| Tag | Content |
|---|
EnhancerAtlas ID | HS062-12738 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr4:186942540-186943220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr4:186943087-186943098 | GACAGCTGCAG | + | 6.62 | | POU4F2 | MA0683.1 | chr4:186943186-186943202 | TTGATTAAATATGCAT | - | 6.86 | | Tcf12 | MA0521.1 | chr4:186943087-186943098 | GACAGCTGCAG | + | 6.14 |
|
| | 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 |
| GH04I186021 | chr4 | 186942677 | 186943227 |
|
Enhancer Sequence | AGAGTTTAAA TAAATCAGGC TGAAAAATCT CTGAGCCTAT GATAACAATC ACTCATTGAT 60
AGCTTATCAC TTAGGAAGAG GTTTCAAGGG CTAAAAGACG TAATGAAACC CCAACGCAGA 120
ACATGTAAAT GAACAGACTG TCTCTTTCCC CTCATACATC CCACGCTACT CAGTACAGAG 180
GCCAAAGCTC TGTGAATGCA CAGGGCTGGG GAACGAGATG CCATCTGGAA CTGGAGATGC 240
AAAGCCACAT CCCATCCCTG ATCCGTATGG CCCAGGCCCA GCCTGGGAAG GTGTGGGGTA 300
TACTGACTGC GGGGGTCCCA TCACTTCTCC TAGAACGGGT TCTCCGCGCG CTGTGCAGAG 360
AACAATACTG TCCTCTAGCG CTCAGAGATC AGAACTGGAA ATCAAGAAGC TTGTTTTTAT 420
TTCTCCTCCC ATATTGTCAG TGATTCCCAG AGCAATATAC CACTCCCAAA GCAAAGGGAA 480
TGGATTGACA CAGTTCACAA AATCCAGGGC AGAATCATCC TGGCTTTGCC TCCCTTGTCT 540
GGGTAATGAC AGCTGCAGGG TTTTATCTGG TCTTTGGGGC AGTGCAGCAT GTATTTAATC 600
TATCCTTAGT TCAGCTTTGC CAAGGGAGAA TCAAGATTTT TCTATCTTGA TTAAATATGC 660
ATGTAATTTG TCATCAGCTA 680
|
