| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00037 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:1269840-1270570 |
Target genes | | Number: 34 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr1:1270391-1270412 | ACCAGTACCAGGGACAGAGCC | + | 7.58 | | REST | MA0138.2 | chr1:1270471-1270492 | GCCAGCACCATGGACAGAAAA | + | 7.69 | | REST | MA0138.2 | chr1:1270432-1270453 | TCCAGCACCACGGCCAGCACC | + | 8.78 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTGACCCAAC CCTGTGATCT CAGCCCCGGT GAACCCAGAC TTAGCTGCGA TCCCCCCCAA 60
GCCAGCAATG ACCCGTGTCT CGCTACAGAG ACCCTCCCGC TCTAGGTTCT GACCCCAGGT 120
TGTCTCCTGA CCCTGACCCC ACAGTGAGCC CTAGGCCTGG AGCACGTGGA CACCCCTGTG 180
ACCATCTGGG CCCCAGAGCC AAGCTGTGTC CCTGTCCCTC TGTGCCCAGA CCAGGCCTGC 240
CCAGGTAACC CAGACCCACT GTTCTGGAAA GAGGCCCGGA GGGCTCCCAG GGTACCCGCA 300
ACCCACACCG TGAGCTCAGG AAAAGGACGC AGGGAGGCCC CGGCCAGATG GCTGGAAGCC 360
CAAATCAGGC CCTGCCGACC TGACCATGTC CCACCAGGGC CCCCATCCTG CACCCTGCCA 420
GGCACCACAG CAGTGGGAGG CCAGGTGGGG GCACACAGGC ATATGCCCAG GGCAGAGCCC 480
GCCGAGGTAG GGGTGGCACC CAGCTTCCTA CTCTGCCCTT TGCCCAGTGG GTAGACAGCA 540
TCATGACTGT CACCAGTACC AGGGACAGAG CCCAGGTGGG GTGGGGGCGG GGTCCAGCAC 600
CACGGCCAGC ACCGACCACC AGGACCCCGG AGCCAGCACC ATGGACAGAA AACTGCCCAC 660
CAGGATCTGA CGCCAGCACG CCGCCAGGCC CACACAGGGT CTCCGGTCAG AGTCCCAGGG 720
TCAGCTCCCA 730
|
