Variant report

Variant	rs6436910
Chromosome Location	chr2:230998015-230998016
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10199897	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10209232	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10498243	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10933323	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10933324	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10933326	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11676757	0.82[AMR][1000 genomes]
rs11894286	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12694841	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13004807	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1365774	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1365775	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1529377	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1549567	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1549568	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1549569	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1549570	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2396712	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2396714	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4361119	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6436909	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6436912	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6706782	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6707129	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6721137	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6735404	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6754313	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6754451	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007920	chr2:230775427-231065592	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv1001562	chr2:230862717-231187043	Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv536156	chr2:230862717-231187043	Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv498047	chr2:230951712-231250489	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv875942	chr2:230959532-231008980	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv875943	chr2:230960946-231027162	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	5 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	chr2:230992800-230999200	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr2:230994000-230998800	Weak transcription	HSMMtube	muscle
3	chr2:230994400-230998400	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr2:230994400-230998400	Weak transcription	Spleen	Spleen
5	chr2:230994400-231000200	Weak transcription	Brain Substantia Nigra	brain
6	chr2:230994600-231000200	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr2:230995600-230998400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr2:230996000-230999000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr2:230996200-230999000	Weak transcription	Osteobl	bone
10	chr2:230996400-230998800	Weak transcription	HUVEC	blood vessel
11	chr2:230996400-230999000	Weak transcription	NHDF-Ad	bronchial
12	chr2:230996400-231002600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr2:230997000-230998400	Weak transcription	Adipose Nuclei	Adipose
14	chr2:230997400-230999400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood

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