Tag | Content |
---|
EnhancerAtlas ID | HS101-01093 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:33194660-33196040 |
Target genes | Number: 17 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr1:33195458-33195468 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:33195458-33195468 | GGCACGTGCC | - | 6.02 | RREB1 | MA0073.1 | chr1:33195238-33195258 | ACCCCACTCAACAACCACCC | + | 6.31 | RREB1 | MA0073.1 | chr1:33194695-33194715 | GGCTGGGGGGTGGGGTGGGG | - | 6.92 |
|
| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_00938 | chr1:33194530-33196220 | Adrenal_Gland | SE_23116 | chr1:33194873-33195324 | Colon_Crypt_1 | SE_65538 | chr1:33194563-33195662 | Pancreatic_islets |
|
| Number: 2 | ID | Chromosome | Start | End |
GH01I032731 | chr1 | 33194874 | 33195324 | GH01I032729 | chr1 | 33195561 | 33195810 |
|
Enhancer Sequence | CTGAGCCTCA TTCAAGTCAA GTCCACATCC TCCCAGGCTG GGGGGTGGGG TGGGGTGCAG 60 GATGCAGGGG AAGGATGCAC ACACACCTGA CTATGGATCT TGGCTCACTG GCTCTGTGAC 120 CTGGGACCAG TGTCTTCCCT CTCTCAACTT CATTTCATAG AGCTAAGAAC CCAACTTACA 180 GGGCTTCCGT GAATTCTGTG GGAACAGGTA AGTGATCATT AATTGTAGAC AGTTAGTTCC 240 CTGTCCCCTA GTCTCCAATT CCCTCCTCCA GGGCCTGGCA CCAAGCTGAG CAGAGCGAGA 300 AACAGTAAAT ATTTAATAAC AGATGGGCTG AGAGCTCCTA ACTGAAGGGA GATGTGGAGG 360 AGCCGGAGGA CACTTGCTTC CCCAGCAGGG GCAGCTGTGC AGACAGGCCG ACCTGGGCTT 420 CAGGGCTAGT GATAGCCAGA TCCTGAAGGA GTTCTTGCCT TCAGTGACTT CCTGAGGGAG 480 CCACAGCTAC CAGTGGCCTT CCCAGGGTAC CCTAGCCCCA CAACACATCT CTCCTATTTT 540 CTCACTTTGC TGCTCAGATG AACATCAAAT GGATGTGGAC CCCACTCAAC AACCACCCAC 600 TGAATCCCTC TCCACTGCGC CAAGCCTCTC CTGGCACTAT AAATTCAGAG AGGAAGGAGG 660 CCAGCCCTTG CTCTTCAGGG CCTCCCATCT AGCTGCGAGA GTGATGGAAA ACATGTTTGC 720 TAAAATGTGA TAGCTAGCCT GGGCAACGTA GGGAGACCCT GTGTCTACGA ATAATTAGAA 780 AAACTAGCCG GGCGTGATGG CACGTGCCTG TGGTCCCAGC TACTTGGGAG GCTGAGGTGG 840 GAGGATGATC GCCTGAGCCT GGGAGGTCAA GGCTGCAGTG AGTCGTGATC ATGCCACTGC 900 ACTCTATCCT GGGCAACACA GCAAGACCCT GTCTCAAAAA AAATAATAAT AAAAAAAGCT 960 GGGTGGCCGG GCGTGGTCCT GAAGGCTGCA GCTGTGCATG TCATCACTTA GTCACTTGCC 1020 TGGTGGTCAC CTATGAGTCA ATGATTCAAA GGTTTCCATC CCAGGGATAC ATCTGCTTCT 1080 TAATAGGAAT TTACAGGGAC AATCCTTTGA CCAGGGGAGC CACCTAAGGG ACTGAGACTT 1140 GATCCCAGAG CAATCAGGCA GAGACTCTGT GCAGCTTCCT TTCCCTTCCT GCCCAGACAT 1200 GCTGCCCCTC CCTCCGACCC TGGGCCTCCC CTTTGTGAAT TTAGGTCTCT GTGGTTGTCT 1260 GTGGGCTGAG GCAGCAAAAA GAGCATTTTG GAGTGAGCCA GAGCTAAATC CAAATCCTGG 1320 TTCTATTACT AACTAGCTGT GTGACCTTGG TCCAATTTCT TATCTGCTCT GAGTCAGTTT 1380
|