Tag | Content |
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EnhancerAtlas ID | HS061-00132 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr1:6452100-6453310 |
Target genes | Number: 23 | 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 | CCCCTCTGGA AAAGTCAAAA CCGACCTTGA GGTAAGGAGA GGCCCTCGAC CAGGCCAGAA 60 GATGAGACTG AGAGTCAAGA ATCGCCATAG ACCCAGGACT TGCTATATGC CCAGCCTTCC 120 TGGAGATGTC AACATCTACA GGAAAGTAAC TTGCTTCTAT TGGACTTGGC TTGAGCCCAA 180 GGTCAGTCTG TGATGCCCAA CCCCCAAATG TGAGGAACCC ACTACCAAAA CAGAAAGCAG 240 CTCTCACTCC TGGTAGTTCA TCAAGCAGGA TAGGACCGGT CGCAGGCCAC AGAGCCTGTG 300 TGCAGTGGCT GAAAACCTAG ACTCCTTGTC CTCACTTAGC TCATGCACAA ATGCCAGCCT 360 GCTGCTTCCG ATTCTGCCGA AGAGAACTGC AGAGTAACCT TCAGGCTGCC CTCCCCACCT 420 CCTATGGGAA ATGAGCTTGT TCATGATCTC CAGCCTCCAG CTTCCTCTGG GGGCCTGCAT 480 CTATCTACTC AGTACCTGGT GGAAGAAGAG GGGGTGCTCT AGAAGGACAA CCCTTTGCCT 540 CTATTGTGTA AGATGCTTTC AGGCCCAACA GACCACTGAT TCCCTTTTCT TCATAGTAAA 600 CTGTTAGAGG TAGACAGTAT TATCTGTTCT TCCTTTCAAC ACCTGCCCTC CCCCAAACCG 660 AAGCAGTGCA CTGAAGACGG TAGCTCTGCA ACCTCCTCCC ACAGGGGCAC CCACCGAGGG 720 GCTCGCGCGG CTCTGGGCAC CTCCCCTCCA CCTCTGGGGG CTTTGGTTAG CGCAGCACAA 780 CCGCCGAGGT AATGATCCCG AATCCTCGAG GAGGCTAAGC AGGACCACGG GGCTGAGGCT 840 CCGGGATGCT CGGGCGAGGC CCGAGGCGGG GCGGCCCACG GGCGCCGGTC GCCGGGCTCT 900 GGAGCTGTGC ATTGACCTCC GCCCGCCCCG TCCCTGCCTG GCTTTCTCGC CCAAACGGCC 960 CGTGGCGCGG CCGCCGCCCT GGAGATGCGG CCAGGAGGAG CCGGCTGGAG GCGGGCGGGG 1020 GCCGCCCGGC TTGTGCGGCA TCGCGAGTCG CATCCCGGCC GGGCGGGCGT CCGGGGCGGC 1080 GGCGCGGAAG GCCGTGCGGG GAATCGGCGG GCGGGGGCGG CCTCGGCGGG TGGGGACCAC 1140 AGAGCCAAGC GGGGCAGGCC TGGGGCGGTG ACCGGCGCGC CTGGCCGCTG CAGGCTGCGC 1200 GCGGGCCCTC 1210
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