Variant report

Variant	rs10018176
Chromosome Location	chr4:100558148-100558149
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs10003664	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13112253	0.82[YRI][hapmap]
rs28632769	1.00[AMR][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	nsv933074	chr4:100460951-100630600	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100546000-100561200	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr4:100553600-100563400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:100553600-100564200	Weak transcription	Left Ventricle	heart
4	chr4:100553600-100564600	Weak transcription	Psoas Muscle	Psoas
5	chr4:100556200-100560400	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr4:100556400-100563800	Weak transcription	Fetal Muscle Leg	muscle
7	chr4:100557200-100561200	Weak transcription	HMEC	breast

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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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