Variant report

Variant	rs4518909
Chromosome Location	chr1:209330216-209330217
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11586407	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11586451	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12722814	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12755287	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1933612	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4402132	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6658956	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6672407	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6678963	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6692414	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6704132	0.82[EUR][1000 genomes];0.85[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	nsv873137	chr1:209301571-209338673	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv522816	chr1:209325038-209342622	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:209327800-209332000	Enhancers	H1 Cell Line	embryonic stem cell
2	chr1:209328200-209331600	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr1:209328200-209334000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr1:209328400-209331000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr1:209328400-209331200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr1:209328400-209332400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr1:209328400-209334000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr1:209328600-209330800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr1:209329200-209333200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr1:209329600-209330800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:209329600-209335800	Weak transcription	HSMM	muscle
12	chr1:209329800-209330800	Weak transcription	Fetal Muscle Leg	muscle
13	chr1:209329800-209331000	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr1:209329800-209331600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:209329800-209332400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr1:209330000-209333200	Weak transcription	HSMMtube	muscle
17	chr1:209330200-209330600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:209330200-209331200	Weak transcription	Fetal Brain Male	brain
19	chr1:209330200-209333000	Enhancers	H1 BMP4 Derived Mesendoderm 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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