Variant report

Variant rs10219510
Chromosome Location chr12:48377635-48377636
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:48358600-48381400 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr12:48359200-48384000 Weak transcription H9 Cell Line embryonic stem cell
3 chr12:48363400-48383000 Weak transcription Spleen Spleen
4 chr12:48364400-48381200 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
5 chr12:48365200-48381600 Weak transcription Right Atrium heart
6 chr12:48365400-48381000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr12:48366200-48381200 Strong transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr12:48366200-48381400 Strong transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr12:48366200-48381600 Strong transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr12:48372400-48378400 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr12:48374800-48379000 Strong transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr12:48375000-48381600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
13 chr12:48375200-48381200 Weak transcription Fetal Muscle Leg muscle
14 chr12:48376400-48380800 Strong transcription Fetal Intestine Small intestine
15 chr12:48376800-48391000 Weak transcription Fetal Intestine Large intestine
16 chr12:48377400-48378800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
17 chr12:48377600-48377800 Bivalent Enhancer Colonic Mucosa Colon
18 chr12:48377600-48378400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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