| Tag | Content |
|---|
EnhancerAtlas ID | HS101-20797 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr19:2506590-2508390 |
Target genes | | Number: 19 | Name | Ensembl ID |
|
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 |
|
| | 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 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I002506 | chr19 | 2506511 | 2507797 |
|
Enhancer Sequence | TAAATGTCCA TCAATAGTAT ATAATTTTTT TTTTTTTGAG ATGGAGTCTC GCTCTGTTGC 60
CCAGGCTGGA GTGCAGTGGC ACAATCTTGG CTCACTGCAA CCTCTGCCCC CCAGGTTCAT 120
TGCCTGCCTC ATCTTCCTGA GTAGCTGGGA TCACAGGTGC CTGCCACCAT GCCTGGCTAA 180
TTTTTATTTT TTATTTTGGT ATTTTTAGTA GAGACGGGGT TTCACCATGT TGACCAGGCT 240
GGCCTTGAAC TCCTGACCTC AGGTGATCCT CCCGCCTCGG CCTCTCAAAG TGCTGGGATT 300
TCAGGTGTGA GCCACCGCGT CCGGCTAAGC ATGTAAATTA AATTACTCTG GAGTTGTTAA 360
AATGCACTGA TTTTTAAAAA ATTATTATTT TTATATCTTT TTTGTTTTCC TTCATAAAAA 420
TGCAATGACT TAGCAAGCTG TCGGTCATAG GAAGTTAAGC GAAAAAAAAA AAAAGCTAAG 480
CCAGCCTCAG AGCAGTCTGT GTTGAGTGAG TCCAGTTTTA AAAACAAATG GCAAGTGTTG 540
GTATGAAATA GTGCCGATCT CCATTACAGA AGACGGTCTT GGGCACATGT GCGGGAGCCC 600
TACGGTCTGG CTGAAAATGC TGCCCAGTTC TGGCCGTACC ACTTTCTAGC TGTGGACTCA 660
AGGGAGTTGT TTACCTTCTG TCAGTCCATG TTTATTCATC TGCACAATCA ATGCGTAGAA 720
CCATAGCCCT TACCTCACAG CGTTTCCGGG AGGATCAGAT GACACAATCC GAGGAAATGA 780
ACCATTATTG CTACTTACTG TCACTGCTTT CTTCTGAGGC CAACGTTTGG GCACGCCTAG 840
AAGTTTGAAG GATTTGCCTC AGCTGTGAAC AAATGGTGGC TACAGGTGCT GAGAATGGGT 900
CTGAAGAAGG GCGTGGAGGG ATCTTCCCTC CCCTCCCCTC CCCACCCCTC CCCTTCTCTT 960
TCTCTCTCCC TCCCTCCCTC TCTTCTTTTT CTTTCTCTCT CTCCCCTCCC TCCCTCCCTC 1020
TCTCTCTCTT TCTTTTTTTC TCTCTCTCCC CTCCCCCCCT TCTCTCTTTT CTTTCTTTCT 1080
CTTTTTTGAC AGAGTCTCAC TTTGTCGCCC AGTCTGGAGT GCAGTGGTGT GATCTCAGCT 1140
CACTGCAACC TCTGCCTCCC AGATTCACGC CATTCTCCTG CCTCAGCCTC CTGAGTAGCT 1200
GGGATTACAG GCGTGCGCCA CCACGCCCGG CTAATTTTTG TATATTTAGT GGAGACGGCG 1260
TTTCACCGTG TTAGCCAGGA TGGTCTCCAT CTCCTGACCT CGTGATCCGC CCGCCTCGGC 1320
CTCCCAAAGT GCTGGGATTA CAGGCATGAG CCACCGTGCC CGGCCGCATG TGGGTTTTTC 1380
AATGGCTATT ATTTAAGCAT CTTCCATGTC CTTTGTGTGT GTGTGTGTGG TGTGTGTGTT 1440
TTGTGTTTTT TTTGTTTTTG ACAAGAGTCT CGCTCTGTTG CCCAGGCTGG AGTGCAGTGG 1500
CGTGATCTCA GCTCACTACA ACCTCCACCT CCCAGGTTCA AACGATTCTC CTGCCTCAGC 1560
CTCCTGGGTA GGTGGGACTA CAGGTGCATG CCACCACACC CAGCTAATGT TTCTATTTTT 1620
AGTGGAAACG GGGTTTCACC ATGTTGGCCA GGCTGGTCTC GAACTTCTGA CCTCAGGTGA 1680
TCCGCCCACC TCAGTCTTCC AAAGTGCTGG GATTACAGGC ATGAGCCACA GTGCCCAGCC 1740
AAGGATGACT TTTGAATGCT GTATGATTTT ATGTAACTTC TTCTTCTTCT TCTTTTTTTT 1800
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