| Tag | Content |
|---|
EnhancerAtlas ID | HS180-08219 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr11:18033580-18034490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr11:18034225-18034237 | TGCCCCGAGGCA | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35602 | chr11:18032257-18034670 | HepG2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACTCATGTGT ATTTCCCCAA CACCAGCACA TGGGTAGGCA CACAGATGCT CGTTCATTCA 60
TTCGTCAACG AGTATTTACT GGGGACCTAC AATGTGCCAG ACACCAAGAG AGGCACCGTG 120
AACAAGACAG GCACAGCACC CACTCTTACC ACACTTACTT TCCAGCCAGA GAGACTGACG 180
TTAATAATAA ATTATACACA TCATTACAAT TGTGATACGT GCTATGAAGA AGCACAAGAC 240
GCAGCGACTG CTTGTTCCCG TGCATGCTGG TCGGCCACCT GCCACGCTCC TGTGCATGAA 300
CCCTCCTCTC TCCCAGACAC ACATCAAGAT GACCCTGTCT CTCCCAATGC TCCCGTCAAA 360
CCAACAGCAG CCCAACTCCC CCAACACATG CAAGAACCGG TCACAGCAGA GTGTCAGCAA 420
ATAGGCAGGG TCTGTGCCTT GTGCGCGGCC AAACACCGCA GGCCTCACAT CTAAAGGATG 480
CTTTCGCCAG GCTGGGACAG GGTCTCCCTC CTCCAGGCAT CAGGAGTGTG GGGGGCACAG 540
GTGGCCCCAC GGAGCTCTGG GACCGGGCGA TCCTCTCCAC CGAGCCCTCC GCGCTGTCTT 600
CCAGGCGCTA TTCGGGCTGG AGGGCTCTCG CGGAACCAGA CGCTCTGCCC CGAGGCAGGT 660
TCTTCCCGCG GCGCCACAGC CCCTCCGGCC CTGACCCCGC CAGCCGGCAG GCCCCTAAGT 720
CGACCGCGAA GACCCTTCCT TCCCCGCCCG CCCGCTCCTC CTCCGCTCCC CCTCCGCTCC 780
CAGCCCAGGA TCCTTCAACC CAGAGCCCGG CTCGGACCTC AGCCGCCCAG CCCCTGAACT 840
GCCCACGCCG CGGCCAGCAG CTCCCACATC TCGGCGCCCC TCAGGGCCTG CACCGGCCCG 900
GGGGCGGAGT 910
|
