Variant report

Variant	rs7786632
Chromosome Location	chr7:137577761-137577762
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10223970	1.00[CHB][hapmap]
rs10267096	1.00[CHB][hapmap]
rs10272404	1.00[TSI][hapmap]
rs10272604	1.00[CHB][hapmap]
rs11977277	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.87[ASN][1000 genomes]
rs273936	0.95[YRI][hapmap]
rs273938	0.95[YRI][hapmap]
rs273939	0.95[YRI][hapmap]
rs273940	0.95[YRI][hapmap]
rs273941	0.86[YRI][hapmap]
rs28370936	0.87[ASN][1000 genomes]
rs3735018	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs56200577	0.87[ASN][1000 genomes]
rs58258788	0.87[ASN][1000 genomes]
rs6974516	1.00[MEX][hapmap]
rs7786386	0.87[ASN][1000 genomes]
rs7801988	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][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	nsv1022793	chr7:137187383-137619359	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv831150	chr7:137500559-137652808	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv518070	chr7:137534627-137808839	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv608470	chr7:137573187-137577761	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137555600-137583200	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr7:137557800-137583800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr7:137558400-137579200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr7:137558800-137588400	Weak transcription	Stomach Mucosa	stomach
5	chr7:137567200-137583800	Strong transcription	Liver	Liver
6	chr7:137567400-137580200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:137567400-137583400	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr7:137567400-137583800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr7:137567400-137584000	Strong transcription	Fetal Intestine Large	intestine
10	chr7:137568000-137584200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr7:137568600-137584000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr7:137568800-137578800	Weak transcription	Fetal Kidney	kidney
13	chr7:137570200-137577800	Weak transcription	Small Intestine	intestine
14	chr7:137570200-137578600	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr7:137570200-137578600	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr7:137570200-137579800	Weak transcription	A549	lung
17	chr7:137570400-137578200	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr7:137570400-137578400	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr7:137570400-137578600	Weak transcription	Aorta	Aorta
20	chr7:137570400-137579200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr7:137570400-137584000	Weak transcription	Fetal Thymus	thymus
22	chr7:137570400-137585800	Weak transcription	Hela-S3	cervix
23	chr7:137570600-137578000	Weak transcription	HUVEC	blood vessel
24	chr7:137570600-137578600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr7:137570600-137579200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr7:137570600-137580600	Weak transcription	Esophagus	oesophagus
27	chr7:137570600-137580600	Weak transcription	Gastric	stomach
28	chr7:137570600-137583800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr7:137570600-137585400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr7:137570800-137578200	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr7:137570800-137578600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr7:137570800-137578600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr7:137571200-137578200	Weak transcription	Spleen	Spleen
34	chr7:137571400-137578400	Weak transcription	Brain Substantia Nigra	brain
35	chr7:137571400-137579800	Weak transcription	NHEK	skin
36	chr7:137571400-137584000	Weak transcription	Thymus	Thymus
37	chr7:137571600-137578000	Weak transcription	Brain Anterior Caudate	brain
38	chr7:137571800-137588200	Weak transcription	Brain Angular Gyrus	brain
39	chr7:137572000-137578000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr7:137572000-137578000	Weak transcription	Brain Cingulate Gyrus	brain
41	chr7:137572000-137578600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr7:137572000-137583800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr7:137572000-137584000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr7:137572000-137584400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr7:137572000-137585800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:137572200-137578600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr7:137572200-137578600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr7:137572200-137578600	Weak transcription	Colonic Mucosa	Colon
49	chr7:137572200-137578800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr7:137572200-137579000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links