Variant report

Variant	rs12297736
Chromosome Location	chr12:83347077-83347078
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10746259	0.86[JPT][hapmap]
rs10746261	0.86[JPT][hapmap]
rs10862526	0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs10862527	0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs10862528	0.85[ASN][1000 genomes]
rs10862529	0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs10862530	0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs11115492	0.83[CHB][hapmap]
rs11115495	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12320912	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12809082	0.83[CHB][hapmap];0.85[JPT][hapmap]
rs1484991	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs1625397	0.85[ASN][1000 genomes]
rs1682590	0.85[ASN][1000 genomes]
rs1682592	0.87[ASN][1000 genomes]
rs1682593	0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs1682594	0.87[ASN][1000 genomes]
rs1682595	0.85[ASN][1000 genomes]
rs17010128	1.00[EUR][1000 genomes]
rs17010139	1.00[CEU][hapmap];0.83[CHB][hapmap];0.93[JPT][hapmap];1.00[EUR][1000 genomes]
rs17010268	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17727549	1.00[AMR][1000 genomes]
rs1796188	0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs1796189	0.87[ASN][1000 genomes]
rs2019384	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs2403020	0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs2403021	0.87[JPT][hapmap];0.85[ASN][1000 genomes]
rs2403023	0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs3993374	0.85[ASN][1000 genomes]
rs4346031	0.85[ASN][1000 genomes]
rs7295699	0.85[ASN][1000 genomes]
rs7957916	0.87[JPT][hapmap];0.83[ASN][1000 genomes]
rs7965229	0.80[ASN][1000 genomes]
rs7970086	0.86[JPT][hapmap]
rs7971263	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv521849	chr12:83013783-83991479	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv469490	chr12:83089431-83507269	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
3	nsv559542	chr12:83089431-83507269	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	esv2758315	chr12:83101045-83357621	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv2759911	chr12:83101045-83357621	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv832472	chr12:83248283-83419753	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
7	nsv559557	chr12:83334204-83453620	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
8	nsv469495	chr12:83339933-83374779	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
9	nsv559558	chr12:83339933-83374779	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83325600-83348000	Weak transcription	Colon Smooth Muscle	Colon
2	chr12:83331400-83348000	Weak transcription	Brain Hippocampus Middle	brain
3	chr12:83340400-83348200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:83340800-83348400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr12:83342000-83352600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:83343800-83347600	Weak transcription	Brain Substantia Nigra	brain
7	chr12:83346200-83349200	Enhancers	Fetal Heart	heart
8	chr12:83346400-83347400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr12:83346400-83349200	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr12:83346800-83347200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr12:83346800-83347200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr12:83346800-83347200	Flanking Active TSS	NHEK	skin
13	chr12:83347000-83347400	Enhancers	Brain Cingulate Gyrus	brain
14	chr12:83347000-83348000	Weak transcription	Brain Angular Gyrus	brain
15	chr12:83347000-83348400	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr12:83347000-83348800	Weak transcription	HMEC	breast
17	chr12:83347000-83367200	Weak transcription	Gastric	stomach
18	chr12:83347000-83379600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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