Variant report

Variant	rs9495463
Chromosome Location	chr6:139708584-139708585
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:139700600-139709400	Weak transcription	Fetal Intestine Large	intestine
2	chr6:139700600-139713800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr6:139706200-139713800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr6:139706400-139713800	Weak transcription	Osteobl	bone
5	chr6:139708000-139709000	Weak transcription	HepG2	liver
6	chr6:139708000-139709600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr6:139708000-139709600	Weak transcription	K562	blood
8	chr6:139708000-139711600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr6:139708000-139713000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:139708200-139709600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:139708400-139713800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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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