Tag | Content |
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EnhancerAtlas ID | HS145-09318 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr16:70510090-70511050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROD2 | MA0668.1 | chr16:70510375-70510385 | GCCATATGGT | + | 6.02 | Zfx | MA0146.2 | chr16:70510149-70510163 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH16I070474 | chr16 | 70508755 | 70511590 |
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Enhancer Sequence | AGAGACGGGG TTTCACCGTG TTAGCCAGGA TGGTCTCGAT CTCCTGACCT CGTGATCCGC 60 CCGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCGCGCC CGGCCTGTGC 120 TGTGCCTCTC ATGCTTGTTG GAACCAGGTG CTGTGCTTCG TGACTGTGCC TTTCCAGGGC 180 TGTGCTGGGG TAGGGCTGGG CAGAGCTGCT TTGGACCTTC CGCCTGTCCT GGCATCGTGC 240 CCTTACTTGA GATATGATCA CCTGTGCCCC CGCCCCCACC CCCTGGCCAT ATGGTGGGAC 300 AGCAAGAGCC CAACAATGAC TATGATCTAA TGAATGTCAC CAGCGCCAGG CTTCTCACTC 360 CTCCTGGCCA CCGAGCCCCC TGGAACCCAT GGCCAGTGTA GAGCAGCTAC AGCTTGTCTG 420 GTTTCAGGTC CACCTCAGGG TGTCAGGTCC CGTCTCCAGC ACACCCCTGG AAAGAAACTG 480 CTGCAAAGGC CTACTGAAGC CTGACTGTGG TGTTTTCTGT CACTCTGCAG CTCAAGCCTC 540 ACATTTCACT GTAGTGACTC ATATCCCATA ATCGGTAGTC ATTAGCAAAA GGAGCAGATG 600 GGGAAGCATT TTCAGTTTTC TTTTGAGGTG TACCATTCAA GTTCTACATT TGGCCAACGG 660 AAAACTATTT GTTGAGAACC CACTCTGTGG GGCCCCAGGG ATAAAATGAG CAAAAATGGG 720 GTCCCTGCCC TCAAAAGTCC TGTGGTCTCC TGGAGACAGA CATTAATCAA TAACTACTCA 780 GGTGCATGTG TATTACAAAC TGTGCCAAGT GCTTTGAAGC AGAGGGGCAC AGTTAAGTCT 840 TGACATTTCA AGACTTAGCC ACTTTGCAAC TACCAGGTTT TGGCTGCAAA GTTCCAGATG 900 GCTTCTGTCT TTTGCATTTC ATACTTTAAA CCCTTGCAGG CCCTTCCCTA ACTATCAAGG 960
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