| Tag | Content |
|---|
EnhancerAtlas ID | HS133-18536 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr20:5053600-5055130 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr20:5054030-5054042 | TGCCCTGGGGCT | - | 6.11 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr20 | 5054597 | 5054958 | | chr20 | 5053777 | 5054341 | | chr20 | 5053635 | 5054480 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH20I005072 | chr20 | 5052981 | 5055710 |
| Enhancer Sequence | CCAGAAATAG ACTCTGAAGT GAGGATTCAT GTACAAGAGA TTATGAAGGA GGTGCTTCCA 60
GGGGAAACAG TAAGGGAATG AAGGAGGCAG GTCAGGGAAA AGGAGAAAAC TGAGCTAGGG 120
TGGCATTTCA TGTGAGGTTC CAGTCTCAGT CTTGTCCCTT GGGAAGCTGT GGGGTGTCAA 180
TTATGCCTCA GGGTTATCCT TCTTCAAAGC AAGAGATCTG GACTTTCTTC CTCCCACACT 240
ATCACCCTGG TAAATATAAA ATCCCAGCGC TTACACAACA GCTCCAAAAA CTCCAGAAAG 300
ACTCTCCTGA ACGTCACAGG TGTGGGAAAG AACCAGGAAG GTTCTGAAGG TGGGGCACAC 360
AAAGACAATG AGAGAGAATG TGGACACAGG GAGCCCTAGT TGAAGCAGCC TGGAGGTTCT 420
GCATTTTTCC TGCCCTGGGG CTTGGCTTTG GTGGCTCACA CTGAGGGAAC TTCACTGTGT 480
ATCCTGGCTT GGTGCCACTG GCTGGGACTC CAGGGTGTGG TCAGAGCTGC TGGAGGGCAG 540
GACCAGAGCC AGGGCCTGGC TGAGGCCTGG CACCAGGGAC TGTACAGGCG AGGCTGCCTG 600
GGCCCTGGAT GAAGAGCAGT GATGTGAGGT GCCAGCTCAG ACGCCAGAGA TAGGAAAGCC 660
CAAAGGCTAG CCTAAGGCTT GGGTAGTGGG AGTTGATGCA ACAAAGTGGG GGAGACTGAA 720
CAACGGCTTC CTCTCTCTTC CTTTCACTCT TAGACTGTCC TCCTTGAAGG GAATCAGATT 780
ATGCCACCCC AAAATATGCC ACATTGGCAC AAGAATTATT TTGAGCTGAA GCCAATTAAG 840
AAATAGCAGA CACCGGAAGA ACTCTCTGCC TGTGTTACTG TGTTTGCAGG AATACCTGAA 900
GCTGGGAATT TATAAAGAAT AGAGGTGTAT TTGGCTCACA GTTCTGCAAG CTCTACAGGA 960
AGCATGGCAT CAGCCAGGGC TCAGCTTCTG GTGAGGACTC AGGGAGCTGC CACTCATGGT 1020
GGAAGGTGAA GCAGGAGCAG GCATGTCACA TGGTGGGAAC AAGCAAGGCG GGGGAGGGGC 1080
CACACTTTTG CACAACCAGA TCTTGCCTGA ACTCAGAGCA AGAGCTCACT CATTACCATG 1140
AGATGGCACC AAGCCATTTA TGGGGGATCT GCCCCCATGA CCCGAACACC TCCCACCAGG 1200
CCCCTCCTCC AACACTGGGG ATCACACTTC AACATGAGAT TTGAAGGGGG CACACATCCA 1260
AACCATATCA CTGCCCCTCC CATTTCTGCC TAAAAGCAGA ACATAAATTT CCATTTGTAA 1320
GGGTGTCTTT CTCTCCCTAC CAGGAAGAGT AGAATAACGC TTAATCACCA TTATCACTGG 1380
AGATGGTACC AAGATGAATC TGCGTAAATG AACCTTACTA GATACCCCTT ATCTAACCTA 1440
TCTATAGTTT CCCCCTTATA TTTACTTTCC CACAGTTTAC AACCCCTAGA AGCCCAAACC 1500
CATTTTTCTT TGTCTAGTTA CCTCTCCACA 1530
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