| Tag | Content |
|---|
EnhancerAtlas ID | HS158-16231 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr13:110488900-110489810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr13:110489447-110489468 | TCCTCCACCTGCTCCTCCACT | - | 6.26 | | ZNF263 | MA0528.1 | chr13:110489444-110489465 | CTCTCCTCCACCTGCTCCTCC | - | 7.75 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I109836 | chr13 | 110488541 | 110489815 |
|
Enhancer Sequence | GGAGAAAAAA AGCTTAAATT GTAATTGGGT AAAGAGTGAC CTTGGGCTCC TCGTGCCCTC 60
TACCTAGTAA TTGGAGCCCT GCTTGCTGTG TCTGATGCAT TCTCCGTTCA GCCTCATGGC 120
TTCCTGGTCA AAGGGCCCCT CGGCTTCCTC AGGATGGTCA TGAGGGCTGC CTCACCCACA 180
CACCCAGGGC TTTCCGGCTG ATAACCTCGG TCTATCAGTT AGGCTTGTTC AGCTTGCATG 240
TGTCCTCTGT GCAGAACCAA TGCAGAGCGA GCACTTGGAC CTGTGGCAGG TGAAGCTAGG 300
CATTTATTAA CTCAGGCTTC CTGTAAACAC AGGGCACAGG AGCCGTCACA ATGAGAACAT 360
GAAAATGAGA GTTATATGGG AATGAGTGCC TCAAGAGCCA TCCCGTGACT GGTGCTTTAA 420
AAAAGAGAGA AAGTTGTGAG CAGCGAAACC CAGGAGAGAG AAGCAGCATG GGGGCTCACA 480
CCAGGTCGTA GCCCTGCACA CCTGCTGCCA CTCTCACAGC AGTGCTGGCC TCCTCATCCA 540
GCATCTCTCC TCCACCTGCT CCTCCACTCC AGCCTGGAGG TCTCTGCTCT GGTCCTGCTT 600
GCCCATGAGA GGGAAACTCA CACTGTGGCC CTTTTGCTAC TTAGAAGTGC AGCCATTTGT 660
TGGATGGTAA CCCTGTACTC AGTGCTGGGA TGACATGTCA CTTACTTTGT CCAATACAAG 720
TCTCAGTACC ATCTCATGAG GAAAGAACAT GATTAATCCA CCTTCACAGA AGTGGATAAG 780
GAGGCTCAGG GGTCCTGCAG CATTTTCGTG GTCACATGGC TGCTAAGCAG CAGAACCAGG 840
AATACCAAGT CTGTCTGATA CCAGAGCTGG ATTCCAACCG ATTCCCTAGA CATCCTCCCC 900
CCAGGCCAAA 910
|
