| Tag | Content |
|---|
EnhancerAtlas ID | HS050-27876 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr17:13085730-13086620 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr17:13086397-13086412 | TGACCTCTCACCCTG | - | 6.51 |
| | | 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 |
| GH17I013182 | chr17 | 13085837 | 13086583 |
| Enhancer Sequence | ATGCATTTTA CTGTTTATAA ATTATGTCAA TTAAAAAAAG ACAAAAGGAG AAAAGAAAAG 60
AATAAAGTAT ATGTCCCAAG CTTATAGAGC ACCTGCAAGA CCTTGGGTTT ATACTGAGTT 120
CTCTTTGGCT TCAGCCCTTT TCCCTTCCTG TTAGAACACA AAGCTTTCCA GGGGTCACCT 180
GGTTTGTCCC TGGCACTGCT GCTGGGTGTC ACCTCATCAT AAATCCATCC AATGTTGCTG 240
CACATCACTG CTTCCTGGTC CTCAGGAGGC TAATGCTCCT GACAGGTGCC ATCTGACCAT 300
GTCACTACCT GAAGAGCTGA CCTGCTTCAC AGGCAGGGGG ACAGAGTGGC ACATCAGAAA 360
GCCACTGCTA TGCATTTCAC CTACAATTAA GTGCTAAGGA ATAATAGTGG GGCTTTTATG 420
CTACATGCAT GTTTTCCTTT CCATTAAATC TCAGATATGC TGTTTGCATA TCTTAGTTCA 480
GGCTGCTCTG AAATCCATAG GGGGAAAGAA ACCCTTCATT AAGTTCAGCA GCACTGTCCG 540
GCAATGCAGC AGCACTCCTA TTTATTTTTC CTTCTGTAAA TATTTGTGCT CTCTCAGGCT 600
AAGGAGTGGC CTGTGCTAGA GACTAAAATA TCCCCATTTA TATCCTCCAG GTGCAGCAGG 660
AAACGCCTGA CCTCTCACCC TGCCCCTGCA ATGACCTCAA CCTCACTTAT GGGGACCACC 720
CTCTGGGCTG CCCTAATGCA GACCCATGAT CACCTCTCCA GGTTGACTGC TGAATAGCAG 780
GAGAAGATGA ACCTGAAATT GAATGGTTAT TGCAACCCAG TTTTTTCGGT CGAAAGGTGA 840
AGGTTACTTA GCTTTTGTTG CTGCCTTCAA GCTTGTTAAT GAAAAGATGG 890
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