Variant report

Variant rs74105948
Chromosome Location chr13:91739726-91739727
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:91737000-91740800 Enhancers Fetal Intestine Large intestine
2 chr13:91737000-91741000 Enhancers Fetal Intestine Small intestine
3 chr13:91737200-91740600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr13:91739000-91739800 Weak transcription Right Atrium heart
5 chr13:91739000-91740600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr13:91739200-91740800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr13:91739600-91740000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr13:91739600-91740000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr13:91739600-91740000 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr13:91739600-91740000 Enhancers Duodenum Mucosa Duodenum
11 chr13:91739600-91740800 Enhancers Fetal Adrenal Gland Adrenal Gland

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