| Tag | Content |
|---|
EnhancerAtlas ID | HS139-14113 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr12:125110420-125111540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr12:125111271-125111291 | GGTAGGGGGTTGGGTGGGAG | - | 6 | | ZNF263 | MA0528.1 | chr12:125110724-125110745 | TGCCCTCCACACTCCTCCTCC | - | 6.01 | | ZNF263 | MA0528.1 | chr12:125110727-125110748 | CCTCCACACTCCTCCTCCTCT | - | 6.13 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09620 | chr12:125108910-125112362 | CD14 | | SE_23633 | chr12:125110096-125111555 | Colon_Crypt_1 | | SE_29720 | chr12:125110106-125112177 | Fetal_Muscle | | SE_34780 | chr12:125108082-125112444 | HeLa | | SE_57235 | chr12:125109943-125112300 | VACO_400 | | SE_57418 | chr12:125110264-125111017 | VACO_503 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 125110562 | 125110683 | | chr12 | 125110878 | 125111184 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I124625 | chr12 | 125109896 | 125112430 |
|
Enhancer Sequence | AGGTCAGGGC AATTCCGCCA CCAGCCAAGG AGTGTGGCAG CCTCTAGAAG TTGCAAGAGG 60
AAAGGAATGA AGCCTCCTCT GGACCCTCCA GAAGGAACCA GCCCTGCCAG TGCCCTGACC 120
TCATCTCCAT AAGCTCCACT GGGACCTTCT GCCCTCCAGA ACGGGGAGAT AACAATATTG 180
TGTTGCTTTA AGCCTCTATG TTTGTGGTGA TTTGTTCAGC AGCAATAGGA AATCCACACG 240
TCATCCAAAT GCCCTCCTTT ACAGAAAGCT TCTGAACCCG CTCTTGCCTC GGTTGGCAAA 300
CTTCTGCCCT CCACACTCCT CCTCCTCTGG GATGGGTGGG GACAAGTCCT TCACTGGGGT 360
CAGGTTGCCC CAAAGCCTGT CTCCTGGACT TGGAGGCTGC TCCCTCCGAC CTCGGCACCC 420
CCCAAGGGCC AGAGGCCACC ACCTCGAGCA GCCAGCGGGT AAGAGCCAGC CTGCAGGGTG 480
GATACTAAAT ACAATAGGTC TGTGACCACA CACGGCCCCA CCCCCAGGGG CCCAGGCCCC 540
GCTGACCTTC CCACCCCGGG GCACACCCAG CTGCTTCCTC AAAGCCACAG CCCTTTCCTC 600
CAGCCCAGCC TTTGCCCTGG CCCTTTCCTC TTCTGCTCCT GACGTGCCTG ACTCATCCAG 660
CAAGTTCCAG CTCAGAAATC TCTGGGGGAG CCTGGTCCAG CCCCGTTCCA TCCACCCCGC 720
CCTGCTGGCT TCATTTCATT TCATGCACTC AGTAGATGGG CACACAGCTC TCCTCTGTTC 780
TCCTCTGGAA GGCACAGGCA GAGCCCTCAC CTCAGGACCT CCAGAAGCTG ACAATTGGTC 840
GGCGGGAGCA GGGTAGGGGG TTGGGTGGGA GCCTGTGACA TGTTTTAATG AAGTGTAGAC 900
ATTTTAAATA TACAATTCAA AGACTTTTTT AAAAATCTTA AGTACATATG TTTTTAGAGA 960
CAGGGTCTCA CGCTGTGGCC CAGGCTGGAG TACAGTGACA CCATCATAAC TCACTGCAGC 1020
CTCGAACGCC TCAGCTAAAG CAATCCTCCC GCCTCAGCCT CCCAGCCTCC CAAGCAGCTG 1080
GCAGTGCAGA TGTGCACCAC CATACTCAGC TAATTTAAAT 1120
|
