Variant report

Variant	rs73977711
Chromosome Location	chr2:173710851-173710852
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12053036	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12615893	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2194715	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3769292	0.83[ASN][1000 genomes]
rs3769294	0.86[ASN][1000 genomes]
rs3769298	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3769302	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59080171	0.81[ASN][1000 genomes]
rs724997	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73977703	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs956752	0.83[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:21 , 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	chr2:173707600-173711400	Weak transcription	Aorta	Aorta
5	chr2:173707800-173711400	Weak transcription	Lung	lung
6	chr2:173707800-173712000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr2:173708200-173713400	Weak transcription	Thymus	Thymus
8	chr2:173708400-173713600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:173708600-173712400	Enhancers	Right Ventricle	heart
10	chr2:173708800-173712400	Enhancers	Right Atrium	heart
11	chr2:173708800-173713200	Weak transcription	Fetal Intestine Large	intestine
12	chr2:173709000-173711000	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr2:173709000-173711200	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr2:173709200-173714200	Weak transcription	NHEK	skin
15	chr2:173710000-173711400	Weak transcription	Pancreas	Pancrea
16	chr2:173710000-173713200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr2:173710000-173719400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr2:173710200-173713200	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr2:173710200-173714200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr2:173710400-173711400	Weak transcription	Left Ventricle	heart
21	chr2:173710800-173712200	Weak transcription	Fetal Thymus	thymus

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