Variant report

Variant rs11119896
Chromosome Location chr1:212444904-212444905
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:212435200-212445600 Weak transcription Right Atrium heart
2 chr1:212442600-212446200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr1:212442800-212445400 Weak transcription Primary neutrophils fromperipheralblood blood
4 chr1:212443400-212445600 Weak transcription Monocytes-CD14+_RO01746 blood
5 chr1:212443600-212445200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr1:212443600-212445600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr1:212444200-212445400 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr1:212444400-212446400 Enhancers Primary T cells from cord blood blood
9 chr1:212444400-212446600 Enhancers Fetal Intestine Small intestine
10 chr1:212444600-212445000 Weak transcription Pancreas Pancrea
11 chr1:212444600-212446000 Enhancers Stomach Mucosa stomach
12 chr1:212444600-212446200 Enhancers HepG2 liver
13 chr1:212444800-212445200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
14 chr1:212444800-212446600 Enhancers Fetal Intestine Large intestine

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