| Tag | Content |
|---|
EnhancerAtlas ID | HS180-19485 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr16:89322720-89324280 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr16:89323632-89323652 | GGGGGTGTGGTGGGGGGTGG | - | 6.22 | | RREB1 | MA0073.1 | chr16:89323757-89323777 | CGTCTGGGGGTGGTTTGTGC | - | 6.26 | | Zfx | MA0146.2 | chr16:89323547-89323561 | CAGGCCTCGCCCGC | - | 6.65 |
|
| | 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 |
| GH16I089256 | chr16 | 89322877 | 89324252 |
|
Enhancer Sequence | AACAAACTAA CTAGGGCCGG GCGCCATGGC TCTCGCCTGT AATCCCAGCA CTTTGGGAGG 60
CTGAGGCAGG CGGATCACAA GGTCAGGAGA TCGAGACCAT CCTGGCTAAC ATGGTGAAAC 120
CCCGTCTCTA CTAAAAATAC AAAAATGAGC CAGGCGTGGT GGTGGGCACC TGTAGTCCCA 180
GACACTCGGG AGGCTGAGGC AGGAGCATGG TGTGAACCCG GGAGACGGGG CTTGCAGTGA 240
GCCGAGATGG CGCCACTCCA GCCCGGGCGA CAGAGCGAGA CTCCGTCTCA AAACAAAACA 300
AAACGAACTA ATTAAACAAA ACAACAAAAG AAAACCTGGC ATCAGTCCTG GTCACTGTGC 360
TCACGCCAGC CTCTCCATCC CGGCTCCTCT TCCAACTCTG CTTCCTGCTT CAGTGACTCG 420
GATGTCGCCC TTCGCCCCAT GCCCAGGAAA CCGGAGGTGG CAGTGGGGGA AGGGAGGGAG 480
GCGTGGAGAA GATACCCTGT CACCATCTCC ATGCCCCTCC CCGGGACCAC ACAGGTCGCC 540
TGGGCCCTGA CCAAATGGTT CGTTGTCCGC CAAGCCAGAC AGCAGGGCAG GCGCGCTCTG 600
TGCAAAACCG AGTCGTGTGC GGGCCCAGGG TGGCGCTCGG GGCGCTTCCA GCGCACGTCA 660
CCTCATCTGC GTCGTCACCA CTGTCGCCTC CGAAAGCGCA TTCCGTCGTC AAAATACACC 720
ACGAGGTCCC GGGTGCCCTC ACCGCCCTCC CCTTCCTCGC CCTCTCGTCG TTGCTGTTGG 780
GACGGGCTCT CGTCGCCCGC GCTGGGGCGC AGTGACTCAG TGTGACTCAG GCCTCGCCCG 840
CGCTCGGGCT CACGGAGCAG CTGGGACGAC GGGCGTGAGC GCAGAAGCCG CAGAGCCCCT 900
CGCGCGCCTC GCGGGGGTGT GGTGGGGGGT GGCCGCCTCC GGGGACGGGC GGGCTGCGGG 960
GCTCCGACCC CGCGGCAGCG TCTCGCGGCG CCTGAGGCCC CGGTGGGCGT GGGTTCCAGG 1020
CTGCACGGCT GGTTTGCCGT CTGGGGGTGG TTTGTGCTGG GACCCCCGCC TCGCCGCAAG 1080
GACCGACGCT TTCCGTATCC CGGGTTCCTG CTTCGGTGTA CCGGCAGAAT CTGATCACGC 1140
GTGGCCTGGA GAATGCGCCC AGGGTCGTAT TGCCTGGAAG GAGCTCTCAG CCGCTGGGGG 1200
AGCCGGAAGG GAGACGGTTC TGCCCTGGAC GCGGGCTGCT CGGCGGCCCC GGCTCTCCTC 1260
CAACCGGCCA AACCCCGCCT GGTCCCGCCG CCGGTGGCTG CTGCTCCCTC GCCGTCTTCC 1320
TGCCGAGCAG CCGCTGGCGT CTTCTTCCAC TGATCTGCTC CTCTCCACGT CCGGCTGCCT 1380
TGTCGGCCTG CTAGGGTCTT GGGTTTTTAT AGTACCAGGA TGGGGGCATG GCGGGCCAGG 1440
GTGGTCTTGG AAAATGCAAC ATTTGGGCAG GAGAGCAGGA GAGCCTGTCC TCACCGAGGC 1500
CGGGGACCCT CCTTTCTCTA CCCAGCACTT CCCTGCCCCC CTCTCGTATC ACCACCACGC 1560
|
