| Tag | Content |
|---|
EnhancerAtlas ID | HS050-05716 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:209964930-209965610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:209965457-209965468 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr1:209965457-209965468 | GGTGACTCATG | + | 6.02 | | NFYA | MA0060.3 | chr1:209965083-209965094 | AACCAATCAGA | + | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27309 | chr1:209965418-209966066 | Esophagus | | SE_27823 | chr1:209962589-209967032 | Fetal_Intestine |
|
| | 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 |
| GH01I209789 | chr1 | 209962777 | 209966655 |
|
Enhancer Sequence | AAGCCTCTCA AAATCCAAGA GCCTCCTCTA CCAAATCCAT GGCCATTAAC CTCCCTGTTC 60
CACAACTGGC CTTGTCACTA AATCCCCCTG CGTGACTGAT AAATCTGGGA CTCCTACCCA 120
CCTAAGACCT GAATAACCTG GAGCTGGAGC TGTAACCAAT CAGAGCATCC CTATGGGCAA 180
GTAAGTGTCA GCCAATGTTT TTGTTGTTGT TGTTGTTTTA GATCATGTCT CATTCTGTCA 240
CCCAGACTGG AGTGCAATGG CATGATCAGG GCTCACTGCA GCCTCAACCT TCTGCATTCA 300
AGTGATCCTC CCACCTCAGC CTCCCAAGTA ACAGGGACCA TGGGCATGCA CTGCCATGCC 360
CAGCTAATTC TTTAAAAATT TTTTTGTAGA GAGTCTCACT ATGTTGCCAA GGCTATTCTC 420
AAACTCCTGG CCTCAAGCAC TCCTCCCACC TCAGCCTTCC AAAGGGCTGG GATTACAGGT 480
GTAAGCCACC ACACCCAGCT GGGCCAGTGT TTCTTTACTT CTTCCCTGGT GACTCATGGG 540
CTAGCCAGGA AACAGAAACA GAGGATGCCT CTGAGACAGG TAGTTTTTCA ATACATGGCA 600
AAGAAATGAA GTTAGAAAGC AGGACAGGAA AGAGTCTATA ATAGAAGCAG AAGACCGAGC 660
AAGAAAGATA AAGTCTCACT 680
|
