| Tag | Content |
|---|
EnhancerAtlas ID | HS040-02144 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:112190880-112192270 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:112191044-112191063 | CTTCCAGCAGGTGGTGGTA | + | 6.04 | | ESRRB | MA0141.3 | chr1:112191084-112191095 | TTTGACCTTGA | - | 6.14 | | RORA | MA0071.1 | chr1:112191086-112191096 | TGACCTTGAT | - | 6.02 | | SPI1 | MA0080.4 | chr1:112191538-112191552 | TACTTCCCCTTTAT | - | 6.15 | | SPIC | MA0687.1 | chr1:112191538-112191552 | TACTTCCCCTTTAT | - | 6.64 |
|
| | 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 |
| GH01I111647 | chr1 | 112189900 | 112191645 |
|
Enhancer Sequence | CCCCAAAGGG TACCCTGCTT CTGCTGGCTT AATTCTCAGA ACTTTGGTGT CATTGGTCTC 60
AGATACCACT TTGCCATCCA CTATCTGGTG GATGGTCGTC TTTTGGATGG TTCGCATGGA 120
GTTGCTGCTG TCCAGGGCAT CACCAAGATT GAAGTCCTTG CCATCTTCCA GCAGGTGGTG 180
GTAGGTGGCG ATCTCAGCCT CTAGTTTGAC CTTGATATTC AGCAGGGCCT CGTACTCACT 240
CCTGGGCCTG GCGTTGCCCC TCTGCCCGGG TCTGTGCCAG CTCTGACTGC AGTTGCAGCA 300
GGATCCCGTT TAGCTGCTCC ATCTGCAGGA AGTAGAGGGC CTCCACCTCC CTCAGTCTGT 360
TCTACAAACT GGCCTTCACA TTTCTCACTG AGTCCAGGTC AATCTTTAAG GACTGGACTG 420
TATGTCTCAG CTCTGTGAGC GTCATCTTAG CCTCTCCAGC CTCAGCAGAC TGCGTGGTGA 480
CCACTGTGGT GCCCTCCTCA ATCTGCTGAG ACCAGTACTT GTCTAGCTCC TGTCGATTCT 540
TTCAAGCCAG CTCATTGTAT TGGGCCGAGA TGTCTGCCAT GATCTTGCTG TCCTGAGATT 600
TGGGGGCATC TGCCTCCATG GTCAACCCAG AGCTGGCAAT CTGGGCTTGT AGGCCTTTTA 660
CTTCCCCTTT ATGGTTCTTC TTCATGAAGA ACAGCTCTTC GTTGAGAGCC TCGATCTCTG 720
GCTTCAGCTG CAGCCAAGTG ACATTGATGT CATCATTGAC CTTGTGGAGT CCGTGGATGT 780
CACTCTCCAC AGACTGGCAC ATGGCCAGCT CTGTCTCATA CTTGACTCTA AAGTCATCAG 840
TAGCAAGATG GGCATTGTCA ATCTGCAGAA CGATGTGGGC ATTGTCCACA GTATTTAAGA 900
AGATCTGAGC TCTCACGTCC TCGATGGTCT TGAAGTAATG GCCCCAGTCC CTGAGCTGGG 960
GTCCCTTCTT CTCCAGGTGC TCCTGGATTT TGCTCTCCAG CTTCCGGTTC TCGGTTTCCA 1020
GGCTCTCACT CTGTCCAGGT AGGAGGCCAG GCATTGAGGC GTTGCATGGT CTCCTCATTC 1080
TGGATGCCTC CCATTCCTGC CAGCCCCTCG GCCATCCCTG CAGCCAGACC CCAAGCTGTC 1140
CCAGAAGCTG GTGGAGTGGG ACACGGAGAT CTGGGAACCA GAGCCCCCAG CACCTGGATA 1200
GACGCTGGCC AGGCGCCATA GCTGGCTGCC TTGACAGAGC TTAGGGACTG GTAGTTGGTG 1260
GATAAGGTGA AGCGAGTGGT AAAGCTCATG CTCTCTGGGG AGGAGAGTGA GAGGATAGGA 1320
CTCAGGCTTT GCCGACGACC AGAATATTAG ATATTATCAT TGCCTAATAT CCCTTTCTTC 1380
TTTTGCTGTT 1390
|
