Variant report

Variant	rs7096353
Chromosome Location	chr10:23723077-23723078
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:23720439..23723434-chr10:23726111..23729992,4	MCF-7	breast:
2	chr10:23719313..23724177-chr10:23725494..23728219,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000165312	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs11013468	0.97[ASN][1000 genomes]
rs11013473	0.99[ASN][1000 genomes]
rs11013474	0.88[JPT][hapmap];0.86[ASN][1000 genomes]
rs11013476	0.86[ASN][1000 genomes]
rs11013478	0.87[ASN][1000 genomes]
rs11013479	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11013480	0.87[ASN][1000 genomes]
rs11013481	0.88[JPT][hapmap];0.87[ASN][1000 genomes]
rs11013482	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11013483	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11013484	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs11013491	0.81[ASN][1000 genomes]
rs12254101	0.81[ASN][1000 genomes]
rs12571102	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12571351	0.88[JPT][hapmap];0.82[ASN][1000 genomes]
rs12571384	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12572169	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1553905	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs16923233	0.88[JPT][hapmap];0.87[ASN][1000 genomes]
rs16923259	0.88[JPT][hapmap];0.81[ASN][1000 genomes]
rs1995981	0.95[ASN][1000 genomes]
rs2089876	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2089878	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2089879	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2089880	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs35182895	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4442437	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4747470	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4747471	0.87[ASN][1000 genomes]
rs4747474	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4747475	0.88[JPT][hapmap]
rs4748885	0.87[ASN][1000 genomes]
rs4748886	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4748887	1.00[ASN][1000 genomes]
rs4748889	0.87[ASN][1000 genomes]
rs57566783	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58056630	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs58305149	0.86[ASN][1000 genomes]
rs58604095	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58614955	0.87[ASN][1000 genomes]
rs59547906	0.87[ASN][1000 genomes]
rs6482276	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7079349	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs7079490	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7079866	0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs7080700	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7083306	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7084431	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7087230	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7092162	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7097072	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7098076	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7100463	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7100487	0.85[AFR][1000 genomes]
rs7100518	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73602555	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs73602556	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs74122431	0.87[ASN][1000 genomes]
rs74122432	0.87[ASN][1000 genomes]
rs74122435	0.87[ASN][1000 genomes]
rs74122436	0.87[ASN][1000 genomes]
rs74122437	0.87[ASN][1000 genomes]
rs7919581	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9633627	0.88[JPT][hapmap]
rs9633648	0.88[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	nsv825305	chr10:23698620-23740919	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23720200-23723800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr10:23721400-23727400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr10:23721800-23727200	Weak transcription	HMEC	breast
4	chr10:23721800-23727400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr10:23721800-23727400	Weak transcription	NHEK	skin
6	chr10:23722000-23723400	Enhancers	Primary B cells from cord blood	blood
7	chr10:23722000-23726200	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr10:23722000-23727200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr10:23722000-23727200	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr10:23722200-23723200	Enhancers	Primary B cells from peripheral blood	blood
11	chr10:23722200-23723200	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr10:23722200-23725600	Weak transcription	Stomach Mucosa	stomach
13	chr10:23722200-23727000	Weak transcription	Hela-S3	cervix

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