Variant report

Variant	rs7779694
Chromosome Location	chr7:116440788-116440789
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:116375738..116377336-chr7:116438734..116441464,2	K562	blood:
2	7:116339031-116340618..7:116434729-116454408	Hela-S3	cervix:
3	7:116071525-116078307..7:116434729-116454408	H1-hESC	embryonic stem cell:	embryo
4	chr7:116434861..116437169-chr7:116440116..116443011,2	K562	blood:
5	7:116434729-116454408..7:117341506-117356953	Hela-S3	cervix:
6	7:116434729-116454408..7:117641436-117645830	GM12878	blood:
7	7:116434729-116454408..7:116610596-116619447	H1-hESC	embryonic stem cell:	embryo
8	7:116434729-116454408..7:116782481-116788433	GM12878	blood:
9	7:116093970-116105948..7:116434729-116454408	GM12878	blood:
10	7:115967532-115969617..7:116434729-116454408	H1-hESC	embryonic stem cell:	embryo
11	7:116245779-116258944..7:116434729-116454408	Hela-S3	cervix:
12	chr7:116435360..116437038-chr7:116438110..116441034,2	MCF-7	breast:
13	7:116434729-116454408..7:117326534-117332210	H1-hESC	embryonic stem cell:	embryo
14	7:116434729-116454408..7:116580605-116585719	Hela-S3	cervix:

No data

Variant related genes	Relation type
ENSG00000001626	Chromatin interaction
ENSG00000234826	Chromatin interaction
ENSG00000222150	Chromatin interaction
ENSG00000252672	Chromatin interaction
ENSG00000231210	Chromatin interaction
ENSG00000105976	Chromatin interaction
ENSG00000237813	Chromatin interaction
ENSG00000243243	Chromatin interaction
ENSG00000213050	Chromatin interaction
ENSG00000226367	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12533223	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12540703	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17138978	0.92[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17138983	0.92[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17139063	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17139068	0.82[CHB][hapmap];0.91[AMR][1000 genomes]
rs2237716	0.92[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3807996	0.92[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58086374	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61248776	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61657532	0.91[AMR][1000 genomes]
rs6949201	0.96[ASN][1000 genomes]
rs73471107	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73471137	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73471159	0.91[AMR][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	nsv831107	chr7:116414734-116649466	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:116421800-116444000	Weak transcription	Esophagus	oesophagus
2	chr7:116423000-116442600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr7:116424000-116440800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:116424200-116445400	Weak transcription	Left Ventricle	heart
5	chr7:116425000-116440800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:116426200-116440800	Weak transcription	HSMMtube	muscle
7	chr7:116427000-116440800	Weak transcription	NHDF-Ad	bronchial
8	chr7:116427400-116445200	Weak transcription	Pancreas	Pancrea
9	chr7:116429600-116441200	Weak transcription	Fetal Lung	lung
10	chr7:116433200-116442400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr7:116433200-116442600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr7:116434800-116442200	Weak transcription	Brain Substantia Nigra	brain
13	chr7:116435800-116442400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr7:116436200-116442600	Weak transcription	HUVEC	blood vessel
15	chr7:116436200-116442800	Weak transcription	Aorta	Aorta
16	chr7:116436400-116440800	Weak transcription	NH-A	brain
17	chr7:116436600-116443800	Weak transcription	Fetal Muscle Trunk	muscle
18	chr7:116436600-116445000	Enhancers	Hela-S3	cervix
19	chr7:116436800-116442600	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr7:116437000-116440800	Weak transcription	Placenta	Placenta
21	chr7:116437000-116441000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr7:116437000-116442200	Weak transcription	Fetal Muscle Leg	muscle
23	chr7:116437000-116444600	Weak transcription	Fetal Stomach	stomach
24	chr7:116437400-116442000	Enhancers	Fetal Intestine Large	intestine
25	chr7:116438200-116440800	Weak transcription	NHLF	lung
26	chr7:116438600-116440800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr7:116438600-116442200	Weak transcription	Adipose Nuclei	Adipose
28	chr7:116438600-116442200	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr7:116438600-116442800	Weak transcription	Colon Smooth Muscle	Colon
30	chr7:116438800-116440800	Weak transcription	Duodenum Mucosa	Duodenum
31	chr7:116438800-116441200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr7:116438800-116442600	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr7:116438800-116444600	Weak transcription	Colonic Mucosa	Colon
34	chr7:116438800-116448600	Weak transcription	Psoas Muscle	Psoas
35	chr7:116439000-116440800	Weak transcription	HSMM	muscle
36	chr7:116439000-116440800	Weak transcription	Osteobl	bone
37	chr7:116439000-116441000	Weak transcription	Stomach Mucosa	stomach
38	chr7:116439200-116440800	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr7:116439200-116441000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr7:116439600-116441000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:116439600-116441400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr7:116439800-116444600	Weak transcription	Small Intestine	intestine
43	chr7:116439800-116446000	Enhancers	Liver	Liver
44	chr7:116440000-116442400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr7:116440200-116440800	Enhancers	A549	lung
46	chr7:116440200-116441000	Enhancers	NHEK	skin
47	chr7:116440200-116441200	Enhancers	HMEC	breast
48	chr7:116440200-116442000	Enhancers	Fetal Intestine Small	intestine
49	chr7:116440200-116442400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr7:116440200-116443600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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