Variant report

Variant	rs7577347
Chromosome Location	chr2:205718651-205718652
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10190031	0.84[ASN][1000 genomes]
rs10201810	0.92[EUR][1000 genomes]
rs10203289	0.84[ASN][1000 genomes]
rs12328364	0.92[EUR][1000 genomes]
rs12612230	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13393061	0.81[EUR][1000 genomes]
rs13393275	0.85[EUR][1000 genomes]
rs13408553	0.92[EUR][1000 genomes]
rs13422729	0.85[EUR][1000 genomes]
rs16836712	0.92[EUR][1000 genomes]
rs28850029	0.85[EUR][1000 genomes]
rs58687976	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59922842	0.85[EUR][1000 genomes]
rs6435255	0.85[EUR][1000 genomes]
rs6435256	0.81[ASN][1000 genomes]
rs6725702	0.81[EUR][1000 genomes]
rs6726480	0.84[ASN][1000 genomes]
rs6726748	0.92[EUR][1000 genomes]
rs6755344	0.92[EUR][1000 genomes]
rs73068606	0.81[EUR][1000 genomes]
rs73068608	0.81[EUR][1000 genomes]
rs7605954	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998485	chr2:205407813-206184006	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv536122	chr2:205407813-206184006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1010210	chr2:205489653-206076013	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv2757846	chr2:205539832-205841174	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2759111	chr2:205539832-205841174	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv875724	chr2:205572718-205727222	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv875725	chr2:205572718-205760800	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:205717800-205718800	Enhancers	Fetal Stomach	stomach
2	chr2:205717800-205719400	Enhancers	Rectal Smooth Muscle	rectum
3	chr2:205718000-205719600	Enhancers	Colon Smooth Muscle	Colon
4	chr2:205718200-205719200	Enhancers	Duodenum Smooth Muscle	Duodenum
5	chr2:205718600-205725200	Weak transcription	Fetal Lung	lung

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