Variant report

Variant	rs73332580
Chromosome Location	chr17:59968621-59968622
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:59944363..59946403-chr17:59967188..59969654,2	K562	blood:
2	chr17:59967872..59970624-chr20:55729420..55732315,2	MCF-7	breast:
3	chr17:59967952..59972166-chr17:60003800..60006338,4	MCF-7	breast:
4	chr17:59968155..59970837-chr17:60077646..60079984,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000108506	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs12451910	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12452094	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12452732	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12452742	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12600909	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16945692	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2271576	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3744434	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4968408	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4968451	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4968452	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4968454	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4968455	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4968456	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4968457	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4968459	0.84[ASN][1000 genomes]
rs4968460	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4968461	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4988344	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56794817	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58085921	0.85[ASN][1000 genomes]
rs58624595	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59080342	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61169879	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61658218	0.81[ASN][1000 genomes]
rs73332565	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73332598	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73334621	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8080599	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8081917	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9630735	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 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	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:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59941400-59975000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr17:59941400-60004400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr17:59941400-60004400	Weak transcription	Aorta	Aorta
4	chr17:59941400-60004400	Weak transcription	Pancreas	Pancrea
5	chr17:59941600-59979600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr17:59941600-59987600	Weak transcription	Right Ventricle	heart
7	chr17:59941600-60003600	Weak transcription	Stomach Mucosa	stomach
8	chr17:59941600-60004400	Weak transcription	Colonic Mucosa	Colon
9	chr17:59941800-59968800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr17:59941800-59969200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr17:59941800-59971800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr17:59941800-59979200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr17:59941800-59979200	Weak transcription	Brain Angular Gyrus	brain
14	chr17:59942600-60002800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr17:59943600-59989600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr17:59944400-59970000	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr17:59946600-59989200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr17:59947400-59977400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr17:59948000-59972600	Weak transcription	NHDF-Ad	bronchial
20	chr17:59948000-59981800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr17:59948200-59980600	Weak transcription	HMEC	breast
22	chr17:59948200-59986800	Weak transcription	Fetal Kidney	kidney
23	chr17:59950000-59979200	Weak transcription	NHLF	lung
24	chr17:59950800-59968800	Strong transcription	Adipose Nuclei	Adipose
25	chr17:59950800-59981600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr17:59951000-59972400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr17:59951400-59992200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr17:59951600-59989600	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr17:59952000-59969200	Weak transcription	HUVEC	blood vessel
30	chr17:59952000-59971600	Weak transcription	Primary hematopoietic stem cells	blood
31	chr17:59952800-59981400	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr17:59953200-59972200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr17:59953800-59985600	Weak transcription	Small Intestine	intestine
34	chr17:59954400-60003800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr17:59954600-59984800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr17:59955200-59979600	Weak transcription	HSMMtube	muscle
37	chr17:59955800-59971600	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr17:59956800-59970000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr17:59957600-59973200	Strong transcription	Liver	Liver
40	chr17:59957800-59971600	Strong transcription	Fetal Muscle Trunk	muscle
41	chr17:59958000-59987600	Weak transcription	Esophagus	oesophagus
42	chr17:59959000-59996800	Weak transcription	Gastric	stomach
43	chr17:59959600-60003600	Weak transcription	Fetal Heart	heart
44	chr17:59959800-59973000	Weak transcription	Primary B cells from cord blood	blood
45	chr17:59960200-59972000	Strong transcription	Stomach Smooth Muscle	stomach
46	chr17:59960800-59970000	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr17:59962000-59970200	Strong transcription	A549	lung
48	chr17:59962000-59977000	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr17:59962200-59969000	Weak transcription	Osteobl	bone
50	chr17:59962400-59970600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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