Tag | Content |
---|
EnhancerAtlas ID | HS012-12198 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:125110470-125111500 |
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 | TTGCAAGAGG AAAGGAATGA AGCCTCCTCT GGACCCTCCA GAAGGAACCA GCCCTGCCAG 60 TGCCCTGACC TCATCTCCAT AAGCTCCACT GGGACCTTCT GCCCTCCAGA ACGGGGAGAT 120 AACAATATTG TGTTGCTTTA AGCCTCTATG TTTGTGGTGA TTTGTTCAGC AGCAATAGGA 180 AATCCACACG TCATCCAAAT GCCCTCCTTT ACAGAAAGCT TCTGAACCCG CTCTTGCCTC 240 GGTTGGCAAA CTTCTGCCCT CCACACTCCT CCTCCTCTGG GATGGGTGGG GACAAGTCCT 300 TCACTGGGGT CAGGTTGCCC CAAAGCCTGT CTCCTGGACT TGGAGGCTGC TCCCTCCGAC 360 CTCGGCACCC CCCAAGGGCC AGAGGCCACC ACCTCGAGCA GCCAGCGGGT AAGAGCCAGC 420 CTGCAGGGTG GATACTAAAT ACAATAGGTC TGTGACCACA CACGGCCCCA CCCCCAGGGG 480 CCCAGGCCCC GCTGACCTTC CCACCCCGGG GCACACCCAG CTGCTTCCTC AAAGCCACAG 540 CCCTTTCCTC CAGCCCAGCC TTTGCCCTGG CCCTTTCCTC TTCTGCTCCT GACGTGCCTG 600 ACTCATCCAG CAAGTTCCAG CTCAGAAATC TCTGGGGGAG CCTGGTCCAG CCCCGTTCCA 660 TCCACCCCGC CCTGCTGGCT TCATTTCATT TCATGCACTC AGTAGATGGG CACACAGCTC 720 TCCTCTGTTC TCCTCTGGAA GGCACAGGCA GAGCCCTCAC CTCAGGACCT CCAGAAGCTG 780 ACAATTGGTC GGCGGGAGCA GGGTAGGGGG TTGGGTGGGA GCCTGTGACA TGTTTTAATG 840 AAGTGTAGAC ATTTTAAATA TACAATTCAA AGACTTTTTT AAAAATCTTA AGTACATATG 900 TTTTTAGAGA CAGGGTCTCA CGCTGTGGCC CAGGCTGGAG TACAGTGACA CCATCATAAC 960 TCACTGCAGC CTCGAACGCC TCAGCTAAAG CAATCCTCCC GCCTCAGCCT CCCAGCCTCC 1020 CAAGCAGCTG 1030
|