Variant report

Variant	rs8021342
Chromosome Location	chr14:37465301-37465302
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:37464918..37466831-chr14:37480204..37482482,2	MCF-7	breast:
2	chr14:37463868..37466130-chr14:37470349..37471911,2	K562	blood:
3	chr14:37464102..37465757-chr14:37474715..37476835,2	K562	blood:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10129948	0.96[ASN][1000 genomes]
rs10130430	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10131507	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10132205	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10137636	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10141660	0.96[ASN][1000 genomes]
rs10148776	0.89[EUR][1000 genomes]
rs11848465	1.00[CEU][hapmap]
rs11850139	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12050275	1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17105840	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs17105858	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17105860	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17105883	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17105951	1.00[CEU][hapmap];0.89[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs17178080	1.00[CEU][hapmap]
rs2022584	1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2022585	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs2022727	0.93[YRI][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2022730	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2056355	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2139746	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2145131	0.96[ASN][1000 genomes]
rs2180599	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28414995	0.94[ASN][1000 genomes]
rs28540719	0.86[ASN][1000 genomes]
rs61989484	0.94[ASN][1000 genomes]
rs6571771	0.84[EUR][1000 genomes]
rs6571772	0.84[EUR][1000 genomes]
rs7142715	0.95[ASN][1000 genomes]
rs7143069	0.96[ASN][1000 genomes]
rs7147216	1.00[CEU][hapmap];0.96[ASN][1000 genomes]
rs7156230	0.86[ASN][1000 genomes]
rs751202	1.00[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs8011174	0.85[YRI][hapmap]
rs8013390	0.85[EUR][1000 genomes]
rs8019355	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs909015	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.86[ASN][1000 genomes]
rs911008	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs925999	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.93[ASN][1000 genomes]
rs9805891	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534288	chr14:37254539-37697745	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37446200-37465800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:37458000-37466000	Weak transcription	HSMM	muscle
3	chr14:37459400-37465600	Weak transcription	NHDF-Ad	bronchial
4	chr14:37462400-37465800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr14:37462600-37465400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr14:37462600-37465400	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr14:37463600-37465400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr14:37465000-37465600	Enhancers	K562	blood
9	chr14:37465000-37466400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr14:37465000-37466400	Enhancers	NHEK	skin
11	chr14:37465000-37466600	Enhancers	HMEC	breast
12	chr14:37465200-37465600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr14:37465200-37465600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr14:37465200-37467000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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