| Tag | Content |
|---|
EnhancerAtlas ID | HS081-01658 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr1:203576000-203576710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:203576594-203576605 | GATGAGTCACC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:203576399-203576411 | AAACAAACAAAC | - | 6.32 | | JUND | MA0491.1 | chr1:203576594-203576605 | GATGAGTCACC | - | 6.62 | | NFIC | MA0161.2 | chr1:203576579-203576590 | TCTGCCAAGAA | - | 6.02 | | RREB1 | MA0073.1 | chr1:203576623-203576643 | GGGCTGGGGTGGGTTGGGGT | - | 6.03 | | RREB1 | MA0073.1 | chr1:203576622-203576642 | GGGGCTGGGGTGGGTTGGGG | - | 7.16 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_25758 | chr1:203575191-203577246 | DND41 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 203576120 | 203576183 | | chr1 | 203576404 | 203576703 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I203606 | chr1 | 203575245 | 203577382 |
|
Enhancer Sequence | ATCCCAGCTA CTCGGGAGGC TGAGGCAGGA GAATCGCTTG AACCAGGGAG TCGGAGGTTG 60
CAGTGAGCCG AGATCGCGCC ACTGCACTCC AGCCTGGTGA CAGAGTGAAA CTCCATCTCA 120
AAAAAAAGAA AGACCTTGTT AGATAACTTA GCTAGGCATG GTGCCAGGCA CCTGTAATCC 180
CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CATTTGAACC TGGGAGGTGA AGGTTGCAGT 240
GAGCTGAGAT CGCACCATTG CACTCCAGCC TGGGCAACAA GAGTGAAACT CCATCTCAAA 300
AAAAAAACAA GAAAGACATT GTTAGATAGC ATTGAGCATA TCACTTAAAT GGCCTTGGCT 360
CACCCCCTGG GGAAATCATG TTCTTTCAAA GACACTATAA AACAAACAAA CAAAAAAAGC 420
AACAGTAGCT ACAGAGTTCC TGCTCCAGCA ACCAGGAGCC TTGAGGCAGC ACAAGGACAC 480
CGGGGCGGGA GCGTGGCCCA AGAAGCAGAG ACAGCAACAA CAACAGGATG ACTTCATTTA 540
CTGAGTTATC AAAAACCACA ATGTCTGAAA ACCACAATGT CTGCCAAGAA AGAGGATGAG 600
TCACCAAGAC CCACAGGAAA GAGGGGCTGG GGTGGGTTGG GGTGGGCAGC ATGGCATGAT 660
GAGAAAAGCA AGTATTTTGA CAGCACACAG ATTCAAATCC TGACACATCT 710
|
