| Tag | Content |
|---|
EnhancerAtlas ID | HS050-27168 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr16:89429950-89431460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr16:89430191-89430202 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr16:89430191-89430202 | GGTGACTCATG | + | 6.02 | | KLF4 | MA0039.3 | chr16:89430399-89430410 | GGAGGGTGTGG | - | 6.32 | | TFAP4 | MA0691.1 | chr16:89431053-89431063 | AACAGCTGAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_09347 | chr16:89429718-89434557 | CD14 | | SE_18559 | chr16:89429883-89432442 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_26651 | chr16:89429817-89431465 | Esophagus | | SE_31628 | chr16:89429942-89431550 | Gastric | | SE_41566 | chr16:89429954-89430881 | LNCaP | | SE_47239 | chr16:89429316-89432368 | Panc1 | | SE_47827 | chr16:89431015-89431352 | Pancreas | | SE_65322 | chr16:89430841-89432177 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I089356 | chr16 | 89423138 | 89432451 |
|
Enhancer Sequence | TACATAGTTC ACAATTCTGA GTCCAGAATC TAGGAGAAAC CACCAAAACT TTCTTTGCAT 60
TCTGTCAAAT TCAAACGCAC TCTGTGTGCC AAGCCTCACT CACTTTATGT CCACCAAGCA 120
CCACACGCTG CTTCCCGTGT ATGTGGCCCA GGCCCCTGTG AAACAAACAC ACTCTCTGTG 180
GTAGACTGGA AGAACACGGG CCTGCAGGTT CCAGTCAGGA AGTGGAGTGC TAGCCCTATG 240
CGGTGACTCA TGCCTGGAGC ACAGCACTTC AGGAGGCTGC GGCAAGGAGG ACTGACTGAG 300
GCAAAAAGTT CGAGACCAGC CTGGCCATCG TGGCAAAACC CTGTCTCTAC AAAAAAGAAA 360
AAAAAAATTA CCCAGGTATG ATGGCATACA TGCCTGCAGT CCCAGCAACT CAGGAGCCTG 420
AGCAGGAGGA CAGCTTGAGC CCGGGAGTTG GAGGGTGTGG TGAGCTATCA TTGTGCCATG 480
CCACTGCATT CCTGCCCAGC CGACCAAGTG ACACGCTGAT TTAAAACACA CACACACACA 540
CACTCAATGG AAGGCAAAAG AAAAGGAAGA AAAAAAAGAC ATGGAGCCTT TCTTTCCAGC 600
CCTGGAGCCT GGGTGTACCC CAGACTTGCT GGGCCCACGA GGACCCTGCC ACTTCCACCT 660
GTGCCCTCAG GCAACATGTG GGGGCCCACA CAGACTGAAG TATGAAATGG ATTCAGCCCC 720
CATCAGCCTA ATGCAGCTTC ATGAGTGATC CCAGGTATGA CCAGCAGAAA ACCACCAGGC 780
AACACAAGAA TTAAGAGAAC TCATAAATCA TTATTTTCTT AAGACACCAT GTATTGTCTT 840
ACACCGCAAT AGGTAACTGA AACACATCCT ACTCACGGTA AGAACAAGCT GAAATATGGA 900
AAGTTGTTTG AGATGCTACT TAAACACAGA TTTAACTCCA GAGCAGAGCC TTTCCATGTA 960
TTTTTCTTAA CCTATTCGCC CTCAAAACAG CGCTGAGCAC AGCAGTCAGA CCCTAAAGCA 1020
GAGGTGTCCA ATCTTTTGAC CTCCCTGGGC CACACTGGAA GAAGAACTGG CTTGGGCCAC 1080
ACATAAAATA CACCAATGCT AACAACAGCT GATAAGCTTA GAAAAAAATC TCATAACGTT 1140
TACAAATTTG TGTTGGGCCA CATTCAAAGC TGCCATGGGC CGCGGGCTGG ACAAGCTTGC 1200
CCTATCTCAC ACTGTTCCCT GTCAGACTGT AAACACTACT CAGAATCACA CAATCTCATC 1260
TCGGCTCCAA GTGGAAGCTT GCTCAGCACC ACGGCCAACC TGATCCCACT GCAGATGTTC 1320
CAACAGCCTG GCACGCAGAT GGCCCAGGGA AAAGCCTCAT CGAATGCTGA ATACCTGTGA 1380
GATCATTTCT TACAAAGCCA AATGAACAAC ACTATGTTAA TTTTCAAATT TTGGCATGGA 1440
AATCACATTC TAAGACGCTT CCCAAGCTTT CTGGAGGATG CTATGAATTC TGTTTTATAG 1500
GTAACAAGTC 1510
|
