Variant report

Variant	rs9467153
Chromosome Location	chr6:24438037-24438038
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	chr6:24438004..24440295-chr6:24440300..24441957,2	MCF-7	breast:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1042303	0.91[YRI][hapmap]
rs1772256	0.80[YRI][hapmap];0.80[AFR][1000 genomes]
rs28564434	0.98[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28661697	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28706811	0.99[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3181759	0.81[AFR][1000 genomes]
rs56148439	0.86[AFR][1000 genomes]
rs59942835	0.91[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs6456613	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6938894	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs73727666	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7751846	0.87[YRI][hapmap];0.90[AFR][1000 genomes]
rs7752186	0.87[YRI][hapmap];0.90[AFR][1000 genomes]
rs7752603	0.91[YRI][hapmap];0.91[AFR][1000 genomes]
rs7757601	0.88[YRI][hapmap]
rs7768124	0.88[YRI][hapmap];0.90[AFR][1000 genomes]
rs7772115	0.87[YRI][hapmap];0.90[AFR][1000 genomes]
rs7772540	0.91[YRI][hapmap];0.91[AFR][1000 genomes]
rs9461006	0.86[AFR][1000 genomes]
rs9461007	0.89[AFR][1000 genomes]
rs9461008	0.85[AFR][1000 genomes]
rs9461009	0.86[AFR][1000 genomes]
rs9467136	0.87[YRI][hapmap]
rs9467142	0.90[AFR][1000 genomes]
rs9467143	0.91[AFR][1000 genomes]
rs9467144	0.86[AFR][1000 genomes]
rs9467145	0.88[AFR][1000 genomes]
rs9467146	0.86[AFR][1000 genomes]
rs9467147	0.86[AFR][1000 genomes]
rs9467150	0.90[AFR][1000 genomes]
rs9467151	0.83[YRI][hapmap];0.90[AFR][1000 genomes]
rs9467152	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs9467154	0.96[YRI][hapmap];0.99[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9467159	0.99[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9467163	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9467164	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026638	chr6:24347972-24475300	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24417400-24451800	Strong transcription	Liver	Liver
2	chr6:24421200-24448800	Weak transcription	Gastric	stomach
3	chr6:24421200-24459600	Weak transcription	Spleen	Spleen
4	chr6:24423400-24439400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr6:24424000-24456600	Weak transcription	Ovary	ovary
6	chr6:24424400-24445800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr6:24425400-24439600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr6:24426000-24438800	Weak transcription	Brain Substantia Nigra	brain
9	chr6:24426200-24446000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:24426400-24441600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr6:24426400-24446000	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr6:24426600-24438800	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr6:24427600-24439200	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr6:24427600-24439400	Weak transcription	Fetal Thymus	thymus
15	chr6:24427600-24440000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr6:24427600-24440000	Weak transcription	Dnd41	blood
17	chr6:24427600-24441800	Weak transcription	Primary B cells from peripheral blood	blood
18	chr6:24427600-24445600	Weak transcription	Fetal Brain Female	brain
19	chr6:24427600-24456800	Weak transcription	Lung	lung
20	chr6:24427800-24467000	Weak transcription	Brain Germinal Matrix	brain
21	chr6:24428200-24449400	Weak transcription	Fetal Muscle Trunk	muscle
22	chr6:24428800-24445000	Weak transcription	Psoas Muscle	Psoas
23	chr6:24429000-24447800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:24429000-24494200	Weak transcription	Primary B cells from cord blood	blood
25	chr6:24429200-24455600	Weak transcription	Brain Angular Gyrus	brain
26	chr6:24429400-24438600	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr6:24429400-24445000	Weak transcription	Brain Anterior Caudate	brain
28	chr6:24429400-24483800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr6:24429600-24444800	Weak transcription	HepG2	liver
30	chr6:24429600-24455000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:24430800-24448400	Weak transcription	Brain Hippocampus Middle	brain
32	chr6:24432600-24463800	Weak transcription	Fetal Intestine Small	intestine
33	chr6:24433200-24441600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr6:24433600-24451600	Weak transcription	Adipose Nuclei	Adipose
35	chr6:24435800-24438200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr6:24436200-24438400	Strong transcription	Primary T cells from cord blood	blood
37	chr6:24436200-24438600	Strong transcription	Fetal Stomach	stomach
38	chr6:24436200-24438600	Strong transcription	Stomach Smooth Muscle	stomach
39	chr6:24436600-24438400	Strong transcription	Fetal Muscle Leg	muscle
40	chr6:24437000-24438200	Strong transcription	Duodenum Smooth Muscle	Duodenum
41	chr6:24437200-24438400	Strong transcription	Right Ventricle	heart
42	chr6:24437200-24438800	Strong transcription	Brain Cingulate Gyrus	brain
43	chr6:24437400-24438200	Strong transcription	Aorta	Aorta
44	chr6:24437400-24438400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr6:24437600-24455400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr6:24437800-24450600	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr6:24437800-24459600	Weak transcription	Left Ventricle	heart
48	chr6:24438000-24438400	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr6:24438000-24439400	Weak transcription	Thymus	Thymus
50	chr6:24438000-24464000	Weak transcription	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links