Variant report

Variant	rs61576366
Chromosome Location	chr9:14870218-14870219
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10114394	1.00[EUR][1000 genomes]
rs10116665	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12343858	1.00[EUR][1000 genomes]
rs12351267	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28413927	1.00[EUR][1000 genomes]
rs28433528	1.00[EUR][1000 genomes]
rs41313784	1.00[EUR][1000 genomes]
rs58241195	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7848267	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7858575	1.00[EUR][1000 genomes]
rs7868311	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9298708	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs950739	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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	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
4	nsv831518	chr9:14760638-14953501	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv892617	chr9:14791348-14889834	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv1018416	chr9:14846753-14921247	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv613647	chr9:14852141-15016475	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	esv3390567	chr9:14852461-14891880	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14859600-14876600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr9:14860000-14883800	Weak transcription	Fetal Muscle Trunk	muscle
3	chr9:14863800-14870400	Enhancers	Colon Smooth Muscle	Colon
4	chr9:14868800-14870400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr9:14869000-14870400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr9:14869000-14870400	Enhancers	Small Intestine	intestine
7	chr9:14869000-14870600	Enhancers	Fetal Lung	lung
8	chr9:14869200-14870400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr9:14869200-14876400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:14869400-14870400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:14869600-14870600	Enhancers	Duodenum Mucosa	Duodenum
12	chr9:14869800-14870400	Active TSS	Fetal Brain Male	brain
13	chr9:14870000-14870600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:14870000-14870600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr9:14870000-14870600	Enhancers	HepG2	liver
16	chr9:14870200-14870400	Flanking Active TSS	Fetal Kidney	kidney
17	chr9:14870200-14870400	Enhancers	Sigmoid Colon	Sigmoid Colon

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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