Variant report

Variant	rs11946436
Chromosome Location	chr4:15399341-15399342
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	chr4:15396902..15399752-chr4:15401577..15403886,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10004540	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10032808	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11942186	0.82[EUR][1000 genomes]
rs1468737	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16891867	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1861045	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1861046	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1861050	0.82[EUR][1000 genomes]
rs2192359	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2192360	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2192361	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2192362	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28405315	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28517424	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28697056	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3822297	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4698105	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4698106	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4698107	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4698108	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4698380	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4698381	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4698383	0.82[EUR][1000 genomes]
rs4698384	0.82[EUR][1000 genomes]
rs60487386	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61170754	0.82[EUR][1000 genomes]
rs6814988	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6837765	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs723299	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7656974	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7661435	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs971490	0.82[EUR][1000 genomes]
rs9998722	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3448986	chr4:14928802-15805558	Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15378600-15401200	Weak transcription	Primary B cells from cord blood	blood
2	chr4:15384400-15402000	Weak transcription	Fetal Lung	lung
3	chr4:15388200-15400000	Weak transcription	Colon Smooth Muscle	Colon
4	chr4:15388400-15401800	Weak transcription	Fetal Stomach	stomach
5	chr4:15394200-15400000	Weak transcription	Lung	lung
6	chr4:15394400-15401600	Weak transcription	HSMMtube	muscle
7	chr4:15394400-15402400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:15397000-15402200	Weak transcription	Right Atrium	heart
9	chr4:15397600-15399400	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr4:15397600-15399600	Weak transcription	Ovary	ovary
11	chr4:15397600-15399800	Weak transcription	Osteobl	bone
12	chr4:15397600-15400600	Weak transcription	Fetal Kidney	kidney
13	chr4:15398000-15399800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr4:15398000-15400000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr4:15398000-15400400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr4:15398000-15401400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr4:15398000-15402200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr4:15398200-15401800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr4:15398400-15399600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr4:15398400-15400000	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr4:15398400-15400200	Weak transcription	Primary B cells from peripheral blood	blood
22	chr4:15398400-15400200	Weak transcription	Adipose Nuclei	Adipose
23	chr4:15398600-15399600	Weak transcription	Aorta	Aorta
24	chr4:15399000-15400000	Weak transcription	Esophagus	oesophagus
25	chr4:15399000-15400200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:15399000-15400400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr4:15399000-15402200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr4:15399000-15402400	Enhancers	Hela-S3	cervix
29	chr4:15399000-15405200	Enhancers	Placenta Amnion	Placenta Amnion
30	chr4:15399200-15400000	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr4:15399200-15401200	Enhancers	HMEC	breast
32	chr4:15399200-15402400	Enhancers	NHEK	skin

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