| Tag | Content |
|---|
EnhancerAtlas ID | HS050-06352 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:231913500-231914840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr1:231914510-231914521 | CCCAATAAAAC | + | 6.62 | | KLF5 | MA0599.1 | chr1:231914002-231914012 | GCCCCGCCCC | + | 6.02 | | MEF2A | MA0052.3 | chr1:231913891-231913903 | TCTAAAAATAGA | + | 7.22 | | MEF2C | MA0497.1 | chr1:231913889-231913904 | TATCTAAAAATAGAC | + | 6.68 |
|
| | 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 |
| GH01I231775 | chr1 | 231911245 | 231915153 |
|
Enhancer Sequence | ATACTCATAC ACTAATTTTA ATATCTCTGT TATTTACAAA CTGTCATACT TGCTTACAAT 60
AACCCTATAA GGTTTGTTGG GCAATATATT GTTTTTATGC CCATTTTGCA GATGAGGCTG 120
CTGAGGGTCC AAGTTCACAC AGCCGTAAAA GCAGTGCCCT CACGTCTTTG GCGAATTTTT 180
AATGCAGAGG GAATCCAGAG ATGGTTCACA CTGATGGCCT GGGAGAGACC AGGCCTTGGA 240
CAGAGTGCTT AGTCCAGCAA TGGAAAGAAG TCCAGCCCAG CAGAGCCGTG GGTCTGTGGG 300
CCCAAGGAAA AGAGAATGGA TGTCCCTCCA GGCCAGGGAT GGTTGTCTCT GTGTGCCTAG 360
TGTTGCCTGA TTGGATTGGA GCCAAGGTGT ATCTAAAAAT AGACAGCCTG GGAAGACCAA 420
ACAGGCAACT GTCTCAAGTC AGAGAGGTCT GTCAGACGTT CCAAAGAAAG AAATGTGAGA 480
GGAAGAGAAA CTGGAAAGCA AGGCCCCGCC CCAGGGCTAG AGGAACTGGT ATTACTTGTC 540
TGTGAAAAGA GGGTTTGAAC TGGGTGGCGT GGAAGGTCTT TTCTGGTTCT ACAATACTTT 600
GCACTTTAGT ATTTTATGAA ATAAGTTAAA ATAAGCTGCC TAAAAACCCC TCATAATTCT 660
ATTCCTAGGA GCTCTATGTT AAGTTCCTCC TTAAAGTTCC CTGGGCAGGC TGTGACCATC 720
CACAGGCCAC GGTGCTCCAG CTGGCACTTT CCTTAGGGCT GGTCCCTAGA GCATGGACCT 780
GAGCAAAGCC TGCTTTCCAA GCACTGCTGC TGCAGCTCAG AGCTTAGACC TCGCCTCACC 840
ATTGTATATC CTCCCGTTTT CTTCTGGAAA GTCGTCATTA CAGGCAACGT GGAAAAGTTT 900
ACCAGACTAT AATCTGGTAA AGGAGGAAGA GGATTGGAAA AGAAGGAAGA GATTTGAAAA 960
TCCCCCTTAT CTGGCTGGGT ACAGATGCTG CTCACCAGGA AATGTAGGTT CCCAATAAAA 1020
CAGGACCCCC ATTTCCAGTT TTCATTGCGT TGTAAATTAA AAATAAAATC TTAAGCCCCC 1080
AACCACTGAA CGGATTCCCT CTTGGCCAAG GAGACCCCAG AGACTCCATA CAAACTGAGT 1140
TCCCAGCCCC AGTGGGCCGG GAGGTCGGAT TTGCCTTGTT ATAATCCCTC CCTTTTGTAG 1200
CTTAGACATA ACAACAGAGC AGCATCAATG CTAAAACGAG ATCATAAGAA CTGATGGAAC 1260
AGACTCTCGG TGGCAATAAG ATACCAAATT ATAAACAAGA CCTAAGGCCA TGCCAGGCAG 1320
GGATAAGTCT CACACCCCTG 1340
|
