Variant report

Variant	rs1835402
Chromosome Location	chr7:84490170-84490171
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:84488567..84491272-chr7:84499868..84501444,2	K562	blood:
2	chr7:84480748..84484086-chr7:84489031..84492555,3	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10085820	0.92[AFR][1000 genomes]
rs10225298	0.92[AFR][1000 genomes]
rs10225557	0.92[AFR][1000 genomes]
rs10226288	0.92[AFR][1000 genomes]
rs10226313	0.89[AFR][1000 genomes]
rs10227472	0.92[AFR][1000 genomes]
rs10229365	0.92[AFR][1000 genomes]
rs10229476	0.92[AFR][1000 genomes]
rs10229726	0.92[AFR][1000 genomes]
rs10230012	0.92[AFR][1000 genomes]
rs10231227	0.92[AFR][1000 genomes]
rs10234993	0.92[AFR][1000 genomes]
rs10235044	0.92[AFR][1000 genomes]
rs10239054	0.92[AFR][1000 genomes]
rs10241357	0.92[AFR][1000 genomes]
rs10242005	0.92[AFR][1000 genomes]
rs10243021	0.92[AFR][1000 genomes]
rs10243755	0.92[AFR][1000 genomes]
rs10243828	0.92[AFR][1000 genomes]
rs10243859	0.92[AFR][1000 genomes]
rs10244922	0.92[AFR][1000 genomes]
rs10250111	0.92[AFR][1000 genomes]
rs10252528	0.92[AFR][1000 genomes]
rs10252836	0.92[AFR][1000 genomes]
rs10253565	0.92[AFR][1000 genomes]
rs10254493	0.92[AFR][1000 genomes]
rs10256352	0.92[AFR][1000 genomes]
rs10257078	0.92[AFR][1000 genomes]
rs10260523	0.92[AFR][1000 genomes]
rs10264147	0.92[AFR][1000 genomes]
rs10268505	0.92[AFR][1000 genomes]
rs10269671	0.85[AFR][1000 genomes]
rs10271353	0.92[AFR][1000 genomes]
rs10271605	0.92[AFR][1000 genomes]
rs10273534	0.92[AFR][1000 genomes]
rs10273650	0.92[AFR][1000 genomes]
rs10274814	0.85[AFR][1000 genomes]
rs10276443	0.92[AFR][1000 genomes]
rs10279991	0.85[AFR][1000 genomes]
rs10282093	0.92[AFR][1000 genomes]
rs13438389	0.92[AFR][1000 genomes]
rs28457219	0.92[AFR][1000 genomes]
rs28503172	0.92[AFR][1000 genomes]
rs28576399	0.85[AFR][1000 genomes]
rs28667540	0.92[AFR][1000 genomes]
rs4398846	0.92[AFR][1000 genomes]
rs59572545	0.92[AFR][1000 genomes]
rs9656563	0.92[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529344	chr7:83714286-84592857	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv949446	chr7:84003501-84763823	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	esv34238	chr7:84279023-84591966	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv831050	chr7:84355996-84527261	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84487800-84490400	Weak transcription	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links