Tag | Content |
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EnhancerAtlas ID | HS095-17827 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr2:234738420-234740050 |
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) |
Esrra | MA0592.2 | chr2:234738983-234738994 | ATGACCTTGAC | - | 6.32 | Esrrg | MA0643.1 | chr2:234738983-234738993 | ATGACCTTGA | - | 6.02 | HEY2 | MA0649.1 | chr2:234739716-234739726 | GACACGTGCC | + | 6.02 | Npas2 | MA0626.1 | chr2:234739716-234739726 | GACACGTGCC | - | 6.02 | RREB1 | MA0073.1 | chr2:234739051-234739071 | GGGAGGTGGCTGATTTGGGG | - | 6.48 | ZNF263 | MA0528.1 | chr2:234738862-234738883 | GGGGCAGGAGGAGAGGGAGAG | + | 7.18 |
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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 | AGTAAGATAC ATCCTGGGCT TTGTGTCCCA GTCTGGGGCC CGCTGTTCCC CGAGGAAACA 60 GGTCCTTGGG TCTGCTGGCT CGGTGAGCTG CAAGCTTTTC TCTGCCTCAG TTGGTTTTCT 120 CTGAGATCCC AGAGGCCACA GCCTGCTCCC TGCTGTCCTC CATCCCTCAC ACAGGCTGAG 180 GAGAGAGGCC ATCCGAGATG ACCTGCAAAG CCACCTCACT AAGCAGTCTC AGCCCCGTGT 240 CGGGGGACAT GGTGTGGTGG CTGCCTATAG CCCTCCTCTG CCCAAACCCT TTCTTCTAGC 300 AGATTCTGTA ACTGGCAGGT CACTTTTGAG TATTAGGACT CAAAATACCC CAAAGTGGTC 360 TTGTCCACTG CCTGCAGGCC CATGTTGGGA TGGGAGCGGG CCTGGCTTCT CCCTCTCCAC 420 AGCCCAGCTC CTCTGTTGCT TTGGGGCAGG AGGAGAGGGA GAGACAGATT TGTTAGTAAA 480 TGTGCCTTCT CATTTGAGTT GCTGCCTCTC AGGCTAACCC CGGCTGGCTG GGGACCTCAG 540 GATCCTCACT CCCTGCATGG CCCATGACCT TGACCGCCCT CTTCTCTCCC TAGTCTCTGC 600 TTACAGACTT GGGGGGTGGG GTCAGGAAGT GGGGAGGTGG CTGATTTGGG GAGGTTCTGC 660 CCCCGCCTAG TAAGCCTTGG GACGCAGCTG GCCTAACATG AAAGAAATGC AATGGTCATT 720 TTCAGCAGGT GCCTTGGACT CCAGCTCTGG GGTCACAGGA CAAGTACTGT CACTATGAGG 780 GCAGCAGTTT CCAGGTGGGG TGGAGCGGGT GGCCCAGATG GCCTGGGTGG CCCAGGTGGG 840 ATGGCCCAGG TGGCCCAGGT GGGATGGCCC TGGTGGCCCA GGTGGGATGG CCCAGGTGGC 900 CCTTACAGGC AGTGAGGGGG ATTGAGATGC ACACTCCCTA GACCTGGGCT TTGCACTCAC 960 CACCCCAGCT TCTGGACTTT GCCACATCCC TCTGCCACAC CATCCCTGGC CACCCTGGGC 1020 ACAAGGTGTC ACTGCCCAGA GGCTCCTTTT CCTTGCCAGT CCTCACCACC CTCTGTCTTC 1080 AGCCCACACT GTTCTTCCAT GTTTTATCGA CAACTGTCCA GTGGGGTGGG GGGGCTTCAG 1140 GGAAGGAACC AGGGTGCACC CAGCAATGGT GACCGAGAGT GAGGAAAGGG CTACCGAGAC 1200 AGAAGCATTT TGTCTTCCTG CCCTGCCGTC TCCAGAAGCT GTGGCCAGCA GGCTTGGTCA 1260 CAGGCAGATG CTGGTGGACT GGGCCTGGGA GGTGAGGACA CGTGCCCAGT CTTGCCTGCT 1320 CAAGCCCGGC TCCCGCCTCT GATCCCATGG AGGGCTGGGT CCCAGGCAGG GCTGCTGAGG 1380 GCACGAAGGT GCTGGCTGAG GGGGCGGGTG GGGCTGCATC TGCCCCCAAG GGGCTTTCTA 1440 TAAATGTACC TGCAGCCATG TTCAAGCTGG CAGGGGCCCA GGTCCCAGGT GGCCTCCCAG 1500 GAGCCACCAG CCCTGCCTTT CTTTGGCTTG GTGAGGCTTT TCTGGGGCTG CCCTCTGGCT 1560 TCCTGCCAGC CTCACCCCTC TGGGGAACCA CGTGGCCTGG CTGATGGCTC TGCTGCCGTC 1620 CTGTGTCCCT 1630
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