Tag | Content |
---|
EnhancerAtlas ID | HS133-19765 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:60526710-60528600 |
Target genes | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr20:60527212-60527233 | GACGCTGTCCAAGGTACTGAC | - | 8.74 | RREB1 | MA0073.1 | chr20:60528029-60528049 | GCGGTGGGGGTGGGGGGGGG | - | 7.57 | SRF | MA0083.3 | chr20:60527987-60528003 | TTTCCAAATAAGGTCA | + | 6.01 | TFAP2A | MA0003.3 | chr20:60527563-60527574 | AGCCTCAGGCA | + | 6.32 | ZNF263 | MA0528.1 | chr20:60528395-60528416 | CCCACTCCCTCATCCTCCCCC | - | 6.7 | ZNF263 | MA0528.1 | chr20:60528392-60528413 | CCCCCCACTCCCTCATCCTCC | - | 7.69 | ZNF740 | MA0753.2 | chr20:60528038-60528051 | GTGGGGGGGGGGG | - | 6.92 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH20I061952 | chr20 | 60527121 | 60527290 |
|
Enhancer Sequence | AGGCCTGGGA CCGGAGTCCT GGTGGGGGGA CACTCCTTGT AATCAGACTC CCAGGGTGAG 60 GCCCTGTGGT GGGGGTGAGG GTCAGGTGAT CTGCGAAGCA CCCCCCTCCC AGCTTCAAGT 120 GGGGAGCTTA CAGGCCTAGA GGTCAGGGCC TGGCAAACGA CCTGAAAAAT CCAGCTTGAG 180 GCCCTTTCCA GGGAGCCCCA GAGGCCTTCT CTTGGGTCAT TTCCCAGGAT GGGGGTCGCT 240 GTCACTCCTC TGTCCCAGGA GGATTCAGAG AGGTCAGTTC ACAGGCCTAT GCTGGGCAGA 300 GCCACTCATC CACGGCACTG GCCACTCAGC CAGGTATTGA CAGACCCACC CGCAGGGCAG 360 ACAAAAGAGG CATGGCCCAG CCAGCTGCGG GACCCTGCAC CCCCCACTCA CTCACACATG 420 TGCACATGCA CACACATGCA CACGTGCAAA CACACACACA CGCACACACA CACAGCCCTC 480 CTCGGCTCAC AGGGGGCTGC AGGACGCTGT CCAAGGTACT GACCTCCCTG CTGCTGGGCC 540 CCTCGCTGCT GAGCCAGGCA GGGGAAGTCA GCTGGGCCAA CTGGGAGGGT CGGGCAGGGA 600 CAGCACCTGA AATCCCTGCT CAGCCCCCTG TGCCGTTCCT GCCCCTGAGA CCACGGCCAG 660 CCACCCAAGG GCTACCCCTC AGCAGCCTGA GGACACAGCG CCGGCTCTTC ATCTCAAGCA 720 CACGGAGGTG CAAGAGGGAG GGTCTGCGGC CTCGGCAGAG ACAGCCGGAT GCACTGAGAC 780 CCTGGCCTGG GGCAGGCAGG GGCTCCCTCA GGGGGCTCAG AAGGGGTCAA TGCTGCAGAC 840 CACAGGCCGG CCCAGCCTCA GGCACGGTCC ACCTGGCACA GCACACTTCA CAGTGTTGAA 900 TATACTGTTG TATTTGTTTC CTGAGGTAAC AAAGTCCCAC AAACTCGGTG GCTTAAAAGA 960 AAGACATTTA TGCTCTCCCA GTCCTGGAGG CCAAAAGTCT GAGATCAGTA TCCCTGGGCC 1020 GAAATCAAGG GGTCGGCAAG GCTGAGCTCC CTCCGGGGAA TTAGGGGACG AGCCCTCACT 1080 GCCTCTTCCA GCCTCCAGTT CCTTGGCTCA CGCCCACATC ACTCCCGTCT CCACCTCCAT 1140 CTTCACTTCA TCTTAGTGTA ACCTCCCTCC ATCTCCCTCT TACATATGGA CACTTCCCAT 1200 TGGATTTCGG GCCTATGACT AGTCCTGAAA GATCTCATCT TGAGACCTTC AACTTGATCA 1260 TATCTGCAGA GACTCTATTT CCAAATAAGG TCACCTTCAC GGGCTGTTTT TCTTTTAGGG 1320 CGGTGGGGGT GGGGGGGGGG GGATTTTTCA GCTGACCACA ATTGTCAACA TTAAAAAATC 1380 AAGATATTGT AGGGGTCCCA CCTAGATATT GAGGAGGTGG ACAACAGGAG GACTGGGTCT 1440 CTCCTTCATC CCTCAGCTGC CAGGATGGAG GGTTTGGGGG GGGTCATTTC TTACACAGCT 1500 CCCAGTAGGA GATGCTGTGT AGCCTTGGGA GTGTCACTTA GCTACCTCTG GGCTTCCTTG 1560 TCTGTTGCTG GGACCGTGTA TCAGCTAGTT GCTGAGTAAC AAACACAAAC ACGATCTCAG 1620 CAGCACAGAG TCAGCATTTG GTTGGCTGGT CCAGGCCAGG CCGCTGGGGC AGCTGAGCTC 1680 TGCCCCCCAC TCCCTCATCC TCCCCCTGAC CAGCAGGCTA GCCACCCTCA CTGATGGCAG 1740 CAACACAGGA CAGCAGCCTG GTCACCGCAG CTCTCAGTTC AGAGCACCAC ATGCCCCGTG 1800 AACATCCCCT CAGTCAAAGC AAGTCACATG GCTGAACCCA CAGTCAAGGG GCAGGGAATT 1860 AGACTCCACC CCCTTAGTGG GGGAGCTTCA 1890
|