Variant report

Variant	rs1494208
Chromosome Location	chr10:27913876-27913877
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10829306	1.00[CEU][hapmap]
rs11015910	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11015913	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11015914	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11015918	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11015920	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11015925	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11015933	0.87[AMR][1000 genomes]
rs12219722	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1494206	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1494207	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17756469	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17756619	1.00[CEU][hapmap]
rs17756631	1.00[CEU][hapmap];0.82[JPT][hapmap];0.82[EUR][1000 genomes]
rs17829539	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1907383	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1908273	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1908274	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1908275	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1908276	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4405204	1.00[CEU][hapmap]
rs60014356	0.91[AMR][1000 genomes]
rs60633943	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60891419	0.89[AMR][1000 genomes]
rs6482634	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7475183	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7903134	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs980135	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[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	nsv550241	chr10:27569521-28025771	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1045257	chr10:27572440-27926946	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers 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	25 gene(s)	inside rSNPs	diseases
3	nsv1053952	chr10:27659365-27915029	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer 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	13 gene(s)	inside rSNPs	diseases
4	esv3368825	chr10:27864181-28043820	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	nsv894985	chr10:27869503-27957785	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv894986	chr10:27904646-27957785	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27904400-27914000	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr10:27904400-27914600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:27909800-27914000	Weak transcription	Brain Germinal Matrix	brain
4	chr10:27910800-27923000	Weak transcription	Aorta	Aorta
5	chr10:27911000-27914200	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr10:27911000-27914200	Weak transcription	HSMM	muscle
7	chr10:27911000-27914200	Enhancers	NHDF-Ad	bronchial
8	chr10:27912000-27914000	Weak transcription	Osteobl	bone
9	chr10:27912000-27914200	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr10:27912400-27914200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:27912400-27915000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr10:27913200-27915000	Enhancers	Fetal Muscle Trunk	muscle
13	chr10:27913400-27914400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr10:27913600-27914000	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr10:27913600-27914000	Bivalent Enhancer	Fetal Stomach	stomach
16	chr10:27913600-27914200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr10:27913600-27914200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr10:27913600-27914200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr10:27913600-27914400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr10:27913600-27914600	Bivalent Enhancer	Fetal Muscle Leg	muscle
21	chr10:27913600-27915000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr10:27913600-27915200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr10:27913600-27917800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr10:27913800-27914000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr10:27913800-27914000	Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr10:27913800-27914000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr10:27913800-27914200	Enhancers	Adipose Nuclei	Adipose
28	chr10:27913800-27914400	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr10:27913800-27914400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr10:27913800-27914600	Active TSS	H9 Cell Line	embryonic stem cell
31	chr10:27913800-27915000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr10:27913800-27915000	Enhancers	HSMMtube	muscle
33	chr10:27913800-27916000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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