Variant report

Variant	rs4675747
Chromosome Location	chr2:209148777-209148778
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	chr2:209131018..209132806-chr2:209148294..209150467,2	K562	blood:

Variant related genes	Relation type
ENSG00000115020	Chromatin interaction

Extended variants
information (count: 101 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs10171006	1.00[EUR][1000 genomes]
rs10175739	1.00[EUR][1000 genomes]
rs10186531	1.00[EUR][1000 genomes]
rs10197958	1.00[EUR][1000 genomes]
rs10201702	1.00[EUR][1000 genomes]
rs10208004	1.00[EUR][1000 genomes]
rs10210393	1.00[EUR][1000 genomes]
rs10804168	1.00[EUR][1000 genomes]
rs10932256	1.00[EUR][1000 genomes]
rs10932259	1.00[EUR][1000 genomes]
rs11677618	1.00[EUR][1000 genomes]
rs11691208	1.00[EUR][1000 genomes]
rs11695873	1.00[EUR][1000 genomes]
rs12185547	1.00[EUR][1000 genomes]
rs12465862	1.00[EUR][1000 genomes]
rs12478198	1.00[EUR][1000 genomes]
rs12479282	1.00[EUR][1000 genomes]
rs12617521	1.00[EUR][1000 genomes]
rs12618837	1.00[EUR][1000 genomes]
rs12621871	1.00[EUR][1000 genomes]
rs12623816	1.00[EUR][1000 genomes]
rs12694105	1.00[EUR][1000 genomes]
rs12694109	1.00[EUR][1000 genomes]
rs1370370	1.00[EUR][1000 genomes]
rs1437414	1.00[EUR][1000 genomes]
rs1446320	1.00[EUR][1000 genomes]
rs1446321	1.00[EUR][1000 genomes]
rs1465803	1.00[EUR][1000 genomes]
rs1465804	1.00[EUR][1000 genomes]
rs1529979	1.00[EUR][1000 genomes]
rs1561240	1.00[EUR][1000 genomes]
rs16840898	1.00[EUR][1000 genomes]
rs16840910	1.00[EUR][1000 genomes]
rs16840936	1.00[EUR][1000 genomes]
rs1838794	1.00[EUR][1000 genomes]
rs1838795	1.00[EUR][1000 genomes]
rs1838796	1.00[EUR][1000 genomes]
rs1866044	1.00[EUR][1000 genomes]
rs1866045	1.00[EUR][1000 genomes]
rs2028146	1.00[EUR][1000 genomes]
rs2043720	1.00[EUR][1000 genomes]
rs2044457	1.00[EUR][1000 genomes]
rs2118296	1.00[EUR][1000 genomes]
rs2118297	1.00[EUR][1000 genomes]
rs2304544	1.00[EUR][1000 genomes]
rs2363463	1.00[EUR][1000 genomes]
rs2363468	1.00[EUR][1000 genomes]
rs2363469	1.00[EUR][1000 genomes]
rs2363579	1.00[EUR][1000 genomes]
rs2885785	1.00[EUR][1000 genomes]
rs2885786	1.00[EUR][1000 genomes]
rs4673385	1.00[EUR][1000 genomes]
rs4673386	1.00[EUR][1000 genomes]
rs4673390	1.00[EUR][1000 genomes]
rs4673395	1.00[EUR][1000 genomes]
rs4675745	1.00[EUR][1000 genomes]
rs4675750	1.00[EUR][1000 genomes]
rs4675754	1.00[EUR][1000 genomes]
rs4675755	1.00[EUR][1000 genomes]
rs57553077	1.00[EUR][1000 genomes]
rs57797425	1.00[EUR][1000 genomes]
rs6435436	1.00[EUR][1000 genomes]
rs6435437	1.00[EUR][1000 genomes]
rs6435441	1.00[EUR][1000 genomes]
rs6435443	1.00[EUR][1000 genomes]
rs6435444	1.00[EUR][1000 genomes]
rs6435445	1.00[EUR][1000 genomes]
rs6435446	1.00[EUR][1000 genomes]
rs6435450	1.00[EUR][1000 genomes]
rs6705163	1.00[EUR][1000 genomes]
rs6708926	1.00[EUR][1000 genomes]
rs6711933	1.00[EUR][1000 genomes]
rs6713477	1.00[EUR][1000 genomes]
rs6718402	1.00[EUR][1000 genomes]
rs6733607	1.00[EUR][1000 genomes]
rs6734963	1.00[EUR][1000 genomes]
rs6742461	1.00[EUR][1000 genomes]
rs6751982	1.00[EUR][1000 genomes]
rs7564882	1.00[EUR][1000 genomes]
rs7569723	1.00[EUR][1000 genomes]
rs7574324	1.00[EUR][1000 genomes]
rs7576852	1.00[EUR][1000 genomes]
rs7580715	1.00[EUR][1000 genomes]
rs7581075	1.00[EUR][1000 genomes]
rs7605498	1.00[EUR][1000 genomes]
rs893253	1.00[EUR][1000 genomes]
rs893255	1.00[EUR][1000 genomes]
rs893256	1.00[EUR][1000 genomes]
rs9283521	1.00[EUR][1000 genomes]
rs934712	1.00[EUR][1000 genomes]
rs934714	1.00[EUR][1000 genomes]
rs959855	1.00[EUR][1000 genomes]
rs976247	1.00[EUR][1000 genomes]
rs994696	1.00[EUR][1000 genomes]
rs994697	1.00[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	nsv1010531	chr2:208610639-209176782	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv536130	chr2:208610639-209176782	Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv534496	chr2:208814372-209302791	Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	nsv834517	chr2:209006797-209170269	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv584297	chr2:209020181-209316760	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv875752	chr2:209141066-209235373	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209133600-209153400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr2:209134600-209149000	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr2:209135200-209148800	Strong transcription	Dnd41	blood
4	chr2:209135800-209149000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr2:209135800-209150400	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr2:209136000-209149200	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr2:209136000-209149200	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr2:209136000-209149200	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr2:209136000-209154800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr2:209136000-209171800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr2:209136200-209148800	Strong transcription	H1 Cell Line	embryonic stem cell
12	chr2:209136200-209149000	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr2:209136200-209155000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr2:209136200-209155000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr2:209136200-209161600	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr2:209137800-209149000	Strong transcription	A549	lung
17	chr2:209137800-209155000	Strong transcription	Fetal Intestine Large	intestine
18	chr2:209138000-209148800	Strong transcription	Sigmoid Colon	Sigmoid Colon
19	chr2:209138000-209149200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr2:209138000-209149200	Strong transcription	HepG2	liver
21	chr2:209138000-209155600	Strong transcription	Thymus	Thymus
22	chr2:209139000-209155000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr2:209139000-209163400	Weak transcription	Right Ventricle	heart
24	chr2:209139200-209159400	Weak transcription	Small Intestine	intestine
25	chr2:209139400-209180000	Strong transcription	Fetal Thymus	thymus
26	chr2:209139800-209161800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr2:209141000-209149200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
28	chr2:209141200-209180000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr2:209141800-209169000	Weak transcription	Hela-S3	cervix
30	chr2:209143400-209152800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr2:209143800-209150400	Strong transcription	Primary B cells from peripheral blood	blood
32	chr2:209143800-209152800	Weak transcription	Fetal Heart	heart
33	chr2:209143800-209154800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:209143800-209154800	Weak transcription	Brain Germinal Matrix	brain
35	chr2:209144000-209153600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:209144000-209154400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:209144600-209148800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr2:209145400-209152800	Weak transcription	Brain Cingulate Gyrus	brain
39	chr2:209145800-209149200	Strong transcription	Left Ventricle	heart
40	chr2:209145800-209150400	Weak transcription	Psoas Muscle	Psoas
41	chr2:209145800-209150800	Weak transcription	NHEK	skin
42	chr2:209145800-209158400	Strong transcription	Primary T helper cells PMA-I stimulated	--
43	chr2:209146000-209152800	Weak transcription	Colon Smooth Muscle	Colon
44	chr2:209146000-209152800	Weak transcription	Fetal Brain Female	brain
45	chr2:209146200-209148800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr2:209146400-209149200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr2:209146400-209150400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr2:209146400-209152600	Weak transcription	Right Atrium	heart
49	chr2:209146400-209152800	Weak transcription	NHLF	lung
50	chr2:209146600-209150400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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