Tag | Content |
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EnhancerAtlas ID | HS176-15449 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr16:70509950-70511110 |
Target genes | |
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 | GCTGGAGTGC AGTGGTGCGA TCTCAGCTCG CTGCAAGCTC TGCCTCCCGG GTTCACGCCA 60 TTCTCCTGCC TCAGCCTCCC GAGTAGCTGG GACTACAGGC GCCTGCCACC ACGCCCGGCT 120 AATTTTTTTG TATTTTTAGT AGAGACGGGG TTTCACCGTG TTAGCCAGGA TGGTCTCGAT 180 CTCCTGACCT CGTGATCCGC CCGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG 240 CCACCGCGCC CGGCCTGTGC TGTGCCTCTC ATGCTTGTTG GAACCAGGTG CTGTGCTTCG 300 TGACTGTGCC TTTCCAGGGC TGTGCTGGGG TAGGGCTGGG CAGAGCTGCT TTGGACCTTC 360 CGCCTGTCCT GGCATCGTGC CCTTACTTGA GATATGATCA CCTGTGCCCC CGCCCCCACC 420 CCCTGGCCAT ATGGTGGGAC AGCAAGAGCC CAACAATGAC TATGATCTAA TGAATGTCAC 480 CAGCGCCAGG CTTCTCACTC CTCCTGGCCA CCGAGCCCCC TGGAACCCAT GGCCAGTGTA 540 GAGCAGCTAC AGCTTGTCTG GTTTCAGGTC CACCTCAGGG TGTCAGGTCC CGTCTCCAGC 600 ACACCCCTGG AAAGAAACTG CTGCAAAGGC CTACTGAAGC CTGACTGTGG TGTTTTCTGT 660 CACTCTGCAG CTCAAGCCTC ACATTTCACT GTAGTGACTC ATATCCCATA ATCGGTAGTC 720 ATTAGCAAAA GGAGCAGATG GGGAAGCATT TTCAGTTTTC TTTTGAGGTG TACCATTCAA 780 GTTCTACATT TGGCCAACGG AAAACTATTT GTTGAGAACC CACTCTGTGG GGCCCCAGGG 840 ATAAAATGAG CAAAAATGGG GTCCCTGCCC TCAAAAGTCC TGTGGTCTCC TGGAGACAGA 900 CATTAATCAA TAACTACTCA GGTGCATGTG TATTACAAAC TGTGCCAAGT GCTTTGAAGC 960 AGAGGGGCAC AGTTAAGTCT TGACATTTCA AGACTTAGCC ACTTTGCAAC TACCAGGTTT 1020 TGGCTGCAAA GTTCCAGATG GCTTCTGTCT TTTGCATTTC ATACTTTAAA CCCTTGCAGG 1080 CCCTTCCCTA ACTATCAAGG GCCTGTCCCA GAAGCAACTC AAGTTTTGTT ATTTTTAATT 1140 TTTTTTTATT TTTGAGATGG 1160
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