Variant report

Variant	rs3769298
Chromosome Location	chr2:173713951-173713952
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs12053036	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12615893	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2194715	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3769292	0.84[ASN][1000 genomes]
rs3769294	0.88[ASN][1000 genomes]
rs3769302	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59080171	0.83[ASN][1000 genomes]
rs724997	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73977703	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73977706	1.00[AFR][1000 genomes]
rs73977711	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs956752	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533927	chr2:173161637-173796894	Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	esv2760591	chr2:173396905-173719520	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173689200-173723200	Weak transcription	Esophagus	oesophagus
2	chr2:173705800-173714400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr2:173707400-173714800	Enhancers	Fetal Heart	heart
4	chr2:173709200-173714200	Weak transcription	NHEK	skin
5	chr2:173710000-173719400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr2:173710200-173714200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr2:173711000-173714200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr2:173712200-173714600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:173713000-173714200	Weak transcription	Pancreas	Pancrea
10	chr2:173713000-173714600	Enhancers	Fetal Intestine Small	intestine
11	chr2:173713200-173714200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:173713200-173714800	Enhancers	Fetal Intestine Large	intestine
13	chr2:173713200-173714800	Enhancers	Hela-S3	cervix
14	chr2:173713400-173714400	Weak transcription	Fetal Stomach	stomach
15	chr2:173713400-173714400	Weak transcription	Small Intestine	intestine
16	chr2:173713600-173714800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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

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