| Tag | Content |
|---|
EnhancerAtlas ID | HS133-02906 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:178499110-178500110 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr1:178499984-178499995 | TCCTTATCTCT | + | 6.02 | | SOX10 | MA0442.2 | chr1:178499811-178499822 | TTCTTTGTTTT | - | 6.62 |
|
| | 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 |
| GH01I178530 | chr1 | 178498781 | 178499981 |
|
Enhancer Sequence | GGAAAACGTG AGTGGGTGGG GATCAGGACT GGCTATTCTA GAGGACAGGG GTGGGTCCCT 60
TGTAACACAG CATCTCACTC CTGTCAACCT GGTGGCCAAT GACAACAGAG TGAGGGGCAG 120
TTGGCTCACC CCAGCCCTCC CATAGGTAAC AGGTGCGGCA GCCCCAGGCC TTGACGCATG 180
TGGTCATCAG AGAAACATGA GGGTGAGTCA TCTGGGAGCA ATTAAGAGGG GAGGCCCAGG 240
AGGAGGCCAG ACTGTGTCAT CCATCCCATC ACTGCCACAG CACTGGCCCA GTGCCCACTC 300
ACAACATTCC TTCTCCTGGG TCACAGGCCA CAGGCCAGCC CAGAAGGTGG CTGAGGATGG 360
GCTCAGGCAT CCAACACTTC TGACTGGGGC CCAGATCCAT CTCTCTTAAA CTCAGCAGCT 420
CTGAGGATCC CCCAATTCCA TGGCAACGGG CTGCCTACCC ACCTTCCCAA GGGGTGCTAC 480
TCTGACTTGC CACAGTCTAG TCTCAGCAAA CTGAAGCTGT CCTTTAAAAA CATAAATTAG 540
AACATGTCAC TCTTCAGCTC AGAACTTTCC AGTGTTTTCC CACTTCTCTC AGAGCAAAAT 600
GCAAAGTCAA TGGTTCACAA AGCCCTACAG GATCCGCCCT GCTGCCTTCC CCATCCCTAA 660
CCCTGTACAG TATTTCACTT GCACTTTCTA GCCATGCTGG TTTCTTTGTT TTTCTTCAAA 720
CACAACACAT ACCCTCTTGC CTCAGGGCCT CTGCACTTGC AAACCCTACC CCCTCTCACC 780
ACCCTGCCAC CACCATCACT AGAATTCTCA GCCTTCCAGT CGGCCAGCTC CCTCGCCTCA 840
AAGTTACCTT CTCAGTGGCC CCCAGTCCCA GCATTCCTTA TCTCTCTTAC TGTCTGCTTT 900
ATTTTTCTCT CCAGCACTCT TGTCACCAAC TCACATACCA TACAGTTTAC TTATTTGTTT 960
ATTGTCTGTC TTTTTCTACG AGAATCTAAG CTTTTTGAGT 1000
|
