Variant report

Variant	rs11820232
Chromosome Location	chr11:77617633-77617634
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs11822541	1.00[AMR][1000 genomes]
rs11825750	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050891	chr11:77416645-77788002	Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv1037292	chr11:77431583-77745934	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv541092	chr11:77431583-77745934	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv949316	chr11:77454076-77769885	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv520740	chr11:77553638-77997936	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
6	nsv1035753	chr11:77577384-77866386	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers 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	52 gene(s)	inside rSNPs	diseases
7	nsv541093	chr11:77577384-77866386	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv555453	chr11:77577494-77618441	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv975954	chr11:77600915-77617903	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:77577400-77630800	Weak transcription	Fetal Heart	heart
2	chr11:77579200-77625000	Weak transcription	HMEC	breast
3	chr11:77583400-77670600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr11:77583400-77690000	Weak transcription	Colonic Mucosa	Colon
5	chr11:77586600-77625000	Weak transcription	Stomach Mucosa	stomach
6	chr11:77591800-77650400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr11:77592800-77690000	Weak transcription	Small Intestine	intestine
8	chr11:77593800-77625000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr11:77595400-77620000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr11:77595800-77671000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr11:77597400-77625000	Weak transcription	A549	lung
12	chr11:77597600-77629400	Weak transcription	Brain Germinal Matrix	brain
13	chr11:77597800-77617800	Weak transcription	Fetal Kidney	kidney
14	chr11:77597800-77620000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr11:77597800-77624800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr11:77597800-77625000	Weak transcription	Colon Smooth Muscle	Colon
17	chr11:77597800-77625000	Weak transcription	Pancreas	Pancrea
18	chr11:77597800-77625000	Weak transcription	NHDF-Ad	bronchial
19	chr11:77597800-77625200	Weak transcription	NHEK	skin
20	chr11:77597800-77625600	Weak transcription	HSMM	muscle
21	chr11:77597800-77629000	Weak transcription	Aorta	Aorta
22	chr11:77597800-77633800	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr11:77597800-77644200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr11:77597800-77644400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr11:77597800-77669800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr11:77597800-77671000	Weak transcription	Fetal Brain Male	brain
27	chr11:77597800-77678200	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr11:77597800-77690000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:77597800-77690000	Weak transcription	Esophagus	oesophagus
30	chr11:77597800-77690000	Weak transcription	Gastric	stomach
31	chr11:77601000-77618000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr11:77601800-77629800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr11:77602000-77640600	Weak transcription	K562	blood
34	chr11:77602200-77617800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr11:77602600-77625200	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr11:77602600-77644200	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr11:77602800-77690000	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr11:77603000-77625000	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr11:77603000-77637400	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr11:77603200-77618000	Weak transcription	Brain Substantia Nigra	brain
41	chr11:77603200-77622200	Weak transcription	NH-A	brain
42	chr11:77603200-77625000	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr11:77603200-77625000	Weak transcription	Osteobl	bone
44	chr11:77603200-77650200	Weak transcription	Fetal Brain Female	brain
45	chr11:77603400-77617800	Weak transcription	HepG2	liver
46	chr11:77603400-77625000	Weak transcription	HUVEC	blood vessel
47	chr11:77604200-77625000	Weak transcription	NHLF	lung
48	chr11:77604600-77625000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr11:77604800-77644200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr11:77605800-77624800	Weak transcription	Hela-S3	cervix

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links