| Tag | Content |
|---|
EnhancerAtlas ID | HS180-41960 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr6:41528260-41529140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gabpa | MA0062.2 | chr6:41528711-41528722 | GTCACTTCCGG | - | 6.14 | | KLF5 | MA0599.1 | chr6:41528319-41528329 | GCCCCGCCCC | + | 6.02 | | PLAG1 | MA0163.1 | chr6:41528681-41528695 | CCCCCTTTGGCCCC | - | 7.82 | | ZBTB7A | MA0750.2 | chr6:41528711-41528724 | GTCACTTCCGGCC | - | 6 | | ZNF263 | MA0528.1 | chr6:41528322-41528343 | CCGCCCCTCTCTCCCTCCCCC | - | 6.23 | | ZNF263 | MA0528.1 | chr6:41528634-41528655 | TCCCCTTCTCTTTTCTCCTTC | - | 6.86 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27953 | chr6:41527869-41530301 | Fetal_Intestine | | SE_28956 | chr6:41528234-41529979 | Fetal_Intestine_Large | | SE_31492 | chr6:41527801-41529921 | Gastric | | SE_65317 | chr6:41527784-41531346 | Pancreatic_islets | | SE_69040 | chr6:41528062-41531620 | H9 |
|
| | 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 |
| GH06I041560 | chr6 | 41527909 | 41531039 |
|
Enhancer Sequence | CAGCTGCGCG TGCACGTGTG CTCCCGGCAG GACGCGCGCC CAGGAGCGCG CTGGGGGCTG 60
CCCCGCCCCT CTCTCCCTCC CCCGCGGGTA AACTCCGGGC ATCCATCAGT CTGTTAATTG 120
CACTAATTAG AGATCGCAGA GGTGTTAATT GGAAAACCCT GGTATTGTGC CTGTTTGGGG 180
GAAGAAAACG TCAATAAAAA TTAATTGATG AGTTGGCAGG GCGGGCGGTG CGGGTTCGCG 240
GCGAGGCGCA GGGTGTCATG GCAAATGTTA CGGCTCAGAT TAAGCGATTG TTAATTAAAA 300
AGCGACGGTA ATTAATACTC GCTACGCCAT ATGGGCCCGT GAAAAGGCAC AAAAGGTTTC 360
TCCGCATGTG GGGTTCCCCT TCTCTTTTCT CCTTCCACAA AAGCACCCCA GCCCGTGGGT 420
CCCCCCTTTG GCCCCAAGGT AGGTGGAACT CGTCACTTCC GGCCAGGGAG GGGATGGGGC 480
GGTCTCCGGC GAGTTCCAAG GGCGTCCCTC GTTGCGCACT CGCCCGCCCA GGTTCTTTGA 540
AGAGCCAGGA GCCTCCGGGG AAGTGGGAGC CCCCAGCGGC CCGCAGACTG CCTCAGAGCG 600
GAAGAGGCAG CCGCGGCTTT GACCCAGCTT CCTTCCGACG GCATCTGCAG GAGCCTCTAG 660
GCCTGACATA GGCTCCGAGG TGCCCTGGCT CCCCCACGGG GAATGCTGAG GGTTGGGCCA 720
CTAGGTCCTG CCTAAGTGCA GGACCTGAGC CTCAGACAAA TCCTGGACCT GCCAAAATAA 780
CTCGGCCTCC GGTGCTATCT CCCATTTGCC CCCAACATGT GGTAGGAGAG GCATATGGAA 840
AGTCTGGGGT GGGGGATAAG AGCCCAGTAT TAGCGAACCT 880
|
