| Tag | Content |
|---|
EnhancerAtlas ID | HS050-70429 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr9:128726820-128728100 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr9:128727076-128727090 | GCAGCCCAGGCCTG | + | 6.2 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGTTTTTCC TAACCTGAAT TTGATATGCC TCAAGCCTGG AAAATCCTCT TCCCTTAGGG 60
TCTGGTCATC TCTGTGGGGT TCTTAGGTCA TAGAGGTAGA AAAGGTGCTT TGCATGCCAA 120
CTCTGCAGTG AATTAGAAGA CAGGGAGTTC TCCAGGAACT GTGATCACAG AAGAAGAAAC 180
AATGGCTGCC ACATGCTCAT CTAGGAGCTG TATCTAGGCT GGGCAGGGAA TCTAGACAAG 240
AGTTCTCAGC AGCCTGGCAG CCCAGGCCTG AAAGAGGGCA TTTTGGATGG ACTTGCAGAG 300
GAAGTTGCAA ATAGATGTGA GGGAGGCAGG AGGCACCTTA TGACCCACCC TGACATTGGT 360
GTAGGAGGTC CGGGTCTGGG GGCAGCATGG CGGCAGAGGG TGGTTGGTGC TGCAGGCACG 420
GGGAGCCTGC TCACCCTCAC CTCCTCTCCA GAAAGGCCTG CCCCATCACT TCCACTCAGT 480
GTTCCCCAAC TCACGAGGCT GGCACCTCCC TCTTCCTGAC TGACATAAAA ATATGTAGCG 540
ACAAGCTGTC TGCCACAGCA GAAATCTGAT CAGACATTGA TTTCAGCAAT TGCCACTATA 600
GGCCAAGACA TAAGGCAAAT TTGTTTCTGA GTACGGTTAT TGCTGCTGCA GGTCTGAGGC 660
AGGAAGGGCC AGCAGCATGT GGAAGGTGGG AGCAACATCC CAAATAGGAG CCTCAGCCAC 720
AGATAATTGG AATACAGATT TTAACAGTGT GTGCTGCTCT GCGGCTCATG CATTTTCATT 780
CTGGAAGATC CTATTTGGAG GGAAATTCTG GCCTTCACTT TCCAAGGGTT ACAGTAGCTG 840
GCTGTCAGGC GTGTATGGAA AAAGGGTGGG CAACTGCTTC TCTATGGAAA TGATGATTAA 900
GCCGGGGTGA AGTTTAGACT TCATGGAGCC CTGGGTTTCG CTGAGGCATT GCATTGAGCT 960
TCTCCACTGC TCCCTTCTGA AGAGATTTCT TTTTGAGTCA CTTTAGTTTT ACCAGCAGAT 1020
CAAAGGCCGA GCTCGATGCC AGCATGGGCC TCGCTGAAGC CCTTCTTCGG CGTGTTGATT 1080
TATTGCCAAG ACTTTACTTG ATGGGATGGA TTTGTTTTAC ATGCATTTAA TCCCACTTTA 1140
ACACATGCTG CCAACTCCTG CCACAGTGGG TTTAGAAAAT ACATTTTGCT AATGCATCTC 1200
TGCTCTCATG TTGTCATCCG GGTGTTTTAA ATTGGGGAGT AGAATTAATA TGTAGACGTG 1260
CACCCGTTGA ACTGTGTTTC 1280
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