| Tag | Content |
|---|
EnhancerAtlas ID | HS104-28515 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr19:2506380-2508160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| 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 | AGCTAAATCC CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CACTTGAATC CGGGAGGTGG 60
AGGTTGCAGT GAGCCGAGAA CACGCCATTG CACTCTATCC TGGGCGGCAA GAGTGAAACT 120
CCGTGTCAAA AAAAAAGAAA GAAAGAAACA TGTTCATAAG GCACTTTATT GAAAGATAGT 180
GTGTAAAAGT AGCAAAACTC AGAAATAATC TAAATGTCCA TCAATAGTAT ATAATTTTTT 240
TTTTTTTGAG ATGGAGTCTC GCTCTGTTGC CCAGGCTGGA GTGCAGTGGC ACAATCTTGG 300
CTCACTGCAA CCTCTGCCCC CCAGGTTCAT TGCCTGCCTC ATCTTCCTGA GTAGCTGGGA 360
TCACAGGTGC CTGCCACCAT GCCTGGCTAA TTTTTATTTT TTATTTTGGT ATTTTTAGTA 420
GAGACGGGGT TTCACCATGT TGACCAGGCT GGCCTTGAAC TCCTGACCTC AGGTGATCCT 480
CCCGCCTCGG CCTCTCAAAG TGCTGGGATT TCAGGTGTGA GCCACCGCGT CCGGCTAAGC 540
ATGTAAATTA AATTACTCTG GAGTTGTTAA AATGCACTGA TTTTTAAAAA ATTATTATTT 600
TTATATCTTT TTTGTTTTCC TTCATAAAAA TGCAATGACT TAGCAAGCTG TCGGTCATAG 660
GAAGTTAAGC GAAAAAAAAA AAAAGCTAAG CCAGCCTCAG AGCAGTCTGT GTTGAGTGAG 720
TCCAGTTTTA AAAACAAATG GCAAGTGTTG GTATGAAATA GTGCCGATCT CCATTACAGA 780
AGACGGTCTT GGGCACATGT GCGGGAGCCC TACGGTCTGG CTGAAAATGC TGCCCAGTTC 840
TGGCCGTACC ACTTTCTAGC TGTGGACTCA AGGGAGTTGT TTACCTTCTG TCAGTCCATG 900
TTTATTCATC TGCACAATCA ATGCGTAGAA CCATAGCCCT TACCTCACAG CGTTTCCGGG 960
AGGATCAGAT GACACAATCC GAGGAAATGA ACCATTATTG CTACTTACTG TCACTGCTTT 1020
CTTCTGAGGC CAACGTTTGG GCACGCCTAG AAGTTTGAAG GATTTGCCTC AGCTGTGAAC 1080
AAATGGTGGC TACAGGTGCT GAGAATGGGT CTGAAGAAGG GCGTGGAGGG ATCTTCCCTC 1140
CCCTCCCCTC CCCACCCCTC CCCTTCTCTT TCTCTCTCCC TCCCTCCCTC TCTTCTTTTT 1200
CTTTCTCTCT CTCCCCTCCC TCCCTCCCTC TCTCTCTCTT TCTTTTTTTC TCTCTCTCCC 1260
CTCCCCCCCT TCTCTCTTTT CTTTCTTTCT CTTTTTTGAC AGAGTCTCAC TTTGTCGCCC 1320
AGTCTGGAGT GCAGTGGTGT GATCTCAGCT CACTGCAACC TCTGCCTCCC AGATTCACGC 1380
CATTCTCCTG CCTCAGCCTC CTGAGTAGCT GGGATTACAG GCGTGCGCCA CCACGCCCGG 1440
CTAATTTTTG TATATTTAGT GGAGACGGCG TTTCACCGTG TTAGCCAGGA TGGTCTCCAT 1500
CTCCTGACCT CGTGATCCGC CCGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCATGAG 1560
CCACCGTGCC CGGCCGCATG TGGGTTTTTC AATGGCTATT ATTTAAGCAT CTTCCATGTC 1620
CTTTGTGTGT GTGTGTGTGG TGTGTGTGTT TTGTGTTTTT TTTGTTTTTG ACAAGAGTCT 1680
CGCTCTGTTG CCCAGGCTGG AGTGCAGTGG CGTGATCTCA GCTCACTACA ACCTCCACCT 1740
CCCAGGTTCA AACGATTCTC CTGCCTCAGC CTCCTGGGTA 1780
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