Variant report

Variant	rs10494444
Chromosome Location	chr1:165530586-165530587
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

rs_ID	r²[population]
rs10158373	0.82[EUR][1000 genomes]
rs10465551	1.00[ASN][1000 genomes]
rs10494443	0.88[EUR][1000 genomes]
rs10494445	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs1326375	1.00[CEU][hapmap]
rs1590578	0.86[ASN][1000 genomes]
rs1648111	1.00[CEU][hapmap]
rs166949	1.00[CEU][hapmap]
rs16846009	0.86[ASN][1000 genomes]
rs16846405	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs16846410	0.88[EUR][1000 genomes]
rs16846549	0.88[EUR][1000 genomes]
rs16846612	1.00[CEU][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes]
rs16846621	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs16846680	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs16847312	1.00[CEU][hapmap];0.87[TSI][hapmap]
rs184038	1.00[CEU][hapmap]
rs192586	1.00[CEU][hapmap]
rs192587	1.00[CEU][hapmap]
rs2013490	0.88[ASN][1000 genomes]
rs206236	0.82[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs2252583	1.00[ASN][1000 genomes]
rs2433131	1.00[CEU][hapmap]
rs2459240	1.00[CEU][hapmap]
rs2485400	1.00[CEU][hapmap]
rs2485401	1.00[CEU][hapmap]
rs28446600	0.80[ASN][1000 genomes]
rs285411	1.00[JPT][hapmap]
rs285423	1.00[CEU][hapmap]
rs285433	1.00[CEU][hapmap]
rs285434	1.00[CEU][hapmap]
rs285444	1.00[CEU][hapmap]
rs285446	1.00[CEU][hapmap]
rs285447	1.00[CEU][hapmap]
rs285449	1.00[CEU][hapmap]
rs285450	1.00[CEU][hapmap]
rs285451	1.00[CEU][hapmap]
rs285454	1.00[CEU][hapmap]
rs411083	1.00[ASN][1000 genomes]
rs447374	1.00[ASN][1000 genomes]
rs58628453	0.88[EUR][1000 genomes]
rs60128426	1.00[ASN][1000 genomes]
rs6666562	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs72693830	0.88[ASN][1000 genomes]
rs73027004	1.00[ASN][1000 genomes]
rs73027007	1.00[ASN][1000 genomes]
rs73027009	1.00[ASN][1000 genomes]
rs74118817	1.00[ASN][1000 genomes]
rs74120723	0.88[EUR][1000 genomes]
rs74120729	0.88[EUR][1000 genomes]
rs796570	1.00[CEU][hapmap]

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165529200-165530600	Enhancers	Brain Germinal Matrix	brain
2	chr1:165529200-165530800	Enhancers	Left Ventricle	heart
3	chr1:165529600-165531200	Enhancers	Fetal Lung	lung
4	chr1:165529600-165531400	Enhancers	Fetal Heart	heart
5	chr1:165529800-165530600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
6	chr1:165529800-165530800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:165529800-165530800	Bivalent Enhancer	Fetal Stomach	stomach
8	chr1:165529800-165530800	Enhancers	Right Atrium	heart
9	chr1:165529800-165531000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
10	chr1:165529800-165531000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr1:165529800-165531000	Enhancers	Brain Anterior Caudate	brain
12	chr1:165529800-165531200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr1:165529800-165531200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
14	chr1:165529800-165531200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr1:165529800-165531200	Enhancers	Right Ventricle	heart
16	chr1:165530000-165530600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr1:165530000-165530600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
18	chr1:165530000-165530800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr1:165530000-165531000	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr1:165530000-165531000	Enhancers	Fetal Brain Male	brain
21	chr1:165530000-165531200	Enhancers	Ovary	ovary
22	chr1:165530200-165531000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
23	chr1:165530200-165531000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
24	chr1:165530200-165531400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
25	chr1:165530400-165530800	Enhancers	Fetal Muscle Leg	muscle

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