| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00168 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:6398140-6399490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr1:6398642-6398655 | GAATGTTCTAGAT | - | 6.03 | | RFX1 | MA0509.2 | chr1:6398961-6398977 | GGTTTCCATGGTTACC | - | 6.24 | | RFX1 | MA0509.2 | chr1:6398961-6398977 | GGTTTCCATGGTTACC | + | 6.26 | | RFX2 | MA0600.2 | chr1:6398961-6398977 | GGTTTCCATGGTTACC | + | 6.41 | | RFX2 | MA0600.2 | chr1:6398961-6398977 | GGTTTCCATGGTTACC | - | 6.5 |
|
| | 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 |
| GH01I006338 | chr1 | 6398431 | 6399551 |
|
Enhancer Sequence | GGCTTTCATG GCAGAAAATC TGCAAAGCAG ATCCCTTCCT GGCATTTTTG AAGCCACCAA 60
CTCCTGCAAT GACAAAGGGC ACTGCTGACT GGGCCCTCAC AAGCAGGAAG GTCCTAGGAA 120
GCAGGAGAGC GCGGCAGGCC ATCCCTCCTC TCCAGGAAGG GGCCAAGGCT CCACCCCCAG 180
CACAGTCGGA GAAGAGCTGC GATCTCACAG GAGATGGCAG GGAACCCCCA AGGCCCCTAA 240
AGTGGGGAAC CCACCCAGCC CTGAGCCTCT CCCGAGTCGT GGGCGCTGCT CCTGTTGTGG 300
GAGGTGCCCA TACACCCCTT CCTGGGCCAC ATCCTGAGAC CAGCATCCAG GGTCCCTCTG 360
ATGTCAGAGG TGCCTGCTGA GGGAGCAGCA GGCAATGGGA ACGCAGACCA CCTTCCACCC 420
CAGGCCCTTG CTCAGCTCCA TCTGCCCACC TGCCGGAGCT GGGCTGACAC AGCCATTCTA 480
ATCAACCCTG CTGAGGTCCT CAGAATGTTC TAGATGCATA ATCGTGCTTG CTACCGGCCC 540
GTCATGAGGA AGAGGACTCA AGCCCCTCAA ATGGCTGTGA GCTGGCACTC CACGGGGCAG 600
CCACTGCTGA GGAACAGGCA TGGGGAAGAG GAGGAAACCG GCCCAGCCTC TCTGCATGGG 660
AGGACTGGTG ACCTGGGAGG TGGCAGGGAG AGGACCAGGG GCAGGGGAAG AGGCCCGCCT 720
TCCCCCTCAC CTCCCGTCCC CAGCCTGGGT ATAAAAAGAA GCGTGAGCTG GTGAACACTG 780
GAGCCGCCCC CTCCTGCAGC GCCCAGTGGG AAGGGGAAGG GGGTTTCCAT GGTTACCATG 840
GCCAAGGAGG AGAATATTCA GATGAAAGCA GAGGCAAAGG TTCACCCAGT GAGCTTCCAT 900
CTGAGCCTGG TTTCTGGGGC TCCCAGGAGC AAGCACTGTC CTCTCTGGAG CCAACACCTC 960
CCTACGCTTG AGGAGGGCAA GCAGGGCAGG GAGACCTGCA GAGGGGTGGA TGGTGCGTAC 1020
CGGCCTCACA GCCCGCGCCC AGCCCCTGCC ATGGATGAGC TGGCCACGGG CAGCAGGACA 1080
GGCAGCATGA TGTGCTCAGG CCGGACCCAG ACAGCAGGGT TGAGTCCTGC TCTGGGTAAC 1140
TGAACTCGTT TCCTAACCCC TCTGTGCCCC TTTCCTGTCT GCAAAATCAG GGCAATGGAC 1200
ATAGCTGCTC CCAGGGCCAT GGTGGGAGGT GAGAGAGGTC TCATTGGTGG AAAAGGGGCC 1260
AGGCCCTGGA GCGTCCTCTG CCCTCAGGAG GGAAGCAGCT GTGTAGCCAC GGCCCTTACT 1320
GCTCCAGTCA ACACTGTCGC TCCCAGAAGT 1350
|
