Variant report

Variant	rs3923203
Chromosome Location	chr11:66835194-66835195
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:66834695..66837581-chr11:66838108..66840654,2	K562	blood:
2	chr11:66827940..66829622-chr11:66832632..66835357,2	K562	blood:
3	chr11:66792581..66795104-chr11:66833340..66835263,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000173227	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11602157	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12287978	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2282502	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7112925	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][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	nsv555226	chr11:66579572-66845362	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
3	esv1817552	chr11:66751014-66839985	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
4	nsv532287	chr11:66784014-67023899	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66825200-66838800	Weak transcription	Spleen	Spleen
2	chr11:66825200-66841400	Weak transcription	Aorta	Aorta
3	chr11:66825200-66849200	Weak transcription	Colon Smooth Muscle	Colon
4	chr11:66825400-66838800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr11:66825400-66839000	Weak transcription	Lung	lung
6	chr11:66825400-66839000	Weak transcription	Stomach Smooth Muscle	stomach
7	chr11:66825400-66839200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr11:66825400-66849400	Weak transcription	Ovary	ovary
9	chr11:66826600-66839000	Weak transcription	Fetal Intestine Large	intestine
10	chr11:66827600-66841800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr11:66828000-66839000	Weak transcription	NH-A	brain
12	chr11:66828000-66845600	Weak transcription	Osteobl	bone
13	chr11:66828400-66839000	Weak transcription	Right Atrium	heart
14	chr11:66830400-66838800	Weak transcription	Pancreas	Pancrea
15	chr11:66830600-66838400	Weak transcription	A549	lung
16	chr11:66830800-66839000	Weak transcription	Stomach Mucosa	stomach
17	chr11:66831400-66844600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr11:66832000-66841000	Strong transcription	NHEK	skin
19	chr11:66832400-66835200	Strong transcription	Fetal Intestine Small	intestine
20	chr11:66832600-66836800	Weak transcription	Fetal Muscle Leg	muscle
21	chr11:66833000-66835200	Strong transcription	Fetal Stomach	stomach
22	chr11:66833000-66835800	Strong transcription	HMEC	breast
23	chr11:66833000-66841000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr11:66833200-66835600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr11:66833200-66835600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr11:66833200-66835800	Strong transcription	Liver	Liver
27	chr11:66833200-66835800	Strong transcription	Esophagus	oesophagus
28	chr11:66833200-66836000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr11:66833600-66835200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr11:66833600-66835200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr11:66833600-66836000	Genic enhancers	Placenta	Placenta
32	chr11:66833800-66838800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr11:66833800-66841000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr11:66834000-66835200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr11:66834200-66835800	Strong transcription	Gastric	stomach
36	chr11:66834200-66836000	Strong transcription	Placenta Amnion	Placenta Amnion
37	chr11:66834200-66838800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr11:66834400-66839000	Weak transcription	Left Ventricle	heart
39	chr11:66834600-66836600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr11:66834800-66838800	Weak transcription	Right Ventricle	heart
41	chr11:66834800-66843400	Weak transcription	Hela-S3	cervix

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