| Tag | Content |
|---|
EnhancerAtlas ID | HS105-59358 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr4:1172000-1173230 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr4:1172243-1172254 | TCTTCCCGCCC | - | 6.14 | | MYC | MA0147.3 | chr4:1172702-1172714 | GGCCACGTGCTC | + | 6.92 | | Myog | MA0500.1 | chr4:1172411-1172422 | AACAGCTGCAG | + | 6.02 | | Tcf12 | MA0521.1 | chr4:1172411-1172422 | AACAGCTGCAG | + | 6.62 | | ZNF263 | MA0528.1 | chr4:1172185-1172206 | CCCCCTCCCCCTCCCTCATCT | - | 6.56 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_20277 | chr4:1170508-1172131 | CD56 | | SE_65329 | chr4:1172464-1173174 | Pancreatic_islets |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH04I001176 | chr4 | 1170670 | 1172418 | | GH04I001179 | chr4 | 1173041 | 1173190 |
|
Enhancer Sequence | ACCACGGGCT CTGCACACAC CGAGGGCCTC CCTCCGGCCA GGCACCATGG GCTCTGCACA 60
CACCAAGGGC TTTGCTCCGG CCAGGCACCA TGGGCTCTGC ACATATCTGC TTTCTAAAGG 120
CTACTTTAGC CCTTGAGACT TCAGACTCGC AGGGATGGGG CCACATGGTC CAGTGGTTCT 180
CCTGGCCCCC TCCCCCTCCC TCATCTTCAG ACTCGAAGGG ATGGGGCCAC ATGGTCCAGT 240
GGCTCTTCCC GCCCCACTCT CCTCTGTCCC TCCTCTTCAG CACCCGCTGA CTTCCTCCCT 300
GGCCAAGACA CCCCTGGCTG CTCACACCTC AGGGCCTTTG CACGTGCAGC TCTCCCTACC 360
TAAAGGATTC TTCCTGTGCT GCCTTCTTCC TGCCATACAG GCCTCAGGGA GAACAGCTGC 420
AGGCCCCACC CCCCACCCCC AGAGGAGTGC CTGGTCATAC TCTGTCATGC CAGGGTTTTT 480
TTTTCAATCA GAGCTCCTAC AGAGAACTAA GCCTACCATA ACCAGTGTGA GCAGACAGGG 540
ATTTACTATG GGGGCTAAGT GGCTTATAGA ATTGTGAGGA GGGTTGAAGA GAGACTGTGG 600
ACTGAGTGTC CAAGGGTGAC CTCCCACACT GCACAGCAGG ACGGGGCTGC GGAGTGGCAG 660
CTGGTCCCCC CTGTGCAGGA ACCCGCCACC CCAGCAGCAG ATGGCCACGT GCTCCTGTGT 720
CCCTCTTGCC CACATGCCTC CATTCTGGAT TCAGGTTTCT CTGAGCACTT CCGATTGATT 780
GGCAGAGCCT GAATCAGGTC AGGGAATCCA GAGTCTTGGA TTCAGCTTTG CAGCCTCTGC 840
AGTCCAGGAG GACACCCAGA AGGAGGATGT GAATCGTGCC AGTGAGCTGA GCTGCAGCCC 900
ACACAGTGCT CATCCCCCTG CTCTTCTCTG ACTTATTTAG CTGACGCTGA GTGGGGACCT 960
TGCCCGGCTG CTTCACCTCT GGAAGCACGA CTGCAGCCAC CATGCCAGGC TCACGGGAGG 1020
GCCAGCAAAC ACAGCACTCA CTCTTATCAG GTTTCACAGT GGCTCTTCCA GTCCCACCTT 1080
GCAAAGGAGG CCAGGTCACT GCTGGCGAGC CACAGATCTG GGAGGAGAAT CTGCTGCTAC 1140
TATCTGGTTC TAAATACTGT TTTTTCTCCT CTGTGCAACA GTCCGCCTCC CTCGAATATG 1200
AGCCTATCCA TTTTCAGTGA CACTTGCCAT 1230
|
