Variant report

Variant	rs11225132
Chromosome Location	chr11:101989718-101989719
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	chr11:101981472..101985692-chr11:101986825..101990078,4	MCF-7	breast:
2	chr11:101984887..101986803-chr11:101989514..101991065,2	K562	blood:

Variant related genes	Relation type
ENSG00000137693	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10750631	0.85[EUR][1000 genomes]
rs10791563	0.88[EUR][1000 genomes]
rs10895255	0.91[EUR][1000 genomes]
rs10895256	0.92[EUR][1000 genomes]
rs11225139	0.88[AFR][1000 genomes]
rs11225141	0.88[AFR][1000 genomes]
rs1365331	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1426395	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1426398	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1549496	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1820453	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2033081	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2033083	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3752685	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3824930	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61918360	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61918361	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7105334	0.92[EUR][1000 genomes]
rs7106388	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7108820	0.88[AFR][1000 genomes]
rs7128788	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7931899	0.93[EUR][1000 genomes]
rs7932563	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9787758	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs983112	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[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	esv3362945	chr11:101736547-102114246	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv898333	chr11:101832670-102079986	Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1052348	chr11:101987090-102255753	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv556141	chr11:101988061-102207851	Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101983400-101998200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:101983600-101990800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr11:101983600-101990800	Weak transcription	Brain Anterior Caudate	brain
4	chr11:101983600-101990800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr11:101983600-101990800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr11:101983600-101991000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr11:101983600-101998000	Weak transcription	Right Ventricle	heart
8	chr11:101983600-101998200	Weak transcription	Colonic Mucosa	Colon
9	chr11:101983600-102014800	Weak transcription	Pancreas	Pancrea
10	chr11:101984000-101991600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr11:101984400-101991600	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr11:101984800-101991600	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:101985000-101991400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr11:101985200-101989800	Weak transcription	Fetal Brain Male	brain
15	chr11:101985200-101998000	Weak transcription	Gastric	stomach
16	chr11:101985200-102009200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr11:101985600-101991200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr11:101985800-101990800	Enhancers	Fetal Intestine Large	intestine
19	chr11:101986000-101991000	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr11:101986000-101991600	Enhancers	Colon Smooth Muscle	Colon
21	chr11:101986200-101991600	Enhancers	Stomach Mucosa	stomach
22	chr11:101986600-101989800	Weak transcription	Aorta	Aorta
23	chr11:101986600-101990800	Flanking Active TSS	A549	lung
24	chr11:101986800-101991000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr11:101986800-101991800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr11:101986800-101992000	Weak transcription	Psoas Muscle	Psoas
27	chr11:101986800-101992200	Weak transcription	Fetal Muscle Leg	muscle
28	chr11:101986800-101995400	Weak transcription	Fetal Muscle Trunk	muscle
29	chr11:101986800-101995600	Weak transcription	Right Atrium	heart
30	chr11:101987000-101991400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr11:101987400-101991000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr11:101987400-101992000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr11:101987400-101995000	Weak transcription	Placenta	Placenta
34	chr11:101987400-101996600	Weak transcription	Duodenum Mucosa	Duodenum
35	chr11:101988200-101990000	Enhancers	H1 Cell Line	embryonic stem cell
36	chr11:101988200-101991000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr11:101988200-101991400	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr11:101988400-101989800	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr11:101988400-101990600	Weak transcription	Spleen	Spleen
40	chr11:101988600-101989800	Genic enhancers	NH-A	brain
41	chr11:101988600-101990000	Enhancers	Ovary	ovary
42	chr11:101988600-101990600	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr11:101988600-101991000	Weak transcription	HSMMtube	muscle
44	chr11:101988600-101992000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr11:101988600-101992400	Genic enhancers	Fetal Lung	lung
46	chr11:101988800-101989800	Weak transcription	NHLF	lung
47	chr11:101988800-101990600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:101988800-101990600	Weak transcription	HSMM	muscle
49	chr11:101988800-101990800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr11:101988800-102009000	Weak transcription	Stomach Smooth Muscle	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links