Variant report

Variant rs10272629
Chromosome Location chr7:47724208-47724209
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:47718600-47728000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr7:47718800-47725600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr7:47720000-47728000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr7:47720000-47732400 Weak transcription Spleen Spleen
5 chr7:47721200-47728000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr7:47721200-47728000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr7:47721200-47728000 Weak transcription Brain Substantia Nigra brain
8 chr7:47721200-47728200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
9 chr7:47721600-47727400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr7:47723400-47724400 Weak transcription A549 lung
11 chr7:47723400-47728000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr7:47723600-47728000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
13 chr7:47723800-47728200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr7:47724200-47724600 Weak transcription HepG2 liver
15 chr7:47724200-47726200 Enhancers K562 blood

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