| Tag | Content |
|---|
EnhancerAtlas ID | HS101-02380 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:116810170-116811330 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr1:116811016-116811031 | TCTGCTGACTCATCT | - | 6.09 | | REST | MA0138.2 | chr1:116811170-116811191 | AACAGCACCAGGGACAGAAAA | + | 6.18 | | Stat6 | MA0520.1 | chr1:116810687-116810702 | GTGTTCCTGAGAAAT | + | 6.87 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_33703 | chr1:116808541-116812093 | H2171 | | SE_66933 | chr1:116808541-116812093 | H2171 |
|
| | 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 |
| GH01I116267 | chr1 | 116810481 | 116811570 |
|
Enhancer Sequence | AGGACTCCTA ATGTTTGATG TCTTTGGGGC TTTTGCCTTG AAGGACAATG GGGATAGACC 60
TTTGCCTCGG AAAAGGAGCG ACTCAAGTAC AAGGCAGGTA AAACCATGGA AAGCAACAAA 120
AGATCAGGGG ACCCTTAGGC TGCTGTGAAG ACCGTACCAT GAAAATCGAG ATAAGGTGGT 180
GCTTTCCTCA GTCAGCAGGA GCACCCAGTC AAACAGAGCA CCTGGCCCCC GCCCAGCGAA 240
TGAAGAGTGG TTGATTCATG AAGAGCCTGG AATGGAGACA GCACCTGTCA GAAGAGGTGA 300
TGGGGCATGA GTATGTGTAC CAGGTTCAGA GTTCGGGCTC CTTCAGTCCA ACTGACCAAT 360
AGGAGAAAAC GCTGAAAAGA GACGGTGATT CAGGGCTGGC AGTGAGGAAG TCCCCAACTT 420
TATCAATGTA CCTGAATTAT TGTTTGGTTC TTCCTGTCTT TGGCTTTTGA TAGTTGTGGT 480
CCTCAGCCAA GAAGAGACAG AGGAAATGGA ACAGAGGGTG TTCCTGAGAA ATATGGGGGA 540
GGAAGAAGTT ATTGTCAACT GGCGCTCCCG CCTGCAATTA TTGTGGTGTT GGCGTTCCTC 600
ATACTTCCCA GTGCCGTCCC CACCACTCAT TGTGCTGGCT TGGAGGCACT CGGTTCAGAG 660
TCTTCAAACC CTCCTCCTCA GCCTTGGCCA GGCTGTCTGT CTCCTCAGGG CAGCCAAAGA 720
AGATGAGCTC ATTTCCAGAA CCCAAGAGGT GGCTCTGACC CTCTCTTCCC AGTTATTGCT 780
GAAGTTGGGT GGCTGAAACC AGTCAGGGCA TCATGCTGGC ACCAGGCCAG TCTTGCATCA 840
GGCAAATCTG CTGACTCATC TCTCTCTTCT AAACAAGCTC TGAGAGTTGG CATGCAGGAA 900
GCAGCACCAA GGAGTCTGAT GGCGTGGGCC ACCTGGCAGG GACTGACCAA GGGGAGGCGA 960
GGAGCAGCAG CCACCTGCCA CCCCAATCCC ACATTCTTCT AACAGCACCA GGGACAGAAA 1020
ATATGTGCCT ACCCAAGAAT TTCAGGGCCA CAAGTAGAAA CAAGTATATC ATAACAGGGA 1080
AGGTTGCAAC ATGAGAAATA TGCTTTCCCT GAGAAAAGTG GATAACTTGA CTTGAATGAT 1140
CTTCAAAAAT TATGTTTGGT 1160
|
