Variant report

Variant	rs4768446
Chromosome Location	chr12:43139715-43139716
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1000413	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10128809	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10161278	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10506215	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10785374	0.87[EUR][1000 genomes]
rs10785375	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10785376	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10880360	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10880361	0.82[EUR][1000 genomes]
rs11181669	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12425497	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12578732	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12816928	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12830101	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3921403	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4768445	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4768447	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7305756	0.87[EUR][1000 genomes]
rs7310956	0.88[AMR][1000 genomes];0.93[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	nsv1044790	chr12:42672255-43344184	Enhancers Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
2	nsv541483	chr12:42672255-43344184	Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
3	nsv832389	chr12:43003361-43173896	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:43133200-43139800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:43137800-43140200	Weak transcription	Pancreas	Pancrea
3	chr12:43138800-43140800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:43139000-43139800	Weak transcription	Fetal Lung	lung
5	chr12:43139000-43140000	Weak transcription	Adipose Nuclei	Adipose
6	chr12:43139000-43140000	Weak transcription	HSMM	muscle
7	chr12:43139000-43140200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
8	chr12:43139200-43140800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr12:43139400-43140400	ZNF genes & repeats	HMEC	breast
10	chr12:43139400-43140600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
11	chr12:43139600-43140400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr12:43139600-43140600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr12:43139600-43140600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr12:43139600-43140600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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