Variant report

Variant	rs8024160
Chromosome Location	chr15:32981978-32981979
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12438604	0.90[YRI][hapmap]
rs16965254	0.88[CEU][hapmap];0.90[JPT][hapmap];0.96[EUR][1000 genomes]
rs28417809	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6494587	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.92[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7177843	0.90[YRI][hapmap]
rs7178316	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7181171	0.82[LWK][hapmap]
rs7494781	0.86[CHB][hapmap]
rs8043234	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422296	chr15:32798938-33221215	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv469587	chr15:32821940-32986579	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv482780	chr15:32821940-32986579	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv456785	chr15:32926076-33352989	Genic enhancers Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv568913	chr15:32926076-33352989	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv482680	chr15:32958401-33154005	Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv568915	chr15:32965357-32994056	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv456787	chr15:32968923-33023951	Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv568916	chr15:32968923-33023951	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:32964600-32990800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr15:32964800-32993800	Weak transcription	Fetal Brain Male	brain
3	chr15:32965000-32983600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr15:32970000-32982600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr15:32973200-32986000	Weak transcription	Brain Germinal Matrix	brain
6	chr15:32975000-32983200	Weak transcription	Brain Substantia Nigra	brain
7	chr15:32975000-32983400	Weak transcription	Brain Angular Gyrus	brain
8	chr15:32975200-32983400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr15:32975200-32983800	Weak transcription	Brain Anterior Caudate	brain
10	chr15:32975200-32986000	Weak transcription	Brain Hippocampus Middle	brain
11	chr15:32977000-32983800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr15:32978000-32982400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr15:32978400-32983400	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr15:32978400-32984000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr15:32978600-32982600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr15:32978800-32996400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr15:32980400-32983800	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr15:32980600-32991200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr15:32980800-32982600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr15:32980800-32982600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr15:32980800-32982600	Weak transcription	NHDF-Ad	bronchial
22	chr15:32980800-32982800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr15:32980800-32983600	Weak transcription	Liver	Liver
24	chr15:32980800-32986600	Weak transcription	HSMM	muscle
25	chr15:32980800-32990600	Weak transcription	Fetal Brain Female	brain
26	chr15:32980800-32992400	Weak transcription	Stomach Mucosa	stomach
27	chr15:32980800-32993600	Weak transcription	Pancreas	Pancrea
28	chr15:32980800-32996200	Weak transcription	HSMMtube	muscle
29	chr15:32981200-32983000	Enhancers	NHEK	skin
30	chr15:32981400-32983000	Enhancers	HMEC	breast
31	chr15:32981600-32982000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr15:32981600-32983400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr15:32981800-32982000	Enhancers	Fetal Kidney	kidney
34	chr15:32981800-32983000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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