Variant report

Variant	rs370058216
Chromosome Location	chr6:13882469-13882470
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3420238	chr6:13880473-13885771	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
2	esv3400999	chr6:13881864-13884220	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv3379567	chr6:13882226-13884187	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
4	esv3473819	chr6:13882414-13883965	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv3352061	chr6:13882450-13883941	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13880200-13882600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:13881400-13882600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:13881400-13882600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:13881600-13882600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:13882400-13884600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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