| Tag | Content |
|---|
EnhancerAtlas ID | HS133-03593 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:222719580-222721060 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:222719935-222719947 | AAATAAACATTC | - | 6.74 | | RREB1 | MA0073.1 | chr1:222720358-222720378 | CCCCCAAACACCCTCTTCCT | + | 6.05 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AACTATACTT TAGCACGGTG TGATCAAAAG GCACAAAACT TGGAGCCTGA GCATCTGGCT 60
CTGTGCCCCA GGATTGTTTT ACCTTGGGTA AGTCATCTAA ACTCTTGAGC CCTCATCAGT 120
AAAATGAGGA TCATAACAAC TGCCTGCAGA ATCATTGCTG GGTACACACT ACATACGTTG 180
GGGAAGAAAG AGGACCTTAT AAATGTGAAT AAATAAACAC GTGTAGGACT GTTTGGCTGA 240
AATTGTTCTT ATTCCTCAAA TCCCTAAAAC AACAGAGCTG CTGACTTTGA CTTTCTGAAA 300
CCTCATGCAA GAGGGAAGGG TCAGGGGTAT AAATTTTTAC CAGGGATGAT CTCAGAAATA 360
AACATTCTCA GTGCTGCTTG TAAAAGCTCA GCTTCTACCC TAATGGGAAT CCTAGAGTTA 420
ATTCTCCAGG AAACAGCTGT GGAGTGGTGT CTAAGAGGAC AGCCCCAGGC GGTGCCACCC 480
AGGTGGCTGA CTTTCTGGGC CAGGCTCAGC TGTAATTCTC TCCTGGACTC TGGGAAGCTC 540
GGTTAACCAC TTCACGCCCT ATGTGGGAGT TACAGTGGTC TGCAGGCTCA GGAACAGTGG 600
CGCCAGGAGT CATGAACAGA TGCCTGTGGA TAGCCAAGTC ATTGTGCTGA CAAGCCCAGG 660
GGGTCTCAGT TCAAAAGGCT GCCTGGACTT CTTGCCTCTC CTCCCCAACA TCATTAGAGG 720
GGTCCTCCCC AGGCAGCCTC TTTTATCAGC TTTCCAAATG CTGACCTCTC CCCATTAACC 780
CCCAAACACC CTCTTCCTAC AAAGTCTGTG TGTGCAGCCT ACACCCGTCT TGTTTTCAGG 840
CTGAGCTCAA TCAAAACGAT GCCTCCCAGG CATGTGGATT TTGGCTGTTG GGCAACCAGG 900
AGAAGCAGAA ACTCTGTGAG TCACTGCTAC TCAGCAGCTT GCATCTCTCT CTTCCAGCTC 960
TGGAGTGCTG GGCAGACAGA ACTCTGGAGA GAGTCTCCAA CCCCTGCCAC CGCCAGGGTG 1020
ACGCCAGAGA TGCCCTGGCA CAAATCACCC AGATGAAAAG GACTGGACCC CAGCAGATGC 1080
CACCACTCCC TCCCTTAACG CGCTCGGTAA ATTCCACGGG TTTAAGTGCC TAGCTCTCTG 1140
AGCACCGCAG AGGATGCAAA TAATTATTTG CCATGCACCA CAGAGGGAGT GTGGCAAATA 1200
ATGGCTGCTC TGAGAGCTCC AGGAAGAGTG TCCCTCTCAT TCTCCTGGAG CCTGGAGAAG 1260
AATCAGGGCC AGCAGAATCC CAGAGGGAGA GCTTTGGGGA ACCCATGGAG ACCAAATTCA 1320
GCACACACTC ATGTCAGTGT GCGTGTCCAA AGCCGGCAGC TCCAAGATGA GGCACCCGGC 1380
ACATGAACTT CTAAAGGGCT GGGCTCCCAA AGCACCCTCC GCTCAGGACC CACACCATGC 1440
AGCCCAGCAC CCAAACCCCT GGGGCTGGAA GGCACTTTTC 1480
|
