Variant report

Variant	rs8015330
Chromosome Location	chr14:65602183-65602184
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:65600572..65603233-chr14:65606608..65608580,2	MCF-7	breast:
2	chr14:65600313..65602525-chr14:65607232..65610149,2	MCF-7	breast:
3	chr14:65588712..65590660-chr14:65602083..65604440,2	K562	blood:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10873180	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10873181	0.84[EUR][1000 genomes]
rs10873182	0.84[EUR][1000 genomes]
rs10873183	0.82[EUR][1000 genomes]
rs10873185	0.82[EUR][1000 genomes]
rs11158572	0.88[ASN][1000 genomes]
rs11158573	0.88[ASN][1000 genomes]
rs11158574	0.86[CEU][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs11158577	0.84[CEU][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11158578	0.84[EUR][1000 genomes]
rs11623603	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11625045	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs11626156	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11626496	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11627859	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12100605	0.86[EUR][1000 genomes]
rs12147959	0.85[ASN][1000 genomes]
rs12880781	0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs12884836	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12887607	0.84[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs12888794	0.86[ASN][1000 genomes]
rs17102423	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17825846	0.88[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1953228	0.86[ASN][1000 genomes]
rs2898863	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34062462	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35002541	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35176994	0.91[ASN][1000 genomes]
rs35769504	0.91[ASN][1000 genomes]
rs4902358	0.94[JPT][hapmap]
rs4902363	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4902364	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4902365	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4902367	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55658675	0.86[ASN][1000 genomes]
rs61987428	0.83[EUR][1000 genomes]
rs61987429	0.84[EUR][1000 genomes]
rs7143495	0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs7144259	0.94[JPT][hapmap]
rs7154852	0.86[ASN][1000 genomes]
rs7161394	0.81[CEU][hapmap];0.80[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs762810	0.94[JPT][hapmap]
rs8004805	0.92[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8009396	0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs8009714	0.88[ASN][1000 genomes]
rs8018788	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs8181937	0.86[ASN][1000 genomes]
rs8181938	0.86[ASN][1000 genomes]
rs8181939	0.83[CEU][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs868814	0.96[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs884683	0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs942627	0.81[CEU][hapmap];0.80[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832816	chr14:65473244-65644645	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	esv1833060	chr14:65594460-65607642	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	esv989058	chr14:65601785-65607798	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65596800-65602600	Enhancers	Fetal Intestine Small	intestine
2	chr14:65597800-65602600	Enhancers	Fetal Intestine Large	intestine
3	chr14:65598200-65602200	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr14:65598800-65604400	Weak transcription	Colonic Mucosa	Colon
5	chr14:65598800-65604400	Weak transcription	Osteobl	bone
6	chr14:65601400-65602400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr14:65601400-65602400	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr14:65601600-65602200	Enhancers	Primary T cells fromperipheralblood	blood
9	chr14:65601600-65602200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr14:65601600-65602400	Enhancers	Fetal Thymus	thymus
11	chr14:65601600-65602400	Enhancers	Dnd41	blood
12	chr14:65601600-65605400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr14:65601800-65602200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr14:65601800-65602200	Enhancers	Thymus	Thymus
15	chr14:65601800-65602200	Enhancers	NHEK	skin
16	chr14:65602000-65604400	Weak transcription	HMEC	breast
17	chr14:65602000-65604600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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