| Tag | Content |
|---|
EnhancerAtlas ID | HS040-03319 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr1:222439300-222440490 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr1:222440229-222440244 | TGCTGACTCATTTTT | - | 6.31 |
| | | 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 |
| GH01I222265 | chr1 | 222439281 | 222440206 |
| Enhancer Sequence | ATTTACAGCC AAAGTTGGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 60
TGTGACTTTC TCTTTTATGC ACATGGTGTT TTCAAGAAAA AAAAAATCCA AGATATAAAA 120
GCCTGACATC ACCACAGGAG CCGTAAAACA TTCGGACAGA TTCTGCATGG CCTGCTTCCT 180
CCATGGGCCT TCCTGGATCC TCAGAAAGTA CCCAGGTCAC CCAGACACTG AGCAGCAATG 240
ACAGCCCTCA CTGCTCTCCA TCCTCCTGGG GTTGGCTTCT CCCCACCCGA CTCGACCCTT 300
CCCAGCAAGA GCAAGGGGTG TTTTCCTAGT GGTCCACCTG CCAGCCAAGG TGGGTCTGAA 360
GGGGAAGTAG CAGGAACTGA GTCCCACAGA GAAGACTCTG GGCTCACACA TCCCCCATCT 420
CAGAGCAGGG CTCTCTAAAA GCAGTTCACC CAGTGAAACA AAAATGACGA CACTGGGGAA 480
CACTCAGCTC AGTTTCAAGG CAACCAGGAA AAATAATCAC AAATTAAGAG AGCTCCCTCC 540
CTCCTTTAAA TGCAAACTCA GCACGTGGAG GAGGAACGCA GTCCAGTCTT CGGTGCGAAC 600
TGCCACAAGC TCTCTCTGAA GAACTGCAAG TGCCTTCCTC TTCCTGAAGT GCTCACCTCC 660
TGGTGAGCTG CCCATCCCAG TTCAAGCAAA GAAAATACTC CCAGCATGAA TGAGAGAAAT 720
TCAAAGAGAA GAGGCCTTGC TGCCTCCCGG TGAGAAAACC GACTGAGGGG CAAAGAGCCC 780
AGGGATCTCC CTAGCCTGTC CCACGGCTCA CAGTCCATGA GGAAGCATAA GAGTCTTGAA 840
CTTCATCCTA ACGCTGGAAA TCTAAACTTT TTCTTTTTCA TCTTCAGAGC ACCTATTGTT 900
TTTCTTTAGA CTGCTCTAAC CTGCCTCCCT GCTGACTCAT TTTTGTCATG TATTCTGTGA 960
AGAAAGATAA TAGACCAAAT TATTCTGAAG CATAACTGCC TGTTAAAAGT CAGAAAAAGA 1020
ACTTGCCCAG CCTCCTGCTC TGTAGCAAGC ACGCCTCCGC AGGGTGGACG GGAGGCAGGC 1080
CAAGCCTACA GGCTGGTGGA GAGCCCTCTT CCTGCAGATA AAAGTGGCAG AAACACTCCT 1140
CCCATCAAAA GAAGTCAAAT GAAGGTTAAT CTTTTGCATC CCCAATCTTC 1190
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