| Tag | Content |
|---|
EnhancerAtlas ID | HS050-17207 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:114287750-114288610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr12:114288185-114288196 | AAATCACAGCT | + | 6.14 | | Myog | MA0500.1 | chr12:114288306-114288317 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr12:114288306-114288317 | GACAGCTGCAG | + | 6.14 | | ZNF263 | MA0528.1 | chr12:114287848-114287869 | CTTTCCTTCCAACCCTCCTCT | - | 6.19 |
|
| | 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 |
| GH12I113850 | chr12 | 114288009 | 114288811 |
|
Enhancer Sequence | GGGGAAGAGG GAGGAGAGAG GTTGGTGCTG CGTACCTCCC CCTCCCTGCA GGGCTATAGC 60
TCCTGCTCAA GGCCTCTCCT CAGCAGCTCC AGCCCTGGCT TTCCTTCCAA CCCTCCTCTT 120
GGCCTAAGGG AGATGACAGT TCTGGGGGCT TCGCCATCCC TGGGGAATCC CTTAGCCCTA 180
CCTATGCCTC CATAAATACC TCTTCATTCA CACCACCTGG GGGTGGGGAT AGATTCTGTT 240
TCTTGCCAGA TCCCTGGCAG GATCTGGAGT CCCTTTGCCT TGACCGGGGG ACAGGTGGAT 300
TTCCTACTTC AGATGGGGTG TCTCGCATGC CTTGGCCCTA CTCAGAATTT GAGGCCTACC 360
CAGGAAAGCT CTGAGCAGGT CTAGCCAGAC TCCAGGGCTG CCCTCATGAT CCAGCTCTCT 420
GGCTCTGCTG TCCTGAAATC ACAGCTCTTT GAGCTCCTCT GACTCAAGCC ATGGACTCCA 480
GGCATCAAGA GGCCTGGCCT CCTGCCGCCT TTTCTGAATT CCCTTAGAAG GCAATCTGCT 540
AAGGTGGTGT GGGGTTGACA GCTGCAGGCT AGACTGTGGC CCAGCCTGGT GGCCTCTTTC 600
AAGAACTGGG AAGGCATTGG AAGGCTGCCA TTGCAGCACT GGGCCTGACC TTTCTGCAGC 660
TTCCCTGGAG ACAGACCTCC TCTCAGCAAC AAAAGGCATT GCATGCCCTT GGCAGGACTT 720
CCATCCCAAG GGGCTGCGAA GAACTGCCCA GGGCCACGGC TTCTGGGCAG AGCTGAGGAC 780
AGTATTCCTG TCTTTAGAAC TCTAAGGCAT TCTCCTGGCC CCTTCTGCTC CTCAGGGAGC 840
TGTCCCTGGC AAAGCCAGAG 860
|
