| Tag | Content |
|---|
EnhancerAtlas ID | HS180-12680 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr12:122047940-122048810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:122048002-122048023 | AAAGAAAAAGAAAAAGAAAAT | - | 6.01 | | IRF1 | MA0050.2 | chr12:122047996-122048017 | AAAAAAAAAGAAAAAGAAAAA | - | 6.09 | | IRF1 | MA0050.2 | chr12:122048786-122048807 | TCTTTCTTTCTCTTTCTTTCT | + | 6.76 | | TFAP4 | MA0691.1 | chr12:122048418-122048428 | ATCAGCTGTT | - | 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 |
| GH12I121609 | chr12 | 122047874 | 122049676 |
|
Enhancer Sequence | GCCGAGATCG CGCCACTGCA CTCCAGCCTG GGCGACGGAG CGAGACTCCG TTTCAAAAAA 60
AAAAAGAAAA AGAAAAAGAA AATGCTAGGG GCTAGAACTG ACTGGGTTTA TTGATGAATT 120
GGATATTGTG GGGAAGGGTG CAGTCTAGGA AAGTGACTGC AGCGTGACTC CTGGGGTGAT 180
CAGAACTACA ATTTCTCCAG CTTCTCTGGG GCCTCACAGA GCCACACTGT GTTTGACAGG 240
CTGTTCCCAG GATGCGGGTG TTTTTATGTG ATTAGGCTGG AACTGTTCTC TGGGAAATAA 300
ATGCCCTCAG TCTAAAGGGC TTTTACGAGC CAGGGCAGGG GATTAAAGGC GGCCGGGCTG 360
TGGAGAAATC CCAGGGTTAG GAGACAGCTG AGCATGGAGA CTTTTAATCT AAACCTTAAA 420
CGTTTTTATT TTCCACTCCT TGAACTCAGG GTGTCACTTT AAATACATGT TTGGCAACAT 480
CAGCTGTTCT ATTTTTCTTT TTAATTATAC AAAGCGAGAT CCTGGAAATG GCTCAGCCCC 540
AGGCTGGGGG AGGCAAGGGA AGTTTGGCAA TGGTAGGAGG CAGAGAAACC AACTAAAAAT 600
CTAGTGGATT TGAAATCCTT TTGAGGGAGC ACAGAGGCCA AACTTCGAGC CACCCTGAAC 660
TTGGTAAGAG CTGCCCTGAC TCAGGATTTC TAAAAGGAGA CCGACAGACT CACCAGCTTA 720
GAATGGAGAG AGGACAGATG GACACGTCTC CAAGACAAAA ATATCACCAG CCCTAGCACT 780
GTTCCTGTAC CTCGAATTTA TTCCCAGGCC CTGTCCTGTT AGCTCAGCTC TTTTCATTTC 840
TTTTCTTCTT TCTTTCTCTT TCTTTCTTTT 870
|
