| Tag | Content |
|---|
EnhancerAtlas ID | HS158-01312 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr1:31319820-31320950 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6 | MA0677.1 | chr1:31320725-31320739 | CAGGTCATAGGTCA | + | 6.56 | | Rxra | MA0512.2 | chr1:31320725-31320739 | CAGGTCATAGGTCA | + | 6.06 |
|
| | 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 |
| GH01I030846 | chr1 | 31319734 | 31321163 |
|
Enhancer Sequence | GTGGCAAGCA ACTGGGTCCA CCCCAGGGGG CCTGAGGCCA GCCCCAGCCT GCCATTAACC 60
TGTTGTGTGG TTTGAGGCAT GTCCCTTCCC CTCTCTAGCC TCAATTTCCC CATTTCAAAA 120
TGGGAGAACT GGGCCAGATG CTATGGGACT TTATTCAGCT TTGACTGGCT GGTGCAAATC 180
CTGACGCTGC TACCTATGAG CTGTGTGACC TGGGGCGGCT ATTGGACAAA CCTTTGGCTC 240
AGTTTCCTCA TCTGTAAAAT AGGGGTAATC GTGGAGCTGC CTCATAGGGT TCTGAGGACT 300
GGATGGGCTG TTACTTGTAG GGCGTTCAGC AGAGTCTGAC AGGAAGGCAC AGACAAAAGC 360
CATCAGTGAC GCTGTTATGC TAAGCTCTGA GAGTCCACGA GTCCTGAGTC CTGCTTCTGC 420
GCGCCTCTGT GTGCTGGGTG ACCTGAGGCA GGTGCCTTCC CCTCTTGGGG CCCAGCAGGT 480
CTGAGAGTTG CCTTCAGAAG CTGGGCCTGG CTGTGACAAG AGAGTGAGTC CCTTCCTGGG 540
CTGGGAGGGG GAACAGGAGC GGACGGAGTC AGCCGGTTTC CTGCAGCCGG GGCAGTGACC 600
TGGGCAGCAG GGACTTCCTG TTTCCCAGAG GGAATCCGGG CCACTGCATC CAGCCCCTCC 660
CTCCCCTCCC TGCAGCTCCC CTCTGTAATG GAGGAAACTT GTCGCTGGGG CAACCTTCCC 720
TGCGTCATCT CCCGGGGCGG GCGGCCCTGT GTGGGTGAGA GAAGCACCAG CAACAATCGC 780
CCTTTGTCTC CAGCTCAGCT GCTCCCAAAG CGCTTTCTGA CCTTGCCCTC GTCTCAGCCC 840
TGAGAGTCTC ATGCCCATTT TCCAGATGAG GAAACTGTGG CCCAAGGAGG TGAGGTGACT 900
TGCCCCAGGT CATAGGTCAC AAGGCTGGTG AGAAGTAAGG CTGGGATTAA AACCTGAGTC 960
TTCTGAAAAC ATGGGCCAGC TTCATCTGGG GCCCTCGGCA CCCAGTGGAC CCTCAGTCAG 1020
GGCCCCCGAG ACACTGTCAG AGCCTGGAGC TTGACTTTTC AGTGCCCTGA TGACCTAGGA 1080
TGTGATCCTC GGCCACTGTC GCCTCCCCAG CTGGAGCCCT GAGGAAGGAG 1130
|
