Variant report

Variant rs463957
Chromosome Location chr22:22372864-22372865
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22365800-22375600 Weak transcription GM12878-XiMat blood
2 chr22:22365800-22376400 Weak transcription Primary B cells from peripheral blood blood
3 chr22:22370600-22374400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr22:22372400-22374800 Bivalent Enhancer K562 blood
5 chr22:22372600-22373000 Bivalent Enhancer H1 Cell Line embryonic stem cell
6 chr22:22372600-22373000 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
7 chr22:22372600-22373200 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
8 chr22:22372600-22373200 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
9 chr22:22372600-22373400 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
10 chr22:22372600-22373400 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
11 chr22:22372600-22376800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr22:22372800-22373200 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
13 chr22:22372800-22374400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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