Variant report

Variant	rs17774510
Chromosome Location	chr10:50487923-50487924
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:50487004..50489223-chr10:50490139..50491748,2	K562	blood:
2	chr10:50486341..50490771-chr10:50506621..50509416,6	K562	blood:

Variant related genes	Relation type
ENSG00000177354	Chromatin interaction
ENSG00000236208	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10745261	1.00[ASN][1000 genomes]
rs10776572	1.00[ASN][1000 genomes]
rs10776573	1.00[ASN][1000 genomes]
rs1475255	1.00[ASN][1000 genomes]
rs1924490	1.00[ASN][1000 genomes]
rs1924492	1.00[ASN][1000 genomes]
rs2104346	1.00[ASN][1000 genomes]
rs6537536	1.00[ASN][1000 genomes]
rs7080017	1.00[ASN][1000 genomes]
rs7916873	1.00[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	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv895376	chr10:50480164-50557211	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50485200-50488400	Enhancers	Left Ventricle	heart
2	chr10:50485600-50488400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:50485600-50488400	Enhancers	Fetal Muscle Leg	muscle
4	chr10:50485600-50488400	Enhancers	Right Ventricle	heart
5	chr10:50485800-50488200	Enhancers	Psoas Muscle	Psoas
6	chr10:50485800-50488200	Enhancers	Right Atrium	heart
7	chr10:50485800-50489200	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr10:50485800-50495000	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr10:50486000-50490400	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr10:50486200-50488200	Enhancers	HSMMtube	muscle
11	chr10:50486400-50488000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr10:50486400-50488400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr10:50486600-50488200	Enhancers	HSMM	muscle
14	chr10:50486800-50488200	Enhancers	NHDF-Ad	bronchial
15	chr10:50486800-50488200	Enhancers	Osteobl	bone
16	chr10:50486800-50489000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr10:50487200-50490800	Enhancers	Fetal Heart	heart
18	chr10:50487400-50488000	Enhancers	Fetal Muscle Trunk	muscle
19	chr10:50487400-50490400	Weak transcription	K562	blood
20	chr10:50487600-50488000	Weak transcription	Primary hematopoietic stem cells	blood
21	chr10:50487600-50488400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr10:50487600-50488400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
23	chr10:50487800-50488000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
24	chr10:50487800-50488800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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