Variant report

Variant	rs7285542
Chromosome Location	chr22:31134552-31134553
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:31031534..31034276-chr22:31133621..31135722,2	K562	blood:

Variant related genes	Relation type
ENSG00000100036	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11913598	1.00[AMR][1000 genomes]
rs11914209	1.00[AMR][1000 genomes]
rs7291536	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8138084	1.00[AMR][1000 genomes]
rs8141399	1.00[AMR][1000 genomes]
rs8142043	1.00[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	nsv915818	chr22:30708245-31346302	Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31114000-31140600	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr22:31115600-31149400	Weak transcription	Brain Hippocampus Middle	brain
3	chr22:31117000-31140200	Weak transcription	Pancreas	Pancrea
4	chr22:31118400-31138600	Weak transcription	Fetal Brain Female	brain
5	chr22:31123000-31137200	Weak transcription	Gastric	stomach
6	chr22:31126600-31136200	Weak transcription	K562	blood
7	chr22:31128200-31139600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr22:31129000-31136800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr22:31129000-31137200	Weak transcription	Brain Substantia Nigra	brain
10	chr22:31129000-31144800	Weak transcription	Brain Angular Gyrus	brain
11	chr22:31129000-31149400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr22:31129000-31149400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr22:31129200-31138800	Weak transcription	Brain Cingulate Gyrus	brain
14	chr22:31129400-31137400	Weak transcription	Brain Anterior Caudate	brain
15	chr22:31129800-31137000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr22:31130400-31136200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr22:31130600-31135800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr22:31131600-31137200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr22:31134000-31135600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr22:31134000-31135600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr22:31134000-31141600	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr22:31134200-31134600	Enhancers	NHDF-Ad	bronchial
23	chr22:31134200-31135200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr22:31134200-31135400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr22:31134200-31135400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr22:31134200-31135400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr22:31134200-31135600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr22:31134200-31136400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr22:31134400-31135000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr22:31134400-31136200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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