| Tag | Content |
|---|
EnhancerAtlas ID | HS133-22301 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr3:49863030-49863870 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mecom | MA0029.1 | chr3:49863829-49863843 | TTTTATCTTTTCTT | - | 6.38 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CACTCTGTTG CCCCGGCTGA ACTGCAGTGG TGTAATCACT GCTTACTGCA GTCTCCAACT 60
CCTGGAATCA AGCAATTCTC CTACCTCAGA CTCCCTAGTA GCTGGGAGTC TGCAGGCATG 120
CACCACCACA CCTGGCTAAT TTTTAAAATT TTCTGTGGAG CCAGGGTCCC ACTATTTTGC 180
TCAAGCTGGT CTCAAACTCC TAGGTTCAAG TATTCCTCCT GCCTCAGCCT CCCACAGTGT 240
GAGCCACTGT GCCGGGCCTC TATTATCTCT GTAGTCAGCC AGTGAGTGAG CTGACAAAGA 300
TTTTCTGGCT TAAAAAACAA ACAAAAAAAG GCACGAGTCC TTTAAATCTT CTGATATGTT 360
GCCAAGGTGG GGTTGGGTGG GGTATTAATG CAGGAATTGC ATCTAAGAGG CTGAATGAAA 420
CCAAGGCAAG CATCTCAGAG TACCTCCAGG TCCGTCAAAG CGCACAACCC CAGCATTTTT 480
GGAGGGCAAG GTTCCCGTGC CTGTTCTGGC ACCAGTCAGC TGCTTTCAGA ACTGGTGCTG 540
CTATCCCCAC AGCCGGATGG GGCTGAGGAA TGGGAGAAGT AGCTGCTTGA TTCACACTAC 600
TCTCTTCATC AAGCAACCCC CTTGTTAAAT TTCCGGGTTC TGAAACAGTT GATTACAATC 660
ACTGCTCTTT TCAGCTCAAT GGTTGCTTTG ATTCAGGAAC CAACCCCTAG AGCTTCCAAT 720
TCCACCATTA TGCATGCCTT CGCTCCACAC TCTTTTGATT ACTATAGCTT TGTAGTTAAG 780
TTTTTAAATT GGGAACAACT TTTATCTTTT CTTTAAAACA ATTTTAAAAA ATGTTTTGGC 840
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