Variant report

Variant	rs6743095
Chromosome Location	chr2:171794628-171794629
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	chr2:171788393..171792186-chr2:171793028..171799958,7	MCF-7	breast:
2	chr2:171783893..171791751-chr2:171794157..171800017,11	MCF-7	breast:

Variant related genes	Relation type
ENSG00000115806	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1035839	0.98[EUR][1000 genomes]
rs13017649	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13028361	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2676139	0.98[EUR][1000 genomes]
rs2676143	0.95[EUR][1000 genomes]
rs2676145	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2676158	0.93[EUR][1000 genomes]
rs2723253	0.91[EUR][1000 genomes]
rs4668353	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4668356	0.93[EUR][1000 genomes]
rs6711510	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6746413	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6753513	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7608813	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs966181	0.98[EUR][1000 genomes]
rs999837	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431801	chr2:171721493-171966493	ZNF genes & repeats Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:171787000-171810400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:171787200-171795200	Weak transcription	Ovary	ovary
3	chr2:171787400-171806000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr2:171787400-171806000	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr2:171787400-171806000	Weak transcription	Esophagus	oesophagus
6	chr2:171787400-171806000	Weak transcription	Psoas Muscle	Psoas
7	chr2:171787400-171807200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr2:171787400-171808200	Weak transcription	Aorta	Aorta
9	chr2:171787400-171810000	Weak transcription	Small Intestine	intestine
10	chr2:171787600-171796600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr2:171787600-171806800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr2:171787600-171807600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr2:171787600-171829800	Weak transcription	Right Atrium	heart
14	chr2:171787800-171795000	Weak transcription	Adipose Nuclei	Adipose
15	chr2:171787800-171795800	Weak transcription	Primary B cells from cord blood	blood
16	chr2:171787800-171798800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr2:171787800-171806000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr2:171787800-171806000	Weak transcription	Stomach Smooth Muscle	stomach
19	chr2:171787800-171806200	Weak transcription	Fetal Kidney	kidney
20	chr2:171787800-171806600	Weak transcription	Fetal Brain Female	brain
21	chr2:171787800-171807000	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr2:171787800-171807400	Weak transcription	Brain Germinal Matrix	brain
23	chr2:171787800-171809200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr2:171788000-171805800	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr2:171788000-171806000	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr2:171788000-171806000	Weak transcription	Brain Substantia Nigra	brain
27	chr2:171788000-171806200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr2:171788000-171806600	Weak transcription	Fetal Lung	lung
29	chr2:171788000-171806800	Weak transcription	Brain Anterior Caudate	brain
30	chr2:171788000-171806800	Weak transcription	A549	lung
31	chr2:171788000-171807600	Weak transcription	Brain Hippocampus Middle	brain
32	chr2:171788000-171808400	Weak transcription	Brain Angular Gyrus	brain
33	chr2:171788200-171795600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:171788200-171806200	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr2:171788400-171805400	Weak transcription	HUVEC	blood vessel
36	chr2:171788400-171805600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr2:171788400-171806200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr2:171788800-171795400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr2:171789000-171795800	Weak transcription	Rectal Smooth Muscle	rectum
40	chr2:171789000-171805600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr2:171789200-171795200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr2:171789400-171798800	Weak transcription	NHDF-Ad	bronchial
43	chr2:171789400-171805400	Weak transcription	Hela-S3	cervix
44	chr2:171789400-171805800	Weak transcription	Osteobl	bone
45	chr2:171789400-171806000	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr2:171789600-171810000	Weak transcription	Stomach Mucosa	stomach
47	chr2:171790600-171795600	Weak transcription	Colon Smooth Muscle	Colon
48	chr2:171790600-171806000	Weak transcription	Duodenum Mucosa	Duodenum
49	chr2:171791200-171795200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr2:171791200-171799000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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