Variant report

Variant	rs7121697
Chromosome Location	chr11:33652823-33652824
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:33651094..33655040-chr11:33655885..33660180,5	MCF-7	breast:

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11032322	1.00[EUR][1000 genomes]
rs11032323	1.00[ASN][1000 genomes]
rs11032334	1.00[CEU][hapmap]
rs11828443	1.00[MEX][hapmap]
rs11828494	1.00[MEX][hapmap]
rs12285827	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12288810	1.00[CEU][hapmap]
rs12291756	1.00[MEX][hapmap]
rs2272066	1.00[JPT][hapmap]
rs4333997	0.82[YRI][hapmap];0.81[AFR][1000 genomes]
rs6484659	1.00[MEX][hapmap]
rs7115000	1.00[MEX][hapmap]
rs7945032	1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044478	chr11:33008435-33656273	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
2	nsv1050944	chr11:33043155-33656273	Flanking Active TSS Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv540993	chr11:33043155-33656273	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv869418	chr11:33053073-33662479	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
5	nsv832112	chr11:33469782-33683052	Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv832113	chr11:33609202-33767781	Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33640600-33666400	Weak transcription	Brain Germinal Matrix	brain
2	chr11:33640800-33673600	Weak transcription	Fetal Brain Male	brain
3	chr11:33642600-33673600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr11:33642800-33657400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr11:33643000-33673600	Weak transcription	Brain Angular Gyrus	brain
6	chr11:33644400-33654400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:33644400-33654800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr11:33644600-33657600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr11:33652200-33653400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr11:33652200-33654800	Enhancers	A549	lung
11	chr11:33652200-33654800	Enhancers	NHEK	skin
12	chr11:33652200-33655200	Enhancers	HMEC	breast
13	chr11:33652200-33659600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr11:33652400-33653000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr11:33652400-33653000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr11:33652400-33653000	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr11:33652400-33653000	Enhancers	HUVEC	blood vessel
18	chr11:33652400-33653200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr11:33652400-33653200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr11:33652400-33653200	Enhancers	Fetal Thymus	thymus
21	chr11:33652400-33653200	Enhancers	HSMM	muscle
22	chr11:33652400-33653200	Enhancers	HSMMtube	muscle
23	chr11:33652400-33653400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr11:33652400-33653600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr11:33652400-33653800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr11:33652400-33654200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr11:33652400-33656200	Strong transcription	Fetal Brain Female	brain
28	chr11:33652400-33659200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:33652600-33653000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr11:33652600-33653000	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr11:33652600-33653200	Enhancers	Esophagus	oesophagus
32	chr11:33652800-33653000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr11:33652800-33653000	Enhancers	Placenta	Placenta
34	chr11:33652800-33654400	Weak transcription	Osteobl	bone
35	chr11:33652800-33654800	Weak transcription	NH-A	brain
36	chr11:33652800-33656400	Weak transcription	Placenta Amnion	Placenta Amnion

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