Variant report

Variant	rs16927404
Chromosome Location	chr11:35381329-35381330
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:35373926..35376824-chr11:35378507..35382009,3	MCF-7	breast:

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs7114489	0.84[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045837	chr11:34893992-35395190	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv832120	chr11:35277410-35490304	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	esv2758264	chr11:35319320-35480522	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv2759819	chr11:35319320-35480522	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv430372	chr11:35376124-35430324	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35367000-35385400	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr11:35370200-35384200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr11:35374400-35381400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr11:35374400-35381600	Weak transcription	Pancreas	Pancrea
5	chr11:35374400-35384600	Weak transcription	Psoas Muscle	Psoas
6	chr11:35374400-35384600	Weak transcription	Right Ventricle	heart
7	chr11:35375000-35383600	Weak transcription	Left Ventricle	heart
8	chr11:35376400-35384400	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr11:35376600-35385000	Weak transcription	HSMM	muscle
10	chr11:35377000-35381400	Weak transcription	Brain Angular Gyrus	brain
11	chr11:35377000-35383800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr11:35377000-35384600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr11:35377000-35384600	Weak transcription	Right Atrium	heart
14	chr11:35377200-35384400	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr11:35377200-35384800	Weak transcription	Osteobl	bone
16	chr11:35379000-35381800	Enhancers	NHLF	lung
17	chr11:35379000-35382000	Enhancers	Hela-S3	cervix
18	chr11:35379200-35382000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:35379400-35382200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr11:35379400-35382400	Enhancers	NHDF-Ad	bronchial
21	chr11:35379800-35382200	Enhancers	Adipose Nuclei	Adipose
22	chr11:35379800-35382200	Enhancers	Brain Anterior Caudate	brain
23	chr11:35379800-35384600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr11:35380200-35381800	Flanking Active TSS	HepG2	liver
25	chr11:35380200-35382200	Flanking Active TSS	Liver	Liver
26	chr11:35380400-35381800	Enhancers	Brain Germinal Matrix	brain
27	chr11:35380400-35382000	Enhancers	Brain Hippocampus Middle	brain
28	chr11:35380400-35382200	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr11:35380400-35382200	Enhancers	Colon Smooth Muscle	Colon
30	chr11:35380400-35384800	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr11:35380600-35381400	Weak transcription	Fetal Brain Female	brain
32	chr11:35380600-35381800	Enhancers	Rectal Smooth Muscle	rectum
33	chr11:35380600-35383600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr11:35380800-35381800	Enhancers	Fetal Brain Male	brain
35	chr11:35380800-35382000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr11:35380800-35382000	Enhancers	Brain Substantia Nigra	brain
37	chr11:35381000-35381800	Enhancers	HMEC	breast
38	chr11:35381000-35382200	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr11:35381000-35384600	Weak transcription	Aorta	Aorta
40	chr11:35381200-35381400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr11:35381200-35381600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr11:35381200-35381600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
43	chr11:35381200-35382000	Enhancers	Fetal Muscle Leg	muscle
44	chr11:35381200-35384600	Weak transcription	Duodenum Smooth Muscle	Duodenum

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