Variant report

Variant	rs6760497
Chromosome Location	chr2:211455953-211455954
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10180357	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11684318	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12991680	0.92[EUR][1000 genomes]
rs13385991	0.90[EUR][1000 genomes]
rs13414563	0.81[EUR][1000 genomes]
rs2302911	0.87[EUR][1000 genomes]
rs2371001	0.85[EUR][1000 genomes]
rs28499505	0.83[EUR][1000 genomes]
rs4309518	0.93[EUR][1000 genomes]
rs6435577	0.83[EUR][1000 genomes]
rs6714124	0.83[EUR][1000 genomes]
rs6755648	0.83[EUR][1000 genomes]
rs7422569	0.92[EUR][1000 genomes]
rs7576225	0.89[EUR][1000 genomes]
rs7583733	0.83[EUR][1000 genomes]
rs7588072	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9288418	0.95[AFR][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	esv3398091	chr2:211315261-211634200	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1013658	chr2:211447246-211809945	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv536135	chr2:211447246-211809945	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211438400-211459600	Weak transcription	Small Intestine	intestine
2	chr2:211442400-211484200	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr2:211442800-211477800	Strong transcription	Liver	Liver
4	chr2:211448600-211480800	Weak transcription	Aorta	Aorta
5	chr2:211448800-211460200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr2:211448800-211475400	Weak transcription	Ovary	ovary
7	chr2:211449800-211458200	Strong transcription	Hela-S3	cervix
8	chr2:211449800-211467000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr2:211450000-211457600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:211450000-211458600	Strong transcription	Fetal Intestine Large	intestine
11	chr2:211450000-211466800	Weak transcription	HepG2	liver
12	chr2:211450200-211481400	Strong transcription	Duodenum Mucosa	Duodenum
13	chr2:211450800-211456600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr2:211455000-211457200	Weak transcription	Fetal Intestine Small	intestine
15	chr2:211455800-211456400	Enhancers	Brain Substantia Nigra	brain

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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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