Variant report

Variant	rs10059433
Chromosome Location	chr5:179954615-179954616
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:179943961..179945573-chr5:179952586..179955313,2	MCF-7	breast:
2	chr5:179954302..179955834-chr5:179973302..179975583,2	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10072835	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10077152	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13357229	1.00[CEU][hapmap];0.92[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17080355	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17080395	1.00[CEU][hapmap];1.00[GIH][hapmap];0.84[LWK][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes]
rs28522110	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6872162	1.00[AMR][1000 genomes]
rs6880907	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs6883791	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7723088	1.00[CEU][hapmap];0.92[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9329113	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023914	chr5:179649883-180040672	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv537983	chr5:179649883-180040672	Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv1030697	chr5:179710469-180686563	ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	184 gene(s)	inside rSNPs	diseases
4	nsv1026417	chr5:179721376-180291360	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
5	nsv1031836	chr5:179742033-180676122	Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
6	nsv537984	chr5:179742033-180676122	Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
7	nsv949199	chr5:179743553-180696889	Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
8	nsv1023537	chr5:179791679-179982822	Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	nsv537985	chr5:179791679-179982822	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
10	nsv1019519	chr5:179866730-179959408	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv830564	chr5:179867394-180010096	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
12	esv1810959	chr5:179945112-179997861	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179923600-179957000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:179924600-179957000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:179929000-179959200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr5:179933800-179959000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr5:179934200-179956600	Weak transcription	Rectal Smooth Muscle	rectum
6	chr5:179936800-179956200	Weak transcription	Fetal Muscle Trunk	muscle
7	chr5:179938800-179956600	Weak transcription	HSMM	muscle
8	chr5:179942000-179956400	Weak transcription	Brain Germinal Matrix	brain
9	chr5:179942000-179958800	Weak transcription	Esophagus	oesophagus
10	chr5:179942600-179959000	Weak transcription	HepG2	liver
11	chr5:179946000-179958400	Weak transcription	Lung	lung
12	chr5:179946200-179960800	Weak transcription	NHLF	lung
13	chr5:179946400-179956800	Weak transcription	Osteobl	bone
14	chr5:179946600-179956200	Weak transcription	NH-A	brain
15	chr5:179946800-179959000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr5:179947000-179958000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:179948400-179956600	Weak transcription	A549	lung
18	chr5:179949000-179956800	Weak transcription	HMEC	breast
19	chr5:179949600-179956400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr5:179949800-179958800	Weak transcription	Aorta	Aorta
21	chr5:179950000-179956600	Weak transcription	Primary hematopoietic stem cells	blood
22	chr5:179950200-179955600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr5:179950200-179956600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr5:179950200-179956800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr5:179950200-179958600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr5:179950200-179959000	Weak transcription	Brain Cingulate Gyrus	brain
27	chr5:179950200-179959200	Weak transcription	Brain Anterior Caudate	brain
28	chr5:179950200-179959200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr5:179950200-179959800	Weak transcription	Left Ventricle	heart
30	chr5:179950200-179975200	Weak transcription	Psoas Muscle	Psoas
31	chr5:179950200-179984400	Weak transcription	NHDF-Ad	bronchial
32	chr5:179950200-179992000	Weak transcription	Right Ventricle	heart
33	chr5:179950400-179992400	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr5:179950600-179959400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr5:179950600-180004000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr5:179950800-179956200	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr5:179950800-179956400	Weak transcription	Fetal Brain Female	brain
38	chr5:179950800-179956600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr5:179950800-179956600	Weak transcription	Brain Substantia Nigra	brain
40	chr5:179950800-179959000	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr5:179951000-179956200	Weak transcription	Primary B cells from peripheral blood	blood
42	chr5:179951000-179956200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr5:179951000-179956600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr5:179951000-179959200	Weak transcription	Fetal Brain Male	brain
45	chr5:179951000-179959400	Weak transcription	NHEK	skin
46	chr5:179951000-179991800	Weak transcription	Small Intestine	intestine
47	chr5:179951200-179959200	Weak transcription	Stomach Smooth Muscle	stomach
48	chr5:179951400-179959200	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr5:179951600-179956200	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr5:179951600-179956600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links