| Tag | Content |
|---|
EnhancerAtlas ID | HS050-48681 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr3:129065600-129066510 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr3:129065742-129065753 | AACAGCTGCAG | + | 6.02 | | Tcf12 | MA0521.1 | chr3:129065742-129065753 | AACAGCTGCAG | + | 6.62 |
|
| | 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 |
| GH03I129346 | chr3 | 129065661 | 129065810 |
|
Enhancer Sequence | CCAGAGTCAA TGGGAATGTA CTGCATTGCA AAACACCTGA GAGAGTCCAT GTCAAATGTC 60
TTTTTGCATT TACATTAGAG AGGACGAAGG CCCTGAGGTC CAAGAACATT GAAACCTGAC 120
AGGTCAGTCA TGCGTGTACT CCAACAGCTG CAGGTAGGGG CCAGGCAAGA TGTCCACACT 180
GCCGTGGCTT CAAAGGCATC CTATCCCAAG GGGTGAACTG AAGGACAGCC TGGAGCTTCC 240
TGGAGACCAG AGGGCCCCTC CACCCTACCT GGAGCAACGC CAGAGCCTGG ACTATTTCCT 300
GCAGCACTTC TCCCCTGCCC TGCTCTATTT TATCTTTTTT AATAAAGATG ACTCCTGATA 360
AACGACTGTT TCTTCCAAAT CTTGTAGTAG CATTGGAAAG GTGGCAGATG GGTCACAGAC 420
ACTCTGCTGC TTTGCGCCCT CCCTGCACAG AACGGGGGCT GTGCACACTC TAATTTAGGC 480
GGCATGCAGT CATGTGATCC TCTCAGTTAC TCAGAAAAAC TGAAAGGAAA AGAGACCTCA 540
GAGAAGAATC TGAGTGACCC CACCCGCAGC AAATCTTTAG CAGTGGCTCT GAAGGGCTGA 600
GGCTCTGAGC AGGTGCAGGG GCAGAGTCCT ACGCATTGTG CATGGCCTCC CCACACTCAC 660
ACTGCCCGGT GAGCATTTTC AGAAGGACAA GTGGCCCCTT CAGGTCCCAT TTGCCTATGT 720
TAATCATGCT GAGAGGTCCC CAGGAAGGTC CCGAAGTCCT AGGAACCAGG CTGTGCTGGG 780
GTCAGAGTGA CGGGGGTGTG GTCCTCAAAG CGCCTTAGGG GGCTACTTGT GCTGCTGGGC 840
TCCTGGCTGT CTAGTGCGGC ACTGGCCTTT CTGCTGCGAT GGTTTCCCCT TTTGATAACA 900
GCGGCACAAA 910
|
