Variant report

Variant	rs12734254
Chromosome Location	chr1:77408265-77408266
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11162233	0.89[CEU][hapmap];0.90[CHB][hapmap];0.89[TSI][hapmap];0.85[EUR][1000 genomes]
rs1252579	0.88[CEU][hapmap];0.90[CHB][hapmap]
rs12722889	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1273142	0.88[CEU][hapmap];0.90[CHB][hapmap]
rs12731790	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs12734069	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[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]
rs12734482	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1357331	0.92[CEU][hapmap];0.84[CHB][hapmap]
rs1403244	0.88[CEU][hapmap];0.90[CHB][hapmap]
rs1522621	0.88[CEU][hapmap];0.95[CHB][hapmap];0.86[CHD][hapmap];0.80[JPT][hapmap];0.85[ASN][1000 genomes]
rs1522622	0.88[CEU][hapmap];0.90[CHB][hapmap]
rs1533849	0.83[EUR][1000 genomes]
rs1546319	0.89[CEU][hapmap];0.90[CHB][hapmap];0.89[TSI][hapmap];0.85[EUR][1000 genomes]
rs17368584	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1766286	0.88[CEU][hapmap];0.90[CHB][hapmap]
rs2350526	0.88[CEU][hapmap];0.90[CHB][hapmap];0.81[TSI][hapmap]
rs34701857	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4949753	0.88[CEU][hapmap];0.90[CHB][hapmap];0.82[EUR][1000 genomes]
rs4949754	0.85[CEU][hapmap];0.90[CHB][hapmap];0.82[EUR][1000 genomes]
rs6703662	0.89[CEU][hapmap];0.90[CHB][hapmap]
rs71658713	0.81[EUR][1000 genomes]
rs71658714	0.81[EUR][1000 genomes]
rs7535901	0.80[EUR][1000 genomes]
rs9660283	0.90[CHB][hapmap]
rs9662288	0.88[CEU][hapmap];0.94[CHB][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9727199	0.89[CEU][hapmap];0.90[CHB][hapmap];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003826	chr1:76965331-77656929	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv535006	chr1:76965331-77656929	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv999350	chr1:77375536-77430222	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv871501	chr1:77382835-77444267	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
5	nsv1005548	chr1:77388792-77430739	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS	n/a	n/a	inside rSNPs	diseases
6	nsv1006696	chr1:77391700-77430739	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12734254	TYW3	cis	parietal	SCAN

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77393400-77429000	Weak transcription	Aorta	Aorta
2	chr1:77400400-77412000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:77405000-77410600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:77405200-77408800	Enhancers	HSMM	muscle
5	chr1:77405200-77410400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:77405400-77410400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr1:77405400-77427000	Weak transcription	Fetal Stomach	stomach
8	chr1:77405600-77410400	Weak transcription	NHLF	lung
9	chr1:77405800-77410400	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr1:77406000-77410200	Genic enhancers	Cortex derived primary cultured neurospheres	brain
11	chr1:77407200-77408400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr1:77407400-77409400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:77407400-77410200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:77407800-77411200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:77408000-77408400	Enhancers	Muscle Satellite Cultured Cells	--
16	chr1:77408000-77408400	Enhancers	NH-A	brain
17	chr1:77408000-77408400	Enhancers	NHDF-Ad	bronchial
18	chr1:77408000-77408800	Enhancers	HSMMtube	muscle
19	chr1:77408000-77409000	Enhancers	Osteobl	bone
20	chr1:77408000-77411000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:77408200-77408400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr1:77408200-77408600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:77408200-77410000	Enhancers	Ovary	ovary

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