| Tag | Content |
|---|
EnhancerAtlas ID | HS050-17852 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:132662580-132663900 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr12:132663148-132663162 | TGTCCCTTGGGATT | - | 6.24 | | KLF16 | MA0741.1 | chr12:132663670-132663681 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr12:132663670-132663680 | GCCCCGCCCC | + | 6.02 | | Myod1 | MA0499.1 | chr12:132663005-132663018 | TCCAGCTGTCCCT | + | 6.16 | | SP4 | MA0685.1 | chr12:132663667-132663684 | CGAGCCCCGCCCCCTCC | + | 6.16 | | ZNF740 | MA0753.2 | chr12:132662876-132662889 | CCGCCCCCCCCAC | + | 7.82 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr12 | 132662941 | 132663228 | | chr12 | 132663524 | 132663727 | | chr12 | 132662936 | 132663290 | | chr12 | 132663332 | 132663875 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I132178 | chr12 | 132662746 | 132663750 |
|
Enhancer Sequence | AAAGGCAAAA ATTACCTTTA TTGAGGTATG ATTTACGTAC AATAAAATGT GCATTTAAAA 60
AAGTATTTTT TCTGCCGGGC ACAGTGGCTC GCGCCTGTAA TCCCAGCTCT TTGGGAGGCC 120
AAAGTGGGAG GAGTGTTTGA GGCTGGGAGC TCGAGACCAG GCTGGGCAAC ATGGCAACAA 180
AAAAAATTAA AAACTTAGCT GGGTATGGCG GTGTGCACCT GTAGTCCCAG TGACCGGGGA 240
GGGTGTGACG GGAGGGTGGG GAGCCCGGGA GTTTGAGGCT GTACTGAGCT CAGAACCCGC 300
CCCCCCCACC CCCTGCACTC CAGCCTGGGC GACAGAATGA GACCCCTGAA AAGTGTTGGT 360
TTCTGACTTT TTTCGTTTTT GAAATCGTTT CCGGCTGGCC CAAGTCGAAA AATAATGCAG 420
ATGTCTCCAG CTGTCCCTGA GAACACTTCC TGTTCCTTGA TCTGTGGCTT GTGATTCTCC 480
CCCCGCCCCC ACTCCCCTTA CATGGGGCTG TGGCTGCCCC CAGCCTTTCC CTTTCGTGAC 540
CTCAGGATTG TATGACTGCA GGTTGGGCTG TCCCTTGGGA TTCAGGGCCT CAAATGTACC 600
TGCTGACCAG TTGAAGAGTG CTGACCAGCT GTCCTGCTGA ACACCTCTCA ATCTGGATTT 660
TTGACATTTC CCTGTGATTA AATTCAGGGA ATCCAGCTTT GGTGACAGAG CCACTGAAGC 720
AAGGCTGTTC CCTGCTTGGA GACGCACCCA CTTTACACGT GTAGGGTGGC GAGTCTGACA 780
AACGCAGCCA CAGGCAGCCC CCACCGGGGG AGCCGGACGT TTCCATCCAC CCAGACAGCA 840
GCGTTCACGC CCAGGACCAT GTGGGCCTGC GCCCCGGGCC GCACCTGCCT CTCCTGCATT 900
CCGTGTCTGG CATCTTGTGT CGTTGCCACC CTGCGTGCCA TGTCTGGCTT CTCTCTCTCA 960
GCGAGTGTCC TCCGTGTCTC CGAGTCGCGC CCGTTCTGTT GTGCGTAAAT GCCGTTCTCA 1020
GAGCTGTTGT TTGTTTAGGG ATGTATCATG TTTTCAGCTT AACATTTGTG CCATTCGTGT 1080
GCCCTGGCGA GCCCCGCCCC CTCCAAGTTA CTGGCGTGCT GTGGGCGTTC TCGGGTTTCT 1140
ACTCTTCCTG CTGTCGCCAG CGCAGCCGAA GCACCAAGCA GGAAGCTCTG CCGAGTTCTT 1200
GGCTTCAGGT AACGTGTCAG ACCCAGGGCA TGAGCTCCAG TCCCTCTTGC CTCCACAAAG 1260
GACAGCACAT TTCCAGTTCA GGGTGCTGTG GCCGACACCG TGCGTGTGGC TGGGGCCAGT 1320
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