Variant report

Variant	rs10248345
Chromosome Location	chr7:87344608-87344609
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:87344474-87344630	K562	blood:	n/a	n/a

Variant related genes	Relation type
ABCB1	TF binding region

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10215700	0.88[ASN][1000 genomes]
rs10215973	0.88[ASN][1000 genomes]
rs10216040	0.91[ASN][1000 genomes]
rs10225955	0.86[ASN][1000 genomes]
rs10230718	0.88[ASN][1000 genomes]
rs10231033	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs10231094	0.84[ASN][1000 genomes]
rs10232449	0.95[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs10235854	0.91[ASN][1000 genomes]
rs10239922	0.88[ASN][1000 genomes]
rs10244734	0.88[ASN][1000 genomes]
rs10245617	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs10245767	0.88[ASN][1000 genomes]
rs10247258	0.93[ASN][1000 genomes]
rs10249603	0.91[ASN][1000 genomes]
rs10252226	0.93[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs10253864	0.91[ASN][1000 genomes]
rs10255051	0.91[ASN][1000 genomes]
rs10256319	0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10258021	0.95[ASN][1000 genomes]
rs10259182	0.93[ASN][1000 genomes]
rs10261685	0.91[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs10263074	0.91[ASN][1000 genomes]
rs10264991	0.86[ASN][1000 genomes]
rs10266417	0.91[ASN][1000 genomes]
rs10268868	0.88[ASN][1000 genomes]
rs10269158	0.88[ASN][1000 genomes]
rs10275831	0.91[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs10276409	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs10278483	0.95[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs10280397	0.91[ASN][1000 genomes]
rs10280686	0.81[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs10280904	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs10281645	0.84[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs10486997	0.86[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs10487000	0.91[ASN][1000 genomes]
rs11972683	0.95[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs11982729	0.91[ASN][1000 genomes]
rs12532279	0.93[ASN][1000 genomes]
rs12532358	0.91[ASN][1000 genomes]
rs12533477	0.88[ASN][1000 genomes]
rs12535013	0.88[ASN][1000 genomes]
rs12537294	0.86[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12538627	0.91[ASN][1000 genomes]
rs13437761	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs13438341	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs17149840	0.91[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs17149864	0.89[ASN][1000 genomes]
rs17149924	0.91[ASN][1000 genomes]
rs17149946	0.91[ASN][1000 genomes]
rs17149963	0.91[ASN][1000 genomes]
rs17150006	0.91[ASN][1000 genomes]
rs17150008	0.91[ASN][1000 genomes]
rs17169578	0.93[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2041049	0.88[ASN][1000 genomes]
rs2106522	0.86[ASN][1000 genomes]
rs2188523	0.95[ASN][1000 genomes]
rs2214101	0.86[ASN][1000 genomes]
rs2373574	0.93[ASN][1000 genomes]
rs28375568	0.91[ASN][1000 genomes]
rs28379741	0.91[ASN][1000 genomes]
rs28470575	0.86[ASN][1000 genomes]
rs28535601	0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs28535947	0.91[ASN][1000 genomes]
rs28537604	0.88[ASN][1000 genomes]
rs28546778	0.88[ASN][1000 genomes]
rs28572147	0.93[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs28624877	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs28627774	0.88[ASN][1000 genomes]
rs28666506	0.91[ASN][1000 genomes]
rs28742881	0.91[ASN][1000 genomes]
rs28774398	0.93[ASN][1000 genomes]
rs28879532	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs28890472	0.91[ASN][1000 genomes]
rs4148727	0.93[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs4148729	0.91[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6465117	0.86[ASN][1000 genomes]
rs6948061	0.88[ASN][1000 genomes]
rs6952943	0.88[ASN][1000 genomes]
rs6955897	0.86[ASN][1000 genomes]
rs7794263	0.91[ASN][1000 genomes]
rs9655953	0.82[AFR][1000 genomes]
rs9655954	0.88[ASN][1000 genomes]
rs976602	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888677	chr7:86802025-87781111	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv464622	chr7:86832603-87541248	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv607725	chr7:86832603-87541248	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv1015862	chr7:87075394-88049798	Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	nsv607729	chr7:87326929-87352572	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv888695	chr7:87328502-87430669	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv607730	chr7:87330423-87352572	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv1814479	chr7:87338467-87346819	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv3340641	chr7:87343816-87345864	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
10	esv3436890	chr7:87344166-87345464	Enhancers Weak transcription	TF binding region	1 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	chr7:87332600-87360000	Weak transcription	Liver	Liver

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