| Tag | Content |
|---|
EnhancerAtlas ID | HS040-03653 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:235805220-235806760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:235805837-235805848 | ATGAGTCATCC | - | 6.62 | | JUN(var.2) | MA0489.1 | chr1:235805832-235805846 | AAAGAATGAGTCAT | + | 6.6 | | JUNB | MA0490.1 | chr1:235805837-235805848 | ATGAGTCATCC | - | 6.62 |
|
| | 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 |
| GH01I235641 | chr1 | 235804920 | 235807008 |
|
Enhancer Sequence | ATTCATGTAC TTGTTTAAAC TACTTTTGAT TTTCTGACTT CTTATCATTG GTCTGATTCC 60
TCCACCGTAA CAGAACTTCC ATGAGGGCGG GGATTTTTCG CTTCCCCCGC AACTGCCTGC 120
GTTTTCGTAG CCCTAGAGCT TCCAACGTAC AGTGCGGAAA AGCAACATAA CACACTAAGA 180
ACCGTGCGGA AAAGGAGAGA AAACCAGACC GCAGGGGCAT TTCACAGCTA ACCACAGCGG 240
TCCGAGGCGA ACGCAGGGTG GAAGAACCCG AGCGAGGCCC GGCAGGGGCG GGGTGAGCCT 300
TGGCCCCGCT CCCGTGCAGG TGTCGCGGGT AAGCTGCCGC GGTTACTGTG AAGCAGGGCC 360
AAGGCCAGCC CTCCGCCTCG AGGCCACTGG TGCTTGGGGG TGGGAAAAGA GTGACCGGGG 420
GCAACTGAGC AAAACATAGA ACAGAAACTC CCTCTCGAAT AGAGACCCAC GCACGGAAGG 480
ATGATACACT GTGATTCCCC GACGTGGGCC TGCAGCAAGA GACGGGTGCT AACAGCGTCC 540
GAGCCAATCC GTAAGCATCA GAGGGACAAA GAAATCATAA ACAAGAGGCA GGATGCAACT 600
GCTTCAACGC AGAAAGAATG AGTCATCCAG GAAGGCGAGG TGGTGGCGGG TTGGCTGTGG 660
TTTTGCAGAG GCGGGCAGGA GGGGCAGGGG GCCAGGGAGA GGGCAGGGTT GGGAGGGTCT 720
CTTTTAAGGG AATCCTATGC ATGAAAGTCT GTGTAAGAAA GGGTGTGCCT CCTACAGAAG 780
GATATTTGTT TTGTCCTAAA CTTGCCGTGT GTTCTTGGAG GCGCGGGCCT CCCTGCTGTC 840
ATCACACCTC GGATCACCCC AGGCAATCTC GCCCCTGTGG CTTCACCTGG GTCCAGCCAG 900
ACCTCTGCTC AGCTCTGCAC GTACATGCCC CCTCGATGTC ACCTCCTGAC TTGGCAAGTC 960
ATACACCCTC TCTCTACTTG CCCAGCTTCA TTCACAAAAC CAGGTCACAT TACCCCTCGT 1020
CCATCCATGC TCAGTCTGGA AACCCTGGGA TCCCAGACAC CAGCCTCTCC CTGGCCCTCT 1080
GTTTCCAATC AGACGGCCAC CCCGACTGAC GCTGGGGCCG GGGCACCCTT GGGCGTTATC 1140
CAGTCTCCCT GTCCTCCCTC TCCTGCCCCA CGCCTCCGAC CTTCCCCACA TGGCAGTCAC 1200
AGCCAGACGG CCAAGGTGGG GCCTGCTGCT TCCTGCTTCT GCCTGACAAT GGCCCTGGAT 1260
TCCCCATTCT TCACGGTCAG TCTCACCTTC ACACCCCGGC TCTGAGCAAC CTTTCTGCTC 1320
TCTCCACTCC TCTTTCATGA CCCTGGGCCC CTGCTGGCCG CCCTGCCTGG AAAGCCCTTT 1380
CTCATTTGTC TGGCTTGAAA AACCTGCCTC AGCTCACCAG GGCCAGCTCA AGACTCCCTC 1440
TGTTGTCACA CGCTTTCTGC ACTGCTATCA GAAAGAACTA ACACTCTCCC TGTCTGTGCA 1500
CTAATCCAGG GTAGGTGGGC TGTTTTCACA CATGCACCCC 1540
|
