Variant report

Variant	rs74074832
Chromosome Location	chr12:33143759-33143760
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11052417	1.00[AMR][1000 genomes]
rs55671927	1.00[AMR][1000 genomes]
rs55825139	1.00[AMR][1000 genomes]
rs56287051	1.00[AMR][1000 genomes]
rs58598352	1.00[AMR][1000 genomes]
rs59120557	1.00[AMR][1000 genomes]
rs74072482	1.00[AMR][1000 genomes]
rs74072985	1.00[AMR][1000 genomes]
rs74072990	1.00[AMR][1000 genomes]
rs74074808	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74074827	1.00[AMR][1000 genomes]
rs74074828	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075503	1.00[AMR][1000 genomes]
rs74075504	1.00[AMR][1000 genomes]
rs7964975	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530421	chr12:32825335-33465991	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv1054440	chr12:32872999-33150460	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv832367	chr12:33063644-33298967	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1039909	chr12:33132909-33244419	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1053849	chr12:33132909-33279169	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:33140400-33144400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr12:33140600-33164800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:33141600-33143800	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr12:33141600-33147200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:33142000-33144400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr12:33142200-33144200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:33142800-33144600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:33142800-33147000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr12:33143000-33144000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr12:33143000-33147200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:33143000-33147800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr12:33143000-33149800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr12:33143200-33143800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr12:33143200-33146600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr12:33143200-33147000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr12:33143400-33143800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr12:33143400-33144400	Enhancers	Placenta	Placenta
18	chr12:33143600-33144000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr12:33143600-33147000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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

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