| Tag | Content |
|---|
EnhancerAtlas ID | HS133-03997 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr1:244317980-244319550 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:244318717-244318735 | GGAGGGAGGGAGGGAGGG | + | 6.03 |
| | | 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 |
| GH01I244154 | chr1 | 244317838 | 244319404 |
| Enhancer Sequence | CATGGGAGCA GTTTGTGTGC TGAAGCCTAT AGCAGACATA GAGTCCACGG ACATTGTTTT 60
ATCTACCTTG TAAGCTCAGC CCATTTGCTG GATTGGGAAA TAAAAAGGAC TGAGTTTATC 120
TTCCAGCCTT CTTCATTTAA GTGTCCTATA TAGTCAATGA TTTACACACT GTGCTCCTGT 180
AGAAACGCTG GGGTCCTACC AACCCATTGT TCACAGACAG CAAATTCTGA CTTGTTTTTC 240
AGTAGAAGTG ACACCCTGCC GTCAGTTCAA CCGTCCCTTT CTTGTCCTGT CTCCCCCTGT 300
GATCATCAGA GGCTCACATT TATGAGCCTT CTGGAGTCAC AGAACAAGTG TGTGCAACTA 360
ACCAGCCCAC CTGGACGTCA GACTTGCCTC GTGACCTTGG CTCAGGTTAT GCTTAACAAC 420
TGGCAGAAAG GTAACTGCCA GAGCCGAGCT GGACATAACA CACGATCCAC AGCCCACAGC 480
CAGGCGTGGC TTCAGCAGCC CCTGGACCCT GAGGGCATGG GGCCCATGCC GGGCTTTGTG 540
GGCAGGATGT GTGCAGGGGG CCGGCAGCTG CTTTGTGCCA GCACAAGTGG GACAGCTGCA 600
ATGAATGGGC CAAAGAGCCA CCTCAAAGGC ACACTGTGCC CAACTTCAAA CACACGGCCT 660
TGCTGCGGAC AGCTGAGGAA CAGCAGCAGC GGCGGCAGCG GCAGTAGCAA CAAACAGGCC 720
GCCTGGGCCC AGCTTTAGGA GGGAGGGAGG GAGGGACTCC CCACTGTGCA GGGCAGCCCG 780
CTGGCAGCGT TGGACAATGC CCAGTCCACA GCAGCTGCAA CCGCCGGCCA AAAGCGATCT 840
GCACATGCGA TCCGACTGAC CTCAGCTCAG TCAGAGTAAG GGACATCGAT CTCTAAGGTC 900
CCACCAGATT GTATCTGTAA CGGGCGTACA GGCGATGTTG CTATGTTCTG GTTCTACCTA 960
CCTCCATTAG AATGTTTTCC GAATCTGCTA AGGACCACCG ATAGGACCCC AGCTATGGAG 1020
CTGTCAGCGT AAATATAGAG GCTGGTTACA TGGGCTCCTC AAACTCTCCC ACCGTATAAC 1080
CCTGCTTGAT TCATTCCTGT TTCTTTCCCC GACGCCAGTG TCTCCAGGAG GAGTGGGCAT 1140
CACAGGCGGC TGCGTGCTTA TTACCCCCTC TTCCTGCCGT GTAGGGGTGG TGGAAGTTGT 1200
TGGGATAAGG CACACAGATG CTCCACCACT GAGGACGTCC TTTGATTGAA TTGTATTAGT 1260
TCTCTCTAAA TGGGTACTCC CCTTGCATCC TGTGCGTTAC CATGCTGTTT ATATTAACAC 1320
CCAGCACTCA GCTCATCCAT GATGAACGCT CAGAGAAAAG TGGGTGGGCT CAAACATAAT 1380
TCGATCACTA AGAGCGAATG TTTAAGAGAG GCTGATACAC TAATCGCTTA GTGATACACA 1440
CACACCCCCC ACCAGATGTT TGAAAGGAAA AAAGATTTTT GACTTCTCCC AAGGGATTGA 1500
GAAATAAATG TATGGGCAAG AGGTGTCTAG TCTACATATG CAGTTGCTGA TATTATTCCA 1560
CGACTAGTTT 1570
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