| Tag | Content |
|---|
EnhancerAtlas ID | HS050-01289 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:26354740-26355680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HINFP | MA0131.2 | chr1:26355357-26355369 | CAGCGTCCGCTG | + | 6.18 | | NR2C2 | MA0504.1 | chr1:26355622-26355637 | AGGGGGCGAAGGTCA | + | 6.15 | | ZNF263 | MA0528.1 | chr1:26354959-26354980 | CCCTCCCTTTATCCCTCCCCT | - | 6.17 |
|
| | 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 |
| GH01I026028 | chr1 | 26355101 | 26355250 |
|
Enhancer Sequence | ACTCAACCCT ATCTGTGACC CTGAGCCAGT CCTTGGGTCT CTCTGGGCCT CAGTTTCCCC 60
ATCTGTTCAA TGGGGCATGG CCCCGAGGCT GCCTAAGTAC TCCCAGGTCT GCTTCTTGGA 120
GGTTCAGGCT CAGAGCCAAA CAGGCTGTAA CTGAGGAGGG TCCTAGTACC CTCTGGGCCC 180
TAGTCATGAG TCCCACACTG AGCAGGCCTG TGTCCTGGTC CCTCCCTTTA TCCCTCCCCT 240
GGCTGGGTTG CAGGCAATGG TCCCCTGGGT GGACAATTGC CAGGCTGGCT CTGAGGAGGC 300
TGGGACTCCT GCCCTCCCCC ACAGGCACAC ACAGCCTGAG TGTGGCCCTG GGCTAGGGTG 360
GTGGAGGGGG TAGGTGGGAG GAACAGAGGG AGCCTGTCCT CTGGGCCAGG GGACCTCTGG 420
GCAGCAGTTT CCTGTGTGGT TCCAGGCTGG GGGCCCAGCC CACCTCATGA CAGAGGAGCC 480
TTTCACGGGC CTGGCTTTTA GCATCGGGGA GGGCTGGGCT CAGAGGCCAC GCAGGCAAGG 540
GGTGCTGAAA GTCTGCCTGT GGCCGAGTGG GGGAGGGCAG ACGTGCATGT CTAAGTCAGG 600
CAGGGCCTCG GAAACATCAG CGTCCGCTGC CTCCCATTTT ACAGATGAGG AAACTGAGGC 660
CAGAGAAAGG CAAGGGAGGT GTCTAAGGCC ACTGAGGGCA GAGGCAGAGC TAGAATGCAG 720
GGCTCCTGCC TCCTAGTCCA ACCACAGATG CGTGGCTGGT GTGATGCTTG TGTTTGTGTT 780
AGTGCGTCAG TGTGCGGCTG TGCATATGCA TGAGTGGGTT TACACATTTG GGAGTGTGGG 840
TGTGGGGTGC AGGGGTGTGG GGTTCTCCCA TTGAGGGAGC CCAGGGGGCG AAGGTCACTG 900
TCCAGGCTCA TGTGTGGTGG GACCTCCCCA TGTGCCTCTT 940
|
