Variant report

Variant	rs2070704
Chromosome Location	chr1:160112138-160112139
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1046995	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10494336	1.00[CHB][hapmap];0.93[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1063125	0.81[ASN][1000 genomes]
rs10908761	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12136519	0.92[ASN][1000 genomes]
rs16831388	0.90[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs16831438	1.00[CEU][hapmap];0.90[CHB][hapmap];0.93[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16831441	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];0.93[JPT][hapmap];0.93[MEX][hapmap];0.94[TSI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17846707	0.85[ASN][1000 genomes]
rs2070702	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2070703	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753267	0.90[CHB][hapmap];0.93[CHD][hapmap];0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs3747625	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55967674	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56199408	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs58313172	0.85[ASN][1000 genomes]
rs9660305	0.85[ASN][1000 genomes]
rs9661252	0.81[ASN][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	esv3327316	chr1:159985477-160151281	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	esv1820784	chr1:160029416-160159395	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv534165	chr1:160029416-160187302	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv872490	chr1:160083012-160121488	Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	esv3453724	chr1:160098374-160136495	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	esv3453725	chr1:160098456-160136351	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160088000-160146200	Weak transcription	Spleen	Spleen
2	chr1:160090600-160112600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:160092400-160112200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
4	chr1:160097200-160112200	Weak transcription	Brain Germinal Matrix	brain
5	chr1:160098600-160112200	Strong transcription	Fetal Muscle Trunk	muscle
6	chr1:160100000-160114800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:160103400-160118000	Weak transcription	Right Atrium	heart
8	chr1:160106600-160114200	Weak transcription	Adipose Nuclei	Adipose
9	chr1:160106800-160121600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:160107000-160112200	Strong transcription	Colon Smooth Muscle	Colon
11	chr1:160107000-160112800	Weak transcription	Brain Cingulate Gyrus	brain
12	chr1:160107400-160114600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr1:160107600-160121400	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr1:160108600-160112800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr1:160108600-160113000	Strong transcription	Stomach Smooth Muscle	stomach
16	chr1:160108800-160112200	Strong transcription	HSMMtube	muscle
17	chr1:160109000-160112200	Strong transcription	Aorta	Aorta
18	chr1:160109800-160114800	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr1:160110200-160113000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr1:160110200-160113400	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr1:160110200-160114800	Weak transcription	Fetal Stomach	stomach
22	chr1:160110400-160114400	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr1:160111000-160113400	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr1:160111200-160114400	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr1:160111600-160112200	Strong transcription	HUES48 Cell Line	embryonic stem cell
26	chr1:160111600-160113000	Strong transcription	Skeletal Muscle Male	skeletal muscle
27	chr1:160111600-160113200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr1:160111800-160112600	Strong transcription	Skeletal Muscle Female	skeletal muscle
29	chr1:160111800-160113000	Genic enhancers	Cortex derived primary cultured neurospheres	brain
30	chr1:160111800-160113400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:160111800-160114800	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr1:160111800-160117600	Weak transcription	Left Ventricle	heart
33	chr1:160112000-160113600	Weak transcription	Right Ventricle	heart
34	chr1:160112000-160115200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr1:160112000-160115200	Weak transcription	Fetal Muscle Leg	muscle

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