Variant report

Variant	rs7847385
Chromosome Location	chr9:16181267-16181268
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10113994	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10116579	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10122731	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10122861	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10125408	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10962317	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10962318	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12341541	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12348548	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12352516	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28454050	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55654095	0.94[AFR][1000 genomes]
rs61377525	0.95[EUR][1000 genomes]
rs7022294	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7028997	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7029038	0.94[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7029598	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9406585	0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949463	chr9:15970668-16377360	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv429999	chr9:16102066-16389100	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr9:16172800-16182800	Weak transcription	Ovary	ovary
2	chr9:16178800-16185000	Enhancers	Primary T cells from cord blood	blood
3	chr9:16179600-16181400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr9:16179600-16181400	Enhancers	Osteobl	bone
5	chr9:16179800-16182000	Enhancers	Colon Smooth Muscle	Colon
6	chr9:16179800-16184800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr9:16179800-16184800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr9:16179800-16192000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr9:16180000-16181600	Enhancers	Rectal Smooth Muscle	rectum
10	chr9:16180000-16183600	Weak transcription	Fetal Thymus	thymus
11	chr9:16180000-16184200	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr9:16181000-16182400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr9:16181000-16184800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr9:16181200-16182200	Enhancers	Fetal Heart	heart

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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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