Variant report

Variant	rs1527879
Chromosome Location	chr2:183485158-183485159
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:183484463..183486734-chr2:183489147..183491693,3	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10173603	0.87[ASN][1000 genomes]
rs10184790	0.89[ASN][1000 genomes]
rs10198603	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10198921	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10201351	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10210679	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10211212	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10803958	0.88[ASN][1000 genomes]
rs10803959	0.89[ASN][1000 genomes]
rs10803960	0.90[ASN][1000 genomes]
rs10931026	0.90[ASN][1000 genomes]
rs11682887	0.91[ASN][1000 genomes]
rs12693319	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13392185	0.90[ASN][1000 genomes]
rs13403435	0.91[ASN][1000 genomes]
rs13410733	0.90[ASN][1000 genomes]
rs1527880	0.83[EUR][1000 genomes]
rs16823439	0.91[ASN][1000 genomes]
rs1918702	0.91[ASN][1000 genomes]
rs2141269	0.91[ASN][1000 genomes]
rs56963248	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs66915042	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6720813	0.90[ASN][1000 genomes]
rs6720841	0.90[ASN][1000 genomes]
rs6749127	0.90[ASN][1000 genomes]
rs7560943	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7577378	0.90[ASN][1000 genomes]
rs7590115	0.90[ASN][1000 genomes]
rs7590242	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533782	chr2:183059730-183500040	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1009882	chr2:183213152-184171519	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	esv2830429	chr2:183300759-183545378	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2757842	chr2:183437700-183835084	Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	esv2759104	chr2:183437700-183835084	Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	nsv875480	chr2:183442443-183489249	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv1837855	chr2:183452578-183499313	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv999603	chr2:183465151-183551522	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183459600-183493800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:183478600-183486000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr2:183481400-183485600	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr2:183482000-183485600	Weak transcription	K562	blood
5	chr2:183482000-183485800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:183482000-183485800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:183482000-183487000	Weak transcription	Fetal Stomach	stomach
8	chr2:183482400-183486800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr2:183482600-183485400	Weak transcription	HSMMtube	muscle
10	chr2:183483400-183485600	Weak transcription	Rectal Smooth Muscle	rectum
11	chr2:183483600-183485800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr2:183483600-183486800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr2:183484200-183485600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr2:183484200-183485600	Weak transcription	Colon Smooth Muscle	Colon
15	chr2:183484200-183490200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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