Variant report

Variant	rs10961576
Chromosome Location	chr9:14561712-14561713
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1004800	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs10491770	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10961563	0.85[AMR][1000 genomes]
rs12686209	0.81[ASN][1000 genomes]
rs2026648	0.87[AMR][1000 genomes]
rs7028679	0.81[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	nsv1029491	chr9:14033607-14942373	Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv915804	chr9:14182608-14903050	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv831517	chr9:14512924-14738206	Enhancers Genic enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv613637	chr9:14524438-15011915	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers 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	11 gene(s)	inside rSNPs	diseases
5	esv3362157	chr9:14542189-14791977	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers 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:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14556600-14561800	Weak transcription	Fetal Muscle Leg	muscle
2	chr9:14559000-14562000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr9:14560400-14561800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr9:14561200-14563000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr9:14561400-14562400	Enhancers	H1 Cell Line	embryonic stem cell
6	chr9:14561400-14562400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:14561400-14562400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr9:14561400-14562400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr9:14561400-14563000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:14561600-14562400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr9:14561600-14562400	Flanking Active TSS	HepG2	liver
12	chr9:14561600-14562600	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr9:14561600-14562800	Enhancers	Fetal Kidney	kidney
14	chr9:14561600-14563200	Enhancers	iPS-15b 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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