| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00402 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:10569970-10572190 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:10571394-10571412 | CCTCCCTTCCTTCCTGCC | - | 7.82 | | EWSR1-FLI1 | MA0149.1 | chr1:10571398-10571416 | CCTTCCTTCCTGCCTCCC | - | 7.88 | | ZNF263 | MA0528.1 | chr1:10571397-10571418 | CCCTTCCTTCCTGCCTCCCCC | - | 6.33 | | ZNF263 | MA0528.1 | chr1:10571393-10571414 | CCCTCCCTTCCTTCCTGCCTC | - | 6.63 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_20679 | chr1:10569696-10574662 | CD56 | | SE_33671 | chr1:10568472-10571497 | H2171 | | SE_36701 | chr1:10569594-10572189 | HMEC | | SE_47404 | chr1:10566553-10580264 | Panc1 |
|
| | 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 |
| GH01I010507 | chr1 | 10567258 | 10578342 |
|
Enhancer Sequence | ACTTACTCAT TACTAACTGG TCTCTCCTGC TTCCCTTTGT CTGTGAACTA AATACAGGGG 60
GCCTCAAGAT AATTGGTAGC TCCATCACTG ACCCACCAAT TATAGATCAG CAGGGAAGGC 120
AGCCCAGGGA TGGTTTGTGG TTGGCACAGG CTGCCCACCT AGAAATGTGA GTTATTCTCT 180
ACCTGCCACC AAGTTGGGCT TGACTAGATC GATCCTTTCC TAATTTTGGA CTTTGGCATC 240
TCTAATTGCA TCACACGGCT CCCTGGTTTA CAGGTTTCAG CCTCATTTCA TCCCTACACG 300
TGCTGCTGGT GTCTTTCTTA GTTCATGCCT CCTTGGCATG TCTACAAAGT ATTAATTTGC 360
AGAGGTTTTG TTTGTATTTT CCTTTGAGGT TCCCTGGTGC CTAGAATGGT TAGATGGCAG 420
GCTGCAGATA AATAATTCTG TTGAAACAGC AGGTTTCTGT GCATTTTTGT CTGGTGTGTC 480
CAAGTAAAGG CAAGTCTTTG TGGGCACCAT ATTAAGCCCC CTTTTTGAGC ATTTATCTGA 540
TTTGTGTTCC AGCTTATCTA CTTTGCTCTG GCATGGAGAA GGAAAAGTCC CATTTCCTGC 600
TAGGCTGCCA GGCACTTATG TAAGACTTTT AGGTGCCAAA GTAGGAAAGG AGTCCCTGTG 660
TTGTATGGCC GTATATATTT TGCATGTGTG TTTCCTGGCT GTTTGGCACC TAGGCACTTT 720
GCTAAGCCCT GTATGGGTTG GGCATATACC GTATTGCTCA GCTCCTGGCA GAAAATAGGC 780
ACTCATACAT ATTTGTGGAA TGAGTGAGTG TGTGTGCTCA CTTATGTGCG ATGGAGATGA 840
TGAGCCAAGG AGTTGGATTG CACAGTTGCT GCCTGGCGTC CTGCTAGGAA CTTAGGGTGC 900
AACATTCCCA CTGGGCCACA CATATGCCGA TGTTCAGTGG ATGACTGCTA CGCAAGCAAC 960
ATAAAGAGGC CATTTTATGA AAGGGAACAT CAGAGGAAAC ATTATAACTG AGACCTTTAT 1020
AGCCTTTCCA TTATTATGGT TTAAATCTTG ACAGTCTTTA TTTGCAATGA CACTGGGACC 1080
AGTAAAGACA ATGCTCACTC CCACCTCCTC GTTCTCCACA TCCTGTTCCG TAGCTGTGGT 1140
GCACCGATAG GCATCGTTAA ATGTGCAGGC AGCAGAGCTG CTGGTTTGTC TAGAAACAGC 1200
CCCTTTTGAC TCAGAAGTTG GAACCCAGAT GACTCACCAT TCTATTTGTT TTATTGCAAC 1260
TGTCATTTCA TAAAATGCCC TGACAGCTTT AAACTGTAAA TGCCAAAGTG AGGTTTTTGT 1320
CTTTTTTATT TTGTTATCTC CTGTTTTTTC TAATCTTTTA TATTTCTATT TTCTCCTTTC 1380
TTTTCAGACT TATTTTCTCT TTCATTACTG TCTCTTTCTC TGTCCCTCCC TTCCTTCCTG 1440
CCTCCCCCCT TTGATGACTC TAATGGCATG AGTAGTTGAA GTGGTTTTTG CTAACATCAT 1500
GGTGCGTTCT TTCCAGCTTT AATGCTATCT GATTGAGCGT GTCTCCCCTC AGATTTTTGT 1560
GTAGGGTTTA GAAATGGAAA TGACCATGCA CATCAGAGTT TAAATTTTCC TAGGAAAGTC 1620
TGCCATGAAC TGTAGGACCT ATAACTTCTA GAGATGGAGG GACCCCTGAC ATCTGTGGAC 1680
TATGGACTCC TGACTTCTGT GGACTCTAGA ATTTATGACT TCTGTGGATT GTGGGGCCTC 1740
TGACTTCCAT AGACCGTGGG ACTGTGACTT CTGTGGACCC AGGGACCTCT GAATTCCATG 1800
GACTGTGAGA CCTCTGACTT CTGTGGCCTG TGAGATCTCT GACCTCTGTG GCCCGTGGGA 1860
CCTCTGACTT CTGTGGTCTC TGGGACCTGT GACCTCTTTG ACTTCCAAGT CTTCTGTGGA 1920
CTGCAGGACC TCATCAACAC GTGTATTGCC AGAAGAGAGG CTTGATTGTG TTAACCTGTT 1980
TCTCTCCAGA GGTGTCACAT ACTAGAATTT CTGCTCAGTC TTATGGCTTA GGTGGGGTGT 2040
TGAGTCTAAA TATATATATT TTTTGAGACG GAGTCTTGCT CTGTCACCCA GGCTGGAGTG 2100
CAGTGGCATA ATCTTGGCTC ACTGCACGCT CCGCCTCCCG GGTTTACGCC ATTCTCCTGC 2160
CTCAGCTTCC CGAATAACTG GGACTACAGG CGCCTGCCCC CACGCTCGGC TAATTTTGGT 2220
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