Variant report

Variant	rs2252906
Chromosome Location	chr8:11499205-11499206
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	chr8:11490989..11493930-chr8:11499186..11501140,2	K562	blood:
2	chr8:11472906..11474859-chr8:11497875..11500697,2	K562	blood:

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10088181	1.00[EUR][1000 genomes]
rs10091294	1.00[EUR][1000 genomes]
rs10094355	1.00[EUR][1000 genomes]
rs10094630	1.00[EUR][1000 genomes]
rs10096015	1.00[EUR][1000 genomes]
rs10096526	1.00[EUR][1000 genomes]
rs10097076	1.00[EUR][1000 genomes]
rs10100742	1.00[EUR][1000 genomes]
rs10101788	1.00[EUR][1000 genomes]
rs10101900	1.00[EUR][1000 genomes]
rs10102714	1.00[EUR][1000 genomes]
rs10103483	1.00[EUR][1000 genomes]
rs10105409	1.00[EUR][1000 genomes]
rs10106250	1.00[EUR][1000 genomes]
rs10108287	1.00[EUR][1000 genomes]
rs10109678	1.00[EUR][1000 genomes]
rs10109971	1.00[EUR][1000 genomes]
rs10111542	1.00[EUR][1000 genomes]
rs10112464	1.00[EUR][1000 genomes]
rs10113255	1.00[EUR][1000 genomes]
rs10216815	1.00[EUR][1000 genomes]
rs2127130	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2127131	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2244775	1.00[EUR][1000 genomes]
rs2252818	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2252908	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2252914	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2264307	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2409812	1.00[EUR][1000 genomes]
rs28394863	1.00[EUR][1000 genomes]
rs28472428	1.00[EUR][1000 genomes]
rs28505660	1.00[EUR][1000 genomes]
rs28665608	1.00[EUR][1000 genomes]
rs4841582	1.00[EUR][1000 genomes]
rs5027656	1.00[EUR][1000 genomes]
rs55951800	1.00[EUR][1000 genomes]
rs57782848	1.00[EUR][1000 genomes]
rs58467083	1.00[EUR][1000 genomes]
rs59035560	1.00[EUR][1000 genomes]
rs60419043	1.00[EUR][1000 genomes]
rs61265429	1.00[EUR][1000 genomes]
rs73533953	1.00[EUR][1000 genomes]
rs73545766	1.00[EUR][1000 genomes]
rs73663183	1.00[EUR][1000 genomes]
rs73663184	1.00[EUR][1000 genomes]
rs73663185	1.00[EUR][1000 genomes]
rs73663187	1.00[EUR][1000 genomes]
rs73663190	1.00[EUR][1000 genomes]
rs73663191	1.00[EUR][1000 genomes]
rs73663201	1.00[EUR][1000 genomes]
rs7831152	1.00[EUR][1000 genomes]
rs7841968	1.00[EUR][1000 genomes]
rs8191510	1.00[EUR][1000 genomes]
rs8191543	1.00[EUR][1000 genomes]
rs8191573	1.00[EUR][1000 genomes]
rs8191669	1.00[EUR][1000 genomes]
rs8191682	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1017865	chr8:11377795-11579954	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11491000-11499600	Weak transcription	Right Ventricle	heart
2	chr8:11498200-11499400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
3	chr8:11498200-11499600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr8:11498200-11499600	Enhancers	Primary B cells from peripheral blood	blood
5	chr8:11498200-11499800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:11498200-11500600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:11498400-11499400	Enhancers	Gastric	stomach
8	chr8:11498400-11499600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
9	chr8:11498400-11499600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr8:11498400-11499600	Enhancers	Primary B cells from cord blood	blood
11	chr8:11498400-11499800	Enhancers	Ovary	ovary
12	chr8:11498400-11500600	Bivalent Enhancer	Fetal Stomach	stomach
13	chr8:11498400-11500600	Enhancers	Stomach Mucosa	stomach
14	chr8:11498400-11502400	Enhancers	Pancreas	Pancrea
15	chr8:11498600-11499400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr8:11498600-11499800	Enhancers	Fetal Intestine Large	intestine
17	chr8:11498600-11500600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr8:11498600-11500800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:11498600-11500800	Enhancers	Fetal Intestine Small	intestine
20	chr8:11498800-11500200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:11499000-11499400	Bivalent Enhancer	Fetal Kidney	kidney
22	chr8:11499000-11499600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:11499000-11499600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr8:11499000-11499600	Bivalent Enhancer	Fetal Lung	lung
25	chr8:11499000-11499600	Enhancers	HSMMtube	muscle
26	chr8:11499000-11500000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
27	chr8:11499000-11500000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr8:11499000-11500400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr8:11499000-11500400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr8:11499200-11499400	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
31	chr8:11499200-11499400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr8:11499200-11499400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
33	chr8:11499200-11499400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
34	chr8:11499200-11499400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
35	chr8:11499200-11499600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr8:11499200-11499600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr8:11499200-11499600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr8:11499200-11499600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
39	chr8:11499200-11499600	Bivalent Enhancer	NH-A	brain
40	chr8:11499200-11499800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr8:11499200-11499800	Flanking Active TSS	Brain Germinal Matrix	brain
42	chr8:11499200-11499800	Bivalent Enhancer	Placenta	Placenta
43	chr8:11499200-11499800	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
44	chr8:11499200-11500000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
45	chr8:11499200-11500000	Flanking Active TSS	Duodenum Mucosa	Duodenum
46	chr8:11499200-11500000	Flanking Active TSS	Fetal Heart	heart
47	chr8:11499200-11500200	Flanking Active TSS	HepG2	liver
48	chr8:11499200-11500600	Enhancers	Liver	Liver
49	chr8:11499200-11500600	Enhancers	Left Ventricle	heart
50	chr8:11499200-11500800	Bivalent Enhancer	Fetal Muscle Leg	muscle

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