| Tag | Content |
|---|
EnhancerAtlas ID | HS150-03006 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr12:54555130-54556180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr12:54555241-54555256 | GGAGGGCAGAGGGCA | + | 6.45 | | ZNF263 | MA0528.1 | chr12:54555659-54555680 | GGGGGAGGGGGACAGGAAAGA | + | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I054160 | chr12 | 54554333 | 54556212 |
|
Enhancer Sequence | AGGGAGGTAC AAGGCAGAGC CCCAGACCAA GGGCCAACAG GCCCCAGCCT GTACCTCTCA 60
GCTGGGTCCC AGTGAACTTG GGCCTCCAAG GGGCCTTCCC CAGGCACCAG GGGAGGGCAG 120
AGGGCAGGGC TGGGCCTGGA CTTGCAGGAT GCTCAACAGA GTTTGCCCTA CCTAATTCCC 180
ACACCCCTCC TCTTGTACTC TTTCCCATCT CCCCAGCCTC TGCTTCTCTC TCCACTTCTC 240
CCACTGTTCT TCCATCTTTG CCTATATTTT CTTCTAATTC TGTTCATCTC TCCCTTTCTC 300
TCTCCATATT CCCGCCTCTC TCCTTTACCT TTTGCCTTCA TCTGTCCCTC TACATCCACC 360
TGTTCTTCTT TCCAGCCCTT CTCTTCCCCT ACCCCAAATC CCTGGGCCTC AGGAGGGACC 420
CTGATCCCAC CAAGGAGCCC TCAGAGGCAG AAAGTCCCCT GTCAGCAGAA CTCTGGAGCT 480
GGCTGCTGAT TCAGTGACTG TAATCTCCCA GGCGGAGGCG GCAGTGGTAG GGGGAGGGGG 540
ACAGGAAAGA TAAATGAGGA GCATAAGAAC AAAATGGCAC AGACACTGGG GACAGGCTCC 600
AGGCTGAGCA AGGTTCTGGG GAGCAGAACC AGAGCCCTGA GCTACAGCCC AATCCCACCA 660
CCGCAGGCTG GTCAGTTGAG TGCAGGAAGT GCTTTCTGGC TACCAGCAAG TGACAGCACC 720
ACAGGGGAGA ACATGGCAAA GAGAAGGGAG CAGGGGACAG GCAGGGAGTG GCAGGGAGAA 780
GCCACCAAAG GAGTCAGAGA AAGAGGGGAG GAAGCCAGAG AAGCAAGGAA CACTGATAGA 840
ACAATGACCC CTCCAGTCCC ACTGCACCCC CAGATCCAGT GTGGACCCCT GCAGTCATAT 900
CATATTCCTG AGCCAGGGCC ACACATGGAA GGTTTGAGGG TTCCAACCAC AGCTTCCACA 960
AGTCTCACTT TTAGGGAGTA CCTTTATCCT TCAGGGTTCT TCCACCCTGA CTTTGGCCTA 1020
CTTTTTGGAG GTTTCACTCA GCCTCCGCTC 1050
|
