Variant report

Variant	rs10119816
Chromosome Location	chr9:95944372-95944373
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:95927482..95929226-chr9:95942592..95945216,3	MCF-7	breast:
2	chr9:95936164..95938359-chr9:95942679..95944798,2	K562	blood:
3	chr9:95943032..95944544-chr9:95948872..95951081,2	MCF-7	breast:
4	chr9:95943290..95945540-chr9:95952949..95954790,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1111776	0.84[AMR][1000 genomes]
rs12684392	0.84[AMR][1000 genomes]
rs1891970	0.84[AMR][1000 genomes]
rs2169756	0.84[AMR][1000 genomes]
rs3847306	0.88[EUR][1000 genomes]
rs56161352	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56311541	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58228786	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58965550	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59630789	0.86[EUR][1000 genomes]
rs60316441	0.85[EUR][1000 genomes]
rs6479458	0.95[ASN][1000 genomes]
rs7024425	0.90[ASN][1000 genomes]
rs7025514	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7031917	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7035727	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7042492	0.84[AMR][1000 genomes]
rs73651371	0.86[EUR][1000 genomes]
rs73651377	0.96[EUR][1000 genomes]
rs73651379	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73651380	0.96[EUR][1000 genomes]
rs73651381	0.96[EUR][1000 genomes]
rs73651384	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7853075	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9657693	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526296	chr9:95708192-96030392	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv893576	chr9:95789960-96158277	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv893580	chr9:95855100-96099377	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv824983	chr9:95902154-95978408	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv430082	chr9:95905745-96095045	Genic enhancers Enhancers Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv614880	chr9:95930572-95978265	Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95907200-95944400	Weak transcription	Right Atrium	heart
2	chr9:95940800-95944400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:95942000-95944400	Weak transcription	Fetal Intestine Small	intestine
4	chr9:95942000-95944400	Bivalent Enhancer	HepG2	liver
5	chr9:95943000-95944600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
6	chr9:95943000-95945600	Weak transcription	Esophagus	oesophagus
7	chr9:95943000-95945600	Enhancers	Right Ventricle	heart
8	chr9:95943200-95944400	Weak transcription	Gastric	stomach
9	chr9:95943200-95945200	Enhancers	Psoas Muscle	Psoas
10	chr9:95943200-95945400	Weak transcription	Spleen	Spleen
11	chr9:95943800-95945000	Enhancers	Fetal Heart	heart
12	chr9:95944000-95945800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr9:95944200-95944400	Enhancers	Brain Anterior Caudate	brain
14	chr9:95944200-95944400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
15	chr9:95944200-95945200	Enhancers	Duodenum Mucosa	Duodenum
16	chr9:95944200-95945800	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr9:95944200-95946000	Enhancers	Left Ventricle	heart
18	chr9:95944200-95946000	Enhancers	Pancreas	Pancrea

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