Tag | Content |
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EnhancerAtlas ID | HS159-05972 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr8:29132490-29134270 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr8:29133803-29133816 | AGGGACAGCTGCT | - | 7.52 | Myog | MA0500.1 | chr8:29133806-29133817 | GACAGCTGCTG | + | 6.14 | Myog | MA0500.1 | chr8:29133603-29133614 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr8:29133806-29133817 | GACAGCTGCTG | + | 6.02 | Tcf12 | MA0521.1 | chr8:29133603-29133614 | GACAGCTGCAG | + | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_24465 | chr8:29133235-29133910 | Colon_Crypt_2 | SE_28216 | chr8:29132632-29134436 | Fetal_Intestine | SE_29296 | chr8:29132633-29134434 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I029274 | chr8 | 29132419 | 29134330 |
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Enhancer Sequence | CCAAAGTGTT CACTGTCTGG ATGAACATCA ATTTACAACC CCCATCCCCA CTTTGTTGAA 60 AAATGTCTCT AAAGAACAGC ATCAATAATA AATCTCTGAT AGGCCTAGTT CATCTCCATA 120 AATCATTCAG GGACAGAGGT CAGGAGATAG TATTCTTTTG ATATTATTTA AGGCAGATTG 180 TACAGTTCAG GCCCCATTAG TGAGCACAAA AGGACACCCA TAAAATATTC ACAGGCTGTG 240 GTACAAACGC ATTGACTGCC TGGGGCACCC ACCTCCGGAG GGATTAGATT AGTCAGAAGA 300 ACTTGCGGTT GCAGCCTACA TGCTCCCTTA AGCTCAGAGG TTCCCATAGC TCATCAGCAA 360 ATCTGATCTA GAATTTTCCA GGGATTTCAA AAAATCCACA GGAGAAAGAG TGAGATAAGC 420 CAGAGGTAAA GAAACTATTT TGCCCAGGGC CCCTAGCCTA AGGAGAAGCA ACTGACTTTT 480 TCCCCCCAAG AATAATGTGG ACAAGGAGCA AAGCTCTCCT CTGAGAAATA TTAGATAAAT 540 TAAGAGTTGG ATAAAAAGAA ATCTGGCAGA GGTAGGCCTG GGGAGGAGTC CAGCCTACAT 600 CCATATACAA AGACACTCTC CTCCCTGTAT TCATTATCAA TATTTTAAAA ATCAAATATA 660 ATTCAATTTA ACCAATATTT GACTGCATAT GTAATAAATG CAAGGTACTT GCCCAACAGG 720 GAATTAAAGT GAATATGACA CACTTGACAT TTCCAGAAAG TTAGAATTTG TTTGAAGGTA 780 ATTATGCTGT TACAATGGAA TCAAATGTCC GTAGAATTCC TACTTTGTTA CCAGGCAGGT 840 AAACAAGAGC TTGTTTTCCC AAGCATGTCA CATGTTGCAC CTGCAGGTGG GTGGTGGAGG 900 TGAGGCCTGA GCCTAGGAGC AGAGGAAGAA GAACCAGTCA CCCCTGATTC AGATCTAGAA 960 GGTGTCACTT AGGCAGGAAA CATGAGAATG GGTGGGCAAT CCTGCTTCTG GAGGGAAGAG 1020 AAGGTCGGAG AAAATGGCAC AAGCTCCAAG AGATGTCGCC TGCGGTTTTA ATCTTCTGGC 1080 TGCTGGGCAT GAAGCAGTTA AAGAGAAACC CAAGACAGCT GCAGCCAGGG GCTCCATAAT 1140 AGCCACGCAG AGGAAGCGCA TAGAGGTCAT TTTTCTATGC CACGAAGGGA GACTTGTTTC 1200 AGCTGAGACC CAATCTGGAT GCTGTTCTGC TCACCAGGAA GCCAGGAGCT ATAAAACCCT 1260 CCCAGTGCCA CAGCATGCGT GACTCAGAGG CAGCTGAGCA GGACCCAGAA CAGAGGGACA 1320 GCTGCTGCGG GCTCACCCTT TTCCATCTTC TACGGGAGGA AAGCACAAGC CTCCCTAGAA 1380 ACAGGATGAT TTAGCCATCG TTTACCAATA TAAATTCCAG ACAAATGAAA GGCTTGGTAT 1440 AAAAACTAGA AAAACTAAAG AAAAGAAAAG TGAATATTTA GCTGATCTCG AGCAAAGGGA 1500 GAAGGCATCA GTAATAGTAA CAGTACTGAG ATACTTGCTC AAAGTCTATC TAGGTGGAGC 1560 TGGGACTCAA ACTTAGAACT CCAGAGCCTC ATTCTTTTTT TTTTTTTTTG AGATGGAGTT 1620 TTGCTCTTGT TGCCCAGGCT GGAGTGCACT GGCGCGATCT CGGCTCACTG CAACCTCTGC 1680 CTCCCGGGTT CAAGCAATTC TCCTGCCTTA GCCTCCCATG TAGCTGGGAT TACAGGTGCC 1740 CGCCACCATG CCTGGCTAAT TTTTGTATTT TTTTAGTAGA 1780
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