Variant report

Variant	rs4709731
Chromosome Location	chr6:164055651-164055652
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1540949	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4709000	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4709730	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6902395	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7744302	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7749197	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7751246	1.00[ASN][1000 genomes]
rs7754222	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7764847	1.00[ASN][1000 genomes]
rs912028	1.00[ASN][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	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	esv2758092	chr6:163992064-164161903	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	esv2759490	chr6:163992064-164161903	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	esv3422917	chr6:164054362-164058660	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164048000-164061600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:164050400-164055800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:164052200-164073000	Weak transcription	Fetal Heart	heart
4	chr6:164055000-164056200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr6:164055200-164056000	Enhancers	Placenta	Placenta
6	chr6:164055200-164056200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:164055200-164056600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:164055200-164057200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:164055400-164055800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr6:164055400-164056200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:164055400-164057000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr6:164055400-164057200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr6:164055400-164057600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr6:164055400-164057600	Enhancers	H1 Cell Line	embryonic stem cell
15	chr6:164055600-164055800	Bivalent/Poised TSS	HepG2	liver
16	chr6:164055600-164056000	Enhancers	Esophagus	oesophagus
17	chr6:164055600-164056000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr6:164055600-164056000	Enhancers	HMEC	breast
19	chr6:164055600-164056200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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