Variant report

Variant	rs11073078
Chromosome Location	chr15:35331860-35331861
allele	A/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:8)

rs_ID	r²[population]
rs1471200	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62005094	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6495738	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6495739	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6495742	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7402595	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7494870	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9920674	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350109	chr15:34668106-35534229	Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv522411	chr15:34953986-35462981	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:35312400-35335000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:35328200-35333000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr15:35330600-35333400	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr15:35331000-35332800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr15:35331400-35332400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr15:35331600-35332000	Enhancers	Placenta	Placenta
7	chr15:35331600-35332400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr15:35331600-35333000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr15:35331600-35333200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr15:35331600-35333600	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr15:35331600-35334800	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr15:35331600-35335200	Weak transcription	Primary B cells from cord blood	blood
13	chr15:35331600-35335400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr15:35331600-35335600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr15:35331600-35335600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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