Variant report

Variant	rs9461570
Chromosome Location	chr6:30099458-30099459
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
TRIM40	TF binding region
ENSG00000231226	Chromatin interaction
ENSG00000204616	Chromatin interaction
ENSG00000204619	Chromatin interaction
ENSG00000204614	Chromatin interaction

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30096200-30100400	Enhancers	Fetal Intestine Large	intestine
2	chr6:30097000-30100400	Enhancers	Fetal Intestine Small	intestine
3	chr6:30098600-30099600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:30099000-30103600	Weak transcription	A549	lung
5	chr6:30099400-30101800	Enhancers	HepG2	liver
6	chr6:30099400-30103200	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr6:30099400-30103400	Weak transcription	Hela-S3	cervix

Quick Search:

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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