| Tag | Content |
|---|
EnhancerAtlas ID | HS060-21175 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr2:242175010-242176020 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr2:242175994-242176014 | TGGCGGGGGGTGGAGGGGGG | - | 6.37 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGCAGGGAGG ATGGTCATGG TTAGGCCGTG GGAGCTGAGA GCAGAGTGAC GTTGTAAGCT 60
CAGCAATGGG GCTCCACGAA ACACAAGGCA AACAGCCCTA TGACAACAGC AATGTGCCCC 120
ACCCGACAAT GCCACCAGGA CCTTTAACTC AATAGAAAAG AATAGGAAAA GATTTGCATT 180
AGGCTAATGC TGGCAGACAG AAATTCCAGA CCCTTCATCC CAAGCCTACC CTCCTGAATT 240
ACAGCAGCCC CTTCAGGCCC ACGTAGGAGG AGAGGCCCTG ACTCCTGGCA CATCCTCGGG 300
GTCATGACGG CTTTGACCGA TGCCCATGAG GTGCCACAAG GGACTCTCGG ACCACTACTC 360
ACCTTCCCTG CCCTGTCCCT TGGGATCAGG ACGGCTTTGG CTAATGCCCA CGAGGTGCCA 420
CAAGGGACTC TCAGACCGCT GCTCACCTTC CCTGCCCTGT CTCCCCCACC GCCCTTCACC 480
TCCAGAACCT GCTTTCTTGC CACAGCATTT ACCATCACTT GCCACAGGAT ATATCTGCGT 540
TGACTGCTTG TCTCTCCACG GCAACGTGAG AACTATTTTT GTGTGCTGTG GCACCGCAGC 600
ACTGAGAGCA GCATCCAGTA CGCAGGTGGC ACTCGACACT GACTGCACAC AAGGTGAGCT 660
AGGCCTGATA ACCCCACTCA CGCGGGGGGA GACGTTGCAA CTGGAGGTCA CATTCATCCC 720
CCTGCAGCTG AGACCCTTCC ACAGCCCCCG CACCCACCGT GGGCCTGAGA GGCCGGATCC 780
CATGCAGCTG TCCCAGAAAG GGGCTATAGA ACCCCGAGCC TTGGTGAAGG GAAGTGGCCT 840
CCCCAAACTC TGTGTCCAGC CGAGAAGCAC AGCCCGTGCG CACACGGTAG GAGCAAGAGG 900
GCTACCTCCA CTGCCACTGC CGCTTGGGCA ACCGTCCATC CCATCCAGGC CACGCGTCTC 960
CCCAGGTGCC TGCTGACTGG GCCTTGGCGG GGGGTGGAGG GGGGCACATG 1010
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