Variant report

Variant	rs9446296
Chromosome Location	chr6:71493883-71493884
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10214715	0.94[AFR][1000 genomes]
rs9446295	0.84[AFR][1000 genomes]
rs9446298	1.00[AFR][1000 genomes]
rs9455206	0.94[AFR][1000 genomes]
rs9455223	1.00[AFR][1000 genomes]
rs9455228	1.00[AFR][1000 genomes]
rs9455231	1.00[AFR][1000 genomes]
rs9455233	1.00[AFR][1000 genomes]
rs9455234	1.00[AFR][1000 genomes]
rs9455235	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932111	chr6:70736835-71633094	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv1027049	chr6:70961610-71561488	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv524328	chr6:70961833-71558805	Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv917312	chr6:70961903-71601688	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71444800-71523600	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr6:71447800-71500600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr6:71466400-71494800	Weak transcription	Small Intestine	intestine
4	chr6:71466400-71508800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:71468800-71532200	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr6:71473000-71515600	Weak transcription	Left Ventricle	heart
7	chr6:71473800-71520200	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr6:71474600-71568800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr6:71474800-71515000	Weak transcription	Duodenum Mucosa	Duodenum
10	chr6:71475000-71515200	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr6:71481200-71495800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr6:71481800-71515000	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr6:71482200-71515600	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr6:71483000-71515200	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr6:71487600-71515600	Weak transcription	Thymus	Thymus
16	chr6:71489000-71494200	Weak transcription	Colonic Mucosa	Colon
17	chr6:71489000-71494400	Weak transcription	Fetal Intestine Large	intestine
18	chr6:71489000-71506000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr6:71489000-71517400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr6:71489000-71521800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr6:71489200-71494400	Weak transcription	Esophagus	oesophagus
22	chr6:71489200-71517800	Weak transcription	Fetal Thymus	thymus
23	chr6:71489400-71494200	Weak transcription	Lung	lung
24	chr6:71489400-71496600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr6:71489400-71515000	Weak transcription	Liver	Liver
26	chr6:71489600-71494000	Weak transcription	Stomach Smooth Muscle	stomach
27	chr6:71489600-71495200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:71489600-71515600	Weak transcription	Primary T cells from cord blood	blood
29	chr6:71490400-71515600	Weak transcription	Pancreas	Pancrea
30	chr6:71491800-71526200	Weak transcription	HSMM	muscle
31	chr6:71492000-71504000	Weak transcription	Primary B cells from cord blood	blood
32	chr6:71492000-71522200	Weak transcription	Brain Angular Gyrus	brain
33	chr6:71492400-71508800	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr6:71492400-71563600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr6:71492800-71515600	Weak transcription	Aorta	Aorta
36	chr6:71493000-71515600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr6:71493000-71526000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:71493200-71502000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links