| Tag | Content |
|---|
EnhancerAtlas ID | HS188-06501 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr19:36192640-36193820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr19:36193359-36193370 | GGCCAATCAGA | + | 6.02 | | NFYB | MA0502.1 | chr19:36193471-36193486 | GAGCCAGCCAATCAG | + | 6.04 | | TFAP2A | MA0003.3 | chr19:36193108-36193119 | CGCCTCAGGCT | + | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_19716 | chr19:36192977-36193968 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_59463 | chr19:36184851-36210443 | Ly3 | | SE_61403 | chr19:36184821-36210454 | HBL1 |
|
| | 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 |
| GH19I035701 | chr19 | 36192703 | 36194302 |
|
Enhancer Sequence | CCTCACGGGG TTATTTAGGT TTCAACGAGT TGATGCACAA GCGTGGCACA TGGAAAGGGC 60
TCGGTAAACA CGAGGTGCTA TTACTCCCAC CACAGTGCCA GTCCTTCTCC CTTTTTTACT 120
TTATTTTTTA TTTTTATTTT TTGAGATGGA GTCTTGCTCT GTCGCCCAGG CTGGAGCGTA 180
GTGGCGCCAT CTCCGCTCAC TGTAACTTCC GCCTCTCGGG TTCAAGCAAT TCACCTGCCT 240
GGGCCTCCCG AGTAGCTGGG GTTACAGGCA TCCCCCACCA CGCCCGGCTA ATTTTTGTAT 300
TTTTAGTAGA GACGGGGTTT CACCATATTG GTCAGGCTGG TCTCGAACTC CTGACCTCAG 360
GTGATCTGCC CGCCTTAGCC TCCCAAAGTG CTGGGATTAC AGGCGTGAGC CACCACGTCC 420
GGCCCCTTCC CCCATTTTAG CGGTTTCGCT CCCTATCGGG GCCAGGGACG CCTCAGGCTG 480
TCTCGGTCAG GACCTACAGC TCCGGTTGTT GTCCCAGGCT CTTCCGCGAG GTGCTCTCCT 540
GTCTCCTGAC CACCCCCATT CCTCCCCACT CCAGCTCCTC AGCGAGCGGC TGCGAAGGAC 600
GCGCACAACA ACACTCCGCG CAGCGGGAAG GTACCGAACT CGCATCGCAG CCTGAAACTG 660
CTCAACTAAG CTCCCGCCCC GCTGCTCTCT GGTCAATCTA AAGCGAAGAC GAGCCTTAGG 720
GCCAATCAGA AGCGACAGCG GTGGAGTCAT GCCCGCCTGC TTGAGGCGCC CTGGCGTCTC 780
ATTGGCTATG CTTGAGAACG AATCCCAGGC TAAGCCACTT AGAAAGGAGC GGAGCCAGCC 840
AATCAGCGGT GCAACCGCCG CGGGGGCCGG GCCAGAAGCC CCGCAGACAA GCACCTCGGG 900
AGACTGGCGA GGGGCGAGCT CGCAGCTTGT TAGCCCCGAA GCCCTGCCCA GGGGGAAACC 960
CTGCTGGAGG GAGTCTAACC CCCGGGCCAG TTAATGTTGG GGCAGCGCAA TCGGCCGTTC 1020
CCTCTGCGGT ATGGTTGGAG GTGGGAGTGC TGACACGTCC GCGCGCAGTT ACTCCTGGCT 1080
GAGCATACAG TCGAGGTGGC AGTGGGAATT GGAAGTGCAA GTGTCACGCT GCCAATCACG 1140
GGGCAAGGCA CTGCCCCCCT CTTGTGTCTT TCCTGTCCCT 1180
|
