| Tag | Content |
|---|
EnhancerAtlas ID | HS044-05762 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr17:48508080-48509050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr17:48508279-48508290 | GACAGCTGCTG | + | 6.14 | | Tcf12 | MA0521.1 | chr17:48508279-48508290 | GACAGCTGCTG | + | 6.02 |
|
| | 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 |
| GH17I050430 | chr17 | 48507850 | 48509572 |
|
Enhancer Sequence | GTACATTAAA ATGATATAAG CTATTGATTC ATTATACTTT GTTCTTTGTA TCACAAATTT 60
TGTTAACATG AAAGTAATGG GTAAAGCAGC TAGTTAGGAG CAAAATGCCT TTAAACAATT 120
GTCCCTGGGA AGGAAGGAGC ATGACTGAAG TCTCATGTCT CTCTGGGCTT GACACATTTT 180
GCATACATCA CATAGCTCAG ACAGCTGCTG AGCTATTTTT CTGTTCTTGT GACCAACAGT 240
TTACACACAC ATGGAAAACT ACAAAATGCT GTTTCTATAC AAGCGCCTTG TATTAAGCCT 300
GGAAGTGTTA TGGGTGGTAA CCATAAATAG TTACAAGAAA TAGACTCTTC CCATAATTTC 360
CAAAACATGA TTTATGAATG ATTTGGTAAC GATATCCCTA TGCATTCCAC TGGGGATCCT 420
CCAGTCTAAA TGTAACAGTA GAAAATAACT ATGAACTTGG CTGCTGGAAT CAGTGAATGG 480
TACACATCTG TTTTAGTTAC CCTCCTCTGC TTTGAATGCT GTACATTGCT GCAGTGTACT 540
GTGAAGCATG TAAAGGTAAT AAAAAGATGA ATGAGTTTGT TTTCATTGAC AGAGCTGTTT 600
TTCTAGAAGG AGTCTACAGG GGAAGTCCAT AGACACACTG ATTCAAGGCA GAAAGTTTGC 660
AGTGCCATTA AAGATGTCAA TCAAAGCAGG AGGAATCTGG TTTGTGGAAA TGGGAGGGGG 720
AGACTTCCCA AAGAGCCTGG GGTTAGAACC TGATCCCTGA AAGGTTAGGT CTGCAGTTTG 780
AAGCCTTTGT ACTTCCGTGA AATCTCACTT GTGCTTCAAT CGTTGTGAAC CCTGGTGCCA 840
TCATAGCTTG CTATAATCTC AAACTTCTGG GCTCAAGCAT TCCTCCCATC TCAGCCTCCC 900
AAGTAGCTAG GACTACAGGC AAGTGCCACC ATACCCAGAT CATTTTAAAA TTTTTTGTAG 960
AGATGGGGTT 970
|
