| Tag | Content |
|---|
EnhancerAtlas ID | HS145-11448 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr19:5045900-5047200 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr19:5046496-5046509 | AGGAACAGCTGGT | - | 6.04 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_41729 | chr19:5045841-5049299 | LNCaP | | SE_65334 | chr19:5045698-5050618 | 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 |
| GH19I005045 | chr19 | 5045762 | 5050235 |
|
Enhancer Sequence | GTGAGCTACC GCGCCTGGCC ATCTTTTTCT GTTTTTTAAC CATGCTGTTT GTTTTCTTCT 60
GGTTAAATTT GAGAGTTTGC TGTGTATTTT GGTTATCAGT TGTGACTTGC AAGTATTTTC 120
TTTCTGACTG GGGCTTGTCT TTCTCTTACG GATCCTGCCT GATTGTTTTC AAGTGAAAGT 180
TCAGCCTCAG ACTCCAGTGC ATGAGAGCCT CTGGGTTGGC TGGCCTGCAC TGCCTGCACT 240
TGGCCTGTAG TGATGACCCG GGAGGGACTC TGCAGCCGCA CGCAGGCTGT GCCAGCCCAG 300
GCCGACCTGC CACAGGTGCC AGGGGAAGCT TCAGGGCTTC CTTGCCATGT GTTTGCCATG 360
CCTAGCCTAT GCACTAGCCT ACTTTTACAG CGGGGGAAAC AGCCCACAGC AGAGAAGCGA 420
CTTGCTGTGG TCCCAGGATG AATTTGCGCC CAGCTCAGCC TGTGCCTGGG GCCTCCCTCT 480
GCCCCATCTG GGTCTCATCA CTGCCTCCCT CCTCACCTCT TCTGGGCTCC TGCCAGGGCT 540
CACCTTGCAA AGGAACCGCT GGTCTTGCCA AGTCTGAGGG CCGGTCGTGC AGGTGCAGGA 600
ACAGCTGGTG GGGGGTGGAT TCAGGCTGTG AGAGCAGCTC ACGTTCATGT GTGTCTGGGC 660
TCCTCTCGGC CTCTCAGCAG GCCATGAGCC TCTCCGGGGA CTGCAGTGAC TAATGTGTAT 720
TTTATGAGCT CTTGGGACAG GACGGGGTTT GTTTGCTTGT GGCATTAAGA ATAGATGTGC 780
CTGGTGGGTG GGGATTCCGT CCTTGTTTGC CTAGTTCTGA AAACTGTCTT CGTCTCCTCG 840
GTCAGAAGCT GTGGAAGGGC TGTCACTGGG CCTTGGCTCC GGTACCATCG CTGGGTTAGC 900
CCCAAGTGGT GACTGTTTTT CTCCTTCCGT GTCATTGACT TAGAGGCGTG TTAATTATGC 960
ACTCCCAAAC TGCAGGCTTC ACAACAAGGC CTCCACCCAG CAGGAAGCAC GCAGCTCAGT 1020
GGAATCTGAC AGGCCCTGCC TGCCTGGTGC ACGCTGGCAT GTGCGATGGG GCCCTTCCTG 1080
GAAGGGCCAA GCTGGCGGTG AGCCCTTCAG AAAAGGTGTC TGGGCTGGGT ATGGCGGCTC 1140
ATGCCTGCAG CCCCAGCGCT TGGAGGGGCC AAAGTGGGAG GGACCATTGA GCCCAGGAGT 1200
TCGAGACCAG CCTGGGCAAC AGAGTGAGAC TTCATCTCTA CACAGAAAAA AGTAAAAATT 1260
AGCCAGGTGT GGTTTCTCAC GCCTATAGCC TATAGTCCCA 1300
|
