Variant report

Variant rs73121583
Chromosome Location chr4:30789926-30789927
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:30779200-30790600 Weak transcription Fetal Lung lung
2 chr4:30784600-30790600 Weak transcription Aorta Aorta
3 chr4:30785400-30790800 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr4:30785600-30790200 Weak transcription HUES48 Cell Line embryonic stem cell
5 chr4:30785600-30790400 Weak transcription HUES64 Cell Line embryonic stem cell
6 chr4:30785600-30790800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr4:30785800-30790600 Weak transcription H9 Cell Line embryonic stem cell
8 chr4:30786000-30790600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr4:30786000-30790800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
10 chr4:30788000-30790600 Weak transcription Colon Smooth Muscle Colon
11 chr4:30788200-30790400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
12 chr4:30788200-30790800 Weak transcription Fetal Adrenal Gland Adrenal Gland
13 chr4:30788200-30791000 Weak transcription Rectal Smooth Muscle rectum
14 chr4:30788400-30790200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr4:30788400-30790800 Weak transcription Ovary ovary
16 chr4:30788400-30791200 Weak transcription Fetal Stomach stomach
17 chr4:30788600-30790600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
18 chr4:30789800-30790400 Weak transcription Fetal Intestine Small intestine
19 chr4:30789800-30791200 Enhancers Fetal Heart heart

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