Tag | Content |
---|
EnhancerAtlas ID | HS098-03448 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:151973580-151974580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr1:151974514-151974525 | GGCTGTGATTT | - | 6.02 |
|
| Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
SE_00284 | chr1:151972648-151974621 | Adipose_Nuclei | SE_09689 | chr1:151972965-151974663 | CD14 | SE_26790 | chr1:151973331-151974796 | Esophagus | SE_28908 | chr1:151973538-151974845 | Fetal_Intestine_Large | SE_33866 | chr1:151973379-151974671 | HCC1954 | SE_34778 | chr1:151973487-151974621 | HeLa | SE_35880 | chr1:151959933-151975921 | HMEC | SE_43050 | chr1:151973511-151974470 | Lung | SE_45267 | chr1:151973586-151974269 | NHLF | SE_47215 | chr1:151973376-151974895 | Panc1 | SE_56104 | chr1:151972738-151974921 | u87 | SE_64341 | chr1:151973031-151974940 | NHEK | SE_67706 | chr1:151972738-151974921 | u87 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGATGAGGAG AAGCTGGGTC TGTTAGAGGA ATTGAAAAAC CACTAGTGTG TCTGAAGCAA 60 GGCAAGTGTG ACATGGGATG AGGCCGAGAG GGAGTACAGC TGAGCTACAG GGATCTGGTC 120 AACCCTTTTT GTTGGTAATG GAAAAAATAA AACAATTATG TAATATAGTG GTTGTAAGTG 180 CAGACTCTGG AGTTTCAGAC AGGCTTGGGA GGAAATCACG TTTTCTCTGC CCCTCATTAG 240 CTGTGTGATC TTGGACATGT CCTTTTCCAA GGAGAAGACA ACTTACTCTT CACCTTCAGT 300 GAAGTGATCA GGCAGAACGG AATGCTAGCT TGTCTGAATC CCAGTGTTTG GCACTCGGGG 360 AGAACTCTGC AAGACATGAC CTGCCTATCA TGGACTGTGG TCTGCCAGAC TGATAGGGTG 420 CATTTCTCCT CTCTTCATTA AAACTTGAGA GCAAGTGGTG TTCCAGGCAA ACATTTGGAT 480 GCTGTGTCAA AGGGAAACAG TTACTGAAGC CACAGATACT CTTTGTTCAT TGATGATACT 540 GGAATGTGGC TGGGGAGAGC TCAGACCCAC AGAAATTGGA CTCTGTGGGG CCCCAGTGAC 600 TCAAACCCCT TGTGAAATGC TGGCTGCTTG GTATGAACTG ACGCCTCAAC AATGTTAGCA 660 GCAGCTAGCT CTGGGGTTTC TGGGCAGTCC TATTGGCTGA AAGCTGGGGA GGCTGCCATA 720 AGGCTTTCTG GAAATATTTA AAATGGACAA TTTACTGGGA AAGGGTGTGT TCTTGCTTTG 780 TAGCTAATGC TGTGGGACCC TCTGGTGGCC ACAGTGGGAA TAGCTTGACA GTGGGGTTTA 840 CTTTCTCTTG AGTGGCCCAG GCAGGAAATC CTTGGCTGGA AACCAGAGGA TTGAATATGG 900 GGCTGGAAAG ATTACCTAGT TGGCTTGAGA TGGAGGCTGT GATTTAGGTT GACATCCTAC 960 CCCATTTTCT CTTGCTTTTG GCAGCATTTC TCTGGGCTTG 1000
|