Variant report

Variant	rs4899186
Chromosome Location	chr14:66333015-66333016
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:66332081..66334699-chr14:66335847..66337619,2	MCF-7	breast:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10151785	1.00[AFR][1000 genomes]
rs2022846	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2154237	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2186100	0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2318304	1.00[AFR][1000 genomes]
rs4131565	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4899185	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4902422	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4902428	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4902429	0.96[ASN][1000 genomes]
rs4902430	1.00[AFR][1000 genomes]
rs6573636	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6573639	1.00[ASN][1000 genomes]
rs6573640	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7160048	1.00[AFR][1000 genomes]
rs8008391	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs8014173	0.94[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs8015322	0.94[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs8019249	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043943	chr14:65782466-66698411	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
2	nsv542120	chr14:65782466-66698411	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
3	esv3366524	chr14:65924360-66423862	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
4	nsv1045000	chr14:66010886-66372518	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1042671	chr14:66010886-66399888	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv817409	chr14:66220075-66990168	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
7	nsv564953	chr14:66287921-67046960	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
8	nsv1050485	chr14:66308283-67109270	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
9	nsv832820	chr14:66310846-66362845	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv530775	chr14:66316836-67079049	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
11	nsv530793	chr14:66317036-67078908	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66328200-66333600	Enhancers	Primary T helper cells PMA-I stimulated	--
2	chr14:66330600-66334400	Enhancers	Thymus	Thymus
3	chr14:66331400-66334400	Enhancers	NHDF-Ad	bronchial
4	chr14:66331400-66335200	Enhancers	Primary T cells from cord blood	blood
5	chr14:66331800-66333800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr14:66332000-66333200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr14:66332000-66334600	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr14:66332000-66336000	Enhancers	Dnd41	blood
9	chr14:66332000-66337400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr14:66332000-66344000	Weak transcription	Gastric	stomach
11	chr14:66332200-66333200	Weak transcription	Brain Germinal Matrix	brain
12	chr14:66332200-66333800	Weak transcription	Small Intestine	intestine
13	chr14:66332200-66334200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr14:66332400-66333400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr14:66332400-66333800	Weak transcription	Fetal Thymus	thymus
16	chr14:66332400-66334600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr14:66332400-66343600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr14:66332600-66334000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr14:66332600-66335000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr14:66333000-66333200	Enhancers	Lung	lung
21	chr14:66333000-66333600	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr14:66333000-66334000	Enhancers	Fetal Stomach	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links