| Tag | Content |
|---|
EnhancerAtlas ID | HS128-10478 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr19:2488820-2490100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr19:2488824-2488842 | TACGCCTTCCTTCCTTCC | - | 6.45 | | EWSR1-FLI1 | MA0149.1 | chr19:2488828-2488846 | CCTTCCTTCCTTCCACCT | - | 6.56 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_24383 | chr19:2488019-2489749 | Colon_Crypt_2 | | SE_25170 | chr19:2487722-2489940 | Colon_Crypt_3 | | SE_27369 | chr19:2488366-2489529 | Esophagus | | SE_31940 | chr19:2488633-2489386 | Gastric | | SE_43297 | chr19:2487788-2489849 | Lung | | SE_50943 | chr19:2488184-2490012 | Sigmoid_Colon | | SE_54295 | chr19:2488527-2489543 | Spleen | | SE_65706 | chr19:2488397-2489169 | Pancreatic_islets |
|
| | 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 |
| GH19I002487 | chr19 | 2487747 | 2490069 |
|
Enhancer Sequence | TTATTACGCC TTCCTTCCTT CCACCTCACC CCCTGGCCAG ACACTCTGGG GGTGGAGAGG 60
GGCGCTGACC CAGGCCCCAG ACGCCCCTCC CGTCCGCCCT CCCTAGCAGG CAGGAGTCCC 120
GGCTTTCCCG TTCCTTAAAT TGGATAATTG GAGACAGAGG CGGGTGCTCG AGACGGAGAA 180
ATCCCCAAGT GGGCGAAAGG CAAGGGGCCT GTCCTAGTTT CCCTGCACTG GGGGCCCCCA 240
CCCTCGCCAG CGCTCCCTCC GGTGCGCCCT GGGCGCGCAG TCTGTGCGCT CGGGAGCCCC 300
CAGCGCCGGC TGTCGACCCC CTCCAGAGCC CGGCGGTGCC AGCCTCCCTC TGTTGCCCGC 360
CAGGCGCGGT GTCTGCGGCC GCCCCGGCAG GAGGGGTTGG GGGGTCCGGG CCGGCGGCAG 420
CTCCGGCGGC GTCTCCCTCC TCCAAGCCCC TGGCGGCGGG CGGCCGGGCC GAGGGCGGGG 480
CGTCTGCACA GACCCTCCTT TTGTGAGCGG CGCCTTCCCC GGGCGGCCTG GCGCGCAGGG 540
CTCGGGCACT GCGCCAGGGC CCGGAATAGC CTCCCTGCCC GGCCGCCCGC CCCACGCCCC 600
GGCGGAGCCG CCTGACCTGC CCGGTCGGGC GCAGAAGAGC CTGGGGCCGC GGTGGCACAG 660
GAACCGGGTG CGTGCTCAGC TGCACGGGGC TGCAGCCGCT ACTCTCCGCT GGGCCGGCAC 720
TGGACGCGTG CAGCCGGGCC TACTGTGCGC AGCCCGTCTT TTGTGTGAAA ACGCCCGCTG 780
TGTGCAGATC TCCGTCTTCG TGCAGGGCCT ACTGTGCGCC GCACCCCCCT TCCATGCAAA 840
GCCTACTGTG TGCAGAACCC CATTTGCCTG CAATGCCTAC TGTGTGCGGC CCCTCTCCTG 900
CGTGCAAACG CCTGCTGTGT GTGACCCTTT TCTTGCATGC AAGGCCTACT GTGTGCAGAG 960
CCCTACCTTC TTGCAGTGCC TACAGGGTGC AGCCCCTCTC CTGCGTGCAG ACGTCCACTG 1020
TGTGCAGATC GCTGTCTTCG CGCTGGGCTT ACTGTATGCA GCACCTCTCT TCCATGCAAA 1080
GCCCACTGTG TGCAGAGCCC CACCTGGCCG CAATGCCTAC TGCGTGCAGA CACCCAGATA 1140
CATACAAAAC CGACTGTGTG CAGGCATCCA CCTACATGCA AACACCTGCA CCTGCACTCG 1200
TGCAAACACC CACCGTGCAC AGGCACCCAC TGACAAACAT TCATGTGAGG AGCCCCCAAG 1260
CTCCCACACT CCCAAACGGC 1280
|
