Variant report

Variant	rs7577807
Chromosome Location	chr2:67285087-67285088
allele	A/C
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:9)

rs_ID	r²[population]
rs55853434	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55868434	1.00[ASN][1000 genomes]
rs6735857	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73937627	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7567815	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7583036	1.00[ASN][1000 genomes]
rs7586922	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7603889	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7608252	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008584	chr2:67168244-67703601	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv535775	chr2:67168244-67703601	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	esv2756926	chr2:67266707-67337017	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2759058	chr2:67266707-67465662	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	esv34381	chr2:67273120-67316250	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67277600-67286600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr2:67282000-67285800	Enhancers	Hela-S3	cervix
3	chr2:67282000-67285800	Enhancers	HepG2	liver
4	chr2:67283600-67285800	Enhancers	Liver	Liver
5	chr2:67283600-67292200	Weak transcription	Colon Smooth Muscle	Colon
6	chr2:67284600-67285400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr2:67284600-67286000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr2:67284800-67285200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:67284800-67285200	Enhancers	Small Intestine	intestine
10	chr2:67284800-67285600	Enhancers	Fetal Lung	lung
11	chr2:67285000-67285200	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr2:67285000-67290000	Weak transcription	Pancreas	Pancrea

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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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