| Tag | Content |
|---|
EnhancerAtlas ID | HS180-05041 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:236322750-236324120 |
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 | ATCAGGAGTT CAAGACCAGC CTGATCAACA TTGTGAAACC CCGTCTCTTT TTGTATTTGT 60
AGAAATACAA AAATGAGCCA GGCATGGTGG CGGGTGCTTG TAATCCCAGC TACTCGGGAG 120
GCTGAGGCAG GAGAATCACT TGAACCTGGG AGGCAGAGGT TGCAGGAAAA AAAAAAAGAA 180
AAGAAAAAAA ATAGGCAAGC GGGAGTTCAA AGGGTGGGAA CAAATCAGTG ACGCGTGAAC 240
AGACTGATTT ATGAGGGCAG GGGGCAGAGT CCAGCAGCTG CTCAAAGGCC TTTATGCTTC 300
TGTCGAAACA AGTACGTCAC ATGCAGAGCT CTAGGCCTTC CTGTGTCATC CGAAAGGATG 360
GGGTGAAGGC CTGGGTTACC AAGGGGGCAC AAGTCGCCCA CAGGTCCGGG ATGAGGAGGC 420
CTTGGCCCAC TGTGGGAGCG GGTGGTGCGG AAAGCCCATG AGGGCTCTCG AACATTCCCC 480
AGCGCCTGAC AGCGGCCAGC TGGGGACATC TCCCAGCCGT GGCTCAGCCT TCAACAAGTC 540
AAAAAGCCAG CATCACCCAC AGCGTCATCC CCAGATCTAT TCTAGGTTCT GAGGTTCTAG 600
GTGGGACTTT CAAAAGCAGA AGAAACGATG CTAAAACCGA AAGGAATTTG CCATTAGGGA 660
GAAATGCTTT ATTTTCACCA GATGACAAAC TTCAGGGTTT CTGATCAAAG TTGCTGCAAT 720
TTCTTCTTTC TCCTTCAGGC CTGATTCTGC TCCCCTCCCC TGTCCTCCCA TCCTTCTTGC 780
CACAACGGGG GAAGCCCTGA AAAACCCCGG TGTTTTCATA GGCTGTGTGG AGCCCAAGGA 840
AGGGGAGGGA AAGGAAGTGG GGCTCATTTA CCACCATTCA GTTCCTGATC GGGTTCCCCA 900
AGAAGCAGCT GGGACTCTCC AACCCAACCT CACTTCCCCG GGGTCCCTGT CATTAGGCAG 960
ATGGCACTCC CATGGCTGTC CCTGCCATGT TCCCTCAGAC CCCTCCTTGC TGCCTCAGTT 1020
TCTCAGCCCT CCACCCTTCC CTGCCTCCTG CCTCTCCCTG TCTGCCCTTC TCGGGACCCA 1080
GGCTCCTTCT GTCTGTCCAC AAGCATGCTC AGGTCTCCCC ATCTTAAAAA CAAGGTCTGG 1140
ACCCCCTGAA TAACCTCTTT CTTGCATTTC ACAAACATGC GCTTTTGGAA AGCAGTTTAT 1200
GCTCTTGAAT TGACTCACTG CTCCCACTTC CTCCTGCTGC CATCCAGGGT CTGCCTGTTC 1260
CCCCTCCAGC CTCCCCGTCA GTCGAGCCTG CCCTTGGCCA GGCCCTGTGG CAGCTTAAGG 1320
TGAAGTGGTC CAGCCTGTCA GCCGCACTGG ACACCCTGAC TGTCTCCTGC 1370
|
