Variant report

Variant rs571176997
Chromosome Location chr22:33459864-33459865
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:33454800-33465000 Weak transcription Fetal Brain Female brain
2 chr22:33457200-33460000 Enhancers H9 Cell Line embryonic stem cell
3 chr22:33457200-33460000 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr22:33457200-33460000 Enhancers iPS-18 Cell Line embryonic stem cell
5 chr22:33457600-33461000 Enhancers HUES64 Cell Line embryonic stem cell
6 chr22:33457800-33460200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
7 chr22:33458400-33460200 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr22:33459000-33460000 Enhancers HUES6 Cell Line embryonic stem cell
9 chr22:33459000-33460200 Enhancers HUES48 Cell Line embryonic stem cell
10 chr22:33459600-33460200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr22:33459600-33460200 Enhancers Fetal Brain Male brain
12 chr22:33459800-33460000 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
13 chr22:33459800-33460200 Bivalent Enhancer H1 Cell Line embryonic stem cell
14 chr22:33459800-33460200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell

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