Variant report

Variant	rs73015159
Chromosome Location	chr2:149126061-149126062
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs57084762	1.00[AMR][1000 genomes]
rs57577804	1.00[AMR][1000 genomes]
rs58448454	1.00[AMR][1000 genomes]
rs60639125	1.00[AMR][1000 genomes]
rs60679558	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73009282	1.00[AMR][1000 genomes]
rs73009297	1.00[AMR][1000 genomes]
rs73011215	1.00[AMR][1000 genomes]
rs73011217	1.00[AMR][1000 genomes]
rs73011296	1.00[AMR][1000 genomes]
rs73013015	1.00[AMR][1000 genomes]
rs73013043	1.00[AMR][1000 genomes]
rs73013055	1.00[AMR][1000 genomes]
rs73013085	1.00[AMR][1000 genomes]
rs73015113	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73015118	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73015121	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73015125	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73015128	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73015131	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73015144	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73015150	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73015188	1.00[AMR][1000 genomes]
rs73017110	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73017112	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73019204	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73019217	1.00[AMR][1000 genomes]
rs73019220	1.00[AMR][1000 genomes]
rs73021555	1.00[AMR][1000 genomes]
rs73021569	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009608	chr2:148897348-149133718	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2753542	chr2:149004714-149268503	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1012275	chr2:149031668-149316793	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1012123	chr2:149078500-149151358	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv583289	chr2:149091754-149170115	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv875277	chr2:149094415-149178974	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv875278	chr2:149094415-149201775	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv875279	chr2:149111470-149201775	Enhancers ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv875280	chr2:149115432-149198275	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv875281	chr2:149115432-149206943	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv583290	chr2:149117734-149170115	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:149100800-149137000	Weak transcription	Primary T cells from cord blood	blood
2	chr2:149102800-149136600	Weak transcription	Primary B cells from cord blood	blood
3	chr2:149120400-149128800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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