Variant report

Variant	rs7515757
Chromosome Location	chr1:185211616-185211617
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10218494	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs10494582	1.00[ASN][1000 genomes]
rs10798007	0.82[ASN][1000 genomes]
rs11804954	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12240005	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12240119	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16823862	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16823869	0.96[ASN][1000 genomes]
rs16823875	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs16823884	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs16823891	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs3766713	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs3766716	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs3895195	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs57927210	0.93[ASN][1000 genomes]
rs57960155	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs58031282	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs58292874	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs58685423	0.85[ASN][1000 genomes]
rs59035619	0.96[ASN][1000 genomes]
rs59227355	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs59611551	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs60064915	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs61573899	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6672580	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6679946	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6687946	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7516303	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7540216	0.81[AMR][1000 genomes]
rs7555243	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs953701	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs953702	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001323	chr1:184525419-185315876	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
2	nsv535222	chr1:184525419-185315876	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
3	nsv548398	chr1:185136458-186003094	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185127600-185218200	Weak transcription	Right Ventricle	heart
2	chr1:185170800-185218200	Weak transcription	Pancreas	Pancrea
3	chr1:185175600-185217000	Weak transcription	Fetal Stomach	stomach
4	chr1:185192600-185218600	Weak transcription	Aorta	Aorta
5	chr1:185192600-185221000	Weak transcription	Fetal Intestine Small	intestine
6	chr1:185193600-185213200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr1:185193600-185213400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:185193600-185214600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr1:185193600-185219200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:185193600-185219400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr1:185193800-185220400	Weak transcription	Brain Hippocampus Middle	brain
12	chr1:185193800-185263600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr1:185194000-185218600	Weak transcription	Lung	lung
14	chr1:185194200-185213400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:185197200-185218200	Weak transcription	Left Ventricle	heart
16	chr1:185197600-185220400	Weak transcription	Ovary	ovary
17	chr1:185199800-185213200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:185202400-185218800	Weak transcription	Brain Anterior Caudate	brain
19	chr1:185206400-185218200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr1:185207600-185211800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr1:185209000-185218800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr1:185209600-185213400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:185210400-185218400	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr1:185210600-185250400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr1:185211000-185213200	Weak transcription	K562	blood
26	chr1:185211000-185215800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:185211200-185214400	Weak transcription	HSMMtube	muscle

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