| Tag | Content |
|---|
EnhancerAtlas ID | HS133-08538 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr13:40955880-40956890 | Target genes | | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIA | MA0670.1 | chr13:40956196-40956206 | ACTTGGCACC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGACCTCGT GATCTGCCCG CCTCGGTGTC CCAAAGTGCT GGGATTTACA GGCGTGACCC 60
CCACGCCCGG ACCTAAATCC ATTATCCAAA GCTCAGGCTG CCTGGATTTT GGAAACCTAA 120
TCTTGTTGAA CTTCCCTGTT TCCTGAGTTG TGTCACATGC TCCAGTGATG TGCCCCCAGT 180
GACAAGCTGT CCAGTTCTTC ACAAACAAAG GCTAGAAAAG TCCAGTGGAT GACCTTCCAC 240
ATCTGGGACT GTCGGTGGCC AGGCCTGGAG TGGCTCCTCC CCTTCTCGTC CCCTCAGCGC 300
AGCTTCCGTC CCACAGACTT GGCACCAGCC ACCACCTCTG CCCCAGATCC TTCCGCTCCC 360
CTTCCCAGGG AGAATGTGTC CTGCCAGCTC TTGCCCCACC AAATGAGGAA CGGGGACTTT 420
GCCGCTGTCC CATTCTGAGA GGTTTGCTCA TGCAACCAAC CCTCCCCTGG GGCCTCAGAC 480
CAAGGCTGTC TCGGCCCAGC CCTGGACCTC AGCCTTAGCT AGGACACAGG AGCGGTCCGC 540
CTGCTCTGTC CGTCCTCGCA ACTGCCTCCG AGTCCAGCAC CCCAGTTCTC AGGCCCAGCC 600
CCGTTTCCTC CTGTCCTTTT TGGTTCTGTG GGTGGCAGAG GCCAGGCAGC GTTTTGGGGT 660
GGGAGCACTG GAGGAGTCCA GGTGAAGTAG GATCCGCCCA TCAGTTCTGA GCCCTGAGTT 720
GACCAGGTTG TCTCCGAGCA GCCCGCCCTG GGCTGGGAGG CCTTAGCCCA ACCCTCCCAC 780
CTGACCCAGG GCCGCAGCGA CTGCCTGCCG CTCTCCCCGC CTCGCCTACG CCTGTTAGGC 840
CTGGGAGAAA CCGAAACCCT CCTCTGCAGA CCATCAGTCA GGGTGACGCA GCAACCTCAC 900
AGCCTAGGGT CTAGCACATT TAAAACATTA AAGCGTCTGC TCCATTTAAC TTTAGGTGAA 960
TGAGCACTCT GCCTCTCTCC CTGCCTTTTC TACCAACAGC CCCTGAGTTA 1010
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