Variant report

Variant	rs3886463
Chromosome Location	chr2:171779492-171779493
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10930447	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11899713	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11904750	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12465605	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12468326	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16859026	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16859028	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16859076	1.00[EUR][1000 genomes]
rs17505447	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17608242	0.90[EUR][1000 genomes]
rs2081766	0.88[AFR][1000 genomes]
rs2081767	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2081768	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2356422	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3770436	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57556696	1.00[ASN][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	nsv431801	chr2:171721493-171966493	ZNF genes & repeats Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:171774600-171779800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr2:171775000-171784800	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr2:171775400-171779600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:171778000-171779600	Enhancers	HepG2	liver
5	chr2:171778200-171784800	Weak transcription	Right Ventricle	heart
6	chr2:171778400-171785000	Weak transcription	Right Atrium	heart
7	chr2:171778600-171780000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr2:171779000-171784600	Weak transcription	Fetal Heart	heart
9	chr2:171779400-171779800	Enhancers	Primary B cells from peripheral blood	blood
10	chr2:171779400-171781400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr2:171779400-171781800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links