Variant report

Variant	rs62463677
Chromosome Location	chr7:101367057-101367058
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:101365013..101367690-chr7:101372321..101375439,3	MCF-7	breast:
2	chr7:101365806..101367484-chr7:101370262..101372822,3	K562	blood:
3	chr7:101364262..101367929-chr7:101368962..101372975,5	MCF-7	breast:
4	chr7:101363569..101367486-chr7:101367567..101371455,4	MCF-7	breast:
5	chr7:101360823..101364160-chr7:101364363..101367581,3	K562	blood:
6	chr7:101366199..101374490-chr7:101455423..101462621,17	MCF-7	breast:
7	chr7:101360484..101362871-chr7:101366884..101369233,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000257923	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10270145	0.82[AMR][1000 genomes]
rs10278430	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11771998	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11772618	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1636441	0.82[AMR][1000 genomes]
rs2529183	0.80[AMR][1000 genomes]
rs4276617	0.80[AMR][1000 genomes]
rs4436052	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4535653	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4602818	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4642556	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56381219	0.84[EUR][1000 genomes]
rs60702821	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62463667	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62463668	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62463669	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62463670	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62463671	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62463672	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62463674	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62463675	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62463676	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62466310	0.82[AMR][1000 genomes]
rs62466312	0.88[AMR][1000 genomes]
rs62466345	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62466346	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62466347	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62466348	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62466349	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62466350	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62466351	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62466354	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62466355	0.80[AMR][1000 genomes]
rs62466356	0.80[AMR][1000 genomes]
rs62466357	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62466358	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62467460	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62467463	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62467464	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62467465	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62467466	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62467468	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62467469	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs757820	0.82[AMR][1000 genomes]
rs757821	0.82[AMR][1000 genomes]
rs757822	0.82[AMR][1000 genomes]
rs7785622	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7796161	0.91[EUR][1000 genomes]
rs7811421	0.88[AMR][1000 genomes];0.84[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	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
6	nsv1021797	chr7:101342353-101466957	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv539046	chr7:101342353-101466957	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101332000-101376800	Weak transcription	Right Atrium	heart
2	chr7:101364200-101369000	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr7:101364800-101382400	Weak transcription	Thymus	Thymus
4	chr7:101365600-101371200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr7:101365800-101367200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr7:101366000-101371400	Weak transcription	Colonic Mucosa	Colon
7	chr7:101367000-101367800	ZNF genes & repeats	Fetal Intestine Small	intestine

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