Variant report

Variant	rs2531071
Chromosome Location	chr7:149984010-149984011
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:1)

rs_ID	r²[population]
rs71537936	0.87[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889435	chr7:149585379-150013393	ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv889452	chr7:149838371-150003208	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1034409	chr7:149844639-150447071	Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
4	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
5	nsv970966	chr7:149961366-150002640	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
6	nsv1015582	chr7:149967986-150285104	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149959200-149986200	Weak transcription	Lung	lung
2	chr7:149974200-149989000	Weak transcription	Esophagus	oesophagus
3	chr7:149976400-149993200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr7:149978200-149985000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:149978800-150000000	Weak transcription	Pancreas	Pancrea
6	chr7:149979400-149987800	Weak transcription	Right Atrium	heart
7	chr7:149981600-149990800	Weak transcription	Fetal Intestine Small	intestine
8	chr7:149983000-149995600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr7:149983200-149990800	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr7:149983400-149996600	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr7:149983600-149984200	Enhancers	Liver	Liver
12	chr7:149983800-149985000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:149983800-149987400	Weak transcription	K562	blood
14	chr7:149984000-149984200	Enhancers	Colonic Mucosa	Colon
15	chr7:149984000-149984600	Enhancers	HepG2	liver
16	chr7:149984000-149985000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr7:149984000-149985000	Weak transcription	Dnd41	blood
18	chr7:149984000-149987400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:149984000-149989000	Weak transcription	Rectal Mucosa Donor 31	rectum

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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