Variant report

Variant	rs372058243
Chromosome Location	chr6:13884001-13884002
allele	A/G
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	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	nsv511850	chr6:13882512-13884124	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13882400-13884600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:13882600-13885000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:13884000-13886000	Enhancers	Fetal Brain Male	brain

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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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