Tag | Content |
---|
EnhancerAtlas ID | HS133-10058 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr15:52395040-52396390 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr15:52395238-52395250 | AAACAAACAAAC | - | 6.32 | Lhx3 | MA0135.1 | chr15:52395719-52395732 | AAATAATTAATTC | - | 6.22 |
|
| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_34917 | chr15:52390348-52397300 | HeLa | SE_36219 | chr15:52394942-52396179 | HMEC | SE_44451 | chr15:52392249-52396098 | NHDF-Ad | SE_64511 | chr15:52395182-52396161 | NHEK |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr15 | 52395777 | 52396019 | chr15 | 52395443 | 52396148 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH15I052099 | chr15 | 52391546 | 52397067 |
|
Enhancer Sequence | CTGGGCAACA AAATGAGACC CTTGTCTCTA CAAAAAAATA CAAAAATTAG CTGGGCATGG 60 TGGTGGGAGC CTGTAATCCC AGCTACTCGG GATGCTGAGG CACGAGAATC CCTTGAGCCT 120 GGGAGGCGGA GGTTGCAGTG AGCTGACATC GCGCCACTGC ACTCCAGCCT GGGCAATAGA 180 ATGAGACCCT GTCTCAAAAA ACAAACAAAC AAAAAACTGC ATAATGAGTA CATGTAGGTT 240 CATTTTATTT TTCTCTCTAT TCTTTTGTAT GTTGGAAAAT GTACATGAAA AAAGGTTTTA 300 AAAATCATCT CAATTTTACT TCCTCTCCAA TGATTACATT CCTTCTTTCC TTTTATAATA 360 ATGATCCTTG AAATCGTTTC TCTACATGCT GACTGATTTT TCTCCTCCCA TACTCTCTTG 420 AACCCACTTC ATTCAGGCTT TCCCCCGCTA CCATTCCAGC AAAATTGCTT TTCTTAAGAT 480 CATGAATGAC CTCCACATTG TTAAATCCAG TGGTTATTTC TCAGTCCTTA TCTTACATGA 540 CCCTCAACTA AACTGGATAG TTATCATTCC TTCCACCCTA AACACTTTCT TCACCTCACT 600 TCCAGGACTG CAGCCTAGCA GGGAACTTGT AGTTGTCAAC AGTATTAATG TTTTTCTTAC 660 CTCCTTAACT CCATCAATTA AATAATTAAT TCTGAAACCC AGACTGTAGA TTTGATTCCC 720 ATCCTGGTGT TAGTTTTGTA CAAAGAAAGG ATGTGTTCCC AGGCAGAATG CAAATGTTGG 780 CAGTGGGTCA CAGGAGTGAG GCTGAGTCAT AACCATTAGT AAGACAGCTC AGAAATCAGG 840 GCCAGCTCAT GACAGGTCTG CATGATCAGT AGGAAAGGAT GTTCCTGTGA CCATCTGAAC 900 AGGGGCCCAC AGCAGCCCCA AGAGAGCTAC TTGCTTAGAA GCTGAAACGG GGGTGTATGT 960 TTTGTTTTTT TTTTTTTGAG ACAGAGTCTC ACTCTGCTGC CCAGGCTGCA GTGCTGTAGT 1020 GTGCTCATGG CTCACTGCAG CCTCAACCTC CTTGGGCTCA AGTGATCCTT CAACCTACAG 1080 CCCCCTGAGT AGCTGGGACT ACAGGTATGT GCCACCACAC CCAGCTGAAT TCTTTTTTTT 1140 GAGACAGGAT CTCCTCTGTC ACCCAGGCTG GAGGGCGGTG GCACGATCTC AGCTCAGTGC 1200 AGCCTCAACT CCCTGAGCTC TAGCAATCCT CCCACCTCAG CCTCCCAAGT AGCTGGGACC 1260 ACAGTCATGC ACCACCATGC CCAGCTAATT TTTGAATTTT TGTAAAGATA GGGTTTTACC 1320 ATGTTGCCCA GGCTGGTCTC AAATTCCTGA 1350
|