Variant report

Variant	rs2884124
Chromosome Location	chr1:210105775-210105776
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:210103690..210106151-chr1:210106770..210109170,2	K562	blood:
2	chr1:210099710..210101405-chr1:210104542..210107645,3	K562	blood:

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs1028325	0.86[EUR][1000 genomes]
rs1040423	0.89[EUR][1000 genomes]
rs10779516	0.84[EUR][1000 genomes]
rs10779517	0.83[EUR][1000 genomes]
rs10779518	0.83[EUR][1000 genomes]
rs10863799	0.86[EUR][1000 genomes]
rs1099863	0.82[EUR][1000 genomes]
rs11119363	0.87[EUR][1000 genomes]
rs11119369	0.87[EUR][1000 genomes]
rs11119370	0.89[EUR][1000 genomes]
rs11119374	0.81[EUR][1000 genomes]
rs11119376	0.82[EUR][1000 genomes]
rs12025114	0.80[EUR][1000 genomes]
rs12078439	0.84[EUR][1000 genomes]
rs12079815	0.84[EUR][1000 genomes]
rs12083466	0.86[EUR][1000 genomes]
rs12092530	0.87[EUR][1000 genomes]
rs126277	0.80[EUR][1000 genomes]
rs1387933	0.81[EUR][1000 genomes]
rs170557	0.82[EUR][1000 genomes]
rs2205987	0.81[EUR][1000 genomes]
rs2205988	0.84[EUR][1000 genomes]
rs2205989	0.81[EUR][1000 genomes]
rs227169	0.81[EUR][1000 genomes]
rs227172	0.82[EUR][1000 genomes]
rs227174	0.82[EUR][1000 genomes]
rs227179	0.81[EUR][1000 genomes]
rs227181	0.82[EUR][1000 genomes]
rs227182	0.82[EUR][1000 genomes]
rs227191	0.82[EUR][1000 genomes]
rs227193	0.82[EUR][1000 genomes]
rs227196	0.82[EUR][1000 genomes]
rs227197	0.82[EUR][1000 genomes]
rs227201	0.81[EUR][1000 genomes]
rs227203	0.81[EUR][1000 genomes]
rs227204	0.82[EUR][1000 genomes]
rs227205	0.82[EUR][1000 genomes]
rs227209	0.81[EUR][1000 genomes]
rs227211	0.81[EUR][1000 genomes]
rs227217	0.80[EUR][1000 genomes]
rs227218	0.81[EUR][1000 genomes]
rs227219	0.81[EUR][1000 genomes]
rs227224	0.82[EUR][1000 genomes]
rs227226	0.80[EUR][1000 genomes]
rs227228	0.82[EUR][1000 genomes]
rs227230	0.82[EUR][1000 genomes]
rs2357212	0.90[EUR][1000 genomes]
rs2636376	0.82[EUR][1000 genomes]
rs2743889	0.82[EUR][1000 genomes]
rs4282820	0.84[EUR][1000 genomes]
rs4454550	0.86[EUR][1000 genomes]
rs4462143	0.89[EUR][1000 genomes]
rs6540567	0.82[EUR][1000 genomes]
rs6540568	0.87[EUR][1000 genomes]
rs6540569	0.89[EUR][1000 genomes]
rs6540570	0.87[EUR][1000 genomes]
rs6540573	0.83[EUR][1000 genomes]
rs6662445	0.87[EUR][1000 genomes]
rs6667057	0.89[EUR][1000 genomes]
rs6678081	0.86[EUR][1000 genomes]
rs6702257	0.80[EUR][1000 genomes]
rs6702961	0.89[EUR][1000 genomes]
rs701947	0.82[EUR][1000 genomes]
rs701948	0.82[EUR][1000 genomes]
rs724054	0.87[EUR][1000 genomes]
rs7514257	0.82[EUR][1000 genomes]
rs7525980	0.82[EUR][1000 genomes]
rs7528647	0.89[EUR][1000 genomes]
rs7530426	0.83[EUR][1000 genomes]
rs7544033	0.89[EUR][1000 genomes]
rs7547709	0.82[EUR][1000 genomes]
rs7549523	0.87[EUR][1000 genomes]
rs7549696	0.87[EUR][1000 genomes]
rs846551	0.82[EUR][1000 genomes]
rs846552	0.82[EUR][1000 genomes]
rs846554	0.82[EUR][1000 genomes]
rs846555	0.82[EUR][1000 genomes]
rs9429827	0.89[EUR][1000 genomes]
rs9429829	0.86[EUR][1000 genomes]
rs9429830	0.87[EUR][1000 genomes]
rs9430020	0.83[EUR][1000 genomes]
rs9430024	0.89[EUR][1000 genomes]
rs9430026	0.81[EUR][1000 genomes]
rs9662387	0.90[EUR][1000 genomes]
rs986057	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999901	chr1:209600631-210205379	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv1014034	chr1:209759648-210501731	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv873140	chr1:210068117-210335644	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv1844866	chr1:210078078-210108473	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv1825811	chr1:210082206-210135806	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210100200-210107800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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