| Tag | Content |
|---|
EnhancerAtlas ID | HS180-32688 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr3:18767040-18767700 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPB | MA0466.2 | chr3:18767503-18767513 | ATTGCGCAAT | + | 6.02 | | CEBPB | MA0466.2 | chr3:18767503-18767513 | ATTGCGCAAT | - | 6.02 | | RUNX1 | MA0002.2 | chr3:18767198-18767209 | TTCTGTGGTTT | + | 6.32 | | ZNF263 | MA0528.1 | chr3:18767238-18767259 | GGAGGCGGAGGGGAAAGGAGG | + | 7.03 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_18730 | chr3:18763374-18769766 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20677 | chr3:18763711-18769948 | CD56 | | SE_22750 | chr3:18763516-18769686 | CD8_primiary |
|
| | 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 |
| GH03I018722 | chr3 | 18763866 | 18769778 |
|
Enhancer Sequence | GCTTTCTGTT GCCTTCAGGT GGATGAACAC TTTCATAGGC AAGTAAAATA GATTGTTACA 60
CCTGACTTAT TTACACAAAG TAAAAAATAG GTTACAGCCT TTTAATTTAA GCTGATCAAC 120
TTTATTATTT CTCTTTGGAT GAAAGCATGT GCAATGTTTT CTGTGGTTTG GGTGTAATTT 180
CCTGCCAGAG GGGGATGTGG AGGCGGAGGG GAAAGGAGGG GTTGCTGAGT TTTGCCATCA 240
AATTCTTAAG TCCAGCTGCT CTCTTTTAAG TGTCAATGAC CTTACTCTAT AGCATCCAGA 300
CTGGTCAAGG TCCCTATAAT GAGAAAACCA AATTACAGGT ATGTAATTTT CACAGTTTTC 360
TGCCGGGATC TCCAAGTTGG TGACAAATTG ATATACTACT GTCTGTACGG AAGACTGCTT 420
TCAGAAAACA GGCCACTCTC AGTTGAAACA CTATGCCTGA AGGATTGCGC AATTTTAAAC 480
TTCCGAGATA TAAAAAACAT CCTTCACCCA AGTCTCTTGT AGAATGTTGA ACTATAGAGC 540
ATATTGTTTA AGCTTGGAAA GCCCTGCCAG AACAACAAGA TGTGAGAAAA ATCTTCAGGC 600
ACCAGGAACA AGGAGATCAT GGAAAAGCAA CTAACAATGG GAAGATAACG TATGTCATGG 660
|
