Variant report

Variant rs73459893
Chromosome Location chr13:39309986-39309987
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:39294800-39325000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
2 chr13:39298200-39339600 Weak transcription Fetal Adrenal Gland Adrenal Gland
3 chr13:39304800-39310400 Weak transcription Rectal Smooth Muscle rectum
4 chr13:39308000-39317600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr13:39308400-39310600 Enhancers Fetal Intestine Small intestine
6 chr13:39309200-39311200 Enhancers Fetal Intestine Large intestine
7 chr13:39309600-39313200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr13:39309800-39310200 Enhancers H1 Cell Line embryonic stem cell
9 chr13:39309800-39310200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr13:39309800-39310200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr13:39309800-39310200 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr13:39309800-39310200 Enhancers Stomach Smooth Muscle stomach
13 chr13:39309800-39310400 Enhancers HUES6 Cell Line embryonic stem cell
14 chr13:39309800-39310800 Enhancers Fetal Kidney kidney
15 chr13:39309800-39311200 Enhancers Pancreas Pancrea

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