Variant report
Variant | rs1957422 |
---|---|
Chromosome Location | chr14:65360358-65360359 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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(count:3 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs1003370 | 0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10151551 | 0.82[EUR][1000 genomes] |
rs10162522 | 0.82[EUR][1000 genomes] |
rs1122339 | 0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs11844283 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12147448 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs17093568 | 0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1951489 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1957420 | 0.84[ASN][1000 genomes] |
rs1957430 | 0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1957433 | 0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1983769 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2016653 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2104170 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs230721 | 0.82[EUR][1000 genomes] |
rs230722 | 0.82[EUR][1000 genomes] |
rs2884307 | 0.82[ASN][1000 genomes] |
rs35179634 | 0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs368818 | 0.82[EUR][1000 genomes] |
rs374461 | 0.82[EUR][1000 genomes] |
rs375797 | 0.82[EUR][1000 genomes] |
rs3813424 | 0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs389370 | 0.82[EUR][1000 genomes] |
rs395112 | 0.82[EUR][1000 genomes] |
rs397901 | 0.82[EUR][1000 genomes] |
rs399508 | 0.82[EUR][1000 genomes] |
rs406811 | 0.82[EUR][1000 genomes] |
rs424222 | 0.82[EUR][1000 genomes] |
rs426044 | 0.82[EUR][1000 genomes] |
rs435006 | 0.82[EUR][1000 genomes] |
rs4899151 | 0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4902323 | 0.82[EUR][1000 genomes] |
rs55983720 | 0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs58989463 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs61989891 | 0.82[EUR][1000 genomes] |
rs6573584 | 0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7149121 | 0.82[EUR][1000 genomes] |
rs7149446 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7158624 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs72625650 | 0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs762072 | 0.82[EUR][1000 genomes] |
rs8008229 | 0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs8013371 | 0.81[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs8022462 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9323455 | 0.82[EUR][1000 genomes] |
rs9323456 | 0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3693169 | chr14:65344400-65381068 | Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
2 | nsv1311 | chr14:65352722-65379802 | Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | nsv510638 | chr14:65353025-65368298 | Enhancers Bivalent Enhancer Active TSS Weak transcription | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
4 | esv993830 | chr14:65357515-65363884 | Enhancers Weak transcription Active TSS | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
5 | esv3530154 | chr14:65360044-65363951 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | esv9140 | chr14:65360143-65363797 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | esv3391571 | chr14:65360199-65364497 | Enhancers Weak transcription Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
8 | nsv512363 | chr14:65360222-65363601 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
9 | esv3530153 | chr14:65360263-65363644 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
10 | esv3443608 | chr14:65360286-65363621 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
11 | esv3523216 | chr14:65360292-65363649 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
12 | esv3523214 | chr14:65360312-65363577 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
13 | esv3530157 | chr14:65360318-65363613 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
14 | esv3530156 | chr14:65360326-65363624 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
15 | esv3523215 | chr14:65360328-65363590 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
16 | esv3530152 | chr14:65360332-65363568 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
17 | esv3523217 | chr14:65360339-65363588 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
18 | esv3324101 | chr14:65360348-65363560 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:65358600-65368000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |