| Tag | Content |
|---|
EnhancerAtlas ID | HS133-09731 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr14:104042480-104043990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr14:104043866-104043877 | ATATTTACATA | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 104043691 | 104043827 | | chr14 | 104042726 | 104043413 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I103576 | chr14 | 104042351 | 104043998 |
|
Enhancer Sequence | AAAAATACAA AAATTAGCTG GTCGTGGTGG CACTTGCCTG TAATCCCAGC TACTCAGGAG 60
ACTGAGGCAG GAGAATCACT TGAACCCAGG AGGCGGAGGT TGCGGTGAGC CGAGATTGCG 120
CCACTGCACT CCAGCCTGGG TGACAGAGCG AGACTCTGTC TCAAAAAAAT AAAAAAAGAA 180
AGTCGATTGT TTATGGATTA AAGAGTTAGA TACATAGTTC GCAGCTGTAG AGCATCTAAT 240
AGGATATAAC AGACTCACCA TTATCTGGAG GAATGATACC GTCCTGAGCT TGAGGGTGAA 300
GACAGAGATA TTCAAGAACA TAAAAGCTGA AAACGTCTGT GTTAAGACTC CTTTTGATCC 360
AGGTTTCTGG ACAGGAGAGT TTGCTGAGCA TATGTGGAGG TGGCTCAGTA CCCAGAGGCG 420
GGTGGAGCTG GCCCCAGTCA TGGCCTGTGC TCAGACGCTA GGACCAGAGC AATTTCTTCC 480
TCATGTTTAA ACTTTTCTCC TAGGCCACTG CCTTACCTTT CTCATGCTAT AAACTGGCTT 540
TCTCTGCCTC CTTGTTTATC CCTCCTAAGT TCAAAGAAGC AGTCAGCTGA GGAGGCTGCC 600
TTTCCTCAGG CTGGCTCCAG CCCGGTTGGG AGGTGCCCGG ATTAGCTGAG GCAGAGGTGG 660
GGCTTGTGCA GAGAGCCTGG CTGCTGCCAT GGAGACGGGA GGAAGCAGGC AAAAGAGCAG 720
GCCTGCTGGC AAAGGATCAG AGGGCTGGGT AGGCGCAGGG ATCAGTGTCC CGGAAATGTG 780
AGGAAGGGCA AGTGCTGGCA GCAAAACAAC ATGGGCAATT TGGACTTCAG GAAAAGCTGC 840
CACAAATACT CAGAAATAAC ACACATTTAT AGACAAATAA CGTGACTACA AGAAGAAAAA 900
ATTGTTCAAA CTCTAAATTT TACAAGGCAT ATTTGTTTAT TTTTTTGAGA TGGAGTCTCA 960
CTCTGTCACC AGGCTGGAGT GCAGTGGCGT GATCTCGGCT CACTGCAGTC TCCACCTCCG 1020
GGTTCAAGCA ATTCTCCTGT CTCAGCCTTC CAAGTAGCTG GGATTATAGG CACCCGCCCC 1080
CACACCTGGC TAATTTGTGT GTGTGTGTGT GTTTCGTAGA CGGAGTTTCA CCATGTTGAC 1140
CAGGCTGGTC TCAAACTCCT GACCTCAAGT GATCTTCTCA TCTCAGTCTC CCAAAGTGGT 1200
GGGATTACAG GCATGAGCCA CCGCGCCCAG CCTACAGTGC ATATGCAACA AGAAGTCATC 1260
ATTTCATGCT TACTCAGTTC ATGGGGGAAT GTTTTCAGTC TTGAGACTCA GTGCTGGCGG 1320
AGTTACATCA AAGGTGGATG GCAGCAGAAA ATCCTCAGCC CCTTTTCCAG AAGAATTTAG 1380
CTACACATAT TTACATATAC CCCAGGAAGC AGGCAAATGA TGCTCATGAA TCATCTCTAA 1440
GAATTCATGT GAGAGCCAGG CTTGGTGGCT CATACCTGTA ATCCCACCAC TTTGTGAGGC 1500
TGAGGTGGGT 1510
|
