| Tag | Content |
|---|
EnhancerAtlas ID | HS101-15164 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr15:65042580-65043750 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr15:65043315-65043330 | GAGGTCAGGAGTTCA | + | 6.22 | | Zfx | MA0146.2 | chr15:65042998-65043012 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_41026 | chr15:65037653-65044857 | Left_Ventricle | | SE_48862 | chr15:65037665-65043189 | Right_Atrium | | SE_48862 | chr15:65043401-65044905 | Right_Atrium | | SE_54599 | chr15:65037420-65046338 | Stomach_Smooth_Muscle | | SE_68765 | chr15:65042047-65042965 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I064750 | chr15 | 65041977 | 65042894 |
|
Enhancer Sequence | CTGCGGAGAG AGGTGGCTGT TACCGTGGAA GGTCAGAAGC GTATGTTGTG CTAGCCCAGC 60
GCTGCCACCT CATCAGCCCC CGCGTTCCCC TGAGTCATTC TCACACCCTT CTCCCTGTCA 120
ACATCAACCC ACCCTGACCT CCGCCACTGC CAAACGTCCA CCGCCCTGCG TTCTGAATCA 180
CGCGGTCTAG CACATAGGGT GGGCATCACG CGGCAGCACT CATCACTTCA GGCAGAAATT 240
CCCATTTGCT CCACTAACTA GTAACCCGAG AGCACAGACC TTACCTTTTA AGTTTTCTCA 300
TCTGCAAACT GAAAAGGCTA CACTGAATCT CAAAGATTCT TTATATAACC ACATATATTT 360
AAAGATTCTT ACTGTTAGCT GGGCATCATG GCTCACGTCT GTAATCCCAG CACTTTGGGA 420
GGCCGAGGCG GGCAGATCAC AAGGTCAAGA GATCCAGACC ATCATGGCCA ATATGGTGAA 480
ACCCCATCTC TACTAAAAAT ACAAAAACTA GCCAGGCATG GTGGAGGGTG CCTGTAGTCC 540
CAGCTACTCG GGAGGCAGAG GCAGGAGAAT CGCCTGAACC CAGGAGGCGG AGGTTGCAGT 600
GAGCCGCACG CCACTGCACT CCAGCCTGGG CAACTGAGTG AGACTCTGTC TCAAAACAAA 660
ACAAACAAAA AGGACAAGCG CCGTGGCTCA CACCTGTAAT CCCAGCACTT TGGGAGGCCG 720
GGGCGGGCGG ATCACGAGGT CAGGAGTTCA AGACCAGCCT GACCAACATG GTGAAACCCC 780
ATCTCTACTG AAAACACAAA TATTAGCCGG GCATAATGGC GCATGCCTGT AATCCTAGCT 840
ACTTGGGAGG CTGAGGCAGG AGAATTGCTT GAACCCAGGA GGCAGCGGTT GCAGTGAGCC 900
GAGATCAAGC CACTGCACTC TAGCCTGGGC GGCAGAGCAA GACTCGTCTC GAGGAAAAAA 960
AAAAAAAGAT TCTTACTGTC TCCATTTAAC TGGCGAGGAA ACAGAGGCTC AGAAGGCAGC 1020
ATGTGAATTC GCAGAACCAG GACACGGGCT GGACCTGCCC CCACAGCTTC TGCCACGCCT 1080
TCCCGCATCA TCCTGCTGCC CTGCCCGACC CGAGATTCAC TCCCGCTGCT TCTCCAGGGT 1140
CCCAGGCTCT ACCCAGGGGG CGGCTGGGTC 1170
|
