Variant report

Variant	rs11808814
Chromosome Location	chr1:211604173-211604174
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10458470	1.00[YRI][hapmap]
rs10465662	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11119725	1.00[YRI][hapmap]
rs11804883	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11806151	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11811760	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12085730	0.85[LWK][hapmap]
rs17017360	1.00[LWK][hapmap]
rs2289758	0.85[LWK][hapmap];1.00[YRI][hapmap]
rs35949128	0.85[AFR][1000 genomes]
rs3738202	1.00[YRI][hapmap]
rs41473244	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1824154	chr1:211565640-211614280	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	n/a
2	nsv945612	chr1:211593276-211615726	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211581400-211608200	Weak transcription	Primary B cells from peripheral blood	blood
2	chr1:211589600-211608800	Weak transcription	GM12878-XiMat	blood
3	chr1:211590400-211604400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:211590400-211607200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr1:211590400-211607600	Weak transcription	Left Ventricle	heart
6	chr1:211590400-211609000	Weak transcription	Primary B cells from cord blood	blood
7	chr1:211590600-211605600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr1:211591000-211607400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:211592200-211605600	Weak transcription	Fetal Intestine Small	intestine
10	chr1:211594800-211605800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:211594800-211606200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:211594800-211607200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:211594800-211608400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:211595400-211605800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:211596400-211609200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr1:211597800-211607800	Weak transcription	Ovary	ovary
17	chr1:211600600-211608000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr1:211601200-211605600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:211602400-211605600	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr1:211603000-211606400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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