| Tag | Content |
|---|
EnhancerAtlas ID | HS141-07774 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr17:18721090-18721750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr17:18721286-18721297 | GCGCATGCGCG | + | 6.02 | | NRF1 | MA0506.1 | chr17:18721285-18721296 | CGCGCATGCGC | - | 6.02 |
|
| | 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 |
| GH17I018818 | chr17 | 18721313 | 18721714 |
|
Enhancer Sequence | AGGGTTAGAG AATGTAGGAG TTGACCCAAG GTCAGGGTGC ATCTAGTACA TGATGGATCC 60
AAGGTTCCTA TCTGGACAGT CTGCCTTAGG CTTACAGTGC TAAGCACCAC ATGCAGTTTC 120
CCCAATCATA CACCTTAGGA CACCACCTTT GTATGTGGGT CTCGTGCCAG AGATGAACGT 180
GGGCGCATGC ACATGCGCGC ATGCGCGCGC GCGCACGCAC ACACACACAC ACACACACAC 240
ACACACACAC ACACGGAGAG AGATTTATTT CAAGGAGTTG GCTTACACAG TTGTGGGAAC 300
TGACAAATCC AAATTCTGTC GGGCAGGCCA GCAGGCTGGA ACTCTCAAGC AGGAGCTGAT 360
GTTGCAATCT TGAGGTCAAC TTTCTACTTC CTCAGGAAAA TCTTAGTTTT GTTCATAAGG 420
CCTTTAACTG ACTGGCTGAG ACATTCCCAC ACAGTAAAAG AGCAACCTGT TTTACTCAAT 480
GTTAACAGAT TGTAGATGTT AGCCACATCT ATAAAATAGC TTCAAAGCAA ACAACACCTA 540
CATTAGTGTT TGATTAAATA ACTCAGTACT AGCCAAGCTG ACACAAAAAA TTAACCATCA 600
CACGCTTCCA GCTGTCTGTA AACGCTATGA CAGCAGGAAG CCTATCTTTG TCATTCGCCT 660
|
