Tag | Content |
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EnhancerAtlas ID | HS120-03198 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr19:11009660-11010390 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr19:11010306-11010317 | TGGGTGTGGCC | - | 6.62 | TFAP2A | MA0003.3 | chr19:11009971-11009982 | CGCCTCAGGCA | + | 6.62 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_23673 | chr19:11008924-11010460 | Colon_Crypt_1 | SE_24532 | chr19:11008947-11010425 | Colon_Crypt_2 | SE_30825 | chr19:11008999-11010458 | Fetal_Muscle | SE_48197 | chr19:11008793-11011250 | Psoas_Muscle | SE_51520 | chr19:11008746-11011610 | Skeletal_Muscle | SE_68858 | chr19:11008941-11010261 | H9 |
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| 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 |
GH19I010898 | chr19 | 11009109 | 11010781 |
|
Enhancer Sequence | CAGAGGCTCG GGAGTCTCCT GAACAAAGAG AGGAACACGG CTTAGCTTGT TTTTTTTTTT 60 TTTTTTTTTG GTTTGTCAGT ATTTCCCAGG TGTCTTCTGT GTGCCAGGGA CTAACTTGGG 120 GATAAAGCTG TGACTTTGAG AAGCTGCCGG CTCCGCGGGC TTTAGCAGCT GCTGCTGTGA 180 TGAAGCGATC CACTTGCCCT CAGCCCCGGC ATCTTTGGCC CAAGCCCAGC CCTAGCCCTG 240 GCTGGGCACA GCCAGGCTTC ACTTGGCCAC AGGTCCTGTA GTTGCCTGCC TGGCGCCAGG 300 TCAGAGAGGG ACGCCTCAGG CAACATCGGG TTGCCAGGCT GCTTGGTAAA CAGGCCTCCC 360 TGGGCCCACT TGCTGTCGCC CAGGTGTGGC TAACAGATCG ACAGTATCTC CTGCCCCAGG 420 ACGGGTATGA GTGTGGGCAC CATGCCAAGG TTGGATGTCC CTTCCTGGGA CCCACCCACA 480 GCTGGGAGCA CTTTATCTTG GGCCTCTGTG GGTGTAGTGA GGCTGTGAGT CTGGGGCAGT 540 GGCCTGCTGA CACCCTCCTG GCAGGGCTCA GGAGGTTCCT CCATGCCCTG CCCTCAGGAG 600 GGCGGCACCT GGCTCCTGGG GTGGGAGAGA GTCTGGCAGG ACTGGCTGGG TGTGGCCGGG 660 GAGCTGCCCT TCAGGTCTCA TATCTGTAGG CCCTCATACC TGGACTCGTC AGTTAGGAAC 720 AGTTTTCTTT 730
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