Variant report

Variant	rs10761318
Chromosome Location	chr9:96905904-96905905
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:96905663..96907940-chr9:96926715..96928230,2	K562	blood:
2	chr9:96904108..96906275-chr9:96917076..96919477,3	K562	blood:
3	chr9:96900996..96905420-chr9:96905582..96911723,7	K562	blood:
4	chr9:96905504..96908787-chr9:96918594..96920364,3	MCF-7	breast:
5	chr9:96904365..96907195-chr9:96908218..96912337,3	MCF-7	breast:
6	chr9:96899016..96906502-chr9:96926750..96931118,14	MCF-7	breast:
7	chr9:96901943..96905386-chr9:96905431..96909431,4	K562	blood:

Variant related genes	Relation type
ENSG00000269946	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10821299	1.00[AFR][1000 genomes]
rs10821302	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10821303	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10821304	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55990139	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7854962	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7866254	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[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	nsv482457	chr9:96813852-96996170	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	217 gene(s)	inside rSNPs	diseases
2	nsv831655	chr9:96834042-97042009	Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	218 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96900400-96907400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr9:96902800-96906400	Weak transcription	Pancreas	Pancrea
3	chr9:96903000-96912000	Weak transcription	HepG2	liver
4	chr9:96903200-96906200	Weak transcription	Gastric	stomach
5	chr9:96903400-96906400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr9:96903600-96906200	Weak transcription	Stomach Mucosa	stomach
7	chr9:96903800-96906400	Weak transcription	K562	blood
8	chr9:96903800-96909200	Weak transcription	Hela-S3	cervix
9	chr9:96903800-96910800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr9:96904000-96906600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr9:96904000-96912800	Weak transcription	NH-A	brain
12	chr9:96904000-96927200	Weak transcription	Thymus	Thymus
13	chr9:96904400-96906400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:96904400-96907800	Weak transcription	Fetal Lung	lung
15	chr9:96904400-96909000	Weak transcription	Colon Smooth Muscle	Colon
16	chr9:96904400-96912600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr9:96904600-96906200	Weak transcription	Aorta	Aorta
18	chr9:96904600-96906400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr9:96904600-96906400	Weak transcription	Esophagus	oesophagus
20	chr9:96904600-96906400	Weak transcription	Psoas Muscle	Psoas
21	chr9:96904600-96906600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr9:96904600-96906600	Weak transcription	Fetal Stomach	stomach
23	chr9:96904600-96906800	Weak transcription	Fetal Muscle Leg	muscle
24	chr9:96904600-96913200	Weak transcription	Adipose Nuclei	Adipose
25	chr9:96904800-96906400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr9:96904800-96910200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr9:96904800-96912000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr9:96904800-96912000	Weak transcription	Spleen	Spleen
29	chr9:96905000-96906600	Weak transcription	NHEK	skin
30	chr9:96905400-96906600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr9:96905400-96907400	Enhancers	Lung	lung
32	chr9:96905800-96906200	Weak transcription	Placenta	Placenta

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