| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00085 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:2279360-2280920 |
Target genes | | Number: 33 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZEB1 | MA0103.3 | chr1:2280072-2280083 | CGCACCTGCGC | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTCACTCCAC ATCCTCGAGT GCATTTTACA AACCGGGAAG TTTTTCGCCT CACGTAACCC 60
AGCACAGCCG TCCCGGGGCA GGGCACGCCT CGGGGTCAGA CCCCAGCCTG GGCTTCCCCG 120
TGGCCCAGTG ATGTCCCTCG CAGGAAGGAG ATCAGCCTGG GACCACACAT TGCAGCGAGC 180
TCTCATTGTG TCTTCAGTCT CCGTCGGTCT GGAACATTCC CGGGCCTTTC CCTGACTGCC 240
ATGGTCCTGG CGTCTTCGAA GCTTCCAGGC CAGGCCTTTC AGGGAAGGTT CCCCCGTGTG 300
GCCGTGTCTG AGGTCTCATC ACAGAGAGAC CCGGGTTACG CATCTTTGGC AGGAGAGGCA 360
TGGATGCGAC GCTCATGCCT TTCATGGATG GCTCTGCTCA GCCCACGCTG CCAGGTGGGG 420
CAGGATTTTC ACTGACCCAG AACCAGTGGA GTCCACCGTG AGGCTGGTGG CGCGTCTCCG 480
TGGGGAGCTG ACTCCTCCTC CCTCTGCCCT CCATGGGGGA AGTGCCTCCA TCCTGCCCCA 540
GCCTGGATCC GCCGCTTCTC CAGGGAACCC CGGTTCTTTT CAGACGCGCA CCTGGGTACT 600
GTGTCCGCTC CTGCCTGCTG GGGAGCCGCT GCCCACGGGC CCTGCCAGAG CCGGAGAGTG 660
CACACACACG CATGCGCACA TACGTGCACC TAGGCAGGCA CGCACGCACA CACGCACCTG 720
CGCAGGCACG CACACACGCA CGCACACGCA CACCTGCGCA GGCACGCACA CACACGCACG 780
CACACGCACA CCTGCGCGGG CACGCACACG CACACCTGCG CGGGCACGCA CACACACGCA 840
CACCTGCGCA GGCACGCACA CACACGCACG CACACGCACT CCTGCGCGGG CACGCACACA 900
CACGCACGCA CACGCACACC TGCGCGGGCA CGCACAGTCA TGTGCACGCA CACACAGCCA 960
TGTGTACGCA GACATGCACA CAAACGCACA GGTTCACTTT CTATGATGCA AACCCCCAGT 1020
CCACACCCCT GAGTGCCAGC CCACGGGTTC CTTCTTGTCC CCACTTCTTT GTGTCCACAG 1080
GCCCTGCTGC ACCCCTCAGC ACAGGGACAC CCCATGGATG CTGCCTCCAT CACCCCCTCA 1140
GGCCCTGTGC TTGGGGGCTT CCCTGCTCCA TTGGGCCCAA CGCCCAGAGC AGGGGCTCGG 1200
AGACCCCGCT GGCCACCCCA CTTGGCAGGA CTTGATGGCT TTGGGACTGA ATTGTTCCAG 1260
GCGGGAAGGG GAGGGAAGAA CAGGAAAGAA CCTCAGAGAA GAGAAAAGGA CCTGTGGAGG 1320
AGGAGGGAAC CTGAAAGCTT AAGCTTTTAC CCAAAAGAGC AGCCACCTCC AAGGAGGCTG 1380
CTTAACCCCA AGGGAGGGGT GCTCCACCCG CCTGCCGACC AAAGAGCCCC TCAGCACCCA 1440
CAAGGCTGCC TGAAGGCAGA GAATTAGCCT TGCTCCCAGT CCCGGCCCCT CTGACATCCC 1500
TGCTTAGTTT TAGCCACACG CACATCCCGA AGTCTGAGTT CATTTCCATT TTCATCTACT 1560
|
