| Tag | Content |
|---|
EnhancerAtlas ID | HS108-04728 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr10:3580710-3581830 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr10:3580778-3580794 | CCTTAAGTAAATATTT | + | 6.05 | | FOXC1 | MA0032.2 | chr10:3580781-3580792 | TAAGTAAATAT | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_44461 | chr10:3579873-3585720 | NHDF-Ad |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I003537 | chr10 | 3579994 | 3582614 |
|
Enhancer Sequence | AGACATTGTT TTTCACTTTT ATTATTATAC ATCAAAGATA TGGTATTTTC CATGTATGTT 60
CATTTAGTCC TTAAGTAAAT ATTTGTCGAT TACATCATTG GATCTTCACA GAAGTGGCTC 120
CTGACTAAAC AACACTGTAT TGTAAGAGAA ATGGCATCAT TTTTTAGCAT ATTTTCTCTT 180
TAGAAAAGAA GACAGAGATT TGAATTTGGG CGACACACAT AATAAAATGG ATGTTTTCTT 240
TTTAACAACC AAATCATACT CGAATTACAA AACCCTCCAG GCATTATCAG TTAATGCAAA 300
CACAGGAGGA AGATTTCTGC TCTCCGATTA CATAAAACGT CTCCCCATTC CCAAGATCCT 360
GGAGCCTCTC TCCCAGCGTC AGCTGTGGAC CGCGGGTTTT GCAGAACGGG AATTCAGGCA 420
CTGTGATCTC AGCCAGTGAG GAGGTCAGAT CAGGGCCCCA GGTTTGCCTG GTGGACCTTC 480
CGAGTGGAAA GCAGCCAATG ATTTGTTACC ATGCAGGACA GCCGCCTCCG GGAACCCGTG 540
TGTGGCCCGG GTGCCACGCA GCCTCGCGAC CCCTGCCTCT CTTCACTGGC TTGTTCTCTG 600
CCTCAGTCAG AGCCAATGAC TTAGTGGCAT CACAATTTTC TCAAACTTGC CAGAACTTTC 660
TGGAATGTAC TTAAAGAAAG CCATGACTCT GCCTCTTGTT AGCTGACATT CATTAGAGGC 720
TTTGTGTCAG AGCTGGAAGC CATGAGTCAC ACTTGCTGAT ACAAGGGGAG ATCTCAGCAG 780
GAGGAACGGG CCTCGTGGTG CCCGTGCGCT TCCTGGAATT GTGCTGTAAG TGAAATGAGA 840
TGCTGGTGCC TGGGAGACCA GAGCTCAGCC CACATGGACT CCTCTGACAC TTCGTCTACA 900
CTTAGAAACC TCCAAGCAGG CACAGGCCAG GCGCAGGTCA CTTTCTTCAG CCCCATCTCC 960
CCAGGCAGCC CCAGAGGCGG CGGCAGTGGG CTCCCAACTT CATGAATCCG CTGGAGCACG 1020
GAGATGTGGC GTGAAAACAT GTCACACTCC TGGAGACGTG CATGAAGCCT CCTGGTGGCC 1080
TCAGAGTGTC TGGGGCCACC GGTCCTTTGA GATTTTAAGG 1120
|
