| Tag | Content |
|---|
EnhancerAtlas ID | HS133-27281 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr6:106441800-106443230 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr6:106442842-106442853 | GAGAGGATTAG | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 106442094 | 106442641 | | chr6 | 106442778 | 106443178 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH06I105991 | chr6 | 106439475 | 106446468 |
| Enhancer Sequence | ACTTGGAAGG GTAAATGAAT TGCAGAGTCG GATACAGCTA ATTTGGGGGA ATGTAAGCTG 60
GATGTCTTTT CCTAATTTAT GAAACGTGAA CGGGGGTAAG GTATTTATTT GTACGCTAGT 120
TGAAGTGGGG CAGGAGCACT GATTCCTGGA CAGTCACTCA AAAGCTGCGC CCAAAGTTTT 180
AAAAAGCGCG GGGACGGTGG AGAGGGAGGC GAAGAGCCCG CGCTGCTGGG CTGGGCTCGG 240
GTGCCGCGCT GGGGACGCCG CATCTACTGA GCGGTCGCCG AAGACGCCGG GAGGCGAGGG 300
GCGAGGTAAG ACGCCGCCTA AAGAGGCCCG GGCTCTCCCC CGGGGTCGTT GTTGGAAAAG 360
CAAATTCCAC GGTGAACTCT ACCAAGCTCA GCGCGTACAC AGCTAGCGGC TCTGGATTGG 420
ACTGCATTCG CCTAAATTGC GTAATTAAAA AAAAAAAATA CACCACTGCC ACCCTACAGC 480
GACGCTTCCG CTGGAAGACG AGCGGGGACG CGTGACAGCG CGGGGATAGC TTTTCTATTA 540
CGTTTCTTGT TCTCCGAGCT CGAGCCCCCT TTTAAAAAGT CGCTCACCAA AAACGGGGTG 600
GGGGATGGAG GTGGGGACGA GAAGTTTCCG AATGCTGAGT TCATTTGGAC GAGGTGAGGA 660
GAACTAGGGT CCTAACAGCA GGTCCAGAGG ACTCTCGAGA TAGGTTTAGA GCCCGTCCTT 720
TTGTCTGGAG TGTCGCGGGA CTCCAGAAGT GGGTTGTGCA AGACAAACTT CCAGATAAAT 780
CTTTGCCCGG ATCCTCCTGC GGTCAAAGCA TCAGTCCTGC CCGTAACTTC CTAACGACAT 840
CTTCTTGGAG CAGATTCCGC GGCGGGGATG GCTGGGTGTG CAAACCGAAA ACAGTTTGTC 900
AGCCCTCCAG TCCCGCCGCG TCGGGAATGC GAGCCCGGCC ACGCGGTCCG ACCGGGTCCG 960
GGGACGGCGC GCTTGTCGCG GGAGCCTCCC GGCTTGCGGA GGGCTTGAGT TTTTTGGCGG 1020
AGACAGAGGA AAGCCTCTGG TCGAGAGGAT TAGAGCGCGC GTTTTCTCCG CCGAGCACGC 1080
TGCCCGACGC CGTCGCAGCC GCGCACTTCC CGGTTTTGAA AGCCAGAGAG ATGAGTCAAG 1140
CGCAAAAGCT CCGGAGTGAC AATGCGAGCT TTTGGCCAGC CTCATCCTCC TCCCCATTCC 1200
CTTGCCTTCT TTTAGGTCTT CGGTTCGTGA CAAGTGCATA GGTTAGGCTT GCACGGAAGA 1260
GGGTCGGGGC AGGTGCCAGC TCAGGGCACC TACCCGGCGT TGTCACGTTC CCTTTGGGAT 1320
CAATGATCTT TCATAACTAG GCTGGGCATG TTCGTGCAGC CCTCTGGGCA CTCTGGGGGA 1380
CGTTCTCATA AGGCTTTTTT TCTTTTCTTT TCTACCTTTT AACAGAACCT 1430
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