Variant report

Variant	rs207434
Chromosome Location	chr2:31555032-31555033
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:30884239..30886249-chr2:31553808..31556092,2	K562	blood:

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs207440	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs207445	0.91[AMR][1000 genomes];1.00[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	nsv948552	chr2:31118599-31595424	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv949028	chr2:31502801-31665108	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
3	esv2762446	chr2:31521093-31610311	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31547800-31556200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr2:31548000-31556000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:31548000-31556000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr2:31548000-31556200	Weak transcription	Liver	Liver
5	chr2:31548000-31556400	Weak transcription	HMEC	breast
6	chr2:31548000-31557600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:31548000-31558400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr2:31548000-31634600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr2:31548400-31558600	Weak transcription	NHEK	skin
10	chr2:31552400-31556000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr2:31552800-31557000	Weak transcription	Fetal Intestine Large	intestine
12	chr2:31553400-31556200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
13	chr2:31553400-31556800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr2:31553400-31559600	Weak transcription	Duodenum Mucosa	Duodenum
15	chr2:31553600-31560200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr2:31554000-31555400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr2:31554000-31556400	Enhancers	Fetal Heart	heart
18	chr2:31554400-31556200	Weak transcription	Primary B cells from peripheral blood	blood
19	chr2:31554600-31555600	Weak transcription	Right Ventricle	heart
20	chr2:31554600-31556400	Weak transcription	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links