Variant report

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs151643	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs151647	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs151659	1.00[EUR][1000 genomes]
rs187066	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs192130	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2182852	1.00[EUR][1000 genomes]
rs239499	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs239503	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs239510	1.00[EUR][1000 genomes]
rs239559	1.00[EUR][1000 genomes]
rs239561	1.00[EUR][1000 genomes]
rs239565	1.00[EUR][1000 genomes]
rs240215	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs240223	1.00[EUR][1000 genomes]
rs240227	1.00[EUR][1000 genomes]
rs2490225	1.00[EUR][1000 genomes]
rs2490229	1.00[EUR][1000 genomes]
rs2490231	1.00[EUR][1000 genomes]
rs2490233	1.00[EUR][1000 genomes]
rs2490237	1.00[EUR][1000 genomes]
rs2490238	1.00[EUR][1000 genomes]
rs2490242	1.00[EUR][1000 genomes]
rs2505931	1.00[EUR][1000 genomes]
rs2505933	1.00[EUR][1000 genomes]
rs2505934	1.00[EUR][1000 genomes]
rs2505936	1.00[EUR][1000 genomes]
rs2505938	1.00[EUR][1000 genomes]
rs2505941	1.00[EUR][1000 genomes]
rs2505943	1.00[EUR][1000 genomes]
rs2505947	1.00[EUR][1000 genomes]
rs2769338	1.00[EUR][1000 genomes]
rs2997392	1.00[EUR][1000 genomes]
rs2997393	1.00[EUR][1000 genomes]
rs6454141	1.00[EUR][1000 genomes]
rs6912898	1.00[EUR][1000 genomes]
rs6925435	1.00[EUR][1000 genomes]
rs7748996	1.00[EUR][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	nsv1028607	chr6:79853272-80767716	Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv1032347	chr6:80284809-80694778	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:80687800-80696400	Enhancers	Fetal Thymus	thymus
2	chr6:80691000-80694800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr6:80691600-80696200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr6:80692800-80695000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr6:80693200-80695800	Enhancers	Dnd41	blood
6	chr6:80693400-80694200	Enhancers	Liver	Liver
7	chr6:80693400-80694200	Enhancers	Fetal Intestine Small	intestine
8	chr6:80693400-80694400	Enhancers	Fetal Intestine Large	intestine
9	chr6:80693600-80694600	Enhancers	HepG2	liver
10	chr6:80694000-80694600	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr6:80694000-80694600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:80694000-80694600	Flanking Active TSS	Thymus	Thymus
13	chr6:80694000-80694800	Enhancers	Primary T cells from cord blood	blood
14	chr6:80694000-80694800	Enhancers	HMEC	breast
15	chr6:80694000-80694800	Enhancers	NHEK	skin
16	chr6:80694200-80694600	Enhancers	Fetal Kidney	kidney

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