| Tag | Content |
|---|
EnhancerAtlas ID | HS158-04866 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr1:214150110-214151270 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr1:214150442-214150457 | GGTTAATTATTGACT | + | 6.07 | | HNF1A | MA0046.2 | chr1:214150442-214150457 | GGTTAATTATTGACT | - | 6.68 | | HNF1B | MA0153.2 | chr1:214150443-214150456 | GTTAATTATTGAC | - | 6.25 | | HNF1B | MA0153.2 | chr1:214150443-214150456 | GTTAATTATTGAC | + | 6.41 | | ZNF263 | MA0528.1 | chr1:214151057-214151078 | GGGGGAGGGGGAAAGTGGGAG | + | 6.52 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_65842 | chr1:214150319-214151482 | Pancreatic_islets | | SE_68033 | chr1:214146367-214176127 | TC32 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I213976 | chr1 | 214150320 | 214150779 | | GH01I213977 | chr1 | 214150941 | 214151090 |
|
Enhancer Sequence | GGATTTGATT CAAACCAACC TGGAACCAGA TTGGATCTCC AAGCTGTTCT GTGTATACAC 60
ACACACACAC ACACACACAC ACACAGACAC ACACGCTGAG ATTTCCAAAA GTGAAATTTC 120
CAGAAGTTAT CCTACAGAGT TAACCCCAGA AAGGACTTCA CTGGCAGACA CAGGCATAAC 180
TTTACTCCTT TTGTGATGAC CCATGAGTGG GGTCTATGGC AGTCTGAATA GATGGGCCTT 240
TCTGTTGAAA GATTCTGCCT AATCCTTCCC ACCAAAGCAG GGTTCTAAAG GTGTCAGCAG 300
GATTTGGCTG ACTGGATCGT TAATGGAGCT ATGGTTAATT ATTGACTGAT TAGGGATTTA 360
CCTTATCTTT CCGTCAGGAG CTGGCTCAAG ACTTAACGGT AAGCAATTTA GAGCCAGGGT 420
GAACCTACAC ACATGCCTTT TTCTTCTTTT CCTTTGGGTC ACTTTAGCTT GCCCCTCCCC 480
ATAATTCACA TTCAGGACAG AATGGCCAGT CCTTACAAGG CGTGGGAGTC CTCAAGAGCA 540
CCGAAAATGA GAGGGGCCAG GTCCACGTGA CAAGTGTCCA GAGACAGAGG CTTAGAGAAA 600
TGTGCCTTTT GCAAAACAGT GTTTATGTGT AAAGGTTTTC CAGTTAAGTC CCTGGGAGAA 660
AAAAAAAAAA AAGCACTTGC TTTTTGTCTC TAAAAGGTCT GGTGATGCCC GTGGGTGAGA 720
ATCCACCCCG CACTCCCCAA GGCCCCTTGG CAAAGCCAGG GAATGAGTAC AGGCAGCTCA 780
GGCCCAGCTG CCCCAGATAA GAGGTGGCCC GTGTTAATGC ACAGGCTTCC TCTGCACCTC 840
AGCAGGGCCT TCCTTTTCTA AACAGTCTCC CTTTAATGTT GGCGAATGTT GTTTTTCCAT 900
TGACTCAACA TCTCGCCTGG TGGTAAGCCA GTGAGGAAAG TTGCAGCGGG GGAGGGGGAA 960
AGTGGGAGAG AGTGATGCCA AAGCAAAAGA GCGGGACGGT CAGCCAGGTT TCCAAACAAG 1020
CTAGACACCT GCTTTGGAAA GACAGTGACC AAGCCTAGAC TTCTGGCTTC CTCTTCACTT 1080
TGATCAGCCT TTTGTTCCCT GCGGGTCTGT GATGGGCTCC CTGCCCCTCC CCTCACCACT 1140
GCCCCCTTCA CTGGGAGCTA 1160
|
