| Tag | Content |
|---|
EnhancerAtlas ID | HS133-25986 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr5:178068660-178070390 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr5:178069575-178069585 | GCTAATCCCC | + | 6.02 | | Stat6 | MA0520.1 | chr5:178069835-178069850 | TTTTTCCTGAGAACT | + | 7.26 | | TFAP2C | MA0524.2 | chr5:178069693-178069705 | TGCCCCAGGGCA | - | 6.44 | | TFAP2C | MA0524.2 | chr5:178069693-178069705 | TGCCCCAGGGCA | + | 7.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I178641 | chr5 | 178068881 | 178070273 |
|
Enhancer Sequence | GGGATCTTGA CTCTTTTTCT TGCCTTCTAA TCTCTCGGCA CAAGACGCTC AAATGAATGG 60
GCAACAGGTC AGCTGTAGCT TGAAGTTTAA TGGGACATTT TCTGTGTCTT TCTGCATCGT 120
CCCTCTGAGA CCTGAGACCT CTCAACCCAC AGAGTGTAGA ATTGTGGGGA AACAAAGCAC 180
AGACTCTCCT CGTGGTGTTT TTGCCACATC ACAGATATCT CTAATACTGT AGGGTCTTCC 240
AGATTTTATA GCCCAAGGGA CAGGGCTGTG TACACCAAAG CTGAGACCTG CTCCGTAGTC 300
ATTTCCCGCT CTGGGTCTCA ATCCCGAGTA GCTTCTCCTA TGGTCATGGC TGGCCTCAGA 360
GGACGGCCCC CACTGAGCTT CTCGGTTATG CTGGTGACCT TCTCATCGGC ACTTTCCTTA 420
TCTCCTTGAA GGATGGAGCC TCTTCGAGGC CCTCTCACAA GGCAGAGTCA GCTGATGAGT 480
AGAGCACACC CTCTAGCATA TCTCCTTCTG GGTCTTATGT TCCCCTCATC TGCCATTTTC 540
CACAGCATTT GCAGCATTTG CACTTCCTGC AGGGTGACAG GCACTTTCCC CAGGCTTCAT 600
CTGTAGCAGC ACGTTAGCTT TGTCTCCCAG GGGCCTTGCC TCGGTGTTAG ATCCTGTGTC 660
ACAGCAGAGG GCTCCCGTAT CAATAAACTC GCCCTCCCAG GCTTCTGTTG CACAGCTCTC 720
AATGAGCACC TTTGGGATCC AGCCCATGTT TCCTCTTTCA GCTCCTGCCA GTGCTGTGAA 780
GCAAGTTCAC TGTGCTCTAG TTACCACACT GTCTGAATCT GGTAAGACAG AACACCCACA 840
TATAAATTAC ATGAAGAGGG TTTGTTACTT ACTCATAGGA AGCAAGGGAC AACGGAAGCC 900
CAGGATTCAT TGGAAGCTAA TCCCCAGGGC TCAGGAAAGC CCCCTGAGGT TGGATTGGAG 960
TCTTGCTGTG GTGTGTATGC TCCACTTGGA CTGCAGCCAA AGGGCCATGG AAGAAAGTGC 1020
AACCTGGGTT TTATGCCCCA GGGCAACATG ACTCACTGGA ATAAGGCATT GAAGGACATC 1080
CTGTTTCTGG GGTAGGGGGG ACTGGAACAG AGCCCAGGCC TTTCCAGCCA GCTTCTCCTT 1140
ATCTCACATT GTTGTGTTCC CAGCACATTC TATGGTTTTT CCTGAGAACT GCAAGTAAGA 1200
AAGAGGAGAG AACTGGGTTG GTCCAAGGCC ATCTGCAGAA CTGTCCTGCA AGTACTTGTT 1260
GGCAAGGTCC TGCAGTTCCT TTGCCTACGG TTCTTTCCTT CCCTTAAGAG GCCCAGCACT 1320
TGCCTGGCCA GATTATGTTG TAGCTTGACC CTAGTTACTG GTCTTGGGAC TGGGGAAGAG 1380
GGGATTGATC CTGAGAAGGG TGCATGCTTT CCTTTAAAGC AGAAGCCTCC AGATCTTCTT 1440
TACATCTTCA AGCATGGAAG CAGCACTGAC CTTTAACAGG GAAGAACGGG CCACTTCTGC 1500
AGACCCAGGA GGTTCAGAGC AATCTAATAA TGCAAGATTT TTTAGTGCGT CAACACAGAT 1560
ATCCCTATTT CCAGTGTCAG GCTCCTATTC CTTCCCAATT AGGATCCTGA CTTTGGCATA 1620
GTAAACCTAC TGGAGTTGAG CATCCAACCT TCTCTGGAAT TCTACTATTC TTATGTCTAA 1680
GTCCTGTGAG TACTTGCCAT GTTCTCTTTC TTGGCTTAGT GATTGCTTTT 1730
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