| Tag | Content |
|---|
EnhancerAtlas ID | HS101-01193 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:38197710-38198540 |
Target genes | | Number: 17 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:38197750-38197762 | GTTTGTTTGTTT | + | 6.32 | | Gata1 | MA0035.3 | chr1:38197763-38197774 | ACAGATAAGGA | - | 6.14 | | Hnf4a | MA0114.3 | chr1:38198181-38198197 | GACGGACTTTGACCCA | - | 6.59 | | NFYA | MA0060.3 | chr1:38198202-38198213 | GGCCAATCAGA | + | 6.02 | | NFYB | MA0502.1 | chr1:38198197-38198212 | AGCTGGGCCAATCAG | + | 6.42 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AACTGTCCTG CAAGGCTCAG AGGACAGAAA GTATTATCTT GTTTGTTTGT TTCACAGATA 60
AGGAAACCCA GTTCAGAGGG GTAAAGACTC CCCCAAGGCC CCAGCTGGAG CCATCACTGA 120
TGAGCGCCTA CTCAGTGCCA GCTTCTGCAT GAGACCCTTT GCCTCCTGTG AGCCTCACAA 180
CAGCCCTGTG GAGTCAGCAT TTCCATCTCC TTTTTAGGTG AGGTTCACAT CAAGGAAGGG 240
GCTGGTGCAC CCTCTGAATC CCTGCAGAGC CCGTGTTTTT TGCTCGACAT CATGCTGCCC 300
CCCGCTCCAC CCCAACACAC CTGACAATGG CATACTAGAG ATGCTCCTCC CGTCGTTTCG 360
TCCCTGCCCA CACCTTATTA GAGGCCCTGC CATATCCACA GCCCCAGAAA GTTATTCTCC 420
CCACTGATAT TCGGTGGCTC CAGCTTTCTG ACCATAGCAT TCAGGAACTG GGACGGACTT 480
TGACCCAAGC TGGGCCAATC AGAATCTCTC TTCCAGGCAT CTCAACAATC CATTGAAAGA 540
CAGAGAAGCA GTGGCTTCAG GACCCACAAG GTAGGGCAGG CTAGGGGCAG AGAGGAGGAA 600
GGAGCAAGGC TGCCTACCTG GGCATTGGCA ACGTGCCGTA AGCAAGCCCC TCTGCATCAT 660
GGGCTGGACT GGTGTGCAGA GAGAGGTTGA GATGAGCAGC ACTGTGGCTC CAGAGGGGAG 720
CTGCCAGACA CCCGCCCAGG TCCAGTGGCC CAGCAAGGCT TCTACTCAGC AGGCTCCATG 780
AGAGTACACT GAAGCCTTTC AAATATAGCC CTTTTATACT TGTTCTTTTT 830
|
