Variant report

Variant	rs12569869
Chromosome Location	chr10:44850323-44850324
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10508884	0.89[ASN][1000 genomes]
rs11238991	0.91[ASN][1000 genomes]
rs11815919	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12573553	0.89[ASN][1000 genomes]
rs17156139	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2028101	0.91[ASN][1000 genomes]
rs34050695	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs34066403	0.87[ASN][1000 genomes]
rs34386578	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36095821	0.91[ASN][1000 genomes]
rs4366439	0.91[ASN][1000 genomes]
rs56376391	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7904065	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038511	chr10:44596885-44870030	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1052337	chr10:44821390-44865015	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	nsv1054649	chr10:44848921-44889713	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44838600-44867400	Weak transcription	Spleen	Spleen
2	chr10:44846600-44850800	Enhancers	Fetal Lung	lung
3	chr10:44847000-44852000	Enhancers	Pancreas	Pancrea
4	chr10:44848000-44851800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr10:44848000-44851800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr10:44848200-44851400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr10:44848200-44852200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr10:44848200-44853600	Weak transcription	Brain Substantia Nigra	brain
9	chr10:44848200-44858600	Weak transcription	Psoas Muscle	Psoas
10	chr10:44848200-44864600	Weak transcription	Fetal Kidney	kidney
11	chr10:44848200-44865000	Weak transcription	Osteobl	bone
12	chr10:44848400-44851800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr10:44848400-44851800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr10:44848400-44865000	Weak transcription	Right Atrium	heart
15	chr10:44848400-44867400	Weak transcription	Adipose Nuclei	Adipose
16	chr10:44848400-44867600	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr10:44848600-44853800	Weak transcription	Ovary	ovary
18	chr10:44848800-44851600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr10:44849000-44851600	Weak transcription	Fetal Stomach	stomach
20	chr10:44849000-44851800	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr10:44849400-44869000	Weak transcription	Right Ventricle	heart
22	chr10:44849800-44864800	Weak transcription	Left Ventricle	heart

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