Tag | Content |
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EnhancerAtlas ID | HS139-28124 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:26231570-26232310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TP53 | MA0106.3 | chr2:26231909-26231927 | GACAAGCCAGGGCTTGCT | - | 6.15 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_09566 | chr2:26230391-26233253 | CD14 | SE_26712 | chr2:26230608-26232892 | Esophagus | SE_28420 | chr2:26231425-26232647 | Fetal_Intestine | SE_29154 | chr2:26231420-26232678 | Fetal_Intestine_Large | SE_32014 | chr2:26231685-26232630 | Gastric | SE_35193 | chr2:26230790-26233105 | HeLa | SE_36382 | chr2:26230622-26233114 | HMEC | SE_64640 | chr2:26230706-26232972 | NHEK |
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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 |
GH02I026007 | chr2 | 26230471 | 26233268 |
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Enhancer Sequence | AGACACCACA TACAGGAATA AAATGTACTG AGGAGACAAA AGAGTGTCAA CCCAAGGATC 60 TCTTTCAGAG GGGTTCCCTT AACTCTGGCA GGCCATGAGG ATGATGCCTG GGAGCCCCAG 120 GATTCTCCTG TTACTTTCTT GTGTCCTCAG AAACCACCCT GGTGACTCAG TAACACAAAC 180 CTAGGGTGTT GAGTGGGTGG GGCACCGCTT CCCACCCCAG TTTATCTGGT TTTCCCAGGC 240 AGAATAGTAC ACTGAAGCTG TAGGCAAAGA GGAAGCCCAA GATAGGGGAA GGCCAGGGTG 300 TTGGTTCCTC AGTTTGTTGA AATCAGAGTC ATGAAGCAAG ACAAGCCAGG GCTTGCTCAG 360 CATTTCTCCT TCCTGGCATG GGTTCACCTC AGCCCCAATT CAGTGGCAGC TCTGTTGGTT 420 CAGAGGGGTG AGGTATCCAA GAGGAGGAAG CTTGTACAAT CCTGCTAGCA GGGGAGGGCT 480 GATGGTAGGG TGGAGTTTCA AAGGAAGCCT CTGACATCTG ACAAAGGCTG AGTCAGTTAT 540 ATTGCCCCAT CTCTGAATCT GGCTTCTCCT GCTCCTCTAC CCTACCCATC CTGCCTTCCA 600 GACACACCAA AGTTCTTTTT ATCCCTGACC ATGACAGGCA TGGCTGCTGT GTGCAGCTTC 660 ATAGGTTGTG CACTGCACAG TTCCAGGAGG TGCTATTCCC ATAGACAAAG GAGTGAATAA 720 CAACTCCAAG AATCATGCAC 740
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