Tag | Content |
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EnhancerAtlas ID | HS060-10913 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr14:104173550-104174850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr14:104174588-104174609 | GCTTCCTGCACCCCCTCCTCT | - | 6.07 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_06305 | chr14:104174102-104176790 | Brain_Hippocampus_Middle | SE_08167 | chr14:104174151-104176650 | Brain_Inferior_Temporal_Lobe | SE_26911 | chr14:104174260-104175004 | Esophagus | SE_41604 | chr14:104172818-104173858 | LNCaP | SE_41604 | chr14:104173873-104176727 | LNCaP | SE_53673 | chr14:104174041-104176901 | Spleen | SE_60612 | chr14:104145010-104184512 | DHL6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I103703 | chr14 | 104169745 | 104175345 |
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Enhancer Sequence | TGCTAAAGGG CAGGGATAGT GTCAGGCCTG ACTCTCCTGG GCCTGCGGGC AGGGCTGGGG 60 ACTGCGGGAG GCATGGTCAG CCTGCCTGTG CCAGGTGCAG TGTGGCTGGA GCACAGGTGC 120 CTGCGGTCAT GGGGGTGAGC AAGGTGCTGA GGGCAGGGAG GGGGGCCCAG CCGGGAAGGG 180 CGGGTGCACC TGAGATGCAG AGTCAGGGGG AGCCCCAGGG CCACCATCAC ATGCCCGCAG 240 GGATCCCCCT ATGGGGCAAT TGCAGCACCA GACGCCTTCA GCCAAAGCTT CCAGAGAGCC 300 CCGAGGCGCT CCCTAACAGC CTCCATGTGA AGAAAAAGGC ACAGCTCTGT CCAGCTGGGA 360 TGCCCTGGGG TGCTGAACAG TTCTCAAGCG GCTTTAATGG GCTCCCGCAG GCGCGCACAC 420 ATGCACACCA CATGCCGTCA GTTCTCTGTG ACAGATACCA TTCTGGAGCA ATGCTGGTCT 480 CAGCCTCTTG GCTAAAGGGC CTTGGATGAG CCATTTGACA CAGCCTCCTC CACGACACCG 540 AAGCCCCTCA GGGCAAGGCT CAAGGTGGGA CATGCGGTGC AGGCTGCGCT CTTGGCCTGG 600 GGCCTGGGCC GGGAGGAGCA GCCCCTCCCT TGGAGTCTGC ACACTGCCTT GGGCACCCCG 660 TCCAGGTGGA GCAGGCCACC CTGACTGTGA GGCCTGCCCA GAGCCCTGCC CACAGCACCG 720 TGTGTGTGGC CGTGGCACCT GCCCACCACG GCAGCCCCAA GTTCAGCACG TTCCTCGGGG 780 CCTGGGCCAC TGAGCCACCT GCAGGGGAGA GAGGGCCCTG CTCATGCCAG GACCCCGCTG 840 CCTACTAGGG CCTGCTGAGA TGCAGGGATG GAAACCTTGT CCGTCCAGGC GCATGGGGTT 900 CCCTGGGTAC CTCCTTCCCC TGCTGAGACC TGGTTTCCCA CACGTGGTGG TGGGACCGTG 960 GCCAGGGCCC CATCTCACAC CGTTCCCACC CTGCCAGAGC CTGAAGGGCT CTGGGTGCTG 1020 ACTGCCAAAT CCACCCCTGC TTCCTGCACC CCCTCCTCTG GTCCATGGAG CAAGGTCCCC 1080 AGGAGGTCCC ACAGCCCGTG TCCACCTCAC GCATCTTCTG ACCCGATGCT GTGACCACAG 1140 CCCCATGGGT GTAGGACAAG CAAGATGGGA ACTCTGGGGC TGGAGCAGCT GCCACACGCC 1200 CTGAGGCTGG TCCCTGGGTG AAGTCTGCAC AGCCCCTGCC CTGCACCACT GGGACCATGA 1260 TGCTGGAGCC ACATGTCACC CCTGGCAGAG ATGCCAGGGC 1300
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