Tag | Content |
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EnhancerAtlas ID | HS133-29555 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:118150970-118153100 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ONECUT1 | MA0679.1 | chr7:118152979-118152993 | ATTATTGATTTATT | - | 6.36 | ONECUT2 | MA0756.1 | chr7:118152979-118152993 | ATTATTGATTTATT | - | 6.53 | ONECUT3 | MA0757.1 | chr7:118152979-118152993 | ATTATTGATTTATT | - | 6.82 | TBX21 | MA0690.1 | chr7:118152915-118152925 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr7:118152915-118152926 | AAGGTGTGAAA | + | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 118151968 | 118152121 | chr7 | 118151130 | 118151516 |
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Enhancer Sequence | TTTGGTTTTC TTTTTTTGAG ATGGAGTCTC ACTGTATCTC TCAGGCTGGA GTGCACTGGC 60 ACAATCTCGG CTCACTGTAG CCTCCGCCTC CTGGGTTCAA GTGATCATCT TGCCTCAGCC 120 TCCCGAGTAG CTGGGATTAC AGACACGCAC CACCCTGCCT GGCTAATTTT TCTATATTTA 180 GTACACACTG GGTTTTACCA TGTTGGCCAG GATGGTGTTG ATCTCCTGAC CTAGTAATCC 240 ACCCACTTCA GCCTCCCAAT GTGCTGAGAT TACAGGCATG AGCCACCATG CCTGGCACTA 300 TCTTTCATAT TTTAAAAATC TTTTTACCCC ATATCATCCT TCAGCTACCA TCCTATTTCT 360 ATGCTCTCCT TTATGGCAAA CCTCTTTGAA AGAGCTCTTT GTTCCCGTTG TCTTTTCCCT 420 TTCTCCCCGA GACAGCCCTT GGATGTAATC ATGAGTCATG TGAAGTGACA CTGCAGCAAT 480 ATTGACAGTC CTTTAAATTG TGCATATAGA TATTTACTTT TTCCATAAGA TTCTTTATTC 540 TTATCATCTT GATTAATGCT TTTATCTGCA GTGAATTTGT TAGCAAGTTA ATGTACTCTT 600 GTCAATAAAA TGGAAGATCA CATGAACTTT TCCCTCCCCA TTAATTGTTT CCCATCATTA 660 CAGACGTTGG GTAAAATTAG AAGTATTTAT ACTATTTAAA TAATGCCTAA ACTATTATTT 720 TTAAGTGTTA CAGATAAACT GCTTATAGTC CACAACTGTT ATGATTATCT TAATGAATGA 780 ATCATGGGCT CTGAAACATG GGAATAACTT ATAATTGAGA AATAATATTG ATCATACCAC 840 TGCACTCCAG CCTGGGTGAC AGAGCAAGAT TCCATCTCAA AAAAAATTAT AATATTAATG 900 TTCAAGGAGC TCAAATTCTA TTGGCAAAAT TCAGGATAGA AATCCTCACT AGAGATAAAA 960 ATTTTTGAGT AATCATCATA TGAATAGTCC ATTGTTCAAA GATTGTTTGT TGACTTGTCT 1020 CTCCTTGTAT ATTGGTTGGA AATAAAATCA GTCCCTTGCA TACATCAGTC TCTCTCTGAG 1080 ACTTTTCTAG TCCGTTGGGA AAAAATGTGA ATTCCTCTAT TAATAACACA TTGTTTAAAG 1140 GCAAACAGTT TTGATATTTC CTGATAAATG GAGGAACAAA TAAAGAAACA GTAGGTTATA 1200 AAATTACTAT TGTTATATTA TCATCTATAT ATTAATAGTT TTTCTTTGTT TATATATGTG 1260 GACCTTTGAA ATCATGTAAC TCTTGTTTTC ATATAGGTGT GCTGAAGCCC TATCCCCAAG 1320 ATGACTATAT TTGGAGACAG GATTTTTGGA GGTAATTAAG GTCCTAATAG TAGGGTCCTG 1380 GTTCTATAGA ATTGGTAGCC TTATAAGAAG AAGAGAAAGA GCAATATTTC TCTCTCCATG 1440 TGCATGAACT GAGGAAAGGC CATGTGAGCC ACACAGTGAG GAGAATGGCA CTCTGCAAGC 1500 CAGAAAATGA GCCCTCACCA GAATCCAGGC ATCCTGGAAC CCTGATCTTT AACTTCTAGC 1560 CATTGGAACC AACAGAAAAT AAATTTCTGT TGTTTAAACC ACATACTCGG CTGGGAGCAG 1620 TGGCTCACAC TTGTAATCCC AGCACTTTGG GAGGATGAGG TGGGCAGATC ACTTGAGGAC 1680 AGGAGTTCGA GACCAGCCTG GTCAACAGGC GAATCCCATC TCTACTAAAA ACACAAAAAT 1740 TAGCTGAGTG TGGAGGTGCA TACCTGTAGT CCTAGCTACT CAGGGGGCTG AGGCTGGAGA 1800 ATCACTTGAG CCCGGGAGGC TGCAGTTGCA GTGAGCCAAG ATCATGACAC GATACTCCAG 1860 CCTGGGTGAC AGAGCGAGAC TCTGTCTAGA AAACAAAACC AAACCAAACA CCTACTCTAT 1920 GGTATTTTCT ATGTCAGCAT AAGACAAGGT GTGAAAATGG GATATAACTT TATTTTTTTC 1980 CAAATTGATG AACCGTCATA TCAGTATTAA TTATTGATTT ATTTGGCTCT TTGTTTTTCT 2040 TTTACAAAAT TGCCTCACAT ACTAAACAAT ATTTATTATA CTGTTTTAAC CTTAAAATGA 2100 GCTTGCTATT TAGGCAAGTT CTTTTTGGGG 2130
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