Variant report

Variant rs728908
Chromosome Location chr1:173488449-173488450
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173487200-173488600 Enhancers Primary T helper naive cells fromperipheralblood blood
2 chr1:173487400-173488600 Enhancers Primary T cells from cord blood blood
3 chr1:173487400-173488600 Enhancers Dnd41 blood
4 chr1:173487600-173488600 Enhancers ES-WA7 Cell Line embryonic stem cell
5 chr1:173487600-173488600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr1:173487600-173488600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr1:173487600-173488600 Enhancers HUES64 Cell Line embryonic stem cell
8 chr1:173487600-173488600 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr1:173487600-173488600 Enhancers Fetal Kidney kidney
10 chr1:173488000-173489600 Weak transcription HUES48 Cell Line embryonic stem cell
11 chr1:173488200-173488600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr1:173488400-173490200 Enhancers ES-I3 Cell Line embryonic stem cell
13 chr1:173488400-173490800 Weak transcription iPS-20b Cell Line embryonic stem cell
14 chr1:173488400-173495200 Weak transcription Cortex derived primary cultured neurospheres brain
15 chr1:173488400-173496000 Weak transcription Right Atrium heart
16 chr1:173488400-173496800 Weak transcription iPS-15b Cell Line embryonic stem cell

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