Variant report

Variant	rs16827685
Chromosome Location	chr3:157182953-157182954
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:157175083..157179044-chr3:157180593..157185169,5	K562	blood:
2	chr3:157181063..157183847-chr3:157192329..157195122,2	MCF-7	breast:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11915662	0.94[YRI][hapmap];0.86[AFR][1000 genomes]
rs11923416	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11924914	0.94[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11928409	0.94[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11928417	0.94[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16827563	0.81[YRI][hapmap];1.00[AMR][1000 genomes]
rs16827677	0.94[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16827681	0.94[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16827690	0.94[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16827766	1.00[AMR][1000 genomes]
rs55695446	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56108012	1.00[AMR][1000 genomes]
rs56247352	1.00[AMR][1000 genomes]
rs56682605	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57705005	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59369651	1.00[AMR][1000 genomes]
rs60821393	1.00[AMR][1000 genomes]
rs60922199	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6776505	0.94[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6788044	1.00[AMR][1000 genomes]
rs6791405	1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6791497	0.94[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6793548	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6794570	0.94[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6799588	1.00[AMR][1000 genomes]
rs6801619	0.94[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6804490	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73876303	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73876318	1.00[AMR][1000 genomes]
rs73876319	1.00[AMR][1000 genomes]
rs73876327	1.00[AMR][1000 genomes]
rs73876330	1.00[AMR][1000 genomes]
rs9680932	0.94[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9682235	0.88[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]

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	esv2757900	chr3:157090166-157254684	Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active 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	7 gene(s)	inside rSNPs	diseases
2	esv2759193	chr3:157090166-157254684	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:157160400-157195000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:157161200-157186600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr3:157164600-157185400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr3:157170200-157187000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:157179400-157184800	Weak transcription	HSMM	muscle
6	chr3:157180200-157186000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr3:157180400-157185400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr3:157180800-157186000	Enhancers	NHDF-Ad	bronchial
9	chr3:157181000-157186400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:157181200-157184400	Enhancers	NHLF	lung
11	chr3:157181400-157183800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr3:157181400-157183800	Genic enhancers	HUVEC	blood vessel
13	chr3:157181600-157183600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr3:157182000-157183000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:157182200-157183000	Enhancers	Brain Germinal Matrix	brain
16	chr3:157182200-157185400	Weak transcription	Lung	lung
17	chr3:157182400-157184600	Weak transcription	NH-A	brain
18	chr3:157182400-157185000	Weak transcription	HSMMtube	muscle
19	chr3:157182600-157183200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr3:157182600-157183400	Weak transcription	Osteobl	bone
21	chr3:157182600-157184600	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr3:157182800-157183000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr3:157182800-157183000	Enhancers	Fetal Stomach	stomach
24	chr3:157182800-157184600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr3:157182800-157190400	Enhancers	Primary neutrophils fromperipheralblood	blood

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