| Tag | Content |
|---|
EnhancerAtlas ID | HS133-03247 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:203576120-203577210 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
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: 3 | Chromosome | Start | End |
| chr1 | 203576120 | 203576183 | | chr1 | 203576282 | 203576863 | | chr1 | 203576404 | 203576703 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I203606 | chr1 | 203575245 | 203577382 |
|
Enhancer Sequence | AAAAAAAGAA AGACCTTGTT AGATAACTTA GCTAGGCATG GTGCCAGGCA CCTGTAATCC 60
CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CATTTGAACC TGGGAGGTGA AGGTTGCAGT 120
GAGCTGAGAT CGCACCATTG CACTCCAGCC TGGGCAACAA GAGTGAAACT CCATCTCAAA 180
AAAAAAACAA GAAAGACATT GTTAGATAGC ATTGAGCATA TCACTTAAAT GGCCTTGGCT 240
CACCCCCTGG GGAAATCATG TTCTTTCAAA GACACTATAA AACAAACAAA CAAAAAAAGC 300
AACAGTAGCT ACAGAGTTCC TGCTCCAGCA ACCAGGAGCC TTGAGGCAGC ACAAGGACAC 360
CGGGGCGGGA GCGTGGCCCA AGAAGCAGAG ACAGCAACAA CAACAGGATG ACTTCATTTA 420
CTGAGTTATC AAAAACCACA ATGTCTGAAA ACCACAATGT CTGCCAAGAA AGAGGATGAG 480
TCACCAAGAC CCACAGGAAA GAGGGGCTGG GGTGGGTTGG GGTGGGCAGC ATGGCATGAT 540
GAGAAAAGCA AGTATTTTGA CAGCACACAG ATTCAAATCC TGACACATCT CTGAGGCCTT 600
CAGCTCTCTG GGTCTCAGCT TCCTTTATCT TTAGTTTTTA TTTATTTTTA TTTCAAAAGA 660
AATGAGATGG AGTCTTCTCT GTTGCCCAGG CGGGAGAGCA ATGGTGCAAT CTTGGCTCAC 720
TGCAACCTCT ATCTCCTGGG TTCAATTGAT TCTCCTGCCT CAGCCTCCCG ATTAGCTGAG 780
ATTACAGGTG CATGCCAGCA CACCGGCTAA TTTTTGTATT TTCAGTAGAG ATGGATTTTA 840
CCATTTCGGC CAGGCTAGTC TCGAACTCCT GACCTCAAGT GATCCACCCA TCTGGGTCTC 900
CCAAAGTGCT GAGATTACAG GTGTGAGACA CCATGCCCAG CCCTCAGCTA CCTTATCTTT 960
AAAAATGGGA AAGAGCCAGG CACAGTGGCT CACATCTGTA ATCCCAGCAC TTTGGGAGGC 1020
CAAGGCAGGT GGATCACGTG AGGTCAGGAG TTCGAGACCA GCCTACGTGG TGAAACCCCA 1080
TCTCTACTAA 1090
|
