| Tag | Content |
|---|
EnhancerAtlas ID | HS133-09377 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr14:67797720-67799490 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mecom | MA0029.1 | chr14:67799230-67799244 | GAGATAAGACAAAA | + | 6.11 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 67798772 | 67799184 | | chr14 | 67798477 | 67798770 |
| Enhancer Sequence | TCTGATTGTA TTTATTCTAC TTAAGTTTTT TTCTCCTGTG ATATTTCTTT CTTTTTTTTG 60
AGACAGAGTC TCACTCTGTC GCCCAGGCTG GAGTGCAGTG GCACAATCTT GGTTCACTGC 120
AACCTCTGCT TCCTGGGTTT AAGTGATTCT CATGCCTCAG CCTCCCAAGT AGCTGGGATT 180
ACAGATGTGC ACCATCACGC CTGGCTATTT TTTGTATTTT TAATAGAGAC GGGGTTTTGC 240
CCTGTTGGCC AGGCTGGTCT CAAGCTCCCG GCCCCATGTG ATCCACCTAC CTTGGCCTCC 300
CAAAGTGCTG AGATTACAGG CGGGGGAGCC CCTGCGCTGG TATTGGTATT TCTAATAGTG 360
CTTTATTACT CAATGATAGA AGTGCTGAAG TAAAACAGAT TTTCAATTTT AACTCTATAA 420
AATTGTGCTA AGAAAATGAT GGCGTTACAA AATGTAACCA ACCGGTTATC TAGTTGCATT 480
CTGAATCTCT GAATCTGTTC TGCTAGTATG AAGGCTTGAG AGTGGCTATC TAGCAGTATG 540
AACTTATTGT CAGTTTTGCC TAGTTCAGCT AAAAATTTTG AGCTAAAACA TTTTGTTTCA 600
TCTTAGTCGT GGATTGTAAT TTGAAAGAGA ACTTCAGACA TGAAGTACTA AATAAGTGAT 660
ATAAGCCATT TTGGCACAAA ATGGAATAAC AATGCCTTAA ATTTGATAAA AACTAGGTGG 720
ATTCGGGCTT TATCATTTTC ATTTCAACTC CAATACCACA AAGTTTCAGT TCTCTGTGGA 780
GTCCTAGAAT GTTCTTCCAA TAATCTTGAG CTTACGGTAG ACATAAGTTT TAGCAAAAAT 840
GTCAGTGTGT TCAGTTACAG TGGTGAAGTA GATTCCCTGC TGGGAACAAA GGATTCTGTG 900
TGCCATATTC AGATGTACAA CATTCCAGAA TGAGAGTCAT GCAAGAAACT GCCTCAGGAC 960
AAGCCAGAGT TGTCATATTT TTAATATGTT TTCTTACTGT TACAGAAGTT CAAACAGTTG 1020
AATGATATAA ATTGTTTTGT ACTATGGGTC CAATATAGTA TTGATGTGTG ACTTTTATAT 1080
CTGAGACATT TTGTCTTGAG TTTAAGTTAG TTGTCTTCAT TGGCAGGGGT GATTTGAGGT 1140
GAGTTTCACT TTCTTGAACC CATGTGCCTG ATAATTAGAG GGTTCAGGAT AAGTTTTGCA 1200
CATAGCCTTG CTGCCTGCTT ATCTTTGTAA AATGGCCCTT TCCTTCAGTC AGTATTTTAA 1260
AGTAGGCTAC TCTATATAGT TTCCCAAACT CTGGTAGGAT ACTTTTAACT CTCTGCAGCA 1320
GATAGTATAG GGCAAGGGCT CTTTACTAGA GCCAAAAGTA AATGGCATTT TAGGTCCTTG 1380
CTCCAACCAG AAAGGTTCAC TCCATATTAC AGATGTTACT ATTAGGAAGA GGTTATAGTG 1440
TCTAGAATGT TTGAAAACAA ATGTTTGTAG GGAAACAGTG TGTGTTCTTG AAGCTTGTAG 1500
TTTTGTTGGT GAGATAAGAC AAAATATGTG AAAACCTAAA TAGTGGTATA AAACAGGATA 1560
TATTGAGTCC CAGATGGTTC ATAATATGAG TCGTGAAGAT GCCAAAGCAA AGGTAACCAT 1620
TGTGGCCGTG ACAGGGTTGG AAAGGAGCTC CTGAGGTTGG GAGAGACAGA AGGAAAGCTA 1680
TGAAGGTCGC TCCTTGTTCT TTGGCCATCT CTGACTCATC CTATATTATT TGGTTAGGAA 1740
AGGAATTATC TCACAGTTTT TATCTTCTGT 1770
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