Tag | Content |
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EnhancerAtlas ID | HS154-04697 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr12:12110930-12112790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxa2 | MA0047.2 | chr12:12112138-12112150 | TGTTTACTTTGT | + | 6.18 | NKX2-3 | MA0672.1 | chr12:12112739-12112749 | TTCAAGTGGT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 12111056 | 12112677 | chr12 | 12111679 | 12111898 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I011958 | chr12 | 12110940 | 12112751 |
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Enhancer Sequence | GCCTTCAGCC TCCTGCCTCT TTACTGCCTT CATTCGCACT TCTTTGAGTC AGGTTGGCAA 60 ACCCCTTCAT AATCCGCCCA ATCTAGTTTT CCAGCCCCCA ATACTCTCCT GACCTATAAA 120 TTCGCTTTCT GCATTGGCCA CAATGAACTC CTCCCAGGTG GCAGCTCTTT GGATCTCTCT 180 ATCCTTCCTT TCTTTGTGCT CTTTTCCTGG AATGTCCTTC TCTTGTCATC CTACCCAAGA 240 CAATCAGTTT CTCCCTCTAT CGCTCCTTGA ATTCGCCTCT GATATTGCAC TTGTGTCTGC 300 ATATTGACAG GTTTATGGAA GACACTTCCT AGCCATCTTG TGAGCTCCTT GAAGGAACTG 360 TGTCTTTATC TGTATAGCCC CACCTAGCAG ATGCTCAAGG CATGCTTGTG GAATGAATAA 420 GGGAACAGAT CATTTCTTCT GAGCTGTTTG CAGTCTGGCT AAGCCAATTG AAAGAATGCC 480 TTCTCTTGCA ATCTACAAAT TGAAAAGCCT GTGAGACCCT CAGGACACTC AGGCAAGTTT 540 TCCAGCATAT GTGACAATAC CAAGCCTTAG TGCATTTGCC TCTCACGTGG AGGAGTCTCT 600 TCTAAAAATG AAACAGAGAT GAAGGGTGAG ACTCTTACAG TGGTTCAACT CCCCTAAGAT 660 CCTCTTGTGA TTTAGAAGCA TCTTGGAAAG AAATCCTTGA CACTCGCCTC GCCCACCCTG 720 AGCTATAAGG TAAAGCTCTC GGTGGTAAAC GTGGCTCCCT GGTAGGGAGA CTTCTTTTAT 780 CCTCATTGTT TCTGGAGGGG GAAGTGTTAG CACAGAGACT CCCTGGGAAA CCCGAGGATG 840 CCTCACCACC TCACCATAAC AGCAGGAAAC CCAGAAATGA TTCACAGCTG AAACCTCTGG 900 CCCACATCGA CACATCACAT CACATGGTTG TTTCAACTGG AAACCAAACA GCCATCTGGG 960 CATGATTATC TGTATTTTTG TGAAGGTGTA AATACACAGT GAGTAGGAAG AGTCCAATAA 1020 AACCTATTAT AATGTTGGTG GTGGGCACCA CAAAGAGAGC ACCCCTTAAT AGACATTCCC 1080 TGGTCCAGTG AAAGACATAC TTTGTACTGA GTCCCGCGCC TGGGAGACCT TCCAGGAAAG 1140 TAAATCCCCA GGAGAGAGAG GCATTTCCCA GTAGGTGCTT TGCTTTTTGG TTGTTTTCTT 1200 TTCTTGGTTG TTTACTTTGT TCTACTTTGT TTTTACTACA GTTCTGTCCT ACTGGTGGCG 1260 GAGTGGGACT CCTTCATGAT GTGGCACAGT TTCCTTGAGT TTTAGGAAGA AACGGCCCAT 1320 GTGGCAGATT CAGAAACAAT GAATCAGCAC CTAAACAAAC AGGAAGGTAA GCGGCCCTCC 1380 CAAGGTCACC TGGGTAGTGG CAGGGTGTGA ACCAGAGTCC AGGTGTCCTG ACCACCCACC 1440 ACCGCCTGTC CTCCTCCCTC ATACAAGATC CCTTCTAGGC CAGCGCTGAG AATAAAGGCA 1500 GCGGCATCAT GGGGAGGGGG TGAGGACAGA AGGGTCAGGG AAGGCACTGG GAGGGAGAGG 1560 CAATCCCAAC CCAACTCCAA CAGCCTAGGG TCAAAGCCCA GCTCCACTCC TGGCAGCTGT 1620 GAGACTTTGG TGCATTTAAT GTCCTTGAGC CTCTATTTCT TCACCTGGAA AATGGGATTG 1680 ATGACAATAT GCGTCCCTCC AACAACTAAA TGGCACATCA AAGCTTTGGT TAAAGGGGTT 1740 GGCACATCGT GAGGACCACG TCAGCTCTTA ATACTCCAAT GATGGCTTCC CTATAAGTGC 1800 AGAGTCTTCT TCAAGTGGTG GTTAGCACGG GTTTTGCCTG TTCCTTTAAT CATGGCTGTG 1860
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