Variant report

Variant	rs2901180
Chromosome Location	chr18:28860103-28860104
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16961585	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28361376	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28566128	1.00[EUR][1000 genomes]
rs28786993	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55987465	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56748528	1.00[EUR][1000 genomes]
rs58106182	1.00[EUR][1000 genomes]
rs7234316	1.00[EUR][1000 genomes]
rs7234921	1.00[EUR][1000 genomes]
rs73413204	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73413256	1.00[EUR][1000 genomes]
rs73413259	1.00[EUR][1000 genomes]
rs9947250	1.00[EUR][1000 genomes]
rs9947771	1.00[EUR][1000 genomes]
rs9967347	1.00[EUR][1000 genomes]

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	esv3360998	chr18:28693111-28881812	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1066692	chr18:28856066-29190505	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv543674	chr18:28856066-29190505	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28855400-28860800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr18:28856000-28860400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr18:28856000-28861200	Weak transcription	Left Ventricle	heart
4	chr18:28858800-28860800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr18:28858800-28861400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr18:28858800-28862400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr18:28859000-28860600	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr18:28859000-28867600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr18:28859200-28860200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr18:28859200-28860200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr18:28859400-28861200	Weak transcription	HepG2	liver
12	chr18:28860000-28862800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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Input of quick search could be:

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

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