 13 | a0001c0001t0001g0040 a0001c0001t0001g0102 a0001c0001t0001g0103 others(10): Show |
15 | HG00140.hp2 HG01169.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.680-477delA | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 49542059 | ||||||
| chr19:49542290 | C | T | 5 | a0001c0003t0001g0020 a0001c0003t0001g0028 a0001c0003t0001g0046 others(2): Show |
8 | HG01433.hp2 HG02055.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-263C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49542290 | |||||||
| chr19:49542544 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.680-9G>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 5/6 | chr19 | 49542544 | |||||||
| chr19:49542779 | C | T | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.879+27C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/6 | chr19 | 49542779 | |||||||
| chr19:49542908 | C | G | 21 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(18): Show |
31 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.879+156C>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/6 | chr19 | 49542908 | |||||||
| chr19:49542915 | A | AAGAGAGG others(17): Show |
12 | a0002c0002t0002g0024 a0002c0002t0002g0025 a0002c0002t0002g0064 others(9): Show |
16 | HG01070.hp2 HG01106.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.879+165_880-166dup others(24): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 49542915 | ||||||
| chr19:49542934 | C | CCAGAGAG others(17): Show |
2 | a0002c0002t0002g0026 a0002c0002t0002g0062 |
3 | HG02055.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.880-166_880-165ins others(24): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 49542934 | ||||||
| chr19:49542935 | C | CAG | 4 | a0002c0002t0002g0007 a0002c0002t0002g0060 a0002c0002t0002g0061 others(1): Show |
9 | HG00438.hp2 HG02083.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-167_880-166dup others(2): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 49542935 | ||||||
| chr19:49542969 | C | CAG | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.880-137_880-136ins others(2): Show |
RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/6 | chr19 | 49542969 | |||||||
| chr19:49542982 | A | G | 22 | a0002c0002t0002g0007 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
32 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.880-124A>G | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/6 | chr19 | 49542982 | |||||||
| chr19:49543028 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG02135.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.880-78C>T | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/6 | chr19 | 49543028 | |||||||
| chr19:49543071 | G | A | 7 | a0001c0003t0001g0020 a0001c0003t0001g0028 a0001c0003t0001g0046 others(4): Show |
10 | HG01433.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-35G>A | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/6 | chr19 | 49543071 | |||||||
| chr19:49543093 | A | C | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.880-13A>C | RCN3 | ENSG00000142552.8 | transcript | ENST00000270645.8 | protein_coding | 6/6 | chr19 | 49543093 |