Variant report

Variant	rs2302135
Chromosome Location	chr4:110901147-110901148
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TCF12	chr4:110901123-110902057	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:110734994..110736731-chr4:110899705..110902509,2	K562	blood:
2	chr4:110899256..110901567-chr4:110902882..110905571,2	K562	blood:
3	chr4:110899444..110901234-chr4:110903435..110906853,3	MCF-7	breast:
4	chr4:110811671..110813373-chr4:110899497..110901188,2	MCF-7	breast:

Variant related genes	Relation type
EGF	TF binding region
ENSG00000272795	Chromatin interaction
ENSG00000109534	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10434002	0.94[CHB][hapmap];0.94[JPT][hapmap];0.99[ASN][1000 genomes]
rs11098058	0.92[CHB][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs11098063	0.81[ASN][1000 genomes]
rs11568853	0.94[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs11568862	0.89[ASN][1000 genomes]
rs11568886	0.89[ASN][1000 genomes]
rs11568901	0.94[CHB][hapmap];0.81[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11568910	0.84[ASN][1000 genomes]
rs11568924	0.90[ASN][1000 genomes]
rs11568925	0.90[ASN][1000 genomes]
rs11568927	0.94[CHB][hapmap];0.81[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs11568941	0.94[CHB][hapmap];0.80[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs11568946	0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs11568975	0.94[CHB][hapmap];0.81[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs11568990	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs11568991	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs11569003	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs11569043	1.00[AMR][1000 genomes]
rs11569046	1.00[ASW][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];1.00[AMR][1000 genomes]
rs11569047	1.00[ASW][hapmap];1.00[MEX][hapmap]
rs11569102	0.82[ASN][1000 genomes]
rs11569103	0.82[ASN][1000 genomes]
rs11569129	0.94[CHB][hapmap];0.88[JPT][hapmap];0.82[ASN][1000 genomes]
rs11569142	0.82[ASN][1000 genomes]
rs17040990	0.83[CHB][hapmap]
rs17041036	0.94[CHB][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes]
rs17041134	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1860131	0.94[CHB][hapmap];0.81[CHD][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs2074389	0.94[CHB][hapmap];0.88[JPT][hapmap];0.82[ASN][1000 genomes]
rs2237043	0.94[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2237046	0.99[ASN][1000 genomes]
rs2237047	0.94[CHB][hapmap];0.94[JPT][hapmap];0.98[ASN][1000 genomes]
rs2237048	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2282782	0.88[ASN][1000 genomes]
rs2282783	0.89[ASN][1000 genomes]
rs2282786	0.94[CHB][hapmap];0.88[JPT][hapmap];0.82[ASN][1000 genomes]
rs2298980	0.89[ASN][1000 genomes]
rs2298984	0.90[ASN][1000 genomes]
rs2298987	0.92[ASN][1000 genomes]
rs2298988	0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2298994	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2298995	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2298997	0.94[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs2298998	0.90[ASN][1000 genomes]
rs2299002	0.81[ASN][1000 genomes]
rs3733628	0.94[CHB][hapmap];0.81[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs3756264	0.83[CHB][hapmap]
rs3796942	0.90[ASN][1000 genomes]
rs3796943	0.93[CHB][hapmap];0.93[JPT][hapmap];0.90[ASN][1000 genomes]
rs3796949	0.93[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs3822285	0.94[CHB][hapmap];0.88[JPT][hapmap];0.82[ASN][1000 genomes]
rs4631111	0.87[ASN][1000 genomes]
rs59242631	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6533484	1.00[YRI][hapmap];0.96[AFR][1000 genomes]
rs6854247	1.00[MEX][hapmap]
rs7695064	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs887027	0.98[ASN][1000 genomes]
rs9307346	0.94[CHB][hapmap];1.00[JPT][hapmap];0.90[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	nsv530156	chr4:110721397-110911297	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110860600-110906600	Weak transcription	Psoas Muscle	Psoas
2	chr4:110875600-110909800	Weak transcription	Pancreas	Pancrea
3	chr4:110885800-110909800	Weak transcription	Left Ventricle	heart
4	chr4:110893800-110909600	Weak transcription	Fetal Heart	heart
5	chr4:110895000-110909600	Weak transcription	Fetal Intestine Small	intestine
6	chr4:110895000-110928600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:110898000-110906600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr4:110899400-110909800	Weak transcription	Right Atrium	heart
9	chr4:110899600-110902200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:110899600-110902200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:110899600-110902800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr4:110900000-110901400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:110900000-110901600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr4:110900000-110901600	Strong transcription	Skeletal Muscle Female	skeletal muscle
15	chr4:110900200-110901200	Enhancers	NH-A	brain
16	chr4:110900400-110901600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr4:110900800-110901400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:110900800-110901400	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr4:110900800-110901400	Enhancers	Osteobl	bone
20	chr4:110900800-110902200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:110900800-110902200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr4:110900800-110902200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:110900800-110902400	Enhancers	NHEK	skin
24	chr4:110900800-110902600	Enhancers	HMEC	breast
25	chr4:110900800-110902600	Enhancers	HSMM	muscle
26	chr4:110900800-110902800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:110900800-110905000	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr4:110901000-110901200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr4:110901000-110902000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr4:110901000-110902000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr4:110901000-110902000	Enhancers	NHDF-Ad	bronchial
32	chr4:110901000-110902200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:110901000-110902200	Enhancers	HSMMtube	muscle
34	chr4:110901000-110902600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr4:110901000-110902600	Enhancers	Muscle Satellite Cultured Cells	--
36	chr4:110901000-110905200	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr4:110901000-110929600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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