| Tag | Content |
|---|
EnhancerAtlas ID | HS040-35878 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chrX:9810430-9811190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chrX:9810913-9810931 | AGAAGGAGGGCAGGGAGG | + | 6.1 | | Hnf4a | MA0114.3 | chrX:9810937-9810953 | GCTGGAATTTGACCCC | - | 6.11 | | RREB1 | MA0073.1 | chrX:9810880-9810900 | TGCTTGGGGTTGGGTGGGGT | - | 6.44 | | RUNX1 | MA0002.2 | chrX:9810648-9810659 | GTCTGTGGTTT | + | 6.62 | | ZNF263 | MA0528.1 | chrX:9810853-9810874 | CCCCTCCCTCCTCCTTCCCTC | - | 6.02 | | ZNF263 | MA0528.1 | chrX:9810857-9810878 | TCCCTCCTCCTTCCCTCCCCT | - | 6.16 | | ZNF263 | MA0528.1 | chrX:9810914-9810935 | GAAGGAGGGCAGGGAGGGAGA | + | 7.76 |
|
| | 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 |
| GH0XI009842 | chrX | 9810349 | 9811695 |
|
Enhancer Sequence | TGGGATTCTG ACAGATCGCT CTGAGACATC CTCCTGTTGT TTCCTTTTCA CCACTGCAGG 60
TCTCCACCTG CCCTGGTGTC CTTGGGAGGA AACCCACCGT GGTAGGGCAC ACAGCGGCTG 120
ACTTGTCCTG GTAAATCATA AGCATGGTGG GCTCCGCAGG TGCCTCCCTC CTTTCTGTCC 180
TTGAGTCTGA AGCCAGCACC TTCTTTGATG ACACAAACGT CTGTGGTTTA GGGTTTTCAA 240
AGGAATTCCC CCTCTTCCTC TCCCACCACA AGAAAGGCTG CTGTGGGGAG CCGGTAGCTT 300
GCAGGCTGGG TTGTCTGGTC GTTTGAATTC CACAAGAAAG CCAACCTAGC TGTCCTGGCT 360
TGGGGCGAGG CGGGAGGGCA GGAGTCCTGG ATCTGCCTGT GTCTGTCTGT CCCTGGCTGT 420
CTGCCCCTCC CTCCTCCTTC CCTCCCCTCT TGCTTGGGGT TGGGTGGGGT CTGTCTTAGG 480
GAGAGAAGGA GGGCAGGGAG GGAGAGAGCT GGAATTTGAC CCCAGAGCTG TCTGCAGCTT 540
CCCAGGAGCC CTTTTCAGAC CCTGTCTGGC TCCTTAGAAA GGCTGTGTGG CTCCTGCGTG 600
GCAGGGCCAC CTCATTAAAA ACACCGGCTC AGGGGAGGGT GCTGGTCACT CTTGGGGCCA 660
ACCAGGATGT TTGCATTTGT CCTATGCACA CAGTACAAAG TTGTTGTTTT TTAAATACCA 720
TTTTAGAGGA GTTTTAGCTC TACAGAGAAA TGCAGAGATA 760
|
