Tag | Content |
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EnhancerAtlas ID | HS098-14948 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:125110460-125111340 |
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 |
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| 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 |
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| 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I124625 | chr12 | 125109896 | 125112430 |
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Enhancer Sequence | CCTCTAGAAG TTGCAAGAGG AAAGGAATGA AGCCTCCTCT GGACCCTCCA GAAGGAACCA 60 GCCCTGCCAG TGCCCTGACC TCATCTCCAT AAGCTCCACT GGGACCTTCT GCCCTCCAGA 120 ACGGGGAGAT AACAATATTG TGTTGCTTTA AGCCTCTATG TTTGTGGTGA TTTGTTCAGC 180 AGCAATAGGA AATCCACACG TCATCCAAAT GCCCTCCTTT ACAGAAAGCT TCTGAACCCG 240 CTCTTGCCTC GGTTGGCAAA CTTCTGCCCT CCACACTCCT CCTCCTCTGG GATGGGTGGG 300 GACAAGTCCT TCACTGGGGT CAGGTTGCCC CAAAGCCTGT CTCCTGGACT TGGAGGCTGC 360 TCCCTCCGAC CTCGGCACCC CCCAAGGGCC AGAGGCCACC ACCTCGAGCA GCCAGCGGGT 420 AAGAGCCAGC CTGCAGGGTG GATACTAAAT ACAATAGGTC TGTGACCACA CACGGCCCCA 480 CCCCCAGGGG CCCAGGCCCC GCTGACCTTC CCACCCCGGG GCACACCCAG CTGCTTCCTC 540 AAAGCCACAG CCCTTTCCTC CAGCCCAGCC TTTGCCCTGG CCCTTTCCTC TTCTGCTCCT 600 GACGTGCCTG ACTCATCCAG CAAGTTCCAG CTCAGAAATC TCTGGGGGAG CCTGGTCCAG 660 CCCCGTTCCA TCCACCCCGC CCTGCTGGCT TCATTTCATT TCATGCACTC AGTAGATGGG 720 CACACAGCTC TCCTCTGTTC TCCTCTGGAA GGCACAGGCA GAGCCCTCAC CTCAGGACCT 780 CCAGAAGCTG ACAATTGGTC GGCGGGAGCA GGGTAGGGGG TTGGGTGGGA GCCTGTGACA 840 TGTTTTAATG AAGTGTAGAC ATTTTAAATA TACAATTCAA 880
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