| Tag | Content |
|---|
EnhancerAtlas ID | HS095-06618 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr12:7143930-7145120 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr12:7144847-7144862 | CGCAATGACTTAGCA | + | 6.25 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAACATGTCT GAACAGGATC TAGTTTGAGG CACTAGGAAG GGTAAGAAAT CAGTTTGAAA 60
AGAGCCCCTT GCTCTGTGGC TGGGTAGTGC TGGAGGTTAG CTTCCTCTAG GCCACTGAGC 120
TCTCACGTCA CTGCAGAAGG CCTTATCTGC AGAGACTTCC CATGCCAAGC AGGCCTGCCC 180
CGTCAGAGAG AATGGCAGAA AGCTCGTGTG TGTCCTGGGG AGATGGTCAG AGGGAGCCAC 240
CTTCCAGCTG AACCCCAATA AGTACTCGTA GCTCACGGTG TAAACGCCCT CCAGAGGTTG 300
CAGCTGTATA CCCAAAGGTC CCGGCCAGCC CCTGTGCGCC CCTGTGTTGA CTGGGTTTGG 360
GGAGGACACA GATGGGGGCG TAGGAGGTGT GTAGCCCTGA CTCAGCTTCC TGGTTGCATC 420
CTAGTCTAGT GTTGTTTGAA GTCACGTGGA CGTGGCCTCC CCTTAGAGGC TGGTGAGGGC 480
ATTTGAGGGC AGTTGTGTGC TCCTGGCCTG GGGCTGTGCT TTTGTGGCTG TGTGTGTGTG 540
TGTTGGCGGG GGAGGGAGGG AGGTGCCCTA GTTGTGCACG GTACTCTGCA GCCCAGCGCC 600
CTGCCGAGGC TTCTGCTGAG AGGAGACAGC GTGCTGGCAG TCCTCAGAGC CCTCGCTTGC 660
TCTTGGCACC TCCTCTGCCT GGGCTCCCAC TTTGGCGGCA TTTGAGGAGC CCTTCAGCCC 720
ACCACTGCAC TGTGGGAGCC CCTTTCTGGG CTGGCCAAGG CTGGAGCCCA CTCCCTCAGC 780
TTGCAGGGAG GTGTGGAGGG AGAGGCGCGA GCCGGAACCC GGACTGCGTG CGGCGCTTGC 840
GGGCCAGCTG GAGTTCCAGG TGGGCGTGGG CTTGGCGGGC CGGCACTTGG AGCAGCCGGC 900
CAGCCCTGCC GGCCCCGCGC AATGACTTAG CACCCGGGCC AGTGGCTGCG GAGGGTGTAC 960
TGGGTCCCCC AGCAGTGCCA GCCCACCGGC GCTGCACTTG ATTTCTCACC GAGCCTTAGC 1020
TGCCTTCCCG CGGGGCAGGG CTCGGGACCT GCAGCCTGCC ATGCCTGAGC CTCCCACCCC 1080
CTCCATGGGC TCCTGTGCTG CCCGAGCCTC CCCGACGAGC GCCGCCCCCT GCTCCACGGC 1140
GCCCAGTCCC ATCGACCACC CAAGGGCTGA GGAGTGCAAG CGCACTGCAC 1190
|
| |
|
|
|
