Variant report

Variant	rs2156532
Chromosome Location	chr11:86287743-86287744
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:86285976..86287836-chr11:86291866..86294445,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12099044	1.00[ASN][1000 genomes]
rs12292032	1.00[ASN][1000 genomes]
rs17149180	1.00[ASN][1000 genomes]
rs1945141	1.00[ASN][1000 genomes]
rs34662182	1.00[ASN][1000 genomes]
rs4614483	1.00[ASN][1000 genomes]
rs55642252	1.00[ASN][1000 genomes]
rs56272084	1.00[ASN][1000 genomes]
rs58173252	1.00[ASN][1000 genomes]
rs58968600	1.00[ASN][1000 genomes]
rs59227416	1.00[ASN][1000 genomes]
rs59339534	1.00[ASN][1000 genomes]
rs59415795	1.00[ASN][1000 genomes]
rs61182121	1.00[ASN][1000 genomes]
rs61248687	1.00[ASN][1000 genomes]
rs61372386	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7103556	1.00[ASN][1000 genomes]
rs7103642	1.00[ASN][1000 genomes]
rs72961775	1.00[ASN][1000 genomes]
rs73514376	1.00[ASN][1000 genomes]
rs73528019	1.00[ASN][1000 genomes]
rs7941124	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044081	chr11:86133641-86868560	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv541118	chr11:86133641-86868560	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv898056	chr11:86156848-86304402	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
4	nsv555665	chr11:86230898-86417553	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer 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	esv1808984	chr11:86282680-86301717	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3463631	chr11:86284104-86288702	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3498293	chr11:86285433-86287994	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv555675	chr11:86285994-86288287	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv555676	chr11:86285994-86288584	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv555677	chr11:86285994-86291818	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv555678	chr11:86285994-86305977	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv555681	chr11:86286096-86288584	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv555682	chr11:86286147-86288287	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv555683	chr11:86286147-86288584	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv555684	chr11:86286341-86291818	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86263400-86288200	Weak transcription	Aorta	Aorta
2	chr11:86271000-86291200	Weak transcription	Gastric	stomach
3	chr11:86275400-86299400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr11:86276400-86299800	Weak transcription	Fetal Brain Male	brain
5	chr11:86277400-86289400	Weak transcription	Brain Anterior Caudate	brain
6	chr11:86279000-86289000	Weak transcription	NHEK	skin
7	chr11:86279800-86288000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr11:86281400-86289200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr11:86282000-86288200	Weak transcription	Colonic Mucosa	Colon
10	chr11:86282000-86288400	Weak transcription	Fetal Intestine Small	intestine
11	chr11:86283400-86289400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr11:86283400-86289400	Weak transcription	Stomach Mucosa	stomach
13	chr11:86283600-86288200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr11:86285000-86288800	Enhancers	HUVEC	blood vessel
15	chr11:86285400-86288400	Enhancers	A549	lung
16	chr11:86285400-86288800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr11:86285400-86288800	Enhancers	Right Atrium	heart
18	chr11:86285600-86288600	Enhancers	Spleen	Spleen
19	chr11:86285600-86288800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:86285600-86289400	Enhancers	NH-A	brain
21	chr11:86285600-86290600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr11:86286000-86288200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr11:86286000-86288400	Enhancers	Stomach Smooth Muscle	stomach
24	chr11:86286000-86289000	Weak transcription	HSMMtube	muscle
25	chr11:86286000-86299400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr11:86286200-86288200	Weak transcription	Fetal Muscle Leg	muscle
27	chr11:86286200-86288200	Weak transcription	Pancreas	Pancrea
28	chr11:86286200-86288800	Weak transcription	NHLF	lung
29	chr11:86286400-86288800	Weak transcription	Fetal Kidney	kidney
30	chr11:86286400-86289000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:86286400-86289000	Weak transcription	Fetal Heart	heart
32	chr11:86286400-86290200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr11:86286400-86298200	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr11:86286600-86288400	Enhancers	Muscle Satellite Cultured Cells	--
35	chr11:86286600-86288600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:86286600-86289000	Weak transcription	HMEC	breast
37	chr11:86286800-86288000	Weak transcription	NHDF-Ad	bronchial
38	chr11:86286800-86289800	Enhancers	Fetal Stomach	stomach
39	chr11:86287000-86288200	Enhancers	Hela-S3	cervix
40	chr11:86287000-86288200	Weak transcription	Osteobl	bone
41	chr11:86287200-86288600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr11:86287200-86289400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr11:86287200-86292000	Enhancers	Right Ventricle	heart
44	chr11:86287400-86287800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr11:86287400-86287800	Enhancers	Fetal Muscle Trunk	muscle
46	chr11:86287400-86288400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr11:86287400-86288800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr11:86287400-86288800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
49	chr11:86287400-86288800	Enhancers	Lung	lung
50	chr11:86287400-86291400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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