| Tag | Content |
|---|
EnhancerAtlas ID | HS050-06680 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:245421310-245422430 |
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 | AGACTCTGTC TTAAAAAAAA AAAATGTTGC TCAGAAGCTT CTCGATCTTG TCACATTCTC 60
CGGTGGTGAG TTGAGAGCAG CCCAGGCCTG GGGTCCTAGG GAGCTTGACG TGGCTACTGT 120
TCTAGACAGT GCTGAGTTTG TCATCACCTT GCTTTCATTA TGATTTCCTC CTCCTCGTCA 180
CCACCTACGG TGTTTATGGA GTTCGCTGTA CATGAAGCCC CAGCGTCCAG AGGTGTAAGA 240
CAGAGCCCCT TCTAGGAGCT GCTGTCCATC CCACTGAAAG GCAGGTCTGA CACAGAAGAG 300
ACAAACAACC ATACTGGGCC TCTGGGGCCC CGTGAGATGT GAACTTCAGG TACCAGAGTG 360
CATGCGGGAG GAGGCCTGGG TGCCCTGGGG ACCCAAAGCA GGAGCTCATT TCTGACCTGC 420
CTCTCTCACC AAGCTTCCTT TGCTGAATGC CGTGGGCAAA CAGTGGTGTT GGTATTGGAG 480
CAGGATCAAA GCTCATTCCT GGCTAACCTG CAAAAATGAG CAGGTAAACA AATGGGATCC 540
ATAAAATAGA GACTAAAATG AAAGTTTGTC TTACTGTGAT TAGCAACTGG CCCCTTTCCA 600
AATTCCACCT GCTCTGCGTG GAGCTGTGGC GTCTCATTCC AAGAGCCTTC TCACAGCATC 660
TGACCCGGGC CTGGGGTAAC AGTACACTGG GGTTTGCCAA GGATAACCAT AGCAAGGCAG 720
CTACAGGAGC ACAGCATGGT GGGGGGGCAT GAAATCAGAA CAAGCAGGAC CCACGGGCGG 780
GGGTGAGAGC AAGTGGCTGG GAGGCAGAGG CAGAAGTGAT GGCTGCTGAC TCACCGTGTG 840
TCTGCCAGGT TGCTTAACCC ATCTCCGCTC CGGTTTTCCC ATGCGTGAGC CCTCTGCAGT 900
GTGTGGCATG CTGATCGGCC TCTGGCATGA AGAGTAAAAG CAAGGCCACA TAAAAATCAC 960
AGGTGCCCCT CGCTTCGTGC AACATGTGTG CCAGTCCAGT TTCTGCAACA GCCCCCCAGG 1020
CGCTGAGCCT GCTCCATGGG TTGGGAGATG TTAGACCTCA AGCTGTGCCC CTAGCTGGGT 1080
GGGTATGGGA AGTTACATGG CAGTGCTGGC TGCATTCTGC 1120
|
