| Tag | Content |
|---|
EnhancerAtlas ID | HS133-07120 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:19182720-19185160 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:19185125-19185146 | AATCCAAAAGTGAAAGTCCAA | - | 6.34 | | NFIC | MA0161.2 | chr12:19183544-19183555 | TACTTGGCATA | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_36311 | chr12:19182093-19185438 | HMEC |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I019029 | chr12 | 19182665 | 19185224 |
|
Enhancer Sequence | GCTTTCTCCC CATCTCCACT GTCAGAATAG CAGTTCTCTG TCCCCATCAG GATACCTCAG 60
AGATCCTGGA CTTCATATTC AAAAGAACAG ATGGGAAGCA GTCACTGTAG ACCCTTCATC 120
TTAATTGTCT CAACAGATTT TGGCAGTGTG TTGTTTTCTC TATGATCATT TCTACAGAAG 180
CAAATTCTGT CAATCACCTA GATGTTTTTA GTATGCATAA GGTTGCCATG CCTTTGCCTG 240
TGTCTTATTA TCCACAAACA TGAGGTCTTT TGATATCACA CTTTCATCTA TTCAATCATT 300
CGTTCATCCA AACAATAATC CTAAATGAGC TCCTACTATG TACCAGATGC TTACTATTGC 360
ATTTTGTAAA ATTATTTTTC TGCTATGCAT GATTTCCCTA CTTAGAGATC AGAGCAAAGA 420
AATCCTGTGC AAATGTTCTG CCCAAAACTC TGGGAGGTGA AACCTCGCAG AGGCTCTCTG 480
CACTTCTGAC AGGAGGTCAG CAAGACAAAG GACTGTTTGG GATGCCAAGA ACAGAGAGGA 540
CCTGAGGCAA AACCACCGGG CAGAATTGTG TGGAAGGCTT TCAAGTTTTC CTGTGCCTTT 600
GCATGTCTAC AACATATTTT GAAATCTTTC AGCATAACCA ATGTAATATT ATATAGATTT 660
TGGTTTCAGT TGTAACCCAA GGTTCGGTTA GGTACCCAGA TCACGAACTA AAATCTCAGG 720
AGTAGTCAGC TGGCATTCCA ATCAGAAAGC TCACACTTCA GAGACAGTCA ATATGAACAT 780
ACACTTTCTG CTATTCATGT CTCCATCAAT ATTAGAAGCT TTTCTACTTG GCATAATAAA 840
TGTTAAAAAT GGGGTGTCAT TGTGGAAATT AGTGAACTTC AAGATAACTT GTTCAATGAA 900
CAGAATGAGA AAATCCACCC AGATTTATAA TCTGTCTCCT TAAGGATAAC ACCTGAAAAC 960
TTCACCCTTA AATGAACCTG TGTCCAATCA TTGAGTCAGA AAATTCCTGC TTTCCTGATG 1020
CCAACTTATG GGCACAGGAT TCTGCTGCCT CTGGCTATTG TTGCATTCAA GTAAATACTT 1080
CATGTAAACT TTTCATACAA AGAAGTAGTT GGAGCACCCA AAGAACAGAG AGCTAGGACT 1140
TCATTAATCT TACAGAACAG TTAGTATAAA TATTTTGGGG TCTGCTCACT ATTAAGTATT 1200
TTTTTCAGTA AGGTCTGTAT TTGTGGCATA ATTTTTGGAG AGTGACACTA TTTCATGGTT 1260
GTTACTACTG TATACTAAAA TAATCTAAGG CTGTGCAAAA CCAAACTGGT TTAGGTTAAC 1320
AACAGCCCCC ATGGAAGGCA CAGAATTAGT TGACGGAATG AAGACCTCTG AAGGAATTTT 1380
GTGGTCATGA CAAGGGCGTG GTGCTCCATA AGGACCTTGA GTCATACAGC TGGGGATTAG 1440
TAAGAACATA AGTATTTCAA TGGAAACTAC TGGAAAGCAG GGACTAAGTC TGGAAACCAC 1500
ACAGGACAAT CTCACAGATG ACAGCGTGTA CAACTACTGA CCATGGCCCG GGTACCTCCT 1560
ACTTCCCTGG GGCCATGAGG TTAGTTAAAT TCAGTGAGGG AAAATGAAGT GAAGGACTGC 1620
CAGAAATTGA CTAAAATTAT GGTTACTTCC ATTAGGAAGA ATAGAGTCTC TAGAGAGATA 1680
TCAAATTGGA ATTTAAAAAA CATTTTAATA ATTTTCCTTC CTTACATATC TAAGTCTTGG 1740
GTTTTGAGGA ATTCATACTC ACTATATTCC ATGCAAGGAA GAAAAATTCT GTCTCTCTTC 1800
ATGTTTATCT AAAATACCTT TTATTTTAAG GCTTAACACT AACGGTTACA TTTTCTCCTC 1860
CAGTAGCTCT TCAGAAGTGA CTTCATGAGA ATCTTTTTAG TGACCCAAAG TCTGGTCCAA 1920
CAATCAAGAG AATATTAATG TCTTTTATAT TAGTCCATTT TTACACTGCT TTAAAGAACT 1980
ACCTGAGACT GGGTAATTTA TAAAGAAAGG AGGTTTCATT GAATCACAGT TCTGCATGGC 2040
TGGGGAGGCC TCAGGAGATT TACAATCTTG GGGGAAGGCA AAGGGGAAGC AAGCACATCT 2100
TACATGGCTG CAGGAAGCAG TGGGGGGAAC TGCCAAACAC TTTTAAACCA TCAGATCTCA 2160
TGAGAACACA CTCACTATCA TGAGAACGGC ATGGGAGAAA CTGCCCCTAT GATCCAATCA 2220
CCTCCCACCA GGTCCCTTCC TCTATACCTG GGGATTACAG TTCAAGATGA GATTTGGGTG 2280
GGGACACAGA ACCAAACCAC ATCATCCCAC CCCTAGTGCC TCCAAAATCT CATGTCCTTC 2340
TCACATTTCA AAACACAATG ATGCCTTCCC AACAGTCCCC CAGAGTCTTA ACTCATTTCA 2400
GCATTAATCC AAAAGTGAAA GTCCAAAGTC TCATCGAGGC 2440
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