| Tag | Content |
|---|
EnhancerAtlas ID | HS101-18878 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr17:47337170-47338510 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr17:47338191-47338202 | CATGAGTCACC | - | 6.62 | | FOSL2 | MA0478.1 | chr17:47338192-47338203 | ATGAGTCACCC | - | 6.14 | | JUNB | MA0490.1 | chr17:47338192-47338203 | ATGAGTCACCC | - | 6.32 | | JUND | MA0491.1 | chr17:47338191-47338202 | CATGAGTCACC | - | 6.02 |
|
| | 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 |
| GH17I049259 | chr17 | 47336904 | 47338798 |
|
Enhancer Sequence | GAAGCCAGGG GAGCCCAGAA CAGGATCCAG GGTCTCCCTC CCCCGTGGTC TGGAGATCCT 60
TGACATCTGC CATCCCCTTA GCAGAAGCTG CAGCCAGAGA AAGAGGGCGA CGGTCCCGTC 120
ACATTCTGAG CCCAGCAACG GAGGGCTTTC CAGGCCGGGA CTGCGGGCAG ATGGGAATTC 180
TCCTCTCCTT TCTGCTGGAC GTATCTCCCC TCAGTTTCGC TATCTGTAAG ATGGGGCATT 240
GTCCCTGCCA AACCCGCAGG CCAGGACGGC CTAAGAGGAT CAAACGAGGA GAGGCAACGA 300
GGATTGGTGC CTGGCTTTTC CTGAAAACAG ATTCCTCCCC CGCCCCCGGG ACCTGTCCCA 360
CAGGGGCGTC TGGAAATTCC ACAGAGCCAG CCAGTCTCAG AGTGAAACAA TCGGATCCGC 420
CGCGACACAG CAGCTATTCA GACGTCGGGG GCGGGGGCCG GGCCGCTGAG CGAGCAGAGC 480
AATGCCGCCC TCGCGTCCCC TCCCGGCCCA CGCGGCTGCC CCGGCCGCCC TCCCCGCGGA 540
GCCCCGGCCT CGCACGGGCC TCGGCGCCCG CCGGGCGTCC CCCAAGCTTC CTTGTTTGTG 600
GCCGAGCGAC CGCGGAGCGT GGCACGTTCA GGAAGGACGA GTCGCCCCAC GGCGGGGAAC 660
CGGCGACCGG CGGCAGCCCC AGCCCAACCC CGGCCACGCC TCGTTAGGCG CCACGTCCCG 720
TCCCCGGGCG CCCGGAGCAC TGTGCCCCGC CGGCCCCTGC CCGCCGCTCG CTGTAGGAGG 780
GAGCCTTCTG CGTCGGCTCC CGACACTCGC TCACTGGGGC GCGGGCACTT GAGAGTAGGC 840
AACCTGGGGG CCCCAGAAGG GGATGGGGCT CCGACAGCTT CAGCCGGGCG TCCCCTCAGC 900
TGCCTTAGCT GGCGTCTGAG AGCGACTCCT CCGTCCAGGG CTGACAGTTC CCTTGCCCCT 960
TAAGAGCCAA TCGGAGAATC ATAGGATCTG ACATCCTGTG GCTCAGCCGG GTCTAAGAGC 1020
TCATGAGTCA CCCTGTGTGC TTTGCTGATG AGGAAACCGA GGCCCAGAGA CGGGGGCTGA 1080
CTTATTCGAG CCACGTTTGT GTCTCCTAGC CCTGTGCCCT TTCTCCAACA CTCTACTATC 1140
CTACCTCAAA TCAAATCCAC TCTGGGGCTA AGGACATCTA GAAGTGTGCG TGTGTGTGTG 1200
TGTGTGTGTG TGCGCGCGCG CCAAGAGTGG CTTGGCTACA TTAGGGAAAT GCCAGAAAAA 1260
TGGAAGGTTT CTAATAAAAG CTGCTCTCCA CGGGCCCAGA GTGTGGGGCT CCCACCCATT 1320
GGCTCCACAA ATCACCTGTA 1340
|
