| Tag | Content |
|---|
EnhancerAtlas ID | HS048-03789 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:236322910-236324120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:236323590-236323611 | AGGGGAGGGAAAGGAAGTGGG | + | 6.04 | | ZNF263 | MA0528.1 | chr1:236323776-236323797 | CCCTCCACCCTTCCCTGCCTC | - | 6.11 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_59322 | chr1:236304325-236328173 | Ly3 |
|
| | 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 |
| GH01I236159 | chr1 | 236322441 | 236324399 |
|
Enhancer Sequence | TGCAGGAAAA AAAAAAAGAA AAGAAAAAAA ATAGGCAAGC GGGAGTTCAA AGGGTGGGAA 60
CAAATCAGTG ACGCGTGAAC AGACTGATTT ATGAGGGCAG GGGGCAGAGT CCAGCAGCTG 120
CTCAAAGGCC TTTATGCTTC TGTCGAAACA AGTACGTCAC ATGCAGAGCT CTAGGCCTTC 180
CTGTGTCATC CGAAAGGATG GGGTGAAGGC CTGGGTTACC AAGGGGGCAC AAGTCGCCCA 240
CAGGTCCGGG ATGAGGAGGC CTTGGCCCAC TGTGGGAGCG GGTGGTGCGG AAAGCCCATG 300
AGGGCTCTCG AACATTCCCC AGCGCCTGAC AGCGGCCAGC TGGGGACATC TCCCAGCCGT 360
GGCTCAGCCT TCAACAAGTC AAAAAGCCAG CATCACCCAC AGCGTCATCC CCAGATCTAT 420
TCTAGGTTCT GAGGTTCTAG GTGGGACTTT CAAAAGCAGA AGAAACGATG CTAAAACCGA 480
AAGGAATTTG CCATTAGGGA GAAATGCTTT ATTTTCACCA GATGACAAAC TTCAGGGTTT 540
CTGATCAAAG TTGCTGCAAT TTCTTCTTTC TCCTTCAGGC CTGATTCTGC TCCCCTCCCC 600
TGTCCTCCCA TCCTTCTTGC CACAACGGGG GAAGCCCTGA AAAACCCCGG TGTTTTCATA 660
GGCTGTGTGG AGCCCAAGGA AGGGGAGGGA AAGGAAGTGG GGCTCATTTA CCACCATTCA 720
GTTCCTGATC GGGTTCCCCA AGAAGCAGCT GGGACTCTCC AACCCAACCT CACTTCCCCG 780
GGGTCCCTGT CATTAGGCAG ATGGCACTCC CATGGCTGTC CCTGCCATGT TCCCTCAGAC 840
CCCTCCTTGC TGCCTCAGTT TCTCAGCCCT CCACCCTTCC CTGCCTCCTG CCTCTCCCTG 900
TCTGCCCTTC TCGGGACCCA GGCTCCTTCT GTCTGTCCAC AAGCATGCTC AGGTCTCCCC 960
ATCTTAAAAA CAAGGTCTGG ACCCCCTGAA TAACCTCTTT CTTGCATTTC ACAAACATGC 1020
GCTTTTGGAA AGCAGTTTAT GCTCTTGAAT TGACTCACTG CTCCCACTTC CTCCTGCTGC 1080
CATCCAGGGT CTGCCTGTTC CCCCTCCAGC CTCCCCGTCA GTCGAGCCTG CCCTTGGCCA 1140
GGCCCTGTGG CAGCTTAAGG TGAAGTGGTC CAGCCTGTCA GCCGCACTGG ACACCCTGAC 1200
TGTCTCCTGC 1210
|
