Tag | Content |
---|
EnhancerAtlas ID | HS133-09626 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr14:96013430-96015640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr14:96014137-96014155 | ATTTCCTTTCTTCATTCC | - | 6.11 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35725 | chr14:96012944-96017601 | HepG2 |
|
| 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 |
GH14I095543 | chr14 | 96009947 | 96015300 |
|
Enhancer Sequence | AAGCTTTCAT GTGGGTTCCT GAGAGCCACC GACAGGAAAA GATATATATT AGGGGATGGC 60 CACACAAAAC ACTGATTGTT TTAAAAATTT AACATTCCAC TTAAGAATTG TTTAGTAAAT 120 CTAAAAAGCA GCTTTAAATT GTGCCTAAGA ACCATATAAT AGCTACTATG AAGCAGAGCA 180 GAGGAATGGT GAAGAGAAAA GCCATTTTAA GGTCCAGGGG CTTACAGAGA CGCATGGGGT 240 GACCAGGTGG ACTCTTGTAA AGCCACATTC CTGTCTTATT TCCTGAGAGT AGCATCACTT 300 TAGGTCTGAA AGCTATGTGG GCATTTTGCG TGAGGGGAGC ATTGTTTTCT TGGCGGTTGC 360 CCTGGGAGCC CAGTGCAGGT GAGCTGAGGG CAGAGTCTCC CTTAGGGCAG AGATGCCACT 420 GAAGGTGCAC CTCACCTCAA AGATCCCTAT CCTGGATTCA GTCAGAATAG CCATGTTATT 480 CTCCTCCTTG TGAACCTCCC GGGGCACCCG GTTGTGTCAC AGTGAAGTCT CTCCTATCCC 540 AGAAAGCCTT CCCTGACCCC AGACGGAACA GACCCTTTAA TCCACTCTAC AGCCCTGTTC 600 TTTGTTCATC ACTCCAGGAC CTAACTGCCT GTTACTTGGC TTTATTCAGA TCCCCTCTGG 660 CCAGCATACA GAGTGCCCCA AAAAATACAT TTAGAAAAGA GTGAAGAATT TCCTTTCTTC 720 ATTCCTTTTG GATTAGTCAC AAGAAATGTT AGGCTATTAC AGGTTACAGC CTCGCAACAC 780 CGCAGTAGCT AAGAGCCGGG ACTCAAGTCA CCCTCCCTGG GTTTGCATCC CAGCACTTGC 840 TGGGTGTGCT ACTGACCTCA GACGACTTAG TAACCTCCCT TCCTGCTTAA GTGGGCAAAT 900 AGCAGATGCC ACCGACCTCA GGCGTGTTAC AAGCTTAGAT GACAGCACCC TGTCGAGACC 960 ATGGCTCATA ATGAGCTCTC ACTGTAAGTT GACCTTGACA GTTAATGTTG GATTACACCT 1020 GGACTTGGTA CCGCGCTGTG GTATCCACCA CCGTTCGGAG GGTTTAAGGG AGCAGAGAAG 1080 GACAGGCTGA TGAACACAAC ATCGTTCATG TTTGGTTGCC CCTGGAACAT AGAGACTCAT 1140 TGTTGAAGGC AAAGGACAGA TCTAATCCTT GTGATGATCT ATCAGTGGAC TGCCCAGCAG 1200 CCCTAGGGGA CGGCAGGGCC TTCAGCCAGA AAGAATTCCC TGTAAAGTAT CTTTCCTACG 1260 ATTATAGTTT GACTTACTGC CACCGAGTTT TATTTTTAAA AATACTGCTT CTATTTCATA 1320 CCAAAGTGGA GAGTCTTTTC TGAACCGATA TGTTAGACAG TTATTGTGTT GAGTTATGCT 1380 TCAAAGAATG CAGTTTAACC TTGAGCTAAT TCTAATTTAG CAGTAGCAAG GATTGTGACA 1440 CTGGGTTCTA CTGTACCTCA TTAGCCATTT TCACAGGGAT TCGTTTTGCC AGAAAAAGGA 1500 GGTAGAAATG TTCGCCGGTT CCTAGGAAAT TTGGTGAGCA AATATGGAAA GTATTTCCAG 1560 ATTATTGATG TGTCTTCACT AGTCCTGAGC AAGCTATCAG CTTTGATCAT CACCACCACC 1620 GATGAAGCAA CCTTCCTGGG GAGGCCATGC TGAGCCCGAG TCTATGGGGA CCTCTTCTGG 1680 CTCCAGACCC AGGCTGGGCA GAGGCTGAGA CTTCAGCTGG GTGTCAGATA CCCCTCACCC 1740 CTTGCCCTGA TCTTGGGGGC GTTAGGGTGC TGTCAGAGTC TGACATAGGT ATTAAAATAT 1800 TTCAAATCTC AAGGAGAACT TCAGAGTTCT TCAGTACATT TACAAGTAAA TTGTAATCCT 1860 GGGAAACTAG CAGCACACTT CCTGTTATTC TGGCTTCTTA AATTCTTTTG TTTTTTGTTT 1920 GTTTTTGAGA TGGAGTCTCT CTCTGTTACC CAGGCTGGAG TGCAATGGCG CGGTCTCGGC 1980 TCACTGCAGC CTCTGCCTCC TGAGTTCAAG CTATTCTCCT GCCTCAGCCT CCTGAGTAGC 2040 TGGGATTACA GGCACCTGCC ACCATGCCCA GCTAATTTTT TGTATTTTTA GTAGAGACGG 2100 GGTTTCACCA TGTTGGCTAG GCTGGTCTCA AACTCCTGAC CTCGTGATCC ACCCGCCTGG 2160 GCCTCCCAAA GCCCTGGGAT TACAGGCATG AGCCACCGCG CCTGGCCTTT 2210
|