| Tag | Content |
|---|
EnhancerAtlas ID | HS042-18740 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr17:9259450-9260520 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr17:9259824-9259839 | TGCTCAGTCATGCTG | - | 6.78 |
| | | 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 |
| GH17I009356 | chr17 | 9259718 | 9260117 |
| Enhancer Sequence | AATTACTTAA TATGTAGGTG GTAGGTCCAT TTGTCAAGCA GTAGAAATAG CATCGTTCCT 60
TCCAGTAGCT CAGTGTGACA ATACTGTTTC TTCTATTAAA ACAATGTCTG CATTTTGGGG 120
TTTGCAGAAA TTCACTGTTT GGCATGACTT TAAGAATAGC TCTAACCAAA TGGTCCATGA 180
GAATACATAA AAACCTTTTT CAGTTCAACA GGTCCACGAA GAACCCAATA ATTCTGAAAG 240
AAACATCGAA GGCTGGAAAA ACATGTCAGA TGATTGTCAG GAGAATATAT GTTGCACATC 300
TCAGTGGTGC CCATGTAAGC TGCCTATATG CCAGGTATGA CCTGGTGTCT GCCAGCTCCA 360
CACCTGCCCT TCTCTGCTCA GTCATGCTGG GGCTTGGAGT CTGTGAACTA CCCTTCCCAG 420
GCTCCCCTGC CAGCTGGCTT CCTGTTATGT TCTGCCAAAA TAAGGCACTG TCAGGAGTTC 480
AGAAAGCAAG AAGAGGGGTG AGGCTGTTCC TCTTCCTCTC TTTCCCCATC TGCTTCTGGC 540
AGCATCTCTG CAAGTGTCTG TATTCTAACA GTGTTCCCCA TGGCAGTGGC AGCCTCTCTT 600
TGGCAGTCCC AGAACGAGCA AGGCAGGCCT GCTTCTGCTG CAGCCCAGGG GCCAGGTCCT 660
AGGCATCTCT AGCACTGGCT GAGCGGCAAT CCCAGGAGTA CTGTGGTGTG CAGCAGCGCA 720
TTTGCATCTT TGCTCTCCTA GGCTTAAGGG TGGCAGCTGC TTCACACAAG GACTAATTTC 780
TGGATTACTG CACCTTCCCC TTTTCATTCT CTCCATCCTT TTAACAGTTT TTTTTTTTTT 840
TTTTTTTTTT TTTAGGCAAA GTCTTGCTCT GTCACCCCGG CTGAAGTGCA GTGGCATGAT 900
CTCAACTCAC TGCAACCTCC GCCTCCCAGG TTCAAGCAAT TCTCCTGCCT CAGCCTCCTG 960
AGTAGCTGGG ATTACAGGCA TGTGCCACCA TGCCTGGCTA ATTTTTGTAT TTTTAGAGAC 1020
GGGGTTTCGC CATGTTGGCC AGGCTGGCGG TCTCAAACTC CTGATCTCAG 1070
|
| |
|
|
|
