Variant report

Variant rs17041555
Chromosome Location chr2:111578581-111578582
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:111562800-111604000 Weak transcription Lung lung
2 chr2:111569200-111579600 Weak transcription H9 Cell Line embryonic stem cell
3 chr2:111569400-111585000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr2:111569800-111580200 Weak transcription HUES64 Cell Line embryonic stem cell
5 chr2:111569800-111580800 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr2:111569800-111590600 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr2:111570200-111580600 Weak transcription iPS-20b Cell Line embryonic stem cell
8 chr2:111575000-111579000 Weak transcription HUES48 Cell Line embryonic stem cell
9 chr2:111576600-111579000 Enhancers Fetal Thymus thymus
10 chr2:111576800-111578800 Enhancers Dnd41 blood
11 chr2:111576800-111579800 Strong transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr2:111577200-111579200 Strong transcription iPS-15b Cell Line embryonic stem cell
13 chr2:111577600-111578600 Enhancers GM12878-XiMat blood
14 chr2:111577600-111582200 Strong transcription H1 Cell Line embryonic stem cell
15 chr2:111577800-111578600 Enhancers Primary T helper 17 cells PMA-I stimulated --
16 chr2:111577800-111578800 Enhancers Primary B cells from peripheral blood blood

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