| Tag | Content |
|---|
EnhancerAtlas ID | HS040-01746 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:56898140-56899210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr1:56898488-56898499 | TGTGGATTGGA | - | 6.62 | | ZNF263 | MA0528.1 | chr1:56898614-56898635 | TCCTCTACCCACTGCTCCCCC | - | 6.12 | | ZNF263 | MA0528.1 | chr1:56898611-56898632 | TCCTCCTCTACCCACTGCTCC | - | 6.31 |
|
| | 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 |
| GH01I056432 | chr1 | 56898273 | 56898672 |
|
Enhancer Sequence | GAGACGAGAC AGCACAGGTA TAGGGCTTAA GGAGGGCAAG AGTGATTTCT GTGTTGGTGG 60
TGTTTTTAAA TGCTAACTGG AACAGGAAAA AAAAAATCAG GTGAGAGAGA AACCACAATG 120
CCTGCCAAGG AGTAGCCTGC ATTGTTCGCC CCTGGAAAAG CTGCTGGCTT AGGGCTTTTA 180
AAGCTGGGGA AAGGTCAACC CCTCGCAAAA GAACAAACTG CATGGCCCTG TGACTTCCCT 240
CCTCTAATTC CCATAACTCC CTGTGCTGGT TGCCTCCTCT GGAACGTGGG AAGGTGATCC 300
CTGCCCTGCC AGGGCTGTTT GGGCTGTGTG CTTGTGCTTG CAGGGCTTTG TGGATTGGAA 360
AGTGTAGGCA ACCTGATGAA GAGGGTTGTT TCTGTGTGCT TAGCTCTGCC AGCCTGGCCT 420
CCTGACCTCC CATGCTGTTT GCTCAGCGCT ACCCATGTAC CTTCCCTCAG GTCCTCCTCT 480
ACCCACTGCT CCCCCTTCTT GATTTCACCT TCCAAATCCT CCCATCCTTG ATAACTGCAT 540
TTCCAAGAAG CCCCTGCTGG TGATGTCGGT CTGCACTGAC CTCATGCCCT CAAGATGTCT 600
TCAGACTGGA TGGCACCATG AGAGTCGCTT TCTTTCTTCT GTGTTTTGTT TTCTTTTCCT 660
GTTGTTTTTT TCTCACCTCT CTCAGCAAGG ACCACCTGGT CTCCCACTTC CCCCATATTA 720
TCATTCTCAG AGGGCCTCCC CCAATCTGCC CTCACCCCCA CCTGTTCCGA ATCTAGCCAC 780
ACTTTCATGC CCCAGTCAAG GCCACTCCAT CTGTGTGCAC CAACCTGACA ATTTCAGTTC 840
CCCAAATGTG CCATGCTCTA GCTTTCCTTC CTCATCTTCC TACTTCAGGT CTCAGTTTAG 900
ATGTCACCTC CTTGATCCTC ACCTCCAATT CCGCTCAGAT GAGGTGCCAC TGCTATGAGT 960
TCCCTTGACA CCCTGTGTTT CCCCCATGAC TGCACTGATT CCTGCTGAAA TTAACCAGTC 1020
TATGCCTTTC TCCGGCTCTT GCAAGAAACT GTATGTGAGC CAGGGCTTGT 1070
|
