| Tag | Content |
|---|
EnhancerAtlas ID | HS007-06776 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr17:5429780-5430820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr17:5430337-5430348 | AACAGCTGCAG | + | 6.02 | | Tcf12 | MA0521.1 | chr17:5430337-5430348 | AACAGCTGCAG | + | 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 |
| GH17I005525 | chr17 | 5428792 | 5431941 |
|
Enhancer Sequence | ATGGGGCGAG ACCCCACTCA GGTGTCTGTG TGAAGTGTTC TTGTTCCCAC AGGCAGCACA 60
GAGAGGAGCA AGTGTGACAA AAATGAGGGA ACTCACTTCC TCTTGGAGGG AGGGTTGTGT 120
GGAGAGCAGA GGTCTGTGTG TGCTGAAGGA GATGGGTGGG TGGGGGAACG AAGGACCCGA 180
AGGACAAGGC CAGCTTCATG GATGTGTGGC CTGTGCAGTC ACACAGGGTC CTGAGCTCAG 240
CAGGGCTTGG TGCTTGGTTT CATGTTTGGT GGTCTTGACA TTCTTAATCA TTTTTGAATG 300
AAGAGCTCCG CGCTTTCATT TTGTGCTGGG CCCTATGACT GCTGGAGCTG GTCCTGCAGG 360
AGGGTGAGAA TGCCCATTGC CACGGTGATG AAGCTGAGAG GCTGAAAGCC TCAAGCTCTA 420
GCTATAGTGG GAGAAAACTC ACCATGGAAA GTTAATGACT CATCACCCGT TCAGCGACGA 480
CAGTGATGAA GCACCAGTGC CCAAGTCCTA AATCAGACCC TGTGTCAGGC AGTGAGGTCA 540
TCGTTTCCAG GGCAATGAAC AGCTGCAGCC CAGACAGCAG GCAGCAAGCA TTTCTGGAAG 600
GGGCCCTGCC CGGCCCCAGG GATTGGTTTC CTGGCTGGTC ACAGCTAGCT AAAAGCAGCC 660
TCTGTGCATT TTGCCTCTTG TTCTGTGGCA GGGGTGTCCA ATCTTTTGGC TTCCCTGGGT 720
CACATTGGAA GAAGAAGAAT TGTCTTGGGC CACACATGTA AAATATACTA ACACTAATGA 780
TAGCTGGTGA GCTTTAAAAA ATTCGCAAGA AAGTCTCATA ATGTTTTAAG AAAGTTTACG 840
AATTCACGTT GGGCTTCATC GAAAGCCATC CTGGGCCGCA TGTGGCCCAC AGGCCGCAGG 900
TTGTACAAGC TTGTGTACGG AGTCCAAAGG GAGTAAATCC TATCTGGCCA CAAGGTGAGG 960
CTCAGAATTT GGTCTAGAGA AGGCTAGTGG GACATGGGCT TGGGCAGGAC TGGGGAGGGG 1020
TAGGGGTGTA GCTCTTAGCC 1040
|
