Variant report

Variant	rs61177158
Chromosome Location	chr13:39347125-39347126
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs17058513	1.00[EUR][1000 genomes]
rs2483422	1.00[EUR][1000 genomes]
rs58892971	1.00[EUR][1000 genomes]
rs73455906	1.00[EUR][1000 genomes]
rs73461816	1.00[EUR][1000 genomes]
rs73461845	1.00[EUR][1000 genomes]
rs73461846	1.00[EUR][1000 genomes]
rs73461877	1.00[EUR][1000 genomes]
rs7996253	1.00[EUR][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	nsv832585	chr13:39233307-39424375	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:39338000-39365400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr13:39338600-39351800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr13:39342000-39351600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr13:39342200-39350200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr13:39344000-39347200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:39346600-39365000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr13:39346600-39370800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr13:39347000-39347800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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