Variant report

Variant rs7924240
Chromosome Location chr10:95610515-95610516
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:95608200-95611400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
2 chr10:95608600-95610800 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
3 chr10:95608600-95611000 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
4 chr10:95608800-95610600 Enhancers Fetal Lung lung
5 chr10:95609000-95611000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr10:95609200-95610800 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
7 chr10:95609400-95611000 Enhancers Fetal Brain Female brain
8 chr10:95609400-95611000 Enhancers Fetal Stomach stomach
9 chr10:95609400-95611200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
10 chr10:95609600-95614400 Weak transcription Small Intestine intestine
11 chr10:95609800-95610600 Bivalent Enhancer ES-WA7 Cell Line embryonic stem cell
12 chr10:95609800-95610600 Enhancers Fetal Brain Male brain
13 chr10:95610000-95610800 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
14 chr10:95610000-95611200 Enhancers Cortex derived primary cultured neurospheres brain
15 chr10:95610200-95612000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
16 chr10:95610400-95611200 Bivalent Enhancer H1 Cell Line embryonic stem cell
17 chr10:95610400-95611200 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell

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