Tag | Content |
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EnhancerAtlas ID | HS127-20105 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr21:46901940-46902700 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr21:46902085-46902102 | GAGGTCACCCTGACCTG | - | 7.18 | ESR1 | MA0112.3 | chr21:46902085-46902102 | GAGGTCACCCTGACCTG | + | 7.96 | ESR2 | MA0258.2 | chr21:46902086-46902101 | AGGTCACCCTGACCT | - | 7.17 | ESR2 | MA0258.2 | chr21:46902086-46902101 | AGGTCACCCTGACCT | + | 9.03 | PPARG | MA0066.1 | chr21:46902083-46902103 | TGGAGGTCACCCTGACCTGG | - | 6.24 | REST | MA0138.2 | chr21:46902649-46902670 | TCCTCTGTCCACTGTGCTGCA | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr21 | 46901943 | 46902059 | chr21 | 46902133 | 46902261 | chr21 | 46902342 | 46902475 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I045482 | chr21 | 46902304 | 46903914 |
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Enhancer Sequence | TAAGTCTTCC CTCGAGTCCA GGGTGAGTGG GAACCAGCAC CACACCATGT GGCCCGGGTC 60 CGGGGGTGCC TGGTGACGCC CGTGAAGGGG AAATGCCAGG AATAGCCCCC CATCACAGCC 120 CCACAGCCTG GGGCCTCGCG CTCTGGAGGT CACCCTGACC TGGGCGGCTG GGGCTTGGGT 180 AGAAATTCAT AACCCTGTGA TGATGAGTGG ACTCACGGGT TTTAAGAACA TGGGCACCCT 240 GCGAGATCTG AGATCTTACT CCAAGCTTCC ACGTTGGTTA CGGGGCAGTG GCCATGAGCC 300 TCTGTCGGAC TGACGCAAGG AGCCGGGGCC CCAGGCGTTT GTGGGTGGAC CTGGCGGGAG 360 TCGCCTGCGT CTGGCCCCCT GGGGAGCGGT CTCCAGCATG ACCTCAGATG AGAGCTGCAC 420 TGCTTTGGAC TGAGCAGGGG ACGCGGGCTG TAAATGCCCC TCACTGCTCT AAGCCTGTGG 480 CTGAGCTGAA GGGCCCTTCT TGGGGAGGCA TCCAGGCCCC AGGCCCCACG TGTAGCCAGG 540 TCCAGCATTG GGACCAGGCT TGGCGTCCCT TGTGGCTTCC CTTTCAGGAC CCCAACCACA 600 CCAGAAAGGG GGGATGACAG CGGCAACAGC CTCAGAAACT ATTAAACCGG CACAGGCAGC 660 AAAGCAGGGA CCCGGGTCGG GGCACAGTTC CTGGCAGGGC GATGTGCCTT CCTCTGTCCA 720 CTGTGCTGCA AGTCTGATTT TGTCATAATC CTGCTCTTTT 760
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