Variant report

Variant	rs1452620
Chromosome Location	chr1:215215692-215215693
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10494989	0.86[ASN][1000 genomes]
rs10494991	0.89[ASN][1000 genomes]
rs10494992	0.89[ASN][1000 genomes]
rs10779633	0.87[ASN][1000 genomes]
rs10779634	0.85[ASN][1000 genomes]
rs10779635	0.89[ASN][1000 genomes]
rs12026832	0.89[ASN][1000 genomes]
rs12141327	0.88[ASN][1000 genomes]
rs1377173	0.87[ASN][1000 genomes]
rs1377175	0.89[ASN][1000 genomes]
rs1377177	0.89[ASN][1000 genomes]
rs1452608	0.87[ASN][1000 genomes]
rs1452609	0.87[ASN][1000 genomes]
rs1452610	0.87[ASN][1000 genomes]
rs1584759	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1584760	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1597847	0.83[ASN][1000 genomes]
rs2262937	0.87[ASN][1000 genomes]
rs2601607	0.87[ASN][1000 genomes]
rs2601609	0.83[ASN][1000 genomes]
rs2601610	0.87[ASN][1000 genomes]
rs2601611	0.87[ASN][1000 genomes]
rs2601612	0.87[ASN][1000 genomes]
rs2601613	0.86[ASN][1000 genomes]
rs2601614	0.87[ASN][1000 genomes]
rs2601615	0.87[ASN][1000 genomes]
rs2601616	0.87[ASN][1000 genomes]
rs2601617	0.87[ASN][1000 genomes]
rs2601618	0.87[ASN][1000 genomes]
rs2601619	0.87[ASN][1000 genomes]
rs2601620	0.87[ASN][1000 genomes]
rs2601621	0.88[ASN][1000 genomes]
rs2601622	0.87[ASN][1000 genomes]
rs2601623	0.87[ASN][1000 genomes]
rs2601624	0.87[ASN][1000 genomes]
rs2601625	0.89[ASN][1000 genomes]
rs2601636	0.87[ASN][1000 genomes]
rs2601638	0.87[ASN][1000 genomes]
rs2601639	0.87[ASN][1000 genomes]
rs2601640	0.87[ASN][1000 genomes]
rs2601641	0.87[ASN][1000 genomes]
rs2601646	0.87[ASN][1000 genomes]
rs2802642	0.87[ASN][1000 genomes]
rs2802643	0.87[ASN][1000 genomes]
rs2802644	0.87[ASN][1000 genomes]
rs2802649	0.87[ASN][1000 genomes]
rs2802650	0.87[ASN][1000 genomes]
rs2802651	0.87[ASN][1000 genomes]
rs2802657	0.91[ASN][1000 genomes]
rs2841574	0.91[ASN][1000 genomes]
rs2841575	0.90[ASN][1000 genomes]
rs2841577	0.90[ASN][1000 genomes]
rs2841581	0.90[ASN][1000 genomes]
rs2841587	0.90[ASN][1000 genomes]
rs2841591	0.89[ASN][1000 genomes]
rs2841592	0.89[ASN][1000 genomes]
rs2841595	0.88[ASN][1000 genomes]
rs2841596	0.87[ASN][1000 genomes]
rs2841597	0.87[ASN][1000 genomes]
rs2841598	0.87[ASN][1000 genomes]
rs2841599	0.87[ASN][1000 genomes]
rs2841600	0.87[ASN][1000 genomes]
rs2841601	0.87[ASN][1000 genomes]
rs2841602	0.87[ASN][1000 genomes]
rs2841604	0.87[ASN][1000 genomes]
rs2841605	0.87[ASN][1000 genomes]
rs2841606	0.87[ASN][1000 genomes]
rs2841607	0.87[ASN][1000 genomes]
rs2841608	0.87[ASN][1000 genomes]
rs2841609	0.87[ASN][1000 genomes]
rs2841610	0.87[ASN][1000 genomes]
rs2841611	0.82[ASN][1000 genomes]
rs2841612	0.87[ASN][1000 genomes]
rs2841613	0.87[ASN][1000 genomes]
rs2841615	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4294386	0.87[ASN][1000 genomes]
rs4339836	0.87[ASN][1000 genomes]
rs4348692	0.87[ASN][1000 genomes]
rs4356023	0.87[ASN][1000 genomes]
rs61820010	0.86[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	nsv468105	chr1:215167236-215248417	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv549182	chr1:215167236-215248417	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215206800-215216000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr1:215213800-215216200	Strong transcription	Osteobl	bone
3	chr1:215214000-215219200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr1:215214800-215215800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:215215400-215215800	Strong transcription	NHDF-Ad	bronchial

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