| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00188 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:6928030-6930590 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PRDM1 | MA0508.2 | chr1:6928859-6928869 | GTGAAAGTGA | - | 6.02 | | RREB1 | MA0073.1 | chr1:6928973-6928993 | TTTTGGGGGTTGGTTAGGGT | - | 6.18 | | ZNF263 | MA0528.1 | chr1:6928696-6928717 | GGGGCAGGGAGGGAGGGGGGA | + | 7.19 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I006868 | chr1 | 6928661 | 6929459 | | GH01I006870 | chr1 | 6930261 | 6930460 |
|
Enhancer Sequence | CTAATGTTAA TTTTTTGTGG AGATGGGATC TCCCTATATT GCCCGGCTAG TCTCAAACTT 60
CTGGGCTCAA GTGATCCTCC TGCCTTTGCT TTCCAAAGTG GTGGGATTAT AGGCGTGAGC 120
CACAGAAGCG TGCCTGGCCT GGGTAGTTCT TTTTAATTGT TGAATATACT TGCTGAGGTT 180
AGTTTCTGCT GCAGAAAGCA TTATATAATG TTGAGTTAAC AGCGATCTTG TAAAGAGTTA 240
GTAGAATGTG TAAAGTTTTA CCTGGGAGGC GGAGGCAGCA GTGAGCCAAG ATCTTGCTAC 300
TGCACTCTAG CCTGGGTGAC AGAGCGAGAC TCTTTTTTTT TTTTTTTTAA AAACAAAACA 360
AAACAAAACA AAACAAAACA AAAAACGACT GTATAGGGTT AAAAAACGAC TGTATAGGGT 420
TTTATTTTAA TGGGTTTCTT CAGCTGTCTC CTTTTAGCTT CTATGACTCT GCATTTTCTT 480
GGCTCTTTGT TTTTCATTTC TTTACAGTTC TTCCATGTAT TTTGTTTTGA AAGTAATATG 540
CCTGAGGTGA AAATGGCGGC ATTTCTGTCA TGATTTAACC TTACTAGAAA TGACATTCTT 600
TGTTCTTTGT CTGTTTAGTT GAGAAGTGAA CCAATTCCCT GTGCTTAAAG TACTACTCCT 660
TGGTGTGGGG CAGGGAGGGA GGGGGGAAGA TTTTTAACAT AGAATACAAA TTGAGTTTGT 720
TGGAAAAGGT ATCCCTATAA AATGTTGTCC AGGTAGTTAG AGCTTAATAT GGGTGATAAT 780
TTCCCTAGAA GAATATTCTT TGCTGTAACA CTGATGACTT GATGGACTTG TGAAAGTGAA 840
ACTTGGTGTG TTTCTTCTTT CAGCCTCCAT GTAACTCACA GATAGGGCAG TGTAGAGTAG 900
ATTTCCAGTT TTAGATTAAG GATAGCTTGT ATCCTATGCA AGGTTTTGGG GGTTGGTTAG 960
GGTCTTTGAG TATTTCCTGT CTAATTCACT TACTAGTTAC AAAGAGACAA GCTGTAATGT 1020
AAAAAGTCTT CCTTGAGCTA GACTAGCTTT CTGTACTCTT TGATTTAAAA ATACCTGGTA 1080
GTTCTGCCAG TTGGGGATTT GTTTGGGGTG AATGAAAACC CCTCAGGCTC AGTCTGTTCA 1140
TGCACTGGTG TGTATTAATT CAGTCCATTC ATAGTCATGA GCTGACTGTG CCTTATTGAA 1200
GAAAGGGAGG CTTCTGGAAG AGAGAGGAAG ATGGATAATC TTGGATCCTG AAGCACTGCT 1260
GCTGGCGCCT GGGAGTGGGG CAGGAAGACA GGAGGTTCTG AAGAGAGGGC TTTGTATCCA 1320
AAGTTAAGAC TTAGGCCAGC CCTTGATGGG GAGAGAAGCT ACTCAGGCCC AATAACCTCA 1380
AATAGTTCAG GTTAAATCGA CAGTTGTCAA GTCTAATTCC TCTTTACAGC ATTATTTCTG 1440
TGGGAAAATG TGTGTGGCTT ATATACTTGC CTCAGCAAAC AGACCGGACT CAGAATCAGC 1500
TCTTTGTTGT CATAATTTAA GTGGAATTAG TTACTCCCTA GGGTTGCATT GCCCCTTGGA 1560
TGGCTTCTAG CCTTCTTTTT ACTTATTAAA TTATATTCCA GGTTCCTTGA CTGTGAGGGA 1620
CATAGTAAAC TCCTAGTAGC CTTTACCTTC CCCTCCCTAA ATAGCAAACT CATGTAGAAA 1680
ACATTAGCTA AAATCCTTTG CAGATTTTTT TGAAATCACC TAAAATGTTG TTATTGGCAC 1740
CATTTCATTT GGAGCCATTT TGTCAGAACC ACTAAGTATT TAGGTGAGGC GATTGATTTC 1800
ATTCCCACGT GGGAATTTGG TTGGTTGTAA TATTCAGGCA CTCAGAGCAA TTCCTGCCTG 1860
GACGTCACGT TCAGGTAGTC TGGTGTCTGA AACTTTTGGC AGAGATTAAG CTGATAGAAG 1920
ATTTGGGCTA ACATTTTTTA GTGTGTGAGT TGGTGAATTT TCAAGATGAT TTAGAAGACT 1980
TTAAAAAAGC ATCTGTGAAT ACTGCATCAT CTTGATGTCA AGAAGAGATT GTTATTTAAT 2040
ACATACATGT TTTAGTAATG AAGGAGGTAC ATAGAGATAA TTGATTTGAA CCGGTTTACT 2100
TTTTCCCCTT TTTAATGCAA AATATTTTTG GGAAACAGAA CTTGACTCGT GTTACACTAC 2160
TCGCTTCTTG TTTTTTGTTA CAAACATGCT GAAATGGTCT AAATAATGAT GCTACTAAAA 2220
CAACGTATGC ATTGTTTTCA TGGGGTGTTG ATTCCTTCTG CAGTGTTCAA AATTACTTGC 2280
ATGCCTCCGA GCAACAAACA CATATGTGAC AGACTTTATG TGAGATGAGC ATTCCAGAGA 2340
AATGAAATGC AAGTTTACTT TTCAGTAGCT ATGCAACTTA AAAAAAAAAC ATTGTGTTTT 2400
TTGAAACATG GCTTTAGGGC ACTAACACTC GGACCGAGTG CATGAGCTCT GCAAGTTATT 2460
TTAACAAAAC CTAATCACAG GAACAAACAT CTGGCATTTA TAGAGTTTGT TTATTTATTG 2520
ATTGCCGTAA GCCTCTAGAA AGAATATTCT GTTTCTTTTA 2560
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