Variant report

Variant	rs9591325
Chromosome Location	chr13:50811220-50811221
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	chr13:50811157..50813184-chr13:50814146..50815876,2	MCF-7	breast:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12871645	0.87[CEU][hapmap]
rs12874827	0.87[CEU][hapmap]
rs17074145	0.87[CEU][hapmap]
rs9596264	0.83[AFR][1000 genomes]
rs9596266	0.94[AFR][1000 genomes]
rs9596267	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9596268	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9596270	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035151	chr13:50513535-51167850	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1254 gene(s)	inside rSNPs	diseases
2	esv2753964	chr13:50545399-51421199	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
3	esv2753492	chr13:50550081-51461720	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
4	esv2752608	chr13:50550099-51054499	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1249 gene(s)	inside rSNPs	diseases
5	nsv832608	chr13:50678628-50888413	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
6	nsv900076	chr13:50710579-50912578	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv561631	chr13:50761619-50846748	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50800400-50814400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr13:50804400-50818600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr13:50805000-50818600	Weak transcription	Psoas Muscle	Psoas
4	chr13:50805200-50815800	Weak transcription	Small Intestine	intestine
5	chr13:50808400-50818800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr13:50809600-50811400	Active TSS	Primary T killer memory cells from peripheral blood	blood
7	chr13:50809600-50811600	Active TSS	Rectal Mucosa Donor 29	rectum
8	chr13:50809600-50812200	Enhancers	Primary B cells from peripheral blood	blood
9	chr13:50809800-50811800	Flanking Active TSS	GM12878-XiMat	blood
10	chr13:50810200-50811400	Enhancers	Aorta	Aorta
11	chr13:50810200-50812000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr13:50810400-50811600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
13	chr13:50810400-50812200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr13:50810400-50812400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
15	chr13:50810400-50813800	Weak transcription	HepG2	liver
16	chr13:50810400-50814400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr13:50810600-50811800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr13:50810800-50811800	Enhancers	Osteobl	bone
19	chr13:50811000-50811400	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr13:50811000-50811400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr13:50811000-50811400	Active TSS	Primary T helper cells fromperipheralblood	blood
22	chr13:50811000-50811400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
23	chr13:50811000-50811600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr13:50811000-50811800	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr13:50811000-50812000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr13:50811200-50811400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr13:50811200-50811400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
28	chr13:50811200-50811400	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr13:50811200-50811600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr13:50811200-50811600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr13:50811200-50811600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
32	chr13:50811200-50811600	Enhancers	Fetal Muscle Leg	muscle
33	chr13:50811200-50812000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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