| Tag | Content |
|---|
EnhancerAtlas ID | HS145-21402 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr5:141743790-141744580 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr5:141744253-141744263 | GCCCCGCCCC | + | 6.02 | | MEF2A | MA0052.3 | chr5:141743823-141743835 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr5:141743823-141743835 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr5:141743822-141743837 | TTCTATTTTTAGTAG | - | 6.57 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_34287 | chr5:141741761-141746021 | HCT-116 |
|
| | 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 |
| GH05I142355 | chr5 | 141735231 | 141745153 |
|
Enhancer Sequence | TACGGGCACG CATCATCATG CCCAGCTAAT TTTTCTATTT TTAGTAGAGA CAGTGTTTCA 60
TCATGTTGCT CAGGTTGGTC TCAAACTCCT AGGCTCAAGC AATCCACCAG CCTCGGCCTC 120
CCAAAGTGCT GGGATTATAG GCGTGAGCCA GCACACCTGC CTTGTCTGGA AGCTTTTAGA 180
GTCACTCACA CAGGAAATGC CGTCTTGGCT CTCCAGGGGT TCATGCTGGA TCCAGCAGAG 240
CAGGACCAGA CAAACACCCG ACATCTTCCC GTTTTCACTC ACCCTCCCTG GCATCATGGT 300
TCAGTGGTCA CGGTGGGCCT GGGAGGGCCC CCCTTGGTTC CCCCTGTTTC CCTTACCTTA 360
ACCTTTGCCT CTCTGACTGA GACCCATTAT GCCTCCTGTC TCTGTTGACT CCATATAATG 420
AAAATAATTG AGCCTGTCTC CACCGATAAC TGTCTCGAAA CAAGCCCCGC CCCGGTCATC 480
TGCCTCTGAC TGAACACACC CCGCCCACTG CACAGGGCCT GCCGTAGCCT GCTTCCAGAA 540
CCCAAGCAGG GAGAACCCGT AGGCGAGGTG CACGTTTCAC AGTGAATGAA GGAACTGGGG 600
CTGACACCCT GGTGGACAGC CCTGTGGTTT GCTGAAGGGT GTCTAATGGT TCTGAGACTA 660
AGGTTCAAAA TCTCTGAAAG CGCCTCTAAA CAAAACGTTA ATTACGGTGT TTTTGCATTT 720
CGACTTTGCC CTTCATCCTC AGCCTTCCTT CCTCGATGCT TCCTGCCCTG GTTTTGTGTG 780
GAAGATTCCT 790
|
