Variant report

Variant	rs62466343
Chromosome Location	chr7:101341225-101341226
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:101338626..101341236-chr7:101455601..101457433,2	K562	blood:
2	chr7:101338468..101347550-chr7:101456060..101461227,20	MCF-7	breast:
3	chr7:101339145..101341455-chr7:101342209..101344273,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000257923	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10239715	1.00[ASN][1000 genomes]
rs10269590	1.00[ASN][1000 genomes]
rs10270145	1.00[ASN][1000 genomes]
rs10278534	1.00[ASN][1000 genomes]
rs10447812	1.00[ASN][1000 genomes]
rs11772618	1.00[ASN][1000 genomes]
rs12667267	1.00[ASN][1000 genomes]
rs1619382	1.00[ASN][1000 genomes]
rs1636440	1.00[ASN][1000 genomes]
rs1636441	1.00[ASN][1000 genomes]
rs1636443	1.00[ASN][1000 genomes]
rs1722218	1.00[ASN][1000 genomes]
rs1722224	1.00[ASN][1000 genomes]
rs1722226	1.00[ASN][1000 genomes]
rs1722229	1.00[ASN][1000 genomes]
rs2529183	1.00[ASN][1000 genomes]
rs4263675	1.00[ASN][1000 genomes]
rs4276617	1.00[ASN][1000 genomes]
rs4436052	1.00[ASN][1000 genomes]
rs4490765	1.00[ASN][1000 genomes]
rs4535653	1.00[ASN][1000 genomes]
rs4602818	1.00[ASN][1000 genomes]
rs4642556	1.00[ASN][1000 genomes]
rs4727503	1.00[ASN][1000 genomes]
rs4727504	1.00[ASN][1000 genomes]
rs4727505	1.00[ASN][1000 genomes]
rs4727506	1.00[ASN][1000 genomes]
rs4729747	1.00[ASN][1000 genomes]
rs56381219	1.00[ASN][1000 genomes]
rs62466309	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62466310	1.00[ASN][1000 genomes]
rs62466312	1.00[ASN][1000 genomes]
rs62466344	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466345	1.00[ASN][1000 genomes]
rs62466346	1.00[ASN][1000 genomes]
rs62466347	1.00[ASN][1000 genomes]
rs62466348	1.00[ASN][1000 genomes]
rs62466349	1.00[ASN][1000 genomes]
rs62466351	1.00[ASN][1000 genomes]
rs62466354	1.00[ASN][1000 genomes]
rs62466355	1.00[ASN][1000 genomes]
rs62466356	1.00[ASN][1000 genomes]
rs62466357	1.00[ASN][1000 genomes]
rs62466358	1.00[ASN][1000 genomes]
rs62467460	1.00[ASN][1000 genomes]
rs62467463	1.00[ASN][1000 genomes]
rs62467464	1.00[ASN][1000 genomes]
rs62467465	1.00[ASN][1000 genomes]
rs62467466	1.00[ASN][1000 genomes]
rs62467468	1.00[ASN][1000 genomes]
rs62467469	1.00[ASN][1000 genomes]
rs6957219	1.00[ASN][1000 genomes]
rs6960571	1.00[ASN][1000 genomes]
rs757820	1.00[ASN][1000 genomes]
rs757821	1.00[ASN][1000 genomes]
rs757822	1.00[ASN][1000 genomes]
rs757823	1.00[ASN][1000 genomes]
rs757824	1.00[ASN][1000 genomes]
rs7785622	1.00[ASN][1000 genomes]
rs7799319	1.00[ASN][1000 genomes]
rs7809926	1.00[ASN][1000 genomes]
rs7811421	1.00[ASN][1000 genomes]
rs848644	1.00[ASN][1000 genomes]
rs848645	1.00[ASN][1000 genomes]
rs848646	1.00[ASN][1000 genomes]
rs848654	1.00[ASN][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	nsv933653	chr7:100701931-101515782	Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv1018544	chr7:101225639-101424889	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv539045	chr7:101225639-101424889	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv482758	chr7:101231458-101395219	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv831079	chr7:101273495-101466776	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101332000-101376800	Weak transcription	Right Atrium	heart
2	chr7:101337400-101342800	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr7:101338000-101342000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:101340000-101342200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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