Variant report

Variant	rs528402111
Chromosome Location	chr4:118401027-118401028
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427692	chr4:118262899-118437573	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv482430	chr4:118347180-118497181	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv3446523	chr4:118399604-118401702	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
4	esv3323015	chr4:118400104-118401152	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:118396600-118402800	Weak transcription	HMEC	breast
2	chr4:118399400-118401200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr4:118399800-118402200	Weak transcription	NHEK	skin
4	chr4:118400000-118401200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:118400800-118401200	Enhancers	Left Ventricle	heart
6	chr4:118400800-118401400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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