| Tag | Content |
|---|
EnhancerAtlas ID | HS105-77659 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr8:42122370-42123820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr8:42123319-42123330 | GGGTGACTCAG | + | 6.02 | | JUNB | MA0490.1 | chr8:42123319-42123330 | GGGTGACTCAG | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26990 | chr8:42122587-42124433 | Esophagus | | SE_34968 | chr8:42122667-42124204 | HeLa |
|
| | 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 |
| GH08I042264 | chr8 | 42122049 | 42125756 |
|
Enhancer Sequence | CGGGCCTTAA ACATTTTTTT TTTTTTTGAG ATGGAGTTTT ACTCTTGTCA CCCAGGCTGG 60
AGTGCAATGG CGCCATCTCT GTTTACTGCA ACCTCTGCCT CCTGGGTTAA AGTGATTCTC 120
CCGCCTCAGT CTCCCGAGTA ACTGGGATTA CAGGTGCTTG CCACCACGCC CAGCTAATTT 180
TTGTACTTTT AGTAGAGATG GGGTTTCACC ATGTTGGTCA GGCTGGTCTC AAACCCCTGA 240
CCTCAGGTGA TCCACCCCAC TCGGCCTCCC AAAGTGTTGG GATTACAGGC GTGAGCCATC 300
GTGCCCAGCC CATTTTATTT TCTAAGTAAA GATAGGTTCT TGTTATGTTT CCCACGCTGA 360
TTGTGAACTC CTAGACTCAA GTGATCCTCT TGCTTCAGCC TCTGGGATAG ATGGGACTAC 420
AGGTGCACAC CACCACACCC GGGCAAAAGG GTCATTTTTA TTCTGCTTTC GGAGTTGCTT 480
CTTCGGTTGC TGTTTCTCAG AATAATCTGT ATGCCAAAGA GGCCTATTTT GGGTGGCATA 540
TTCTGGTCTC CTACTGTGAT CTGGCCTCCC AGATAGTCAC CAGCAGACTC CTGCAGAAAG 600
GAAAAGTTGG GACAGGCAGG TAGGAGGGCC AGGCACCACT GACAAGGGGA AGTGCAGAGA 660
GAGGCCTGAG CCCAGGAAGG ACTAGAGTCC GGCAGCTGAG CTGCAACACA GCCCATGGGT 720
CAAAAGTAGG AGCTCAGAAC CAAGGTAAGC CGAAAAGCAT ACCTGTTGGT TTCTTAGACG 780
TCTACACCGG CCCATAGCCT TTGTCTCCGC CACCATGGCC TGAGGTGGCA GCTGCCCTTT 840
CATGACTTCT TCCTCTTTAG TTTGAATTTA CTGGAATAAA AACGTGTGTG TAAAAGTAAA 900
GGGAGCTTAA AAAGTGATTT CCTCCTCTAA GCTCTTGTTC CTCCAGAGAG GGTGACTCAG 960
AGCCCCAAAT CCTTGCCTTT GCTTGTTTCT GCCTAAGTTT GAGGCACAAC AGCCGGCTGG 1020
CCCTGCTCCT CTCAGTTTCT TGATTGGCCC AGGTCCAGTC ACAGAGACAG CAGCTGGCCA 1080
ATTTCCTTTC CTTCCTCTTC TGCAGCCAGC TCTGCATGGA GCCCAAAGGG TCTGCGGCAA 1140
GGTTCATTCT CACCCTCGTC TCCACCAGCC CACCCTCATC TCCCACCAAG GTCCCCAGAA 1200
CAAAGGCAGA CTTCTTCACA TCCTCCGACT TTCTAAACTA GTTTCTCCAA CTTTTCTGGC 1260
AGAGGAGTTT TTGTCTGTTG AAGAAGCAAG TCCTGACCTG CAGAGTCCTT TCTCTGCAGG 1320
GCTGGGATAA AACAAAATCA GATGGGTCAT GAAAGAGTTG CTGAAATCGC TGAACCAGAG 1380
CTGACTATGG GGGCTGGGGT GCTGGGGAAA TCCTCCCCAT CCTCTGTGGT CTGCCTTACG 1440
GCCTCTTATC 1450
|
