| Tag | Content |
|---|
EnhancerAtlas ID | HS184-12733 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr16:82185960-82186910 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr16:82186357-82186372 | TCTGCTGAGTCACCA | - | 6.39 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 82185977 | 82186045 | | chr16 | 82186053 | 82186709 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH16I082152 | chr16 | 82185745 | 82187369 |
| Enhancer Sequence | AGCTTTAACA GTGTTATCAG TCAGAGCTCT TAGCTATAAA CACCAAAGGC TGACCCTGGA 60
TGACTTCAGC AGAGAAGGAA TTTACTGTAA GAACACTGTA GGCTCTTCAT TTCCAAGGGG 120
GACTGGTTCC AGGACCCCTT GTAGATATCA AAATCTGTGA CACAAAGAGC CAGCTGTACT 180
GGGCATCTCA GAATCACCGG GAAGGCTGAA GGGGCAGAAT TGGAAGACGG GCAGAAATAA 240
CGGTCGCTAG GTGGTTGCAC CAGAACCAAA ATCATGCTAG AGAATGACCC TAGGAAAACC 300
ACTGTTGCTG CTGACGGGGC TGAGCACGAC ACCACTGATG GCATTGGGGC AGGTTGCGTT 360
CCCTGGACCA GGATGTTTCT GTCTGCAGCA GAATTTCTCT GCTGAGTCAC CACCACATGA 420
CCGTAAATCC AAGGTGACAT ATCTATCTCC AGCCTGGCCA TAAACCCTAA AGCATGGCAG 480
GAAAGCAAAC ATGTGGCTTT TAAGGCTTGT TTGCCGGAGT AGGCTCTGAT TCTCATAAAG 540
ATTCCCTTAT GCAACAAACA CTTATTAAAC CAAACTGTGT GTATTAAATC AAACTGCGGA 600
AACAGCCACC AGTAAAAGAG CCTCAGCTGG GCACAGTGGC GGATGCCTGT AGTCCCAGTT 660
ACTCAGGTGG CTGAGGCAGG AGAACTGCTC GCATCCCAGA AGTGGAAGTT GCAATGAGTC 720
AAGATTGTGC CACTGCACTC CAGCCTGGGT GACAGTGTCA AACACTCACC TCCAAAAAAA 780
AAGAAAAAAA AGGAGCCTCT GCTCTCCTGG AGGTTACAGT CTATAGAAAG AGGGGCCAAA 840
TAATGAATGA AACATGAAAC ATTTATATCA CACAATGGAT GAAAATAAAG CAGGTTATTC 900
CATCCCTAGC TGTAGGGGAG TAATTGGTAT GGAACTAGCT TTCCTGCACC 950
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