Variant report

Variant	rs4669772
Chromosome Location	chr2:11843277-11843278
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:11842746..11844710-chr2:11858311..11861205,2	K562	blood:

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10180912	1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs12052681	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12465629	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12465630	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12692445	0.82[AMR][1000 genomes]
rs13036247	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4389306	0.83[EUR][1000 genomes]
rs4542816	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4668739	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4669774	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4669775	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62116211	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6432230	0.82[CEU][hapmap]
rs6432231	0.80[CEU][hapmap];0.82[JPT][hapmap]
rs6736021	0.88[CEU][hapmap];0.85[CHB][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7597788	0.85[EUR][1000 genomes]
rs7598716	0.82[EUR][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	nsv1010506	chr2:11430965-12057286	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv535585	chr2:11430965-12057286	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv1003899	chr2:11789374-12248081	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
4	nsv469449	chr2:11808654-11854012	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv580972	chr2:11808654-11854012	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11837800-11845400	Weak transcription	Pancreas	Pancrea
2	chr2:11837800-11848200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr2:11838200-11843400	Weak transcription	HMEC	breast
4	chr2:11838400-11844000	Weak transcription	Lung	lung
5	chr2:11838400-11845000	Weak transcription	Brain Anterior Caudate	brain
6	chr2:11838600-11843400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:11838600-11848000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:11838800-11843400	Weak transcription	NH-A	brain
9	chr2:11839000-11843400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr2:11839000-11843400	Weak transcription	NHLF	lung
11	chr2:11839000-11843600	Weak transcription	NHEK	skin
12	chr2:11839200-11843600	Weak transcription	HSMMtube	muscle
13	chr2:11839400-11843400	Weak transcription	HSMM	muscle
14	chr2:11839400-11843600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr2:11840200-11844000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr2:11841600-11850000	Weak transcription	Brain Substantia Nigra	brain
17	chr2:11841600-11850000	Weak transcription	Ovary	ovary
18	chr2:11841600-11850200	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr2:11841800-11845000	Enhancers	Osteobl	bone
20	chr2:11841800-11850200	Weak transcription	Brain Angular Gyrus	brain
21	chr2:11842200-11847600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr2:11842400-11843400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr2:11842600-11843400	Weak transcription	Esophagus	oesophagus
24	chr2:11842600-11844800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr2:11842600-11844800	Enhancers	NHDF-Ad	bronchial
26	chr2:11842800-11843400	Weak transcription	Psoas Muscle	Psoas
27	chr2:11842800-11844200	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr2:11843200-11844400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr2:11843200-11844600	Enhancers	Muscle Satellite Cultured Cells	--
30	chr2:11843200-11844600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr2:11843200-11845000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr2:11843200-11845600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr2:11843200-11847800	Weak transcription	Placenta	Placenta

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