| Tag | Content |
|---|
EnhancerAtlas ID | HS180-49329 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr9:90181880-90183200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr9:90182810-90182831 | GTTCACTTTCAGTTTCTTTTA | + | 8.06 | | IRF9 | MA0653.1 | chr9:90182814-90182829 | ACTTTCAGTTTCTTT | - | 6.24 | | NFIA | MA0670.1 | chr9:90182123-90182133 | GGTGCCAAGT | + | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_32327 | chr9:90181971-90184905 | Gastric | | SE_35598 | chr9:90182940-90187491 | HepG2 | | SE_54811 | chr9:90182071-90187454 | Stomach_Smooth_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 90182577 | 90182784 | | chr9 | 90182927 | 90183199 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH09I087569 | chr9 | 90182315 | 90182864 | | GH09I087567 | chr9 | 90182866 | 90182964 |
|
Enhancer Sequence | CAAAGAAAAA TAGCAAGAAA GCTCATTAAT GAAGGGTTGC TAATGCAGAG AGAAGCTCCC 60
CAGAATTCAC GTTGGCAGTT AATCTGAAGA TATAGATGGA CTGCTCATGA AATCTAGAGT 120
TCCTTCCAAA ACAAATTATT GTGAGATTAA AATATTCTCT TTCTGTTGGC ACAGCAAGTG 180
AAGGCAAAGT CATGGGAACC TGGTGGACTT TAGAAATGCT TGGCCTCTCC TCCCGTGGTG 240
GCTGGTGCCA AGTCAATCTG TAGCTGATTA TTGTCTCGAA TATGTACTCA AATGAGCTGT 300
GTAGTAGGCC ATCTGCTGTC TCCTCGACTC AGCTGATAGG CCCTGGAAAA GGGAAATCCT 360
GCCAAAATGC AAATATCCTA CTTAACTGAT AATATAGGGA GAGGAGATAC AGGCTGTGGG 420
GGAATGGGGG TAGGGAAGGG AATGGGGCGT GGGGAAGAAA TAAGTGACTG TCTTCACCCT 480
TCCTCGATGT CTTTCCATCC TCCTGTGTTT CTTCCTGTTA GAGAAAGACC AGGTGTGGAT 540
CAGTAGACCC CGCTCACAAT TGGAGTTGCG GGGTCAGACT GGAAGTAGCC AGGGAATTAG 600
GCTCGGTTGT GAGGATGCTT TTTGTAGCCT CTTCATTTGA ATTCAAGAAC CTATAGCCTC 660
TTGGTTTCCA CTGGCACGCT TGCCATGGTA GGAGCCCTTG TTAGGATTAA GCTTTTCTCA 720
GTGCTGGAGA TGGAGTTGTT GCACTCATAG GGCTACCACC TGGATTCCTC AGATTGCCTC 780
CGAATGAGTC TGTGAGCCCC ACCCCACCGG ACCTCCCTCC ATGGCGTCCC TCCCAAGCAT 840
GACTCAAGGG TTCTGAGTTG CTGTGTTGAA TGGATTGGCT AGCGATCGTT TCCATGGGCA 900
TACTGCTCCA TCATTTCCAA ATGCTTTCGT GTTCACTTTC AGTTTCTTTT AATATTTATA 960
GACACCCCAA AAAGGCTGCC ACTATTCAGT TGAAATGGTA ATGCTAAGGA AACTAAGGCT 1020
CCAAGAAGAC GGTCCAAGGT CTCATGGCTA AATGAGTAGA AGACCAAAAC TGTGATTACA 1080
AAGCTGTCAC CAGCTCTGCC CCTTTAGGGT GAGTTACTGA TGAAAGAAGA GTTGGCTCTG 1140
CAGACAGCAG TGAGGAGGAG TGAAGCCACC CAGGCATAAG GCACCGGGGA GCTGCGGGCC 1200
TGTGTCCAGC TGGAGCGCAC GGGGCCATCT GAAGGGGCAG TCGCTATGCA TTGGGCGCTG 1260
ACTGCCTGCA GGCCGTGGGC CAACGCTGCC AGCTCTTCCA AGTCTTCATG CATTGCTGGG 1320
|
