| Tag | Content |
|---|
EnhancerAtlas ID | HS050-24630 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr16:507710-508760 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAX | MA0058.3 | chr16:508259-508269 | ACCACGTGCT | + | 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 |
| GH16I000456 | chr16 | 506628 | 508910 |
| Enhancer Sequence | TAGTTAATGA TTTGTTTAAA AAATATTTGG TTAATGTTTC AGAATAAACA ACTTGGTACT 60
TTGTGTTCAA TTAGTAGCTT CAGTGTGGAA ATTCTTAGGA ATCTTCAGGA CAGATTGGCC 120
AGTCTGGACT CCGGATTAGG TAACTCTCAG GTACCCAGCA AGACTCTCAC ATTCTTAGGA 180
ATGAGCTTAG GAATGAGGAC TTTTGTGAGA TAAGTGGGGA GATGTTTTAT AAACTCCAGT 240
TGTCTCCAGG AAGTTGGTTG ATGATGGACT TCCGAGGCTA GAGTCACGCT AGCACACAGA 300
GCCCTAGGAT TGGGGCGATG GCCCCGGCCT CTTCCGTTGT GAAGGGGAAG CGGAAACTCA 360
GTCTCTGGCT CAGGAATTCC ACACTGTGGG GTCCCTTAGC TGGGGCTGGC CCTGTTTGAG 420
CCTGACTTTA TGAGGCATGT TGGCTGACAG TGGCGAGAGG GCCAGCCACG GGGGCCCGGG 480
CCTTGCTCTG GTGCCCTGTG TGCTTCGGGC TCTCTGGATT GCCTCCTGGG CGATGCTATA 540
GCCTTGCTGA CCACGTGCTA CACCCCCCAT CCTTTTCCTG AAACAGAGCA GCTGTGTCCT 600
GGCATCTCCA GCAGGGCTGC CCTTGAGGGT TCTGTGCTTG CTGCTTGGTA GCAGCCCCGG 660
CATCTGGACT TCACCACAGG GCCTAGGGGG CCTTCCTCGG GTTCACCGAT GCCCACAGGG 720
CCTGGGGGGC CTTCCTCGGG TTCACCGATG CCCACAGGGC CTGGGGGGCC TTCCTCGGGT 780
TCACCGATGC CCACAGGGCC TGGGGGGCCT TCCTCGGGTT CACCGATGCC CACAGGGCCT 840
GGGGGGCCTT CCTCGGGTTC ACCGATGCCC ACAGGGCCTG GGGGGCCTTC CTCGGGTTCA 900
CCGATGCTCA TCTGCCGTAA CCTGCCTGAG GCCCTAGGGT TTTGTCAGTT AATGGATGTG 960
GCTACAGCCA GGGCTCCTGC CAGCCTGTTG CCTCTCCCTG TCCCTGAGCA TTTTCACAGT 1020
CCAGCCCGCC ACCCAAGAGG GGCTTTCTTC 1050
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