| Tag | Content |
|---|
EnhancerAtlas ID | HS098-00183 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr1:7281620-7283080 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SREBF2 | MA0596.1 | chr1:7282566-7282576 | ATCACCCCAT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGTACCAGGC AGACCAGTGA ATGCGTCGTG AAACACCTCT CCAGGCCCGT GGAATGGGGT 60
GGGGAACGCT GGGGTCTCAG TGTGAGCCTG GCCTTTGGAT TCAGACAGTG CTGAATTACA 120
GTCTCAGCCC TGCTTCTTGC TGGCTGTGGG GCTGGGGCCA CATGAACCGG CTAAGCTTTG 180
GCTTTCTCAG AAATAGTTTG GGGATAATGA TTCCTGCCTA GTGGGAAGAT TAAATAAGAT 240
AAAGGAATGG CAAAGTTTTA TCCCATGGTC AGGGAGGATG GTGACTGCCT TGTGCCATGG 300
GTGACCCCTG CCTTCCTTCA GAGGGCATGT GCACAAGCTG GTGCATACAC ACACACACAC 360
ACACACATAC ACACACACAC ACACACACAG GCTTCCTGTA GTCCTCGGTT GCCTGGGAGG 420
CAGCAGTGAC TCTGCCTTCT AGAAGTCGTC TGAACTGTCT GCTTTCCAAA CAGGGGCGAC 480
AGGACTGTGA CTCGAGGTGA TGGGTTGCTG AACTGCTCTG CTGCCAGACA CATTTTGCTG 540
GCTTCTCATA ATGTCACTGA GATCTGGGAA ATGGACCAAG CACGATTTCC AGCTAAATGA 600
AACACTTTGG GGCCATCAGC TAAATAGATG ATGCTTTTGA GAAAACCCCA TGAGCATTGT 660
GTCAGACAGG CCGTGGGACC CTGCAAGCCT GTCTTTTTCT GTGCTCGTCT GGGTGATGAG 720
ACATCGCCCG GGCTGGTTCC ATGAGCACCT CTGGCTGTGA GGACCTGCGT CTTCTGTCTC 780
AATGCACCTG CGGGGAGGCT GAGATTTGAT CCTCATGGAA CATTCAATCC TTTCTGCATC 840
TCGCTGTCTT CCTGCCCTCC TCTTTCTCCC TTCCTCTTGC CTGACTGTTG ACTACAAAAT 900
AGGATATTAT TTAGGAACGT GTCCTTGCCT CCCTCCCTGG CTCTACATCA CCCCATGACA 960
TAGTGGCTGT GCTCAGGCGG AGAGTGAGTT ATGTTTCTGT GGGCAGGAGT GGGTCATGAG 1020
TCCTGAGTCC TCCCTAGACA GCCCCAGCCC TTTCTCTTTG TTCCAAGGGG CCCAGCCACC 1080
ATATTGATTG TTTCATCCCT CTGCACTGCC CAGAGCTGCC TCCTGGAGCA CGCTCTCTTC 1140
TTTCCTGATG GCAACGGTCC CACCTGATGG CAATGGTCCC TGGGCCAGAG GATGCCCATT 1200
GGTCTTCATG GAGAGAGCTT GGGTCAGGCC CACTTGGTCT CCAATCCTGG CTTCGCCGCG 1260
TGCCAGCTCT GCAGTGGTGC CAGCTTATCC TGCTAAGCCT AGCTTCCTCT TCTACGTGGG 1320
TATATCTGCC TCAGGTGCAG CTGTGAGGAT CCGGGGTGAT GCTCATGAGG TGCCCGGCAC 1380
CCTGTGTGGC ACAGAAATGA CCAGAAAATA CCAACTCACC CAATGCCAAG TCTTCACTGT 1440
CCTTAAGATC TCAAACCTTT 1460
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