| Tag | Content |
|---|
EnhancerAtlas ID | HS040-03492 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:229300740-229301590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr1:229301236-229301253 | AAGGGCACTCTGACCTT | - | 6.02 | | ESR1 | MA0112.3 | chr1:229301236-229301253 | AAGGGCACTCTGACCTT | + | 6.08 | | ESR2 | MA0258.2 | chr1:229301237-229301252 | AGGGCACTCTGACCT | - | 6.98 | | EWSR1-FLI1 | MA0149.1 | chr1:229301002-229301020 | GGACAGAGGGAAGGAAGT | + | 6.07 |
|
| | 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 |
| GH01I229164 | chr1 | 229300122 | 229301890 |
|
Enhancer Sequence | GCAGAGACGC AAGGGCAAGA GAGGAGCAGA GGGAAAACCA AAGCGTCAAG ATCGAACTTC 60
TGTGGACCCA TTGAGCACCC AGGGTCCAGG GCCGGGGCCA CCCAAGGGCC AGATCTGCCT 120
TGAGGTGCCT GTCTCCGACC AGAGGGAAAC TCCCATCAGA GCAGGTGTGT TTTGTTTACC 180
AACATCCCCA AGAAGCATTC CGTTCCTCTC ACACCCTTAC TGCATTCCCT CTGTGTCTCT 240
AGATCGCAGG AGGAAGAAAA AGGGACAGAG GGAAGGAAGT CCCCTTAGCT GCTGTAAGAG 300
ATTGGTACAT TTTGTCATTT CTCTGAGCCT GTTTTCACAT CAGCAAATGC AAACAGTGAC 360
CTCCTCCAGT TGTTAGGGGA ATTAAATTAG ACAATGAAGG TGTCCAGAAA ACAGCACCTC 420
AAAATACACC ATGTTGGCAT GTTGATGGTT TTAAGTCAAA GACACAAAAA ATAACGACAG 480
CAGCGGCAGG CACAGGAAGG GCACTCTGAC CTTCTCTAAA GCAGAATGTG AAACTCCCAT 540
GTGGAAGGTG TCTCTGCTTA CTCATAGCTC AAACAATGGG CCATTTTTCA CAGTGCTAAG 600
ACCTGAAATG TAACTTGTTC TACATTAAGT TTGAGGTCTC TAGGCCCTTT ATCTTCTGGC 660
AATGTTTTGT GCCACTGTGA CCTCATAATG TTAATGTTGG GAGAGACTGC GTGGCCCATC 720
AGTGCAGCCC GATGCCTGCC CATTCTCCAT TAACTCACCC CATGCTCGTG GAGACTTTAT 780
TGCATGCTGG ATGCTGTGGT CTCCACGGGA AACGCAAACG TGAAAATGAC CAGATTCTGC 840
CTGAAGTTGC 850
|
