Variant report

Variant rs992036
Chromosome Location chr22:22703958-22703959
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22701200-22706600 Weak transcription Primary hematopoietic stem cells blood
2 chr22:22701400-22706400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr22:22702200-22704000 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
4 chr22:22702200-22704200 Enhancers Brain Cingulate Gyrus brain
5 chr22:22702200-22704400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
6 chr22:22702400-22704200 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
7 chr22:22702400-22704200 Bivalent Enhancer H1 Cell Line embryonic stem cell
8 chr22:22702400-22704600 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
9 chr22:22702800-22704000 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr22:22702800-22704200 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
11 chr22:22702800-22704400 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
12 chr22:22703000-22704400 Bivalent Enhancer H9 Cell Line embryonic stem cell
13 chr22:22703000-22704400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
14 chr22:22703000-22705800 Weak transcription Primary B cells from peripheral blood blood
15 chr22:22703400-22704600 Bivalent Enhancer ES-WA7 Cell Line embryonic stem cell
16 chr22:22703600-22704000 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
17 chr22:22703800-22725200 Weak transcription Right Atrium heart

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