Variant report

Variant	rs2377985
Chromosome Location	chr10:50448001-50448002
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:50446994..50449831-chr10:50450885..50453374,2	K562	blood:
2	chr10:50446413..50449430-chr10:50451528..50453716,3	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10745252	1.00[ASN][1000 genomes]
rs10776546	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10857443	1.00[ASN][1000 genomes]
rs10857445	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10857447	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11593489	1.00[ASN][1000 genomes]
rs12257188	0.86[EUR][1000 genomes]
rs17009530	0.86[EUR][1000 genomes]
rs17009562	0.86[EUR][1000 genomes]
rs17009596	1.00[EUR][1000 genomes]
rs17009606	1.00[EUR][1000 genomes]
rs17451560	0.86[EUR][1000 genomes]
rs2002392	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2377950	1.00[ASN][1000 genomes]
rs2377951	1.00[ASN][1000 genomes]
rs2377952	1.00[ASN][1000 genomes]
rs2377987	1.00[ASN][1000 genomes]
rs2377991	1.00[ASN][1000 genomes]
rs2377992	1.00[ASN][1000 genomes]
rs2889807	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4514329	1.00[ASN][1000 genomes]
rs4838372	1.00[ASN][1000 genomes]
rs4838465	1.00[ASN][1000 genomes]
rs57374856	0.86[EUR][1000 genomes]
rs58131680	1.00[EUR][1000 genomes]
rs6537509	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6537510	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7075088	0.86[EUR][1000 genomes]
rs7094605	1.00[ASN][1000 genomes]
rs73306720	0.86[EUR][1000 genomes]
rs73306721	0.86[EUR][1000 genomes]
rs73306722	0.86[EUR][1000 genomes]
rs73306725	0.86[EUR][1000 genomes]
rs7394346	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7893648	1.00[ASN][1000 genomes]
rs7906560	1.00[ASN][1000 genomes]
rs7909019	0.86[EUR][1000 genomes]
rs7912808	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7913102	0.86[EUR][1000 genomes]
rs7922135	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7923767	1.00[ASN][1000 genomes]
rs9645532	1.00[ASN][1000 genomes]
rs9645533	1.00[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	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

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50445200-50449800	Weak transcription	K562	blood
2	chr10:50445600-50450200	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr10:50447600-50452400	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr10:50447600-50453000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr10:50447800-50448600	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr10:50447800-50450000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr10:50448000-50448200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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