Tag | Content |
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EnhancerAtlas ID | HS059-00138 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:6452120-6453310 |
Target genes | Number: 20 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr1:6452272-6452287 | GAGCCCAAGGTCAGT | + | 6.17 |
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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 | CCGACCTTGA GGTAAGGAGA GGCCCTCGAC CAGGCCAGAA GATGAGACTG AGAGTCAAGA 60 ATCGCCATAG ACCCAGGACT TGCTATATGC CCAGCCTTCC TGGAGATGTC AACATCTACA 120 GGAAAGTAAC TTGCTTCTAT TGGACTTGGC TTGAGCCCAA GGTCAGTCTG TGATGCCCAA 180 CCCCCAAATG TGAGGAACCC ACTACCAAAA CAGAAAGCAG CTCTCACTCC TGGTAGTTCA 240 TCAAGCAGGA TAGGACCGGT CGCAGGCCAC AGAGCCTGTG TGCAGTGGCT GAAAACCTAG 300 ACTCCTTGTC CTCACTTAGC TCATGCACAA ATGCCAGCCT GCTGCTTCCG ATTCTGCCGA 360 AGAGAACTGC AGAGTAACCT TCAGGCTGCC CTCCCCACCT CCTATGGGAA ATGAGCTTGT 420 TCATGATCTC CAGCCTCCAG CTTCCTCTGG GGGCCTGCAT CTATCTACTC AGTACCTGGT 480 GGAAGAAGAG GGGGTGCTCT AGAAGGACAA CCCTTTGCCT CTATTGTGTA AGATGCTTTC 540 AGGCCCAACA GACCACTGAT TCCCTTTTCT TCATAGTAAA CTGTTAGAGG TAGACAGTAT 600 TATCTGTTCT TCCTTTCAAC ACCTGCCCTC CCCCAAACCG AAGCAGTGCA CTGAAGACGG 660 TAGCTCTGCA ACCTCCTCCC ACAGGGGCAC CCACCGAGGG GCTCGCGCGG CTCTGGGCAC 720 CTCCCCTCCA CCTCTGGGGG CTTTGGTTAG CGCAGCACAA CCGCCGAGGT AATGATCCCG 780 AATCCTCGAG GAGGCTAAGC AGGACCACGG GGCTGAGGCT CCGGGATGCT CGGGCGAGGC 840 CCGAGGCGGG GCGGCCCACG GGCGCCGGTC GCCGGGCTCT GGAGCTGTGC ATTGACCTCC 900 GCCCGCCCCG TCCCTGCCTG GCTTTCTCGC CCAAACGGCC CGTGGCGCGG CCGCCGCCCT 960 GGAGATGCGG CCAGGAGGAG CCGGCTGGAG GCGGGCGGGG GCCGCCCGGC TTGTGCGGCA 1020 TCGCGAGTCG CATCCCGGCC GGGCGGGCGT CCGGGGCGGC GGCGCGGAAG GCCGTGCGGG 1080 GAATCGGCGG GCGGGGGCGG CCTCGGCGGG TGGGGACCAC AGAGCCAAGC GGGGCAGGCC 1140 TGGGGCGGTG ACCGGCGCGC CTGGCCGCTG CAGGCTGCGC GCGGGCCCTC 1190
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