Tag | Content |
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EnhancerAtlas ID | HS159-02942 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr19:2506580-2508710 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr19:2508201-2508213 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr19:2508201-2508213 | TCTATTTTTAGT | - | 6.32 | Nr2f6(var.2) | MA0728.1 | chr19:2506835-2506850 | TGAACTCCTGACCTC | - | 6.22 | Nr5a2 | MA0505.1 | chr19:2506827-2506842 | GCTGGCCTTGAACTC | - | 8.25 | RARA | MA0729.1 | chr19:2506832-2506850 | CCTTGAACTCCTGACCTC | - | 6.73 | RREB1 | MA0073.1 | chr19:2508016-2508036 | GTGGTGTGTGTGTTTTGTGT | - | 6.04 | RREB1 | MA0073.1 | chr19:2508007-2508027 | TGTGTGTGTGTGGTGTGTGT | - | 6.16 | ZNF263 | MA0528.1 | chr19:2507593-2507614 | CCCTCCCTCCCTCCCTCTCTC | - | 6.11 | ZNF263 | MA0528.1 | chr19:2507513-2507534 | TTCCCTCCCCTCCCCTCCCCA | - | 6.23 | ZNF263 | MA0528.1 | chr19:2507545-2507566 | CTCTTTCTCTCTCCCTCCCTC | - | 6.23 | ZNF263 | MA0528.1 | chr19:2507581-2507602 | TTTCTCTCTCTCCCCTCCCTC | - | 6.23 | ZNF263 | MA0528.1 | chr19:2507523-2507544 | TCCCCTCCCCACCCCTCCCCT | - | 6.56 | ZNF263 | MA0528.1 | chr19:2507626-2507647 | TTTCTCTCTCTCCCCTCCCCC | - | 6.65 | ZNF263 | MA0528.1 | chr19:2507634-2507655 | TCTCCCCTCCCCCCCTTCTCT | - | 6.69 | ZNF263 | MA0528.1 | chr19:2507549-2507570 | TTCTCTCTCCCTCCCTCCCTC | - | 6.99 | ZNF263 | MA0528.1 | chr19:2507589-2507610 | TCTCCCCTCCCTCCCTCCCTC | - | 7.53 | ZNF263 | MA0528.1 | chr19:2507585-2507606 | TCTCTCTCCCCTCCCTCCCTC | - | 7.54 | Zfx | MA0146.2 | chr19:2506860-2506874 | CCCGCCTCGGCCTC | + | 6.01 | Zfx | MA0146.2 | chr19:2507899-2507913 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_24383 | chr19:2507083-2507568 | Colon_Crypt_2 | SE_25170 | chr19:2506877-2507592 | Colon_Crypt_3 | SE_27369 | chr19:2506975-2507651 | Esophagus | SE_31940 | chr19:2506925-2507690 | Gastric | SE_41828 | chr19:2506999-2507555 | LNCaP | SE_48020 | chr19:2506970-2507608 | Pancreas | SE_54295 | chr19:2506798-2507812 | Spleen | SE_65706 | chr19:2506996-2508346 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I002506 | chr19 | 2506511 | 2507797 |
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Enhancer Sequence | AGAAATAATC TAAATGTCCA TCAATAGTAT ATAATTTTTT TTTTTTTGAG ATGGAGTCTC 60 GCTCTGTTGC CCAGGCTGGA GTGCAGTGGC ACAATCTTGG CTCACTGCAA CCTCTGCCCC 120 CCAGGTTCAT TGCCTGCCTC ATCTTCCTGA GTAGCTGGGA TCACAGGTGC CTGCCACCAT 180 GCCTGGCTAA TTTTTATTTT TTATTTTGGT ATTTTTAGTA GAGACGGGGT TTCACCATGT 240 TGACCAGGCT GGCCTTGAAC TCCTGACCTC AGGTGATCCT CCCGCCTCGG CCTCTCAAAG 300 TGCTGGGATT TCAGGTGTGA GCCACCGCGT CCGGCTAAGC ATGTAAATTA AATTACTCTG 360 GAGTTGTTAA AATGCACTGA TTTTTAAAAA ATTATTATTT TTATATCTTT TTTGTTTTCC 420 TTCATAAAAA TGCAATGACT TAGCAAGCTG TCGGTCATAG GAAGTTAAGC GAAAAAAAAA 480 AAAAGCTAAG CCAGCCTCAG AGCAGTCTGT GTTGAGTGAG TCCAGTTTTA AAAACAAATG 540 GCAAGTGTTG GTATGAAATA GTGCCGATCT CCATTACAGA AGACGGTCTT GGGCACATGT 600 GCGGGAGCCC TACGGTCTGG CTGAAAATGC TGCCCAGTTC TGGCCGTACC ACTTTCTAGC 660 TGTGGACTCA AGGGAGTTGT TTACCTTCTG TCAGTCCATG TTTATTCATC TGCACAATCA 720 ATGCGTAGAA CCATAGCCCT TACCTCACAG CGTTTCCGGG AGGATCAGAT GACACAATCC 780 GAGGAAATGA ACCATTATTG CTACTTACTG TCACTGCTTT CTTCTGAGGC CAACGTTTGG 840 GCACGCCTAG AAGTTTGAAG GATTTGCCTC AGCTGTGAAC AAATGGTGGC TACAGGTGCT 900 GAGAATGGGT CTGAAGAAGG GCGTGGAGGG ATCTTCCCTC CCCTCCCCTC CCCACCCCTC 960 CCCTTCTCTT TCTCTCTCCC TCCCTCCCTC TCTTCTTTTT CTTTCTCTCT CTCCCCTCCC 1020 TCCCTCCCTC TCTCTCTCTT TCTTTTTTTC TCTCTCTCCC CTCCCCCCCT TCTCTCTTTT 1080 CTTTCTTTCT CTTTTTTGAC AGAGTCTCAC TTTGTCGCCC AGTCTGGAGT GCAGTGGTGT 1140 GATCTCAGCT CACTGCAACC TCTGCCTCCC AGATTCACGC CATTCTCCTG CCTCAGCCTC 1200 CTGAGTAGCT GGGATTACAG GCGTGCGCCA CCACGCCCGG CTAATTTTTG TATATTTAGT 1260 GGAGACGGCG TTTCACCGTG TTAGCCAGGA TGGTCTCCAT CTCCTGACCT CGTGATCCGC 1320 CCGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCATGAG CCACCGTGCC CGGCCGCATG 1380 TGGGTTTTTC AATGGCTATT ATTTAAGCAT CTTCCATGTC CTTTGTGTGT GTGTGTGTGG 1440 TGTGTGTGTT TTGTGTTTTT TTTGTTTTTG ACAAGAGTCT CGCTCTGTTG CCCAGGCTGG 1500 AGTGCAGTGG CGTGATCTCA GCTCACTACA ACCTCCACCT CCCAGGTTCA AACGATTCTC 1560 CTGCCTCAGC CTCCTGGGTA GGTGGGACTA CAGGTGCATG CCACCACACC CAGCTAATGT 1620 TTCTATTTTT AGTGGAAACG GGGTTTCACC ATGTTGGCCA GGCTGGTCTC GAACTTCTGA 1680 CCTCAGGTGA TCCGCCCACC TCAGTCTTCC AAAGTGCTGG GATTACAGGC ATGAGCCACA 1740 GTGCCCAGCC AAGGATGACT TTTGAATGCT GTATGATTTT ATGTAACTTC TTCTTCTTCT 1800 TCTTTTTTTT TGAGACGGAG TTTCACTCTT GTTGCCCAGG CTGGAGTGTA ATGGCACGAC 1860 CTCAGCTCAC TGCAACCTCC GCCTCCCAGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCCG 1920 AGTAGCTGGG ATTACAAGCA TGGGCCACCA CACCCGGCTA ATTTTTTTGT ATTTTTAGTA 1980 GAAACGGGGT TTCTCCATGT TGGTCAGGCT ACTCTTGAAC TCCCGACCTG AGGTGATCTG 2040 CCAGCCTCGG CCTCCCAAAG CATTGGGATT ACAGGCGTGA GCCACTGTGC CCGGCCTATT 2100 TTATGTAACT TCTATAGTTA TTATATTTTG 2130
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