| Tag | Content |
|---|
EnhancerAtlas ID | HS180-05132 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:245421340-245422430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr1:245422133-245422148 | TGCTGACTCACCGTG | - | 6.45 | | Zfx | MA0146.2 | chr1:245421386-245421400 | GCAGCCCAGGCCTG | + | 6.2 |
|
| | 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 |
| GH01I245258 | chr1 | 245421378 | 245422509 |
|
Enhancer Sequence | TCAGAAGCTT CTCGATCTTG TCACATTCTC CGGTGGTGAG TTGAGAGCAG CCCAGGCCTG 60
GGGTCCTAGG GAGCTTGACG TGGCTACTGT TCTAGACAGT GCTGAGTTTG TCATCACCTT 120
GCTTTCATTA TGATTTCCTC CTCCTCGTCA CCACCTACGG TGTTTATGGA GTTCGCTGTA 180
CATGAAGCCC CAGCGTCCAG AGGTGTAAGA CAGAGCCCCT TCTAGGAGCT GCTGTCCATC 240
CCACTGAAAG GCAGGTCTGA CACAGAAGAG ACAAACAACC ATACTGGGCC TCTGGGGCCC 300
CGTGAGATGT GAACTTCAGG TACCAGAGTG CATGCGGGAG GAGGCCTGGG TGCCCTGGGG 360
ACCCAAAGCA GGAGCTCATT TCTGACCTGC CTCTCTCACC AAGCTTCCTT TGCTGAATGC 420
CGTGGGCAAA CAGTGGTGTT GGTATTGGAG CAGGATCAAA GCTCATTCCT GGCTAACCTG 480
CAAAAATGAG CAGGTAAACA AATGGGATCC ATAAAATAGA GACTAAAATG AAAGTTTGTC 540
TTACTGTGAT TAGCAACTGG CCCCTTTCCA AATTCCACCT GCTCTGCGTG GAGCTGTGGC 600
GTCTCATTCC AAGAGCCTTC TCACAGCATC TGACCCGGGC CTGGGGTAAC AGTACACTGG 660
GGTTTGCCAA GGATAACCAT AGCAAGGCAG CTACAGGAGC ACAGCATGGT GGGGGGGCAT 720
GAAATCAGAA CAAGCAGGAC CCACGGGCGG GGGTGAGAGC AAGTGGCTGG GAGGCAGAGG 780
CAGAAGTGAT GGCTGCTGAC TCACCGTGTG TCTGCCAGGT TGCTTAACCC ATCTCCGCTC 840
CGGTTTTCCC ATGCGTGAGC CCTCTGCAGT GTGTGGCATG CTGATCGGCC TCTGGCATGA 900
AGAGTAAAAG CAAGGCCACA TAAAAATCAC AGGTGCCCCT CGCTTCGTGC AACATGTGTG 960
CCAGTCCAGT TTCTGCAACA GCCCCCCAGG CGCTGAGCCT GCTCCATGGG TTGGGAGATG 1020
TTAGACCTCA AGCTGTGCCC CTAGCTGGGT GGGTATGGGA AGTTACATGG CAGTGCTGGC 1080
TGCATTCTGC 1090
|
