Variant report

Variant	rs61169879
Chromosome Location	chr17:59917366-59917367
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	chr17:59913331..59919987-chr20:55836222..55842888,9	MCF-7	breast:
2	chr17:59485300..59495746-chr17:59906301..59920408,36	MCF-7	breast:
3	chr17:59916411..59918258-chr17:60141460..60143783,2	K562	blood:
4	chr17:59800153..59801027-chr17:59916762..59917391,2	MCF-7	breast:
5	chr17:59498730..59500384-chr17:59914987..59917975,2	MCF-7	breast:
6	chr17:59910616..59917582-chr17:59936691..59943102,15	MCF-7	breast:
7	chr17:59800583..59801312-chr17:59916811..59917454,4	MCF-7	breast:
8	chr17:59496517..59498736-chr17:59916457..59918359,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000187013	Chromatin interaction
ENSG00000108510	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000136492	Chromatin interaction
ENSG00000226308	Chromatin interaction
ENSG00000101144	Chromatin interaction
ENSG00000121068	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs12451910	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12452094	0.81[AMR][1000 genomes]
rs12452732	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12452742	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12453644	0.83[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12600909	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12601269	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs16945692	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2271576	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2378908	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3744434	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4968408	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4968451	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4968452	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4968454	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4968455	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4968456	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4968457	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4988344	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56794817	0.81[AMR][1000 genomes]
rs58624595	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs59080342	0.81[AMR][1000 genomes]
rs73332565	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73332580	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73332598	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8080599	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8081917	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9630735	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][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	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	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
4	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
5	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
6	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
7	esv2576756	chr17:59916415-59917840	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59863600-59925000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr17:59870400-59933400	Weak transcription	Fetal Intestine Large	intestine
3	chr17:59884200-59933200	Weak transcription	K562	blood
4	chr17:59894000-59922400	Weak transcription	Osteobl	bone
5	chr17:59894800-59922000	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr17:59898800-59920800	Weak transcription	Thymus	Thymus
7	chr17:59898800-59939600	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr17:59898800-59939800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr17:59899200-59919000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr17:59899400-59920600	Weak transcription	Fetal Thymus	thymus
11	chr17:59899400-59924200	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr17:59904200-59927000	Weak transcription	Fetal Kidney	kidney
13	chr17:59904800-59933200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr17:59905400-59923800	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr17:59905400-59931400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr17:59905600-59923800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr17:59905800-59919000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr17:59905800-59920600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr17:59905800-59923600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr17:59905800-59939000	Weak transcription	Primary T cells from cord blood	blood
21	chr17:59906000-59919200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr17:59906200-59921400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr17:59906200-59940200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr17:59906400-59919000	Weak transcription	GM12878-XiMat	blood
25	chr17:59906400-59919200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr17:59907800-59920200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr17:59910000-59921200	Weak transcription	Fetal Muscle Leg	muscle
28	chr17:59910200-59918800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr17:59911200-59921000	Weak transcription	Fetal Stomach	stomach
30	chr17:59911600-59937800	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr17:59911800-59939000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr17:59912000-59919200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr17:59912000-59919400	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr17:59912000-59925600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr17:59912000-59938400	Weak transcription	HUVEC	blood vessel
36	chr17:59912200-59921600	Weak transcription	NH-A	brain
37	chr17:59912200-59939200	Weak transcription	HSMM	muscle
38	chr17:59912200-59939800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr17:59912400-59918400	Weak transcription	Hela-S3	cervix
40	chr17:59912400-59918800	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr17:59912400-59919200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr17:59912400-59919400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr17:59912400-59920400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr17:59912400-59921400	Weak transcription	HMEC	breast
45	chr17:59912400-59923600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr17:59912400-59931400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr17:59912400-59931400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr17:59912400-59938600	Weak transcription	NHDF-Ad	bronchial
49	chr17:59912400-59938600	Weak transcription	NHEK	skin
50	chr17:59912400-59939400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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