| Tag | Content |
|---|
EnhancerAtlas ID | HS101-35637 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr5:132466120-132466800 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr5:132466630-132466644 | GTGAGTCATCCCTT | - | 6.29 | | ZNF263 | MA0528.1 | chr5:132466263-132466284 | GCTCCCTCCCTCTCCTCCCTT | - | 6.09 | | ZNF263 | MA0528.1 | chr5:132466254-132466275 | TCCTCCCTTGCTCCCTCCCTC | - | 6.3 | | ZNF263 | MA0528.1 | chr5:132466317-132466338 | CTCTCTTCTCTCTCCTCCCCT | - | 6.61 | | ZNF263 | MA0528.1 | chr5:132466314-132466335 | TTCCTCTCTTCTCTCTCCTCC | - | 7.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCCACTTATA CTAGTTCATG GCAAAAATTA TTATAAAGAC ATAGGAGTTG ATTTCAGAGC 60
CTGAGACCAG GAAGGAAGCT GGAGCTCGGG AATGGGCGGA GACTAGAACC TGGAAAGTTG 120
TCAATTTCCT CACTTCCTCC CTTGCTCCCT CCCTCTCCTC CCTTCGATTC TTCTCTCTCC 180
CTCCCCCCTT CCACTTCCTC TCTTCTCTCT CCTCCCCTCT TTTTTCTCTG TAGACCAGCT 240
TTCTCTGGCC ATAACGGGGA AGATGGCCAC CCCCACACTC TTTGAGCTTT GCTTGGCTCT 300
CAGTTCCAGT CCCACGAGGA AGTTAATAAC TGAGTCTACC TGGAGAAGAT TCTCACTGAC 360
CCACCTTGGG GCAGGTAATC TTCCCAGGTA ATAGGTCCTG TCACCTCTGG CCAGGGAGAT 420
GTGCTTCTGA GGTGCACACA TGGCTGCCGT GACCCACACT TGTGGTGTGG GAAGGCAGTT 480
TTCAGGACAA TGGGATGACC CATGGGCTGG GTGAGTCATC CCTTTAAGGT GTTTCCCGCA 540
GGAGGCACTT ATGTGACAAA TCCATCACCC AAGTGGGGGA AATGCTTATG GGGCTCCTGT 600
TGCTATTAAT GTGGCTAATC AGACGACATA GGATTTTGCA CTATTGTCTG AGCAGTTTTC 660
CATGTTATTA CAAACATTTT 680
|
