The 2.0 version of rSNPBase

Variant report

Variant rs4809147
Chromosome Location chr19:21781002-21781003
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:21770000-21786600 Weak transcription Primary T cells from cord blood blood
2 chr19:21770200-21786600 Weak transcription Right Ventricle heart
3 chr19:21771000-21786200 Weak transcription Stomach Smooth Muscle stomach
4 chr19:21771200-21786200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr19:21771200-21786200 Weak transcription Skeletal Muscle Female skeletal muscle
6 chr19:21771400-21782200 Weak transcription Fetal Intestine Large intestine
7 chr19:21771400-21785000 Weak transcription Fetal Intestine Small intestine
8 chr19:21777600-21781400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr19:21778000-21783600 Weak transcription Fetal Adrenal Gland Adrenal Gland
10 chr19:21778200-21782000 Weak transcription Primary hematopoietic stem cells blood
11 chr19:21778200-21785800 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr19:21780000-21782600 Weak transcription H1 Cell Line embryonic stem cell
13 chr19:21780600-21781800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr19:21780600-21782000 Weak transcription K562 blood
15 chr19:21780600-21784400 Weak transcription Pancreas Pancrea
16 chr19:21780800-21782000 Weak transcription Gastric stomach
17 chr19:21780800-21782000 Weak transcription Dnd41 blood

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Last update: Aug 31, 2015