| Tag | Content |
|---|
EnhancerAtlas ID | HS101-08929 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:111493780-111494930 |
Target genes | | Number: 19 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr11:111494106-111494124 | GTTTTGGTTACATTTTCC | - | 6.23 | | NFYB | MA0502.1 | chr11:111494484-111494499 | ACGTGAGCCAATCAG | + | 6.46 | | SCRT1 | MA0743.1 | chr11:111494703-111494718 | TGTCACCTGTTGCTC | - | 6.21 | | SCRT2 | MA0744.1 | chr11:111494705-111494718 | TCACCTGTTGCTC | - | 6.36 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_00011 | chr11:111494540-111497038 | Adipose_Nuclei |
|
| | 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 |
| GH11I111622 | chr11 | 111493681 | 111496554 |
|
Enhancer Sequence | ATTGCCCCAC AGCTCACTGA TGCTCTTTTC CATTTTTAAA AAATTCCTTT TTTTCTATTT 60
CATGTTGAGT AGTTGCTATT TCTGTCTTTA AATTCACGAA TCTTTTCTTC TGCCATTAAT 120
CCCATCCAGT GTATTTGTCA TCTCAGACAT TGTAGTATTC TTTTCTATAA ACTTGACTAG 180
GACTGTTTTT TAATGCCTTC CATGTCTTTA CTGATCTTTC TGAACATCTA GAATCCAGTT 240
ATGATAATTT TTAATGTCCA TGTCTGCTGA TTTCCAGCAT CTCTGTCAGT TCTAGGTTGG 300
TTTTGATTGG TTGATGTTTC TCCTCAGTTT TGGTTACATT TTCCTATTTC ATTACATGTC 360
TGGTAGTCTT TGATTGGATG CTAGACATTG CCAATTTTAC CTTGAGCACC ACATATTTTT 420
GTGTTACTTT AGGTTTTCTT GAACTTTGTT CTGGGATGCA GTTAAGCCTA CTTGGAAACA 480
GTTTGATCCA TTTGGGTCTT GCCTTCATAA TTGAAACAGT GCTCAGTCTG GGTCTAGTTA 540
CTTCCCACTT CTGAGTACTC TACTCAATGC CCCATGAATG CTGAGGTTTT TTGGCCTGAC 600
AAGTAGGAAC AGGCACCATT CCTGGCTTTG TGTAAGCACC AGGCAGTGTT CTCTCTCAGC 660
CTCTCAGATG GTTTTTTCTC TGGCCTCTGG TGGTTTTCCC TCACACGTGA GCCAATCAGC 720
ACTCTCCTGA GTGCTCAAGG GACGGATCCC TCTGCAGACC TTTGGACTTC TTTCTGTGTG 780
TAGCTCACTC TTATCTGGGA CTCTCAGCAT TGTCTACTCA ACTCAAAGAC ATTGCTGGGC 840
CACACCTGGG TTTCCCCTCC CTGTGCTGTG GCGTAGAGAT TCTCTCAAGG CATTAGTTGG 900
AACATTCATG GTCTCGCCTC ATTTGTCACC TGTTGCTCAG GGTTCACTTT CCTTTGCCTG 960
ATGTCCAGTG TCTTATAAAC CATTCTCTCA TGTATTTTGT ATTTTTGTTG TTGAAGATGG 1020
GAAGGTTGTT TCAGGCTGGA GGACAAATCT ATCTTAGCCA AAAGCAGAAT TATTTAGTCC 1080
TTTCAAATGT GTTATTAATT TAAGGTATTT TAAAGAGAAA GAACCATATG CACTTCTATA 1140
GTTTTGAAAA 1150
|
