| Tag | Content |
|---|
EnhancerAtlas ID | HS051-08387 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr14:77430880-77432420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mafb | MA0117.2 | chr14:77432260-77432272 | AGTCAGCATTAT | - | 6.14 | | RREB1 | MA0073.1 | chr14:77431152-77431172 | TTGGAGAGGGTGGGTGGGGG | - | 6.16 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_24529 | chr14:77431089-77431884 | Colon_Crypt_2 | | SE_24529 | chr14:77431954-77432400 | Colon_Crypt_2 | | SE_27091 | chr14:77431372-77432306 | Esophagus | | SE_31928 | chr14:77431084-77431952 | Gastric | | SE_65382 | chr14:77430652-77431927 | Pancreatic_islets |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH14I076964 | chr14 | 77431161 | 77431310 | | GH14I076965 | chr14 | 77431373 | 77432400 |
|
Enhancer Sequence | CCAACGTGGA GAAACCCCAT CTCTACTAAA ATACAAAAAA TTAGCGGGTC ATGGTGGCAT 60
GCACCTGTAA TCCCAGCTAC TCAGGAGGCT GAGGCAAGAG AATCTCTTGA ATCCTGGAGG 120
CAGAGCTTGC AGTGAGCTGA TATCACGACA CTGCACTCCA ACCTGAGCGA CAGACCAAGA 180
CTCTGTCTCA AAAGAAAAAA AAAAAAAAGA GGTGACTGAC AGAGAATGAC CCCAGCAAAG 240
GACCAGAGAA GGAGCAGTCC ACGGAGGACC ACTTGGAGAG GGTGGGTGGG GGGAAACCCA 300
GCTCACAGGA GAAGGTGTGG CCGATGGTGT GGCATGCTGC TGAAAGGCCA GGTAGGTGAG 360
AACAGTGGTG AGCACTGTTT CAGTGGTGGT GGTGGCGGAG GGAGAGTGAC AAAAAGCATT 420
TGGTTCTGAG CCTGGGAGTA GCAGGCTGGG GGAGGAGCCT AAGGCTAGGC CGGCTCTCAG 480
GAGCAGTGTG GGCCCCAAAT ATCCTCTTCT GTGATCTTTT TACCTTTTGG CAAAGTGTTA 540
TTTAAATGTA TTTAAATCTT TTAAGGAAAT ATTTCTAATT TTGTGCCAAA ATAAAGCACT 600
GTAAATCCTA GCCACTGTTC CTTTGCTTCC CCAGGGGCCG CAGTGACTGT GTCCAGTCCT 660
TCCTCACCCC GCTGCAGAGT CAGTCCAGGA GGCCTTTACC CACAGCACTG CCACCTCCCT 720
CCACGACCCC TGTCTTTCTC TTCCCCAGAT TAAACGCTCC CACTTCTCTC CATTCTTCTT 780
TCTCCACCCC CAGGCCCATT TCTGCCTCGG TTGCCTGCCT CCAACCACAA TCCAGTTTTT 840
TGGCTCCCAG AGACAGACAT GCCCAGATCT GAACACCACC CACCTGGGTA TGTTCTGCCA 900
GTGTGCAAGG TGGGGCCCTC CAGGCCCTCT CCTCCCCTCC CTTTTTCTAG ATGCCATTTC 960
CTGCTAAAGC CACCTCTCCC ATGGCTATAA ACTACCTTCA ATCAGGGCAC GAACTCTAGA 1020
GCACAAGAGA ACCTGAGATT CTTTAAAACA TTCTAGTTTA ATGTCCTCGT TTTACAGATA 1080
AAGAAAATGG GTACGGCCAA GACCATAGAC CTAGTGATTG TCAGATGAAC AATTAGACCC 1140
ACAGAACCAT CCAAGCTACA GAGGACGCAT TCTGCCTTCC CTTGGATCCT GTGGTTTGAG 1200
GATGGAGGTC TAGGACCGTG GCAGGCTTTT TGTCCCATGA GGGAAGGCCA TGGAGCTGAG 1260
GAAGGGGAAG AACACACACA CCTAATGGAA TCTCGAGAGA AAGTTCAGAC ATCAAAAGAC 1320
AGAAGCGACA GAGACCCAGG TCTGTGGGGA CGCTGTATGG CTGAGTCAAG TCTTGATCAA 1380
AGTCAGCATT ATATCTGGAC TTGCACAGTT TCTGAGCCTT GAAACTCCAT TTCGTTTAAG 1440
TGAGCTTTTA ACTGTCACAG GCAGCTGCAT GCACACACAA GTCCATGTGA TTAGATGTTT 1500
CCAAGAGTCT GGAATAACAT ACCCCAAACT GTTAATAGTG 1540
|
