Variant report

Variant	rs191247742
Chromosome Location	chr8:130710786-130710787
allele	A/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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:130709158..130713272-chr8:130716107..130718644,3	K562	blood:
2	chr8:130709015..130711494-chr8:130712126..130713771,2	K562	blood:
3	chr8:130698168..130701867-chr8:130706682..130711085,4	MCF-7	breast:
4	chr8:130699826..130701651-chr8:130708566..130712426,4	K562	blood:
5	chr8:130700584..130702961-chr8:130710020..130711748,2	MCF-7	breast:
6	chr8:130709112..130710957-chr8:130718766..130720271,2	K562	blood:
7	chr8:130547962..130549604-chr8:130709178..130711041,2	MCF-7	breast:
8	chr8:130703853..130706502-chr8:130708490..130712451,4	K562	blood:
9	chr8:128747402..128749351-chr8:130710399..130712084,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000136997	Chromatin interaction

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	nsv967630	chr8:130710443-130711212	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130705800-130713600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr8:130707200-130713200	Weak transcription	Fetal Lung	lung
3	chr8:130708200-130720200	Weak transcription	Esophagus	oesophagus
4	chr8:130709400-130710800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr8:130709400-130710800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr8:130709400-130710800	Enhancers	HSMM	muscle
7	chr8:130709400-130710800	Enhancers	NH-A	brain
8	chr8:130709400-130710800	Enhancers	NHEK	skin
9	chr8:130709400-130710800	Enhancers	Osteobl	bone
10	chr8:130709400-130711400	Enhancers	A549	lung
11	chr8:130709600-130710800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr8:130709600-130710800	Enhancers	Muscle Satellite Cultured Cells	--
13	chr8:130709600-130710800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr8:130709600-130710800	Enhancers	HMEC	breast
15	chr8:130709600-130710800	Enhancers	NHDF-Ad	bronchial
16	chr8:130709600-130710800	Enhancers	NHLF	lung
17	chr8:130709600-130711600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr8:130709800-130710800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr8:130709800-130710800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr8:130709800-130710800	Enhancers	HSMMtube	muscle
21	chr8:130709800-130711600	Enhancers	K562	blood
22	chr8:130710400-130715400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr8:130710600-130713800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr8:130710600-130716400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr8:130710600-130719800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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