| Tag | Content |
|---|
EnhancerAtlas ID | HS051-17822 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr21:35266300-35267740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PHOX2A | MA0713.1 | chr21:35266418-35266429 | TAATTGGATTA | - | 6.02 | | Phox2b | MA0681.1 | chr21:35266418-35266429 | TAATTGGATTA | - | 6.02 |
|
| | 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 |
| GH21I033894 | chr21 | 35266551 | 35267830 |
|
Enhancer Sequence | AAACATCTTA GTAGTTAATG CACTGTTCAT TTAGGGAGTC CCCATCCTGG TCCAGGCCAC 60
CCTCCTAGAA GCTGGGCGGC AGCTGGACGG GCCTGCCTTG GTGGCATTCA AGCAAGCCTA 120
ATTGGATTAG GTTGGTGCAA AAGTGATTGC GGTTTTTGCC ATTGCTTTTG ATGGCAAACT 180
AACTTTAAGT CATTAAAATA AGACCCAACG CTTATAAAAG AGTTCATATC CACCTCCCAA 240
TAACTTCTTT AGTTCCATGC AGCCTCAATC AGTTCCTCCA TTCAAAGGAA CCCTCTTTAC 300
CCTGGCCCTG GGGGAGCCAT ATTACACCCA CATCATAATT TTTCTGACAC TATGTGTGCT 360
TGTCAAATTT CAGGGTCAGT TTCCCCTTAT TGGATGTCAG GGGTGTTTTG TGAGTTGTGT 420
TTTAATAGGA TTCTGTTCGA TTTTCTATAC CAGCCTATAT TGTTACTATC ATCTGCCTAG 480
TATGAATATT TTAGTATTCA AAGCCCACCA GATAAAGCTG TGTTCAGAAG TGGACTTTTT 540
GGTCAGCCTT GAAAAAAAAA AAATCAGCAT TTCTCTGATA TTTCCTGAGG ATTAACCAGA 600
AACTAAGGTT TCTTTTTAGG CAGTGGTAAG AATGCGTATT TTCTTCTTCC AGAAGTTCTG 660
GTTTTATACT TTTATCTTTT GAAAGAATAA CATTCCTGTG CGACTCTGCT TCTCTTCGCT 720
TTTGCATTTC TCTTTTTTAA CTCAAATCTC TTATTTCCTG CCGTTCCTGT ATCTAAACAG 780
AATGGGGGCC TCAGGCAGAC AGGAACCAAA GAAAGGGTGT AGTGGCTTTG CAGCGTTGGG 840
TGAGCAGCAG CCGCTGCCAT TCTGTGCACT GTCACCGGCG GGGGTGGAGG GTCTCCCTGT 900
AGGAGGAGGA AACTCGCTGT TTTCACTGGC AGATTTCAAG GTGCCGGCTC CACCTACCGC 960
AGCTGCTAGG CATTGCTCTT GTGTAGATCG CAGAAGGAGT TATTGGTGAT GTGGGGTGTA 1020
GGGGAAGACA GGAAAACGGA CTCAGAGCTA GGAATGTGGG CCTGGCAGAG ACCGAAGGCT 1080
GGGTGGGAAG GAAGCTCGCG GCGAGCCTAG GGTTCAAGCC TAGCGCGCCA GGGGTCTCCA 1140
GTGAGACCTT GCTCTTCCCT GCCGCTGAGG CTGGGGCTGC ACGGAGGTCC TCAGGCTTCC 1200
CACCCTTTCT GCATCAGCTT TAGTGTCTGT CGGCTGGGTG GACTGCAGGG CAGGTGACCT 1260
GGAGGAGGCC CTGCTCCCCA GCAAGCGTTC TAGGAGTTAC GGTGTGCTCT ATTGGGATTG 1320
GATTACAGTC TCTACTTGTA GACTTTGACT TCTGGAATTT TAGGTGGAAG GGAATTTTTG 1380
TTGGTGGGAC GCAGCAGCTC AGTGCGTGGT GTGTGCATGC GTGTTTGTGC GTGCGTGTGC 1440
|
