Tag | Content |
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EnhancerAtlas ID | HS108-12756 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr14:105234710-105235680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr14:105235019-105235038 | CGTCCACCAGGTGGCAGCA | + | 7.68 | MYCN | MA0104.4 | chr14:105235333-105235345 | GGCCACGTGGTC | + | 6.52 | MYCN | MA0104.4 | chr14:105235333-105235345 | GGCCACGTGGTC | - | 6.52 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_25196 | chr14:105234645-105235707 | Colon_Crypt_3 |
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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 |
GH14I104766 | chr14 | 105232690 | 105236000 |
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Enhancer Sequence | TGTTCTTGGC TCCCACAGAC CCAGAACATC CTCGCCAGCC TGTGCTCCCT ATGGGGCACC 60 CCCTCCAGTG GAAGTGAGGG CAGCCACGCA CCCCTGGGAA TGCCTTAGAG AGGGGCCAAT 120 TGCCATCGCC AGGGGCCTGA CTCTGCAACC ATCCACACCT ACGGGGAGTC CATTTGAGAG 180 ATGAGGAAGC TGAAGCTCCA GGCCCCTGGC TCGTGCTGGT CACCCAACCA CCCGGAACCT 240 GGTCGCCAAC CCGCTGTCAG TTGCTCGGCA GTGGACTCCT CTCCTGGCTC AGGGCGCGGT 300 TCCGGCAGGC GTCCACCAGG TGGCAGCACC GGCACATTCT GCAGGCTGTT CCGGCTCAGA 360 GCTCGATGTA GTGCTCTGGG GTAACCTGGG CCCCAGCCTG TCCCCTCCCG CCCCCTGCAG 420 CCCCTCCTCC CACCGCCTGC AGCCCCTCCT CCCGCTCTGT CCAGCTTCGA ACAGGCCACT 480 CAGGCCTCCC AGCCTTACTT CCACCGTGGC CCAGGCCATG ACCTTGGCCC CAACTCTGGG 540 CCCTGCCCTA TCTGTCCTTC CTGGTGGTCT GTCTCATTCA CTGCCCTACC CAGGGGAACA 600 GCACCTGGGG CTGGGGGGCA GATGGCCACG TGGTCCAATG GTCTCCTTCA TGGCTGGGGT 660 GAAGCTGGGT GGGGTCAAGG GAAGAAGAGG TGGATCCCAA CGGGGGCAGG GCCAGCCAGG 720 GCCTCCCATC TCCCCTCAGG CCAGGCCTCT GGAGATGGGG GTGGAACACC TTCCATGGGA 780 GGCTGCCCCT GGGAACAGGC CTGTATACTC CCGCCTCGGC CCACCACACA GCCTGTCCCC 840 AAACCTGTTG GGGTGGCGGT GCCCACCAGG AGGAGCTGGG GAGGACCAGC TGCTCTGAGG 900 ATGCTGCTTC CCTCCCAGGA CTCCCCACTC CCTCCCTGGC CACCCACTCT TCCACCCAGC 960 AAAGTGAGCC 970
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