Variant report

Variant	rs10776604
Chromosome Location	chr10:49668241-49668242
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:49667304..49669133-chr10:49726390..49728865,2	K562	blood:

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10745275	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10776605	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11101337	1.00[EUR][1000 genomes]
rs1814473	1.00[EUR][1000 genomes]
rs1822860	1.00[EUR][1000 genomes]
rs1867574	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1867575	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3853761	0.95[AFR][1000 genomes]
rs3867448	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3867449	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3867450	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4012794	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4012795	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4012801	1.00[EUR][1000 genomes]
rs4082089	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4838599	1.00[EUR][1000 genomes]
rs74130282	1.00[EUR][1000 genomes]
rs7478027	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv895372	chr10:49576878-49933488	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49652000-49673000	Weak transcription	HMEC	breast
2	chr10:49653000-49673600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr10:49655200-49677800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr10:49657800-49677600	Weak transcription	HSMMtube	muscle
5	chr10:49661200-49669200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr10:49661800-49668600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr10:49662200-49671800	Weak transcription	Aorta	Aorta
8	chr10:49662400-49672400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr10:49662600-49671800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr10:49664800-49669600	Weak transcription	Osteobl	bone
11	chr10:49664800-49671200	Weak transcription	Right Ventricle	heart
12	chr10:49664800-49671400	Weak transcription	Adipose Nuclei	Adipose
13	chr10:49664800-49671400	Weak transcription	NHDF-Ad	bronchial
14	chr10:49665200-49671600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr10:49665200-49673400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr10:49665400-49670800	Weak transcription	Ovary	ovary
17	chr10:49665400-49671200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr10:49665400-49671200	Weak transcription	Brain Angular Gyrus	brain
19	chr10:49665400-49672200	Weak transcription	Spleen	Spleen
20	chr10:49665400-49675000	Weak transcription	HUVEC	blood vessel
21	chr10:49665800-49671200	Weak transcription	Brain Hippocampus Middle	brain
22	chr10:49665800-49671200	Weak transcription	Fetal Heart	heart
23	chr10:49665800-49671400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr10:49665800-49671400	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr10:49665800-49671600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr10:49665800-49672400	Weak transcription	Brain Substantia Nigra	brain
27	chr10:49666000-49668400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr10:49666000-49668400	Strong transcription	NHLF	lung
29	chr10:49666200-49668800	Strong transcription	Muscle Satellite Cultured Cells	--
30	chr10:49666400-49671400	Weak transcription	Brain Cingulate Gyrus	brain
31	chr10:49666600-49671400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr10:49667200-49668400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr10:49667200-49671000	Weak transcription	Fetal Stomach	stomach
34	chr10:49667400-49668800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr10:49667600-49670800	Strong transcription	HSMM	muscle
36	chr10:49667800-49668400	Genic enhancers	Primary hematopoietic stem cells	blood
37	chr10:49667800-49669000	Genic enhancers	K562	blood
38	chr10:49668000-49668400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr10:49668000-49669200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr10:49668200-49670600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr10:49668200-49670800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr10:49668200-49671400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr10:49668200-49671400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr10:49668200-49674400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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