Variant report

Variant	rs7711892
Chromosome Location	chr5:108066842-108066843
allele	A/C
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	CEBPB	chr5:108066655-108067022	K562	blood:	n/a	chr5:108066832-108066843
2	CEBPB	chr5:108066679-108066995	HepG2	liver:	n/a	chr5:108066832-108066843
3	CEBPB	chr5:108066613-108066957	K562	blood:	n/a	chr5:108066832-108066843
4	CEBPB	chr5:108066727-108066976	A549	lung:	n/a	chr5:108066832-108066843
5	CEBPB	chr5:108066545-108067015	IMR90	lung:	n/a	chr5:108066832-108066843
6	SPI1	chr5:108066054-108066857	GM12878	blood:	n/a	chr5:108066494-108066503
7	NFIC	chr5:108066219-108066903	GM12878	blood:	n/a	n/a
8	GATA2	chr5:108066297-108066929	HUVEC	blood vessel:	n/a	chr5:108066491-108066501 chr5:108066533-108066542
9	CUX1	chr5:108066364-108066872	GM12878	blood:	n/a	chr5:108066681-108066695

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:108060235..108074407-chr5:108078172..108087811,48	K562	blood:
2	chr5:108059312..108068052-chr5:108079113..108087366,42	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FER-3	chr5:108065631-108067538	NONHSAT103128

Variant related genes	Relation type
LINC01023	TF binding region
ENSG00000151422	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10036583	1.00[JPT][hapmap]
rs10037675	1.00[JPT][hapmap]
rs10039132	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10039951	1.00[JPT][hapmap]
rs10041657	1.00[JPT][hapmap]
rs10042152	1.00[JPT][hapmap]
rs10042569	1.00[JPT][hapmap]
rs10050547	1.00[JPT][hapmap]
rs10052208	1.00[JPT][hapmap]
rs10052531	1.00[JPT][hapmap]
rs10054086	1.00[JPT][hapmap]
rs10061811	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10064960	1.00[JPT][hapmap]
rs10065605	1.00[JPT][hapmap]
rs10065611	1.00[JPT][hapmap]
rs10066173	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10070327	1.00[JPT][hapmap]
rs10077917	1.00[JPT][hapmap]
rs10214241	1.00[ASN][1000 genomes]
rs10223256	0.82[JPT][hapmap]
rs10477428	1.00[JPT][hapmap]
rs10477429	1.00[JPT][hapmap]
rs10477432	1.00[JPT][hapmap]
rs10477931	1.00[JPT][hapmap]
rs11741855	0.88[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11748534	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12719099	1.00[JPT][hapmap]
rs13358881	1.00[JPT][hapmap]
rs13359423	1.00[JPT][hapmap]
rs13360253	1.00[JPT][hapmap]
rs1396444	1.00[JPT][hapmap]
rs1423456	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1423459	1.00[JPT][hapmap]
rs17161463	0.96[ASN][1000 genomes]
rs17161466	0.88[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.84[TSI][hapmap];0.88[ASN][1000 genomes]
rs17161505	1.00[JPT][hapmap]
rs17161540	1.00[JPT][hapmap]
rs17161562	1.00[JPT][hapmap]
rs17163941	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs2009646	1.00[JPT][hapmap]
rs2081128	1.00[JPT][hapmap]
rs2113001	1.00[JPT][hapmap]
rs2229085	1.00[JPT][hapmap]
rs28376017	0.96[ASN][1000 genomes]
rs2900037	1.00[JPT][hapmap]
rs35141056	1.00[JPT][hapmap]
rs3805600	1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs3805601	1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs3828655	0.83[ASN][1000 genomes]
rs41508849	1.00[JPT][hapmap]
rs4358573	1.00[JPT][hapmap]
rs4361568	1.00[JPT][hapmap]
rs4479887	1.00[JPT][hapmap]
rs4560594	1.00[JPT][hapmap]
rs4560595	1.00[JPT][hapmap]
rs62361298	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs62361300	0.96[ASN][1000 genomes]
rs6594341	1.00[JPT][hapmap]
rs6859105	0.84[ASN][1000 genomes]
rs6859750	0.84[ASN][1000 genomes]
rs6869591	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6870408	1.00[ASN][1000 genomes]
rs6873130	1.00[JPT][hapmap]
rs6873917	1.00[JPT][hapmap]
rs6888173	1.00[JPT][hapmap]
rs7715658	1.00[JPT][hapmap]
rs7728920	1.00[JPT][hapmap]
rs889269	1.00[JPT][hapmap]
rs9326750	1.00[JPT][hapmap]
rs9326752	1.00[JPT][hapmap]
rs9885265	1.00[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882689	chr5:107595383-108299744	Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:108064600-108071600	Weak transcription	Pancreas	Pancrea
2	chr5:108065000-108068400	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr5:108065200-108067400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:108065200-108067400	Enhancers	Primary B cells from cord blood	blood
5	chr5:108065200-108068400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:108065400-108067200	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr5:108065400-108067400	Enhancers	GM12878-XiMat	blood
8	chr5:108065600-108067000	Enhancers	HUVEC	blood vessel
9	chr5:108066000-108071400	Weak transcription	K562	blood
10	chr5:108066600-108067000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr5:108066600-108082600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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