| Tag | Content |
|---|
EnhancerAtlas ID | HS040-03435 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:227002380-227003560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr1:227003463-227003474 | GGGGGCGGGGC | - | 6.02 | | KLF4 | MA0039.3 | chr1:227003030-227003041 | AGAGGGTGTGG | - | 6.02 | | KLF5 | MA0599.1 | chr1:227003464-227003474 | GGGGCGGGGC | - | 6.02 | | Klf1 | MA0493.1 | chr1:227003032-227003043 | AGGGTGTGGCC | - | 6.32 | | Myod1 | MA0499.1 | chr1:227002636-227002649 | TGCAGCTGTTTCT | + | 6.29 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_54921 | chr1:227001401-227004634 | Stomach_Smooth_Muscle |
|
| | 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 |
| GH01I226813 | chr1 | 227001144 | 227005115 |
|
Enhancer Sequence | AAGTAGGGAT TTCTTTGTAA CTGCCCTGAC CCTGGATTAT GCCCTACTCC TTATTTTGTC 60
TAAAACATTA GCTGGGCATG GTGGCATGGG CCTATAGTCC CAGCTACGCA GGAGGCTGAG 120
TCAGGAGAGT CACTTGAGTC CAGGAGCTTA AGGCTACAGT GAGCTATGAT CCAGCCACTA 180
CACCCCAGCC TGGGCGACAG ATCCTGTCTC TATAAAAGAA AAAAAAAATC CTTGAGAGTA 240
GCTTGGCTTT GCAGAATGCA GCTGTTTCTT GCTTTTGAGG GTGTTTGTTT GCCATTTGAC 300
CCTCTTTTTT TAAACCTTAT GTTTATAAGG GAAAGCCTCT TACAGTAAGT GTGTTTAGGG 360
TTCTAGTTAC AATTAATCTG TGGTCCTAGA GAAGGCAAGA GGGCCGAGGG AAGGGAGAAG 420
AAGGGCTGGC AAGACAGTGA GAGCAGAGAG CTTGTGACTT CACTCCCCCA GGCAGAGGGA 480
AGAGTGACTA AGCCGGACGC TCCATCCAGG CAGGAAAACC GTCCAAGCTT GCTCATTTCC 540
CATCAGCCTC GCACCTGCTG GGATCTCCTG GCTGGCATGG ACTCTGTACA GTCACCTGGT 600
GTCCCCAGCA CAGGACACCC TGGGGCCTTT TTCCTACTCA GTCAGATGCC AGAGGGTGTG 660
GCCGTCATCC AGTTACAGAC GGAGCTAATA ACAAAGTCAC TCTGCCTTTC ATGTGTGCAG 720
CACTTCAAGC ATTTCTAAAT GCTTGCACGC CACTAAGAGA TCTTGCATAA GCACAGGGTC 780
AAGTCCTTTT GATTTATTCA ATAAGACACA AACCAACTTA GAAAGTGAAA ACTCTGACTT 840
TTTGGCATGC ACTTGGTGCT GCTCCACATT TACTGCTGGC CTGTCCCTGT CCCTCCTTGT 900
CTTTGTCACT TAGCTGTGGC CCTTCTTGCA GGAAGACTTC TGGAATTGTC ATATTCCCAC 960
CTCTTTCTCC TTCCTCTGCT TTCTGCAGGT GACACTAAGG AAACTCATCT CAATGCATGC 1020
ACAGGGAACA ATGAAGATGT AGAGGATGTG CTATGACCAT TGCAAACATA GAAAAATTAA 1080
GCTGGGGGCG GGGCACAGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA GGACAAGGCG 1140
AGCAGATCAC TTGAAGTCAG GAGTTCAAGA CCAGCCTGGC 1180
|
