| Tag | Content |
|---|
EnhancerAtlas ID | HS133-10519 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr15:89609700-89612360 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr15:89612152-89612163 | CCACACCCTGC | + | 6.62 | | NEUROD2 | MA0668.1 | chr15:89611904-89611914 | ACCATATGGC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr15:89612218-89612233 | TGAACTCCTGACCTT | - | 6.04 | | SPI1 | MA0080.4 | chr15:89611976-89611990 | AGCTTCCTCTTTTT | - | 6.24 | | SRF | MA0083.3 | chr15:89609731-89609747 | TTTCCAAATAAGGTCA | + | 6.01 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_13697 | chr15:89611215-89612033 | CD34_Primary_RO01536 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I089066 | chr15 | 89609940 | 89612430 |
|
Enhancer Sequence | CTTAACTTGA TTACATCTGC AAAAGACCCT ATTTCCAAAT AAGGTCACAT TCACAGATAC 60
CAGGGGTTAG GACTTGAACA TATATTTTGG GGGGACACAA TTCAACCCAA TACCTTGGGC 120
ATCCTTGTCA CCAAGGCATT CTCCTATCAT ATTTCCTTCC CAAGGCCTGG AGGAACATGG 180
CTGCCTGCTC ACACAAGTAA ATAGGAGGTG CTGGAGGTCT TAAGCCACAG CAGGAGGGCT 240
GGGCAGAAAC CTGTGCTCAG CAAGATACCT TTTCAGTGAA GGGTACCTGT TGCGGCAGGC 300
CAAGAGAGCC ACGGGCCAGC CAAGAGGCCA AGTCAAGCTG TAGTGAAACA GTTCCCTTTG 360
GTGTCTGCAG CTGAGTGCCT GATTGCACAG TGGCATGGCA CAGCTGTGTT AGTCGTCCTT 420
TCTCCAGATG CCATGAAGTC TGGAAAATGT GTCTGGATAC TTGTGAGGTC ACCATACTTA 480
GGGAGTTTGG ACTCTGAATA AACAAGCGGC AGAAAGTCTT GAGATTCACA GCTCTTTCTG 540
CTCCAGATTC TATACAGTTG AGGAAGGAGA TGTGAATTGA TGGTGGGGCC CCATGTTGGG 600
GTGATCAGAC CCAACACCAG GCCATGGGGG CTACGAAGTC CAGTGGAGTT AAAGGAATGA 660
GACAAGACAA GAGTGCATAA AGTGGGATCA GGGGGCCAAT GCTAGTATGG AGGCTGCTAA 720
GGCCCGGAGC TCTGGAAGCC CACACTATTT ATTGGTGATC AAACAAAGAA GCAGGTGGTG 780
AGGATGTGGG GGTTGAAAGA AAGCAGTGTA TCAAGCACAT GATCTACAAC TGTGACAGTT 840
TAGCATTTTC TTTGAAGCAT ATGGAACATG TTCTGCTACT TGAGATAATG GGAAACATGT 900
TCTTCTAGTT TAAGTTACAA TCGATCTAAT AGCCTGGGAG TGCTAGAAGC AAGAAGCCAG 960
CAAGTCTAGA CACATTCCAG AGGCCACAAG GAGTTTTAAG CCCTGAGCCC TGGATTCTGT 1020
CCAAGCCACA AGGGGTTTTA TGCCCTGGGC TTAGATTGTG GTGTGGCAGG GCAGGTTTCC 1080
ACCCTTTGGC ACAGAGCTTG GTGTTCCAAA GGCCATGAGG GGTTTTAGAC CCTGGACCCC 1140
AGGCATGTTC CAAGACTGTT TTACATTATG TCAGCCATGC AAGCCCTGCC TCAGCCTTTT 1200
TCCCAATACT CAGCTTTTCT CGAACACCCC AGATGTCTTC TGTGAGACCT GGCTGGAGTT 1260
CTACAGCACC TCCTGCCTGC TACTATCCTA ACACTCTGTG GAGCAAACTC TATTCACTTG 1320
TTCTCCATCT TTTCCTTCTG GGCTCTGAGA GTCCAAACCT TGAGGTAGGT ACCATGACAC 1380
ATTGGGGTCT CCACTCACAG CCTGATGCCT GTAGATGATC AGCCACTGTG TAATGAATGA 1440
ACTCATTCTT CAATAAACCA GTGAATGATC ACATGAAAGA AACGGTCTAG TGGGACTCTC 1500
TGGCCACAAA TACTGAATCA CCTTCCTCTT CTTTACCATA GAAGAAGGGA GAATTTCTTT 1560
CTCAAAGACC AAACCCTAGA CTTCATAGTC TTTTTCTGTT TTTCTCCCCT ACAGGACTTC 1620
TACCCCTCAG GGTCTCCCAC AGAGCATTCT GTGGGCAACT AACCATCTAA TGTTATTTTT 1680
ATAGGGCCCA AGGGAGAAAT TCTTATACAT ACACACATGT GCGCGTGCAC ACACACACAC 1740
ACACACACAC ACAAACTCTG TGTGTGTGCA TGTATAAATG ATTTCAGTTA TGTACTGCTA 1800
CATAACAAAC CACCCCTAAT GTAAGTAGCA CAAAACAACC ATTTTATTTT GCATACAGAG 1860
TCTTTGAGTC AGGAAATTAG ACAGCAACTA GCAGGGGTGG CTAGCCTCTG CTCCCTGGTG 1920
TCTGAGACCT CAGCTGGAAA GACTTGAAAG CTGAGAATGA CTCAACAATT GGGGGCTAGA 1980
GTCATCCGGA GGCGTCTTCA CCCACATGTC TGGTGGTTTG GCTGGAACCT CAGCTGGGCT 2040
TTCAGCCCAA ACACCTACAC GTGGTCCCTC CATGTGTTCT CTCCACACGG GCTAGCTGGG 2100
CTTCATCAGA CTAGCTGGTA ACTGGGGTCC AAGGGAAGGT GTCCCGAGAA AGCAAAGCAC 2160
AAGTGCATGG CATTTTTATG ACCTGGCCTC AGAAGTCACA GAGCACCATA TGGCATCATA 2220
TGATATTGGT CAAGGTTACA GAGTTTTCCC AGGTTCAAGG CATGAGGAAG TGGGCAAGCT 2280
TCCTCTTTTT TTTTTTTTTT TTTTTTTTTT TTTTGTCAAG AGGGAGTCTC TCTCTGTTGC 2340
CCAGGCTGGA GTGCAGTGAC TAGATCTTAG CTCACTGCAA CCTCCACCTC CCGGGTTCAA 2400
GTGATTCTCC TGCCTCAGCC TCCTGAGTAG CTGGGACTAC AGGCGCATGC CACCACACCC 2460
TGCTAATTTT TGTATTTTTA GTAGAAATGG GGTTTCACCA TATTGGCCAG GCTGGTCTTG 2520
AACTCCTGAC CTTGTGATCC ACTCACCTCA GCCTCCCAAA GGCAAGCTTC TAGAACAGCA 2580
CATGGACAGA AGATATTGGT ATGTCACTTG GAAAACAGTC TGGCAAGCTC TTTTTTTCTT 2640
TTCTTTTCTT TTCTTTTTTT 2660
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