| Tag | Content |
|---|
EnhancerAtlas ID | HS176-15680 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr16:87027880-87028970 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr16:87028323-87028338 | ACAGCTGAGTCATTG | - | 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 |
| GH16I086993 | chr16 | 87027518 | 87029163 |
| Enhancer Sequence | TTTGATTTTA CAAATTTGGA AACTAAGGCT CAGAGAAGTG TGGTTTTACC TCTGAAACAC 60
GCAACTTCCC ACCCACCCAA AATGAGTGAT GGAGAAAGAA CCAACAGGAT TGGGCAACTG 120
TTGGATGTTG AGCAAGAGGG AGAGAAGAGT TGACTCGGAG GTTGGTATAC TCCAAGAAGG 180
CTTCCTGGAG GAAGTGGACA ATTCAGAACA CAGGACCCTT TATCCAAATC AAATACAAAT 240
AGGGAACACT ATTATTAAGT ATTATCTCCT ATCTCTGTAA AAAGCCTTGT GGCCAGGGGG 300
TGTTCTGGAA ATGCTAGTTA ATTTCTGGTT AAATATTGGA TCCCTGGGAG TTCTTTAAAG 360
GCTCGTTTAC CCAGCCTGGA AGTTAAGCCT GTAACTTAAA CGCATTGTCA AAACCAGGAA 420
ACATTTACCC CCCAGTCCAG ACCACAGCTG AGTCATTGGC CAGGAGAAGC TCAGTCTGTG 480
TGCAGAGAGC TGGAGATTAT CTCATCTTCC AGGCACTTGT AGACATCCAA TCTGGACAAA 540
TCATGTCCCA CTCCCAAGAA TCTGCAAGAA ATGGCCTGAT GTGTCTCCCA CAGAACAGCC 600
GATGATGATA ACTCATTGTC ACTCGAGCCA GTGGGCAGAT AATGACCCCG CTGACAGGGT 660
CCAGCCTGCT GCTCCGCCCC AGCAGACATG CTCCAACAAT GGCTTCATCA TCCTCCCCAC 720
CGGGACTGTG TAGATGAGGG AGGTGCCTCC CGCGGTGCAG GCTGTGAGCT CTAAGCAGTC 780
ACGCTGGACG CTGGACCAGT GCCCTGGGCT GCTCCTCCCT GCAGCCCCAC GAGCCCAGGT 840
AGGGATCACC AGAGGTCGTT TCACTCCCAA GTGGAGTGAT AAGTCAGTCC TTCTACAGGA 900
AGATTTCTCA CAAAGTGCCC TACTGCACTG TCAAAGGGTA AAAAGGAGAA AAAAAATAAT 960
AAAGCCAGAG GCAAGGGCTC CAGGCAAGAG CAAGATGACA ATATTTGTAC AGCGGGGTTT 1020
GGAGAGGAGC CCCCGTGAGA GCCCAGCGTC TGAGAGAGCC AGTCCTTTGA ACTGTCCCAC 1080
CCTTTGTTAT 1090
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