| Tag | Content |
|---|
EnhancerAtlas ID | HS092-22836 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr19:39660950-39662800 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr19:39661133-39661144 | TGGGTGTGGCC | - | 6.62 | | ZNF263 | MA0528.1 | chr19:39662775-39662796 | GAAGGAGTGGAGGGAGGGAGC | + | 6.04 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_27062 | chr19:39660312-39661819 | Esophagus | | SE_31899 | chr19:39661027-39661526 | Gastric | | SE_41568 | chr19:39661019-39661980 | LNCaP | | SE_41568 | chr19:39662105-39662849 | LNCaP | | SE_68806 | chr19:39660910-39661933 | H9 | | SE_68806 | chr19:39662005-39662964 | H9 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH19I039170 | chr19 | 39660911 | 39661980 | | GH19I039171 | chr19 | 39662421 | 39662570 |
|
Enhancer Sequence | AGTGGAGAAA ATCACTCCTG TGAAACGCTG GGGGCTTTTT GGTTTTGGGT TTTTTTTTTT 60
CTTCCTGCCA TCTAGAGCAA AATGGCAAGG TTGGGATTTG AACCAATGTC TGTTTCCAAG 120
GCCCGTGCTC TTAACCCCTC TGCTGCCTCC ATGTGAAATC ATAAGAGTTG TGGAGCCGGT 180
GTCTGGGTGT GGCCTGGCAT GAGGCTGGCC TGGCCTGAGC CCGTGCTGGG CCTCTGAAGC 240
CAGCCTTGGA GCCTGGACTC TCTCCCATGG TCAGTGGGGA CCAGGAGGGG CCGCAGGCCA 300
AGGGGAACTC GGCCAGGTTT GCATCCAGCG GGTGGAGATG GGTGTGCCTG GGGACTCACC 360
CTCCCGGTGC CCAGCCCAGC CTGGCGGGGA GAAGCCCCAA GGCCCACAAG TTGGCCATAG 420
ACACAAGTGC AGCCTCAATG TGGTAGCCCA CTGAGGGGTC CGTGTGGTCC TTGCAGGGTG 480
CTTTTGAATG CTTTGACTTC TTTGCCTCCA CTGAGAAAGT GACAGACTTC ACTTCCAAAG 540
CCGTTTCTGG CATCTGGTGA CAGACCAGCT GGAGGCGAGT GGCAGCTGCC TCCACGGGCA 600
GGGCACTGGC TCTTCTGGGC CACAGGCCGC ACCCGACCCA CCTCAGCTCC ACGCCCTGCC 660
TGGCTCTGTG GCCACTTGCA TGTAGGCTTT GCCCCCACCA AGGTGTCTCC AAAAACCCAG 720
CCCCTGCCTG GCTTGCCAGA TGTGAGGCCT GCCTGTGACT GTCCCAGCAG GAGGCAGGGC 780
ACTTGAATTC ACACATGGGG CCTTGTGGCC AGCACTGTCC TGGGGCCCCA TAGGCACTTG 840
TGTTTGCTGC CCTTGACCGG GCCTCAGGCC TCCCAGGACC TTCTCGACTC CCTGTTGGTT 900
TTTTTTTTTT TTTTTTTGAG AGACATTCCT GCTCTGTCTC CCTGGCTGGA GTGCAGTGGC 960
GCCACCTCGG CTCATGCAAC CTTCGCCTCC TGGGTTCAAG CGATTTTCCT GCCTCAGCCT 1020
CCCGCGTAGC TGGGATTACA GGCGCCCACC ACTATGCCCA TCTAATTTTT GTATTTTTAG 1080
TAGAGACGGG TTTTCGCCAT TTTGGCCAGG CTGGTCTCAA ACTCCTGACC TCAGGTGATC 1140
CTCAGCCTCC CGAGGTGCTG GGATTATAGG CGTGAGCCAC TGCTTCTTGC CTCAACGCCC 1200
TGTTCTAACA GCAAAGTCTG GCCTTGTGTC CACCTTGACT TCCTGGGGCC CCTGGGCAAG 1260
GCCCGGCTTC AGGCAGACAG CCACGGCCAG GAGAGACAGG GCAGCGGCAG ACCACGGATT 1320
TTGTGGGATC AGTGTTTTCT ACACGTTACA GGCAGGCCTC TGGCTGGAGG ATGCCTGGCA 1380
GCCCCAGGCA GGGTCCGGGT TTCGTGGGAT CAGTGTTTTC CACACATTAG AGGCAGGCCT 1440
CCGGCTGGAG GACATCTGGC AGCCCCGGGC AGGGTCCTTG TCAGCAGGGC CCACGTTCTC 1500
AGCTCACTGT GGCCTTTGCA CAGACACCTC ACTCACTACG TGGTTTAGCA AAAGTTCACT 1560
GAGCCCCTGC TGTGCGCCAG ATGCTGGTCT AGGTGCTGAG ATGGAGCAGG ACCCGAAGCA 1620
GACAGGAAAA AACAATCCCT GCCCAGAGCA TGCACTAGGC AGAGCCGGGA GCAGACAGAT 1680
GCCTGTGTGC TCTGTATCAG CTGCTGTTAG GTGCTCTAGG TAGAATGCAG GCAGGGCAGG 1740
GGCCGGGGAG GGCAGGGGCT GGCATTTTAG ATGATGGGAG GCCAGCAGAA GCCTCACTGA 1800
GAAGCTGAGT TTTGAGCAAA GACCTGAAGG AGTGGAGGGA GGGAGCCACA 1850
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