| Tag | Content |
|---|
EnhancerAtlas ID | HS050-58582 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr6:42677760-42678870 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr6:42678212-42678228 | TCTTGTTTACTCAGTG | - | 6 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 42677801 | 42677855 | | chr6 | 42678223 | 42678399 | | chr6 | 42678244 | 42678442 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH06I042710 | chr6 | 42678201 | 42678442 |
| Enhancer Sequence | TCTGCAGGCT GGGCTTGCGG ACATTCCCCG TCTCCCCACC TCGCCTCCCT GAGCCCCCAG 60
ACAAGTCACC CTAATGGTCT CCACCAGGCT GTCTCCCCTC ACACTGGGGC TCCCTGAGTC 120
AGGGCTGTGT CTCCCCCTCA GACTGGGGCT CCCTGAAGAC GGGGCTGTGT CTCCCCATCA 180
GACTGGGGTT CCCTGAGGAC GGGGCTGTGT CTCCCCTCAG ACTGGGGCCC CCTGAAGATG 240
GGGCTGTCTC CCCTCAAACT GGGGCTTCCT AAAGACAGGG CTGCGTCTCC CTCATACTGG 300
GAACTTCCCA GTGTATTCCC AGGGGCAACA TCCAGGTCAG CCTGGGGGAA AAGGCCAAGC 360
TTGGTGAACG TTGGGACCTG CCTGGGTCAC CAGCCTGGGA ACTCCTGGGG TCTCTCACTT 420
CTGGAGCTAT CCCTCCCCCA CTCCAAACAT CATCTTGTTT ACTCAGTGCT TGCCCTCATT 480
CCAACCACAG ATTAAGGCTC CTCTCACCCT CTTAAGACAA AGCCAGGCAG AGGAGAGCGC 540
CTTAGTGGTG AGCCGGCTAT TTATATCACA GCGTGTTTCC CAGGCTACGA ATTTCACTCT 600
GCGCGGAAGG GGCCGGGGGC GGTGGAGGAG GAGTCACTAG GGTTTGAAAG GGTCTTGATT 660
AAGATAAGAA CTATGTTCTA GGCCACTCTC CCATAAGCAA GGCACAAAGA GCCTGGGAAA 720
ATGATCACGT CTGAGTTTTT CCAGAAAAAC CAACATAATT TAGTAAGTGA ATCAAATTAG 780
TAAAGCCAGC CATAGGGCAA TGAGCAGGGG TATACCTGAC AGTGGGTCAT GCCAAGCAGA 840
ACGCTGGCTG AGGGACACCT GTGAGACCTT GAGAACTGGC CTAACCTCTC TGAGCCTGAG 900
TTTTCTCATC TAAGAAATGA CATTTTAAAC ACTCGACAGG GGATGGTGGA AATTAAATGG 960
GATCATACAC GTGGAGCATT TGGTACACAC TATGTGCTTA GTATGCTTTG ATGATTGCTT 1020
TTTTGTGTAG TGCTGTGGTT TGAATGTGTC CCCCAAAGTT CCTGTGTTGG AAACGTGAGG 1080
CCCAGCATGA CAGTGGTGAG AGATGGGACC 1110
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