Variant report

Variant	rs10217465
Chromosome Location	chr9:2234922-2234923
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:2226247..2228750-chr9:2234155..2236078,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10119172	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10757276	0.89[ASN][1000 genomes]
rs10757280	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10757293	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10811655	0.89[ASN][1000 genomes]
rs10811672	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10811676	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10811677	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10965284	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10965294	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1924487	0.81[ASN][1000 genomes]
rs2093835	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60884758	0.88[ASN][1000 genomes]
rs7045985	0.84[ASN][1000 genomes]
rs7851755	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7863671	0.84[ASN][1000 genomes]
rs7869382	0.84[ASN][1000 genomes]
rs7870192	0.84[ASN][1000 genomes]
rs7873444	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016148	chr9:1457605-2361750	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv539916	chr9:1457605-2361750	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1020530	chr9:1870197-2658587	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv530929	chr9:1998911-2925112	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv892057	chr9:2144687-2241994	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv892059	chr9:2198627-2255397	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1033628	chr9:2215179-2303623	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv539927	chr9:2215179-2303623	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv892060	chr9:2218129-2261944	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv466078	chr9:2218129-2621030	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
11	nsv613126	chr9:2218129-2621030	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
12	nsv6457	chr9:2228493-2271756	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv892061	chr9:2229694-2262889	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
14	nsv1029947	chr9:2233969-2364269	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2223600-2240800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr9:2230000-2241200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr9:2230200-2241200	Weak transcription	Stomach Mucosa	stomach
4	chr9:2231200-2235600	Enhancers	Fetal Stomach	stomach
5	chr9:2231400-2235800	Enhancers	Fetal Heart	heart
6	chr9:2231600-2235600	Enhancers	Colon Smooth Muscle	Colon
7	chr9:2233600-2235600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr9:2233600-2235600	Enhancers	Ovary	ovary
9	chr9:2233600-2235600	Enhancers	HSMMtube	muscle
10	chr9:2233600-2235800	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr9:2233800-2235400	Enhancers	Fetal Muscle Trunk	muscle
12	chr9:2233800-2235400	Enhancers	Fetal Muscle Leg	muscle
13	chr9:2233800-2235600	Enhancers	Fetal Brain Male	brain
14	chr9:2233800-2236200	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr9:2234000-2235400	Enhancers	HSMM	muscle
16	chr9:2234200-2235000	Enhancers	HMEC	breast
17	chr9:2234200-2235200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr9:2234200-2235200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr9:2234200-2235200	Enhancers	NHEK	skin
20	chr9:2234200-2235600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr9:2234200-2235600	Enhancers	Fetal Lung	lung
22	chr9:2234400-2235000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr9:2234400-2235000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr9:2234400-2235000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr9:2234400-2235000	Enhancers	Brain Hippocampus Middle	brain
26	chr9:2234400-2235000	Enhancers	Colonic Mucosa	Colon
27	chr9:2234400-2235200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr9:2234400-2235200	Enhancers	Brain Anterior Caudate	brain
29	chr9:2234400-2235200	Enhancers	Fetal Brain Female	brain
30	chr9:2234400-2235200	Enhancers	Placenta	Placenta
31	chr9:2234400-2235200	Enhancers	Right Ventricle	heart
32	chr9:2234400-2235400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr9:2234400-2235400	Enhancers	Esophagus	oesophagus
34	chr9:2234400-2235400	Enhancers	Psoas Muscle	Psoas
35	chr9:2234400-2235600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr9:2234400-2235600	Enhancers	Fetal Kidney	kidney
37	chr9:2234400-2235600	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr9:2234400-2235600	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr9:2234400-2236000	Enhancers	Left Ventricle	heart
40	chr9:2234600-2235000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr9:2234600-2235000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr9:2234600-2235400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr9:2234600-2235400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr9:2234600-2235400	Enhancers	Right Atrium	heart
45	chr9:2234800-2235000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr9:2234800-2235000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr9:2234800-2235000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr9:2234800-2235000	Flanking Active TSS	Stomach Smooth Muscle	stomach
49	chr9:2234800-2235200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr9:2234800-2235400	Enhancers	Rectal Smooth Muscle	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links