Variant report

Variant	rs7527891
Chromosome Location	chr1:221267252-221267253
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10218738	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10218739	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1073166	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10746408	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10779421	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10779422	0.81[EUR][1000 genomes]
rs10863580	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10863582	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10863584	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10863585	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10863589	0.86[EUR][1000 genomes]
rs11118645	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11118650	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11118657	0.83[EUR][1000 genomes]
rs12139572	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12568940	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1372665	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1417921	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1442465	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1539139	0.86[EUR][1000 genomes]
rs1867071	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1965817	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1992480	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2378435	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4359036	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4518910	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4532839	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6541171	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6541172	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6541179	0.84[EUR][1000 genomes]
rs6541180	0.81[EUR][1000 genomes]
rs6656408	0.85[EUR][1000 genomes]
rs6656596	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6657690	0.86[EUR][1000 genomes]
rs6664595	0.81[EUR][1000 genomes]
rs6669742	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6677416	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6694121	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6696268	0.87[EUR][1000 genomes]
rs7513152	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7527151	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7545437	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs894361	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9431421	0.86[EUR][1000 genomes]
rs9431432	0.81[EUR][1000 genomes]
rs9431436	0.81[EUR][1000 genomes]
rs989463	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv873199	chr1:221136672-221451217	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221259800-221270000	Weak transcription	Adipose Nuclei	Adipose
2	chr1:221262800-221267400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:221263400-221267400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:221263400-221267600	Weak transcription	NH-A	brain
5	chr1:221263800-221271400	Weak transcription	Placenta	Placenta
6	chr1:221264000-221267400	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr1:221264000-221267400	Weak transcription	A549	lung
8	chr1:221264000-221267400	Weak transcription	HSMMtube	muscle
9	chr1:221264000-221267400	Weak transcription	NHDF-Ad	bronchial
10	chr1:221266800-221267400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:221266800-221267800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:221266800-221268000	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr1:221266800-221268000	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr1:221266800-221268000	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr1:221266800-221268400	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr1:221267000-221267800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:221267000-221268000	Enhancers	Fetal Lung	lung
18	chr1:221267000-221268000	Enhancers	NHLF	lung
19	chr1:221267200-221267800	Enhancers	HSMM	muscle
20	chr1:221267200-221268000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:221267200-221268000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:221267200-221268000	Enhancers	Primary hematopoietic stem cells	blood
23	chr1:221267200-221268000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:221267200-221268000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr1:221267200-221268000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr1:221267200-221268200	Enhancers	Osteobl	bone

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