| Tag | Content |
|---|
EnhancerAtlas ID | HS050-35225 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:10522300-10523490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXF2 | MA0030.1 | chr2:10523333-10523347 | CAAAAGTAAACAAA | + | 6.29 | | FOXP2 | MA0593.1 | chr2:10523336-10523347 | AAGTAAACAAA | + | 6.62 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_31666 | chr2:10522327-10525053 | Gastric | | SE_42393 | chr2:10519311-10523609 | Lung | | SE_47142 | chr2:10520006-10523588 | Panc1 | | SE_51031 | chr2:10520994-10523532 | Sigmoid_Colon | | SE_53236 | chr2:10522189-10523377 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 10522394 | 10523199 | | chr2 | 10522808 | 10523000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I010379 | chr2 | 10519928 | 10531406 |
|
Enhancer Sequence | CCAATCTGAA AAGGCTATGC CTATGGAGGA TTGCAACTCT ATGATATCCT AGGAAAGGCA 60
AAGCGATGGA GATAATAAAC AGATCAGTGG TTCCTACGGG TTAGGAGGGA GGGAGGGATG 120
AGCAGGCAGA GCACAGGGCA TTTTTAAGGC AGTGAAACTG CTCTGTGTGA TACTGTAGTG 180
GGGGAGCCAT GTCATTGCAC AGTTGTCAAA ACCCATAGAA TATACAGCAC CAGCAGTGAG 240
TCCTAATGTA ACCTACGGAC TTGGGTGATA ATGACGTGTG AAGAGACAAG GCGGGTTCAT 300
CCGTTGTAAC AAACAGCCAC CCTGGTAGTA GGGAGGGCAG GAGGTATGTA GAGAACTCTG 360
TGCTTTCCAC GCGATTTTGC TGTGAACTAA ACAGCTCTAA AAAATAAAGT TCATTAATTA 420
AAAAAAAAAA AAAAAAAAAG GGAAATGACC ACATGCAAAG CACTGCGTGG AGGGCCACGC 480
ATCCCAAGCA AGTCAGCTAG AGTAGAGGCA GGAACCAAAC AGCTCTATGA GGTTCTGGAT 540
GAGAAGCCGC ATGCACCACC CCCTCCCTGC TCCCGTGTGG GACCCAGTGA AGACCTCCTG 600
TGCCCGGCTG CAGCTGCTGA GTGTGGGAGT GTGCTCTCCA CAGCAAACCA GCCGTGAAGG 660
CTGCACACCT TCCTGTTTCT GCCCAGCCAC ACCACAGGGC ACTCAGCCCT TTTCCTGAGC 720
ACTTGAAGCT GCGTTTCCTC GAGCTCCTTC CTGTTTAAGA ACAGGAGGGG AGTGGCGGCT 780
CGCTTGTGCA CCACTCTCCA GGGCAGTGGT GTGCGGGACA CCCTGCAGCA CCTTTGACTC 840
CTCCTCTGGG AATGAGGCGT GGTTTAATCT GCAACCCCTT ACCATTAGAG TCTGCAACTA 900
GTCAAAAGGT GAATCTGGCT GGGCGCGGCG GCTCATGCCT GTCATCCCAG CACTTTGGGA 960
AGCTGAGGCA GGAGGACTGC TTGAGCCCAG GAGTCCTGAC CAGCCTGGGC AACATAGTAA 1020
GACCTCCTCT CTACAAAAGT AAACAAAACT AGCCTGGCGT GGTGTCATGT GCCTGTGGTC 1080
CCAGCTACTC AGGAGGCTGA GGTAGGAGGA TCACTTGAGC CCAAGAGGTT GAGGCTGCAG 1140
TGAGCCAAGA TCGCGCCACT GTGCTCCAGC CTGGGTGACA GAGTGAGACC 1190
|
