| Tag | Content |
|---|
EnhancerAtlas ID | HS187-12455 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr19:45224950-45226330 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:45225175-45225190 | TGAACTCCTGACCTC | - | 6.22 | | SPI1 | MA0080.4 | chr19:45225788-45225802 | CAAAAGGGGAAGTG | + | 6.41 | | SPIB | MA0081.2 | chr19:45225790-45225802 | AAAGGGGAAGTG | + | 6.07 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_09606 | chr19:45225026-45227473 | CD14 | | SE_23877 | chr19:45225227-45225635 | Colon_Crypt_2 | | SE_31568 | chr19:45225186-45226205 | Gastric | | SE_34750 | chr19:45225301-45226193 | HeLa | | SE_53360 | chr19:45224892-45226462 | Spleen | | SE_62704 | chr19:45221152-45271677 | Tonsil | | SE_65330 | chr19:45224918-45226537 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 45225441 | 45225906 | | chr19 | 45225274 | 45226089 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I044721 | chr19 | 45225041 | 45229949 |
|
Enhancer Sequence | TGTTTTGTTT TGTTTTGTTT TTTGAGACAG AGTTTCACTC TTGTCTCCCA GGCTGAAGTG 60
CAATGGTGCC CACTCAGCTC ACTGTAACCT CTGCCTCCGG GGTTCAAGTG ATTCTCCTAC 120
CTCAGCCTCC TGAGTAGCTG GGATTACAGG CATGCACTAC CACGCCAAGC TAATTTTTGT 180
ATTTTTAGTA GAGACGGGGT TTTGCCATGT TGGCCAGGCT GGTCTTGAAC TCCTGACCTC 240
AGGTGATCCA CCTGCCTCAG CCTCCCAAAG TGCTAGGATT GCAGGTGTGA GCCATCATGC 300
CCGGCCCTGA TTCAGGTTCT AACAGGATCC CTCTGGCCAT GAGGTGGAAA GAGACTGTTG 360
GGGGCAGAAT TGTAAAGCGA GGGACAAGAA GAGTCAGGGG TCTCCAAGCT TTGAGCCTGA 420
GCCACTGCAA GGATGAAGCT GCCATTTCTG AGGCCAGAAG GCTGCAGGCA GGGCTGGGTT 480
GGAGATTGGA ATGAAGATAG GTCTTGTTTG AGGCCAATGA GGAGGGAGCC TCACCCGAGG 540
CACACAGGCT CCAGGCGGGA AGTTGGCGAC AAGTTGTGGA CTGTGGTTTT CACCCACCTC 600
ATGGGGCCCC CTCATCCTCT CCCCCAACTT CCCCTCACGC CGTGGTGGAG CCAGCTTTGT 660
TTGTTTCCCC CCCATCATCC GTTTCATGAT GGGGAAGACT GGTTTTCCCC TAACCCAACA 720
GACACCTCTT CCCTCAGCCT GTCCCTGACC CTCCCACCTC GGGAAGCCCC GAGCGGGCCT 780
CCCAGAATGT CCCGGCAGGA AGGGGCTGCT GCTACCGTTC ATCCAGCCAG ATGAACCCCA 840
AAAGGGGAAG TGGGTCACCC GTAGTCACCC GGCTCATGGT CAGCTCGGGA CTTCAGGATC 900
TCGTCTCTTC ACTGCACCCA CCACAGCCCT GGGAGGTTTT CCATGCACGC TTCTCATTCT 960
CCCCACATTT CACACGAGAA AACAGGGGCT CCAAGAGAGG CCCACACTCA CCTAAGGAGC 1020
TCGAAAGATA GGGGCATCTG GATTTGAACC CAGGTCCTAG CAGATGTTGT TAGCTCAGAG 1080
GAGAAGGCAG AGAGGGTGAA CAGAACCCAG CCTGCCCTCC CAGATCCAGT GGGAAGGCAG 1140
ACTTGTCCCC AGGTAATAAT AGCCCAGCAG TGTTCACAGC CTGGGATGGA GGAGCCCAGG 1200
AGGCTGCAGG AGCTCAGAGC GCATGCCTGA CCCAGCCTGG GGTCAAGGAG GGCTTCCTGG 1260
AGGAAGGGAC AGCTCATCTG ATACCTAGAG GATGAGTGGG AGTTACTAGG TGTAAATAGT 1320
GCAGGGAGAG GGAAGAGTAT GTGCAAAAGC CTAGGGTTGA GAGGAAACCT AGGGGCTCCA 1380
|
