| Tag | Content |
|---|
EnhancerAtlas ID | HS086-12825 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr9:139755250-139756560 |
Target genes | | Number: 61 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYB | MA0100.3 | chr9:139756155-139756165 | ACCAACTGTC | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27897 | chr9:139741447-139756394 | Fetal_Intestine | | SE_29019 | chr9:139741397-139757349 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGCTCCCAGG GTGAAGTCAG TGTGTCCACA CTTTACCAGC CAGTGAGGGT GGGGGCTGCA 60
AGTGTTAAGT GACGTGCTAG GGGCGCCTGC TTGCTTCTGG ATGCAGCTCA GGAACCAGAG 120
ACAAGGGGAC CCTCTCTCAT CAGGACACAG ACCCACCCAG GACAAGGGCC GGGGCAGGCC 180
CTACCAGCTA GGGGCTCTGC ATCTATTGAG GACAACAGTG AAACTGACCC ACAGCATCAG 240
GGGCATGCAG AGGAGATGAC CCTTAGGGGA CAGGGTGCAT GGAGCAGGCC TGGAAGGGAG 300
AAGTGCCCCA GCTGGGCCCA CTGTCTGTGG TATAGGCCTG AGCTGCCCCA GGGGCTGTGG 360
GTCACAGTAC CCAGGTCACC AGGTGCCCCA GGGCTGTGGG TCGCAGTGGC CAGCTAAGTG 420
GGTGCCTCAA GGCTGCGGCT GAGCCCTTCC CTTTGGCCCC CATGCCTGAG CAGGAGGGTG 480
ACCCTGTGAA GCTGTCACTG GGCCTGGGGC ACCAGCAGAG GACTGCCATC CTAACGCAGG 540
GTCAACGTCA CTAACCTCAG CTCCCAGAGC TCTGCTCCTC CATGTGGGTG ACTTGGCCAC 600
TGCCCCATGG TGAGGGCCTG GTCTTGTGGC TCTGAGGCCT GGCTGTGGGT GGCTGTCCCC 660
AGGGAGGGTA GCGATACCCA GACCTGTGCA GCCAGGCCCC CTCCTGCCCA CAGGAAAGCC 720
CTACCCTGCC TCATGAACAC ACATCTGCCC CCAGGAGCCA TGCGGTGTTG GAGGGCACAG 780
CACAGCACCC TTGCCAGCCG CTAGGCTCCC ATCCGCCCTG GGGACTAAGT CCCAGCGGAG 840
GGCGGCAGTT GGGCACGGCT ACCGCCGTCC CTCGTCTTCA GGTGCCGTGG GGCTGACCAG 900
TGCCCACCAA CTGTCCACGC AGATGGGCGA AGAGGAAATG GCCCTGCAGA GACCTTCAGA 960
GCTCCCCCCG GCAGCCCACT CCCGGGCATC AGTCATGAAA ATTCACCAGC TTTCCCCACA 1020
ACTAGGGGCC TGGGAGCTGA GAGCAGGACC GGACAATCTG GCCCCAGCGC CAAGGGCAGG 1080
AACTTTTCCC AGCTTCTCTT CAGAGCTGCA TCAAAGAAAG CAGCGCCCAG TGACACCGCT 1140
CCTCTTCCTT CCACGCCTCA GGCCTCCACC CCTCACCCTT GTATAAGGTG GTGCTCAGAG 1200
CTCCCCGAGG CCTCTGAGCC ACAACCGCTA CTGGGCAGAC ACCCCAGGAC AGGAAGGTGG 1260
AGTTCTGCAC CCTGATCTGA GGAACGCGAT GTAGGGAGAA AAACAGCCAG 1310
|
