Tag | Content |
---|
EnhancerAtlas ID | HS133-27889 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:2915370-2916770 |
Target genes | Number: 13 | Name | Ensembl ID |
|
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr7:2916059-2916072 | GGGGGCAGCTGCT | - | 6.03 |
|
| 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 |
GH07I002875 | chr7 | 2915376 | 2916288 |
|
Enhancer Sequence | TGTGCCCGGT CAAGTTCCTT CTTCTGATAA GGACTCCATT CACCGGGCTA GGGCCCTTCC 60 TACTCCAGTG TATCCTCATC TAACTAATTA CATCTGCAAT GATGCTATTT CCAAATAAAG 120 TGATGTTTGC AGTTACCAAT GGTTAGGACT TGCGCATATC TTTTGGGGAA TATAATTCAA 180 CTCACAAGAG AAGGTTGTAG CTGCAGGCAC TTGGGGCTCA GTCTTGGTGG CACCCCTCCC 240 TCCAAGAGGC TGTGTGGAAT GTGCTTGAGA ATTGCCCCCG TGAGGCGTGA GGAGCTGCGG 300 CATTGACCCG CCCCCTCCTG CCTGGAGGTG TCTCGGAGCC CTGGGATTTT CCTCCCAATG 360 TGGCATTCAC AGGCATCACA TCACTATCTG GCCATCAGCC ACGGTGGGAG TATTGACACC 420 ACAGACATCA GCGGATGTTA CAAATCAGGC TTCTTTTTCC CCGTGAATCA GCCTCCTGTA 480 CCACTCCGGC CCCTCCCTGG TGCAGGAGCA GTGCAGTGAG CTGATTCATG CGGAGAAAGA 540 TTGGTCTGGC CTGCCCCGTG AACGGTCTGT GTGTGGTCCT GGCCTGAGGA CACCCCAGCG 600 GGCTCATGTG GGGACTGCCT GCAGGTAACC TCTAGACTTG GCTGAGCACC AAGAGTGTTG 660 GCCATAGGGG ACCAGGCAGG TGGACGCCTG GGGGCAGCTG CTGGCTTCCC AGCGGGGCGC 720 TGCCTGAGGC CCGGTTTGCC CAGAGAAGTG AGCAGCCAGC TGTGGCCCGG CAGAGTCCCA 780 GGCCGTGCTG ACAGGTGTGG CCAAAGGGCA AAGGGTGTTA TTATAAAAGA GAATTTACGG 840 CAGCGGCAGC TTGGGCTGGC TGAGCCCACG GGCAGCAGGA GGATGGAGTG GGGCTGGCAG 900 GATGCTGGCA GGATGAAGGA TCTGCATTTC ATTGAGACAG TGGGTTGGAG TCCACGCGGC 960 TGAGATTAAA TAGCCCGTCC CCGGAATGCA GAGAGCCAGA GATAAATCAG ACTTTACTGC 1020 AAGTGGGGTG GCAGGGAGTT AATTAGGAAA GAGAAAAAAA AATACATTTC AACTCACAAA 1080 GAAGCCCAGT GAGCCAGCAG AGAATAGCCC GGCCCCTCCA GGGGTCACTT TGGGGAGGGG 1140 CTGGCATCCC TGGTCCCACC AAAGGGCACA CAGGACTGGG AAGGATGTCA CCTTGGAAGT 1200 GTCAGGGCCC AGTGCAAGAG GGTGAGAATG CTGGCTGCCC CGTGGAGCTG TGCCCGGGCT 1260 GTGCCCCGGC TGGTCTTGGC CTGGGCCCTG CCAGTGAGGT GAGCTGGGTC CTGAACTTCC 1320 AGGTTGGGGA CCAGGTCCTG GAATTGCATC CTGGTGCAGG AGCAGGCATC GCAGGTCACA 1380 TTCAATGAGT GCTCAGAAAT 1400
|