| Tag | Content |
|---|
EnhancerAtlas ID | HS050-40128 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:221968600-221969750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PBX1 | MA0070.1 | chr2:221969219-221969231 | CAATCAATCAAA | + | 6.18 | | ZNF263 | MA0528.1 | chr2:221969148-221969169 | CCCCTCTCTCTCTCCTCACCC | - | 6.15 | | ZNF263 | MA0528.1 | chr2:221969123-221969144 | TCCACTTTCCTCCTCTCCTCC | - | 6.35 |
|
| | 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 |
| GH02I221103 | chr2 | 221968644 | 221969720 |
|
Enhancer Sequence | ATAAACTAGA TTCCTTTCCT TTTAACTGAA AAAAATTAGA GAGGAGTGCT GCCTGGAGCC 60
CTGCCTCCTT GGCGTTGTGC TCTACTTTTT TATCTACACA GGATTTGTGT CAATTTGTTG 120
GTCTTACAAA TGCTCCTATT GTGGGGAGGA AACCATGGGC TGAACACAAG GGCTGCCTGA 180
CTTCCCAGTT TCACTCCAGG AGGCCCACGT CACACCAGCT TCTTCTTGAT GCTGTAGACA 240
CAGTCACAAG GTGTCCACAT GTGTCTTCCT CACACCCATC CGCTGGGAAA CAGGACTCTC 300
CTTCCTGCTC TGCAGGGTGG AAAATAGGAC CCCAGGCAGT CGCTCCCTTG GAGATGGGTC 360
CCACACTCCA TGAAGCTCAG CATGGGCATA AGAGCTGTCT GGCTGCGGTG GCTGCCTGTT 420
TTCAGCAGGG GTCTTCAGCC AGCATTTTCT CCAGGAGGGT AGCACTGAGC TTTCTTCCAG 480
CTGATGGCTC TGGAAGGCAC CACAAGTTCT TTTTGGCGCA TTTTCCACTT TCCTCCTCTC 540
CTCCCACTCC CCTCTCTCTC TCCTCACCCC ACACAGATCC TGTGCTGATT GACTGCCATC 600
GCCAGGCTTC TGTACCAGGC AATCAATCAA AAGAGACCTT CCCACGCGGA ACAGCCGCCG 660
CCCCTCCACC AGACTGCTGC CTCTGACATT TCCTGCGTGC CTGGACTGAG CCTGTTTGGA 720
AGGCTCCAGC CCCCTCCTAT CAGTCTGGGC ACTCAGGGCT CTGGCAGCAG CTGCCGCTCT 780
GAATGTTGAC ACCCTGCCAC GTCAACACTG GCCGGGCCGA TGTTCCTTCA CACTCATCTG 840
CTGAGCCCAA ACTTCCCCTG CTGGCGGGCT CTCCCTGTTT GAATGGGCTC CCAGTCAGAA 900
AGGGCTCCCT GAAGCCTTAG CTCCTTGAAG CTCGCCCCTT GCAGCCTTCC GGCTAGAGGA 960
TGTGGCTGTT GGATCAGCTC AGTGATCCTT GGTTCACAAA AAAAGAAATT CAGTTCAATG 1020
TGGCCTTTCC CAAACCCCCT CAAACAGCGT TCTGTGCAGA TTGAGCCTGC TGGCCTTGGC 1080
ATTGTCCTTC CGACTTGATT TTTCAGACTA TCTTTCCTCT TGTCTGTGAG AATACCATGG 1140
GGCTCAAGGA 1150
|
