Tag | Content |
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EnhancerAtlas ID | HS024-04874 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr14:103999190-104000880 |
Target genes | Number: 13 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr14:103999875-103999886 | CCACACCCTGC | + | 6.62 | NR2C2 | MA0504.1 | chr14:104000853-104000868 | TGCCCTCTGACCCTC | - | 6.66 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_04042 | chr14:103999622-104001771 | Brain_Anterior_Caudate | SE_05960 | chr14:104000109-104002743 | Brain_Hippocampus_Middle | SE_07063 | chr14:103999188-104001357 | Brain_Hippocampus_Middle_150 | SE_24782 | chr14:103998190-103999988 | Colon_Crypt_3 | SE_26871 | chr14:103998538-104004355 | Esophagus | SE_54593 | chr14:103996750-104012040 | Stomach_Smooth_Muscle |
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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 |
GH14I103532 | chr14 | 103999139 | 104004361 |
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Enhancer Sequence | TCCGGGGTTC CGGGAGAGGT ACAGCCTGGG TGGGGGTGGG GCAAGGGTGC AGGACTGAGC 60 TCCTGGGATC TCAGAGGGGT CCAGAGACCA AGCCACACCA TGGCAGTGGC CAGGCCAGGG 120 CCCCACTTTG GCCTGAGGTG AGGAGTGGGT CAGGCTGGCC AGGGGAGGCA GAGCTGGGGA 180 GGATGGTCCC TGGCTGGGCC CTGCTCCTGG TCTCTGGCCT CTCCCAACCC CCTGATGGAG 240 GAAGGTGGCA GCGCCACCCA AGTGCAGGGC AGGCCCGGCC GGAGGAGTCT GGAGTCCCCT 300 CCCTGCTGTT TCCCAAAACC TCTCCTCCCC CAGGCTCTGG AGCCCAGGGA GCTGGCCCCT 360 TTTAGGGAAG ATGCTGGGTG CGGAGGCGGG GCAGCCCTGG GGAAGGTCGG GCCTCAAGCC 420 AGGGAGGTGG CTGGGAGGCC CAGGGTTTTT CCCTTTTCTG GAGAAGGAGC AGCTCAGGCA 480 GCAGGGGCCC CTTCCTTCTT CCCAGCTGAG AGTTGTATTC TGAGAGGGTT GAAGGGTGGA 540 GGTGCTGGGC GCCCCACCCC ACCTCAAAGA TGAGCCGAGG CCTGGTGCGA ACAGCAAGGC 600 TGTGGCCGGG GGTCCCCTGC TGGCTCCAGC CCAGCCCTGA CTCCTGGGTC CTGGTCTCTG 660 CTGAGGTGGG TAGCTGTGGG GATCTCCACA CCCTGCCTCC TAGGCTTCCT GCTCTGGGGA 720 CACTTCTGGG CCTGGACCAT AGTCCCAGGG AGGCTGAACC CGGCAGAGCC TCCCCTGGGG 780 CCCCCCTGCT GCCTTTGTGA CTCCTTCCTC CAGCGTGGCT CGGGGAACCC GCGCCTGCCT 840 CTGGGACCTG TCCCTTTCCC TGCGAGCTCC CCCTTCTGGG TCCAAAGGCT CCTGGCTCAT 900 TCATGGGCCC GGCATCTCCT GCCGGCCACG GGAGCCCGCT GGGGAGGATG CGGCATGCTC 960 AGCCTCTGTG CCCTGTCTAG GCTGTTGTCA CACAGCAGGT GCCTCCTCTA ACCCCGAACC 1020 TCCTGGCGGC CCCGTGTTAG GGTACAGCTG AGGAGACCAA ACCTCAGGGA CGTTTGAGGA 1080 CACTTGCCTG GGCCACATAC CTCTACCCGG CCCTGGCTTC CCCAGGTCCT CCCTGCCAGG 1140 ACAGGGACCC GGGCTGGGTT CTCATTCACT GCAGGCCAGG CCAAGTGAAG CCCGTGGCTG 1200 CCCTGGTGGG AGGCGGCAGG GAGGGGCTGT CATGCTCGGG CTCTGCTTCG AGTAGGCGCC 1260 TCCTGTTCCC GGGAGCAGCG ACAGCCTCTA ATTTCCTGTG ACAGCAGCGG CCCCCGCACC 1320 GCCCCACGCT GCCGTGCTGT CAGAGCTGCT CCGGGCCCAG AGCTCCAGCA GCCCTGTGGA 1380 AGGCAGGAGA GCAGTGCCCG CTGTGGGCCA AGTGAGACAA TGGCAGCGCG GGCTTGACCC 1440 GGTGCCTGGC ACATGGGAGG GCCTGGCATG GCTAAGCTGG GTGACATGAA CAGCGGCGCC 1500 AGGCCCCATG GGGGGCTGTC AGTTGAGGGC CAGGCCCCTC TGCCCTGCAG TCCCAGCTCT 1560 TGGAGAGCTT GCAGTCTGTG TTGGGGCTGT CTTAGGCTGG CCTCAGACCC TAGGGTGGGA 1620 GTCCAGGGAT GCTAGGGCCA GACGGGCCAG GCTCTGCCAC CCCTGCCCTC TGACCCTCGG 1680 GTCCTGTTTC 1690
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