Variant report

Variant rs7684325
Chromosome Location chr4:151938737-151938738
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:151936400-151938800 Active TSS HepG2 liver
2 chr4:151937600-151940600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr4:151937800-151940400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr4:151937800-151967600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr4:151938000-151939800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr4:151938200-151967400 Weak transcription H1 Cell Line embryonic stem cell
7 chr4:151938200-151969000 Weak transcription H9 Cell Line embryonic stem cell
8 chr4:151938400-151939200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr4:151938400-151939200 Enhancers Fetal Intestine Large intestine
10 chr4:151938400-151939200 Enhancers Fetal Intestine Small intestine
11 chr4:151938400-151939400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr4:151938400-151942600 Weak transcription K562 blood
13 chr4:151938400-151967000 Weak transcription ES-I3 Cell Line embryonic stem cell
14 chr4:151938600-151939400 Enhancers Duodenum Mucosa Duodenum

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