Tag | Content |
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EnhancerAtlas ID | HS040-35981 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chrX:48348200-48349750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LBX2 | MA0699.1 | chrX:48348880-48348890 | GCTAATTGGC | - | 6.02 | RUNX1 | MA0002.2 | chrX:48348827-48348838 | GTCTGTGGTTT | + | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI048485 | chrX | 48343798 | 48349762 |
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Enhancer Sequence | TGGGAGGATC GTTTTAGCCT GGGAGATTGA GGCGGCAGTG AGCTGAGATC ATGCTGCTGC 60 CCTCCAGCCT GGACAACAGA GCAAGACCCT GTTTTGAAGA AAAAACAAAA AACAAAACAA 120 AACAAAAAAA GTGCAGTACT TTGCAAGCAA TAAAGATTTC TATTTCTGCA AGAGAGGCTG 180 TGCTCATGCC TGTCCTTACC CCTCTCCTTC CTGCACAAAC ACATCTCAGG AATGCACCTG 240 AGGAAAAGGA GGGAGCCGGG GCCTCCCTCA ACTGCTCAAG GTAGTGCTCC CTTTGTTGTC 300 TGCTGTGAAC TGAATTGTGA ATTCAGCAAA TTCCTTTGTT GAAGCTTTAA TCCTCAATGT 360 GACTGTATTT GGAGATGGGG GTAATTAAGA TTAAATGAGG CCATAAGGGC AGGGTCCTAA 420 TCTGATAGAA CCGGTGTCCT CATTAGAGAG GGAAGAGATG CCTGAGCTCC CTCCCTCTCT 480 CCCTGTGGGC GCACAAAGGA AAAGCCACAT GAGGACAGAG AAAGAAGGTG GCTGTCTACG 540 AGCCAGAAAG AGAAGCCTCA CCAGAAACCA ACCCTACCGG CACCTTGATC TTGAACTTCC 600 AGCCTCCAGA ACTGTGAGAA AATAAACGTC TGTGGTTTAA GCCACCCAGT CTGAGGTATT 660 TTGTTAAGGC AGTCTGAGCA GCTAATTGGC TCTCAGTTTC AAGGCTGATT TCAAGAGACT 720 CGTGTTGGCC AGGTATGAGG GGAGCCAGTG CTCAAGTGAA GGAAGGAAAA TTCAGCACAT 780 CCTCCTCGTC TAGCTGAAGG GGGCTCTGGA GCAGCAGGAG GGGCCCAGGG CAAGCCTGGA 840 ATGAAATCCG TGGCACTCCT GCAGGTTCTG GGGGCGGTGT CCATGGAATA TCCTCTGCCA 900 CATAACAAAA TGACTAATAA TTGCTTGGGG AGCTTTCAGA ACTGCCCCAA GGCTTCCTCT 960 AACACTCCAC CCACACCTGG TTCATGCCAG GTTGCTCGAT GCCTTGGTTC GGGAGAATAG 1020 GTGTGGTGTC ATCTCAGGCT TGGTGGCAGC CCAAGGGAAG GGGCAAGTGT TCTGAGTCTC 1080 TCTAGATGAC ACAGGAGCTG AGGAAAGCTG GAGTGAATTA TGAGTCACAG CCCGTACCTC 1140 ACAAGAAAGT TCTGCCCGAT GCCAGAGCTG GGAGCCATCA CCAGTTATGC AGGGTTGGTG 1200 GAGAAGAGCC TCGGGATAAT TGGTATGCAT GCCCGCACAT AGGTGTGTGC GTACCAGTAC 1260 GTGTGAAGTT ATGCAGGAGT GCGTGGTGTG CTTATGCCCA TGTGTGTGCA CATTAGTCCT 1320 TTTGTGCATG CATGCATACA TGGCACATGT GTGTGCATTC ATGCTTTGCT GTTTTGAATG 1380 CAGGTATGGT TATAAGTGCA TATGGGCAAC AGAAGTTCAA GTGTGAATTC TCATGGAGAT 1440 GCTAGGGTGT AGCAGGCACA TGGGGACCTG TTCCCTGACA GGGGTGTTTG TGAAAAGCAA 1500 CTGTGCATAT GTGTGAGGGT GTACTTATAT ATGAGATTCT ATGTGCAAAG 1550
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