Variant report

Variant	rs73230249
Chromosome Location	chr3:113632405-113632406
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs17666485	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6798319	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72954636	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013506	chr3:112890608-113680951	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv829678	chr3:113446177-113633053	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv877351	chr3:113450495-113637424	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv1013746	chr3:113460162-113646657	Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:113618200-113641800	Weak transcription	Fetal Intestine Large	intestine
2	chr3:113619200-113652600	Weak transcription	Pancreas	Pancrea
3	chr3:113626200-113642200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr3:113626600-113641800	Weak transcription	Fetal Intestine Small	intestine
5	chr3:113629400-113633000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr3:113631400-113633600	Enhancers	Liver	Liver
7	chr3:113631600-113666200	Weak transcription	Esophagus	oesophagus
8	chr3:113631800-113632600	Enhancers	Duodenum Smooth Muscle	Duodenum
9	chr3:113631800-113634200	Enhancers	NHDF-Ad	bronchial
10	chr3:113631800-113634600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr3:113631800-113637000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr3:113632000-113633200	Weak transcription	Osteobl	bone
13	chr3:113632000-113633400	Weak transcription	NHEK	skin
14	chr3:113632000-113634200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr3:113632000-113666000	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr3:113632200-113632800	Weak transcription	NHLF	lung
17	chr3:113632200-113656200	Weak transcription	Duodenum Mucosa	Duodenum
18	chr3:113632400-113632800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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