| Tag | Content |
|---|
EnhancerAtlas ID | HS094-18755 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr19:5926100-5927280 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr19:5926684-5926697 | AGCAGCTGTCTCC | + | 6.21 | | TEAD1 | MA0090.2 | chr19:5927167-5927177 | CACATTCCAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_06265 | chr19:5926533-5928051 | Brain_Hippocampus_Middle | | SE_31728 | chr19:5927085-5927871 | Gastric | | SE_42610 | chr19:5926484-5928110 | Lung | | SE_44587 | chr19:5925185-5928523 | NHDF-Ad | | SE_49179 | chr19:5925872-5928148 | Right_Atrium | | SE_50862 | chr19:5925649-5928073 | Sigmoid_Colon | | SE_53195 | chr19:5925788-5928090 | Small_Intestine | | SE_54795 | chr19:5924181-5930539 | Stomach_Smooth_Muscle | | SE_65343 | chr19:5926997-5927821 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I005925 | chr19 | 5925743 | 5928392 |
|
Enhancer Sequence | TATGAACATG ATAGAAGCAG AATTTCTTGA GGGCCTCTTT CCTACCAGCT GCTATGCTGA 60
GTCTGTCAAA TGCACGATCT GCTTTAATCC TCACGAGGCC TGGGAGGGGG ATGTTAGGGA 120
CCCTGTTTGA CCAACAAGGA AGCAGAGGCT CAGAGGGTTA AGAAACCATG GCTCTGGCTG 180
GGCGCGGTGG CTCGTGCCTG TAATACCAGC ACTTTGGGAG GCTGAGGCGG CGGGGAATCA 240
CTTGAGGTCA GGAATTCGAG ACCAGCCTGG CCAACATGGA GAAATCCCCA CCTCTACTAA 300
AAATACAAAA AATTAGCTGG ATGTGGCAGT GGGCGCCTGT AATCCCAGAT ATTTGGGAGG 360
CTGAGGCAGG AGAATCGCTT GAACCCAGGA GGTGGAGGTT GCAGTGAGCA GAGATCATGC 420
CACTGCACTC CAGCCTGGGC GACACAGCAA GACTTCGTGT CCAAAGAAAA AAAAAGAATC 480
CATGGCTCAA GTTTGCCCTG GAAGGAGAGG CTGGGATTTG ACTGAGACTG CGAAGTGCAC 540
GTAAGCCTCT GACTTCTGCA AGAAGCCAAC CCCACCAAAT TCAAAGCAGC TGTCTCCCCA 600
GACTCAAGGC AGAGATTCCA CAGGGCCTGA ACTCCACAGG CCAAGCCCTT CCCCGCCTCT 660
TGCCCTCCCT CCTTGGAGGG AACAGCCCCT GAGGGACTCA TTATTTTGCC TAAAGCCATG 720
GCAACAGCAA CATCAACTTT CCACGTTTCT CGACTTGGGC TTCTGTTGGA CGGTGAGTAA 780
CAGAAAGGAA AGCAGAAAAC ACAAGCCGGT GCTTTCTGCA TGCTAGAGAG GTTTTTGTTT 840
ATTTCAGGGC CCTCCCCGTC GACACTACTG ACATGTTGAC ACTGGGCCCA GAACATTCCC 900
TGTGGTGTGG CTATCCTGGG CACTGCAAGG GGCGGAGTGG CATCCCTGAC CTCCAGAAGT 960
ACCTCCCAGT TGTGACAACC ACAAAAGTCT CTAGACACAG CCACCGATAC CGCCTCTCGA 1020
GCTTTGAAAG AAGCTTCTTG CCAGTGGAGC TGCTAGAGAT GCCGTAGCAC ATTCCATGTC 1080
TGTGGCTGGG AAAGGTGGTG CTGGCTGACC CTGGTCTTCC TAGAGTCCCA GTGCATGGTC 1140
CAGGGCCACT GTTTCCAACC ACTGCCATCC CTTCCCCACC 1180
|
