Variant report

Variant	rs1884619
Chromosome Location	chr14:33129814-33129815
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:33129614..33131625-chr14:33133095..33135565,2	MCF-7	breast:

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10135562	1.00[CHB][hapmap];0.88[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.93[MKK][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10141122	0.95[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.96[TSI][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10144339	1.00[CEU][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10147066	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10483416	0.95[CEU][hapmap];0.91[GIH][hapmap];0.85[TSI][hapmap];0.81[EUR][1000 genomes]
rs11844389	0.83[EUR][1000 genomes]
rs11846446	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12323757	0.95[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12323763	0.95[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12323766	0.95[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12880113	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs17515243	0.88[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.91[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1956223	0.95[CEU][hapmap];0.88[GIH][hapmap];0.89[MEX][hapmap];0.85[TSI][hapmap];0.82[EUR][1000 genomes]
rs34340539	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4981994	0.80[CEU][hapmap]
rs7141374	0.80[EUR][1000 genomes]
rs71419918	0.81[ASN][1000 genomes]
rs71419919	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7142867	0.83[EUR][1000 genomes]
rs927062	0.95[CEU][hapmap];0.88[GIH][hapmap];0.84[MEX][hapmap];0.89[TSI][hapmap];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045035	chr14:32986003-33543227	Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv542021	chr14:32986003-33543227	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv428624	chr14:33065571-33214223	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv16083	chr14:33129777-33130735	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:33107000-33130600	Weak transcription	Left Ventricle	heart
2	chr14:33113800-33130600	Weak transcription	Right Ventricle	heart
3	chr14:33115000-33134400	Weak transcription	Psoas Muscle	Psoas
4	chr14:33117800-33149200	Weak transcription	Colon Smooth Muscle	Colon
5	chr14:33121000-33134200	Weak transcription	Fetal Muscle Leg	muscle
6	chr14:33126400-33132800	Weak transcription	Esophagus	oesophagus
7	chr14:33126600-33131800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr14:33126600-33134800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr14:33126800-33130200	Weak transcription	HSMMtube	muscle
10	chr14:33126800-33130400	Weak transcription	Aorta	Aorta
11	chr14:33126800-33131200	Weak transcription	Osteobl	bone
12	chr14:33126800-33131400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr14:33126800-33131600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr14:33126800-33131800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr14:33127200-33131600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr14:33127400-33130600	Weak transcription	Brain Anterior Caudate	brain
17	chr14:33127400-33131400	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr14:33127400-33131600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr14:33127400-33136200	Weak transcription	Brain Hippocampus Middle	brain
20	chr14:33127600-33131000	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr14:33127600-33131400	Weak transcription	Brain Angular Gyrus	brain
22	chr14:33128600-33131000	Weak transcription	Brain Substantia Nigra	brain
23	chr14:33129200-33133600	Enhancers	Fetal Heart	heart
24	chr14:33129400-33130000	Enhancers	Right Atrium	heart
25	chr14:33129400-33130000	Enhancers	NHDF-Ad	bronchial

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