Variant report

Variant	rs1531736
Chromosome Location	chr3:98674917-98674918
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs1036674	1.00[AMR][1000 genomes]
rs1082398	1.00[EUR][1000 genomes]
rs1082399	1.00[EUR][1000 genomes]
rs1082400	1.00[EUR][1000 genomes]
rs1082402	1.00[EUR][1000 genomes]
rs1082404	1.00[EUR][1000 genomes]
rs1082406	1.00[EUR][1000 genomes]
rs10935512	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1095913	1.00[AMR][1000 genomes]
rs1095914	1.00[AMR][1000 genomes]
rs1351496	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1383908	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1383911	1.00[AMR][1000 genomes]
rs1440157	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1481633	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1600788	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1818053	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs1822019	1.00[AMR][1000 genomes]
rs1972432	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2099738	1.00[AMR][1000 genomes]
rs2119189	1.00[AMR][1000 genomes]
rs2128053	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2133575	0.95[AFR][1000 genomes]
rs2173598	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2439227	1.00[AMR][1000 genomes]
rs2439230	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2439233	1.00[AMR][1000 genomes]
rs2439234	1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2439235	1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2448985	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2449047	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2454672	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2454675	1.00[AMR][1000 genomes]
rs2454681	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2454683	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2454690	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2470820	0.86[YRI][hapmap];0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2470828	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2470839	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2470850	0.80[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2470856	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2470858	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2470866	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2470868	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2470874	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2470883	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2470884	0.95[AFR][1000 genomes]
rs278375	0.92[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs278377	1.00[AMR][1000 genomes]
rs278378	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs278384	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs278385	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs278386	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs278389	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2922213	1.00[AMR][1000 genomes]
rs2929491	0.86[YRI][hapmap];0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4273318	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4857107	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs5013928	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6440232	1.00[AMR][1000 genomes]
rs6795351	0.98[AFR][1000 genomes]
rs7373983	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858658	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7430403	0.81[AFR][1000 genomes]
rs7626395	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7630797	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs774536	1.00[EUR][1000 genomes]
rs774543	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs774546	1.00[EUR][1000 genomes]
rs774548	1.00[EUR][1000 genomes]
rs828604	0.92[YRI][hapmap];1.00[AMR][1000 genomes]
rs828606	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs828607	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs828611	0.92[YRI][hapmap]
rs828619	1.00[AMR][1000 genomes]
rs828620	1.00[AMR][1000 genomes]
rs828622	1.00[AMR][1000 genomes]
rs828623	1.00[AMR][1000 genomes]
rs828624	1.00[AMR][1000 genomes]
rs866873	1.00[AMR][1000 genomes]
rs965757	1.00[AMR][1000 genomes]
rs974981	1.00[AMR][1000 genomes]
rs974982	0.84[AFR][1000 genomes]
rs9883226	1.00[YRI][hapmap]
rs996199	1.00[YRI][hapmap];0.95[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv591065	chr3:98204198-98766326	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv1007140	chr3:98421229-99202458	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv536663	chr3:98421229-99202458	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv877214	chr3:98445324-98738006	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	nsv1007486	chr3:98597738-99249081	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	esv3440755	chr3:98666311-98680865	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98670600-98675600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr3:98672400-98675000	Enhancers	NHDF-Ad	bronchial
3	chr3:98672400-98675200	Enhancers	NHEK	skin
4	chr3:98672800-98675600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr3:98674000-98676800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr3:98674200-98677000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr3:98674200-98678800	Weak transcription	NH-A	brain
8	chr3:98674200-98679400	Weak transcription	NHLF	lung
9	chr3:98674200-98679600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr3:98674400-98675200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr3:98674400-98676400	Weak transcription	A549	lung
12	chr3:98674400-98677200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr3:98674400-98677600	Weak transcription	HMEC	breast
14	chr3:98674400-98679600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr3:98674400-98679600	Weak transcription	Osteobl	bone
16	chr3:98674400-98681000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr3:98674600-98675000	Weak transcription	Fetal Lung	lung
18	chr3:98674600-98678800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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