Variant report

Variant rs12296768
Chromosome Location chr12:8970079-8970080
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:8960000-8972000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr12:8963000-8970200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr12:8966800-8975600 Weak transcription ES-WA7 Cell Line embryonic stem cell
4 chr12:8967000-8972000 Weak transcription H9 Cell Line embryonic stem cell
5 chr12:8967000-8975000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr12:8967200-8971800 Weak transcription HUES6 Cell Line embryonic stem cell
7 chr12:8967200-8972000 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr12:8967400-8971400 Weak transcription iPS-20b Cell Line embryonic stem cell
9 chr12:8967800-8974000 Enhancers Primary neutrophils fromperipheralblood blood
10 chr12:8968200-8972000 Weak transcription iPS-18 Cell Line embryonic stem cell
11 chr12:8968600-8970800 Enhancers ES-I3 Cell Line embryonic stem cell
12 chr12:8969000-8970400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr12:8969400-8970800 Enhancers iPS-15b Cell Line embryonic stem cell
14 chr12:8969600-8970200 Genic enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr12:8969800-8970400 Enhancers HUES48 Cell Line embryonic stem cell
16 chr12:8969800-8970600 Enhancers H1 Cell Line embryonic stem cell
17 chr12:8969800-8970600 Enhancers Esophagus oesophagus
18 chr12:8969800-8970600 Enhancers Placenta Amnion Placenta Amnion
19 chr12:8969800-8975600 Enhancers Placenta Placenta
20 chr12:8970000-8970800 Enhancers K562 blood
21 chr12:8970000-8972400 Weak transcription Primary monocytes fromperipheralblood blood
22 chr12:8970000-8972400 Weak transcription Primary hematopoietic stem cells blood

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