Variant report

Variant	rs12453644
Chromosome Location	chr17:59900357-59900358
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:59895324..59898456-chr17:59898526..59902353,6	MCF-7	breast:
2	chr17:59476100..59479841-chr17:59897699..59902465,4	MCF-7	breast:
3	chr17:59897032..59900869-chr17:59902920..59905973,5	MCF-7	breast:
4	chr17:59876221..59877900-chr17:59899505..59902130,2	K562	blood:
5	chr17:59897823..59900768-chr17:59908892..59911351,2	MCF-7	breast:
6	chr17:59898858..59900358-chr17:59911804..59913981,2	MCF-7	breast:
7	chr17:59898589..59900592-chr17:59938772..59941762,2	MCF-7	breast:
8	chr17:59477432..59480402-chr17:59899542..59902137,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000267280	Chromatin interaction
ENSG00000267131	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000136492	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11079457	0.90[ASN][1000 genomes]
rs12601269	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16945692	0.83[EUR][1000 genomes]
rs2378908	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4968451	0.84[EUR][1000 genomes]
rs4968452	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs4988344	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61169879	0.83[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs9630735	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3378293	chr17:59744117-60124899	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
2	nsv908673	chr17:59767501-59926645	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	94 gene(s)	inside rSNPs	diseases
3	nsv575841	chr17:59812748-59914681	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
4	nsv575842	chr17:59812748-59927307	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	70 gene(s)	inside rSNPs	diseases
5	nsv908675	chr17:59835864-59937286	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	67 gene(s)	inside rSNPs	diseases
6	esv1794309	chr17:59861640-59907952	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region Chromatin interactive region	32 gene(s)	inside rSNPs	diseases
7	nsv575843	chr17:59869081-59935723	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
8	nsv916786	chr17:59890834-60103687	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59848800-59911200	Weak transcription	HUVEC	blood vessel
2	chr17:59851200-59902600	Weak transcription	Fetal Stomach	stomach
3	chr17:59863600-59925000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr17:59870400-59933400	Weak transcription	Fetal Intestine Large	intestine
5	chr17:59873200-59905000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr17:59874400-59910600	Weak transcription	Hela-S3	cervix
7	chr17:59884200-59933200	Weak transcription	K562	blood
8	chr17:59887400-59901600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr17:59887600-59905200	Weak transcription	Fetal Lung	lung
10	chr17:59887800-59911000	Weak transcription	NH-A	brain
11	chr17:59888000-59910400	Weak transcription	NHEK	skin
12	chr17:59888000-59911000	Weak transcription	NHLF	lung
13	chr17:59888000-59911400	Weak transcription	HSMM	muscle
14	chr17:59891000-59905200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr17:59891000-59911000	Weak transcription	NHDF-Ad	bronchial
16	chr17:59894000-59905200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr17:59894000-59905400	Weak transcription	HepG2	liver
18	chr17:59894000-59910600	Weak transcription	HMEC	breast
19	chr17:59894000-59922400	Weak transcription	Osteobl	bone
20	chr17:59894800-59922000	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr17:59897600-59900600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr17:59897800-59900800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr17:59898200-59912000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr17:59898400-59900800	Strong transcription	Dnd41	blood
25	chr17:59898600-59900600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr17:59898600-59904600	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr17:59898800-59900800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr17:59898800-59904800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr17:59898800-59904800	Weak transcription	A549	lung
30	chr17:59898800-59905200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr17:59898800-59905600	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr17:59898800-59911200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr17:59898800-59914400	Weak transcription	Primary B cells from cord blood	blood
34	chr17:59898800-59920800	Weak transcription	Thymus	Thymus
35	chr17:59898800-59939600	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr17:59898800-59939800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr17:59899000-59905000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr17:59899200-59905000	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr17:59899200-59905000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr17:59899200-59905200	Weak transcription	Primary hematopoietic stem cells	blood
41	chr17:59899200-59905400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr17:59899200-59911200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr17:59899200-59919000	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr17:59899400-59900400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr17:59899400-59902600	Weak transcription	Fetal Intestine Small	intestine
46	chr17:59899400-59904600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr17:59899400-59905200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr17:59899400-59908600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr17:59899400-59920600	Weak transcription	Fetal Thymus	thymus
50	chr17:59899400-59924200	Weak transcription	Primary neutrophils fromperipheralblood	blood

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