Variant report

Variant	rs74087466
Chromosome Location	chr13:51876839-51876840
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs17837212	1.00[AMR][1000 genomes]
rs2897898	1.00[AMR][1000 genomes]
rs56734999	1.00[AMR][1000 genomes]
rs59315390	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59819997	1.00[AMR][1000 genomes]
rs60239593	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74084806	1.00[AMR][1000 genomes]
rs74087455	1.00[AMR][1000 genomes]
rs74087457	1.00[AMR][1000 genomes]
rs74087459	1.00[AMR][1000 genomes]
rs74087464	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74087485	1.00[AMR][1000 genomes]
rs9596501	1.00[AMR][1000 genomes]
rs9596507	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832611	chr13:51766472-51938314	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51853000-51889600	Weak transcription	Brain Angular Gyrus	brain
2	chr13:51867600-51910800	Weak transcription	Pancreas	Pancrea
3	chr13:51871800-51877400	Weak transcription	Fetal Brain Female	brain
4	chr13:51873200-51877000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr13:51875000-51877000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr13:51875200-51880000	Enhancers	H1 Cell Line	embryonic stem cell
7	chr13:51875200-51880000	Enhancers	H9 Cell Line	embryonic stem cell
8	chr13:51875400-51880400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr13:51875400-51880400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr13:51875600-51880400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr13:51875600-51880400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr13:51875800-51878400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr13:51876000-51877000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr13:51876000-51877000	Enhancers	Fetal Heart	heart
15	chr13:51876200-51880600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr13:51876600-51877000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr13:51876600-51877000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr13:51876600-51877400	Enhancers	Brain Germinal Matrix	brain
19	chr13:51876600-51877800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr13:51876800-51877200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr13:51876800-51877600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr13:51876800-51877800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr13:51876800-51878200	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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