| Tag | Content |
|---|
EnhancerAtlas ID | HS180-29213 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr20:2559070-2559790 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr20:2559685-2559700 | TGCTGACTCATGCTG | - | 7.41 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTTATTCCA AATGGATTTG TTTCCACAAT GTGGGGCTGG TGGAGAGCAG TCCCTTGGAG 60
AGTTGACAAA ACAACACCCA GCCATAGAAA GACGGCTGAT CAGGTTTCTG TTTGGTACAT 120
AGTCTGGGTG TCTAGCTGGG AACAGATCAC AGGAGGGGGC AACATGCCTT TCTGACTCTT 180
TTCAGAAAAG CGAGGCTGTT GTTCCCCCAG GAGAAGAATG TTCAGCTATG GGTTGAGATC 240
TCCTTATCAG TTGCACCACC CCTGCAATTT TGCGACAGTT CCTATCAGAG AGAGGCACTT 300
GGCTGTCTGC CAGACGTGGG TCTGAGAGTA GCCAGAGTTC CTTCTACCTT TGAATTTTTG 360
TTTTAAGTTG AAGAAAGTCA TATCAGAGGT TGCTAACTCA ATCGGACCCT CCAAATCAGA 420
AATCGTACAG AGAATTTCTC ACTTTATCTA CAAACTGTCC AAACCAGAAA TTTTATCAGC 480
ACAGTAAGGG GTGGCCCTCA CTTGTCTCTC ACTCCAGGCC TGACGTTGGG GAAGTAAAGG 540
TTTGAACACC TGCCTCTGGC AGCCTGGGCT CAAGGACAGC AGGAGCTGGG GACTGCAAGA 600
CAGCAGCTTC ACCCATGCTG ACTCATGCTG ACCTGTCGGC CTCCTCGTGC CCCTCATCAT 660
GCCCCTTTGT GCTCCAGGTT GACATGTTAA GGAACTGAGA GTTTTACGTC TTTTATTTCA 720
|
| |
|
|
|
