Variant report

Variant	rs72976732
Chromosome Location	chr3:54076439-54076440
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs28385736	1.00[EUR][1000 genomes]
rs4358292	1.00[EUR][1000 genomes]
rs4364155	1.00[EUR][1000 genomes]
rs4687764	1.00[EUR][1000 genomes]
rs55940822	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55971211	1.00[EUR][1000 genomes]
rs59150035	1.00[EUR][1000 genomes]
rs60408413	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61026534	1.00[EUR][1000 genomes]
rs6445623	1.00[EUR][1000 genomes]
rs6797145	1.00[EUR][1000 genomes]
rs72974991	1.00[EUR][1000 genomes]
rs72975002	1.00[EUR][1000 genomes]
rs72976731	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73841260	1.00[EUR][1000 genomes]
rs7623521	1.00[EUR][1000 genomes]
rs7650910	1.00[EUR][1000 genomes]
rs9812910	1.00[EUR][1000 genomes]
rs9863533	1.00[EUR][1000 genomes]
rs9864400	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003621	chr3:53448934-54425322	Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers 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	31 gene(s)	inside rSNPs	diseases
2	nsv1006990	chr3:53849510-54285212	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv1014752	chr3:53912429-54123246	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv1005411	chr3:53927782-54158638	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1014595	chr3:53944473-54846754	Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:54059600-54078000	Weak transcription	Right Atrium	heart
2	chr3:54069800-54078000	Weak transcription	Esophagus	oesophagus
3	chr3:54075800-54078200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr3:54076000-54076600	Enhancers	Left Ventricle	heart
5	chr3:54076000-54076800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr3:54076000-54076800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr3:54076000-54077000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr3:54076000-54077000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr3:54076000-54077200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr3:54076000-54077400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr3:54076000-54077400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr3:54076000-54077400	Enhancers	HMEC	breast
13	chr3:54076000-54077400	Enhancers	NHEK	skin
14	chr3:54076000-54077600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr3:54076000-54077800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr3:54076200-54076800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr3:54076200-54077000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr3:54076200-54077000	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr3:54076200-54077200	Enhancers	Hela-S3	cervix
20	chr3:54076400-54076600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:54076400-54076600	Enhancers	Fetal Muscle Leg	muscle
22	chr3:54076400-54076600	Weak transcription	Gastric	stomach
23	chr3:54076400-54076800	Enhancers	H9 Cell Line	embryonic stem cell
24	chr3:54076400-54076800	Enhancers	Fetal Intestine Large	intestine
25	chr3:54076400-54076800	Enhancers	Fetal Lung	lung
26	chr3:54076400-54076800	Enhancers	Lung	lung
27	chr3:54076400-54077000	Enhancers	Placenta Amnion	Placenta Amnion
28	chr3:54076400-54077200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr3:54076400-54077200	Enhancers	Placenta	Placenta
30	chr3:54076400-54078400	Weak transcription	Fetal Stomach	stomach

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