Variant report

Variant	rs10923778
Chromosome Location	chr1:119783019-119783020
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs12058436	1.00[AMR][1000 genomes]
rs12065477	1.00[AMR][1000 genomes]
rs57903762	1.00[AMR][1000 genomes]
rs58854146	1.00[AMR][1000 genomes]
rs72991462	1.00[AMR][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	nsv932014	chr1:119476480-120471049	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	86 gene(s)	inside rSNPs	diseases
2	nsv831192	chr1:119671172-119843226	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
3	nsv917091	chr1:119688975-120023222	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	esv34089	chr1:119752112-120072961	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:119722000-119784400	Weak transcription	Left Ventricle	heart
2	chr1:119740600-119785200	Weak transcription	Ovary	ovary
3	chr1:119744600-119785000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr1:119749400-119783600	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr1:119760200-119792200	Weak transcription	Spleen	Spleen
6	chr1:119768800-119791800	Weak transcription	Psoas Muscle	Psoas
7	chr1:119771000-119799600	Weak transcription	Fetal Intestine Small	intestine
8	chr1:119779600-119794400	Weak transcription	Gastric	stomach
9	chr1:119782800-119783200	Weak transcription	Rectal Smooth Muscle	rectum
10	chr1:119783000-119783200	ZNF genes & repeats	Aorta	Aorta
11	chr1:119783000-119783200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet

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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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