Variant report

Variant	rs607484
Chromosome Location	chr1:168687512-168687513
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs511187	0.85[CEU][hapmap]
rs512129	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs523447	0.87[ASN][1000 genomes]
rs524705	0.86[JPT][hapmap]
rs528953	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs529949	1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs531706	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs533619	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs534503	0.85[ASN][1000 genomes]
rs542149	1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs544013	0.87[CHB][hapmap];0.85[ASN][1000 genomes]
rs545833	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs553721	0.90[EUR][1000 genomes]
rs573418	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs581753	0.95[CHB][hapmap];0.98[CHD][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs586318	0.83[JPT][hapmap]
rs590033	0.84[ASN][1000 genomes]
rs590875	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs627406	0.86[JPT][hapmap]
rs631451	0.86[JPT][hapmap]
rs635954	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6427145	0.96[ASN][1000 genomes]
rs678629	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs681316	0.90[EUR][1000 genomes]
rs686226	0.91[CHB][hapmap];0.98[CHD][hapmap];0.86[JPT][hapmap];0.90[ASN][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	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
2	nsv831836	chr1:168538779-168716956	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv831847	chr1:168669877-168850129	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168678200-168695600	Weak transcription	Fetal Muscle Trunk	muscle
2	chr1:168679200-168694600	Weak transcription	Fetal Muscle Leg	muscle
3	chr1:168679600-168694600	Weak transcription	Fetal Stomach	stomach
4	chr1:168679800-168694600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr1:168680200-168687600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:168680200-168694800	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr1:168681400-168692400	Weak transcription	Colon Smooth Muscle	Colon
8	chr1:168683600-168687800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:168683600-168687800	Weak transcription	NHEK	skin
10	chr1:168683600-168688000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:168683600-168688200	Weak transcription	Hela-S3	cervix
12	chr1:168683600-168696000	Weak transcription	Left Ventricle	heart
13	chr1:168686400-168688000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:168687000-168687600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:168687000-168687800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr1:168687000-168689000	Enhancers	Pancreas	Pancrea
17	chr1:168687000-168689600	Strong transcription	Adipose Nuclei	Adipose
18	chr1:168687200-168687600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:168687200-168687600	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr1:168687200-168687800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:168687200-168687800	Enhancers	Muscle Satellite Cultured Cells	--
22	chr1:168687200-168687800	Enhancers	HSMMtube	muscle
23	chr1:168687200-168688200	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr1:168687200-168688400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr1:168687200-168689600	Enhancers	HMEC	breast
26	chr1:168687400-168687600	Enhancers	Fetal Lung	lung
27	chr1:168687400-168687600	Enhancers	Ovary	ovary
28	chr1:168687400-168687800	Enhancers	Fetal Heart	heart
29	chr1:168687400-168688000	Enhancers	Placenta	Placenta
30	chr1:168687400-168688000	Enhancers	Right Atrium	heart
31	chr1:168687400-168688000	Enhancers	HSMM	muscle

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