| Tag | Content |
|---|
EnhancerAtlas ID | HS098-18641 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr14:105641970-105642870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr14:105642610-105642623 | AGCAGCTGTCACC | + | 6.41 | | Myog | MA0500.1 | chr14:105642609-105642620 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr14:105642609-105642620 | CAGCAGCTGTC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 105642281 | 105642840 | | chr14 | 105642046 | 105642270 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I105175 | chr14 | 105642028 | 105644289 |
|
Enhancer Sequence | AGGTGATCCG CCTGCCTCGG CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCACCGTGC 60
CTGGCCCAGC GTGGAAATGC TGCCTTTAAC TTGGGAGTCC ACCCATCCAG CCAGGAACGT 120
GCCCAGGTGA AGTCCTTGAG GCTGCTGAGG TGGGAGGGCC CCAGGCTCAA CCCTGAGTGG 180
CCCATGTGCC AGGCTGACAG GTGCAGAGAC TTCCGGTGCT TCTCCCAGTG GAGCGGGCCC 240
TGGCCTCTGG AGGAGGCTGT GGAGGCTGGT GCTCAGCTGG TGGGGGTGGG GGTCTGTGAC 300
ACCCTCCTCC TTCCCCAAGA CCTCAGCTGG GGTCAGGAGC CCATCGTAGC GTCCCTGGGG 360
AAGTGGATGG GCTTCATACC AACATCTAGT CCTGGGAAGG CAACCCCACC CCAGCTGGCA 420
GCCCTCGCGG GGCAAGAGTT GGTGCCTCGA GTTTGGTGGG TCAGGTCCCA AAGCGCAGGC 480
TCTAGTGCCT GTTCCCCAGG AGAGCTGGAG CCACCCCTTC TCCAGCCCAG GACACAGCTT 540
CTCCCTCATT CCTAAGCCAC CCTCTGAGAA CAGAGCTGTG AGTCACCCCC ACCCCCAGCG 600
CCCGGTCTTA ATCCTACAGG AAGTAGAGGC ACCTGTCAGC AGCAGCTGTC ACCCGGCCTG 660
CCTCACACAG CTGGGGGCCG CAGGCTGGGG GCATGGGGCC GAGACGCTGC AGAGAGAGCC 720
CCAAGAGCCC AGATTCTGGC CTGGCTTAGG AGCTGAGGCG CATTCGGTCC AACCCTCCCC 780
TAATCCCATG TTGGAAAACA AGGAGGAATC CATCCTGCTT GCACACTCCC AGGGACGGGG 840
CCCTCACTCT CTCCCATCTC CTGAGTCACA CCACAGGCCT GAGGGCCTGG TCCCACTCAC 900
|
