| Tag | Content |
|---|
EnhancerAtlas ID | HS133-01726 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:64104470-64106950 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr1:64106096-64106109 | GAAGATTCCAGAA | - | 6.2 | | HSF1 | MA0486.2 | chr1:64106101-64106114 | TTCCAGAACATTC | + | 6.62 | | MNX1 | MA0707.1 | chr1:64106707-64106717 | GGTAATTAAA | + | 6.02 | | Sox3 | MA0514.1 | chr1:64105899-64105909 | CCTTTGTTTT | + | 6.02 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I063638 | chr1 | 64103737 | 64104505 | | GH01I063639 | chr1 | 64105135 | 64109949 |
|
Enhancer Sequence | GGTAAGTCAC ACTCCTGTGC TAGCATTTTC CTCCCTGTAA CCACTATTTC CAGTAAAAGC 60
TTAGACTGCT AAGGTAGCAC TGAAATACCA ACGGTAGCCG ATGTGTCCTA AATCAAGGCA 120
CAAATTATTT ATAACAACCC TGATGAAATG TGCACATTTG AAAAGGGGTG AGCACATTCA 180
GCCAGAAAGG CTAATTTTAC TTTCAGAGGA TCATATCGAC TCAGACAGGA AGTTGGGGGG 240
CCTCCTCAGC AGCGTGGTCA TTGAGTCTGC AGGGATTAAA CAGAGCGATA AACAGATTTT 300
TCTTCCTTCG GTGGTCAAAG AAACCTTTAT AAATGTTTTC ATTTCTGAGA AGAAATACGG 360
TGGAGCAAGT CGGTTTTTTG TTTTTATTTA AGAAGAGGTT TCAGCACAGC ATTAAATCTT 420
TCTCTTTTAT AGGCCCAAGT TTTCTATAGC AGAGTAATCA AGGCTAAATG AAGGAAGACC 480
ATGAGGGTGG AACTAAGTTG CTAGGTGATC AAGAAATTAA AAATACATCG TTGTGCCTGA 540
GGATGTTTGT GTAATTGTAT TAATATTAGA GTGAAAGAAG GGTACATAGT ATTCTCAGGG 600
GATGACCCCA GACCTATAGA CCTCACTCTC TGCGCTCTCC TTCCTCCTCT CTGCTTGTCC 660
AAATATTGAC CCGAACTCCC ACCTCCTTCA CGACCTTCTC TGCTACCTCA TGCTGCCTGT 720
ATCAGTCTCT CTTTCCTAAA AGTCTGTTCA GGTGTGTGGC CCTGTCCCAT GTATCAGTCT 780
CCGGCCAGGT TATAAGGTAG TTAAGTGACT GCATCTCTTC TCCTTTTATT CCCTCTACCC 840
AATATTTTTA AGTAAATGTG CTGATCTTGG TCCTATAGTA CTCTACTGTC ACCCTTTAGT 900
GAAGAAAAGA AGATCAAAAT CAAGCATTCT CTCAGCTTTG CAATTGAGTT GCAATTCATG 960
CCAGGTTAAA CAGAACAGAA TACTGACTTC ATTTCCTTTC CTATAAGTCT GGAGGTAGAG 1020
CAGGTAGAAT GAGCTGCTAA ATTGGAGGCA CATATTTACA GAGTTCTAAG CAACTTGATA 1080
TTTTCGAGAG TGGTAATATT CCTTGGCAAT GAACTGCCTT GATAGAATTG GAAGGTATGA 1140
AGAAGGCTGG ATGAGTCTTG GGGTTGAACA ACTTCCACAA CAAAGGCTAG ACAGTTTCCC 1200
AAAGTTGTGG GTGTTTAAAT CAGAGATTAC AAGGCCACTG CTTAGTCCTT TTCTACTTCA 1260
TATAATGGGC ATGGTGCCAT GCTATTCTGA GGGATACTAC ATGAGTGCCC AATGAGCCTA 1320
TGAGGTGGTC TTCTCCCATG AAACTCCCCA CAGGGTCATC TAGTTCAGGC CTGGCTTCAG 1380
TCATTCTTTA TGAATGAAGA TGTCTTTGAA GGCAGCAACT GTGTCAAAAC CTTTGTTTTC 1440
CTGTTCTCCT GTACCAGTAT CAGTGTTGAG CCTAGTGAAA AGATAAAAGT CTAGAGTCAG 1500
GTTTCCCAGA GCATGTGAGT ATGTGGAAGA ATACTAGTTC CATGAGAGGG TTCTAGGGGT 1560
CAAGAAAAAT TGGAAAAATT GGACCACACT TCTCTGTTTT GGATATTCAC AATGATATTA 1620
GCATTTGAAG ATTCCAGAAC ATTCTGCCAT AAAGAATCCT GTTAGTACAG TTTTGCCTAA 1680
ATATAGTTTA CCACTATATA TAATAATTAT GATGATATGA TACAATATCA TCACCACAAT 1740
AATGATTATT ATTATTATCA TTTCGTAGTA TGTACAGTAA CTTCTTTTTC CACAGACCCA 1800
TGTGGGAAGC CTTGGTCAAG AGGGATCAGA GCCCCAGAGC CAAGTAGGAA TCCCTGGTGC 1860
TGACCCACAG GGAACAGGCC TGAAGACAGG ATAGCACAAG CTGCTCCTCT TACACAACAG 1920
GCCTTCAAAT ACAAGAAGCA GCTCTCAGGT CCTTCCTTCT TCAGGCCGTC CATCTTTGTT 1980
TCCTCCAGTC ATTCCTCATT TCACATTGTT TATAGACTCA GTGCCAGACT CTAGGTGCTT 2040
CTGAGTTTGC CAGTGCCACT CTTAGAAGGT GATGCCCAGA ACTGAGCCCA AATCTTCCAG 2100
GGTTGGCCTG GCAAGTGAAG AGTGGGGTGG GATGATTATT TCTAGTGATT AGGACACTGT 2160
ATTTTTCTTG ACATAACTTT CCTTTATGTT AGTTTTTAGG AAGTTGCATA ATACTGTTTA 2220
GCCCACATAA GGTTGTGGGT AATTAAACCC TTAAAGTTTT TACCTAGAAC TATTTGCCAA 2280
GGGAAGTCTC TCATGTTATG TTTGTGGAAT TGATTTCTTT GAACCAAAGT ATTAGACTTT 2340
AGACTATTGT TAAAGTTTGT TCTCATTTAT TAACACATTC AACAAATACC TAGTACCAAT 2400
CATGGTTTTA GCTTCTCCTT GGTATATTTC ATGTCCAAAG AGAGAATGCT CTTCATTATC 2460
ATGAGGATAA TCACAAGCTC 2480
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