Variant report

Variant	rs7506168
Chromosome Location	chr18:45539806-45539807
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12967850	0.82[EUR][1000 genomes]
rs13382003	0.84[AFR][1000 genomes]
rs28594148	0.84[AFR][1000 genomes]
rs4341811	0.86[AFR][1000 genomes]
rs6507796	0.86[EUR][1000 genomes]
rs9946587	0.90[ASN][1000 genomes]
rs9954662	0.83[CHD][hapmap];0.89[JPT][hapmap]
rs9965294	0.80[CEU][hapmap]

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	nsv909616	chr18:45467806-45844500	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1066479	chr18:45505569-45554507	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1055669	chr18:45513090-45559375	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45535200-45549000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr18:45535800-45544000	Weak transcription	A549	lung
3	chr18:45537800-45543200	Enhancers	Hela-S3	cervix
4	chr18:45539200-45544200	Weak transcription	Fetal Thymus	thymus
5	chr18:45539600-45540000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr18:45539600-45540200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr18:45539600-45540200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr18:45539600-45540400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr18:45539600-45540400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr18:45539800-45540200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr18:45539800-45540400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr18:45539800-45547400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr18:45539800-45547800	Weak transcription	H9 Cell Line	embryonic stem cell

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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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