| Tag | Content |
|---|
EnhancerAtlas ID | HS101-03440 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:186587040-186588220 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr1:186587382-186587393 | TGGGTGTGGCC | - | 6.62 | | NFIA | MA0670.1 | chr1:186587613-186587623 | GGTGCCAAGT | + | 6.02 | | POU4F2 | MA0683.1 | chr1:186588106-186588122 | CTAATTAATGATTCAC | - | 6.13 | | SPI1 | MA0080.4 | chr1:186587939-186587953 | ACAAAGAGGAAGTA | + | 6.18 | | SPIC | MA0687.1 | chr1:186587939-186587953 | ACAAAGAGGAAGTA | + | 6.89 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 186587154 | 186587268 | | chr1 | 186587444 | 186588060 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I186617 | chr1 | 186586933 | 186588332 |
|
Enhancer Sequence | GGAAAGAAAG AAAAAGAGGT CTAAAGCATA CTCTGGGAGA ATGGAGAGAA AAACAACTGT 60
GTGATGGAGT CAGGAAAGGA CTTCGTTTGA GCTGATCACT ATTCCCCTCA GACTAAAACA 120
AAGTGTTTGT CCATCTGAAA GTGCTGATCT ACAGTTTTGA GACAGAGGGC AGTGGATGGA 180
CAGTGGATGG GTCGGGTTTT GGCAATGAGA GGGAGCTGAT TTGAATTAGA GGAAGTAAAA 240
AAGTATGGGA GAGTTCTGTG GGGAATCATT AGGACTCCTT AGGAGATAAC AGACGATTCC 300
AAGCAGCAGA TGAGGTGAAG TCGAACTCCA CTGGACCTGT GGTGGGTGTG GCCAGCGTCA 360
TCCATCCAGA GTGAACCCCA ACAGGAGCCA CTCCGGGGCT GGGGCAGGCG GATGATCTGC 420
AGACAAGGCT TTTAATGGGC TATGTTTGGG AAAAATATAT TTTATATATA ATAGATTATA 480
TTTGTAAAGA CTTGTAGTTT CAGGATTTCA TACAAATTAG CTTTCCAGTA TTGAGCCACT 540
GCAGTTAGGG CCCGGTCTCT GTCCAGCAGG CTGGGTGCCA AGTTCAGTGT CACAGCGTTC 600
AGCAGGTGAG ACACTCTTAA TAGGCAGACA CGGTGCCTCT GAACGCACAA CGTGCAGTAA 660
AGGAAATGCA GGCAATCCCT GTAAGGAGGA AGTGGTTAAG GGATCGAAAG CAGCTTGAGA 720
CTTGTGCAAT GCAGTCATTG TCACCGAAAA CTCCAAATGC GTTTTCATTT TCAAATGCTG 780
AATTACACAC AGGATTGCAC AAGGAAAGTC TCAGAAGACT TCCAACCAGA GAGCCTTGAT 840
TCCAACTGGC TTTGCTTCCA AGAGCACATT CGGGACATTT TGAAAACCTG CCCCCAAAGA 900
CAAAGAGGAA GTATTTTGTT GTGGAAATCT GGTGGGTGTT TTTTGTGTGT GAATGGATGA 960
GGAAAACTGC ACGCTCGTTT AATTCAATAA GTTAATATCA TCTGGCAAAA GCATCTCTCA 1020
TACAGGAGGG ATTGAGGGTT TTTAACAAAA CATTTTCCCT ATGGACCTAA TTAATGATTC 1080
ACTCATTTAG TGTTAATGCA CTTACTCATC CTTTAATTTA TTACTCAGAT ATGTTGGCCC 1140
CTCACATCCC ATTTATCTGT TAGAAACAGT CAAGCTTGCC 1180
|
