Variant report

Variant	rs2690896
Chromosome Location	chr7:101351426-101351427
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:101350597..101352580-chr7:101511716..101513955,2	K562	blood:
2	chr7:101346602..101348960-chr7:101350465..101352401,2	MCF-7	breast:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12534998	0.87[ASN][1000 genomes]
rs12535663	0.93[ASN][1000 genomes]
rs1969432	0.86[ASN][1000 genomes]
rs2429068	0.94[ASN][1000 genomes]
rs2529179	0.95[ASN][1000 genomes]
rs2529180	0.82[ASN][1000 genomes]
rs2529181	0.90[ASN][1000 genomes]
rs2529182	0.95[ASN][1000 genomes]
rs2529185	0.81[ASN][1000 genomes]
rs2529186	0.93[ASN][1000 genomes]
rs2529187	0.93[ASN][1000 genomes]
rs2529188	0.94[ASN][1000 genomes]
rs2529189	0.94[ASN][1000 genomes]
rs2529190	0.93[ASN][1000 genomes]
rs2529242	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2529243	0.82[ASN][1000 genomes]
rs2529244	0.82[ASN][1000 genomes]
rs2529245	0.83[ASN][1000 genomes]
rs2529246	0.95[ASN][1000 genomes]
rs2529247	0.99[ASN][1000 genomes]
rs2690890	0.94[ASN][1000 genomes]
rs2690891	0.94[ASN][1000 genomes]
rs2690892	0.94[ASN][1000 genomes]
rs2690893	0.94[ASN][1000 genomes]
rs2690895	0.83[ASN][1000 genomes]
rs2690897	0.82[ASN][1000 genomes]
rs2690898	0.82[ASN][1000 genomes]
rs2690899	0.82[ASN][1000 genomes]
rs2690900	0.82[ASN][1000 genomes]
rs2690901	0.82[ASN][1000 genomes]
rs2690902	0.95[ASN][1000 genomes]
rs940479	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933653	chr7:100701931-101515782	Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv1018544	chr7:101225639-101424889	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv539045	chr7:101225639-101424889	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv482758	chr7:101231458-101395219	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv831079	chr7:101273495-101466776	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
6	nsv1021797	chr7:101342353-101466957	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv539046	chr7:101342353-101466957	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101332000-101376800	Weak transcription	Right Atrium	heart
2	chr7:101349600-101352000	Enhancers	Stomach Mucosa	stomach
3	chr7:101350000-101351600	Enhancers	Colonic Mucosa	Colon
4	chr7:101350000-101352600	Enhancers	Fetal Intestine Large	intestine
5	chr7:101350200-101352000	Enhancers	Fetal Intestine Small	intestine
6	chr7:101350600-101351800	Enhancers	Esophagus	oesophagus
7	chr7:101350800-101351800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr7:101350800-101352200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:101351000-101352000	Weak transcription	Fetal Thymus	thymus
10	chr7:101351000-101352000	Enhancers	Rectal Mucosa Donor 29	rectum
11	chr7:101351000-101352600	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr7:101351200-101352000	Enhancers	Duodenum Mucosa	Duodenum

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