Variant report

Variant	rs920701
Chromosome Location	chr13:76417101-76417102
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs2273996	0.88[CEU][hapmap]
rs7334674	0.83[YRI][hapmap]
rs7996791	0.85[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs9318377	0.88[CEU][hapmap]
rs9530470	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9530472	0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs9530473	0.85[CHB][hapmap];0.85[CHD][hapmap];0.82[GIH][hapmap];0.91[JPT][hapmap];0.84[MKK][hapmap];0.92[ASN][1000 genomes]
rs9530474	0.92[ASN][1000 genomes]
rs9600563	0.81[CHB][hapmap];0.86[JPT][hapmap];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832646	chr13:76300428-76483102	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv2758333	chr13:76321610-76542003	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	esv2759950	chr13:76321610-76542003	Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76387800-76427200	Weak transcription	Ovary	ovary
2	chr13:76391200-76418600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr13:76391200-76431600	Strong transcription	Hela-S3	cervix
4	chr13:76394400-76435800	Weak transcription	Colon Smooth Muscle	Colon
5	chr13:76396400-76432000	Weak transcription	Brain Substantia Nigra	brain
6	chr13:76396400-76436800	Weak transcription	Fetal Brain Male	brain
7	chr13:76399000-76433200	Weak transcription	Small Intestine	intestine
8	chr13:76399800-76433000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr13:76400800-76428400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr13:76404800-76418400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr13:76406000-76428600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr13:76406000-76429600	Weak transcription	Primary hematopoietic stem cells	blood
13	chr13:76406000-76430600	Strong transcription	Osteobl	bone
14	chr13:76406000-76436800	Strong transcription	Muscle Satellite Cultured Cells	--
15	chr13:76406600-76435000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr13:76406800-76427800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr13:76408400-76435000	Strong transcription	HSMMtube	muscle
18	chr13:76408400-76435200	Strong transcription	NH-A	brain
19	chr13:76410200-76419600	Strong transcription	Fetal Intestine Large	intestine
20	chr13:76410400-76417600	Strong transcription	Rectal Mucosa Donor 31	rectum
21	chr13:76410800-76417200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr13:76411000-76420600	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr13:76411200-76418600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr13:76412400-76419200	Strong transcription	Skeletal Muscle Female	skeletal muscle
25	chr13:76412800-76417600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr13:76412800-76419800	Strong transcription	HepG2	liver
27	chr13:76412800-76420200	Strong transcription	Duodenum Mucosa	Duodenum
28	chr13:76413200-76436800	Strong transcription	NHDF-Ad	bronchial
29	chr13:76413600-76419200	Strong transcription	NHLF	lung
30	chr13:76413800-76437600	Strong transcription	HSMM	muscle
31	chr13:76414000-76433000	Strong transcription	Liver	Liver
32	chr13:76414200-76417600	Genic enhancers	Thymus	Thymus
33	chr13:76414200-76417800	Strong transcription	Placenta	Placenta
34	chr13:76414200-76418000	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr13:76414200-76419200	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr13:76414200-76420400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr13:76414200-76433400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr13:76414400-76417600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr13:76414400-76417600	Strong transcription	Gastric	stomach
40	chr13:76414400-76417600	Strong transcription	Pancreas	Pancrea
41	chr13:76414400-76417800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr13:76414400-76417800	Strong transcription	Aorta	Aorta
43	chr13:76414400-76418200	Strong transcription	Fetal Muscle Leg	muscle
44	chr13:76414400-76419000	Strong transcription	Fetal Intestine Small	intestine
45	chr13:76414400-76419200	Strong transcription	Right Ventricle	heart
46	chr13:76414400-76419200	Strong transcription	Sigmoid Colon	Sigmoid Colon
47	chr13:76414400-76426200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr13:76414400-76435200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr13:76414600-76417600	Strong transcription	HMEC	breast
50	chr13:76414600-76420200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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