Tag | Content |
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EnhancerAtlas ID | HS139-47908 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr6:105158510-105159960 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr6:105158883-105158894 | CTTCCCAGAAG | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 2 | ID | Chromosome | Start | End |
GH06I104710 | chr6 | 105158561 | 105158690 | GH06I104711 | chr6 | 105159275 | 105159510 |
| Enhancer Sequence | TCACAGAGAC CAAGAAACAT AAACATAAAA GAAGGCTGTG ATGAAAGTGA GGCTATGTAT 60 GAAATCTTGC TCATACTAGT TTCAAAACTC TATTTATTTG CTGATCCACC ACAGATAAGT 120 TGGTTGTCAG CTTAATGTCA TCTCAGCTTC CATTTCATCT ACAGCTCATG CAGGCTGGGA 180 ATGTAATTTC AGGCATTAGG CTTAAATTTC ACTTAAAGTG GATGTTCCAC TCAGCTTTTT 240 AAAACAGGAA TTGGATTTTA GCATACTACT ATTTCATTCC CCTTGATGCT ATTGTTTCTT 300 CTGTTAAATT CCCGAGTCCA TTCAGAAAGA GGAAAGAGAG AGATGCCTAG ATTCCAAAAT 360 ACCTTTCATT GTTCTTCCCA GAAGACAAAT CTTTTCTATC CAGATTCTAC TGGTGGTCAA 420 TGTTACATGA ACGCAGAGCA GAGTGGTACC TCAAACATTG TTATTGACTT AGCAGTACAT 480 TGGGCACAGA TCAAGTTGCT ATTAAAAGCA ATGTACTCCT GCCTCCTTCA CATATGCCTG 540 GGGTCACTTG TGTTTGGCAC CTATGTGTCC TTATGTTATT ACAAAACCAT ACCCTGGAGT 600 CTTGCTAACT CAGTTTTTTT CTTCACTACA TTCGATGTAA TTTTCACATC AAGGTGTTTC 660 TATAGACTAG ACAGAGTTAG AGTTCAGCTT CTTCCACCCA AAGTGTTTAA ATTTGACTAG 720 ACAGCAGCAA TTGCTTTTTA ATCTAAGCAA ACTGATCTGT CAAAGACAAT CAACTCAGGG 780 AAGTTATTCC AGGAGGATCC TAATAATCCC GATGAGTCAC GCTGCCCTAT GTGAAACTCA 840 GCCACTGAAC TCTTGACATA GCGTGTCACA AGTACTTAGT GGAATAAGTA CATACAGCTG 900 AACTCTGTGT TGACACACAC ACTCTAGCCT CTCGTGCATA ATGATCACTG CATTTAGTCT 960 GGTAGAGGAG CACACTCTTG TGTGTGGTGA TGTCAATTCA TGTTTAATGA TGTTACAGCA 1020 ACTGGGCTTC AAGTTGCATA ACCCACTGTC CTCACAAGCA CTGATCAACA GTATGCTTGA 1080 TTCTCCTAGA TGAAAATAAA GGGTTGTGGT TGTTGTTTAT AATGACCTCC TAGCTTTTTA 1140 TTTATGTATT TATTTTGAGG CAGGGTCTCG CTCTGTTGCC CAGGCTGGAG TGCTGTGGTG 1200 CGAGCATAGT CTACTCCAGC CTCAAACTCC TGGGTTCAAG CAATCCTCCT GCCTCAGCTT 1260 CTTGTGTAGG TAAGATCACT GACATGGGCC ACCACCCCTG GCTAATTTAC TTATTTTTTT 1320 ATAGAGACTG GGGTCTTGCT ATGTTGCTGA GGCTAGTCTC AAACTCCTGG CCTCAAGTGA 1380 TCCTCCTGCC TCATCCTCCC AAAATGCTGA GATTATAGAT GTGAACTACC AAGCCCAGCC 1440 TCACCTCCTA 1450
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