Tag | Content |
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EnhancerAtlas ID | HS105-38985 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:11466250-11467470 |
Target genes | Number: 28 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SREBF2 | MA0596.1 | chr19:11467455-11467465 | ATCACCCCAT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GAGAGGAGGG GGTGGGGGCG CCCCTCATCC CCTCCCGTGG GCTTCCCACC CCCGGTGTCG 60 GTCTCCGGTT CCTGAGGGTT GGGTCCCTCT GGGTCCAGCG CGGGGAGGGG CGGGGGAGGG 120 GAGGCGGCGA GCTGGGGGAG GGGACCGGGC TGGGGGAGGG GACCCCGGGC CGAGGAGCCA 180 GCACCGGTGG TGAGGGCGGC TGTGGGTAAC TGTGATTGTG TGGTTGTCAT TGTGTGTCTG 240 TGTGTGGTTG TGTAACTGTC ATCGTGTGGC TGCATGACTG GGATTGTGTG GTTTCGGGAG 300 GTCCGCGGGT GTGTGTGTGT GTGTGTCACT GTCATTGTGC GGCTGTCGTT GTGGGTGTCA 360 CTCTGATGGT TTGTGTGTGT GTGTCTGGCT ATGCTGTGAC TGCCATTGGC CCCCCGTGTG 420 GCTGCTGTCT CTGTGTGTGA CTGTCTTGGT GTTCGTGTGG TTGTGTGCAT AGGACTGTCA 480 TTGTGTGGCT CCTGTTGTGT GTTCATTCTG ATGGTGTGTA TGTGTGTGTG GCTGTGGTCG 540 TGCGCTGTGC ACCTTTCTTG TGTGGCATTG TGAGTCTGTG TCATGGTCCA TGGATGTGGC 600 CATGTGGTTG TAGATGGCAC CTTGTCTCTC CCCTGTGACT GTTGGTGTGA ATAAGAGACT 660 GTTAGTGTGT GTGTGGCTGT CGCTGAGTGC CTTGTAATTG GGGGTGTGAC GCTGTGATGA 720 GTTCTGTGAC CCCCATTGTG TGCGGTGACT CTTTTCTGTG ACTCTTAAGT GTGTTGCAGG 780 CCTGACTGTG TGTCCCTGAC TGTAGCGGTG TGGGGGCTTG TGTGGGACTG TGATGTGTGT 840 AGGGTCTCCT GACATGTCTC TCTCTGTTTG GCCTGGGGTG GGGGTGGGGA CTTGTTTGAT 900 CTGTTTGGTG TCTCTGACAG GCTATGAGCC CACTGTGTGT GAGTATGCAG TGACATGTGT 960 TGTGTGTGTT GGACACCTGT CTGAACAAGG GGGCCCCTCT TGTTTACTGC AAAGTGGCGC 1020 CCAGCACAGC GCCTGGAAGT CGGCAGGTGC TCGGTCTTCA CTGTGGGATG GGTGAACGCT 1080 ATGCCATGGT TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG GTGCCAGGAT GGAGGCTGCG 1140 GCTGGGTTGT GCTTCCTAAG GGTGACAGCA TGGGTGACTC TGGGTATCTA GGACCTCTGG 1200 CAACCATCAC CCCATATCAC 1220
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