Tag | Content |
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EnhancerAtlas ID | HS040-12748 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr16:1945810-1946590 |
Target genes | Number: 21 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PHOX2A | MA0713.1 | chr16:1945852-1945863 | TAATTAGATTA | - | 6.32 | PROP1 | MA0715.1 | chr16:1945852-1945863 | TAATTAGATTA | - | 6.14 | Phox2b | MA0681.1 | chr16:1945852-1945863 | TAATTAGATTA | - | 6.32 |
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| 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 |
GH16I001895 | chr16 | 1945873 | 1946345 |
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Enhancer Sequence | CCTCCCCTGA AAGCCGCCTG GAAGAACATC TGCCATTTGC TCTAATTAGA TTAAGACACA 60 TGCAAGTGTC CTAGTCCCTG GAATAACCGC TGTTAAGAGT TCCCTTTGAC ATTTGCAAGG 120 GAAGAATCCA CACCCACATG TTCAGCCCGA CCTGCTCTCA ATGGTTTCCC TCCCGTGGGG 180 CCTGTGTCTG GCCTGTCCTG GCCCCACAGG TAATGCCCCC GACCCGGAAG GCATTGTGGA 240 CCCAGATGTG CAACTGACCT GGAACACAGC TGAGTGATAT CAGACTCAAC ATCAGGTGCA 300 GAGCTGTTTG TTCTGTTGGA GAACATTCCA GAGGTTCCAG AAGCTGGCAG GGCTTGGGGC 360 TCACCCGTGT TTCTGTGCCA GGAGCTCTCC CCAAGCACCT GCTGTGACTC AACAAAGCTG 420 CACTGAGCAC AAGCTTGGGT CAGGCCCCGC AAGGGGATCC AGGGAGGAAA CACACAGACA 480 GGGGGTCGCT GCCGTGGGGC AGAGAACAAA CTGGTGCTGC CTGTGCCTGG TGGGCAGAGC 540 CCGGGTTGTC GGAGGCACGT TCAGAAGCTG GGTTCACTCA GTCTGTTCCG TCATGGGATC 600 AATGGGCCCC CTTGGAAAGT TCTGGAGTGA GGGAACCATC ACTGAGGGTG TGCTAGTGGC 660 AGTCCCGCTC TGTCCCCCAG GCTGGGTGCG TGGCGGTGGC AGTCCCGCTC TGTCCCCCAG 720 GCTGGGTGCG TGGCGGTGGC AGTCCCGCTC TGTCCCCCAG GCTGTGAGTG CAGTGGCACG 780
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