| Tag | Content |
|---|
EnhancerAtlas ID | HS105-21597 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr13:28475540-28477060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr13:28476210-28476227 | CAGGTCACTGTAACCCG | - | 6.08 | | IRF1 | MA0050.2 | chr13:28475978-28475999 | AGAAAGAAAGAGAAAGCGGGA | - | 6.59 | | IRF1 | MA0050.2 | chr13:28475929-28475950 | AGAAAGAAAGAGAAAGAAAGA | - | 6.76 | | LHX6 | MA0658.1 | chr13:28476597-28476607 | ACTAATTAGC | + | 6.02 | | SPIC | MA0687.1 | chr13:28475919-28475933 | AGAAAGAGGAAGAA | + | 6.42 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65672 | chr13:28475786-28476442 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I027901 | chr13 | 28475787 | 28476442 |
|
Enhancer Sequence | TGGGTTGGGG GTGTTAAAAA TCAATCCCTG GAAAAGCTAT TTCCTGCTTC TCTCTCTTCT 60
TTCCCCACCC TGCCTCCTCA CCCCCGTTAA ACCTTGGATC TTCAAATCCC TTTCAATCCT 120
CAGAGCCTAG CACTTGTTTT GCCCCAGGGG ATAAAATGTG TGGGGGAAGT AGCAATGAGT 180
ACATAAATCA CATTTTTACA ATAATTTTTC AAAACAGTAA AACAACCAAT AACAGTGACT 240
GTGTCTAATT CATCTTCAAA TCCCCAGTAC TTACACAATA GTGAATGACA CACAGAAGTT 300
ATGAATATAA GAAAGAAACA AAGAAACAAA GAAAGAAAGA GAGAAAGAAA GAAAGAAAGA 360
GATAGAAAGA GAGAAAGAAA GAAAGAGGAA GAAAGAAAGA GAAAGAAAGA AGAAAGAAAG 420
AAAGAAAAAG AAATAAAAAG AAAGAAAGAG AAAGCGGGAA GGAGAATCAA CAAACATTGA 480
GCACGTGCTA TGTGCTGAGC ACTGAGGAAA CATAATTGCA AAGGTGTGGC ATTTTATTTA 540
TATAGTTGGT TATTTACTTA TTTATTTTAG GCATAGCTTA TAAATTGATG GGATCTACAG 600
CTGATGGTGC TGAAGGGACT TAGCTCCATT TGCAAGAATC AAGGAGATTT CCTAGACAAG 660
ACAGAGGCCC CAGGTCACTG TAACCCGTGC TCTCTTTGCT CTCTTTCTCC CGGTCCTCAC 720
TGCCTCTTAC CCAGCCACTC CTCACCAGTG TGAGTGTGGT AGGCTGATGA CATCTCACCC 780
TGCATCCATC CCACTCTTCC TCTTGCTTAA AGTTGGAAGC ATAGCTCCAG CCACATGCCC 840
TCTTTTTGGC AAAGTCTCTC ACCTTAGCAA CATCTCCATG GGCAACAGTC TTAACTAATT 900
CTTCATTAAG GTCACAGGTT CTTGAGTTTC AAGTCATTTC TTCAGGAGTC AGGAGAGTCT 960
TTCACCAGAT GCCACATGAG AAATTGCTGC TGGATTATAT GTCCAAGATG TTACACAAAC 1020
TCTCACCTTT AAATCACCTT CTCTTTTGAT CACAGTGACT AATTAGCAGA GCCAATGTTG 1080
AAATGCAGAT CTTCTGGTTC TTAGTGTGAT GGGCCATTTC TGCTTTTCAC AGTGTTCTCA 1140
GATTTTTCGA GTTCAATCTC AGCGCCATGC CATGTGTGCT GGCCTTCTGG GGACCTATCT 1200
TAACCACCCA TCCTGCACTC TAGGATACAA CTGAATGGCA ACCTTCTTCC TATCCACCAT 1260
GCAGGCCTTA AGAATGCTGT CCTATTCAGA GAATGTCATC ATGTGGACAA AGTCCTGAGC 1320
AATGGATAAG GATGACAACT GATATGACAG CAGGAAGTTT TTTTTCTCAG GTGAGAGGAC 1380
AATGGAAACA GGGGAAAACT CTTCTGTGGA CATCAGCTTC TCAGCAGTGA ATACAAACTG 1440
AGAAATCAAA AGAGAACTTT TTTTTTTTTT TGAGACAGTT TCACTCTTGT TGCCCAGGCT 1500
GGAGTGCAAT GGCATGATCT 1520
|
