Variant report

Variant	rs1160093
Chromosome Location	chr4:46949770-46949771
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

rs_ID	r²[population]
rs10015891	0.89[YRI][hapmap]
rs10017677	0.81[CHB][hapmap]
rs10021503	0.86[YRI][hapmap]
rs10021918	0.81[CHB][hapmap]
rs10023110	0.88[YRI][hapmap]
rs10025240	0.81[CHB][hapmap]
rs10025379	0.81[CHB][hapmap]
rs10027692	0.81[CHB][hapmap]
rs10028342	0.81[CHB][hapmap]
rs10050095	0.81[CHB][hapmap]
rs10517169	0.81[CHB][hapmap]
rs1159396	0.82[YRI][hapmap]
rs1160092	0.86[YRI][hapmap]
rs12508654	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13109080	0.82[MKK][hapmap];0.82[YRI][hapmap]
rs13110516	0.81[CHB][hapmap]
rs13114476	0.81[CHB][hapmap]
rs13115057	0.81[CHB][hapmap]
rs13118711	0.85[YRI][hapmap]
rs13126445	0.81[CHB][hapmap]
rs13138566	0.81[CHB][hapmap]
rs13140528	0.80[CHB][hapmap]
rs1355578	0.81[LWK][hapmap];0.82[YRI][hapmap]
rs1398170	0.81[CHB][hapmap]
rs1398174	0.85[YRI][hapmap]
rs1398177	0.86[YRI][hapmap]
rs1512126	0.81[CHB][hapmap]
rs1512129	0.81[LWK][hapmap];0.81[MKK][hapmap]
rs1512131	0.81[AFR][1000 genomes]
rs1512132	0.83[MKK][hapmap]
rs1512138	0.81[CHB][hapmap]
rs17598809	0.81[CHB][hapmap]
rs17599074	0.81[CHB][hapmap]
rs17641065	0.81[CHB][hapmap]
rs17641171	0.81[CHB][hapmap]
rs2280073	0.83[MKK][hapmap]
rs4560384	0.86[YRI][hapmap]
rs4637372	0.82[YRI][hapmap]
rs6447517	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6818817	0.81[CHB][hapmap]
rs6818913	0.82[YRI][hapmap]
rs6819625	0.81[CHB][hapmap]
rs6824152	0.82[YRI][hapmap]
rs6842375	0.81[CHB][hapmap]
rs6843462	0.84[LWK][hapmap];0.84[MKK][hapmap];0.86[YRI][hapmap]
rs6844842	0.83[MKK][hapmap]
rs6847258	0.81[CHB][hapmap]
rs713287	0.83[LWK][hapmap];0.84[MKK][hapmap];0.82[YRI][hapmap]
rs7655866	0.82[YRI][hapmap]
rs7660277	0.83[YRI][hapmap]
rs7661550	0.81[LWK][hapmap]
rs7665758	0.83[MKK][hapmap]
rs7679715	1.00[CHB][hapmap];0.95[CHD][hapmap];0.82[GIH][hapmap];0.95[JPT][hapmap];0.81[MEX][hapmap]
rs7680308	0.89[YRI][hapmap]
rs7683996	0.81[CHB][hapmap]
rs7691100	0.81[CHB][hapmap]
rs9291292	0.80[CHB][hapmap]
rs9291294	0.86[CHB][hapmap]
rs9291297	0.81[CHB][hapmap]
rs9291298	0.85[YRI][hapmap]
rs953380	0.81[CHB][hapmap]
rs9992220	0.81[CHB][hapmap]
rs9995416	0.82[LWK][hapmap];0.87[MKK][hapmap];0.89[YRI][hapmap]

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:46946000-46950600	Enhancers	Fetal Heart	heart
2	chr4:46947400-46949800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr4:46947400-46952200	Weak transcription	Right Ventricle	heart
4	chr4:46947600-46952200	Weak transcription	Left Ventricle	heart
5	chr4:46947800-46950000	Enhancers	Brain Germinal Matrix	brain
6	chr4:46948000-46950200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr4:46948000-46950400	Enhancers	Fetal Brain Male	brain
8	chr4:46948200-46950000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr4:46948400-46949800	Enhancers	Brain Anterior Caudate	brain
10	chr4:46948400-46950000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr4:46948800-46949800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr4:46948800-46955200	Weak transcription	Brain Cingulate Gyrus	brain
13	chr4:46949000-46949800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr4:46949000-46949800	Enhancers	HUVEC	blood vessel
15	chr4:46949200-46949800	Enhancers	Osteobl	bone
16	chr4:46949400-46950200	Enhancers	Fetal Brain Female	brain
17	chr4:46949600-46955200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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