Variant report

Variant	rs2167695
Chromosome Location	chr10:4753980-4753981
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:4733738..4735615-chr10:4753440..4756163,2	MCF-7	breast:
2	chr10:4748341..4750852-chr10:4751570..4754263,3	MCF-7	breast:
3	chr10:4748910..4750501-chr10:4752014..4754640,2	MCF-7	breast:
4	chr10:4752926..4755618-chr10:4756217..4757722,2	MCF-7	breast:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10795198	0.89[ASN][1000 genomes]
rs10904318	0.89[ASN][1000 genomes]
rs10904319	0.89[ASN][1000 genomes]
rs10904320	0.89[ASN][1000 genomes]
rs10904321	0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs10904322	1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[YRI][hapmap];0.80[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs10904324	0.93[ASN][1000 genomes]
rs10904325	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10904326	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10904327	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10904329	0.92[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs11252666	0.83[ASN][1000 genomes]
rs11252667	0.83[ASN][1000 genomes]
rs11252674	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11252677	0.93[ASN][1000 genomes]
rs11252679	0.98[ASN][1000 genomes]
rs1901635	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36034519	0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs4372341	0.98[ASN][1000 genomes]
rs6601857	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6601858	0.99[ASN][1000 genomes]
rs7079701	1.00[CHB][hapmap];0.87[JPT][hapmap];0.85[ASN][1000 genomes]
rs7090458	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7091473	0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7093111	0.93[ASN][1000 genomes]
rs7895619	0.94[ASN][1000 genomes]
rs7905751	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7923564	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894787	chr10:4385379-4857717	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv1040924	chr10:4734176-4765606	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	4 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	chr10:4738400-4755600	Weak transcription	Right Atrium	heart
2	chr10:4743400-4758400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:4746600-4754200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr10:4746800-4762800	Weak transcription	NHLF	lung
5	chr10:4747200-4754000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr10:4748400-4755400	Weak transcription	Left Ventricle	heart
7	chr10:4749200-4769400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr10:4752600-4754800	Enhancers	Stomach Mucosa	stomach
9	chr10:4753400-4754200	Enhancers	Gastric	stomach
10	chr10:4753400-4754400	Enhancers	Adipose Nuclei	Adipose
11	chr10:4753800-4754200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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