| Tag | Content |
|---|
EnhancerAtlas ID | HS133-19272 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:47668290-47669600 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr20:47669165-47669185 | TGGTGGTGGTTGTTTTGGAG | - | 7.23 | | TP63 | MA0525.2 | chr20:47668723-47668741 | GACATGTTGTGACTTATC | + | 6.33 | | ZNF263 | MA0528.1 | chr20:47669086-47669107 | GGAGGAGGTAGGAGATGAGGT | + | 6.33 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr20 | 47668295 | 47668414 | | chr20 | 47669409 | 47669497 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I049052 | chr20 | 47668941 | 47669090 |
|
Enhancer Sequence | ATGGCATGAT CATAGCTCAC TGCAGCCTTA AAATTCTGAG CTTAACCAGT CCTTCTGCCT 60
CAGCCTCCAG AGCAGCTGAG ACTACAAGTG CTCGCCACCA TGCCTGGCTA ATTTTTATTT 120
ATTGTAGAGA CAGGGTCTCA CTATGTTGCC CACGCTGGTC TTGAAATCCT AGCCTCAAGT 180
GATCCTTCCG CCTCGGCCTT CCAAAGCGCT GGGATTACAG GCATGAGCCA TTCTGCCAGG 240
CCAGAACAAA TCTAAAAATT CACTTTCTTG AAGTACTTTT GAATAAACAA ATTTAATTGT 300
GGCAGTTAAG TTGGTCATTT GTTCATCTGA CATTCATGCA ACTGAGTTCC CACATTATGT 360
TGGGGCTGCT AATGATTGAT CTGAAGGGAT AGTCTCCAGT CTTGACTGGA AACTCATGTT 420
TTGCTGGGTG ACTGACATGT TGTGACTTAT CCTTTAGTTC ATACAACAAA TGCTTACTAA 480
ATATGTACTG TGTGCCAGGT AATGCTGAAG GTCCTGAGCA TACAGACGAA AGTCCCTGCC 540
CTCAGGAGCT TGCAGTCTAG TGTGTGTATG AGACGACAAA GAAGTTTATT TCAAATGAGG 600
GTAATTGCTA ACACAGTAAA ACAAGGATGA TGTAGATGGT AATCGTAGAA GGCCTTTTTG 660
AAGAGTTGAC AGTGGGCTGA GTGCTGAATG GTGTCCATTA TCAAATTAGA GGATGAGCAT 720
TATTATGGTC AGGGAGAACT CTTGTGGCCA GTTTGTAGAA CAGAAGGCTT TTGTGCCTGG 780
AATGTAGCAA GAGCCAGGAG GAGGTAGGAG ATGAGGTCAG TAGATACCAG ATTGCTTAGA 840
CCCTGCTGTG GTAAGGGATT TGGTGGTGGT GGTGGTGGTG GTGGTTGTTT TGGAGATAGG 900
GTCTCACTCC CATTGCCCAG TCTGTAGTGC AGTGGCCTGA TCACAACTCA CAGCAGTCTC 960
AATTTGCTGG ATCTACAGGT GTGTGCCACC ACACCTGGCT AATTTTTTGT ATATTTAGTA 1020
GAGACAGGGT CTTGCTGTGT TAGCCCAGGC TGGTCTGAAG CCGGCTGAAG CAATCCACCT 1080
GCCTTGGCCT CCCAAAATGC TGGGCTAACA GGCGGCAGCC ACTGCACCTG GCCAGGAGTT 1140
TGGGTGTTTA AGACAAGTAA TTATGAGGAA TCTAAGGAGT TTTAGTTGAG AAATATACAA 1200
ATGCTAGAGA AACATAATGA AGAAAGTGAA ATGCAGATTT ATTAAGAAGT GTATTTTTAA 1260
AAATCAAGAA AATAAGCCCT GTGTGGTGGC ATATGCCTGT AGTCCCAGCT 1310
|
