Variant report

Variant	rs370672899
Chromosome Location	chr1:168426982-168426983
allele	-/CTCT
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	esv2500882	chr1:168426298-168429687	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
2	esv2188881	chr1:168426881-168429003	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
3	esv3452563	chr1:168426919-168428923	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
4	esv3452565	chr1:168426919-168428923	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168423000-168430600	Weak transcription	Liver	Liver
2	chr1:168423400-168427200	Enhancers	NHEK	skin
3	chr1:168426000-168435200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:168426600-168435000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr1:168426600-168435200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:168426800-168427000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:168426800-168427000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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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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