Variant report

Variant	rs72900599
Chromosome Location	chr4:111144020-111144021
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10022428	1.00[EUR][1000 genomes]
rs11947429	1.00[EUR][1000 genomes]
rs17041465	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4698822	1.00[EUR][1000 genomes]
rs72900602	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7673060	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	nsv869392	chr4:110945459-111235071	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:111138000-111145800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:111141400-111148800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:111143600-111144600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr4:111143800-111144200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr4:111143800-111144600	Enhancers	HUES48 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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