| Tag | Content |
|---|
EnhancerAtlas ID | HS073-05018 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr16:8944240-8945450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr16:8945029-8945040 | CATGAGTCACC | - | 6.62 | | JUND | MA0491.1 | chr16:8945029-8945040 | CATGAGTCACC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr16:8944963-8944978 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr16:8945265-8945280 | TGAACTCCTGACCTC | - | 6.22 | | Nr5a2 | MA0505.1 | chr16:8944955-8944970 | GCTGGCCTTGAACTC | - | 8.25 | | RARA | MA0729.1 | chr16:8944960-8944978 | CCTTGAACTCCTGACCTC | - | 6.73 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_01141 | chr16:8942170-8944934 | Adrenal_Gland | | SE_27347 | chr16:8942201-8947497 | Esophagus | | SE_65798 | chr16:8944062-8944985 | Pancreatic_islets | | SE_65798 | chr16:8945277-8946472 | Pancreatic_islets | | SE_68855 | chr16:8941535-8945039 | H9 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH16I008847 | chr16 | 8941569 | 8945057 | | GH16I008851 | chr16 | 8945329 | 8945470 |
|
Enhancer Sequence | TCACCCAGGG CTTAAGCCTC AGAGAAAAGG CCTGGGTTGA ACCTGAGCAG TGGGTGAGTG 60
CAGGGCAGGC CTCTGGCTCC CTGGAGGGAG AGGCTAGCCA GGAAGTTGAG CTTGAACCTG 120
ATCCCGAGGG AGAGGTGTGG GGCATGCTCA TGATCTGTCC GGGAAGGTCT CTCCAGCTAC 180
TGGAAGGGGA GTGCCCACAG GGGCCAGGAG AAGGCAGTTG GGCAGATGTT GCCGTAGTCC 240
GGACACATCC AGGCATACGT GGTTTTGAAT CACTTCCTCT CCAAGGGCTG CTGCTTCCTC 300
TCCACCCCTC CCAAGTGTTC TGGCTCTGGG CCCCAGCTGG CCACCTCAGC CCAGGCAGGC 360
TCCTCCAACC TGAACGACAG GCAACCTCCA CGCTGCCTGC CACGGCACCC CAAAGTCAAG 420
ACGTAGAACT CATTCCACCT CCTTCACCCG AGGCTGCTTT CCCAAACGTC TTCCCAGTCC 480
CACCTTCAGT TTTGTTTTTT GTTGTTGTTG TTGCTATTGT TTTTGAGACA AGTCACTGTT 540
GTTGCCCAGC CTGGAGTGCA ATGGCACGAT CTCAGCTCGC TGCAACCTCC GCCTCCCCGG 600
TTCAAGCAAT TCTACTGCCT CAGCCTCCCG AGTAGCTGAG ATTACAGGCC CCTGCCACCA 660
TGCCCAGGTA ATTTTTGTCT TTTTAGTAGA GACGGGGTTT CACCATGTTG GCCAGGCTGG 720
CCTTGAACTC CTGACCTCAG GTGATCCACC TGCCTTGGCC TCTCAAAGTA CTGGGATTAC 780
AGGCATGGGC ATGAGTCACC ATGCCCGGCC TTTTTTTTTG TTTTTGAGAC AGAGTCTCAC 840
TCTGTTATCC AGGCTGGGGT GCAGTGGCAC AATCTTGGCT CGCTGCAACC TCTGCCTCCA 900
GGTTCAAGTG ATTTTCCTGC CTCAGCCTCC CAAGTAACTG GGATTACTGG TATGCACCAC 960
CACGTGCAGC TAATTTTTGT ATTTTTAGTA GAAACGGGGT TTCACTATGT TGCCTAGGCT 1020
GGTCTTGAAC TCCTGACCTC AAGTGATCTG CCCACCTCGG TTACCAAAGT GCTGAAATTA 1080
CAGGCGTGAG CTACCACGCC CGCTCCCCAC CTTCAGCTTT TGCCAAACCC TTCCTTGGCT 1140
ACCCATGTAG TACTCCATAT AGTAAGTAAG TCAGCAAATC TCATTGTTTT GAGCTAAGTG 1200
CCTACGTTAG 1210
|
