| Tag | Content |
|---|
EnhancerAtlas ID | HS051-07716 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr13:111296840-111297980 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr13:111297752-111297765 | CAAAGGTCACGGG | + | 6.82 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09490 | chr13:111296454-111301181 | CD14 | | SE_55064 | chr13:111296525-111298689 | Stomach_Smooth_Muscle | | SE_65828 | chr13:111296832-111297953 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I110644 | chr13 | 111296801 | 111297614 |
|
Enhancer Sequence | TCATGTCGCA GAAGCTCCTT AAAAGCAGTC TTGATGGCAG TGGGCAAACG GAATTCAATG 60
TCAAAAGACA AAGGCTTCAG CAGGTCACTT CAGTCTGGCC TTTCTCCTGG CTTCTATGGA 120
GGGAGGACAC AGCTCTGGCA TCGGCTACCT CACTGCAGAC CATACAACTA TAGGTGCATG 180
AGGAATCTCT TGTGCCTCAG TTTACCCATC AGTCATGTGG GTGGTGACTA GCTCATCAGG 240
CTTCGCGGGT GAAGCATGAC CGTGGAGTAT GGCAGGTGGC GCATGGTAGG TGGAGGCTGA 300
GTGGGCACTG GGCTGGGTTT CTCAGAAAAC GGGGAAATCC TGGTACGTGG CTCACATCAG 360
TTACCAAGCA CAGAGACCCT TGGGTGACAC TAGCCTTAGT TTGCAGGTGC CCCAGAATTG 420
CAAAGCTTGG GAAGGAAAAG CGCAGGACAA AAGCCAGCCT CTTTACTTGT CCCGCCCCTT 480
GCCACAAGAG GCCCCTGTTG CCCTAGAGCT GGGCCAGCCT GGTAGTGCCG GCAGCAGCTG 540
CGGTGAAGGC AGGAGGCCGC GGACGGGCTG AGGAGGAGGA GCTCCCGTGC AGGAGCAGCC 600
TGGCTGCGGG ACCTGCCCCA GCCCGGCCTG GCTGCCTTCA GTGCGGGGCA GCCTGTTCCT 660
GCAGCCGGCT GTGACTCAAA TGCCCGCCCC CCTCAGAGGC GAGCCCTGCG CGTCTGCAGT 720
ATTTGGACCG AAGGCACCCG GCAAGGGCAC ATGGCACCCT GCCCCACCTG CTGGTGCTCT 780
GAAACCCAAC ACTGCACGCA GCCAGGGATG GAGACCTCCA CAGAGATGCT CAACTAACAG 840
AGCATGTGGC CAGAACCCCC AGGTGTTTCC AGAGGTGGGA GAGGCACAAA CAGCCTCGGC 900
TTCCCGGGTC ATCAAAGGTC ACGGGGCTCC TGACGCAGCG CCTCCCAGGG CCTGGCAGGG 960
GACCCTCAGA CGTGCAGGAA CCAAAGCCTG CCGCCGCCTT CACGGTCTTT GTCCCACCTG 1020
CCAAACACTT GCAGTGACCC ACGAGTCCAG GCTCAGACCC CTGGGTGCTT GGTGTGGTCA 1080
TCACACTGGG GTGCAGATTG CATAACAGTG CCTTGGGGTA AATGGGTCTT TCCTTAAAAA 1140
|
