Tag | Content |
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EnhancerAtlas ID | HS102-11377 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr19:2506410-2508250 |
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 | GCAGGAGAAT CACTTGAATC CGGGAGGTGG AGGTTGCAGT GAGCCGAGAA CACGCCATTG 60 CACTCTATCC TGGGCGGCAA GAGTGAAACT CCGTGTCAAA AAAAAAGAAA GAAAGAAACA 120 TGTTCATAAG GCACTTTATT GAAAGATAGT GTGTAAAAGT AGCAAAACTC AGAAATAATC 180 TAAATGTCCA TCAATAGTAT ATAATTTTTT TTTTTTTGAG ATGGAGTCTC GCTCTGTTGC 240 CCAGGCTGGA GTGCAGTGGC ACAATCTTGG CTCACTGCAA CCTCTGCCCC CCAGGTTCAT 300 TGCCTGCCTC ATCTTCCTGA GTAGCTGGGA TCACAGGTGC CTGCCACCAT GCCTGGCTAA 360 TTTTTATTTT TTATTTTGGT ATTTTTAGTA GAGACGGGGT TTCACCATGT TGACCAGGCT 420 GGCCTTGAAC TCCTGACCTC AGGTGATCCT CCCGCCTCGG CCTCTCAAAG TGCTGGGATT 480 TCAGGTGTGA GCCACCGCGT CCGGCTAAGC ATGTAAATTA AATTACTCTG GAGTTGTTAA 540 AATGCACTGA TTTTTAAAAA ATTATTATTT TTATATCTTT TTTGTTTTCC TTCATAAAAA 600 TGCAATGACT TAGCAAGCTG TCGGTCATAG GAAGTTAAGC GAAAAAAAAA AAAAGCTAAG 660 CCAGCCTCAG AGCAGTCTGT GTTGAGTGAG TCCAGTTTTA AAAACAAATG GCAAGTGTTG 720 GTATGAAATA GTGCCGATCT CCATTACAGA AGACGGTCTT GGGCACATGT GCGGGAGCCC 780 TACGGTCTGG CTGAAAATGC TGCCCAGTTC TGGCCGTACC ACTTTCTAGC TGTGGACTCA 840 AGGGAGTTGT TTACCTTCTG TCAGTCCATG TTTATTCATC TGCACAATCA ATGCGTAGAA 900 CCATAGCCCT TACCTCACAG CGTTTCCGGG AGGATCAGAT GACACAATCC GAGGAAATGA 960 ACCATTATTG CTACTTACTG TCACTGCTTT CTTCTGAGGC CAACGTTTGG GCACGCCTAG 1020 AAGTTTGAAG GATTTGCCTC AGCTGTGAAC AAATGGTGGC TACAGGTGCT GAGAATGGGT 1080 CTGAAGAAGG GCGTGGAGGG ATCTTCCCTC CCCTCCCCTC CCCACCCCTC CCCTTCTCTT 1140 TCTCTCTCCC TCCCTCCCTC TCTTCTTTTT CTTTCTCTCT CTCCCCTCCC TCCCTCCCTC 1200 TCTCTCTCTT TCTTTTTTTC TCTCTCTCCC CTCCCCCCCT TCTCTCTTTT CTTTCTTTCT 1260 CTTTTTTGAC AGAGTCTCAC TTTGTCGCCC AGTCTGGAGT GCAGTGGTGT GATCTCAGCT 1320 CACTGCAACC TCTGCCTCCC AGATTCACGC CATTCTCCTG CCTCAGCCTC CTGAGTAGCT 1380 GGGATTACAG GCGTGCGCCA CCACGCCCGG CTAATTTTTG TATATTTAGT GGAGACGGCG 1440 TTTCACCGTG TTAGCCAGGA TGGTCTCCAT CTCCTGACCT CGTGATCCGC CCGCCTCGGC 1500 CTCCCAAAGT GCTGGGATTA CAGGCATGAG CCACCGTGCC CGGCCGCATG TGGGTTTTTC 1560 AATGGCTATT ATTTAAGCAT CTTCCATGTC CTTTGTGTGT GTGTGTGTGG TGTGTGTGTT 1620 TTGTGTTTTT TTTGTTTTTG ACAAGAGTCT CGCTCTGTTG CCCAGGCTGG AGTGCAGTGG 1680 CGTGATCTCA GCTCACTACA ACCTCCACCT CCCAGGTTCA AACGATTCTC CTGCCTCAGC 1740 CTCCTGGGTA GGTGGGACTA CAGGTGCATG CCACCACACC CAGCTAATGT TTCTATTTTT 1800 AGTGGAAACG GGGTTTCACC ATGTTGGCCA GGCTGGTCTC 1840
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