| Tag | Content |
|---|
EnhancerAtlas ID | HS065-01156 |
Organism | Homo sapiens |
Tissue/cell | GM18508 |
Coordinate | chr12:53370520-53371930 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr12:53370981-53370993 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr12:53370985-53370997 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr12:53370989-53371001 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr12:53370993-53371005 | AAACAAACAAAC | - | 6.32 | | Foxo1 | MA0480.1 | chr12:53370687-53370698 | TGCTGTTTACA | + | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_28539 | chr12:53368573-53370700 | Fetal_Intestine_Large | | SE_43402 | chr12:53368192-53371633 | MCF-7 | | SE_47355 | chr12:53367961-53371751 | Panc1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I052974 | chr12 | 53368170 | 53371635 |
|
Enhancer Sequence | GGAGCCATAA GGGATGCAGA CAGAGACTCA AAGACAGAGA CAAGGGCTGA GGGAGGGGGG 60
ATGGAAAGAA CTGGGGAGCC AAAGACTGCA GCGGGGAAAG AATGCAGTGT CCATCCTAAA 120
AGAAGGAAAA TGGAAGTTTC CCAGGGAGGA GGGTGCCTGA TCTTATCTGC TGTTTACATT 180
CCAGAGAGCC CCTGCTTCTG CTTCTCATCT TAATTAGAGA ATACTTGAGA AGCCCTGCCG 240
CCGTGCAGAG AGAAAGGAAT GCAGGCCCCC ACTAAACCCC AGCCTGCCCC CCTCACCCCT 300
GACCTCCTGC TGGCTATGTG GTGGGACTGA TGGGAGTCTG GGTTCTGGAT CCATTTTCTG 360
TTTTCTGTTT TTTTGTCTAC AGTGGGCTGA TCCATTAAGC TGGATTCCTT GAGAGAGTAT 420
GTGAGAGGGT CTGGGAACTG TCAGGGCTCC ACTCCTGCAG GAAACAAACA AACAAACAAA 480
CAAACAAAAT TAAAAAGTAT TAGAAAGAGC CACTGAGAGG AACAGCTGAG ATTCTCTCAG 540
TCAGTCTGCC ATTCACCCCC TCAAACATCG CCCTCACTCC ACCACCATAA TGTCCAGGCA 600
GGGTGCTGAC ACTTCACCGT TCACCTCCCA CCCTGCCCCG GGCTGTCCTC CAAATGTGTG 660
TCAGACACAG TGCTGGGGGA CTTATACTTC TGTCATAGTC TCTGTCTTCA GTAGCATATG 720
GTAAGAGCCA GGATCCGCTA TTAAACATGC TGTGAGTGGG TAGAGACAAA GTCTTGTCTT 780
GTAGGGTGAG CAGGCAGTGA GGTCAGAAAG GGCATCACAG GTAGAGGAAA AAGCATGGGC 840
AGAGGTCTGG AACCCAGTCC CTCTTCATAC CACCCGCTGA CCCTTTCCCC TCCCCCCCAC 900
ATGAGATTTC TCCCCCTCTC TTCTCTCTTC TCTCCCTCAA CAATTCCAGG GTTGCCCACC 960
TGAAAACAAG CTCCCTGGAC CACCTTCCCT TGCAGCTCTC TGTTCCTTCT CTCTTTTTTT 1020
TTTTTTTTTT TTTTTGAGAC GGAATCTCAC TCTGTCACCC AGGCAGGAGT GCAATGGTGT 1080
GATCTCAGCT CACTGCAGCC TCTGCCTCCC AGGTTCAAGT GATTCTCCTA CCTCAGCCTC 1140
ACGAGTAGCT GGGATTACAG GTGCCCACCA CCACACCCAG CTAATTTTTG TATTTTTACT 1200
AGAGATGGTG TTTCACCACA TTGGCCAGGC TGGTCTCGAA CTCCTGACCT CAGGTGATCC 1260
ACCCGCCTCA GCCTTCCAAA GTGCTGGGAT TACAGGCGTG AGCCACTGCG CCTGGCCAGC 1320
TCTCTGTTCC TTCTCATAGC TAAGCATCTT ACATCATTCT CTCTCGTTTT GTTGTTGTTT 1380
TGTTGTTGTT GTTGTTGTTG TTGTTGTTGT 1410
|
