| Tag | Content |
|---|
EnhancerAtlas ID | HS133-32397 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr9:132879680-132881730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr9:132880715-132880730 | TCTGCTGAGTCATGG | - | 7.13 | | Nfe2l2 | MA0150.2 | chr9:132880717-132880732 | TGCTGAGTCATGGAG | - | 7.29 | | ZNF263 | MA0528.1 | chr9:132880928-132880949 | TCCCCAACCCCCGTCTCCTCC | - | 6.12 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_30857 | chr9:132879830-132883526 | Fetal_Muscle | | SE_37721 | chr9:132879339-132883526 | HSMMtube |
|
| | 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 |
| GH09I130117 | chr9 | 132879510 | 132883471 |
|
Enhancer Sequence | AGGCCAGAGG GCAGCTCGTG AACTAAACCC TCCCCAGAAG GGACATTTCA GGCCAGTGTG 60
GTCTCAGGTC AGCCCGTGGC CTGCGTCCTT TGGTGCCTTT CTGGTGACTG AGAGAAGCTG 120
TTCGCCAGAC TTTCAGGCCT GTATCTGACC ACAAACGGGG GAGCTCCTCT GTCCCCCATG 180
CTGAGTGAGC TGGAGCCCAG GACTTAAGCA GATTGTGGAA ATGCCGAGAC TCAGCGTAAG 240
TCAGAGGTAC TCTTAACGCC AGCCAGGCTG TCCATCGTCT TTATTTCTTT AATTTTTGTG 300
TTTGACTCAA AATTCCCTCT GAAGCCCAGC AGAGAGGAAG CAGGCAACAA GGATGAAGAG 360
TAGGTGGGGG TGTTTTAGGC TCTGAGGCTG TCCTTACACT CAGGGAAGGA TTGTTTTAGA 420
AATTTTTCAC GCTTTAAGTG GCTGTTGTGG GCCTTTGCTT CTGTGTGCCG CATAAATCAT 480
GTGGTGTAAA CTCCTTAGAA AGGATTACTG CCTGCTCTTG GGCATCACCC AGCCTTTTGA 540
GTCATGATTG CATCGTCCTG AACTAATCGT CCTGACCTGT GTCGTCCTAA AGTCACTAGT 600
GGACTTTAAG GTTATGAACT GCCTTTCCCT TAGCATGAAG CGTAGGTGTT AAGAGCTTGG 660
TCCTTGGAGG GAGGTGGACT TGGGTTTGCG TATTGGCTTC TCCACTTACA AGCTGGGTAA 720
CTTTGGTCAT TTACTAAACT TCTCCAGGCC TGAGTGTGTC AGGCCTGCTT CCCCCACAGA 780
GGCCATCGTG AGATGAAGCA TGAGAGGTGC CCAGCCCAGC TTCTGGCACA TGGTGATGAC 840
TCAGTTGATG GCAACGACCA GTGCTGTTGT TTTTGTCCTT GTTACAGTTC CAGGATCCTC 900
TTGGGAAGTC AGCTGGGAAG GAGGGGATAA TCTGTCTCCT TGCTGGCCTT CTTAGTTCCT 960
CTTTCACTCA GAGAGGACAG GGGACCACCT AGGGCAGGGG CAGCACCTCC TGTGCACTGT 1020
GGGGGGCGTT GCTCTTCTGC TGAGTCATGG AGAGTATTGA CTTGGGCATT TGCAGGGGCT 1080
GTGGTATTTC CTGCCTCAGT GGGCACTTGT CCTGTTCTCA TCAGTAAGAA GGACTTACCA 1140
GAATCGAGTG TCATGGTTAT TTTCCTCAGA GTGAGTTGGA GGTAGAGGAG CCCACAGGAC 1200
AGGAGGTCAG CCTTACAGGA CCCCCAAGAC CAGGTGGACA TGACACCCTC CCCAACCCCC 1260
GTCTCCTCCT TTTCTCTCCC CTGCAGAGGT TTCAGCATCT TCATAGCCGG GCCTGATTCC 1320
CTAAGATGGG CAGGGGCAGG GGCAGCCTGG GCATCTATAC TTAAAGCTCT TCCGATGATT 1380
CTGTTGCTCA CCCCCATTAA GAACCATTGC TATAAAGGAA TTCTCCTCCA CATGAGGAGG 1440
TCGATGCCTG GAGACAGAGG CAGCAGGCCA AGGGCAGGCA CACCCAGCTG AGATGGGGCA 1500
GGGCTGGAAG GCAGGCCTCC TGGATCCTGC CTGGGGCCTT GTCTCTCTCC CCACACTCAT 1560
TCTTTCACCG TATTTGCTGC TCCTCATGGT GAGGTCAGAA ATAGCCCGCC CAGCCTTGGT 1620
GAGCCTTCGC TCCCACAGGA GCCCAACACC CAGCCCGCCA CAGTCCGGTG AGCAGCAGGC 1680
TGTCGGTGTT CCTAAGTCAG GGAAATCTTT GGAAGAACAA TGGAGGGAGT CGTGGGACCC 1740
CAGGCTGCGA CCTGCTGCCT GGCTGCTCAC TGCATCATGC TGGTTTCACC CTGCTCAGAG 1800
CGGGCTCCAC CCCTGCTCGG CATCCTGACT CATCCTATGC ATATGGCAGC GCTGCTTGCA 1860
GGAGAGCCCA GGCGCCCTGG CAGCCCCCAG GTCCCCATTT GTTCCAGTTT TACTCACTGG 1920
ATTCTTGCCA GAGGTGGCAG CCGCTGTGAC ACAGTATATG CTACATTTGG TATTGGGCTA 1980
ATCCTATATG ACACTAACAC TGTCATGGCA AGTAGCCAAC TGCTCACTGC GAGCCAGCTG 2040
CTTTCTGTGT 2050
|
