| Tag | Content |
|---|
EnhancerAtlas ID | HS139-18331 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr15:45569860-45571390 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr15:45570958-45570970 | CAAATCACAGCA | + | 6.52 | | Gfi1b | MA0483.1 | chr15:45570959-45570970 | AAATCACAGCA | + | 6.62 | | Nr2f6(var.2) | MA0728.1 | chr15:45570677-45570692 | AAGGTCAAGAGGCCA | + | 6.65 | | Nr5a2 | MA0505.1 | chr15:45570671-45570686 | AAGTCCAAGGTCAAG | + | 6.29 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGGATTAGA GAGTGACTCC TTAACGAGTT TGGGGTTTTC CTTTGGGGTG ATGGGAATGT 60
TTTGGAACGA GATAGAGGTG GTGGTTGTGC AACATTGTGA ATATTATGTC ACTGAATTGT 120
TCACTTTAAA ATGGCTGTTT ATGTTATGTG AATTTCACCT CAATAAAAAA AATTTTTAGA 180
AGGATTCAGG TACTTGGCTG AGGCAGGAGA ATGGCGTGAA CCCGGGAGGC GGAGCTTGCA 240
GTGAGCCGAG ATCCCGCCAC TGCACTCCAG CCTGGGCGAC AGAGCGAGAC TCCGTCTCAA 300
AAAAAAAAAA AAAAAAAAAA AAAAGAAGGA TTCAGGTACT TGTATCTTCC CTTAGCTAAT 360
CTACCTCCTT CAATTTCCCA ATTCTCTCAG CTCAGAACCA CTTGGTCGTC TTCTCAGTCT 420
CGATTCCTAT CTTCTCTCCC GTTTTCCAAA CTTGACAGAA AAAGGAAGCT TCAATAAATT 480
GTTTCTTGAA CTACAGATGA ATTTTACTCT ATGCCTGGTT TATTTCTGAG AGGCAGCAGA 540
ATGCAATGGT TACTGGTATT GGACATGACG CCAGATTACT TGAATTCTGA TTCAAGCTCT 600
GCCAGTTATC ACTAAGGTGA TTTTGGACAA GTTCCTTAAC TTCTCTGTGC CTTGGCATCC 660
TCATCTATAA AATAAAGATA GTGAGACCCA CCTTATAGGT AAAGACAGTG ACACTGCTGT 720
AAGGGGATTA TCTGTTTTCT GTTGCTCATA ACGGAATACG TGAAACTGGG TAATTTATAA 780
AGAAAAGGAG TTTATGTCTT AGGAGGCTGA GAAGTCCAAG GTCAAGAGGC CACACCCGGT 840
GAGAGCTTCT TGCCAGTGGG GACTCTGCGG AGTGCAGGGG CAGTGTAAGG CATCGCATGG 900
TGAGGGGGCT CAGTGTGCTA GCTCAGGTCT CCTCTTATAA AGCCACCAGT CCCTCTCCGT 960
GATAACCCAT TAACTCATGA ATGGATTGGT CCATTCCGGA CGGCAGAGCC CTCATGACCC 1020
AATCACCTCT TCAAGACCCC ATTCTCAATA TTGCCACACT GGGGAACAGG TTTCAACATG 1080
AGTTTCCGAG GAGGCATTCA AATCACAGCA GGGAACAAAA CAGTGACTGC TCGCTCCAAG 1140
TCTAATGTAA GGTTAGCTAT TACTATTAGC TGTTACTAAT AGCATTACTA TACTTACTAT 1200
AATACCATAG TTAATAGTAT TATAGATTAT AGTAGTAATA ATACCATTAC TATCATTTAG 1260
GAACCTGAGT TCATGGCTAT CGATTTGTTG AGTAATGTAT GAAATTCAGT TCACACAAGG 1320
AAGCATGAGA GAAGGGGACT CTATCTCCCT CCAGGGCGGG GGCCAACTTT TTAATTCGGT 1380
TTTTAAATTC TCAGGTTCCT ACTTAAAGTA AACCTGGCCT AAACTCTCCC TCTTAGAGGG 1440
CTTCGCTGTA AATGCGGGAA GCATGCCAAT CTCAACACCA GTGTCTGCAG AACACTGTCA 1500
AATGCAGGAG GGAACAGGAA AAACAGGAAC 1530
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