Tag | Content |
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EnhancerAtlas ID | HS154-04716 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr12:13144100-13146900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:13146079-13146097 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr12:13146083-13146101 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr12:13146058-13146076 | CCCTCCCTCCCTCCCTCC | - | 6.03 | EWSR1-FLI1 | MA0149.1 | chr12:13146062-13146080 | CCCTCCCTCCCTCCCTCC | - | 6.03 | EWSR1-FLI1 | MA0149.1 | chr12:13146091-13146109 | CCTTCCTTCCTCTCTCTC | - | 6.25 | EWSR1-FLI1 | MA0149.1 | chr12:13146067-13146085 | CCTCCCTCCCTCCCTTCC | - | 7.08 | EWSR1-FLI1 | MA0149.1 | chr12:13146071-13146089 | CCTCCCTCCCTTCCTTCC | - | 8.13 | EWSR1-FLI1 | MA0149.1 | chr12:13146087-13146105 | CCTTCCTTCCTTCCTCTC | - | 8.32 | EWSR1-FLI1 | MA0149.1 | chr12:13146075-13146093 | CCTCCCTTCCTTCCTTCC | - | 9.42 | Gfi1b | MA0483.1 | chr12:13144327-13144338 | AAATCACAGCC | + | 6.02 | IRF1 | MA0050.2 | chr12:13145885-13145906 | ATGGTGAAACTGAAACAAAAA | - | 6.81 | Nfe2l2 | MA0150.2 | chr12:13145562-13145577 | TGCTGAATCATTCTG | - | 6.78 | ZNF263 | MA0528.1 | chr12:13146083-13146104 | CCTTCCTTCCTTCCTTCCTCT | - | 6.58 | ZNF263 | MA0528.1 | chr12:13146075-13146096 | CCTCCCTTCCTTCCTTCCTTC | - | 6.76 | ZNF263 | MA0528.1 | chr12:13146079-13146100 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr12:13146062-13146083 | CCCTCCCTCCCTCCCTCCCTT | - | 7.05 | ZNF263 | MA0528.1 | chr12:13146071-13146092 | CCTCCCTCCCTTCCTTCCTTC | - | 7.19 | ZNF263 | MA0528.1 | chr12:13146054-13146075 | TTCCCCCTCCCTCCCTCCCTC | - | 7.32 | ZNF263 | MA0528.1 | chr12:13146067-13146088 | CCTCCCTCCCTCCCTTCCTTC | - | 7.38 | ZNF263 | MA0528.1 | chr12:13146058-13146079 | CCCTCCCTCCCTCCCTCCCTC | - | 7.97 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_46589 | chr12:13143937-13147247 | Osteoblasts |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 13145446 | 13145954 | chr12 | 13145478 | 13145960 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I012990 | chr12 | 13143372 | 13147333 |
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Enhancer Sequence | AGGCAGCAGG CAAGGTGAAC CCACTGGGCA GTTACACCAC GCCTGGCCTC TGCTGTTGAT 60 TTATGTATTT TTTATTGCTG TATTGCTATT ATTATTTTTT GAATATTTTC CATCTGTGGT 120 TGGTTGAATC GTGGATCCAG AACCCACAGA CAGGAAGGGC TGACTGTAGC TCTGTTCACA 180 CCGTGCTCCC AGACACAGCA TATCCTCTCC CTAACTCTTG TCTCACTAAA TCACAGCCTC 240 CCAATCTGCT TAATGCTCAG CTCCACTGTC TCTTTTCACA CAAATCCTTC TTTCATCTCC 300 CCATCACCAC TTTCTGCATT GAGGCCCTGT CCTTGGACTA TCCTTTCCCT GGTGTTTACT 360 CATTATGGAC CCCCACAGCT CTCCTTCAGT ACATCTCCTG CTCCTTGCCA CGTGATTGCT 420 CATATAATTT AATTTTGTAT TCCTGGACAT ACTGTAAGGC AGTGTTCTTC ACATTTTGAA 480 AAAAAATCAC AATCCACAAG AAGGAAAGCA TTTTTTACAG CCTGTCTTAT CATGAATATA 540 CACATAGTTA AAGTTTCACA AAGTAATGCT TTACCCTTAT GGATGAGATG CATCCTGGCT 600 TTTTTTTTGT TCCTTCCCCT ATCCTGTTTT CTTCTCTTCT ACTCTACTGG AGTGAATTTT 660 ATTCCATCCC ATTAGAAGAA GGAAAGTTGG TCTATGTTAA TTTTACCATC TGGTAATGAA 720 ACATTATTAT AGTTTTAACA ATCTGCAATA AAGCCTTTAT GGGCAGAAAC TATACCACAG 780 AGCTTTACAT GTGAGAAGTG CAACAGATAT TTATTTGATT AAGGTGCTGT GTCTCCTAAC 840 AATGATTATG AAAAACAGAC ACATGGTAGG GAACCTGGCT GCCCTAGACT GGTCAAATAG 900 GTTTTCATAT AATATCCTAG ACTGAAGATT CACAACTAGG GAAGAGGGTG TGACTCCCAG 960 GGGGACAGAA GGTGTCTCTG GAGGAAGGCA GGACTGTACG GCTGTGAGTG GCAAGTGTAG 1020 TCTCAATGAG CATATTTAAT ATTTATTTTA TTTTTGAGAC AGAGTCTTGC TCTGTCACCC 1080 GGGCTGGAGT GCAGTGGTGT GATCTCTGCT AAGAGCAACC TTCACCCCCC AGGTTCAAGT 1140 GATTCTTCTG CCTCAGCCTC ACAAGTAGCT GAGACTACAG GCGAACGCCA CCACTCCCAG 1200 CTAATTTTTG TGTTTTTAGT AGAGATGGGG TTTTGCCACA TTGGACAGAC TGGTCTCGAA 1260 CTCCTGACCT CAGGTGTTCT GCCCACCTCG GCCTCCCAAA GTGCTGGGAT TACAGGTATG 1320 AGCCACTGTG CCCGGCCTTA ATATTGTAAT TTTAACCCTG AGTGCCAAGT TTGTACTTAA 1380 ATCCCCCTTC ACATGGGGTA GAGGAAATTG CGCCAGACCA GGAATCATGA GGCAGCAAGT 1440 CAGCCTTGAC TGTGGGGCAC CGTGCTGAAT CATTCTGAGG CTGCTGTGAA GCCCTCCATC 1500 TGGTGAATCT GACACTTCCA AAGAGCCTTC AGTAGCAAAC TGTTAAGTAA ACTTAGGGTG 1560 TTTTGCTCTT TCTGTTGCTG CAGAGAATTC CAGAACTCCC CTTTCATTTG AGAGCGCACC 1620 TACCCTTGGC ACTTGTAATG TTTTAAATTC CAGAAACACT ATCCTGTGAA TCACAGAAGT 1680 TCAGAACCTA AAATGGTTTT AAAGTTTACC TAATCTAACT AATTTTATCA AGGAGAAAAT 1740 GAAGAACCAG AGAGACTAAG TTGCTCAAAG TGATGTAACT ACTGAATGGT GAAACTGAAA 1800 CAAAAATTCC AGTTCCCAAA CTCTAGTCTA CTCCAGTCTA ATACTCGTTG CAAGGTTCTC 1860 TAAAGCTATG GGGGGTGAAG TGAGCATTTA AACCTCTGTT TCTTTTCTTT ATCCTCCTTT 1920 CTTTCCTCTC TCTGTCTTTC TTTTTTTCTT TCGTTTCCCC CTCCCTCCCT CCCTCCCTCC 1980 CTTCCTTCCT TCCTTCCTTC CTCTCTCTCT CTCTCTTTCT TTCTCTTTCT TACAGGGTCT 2040 CATGGTTGCT CAAGCTGGAG TGCAGTGGTA CAATCTTGGC TCACTGTAAC TTCAGCCTCC 2100 TGGGCTCACG TGATCCTCCC ACCTCATCCT CCTAAGTAGC TGGGACTACA GGTGTGTGCC 2160 ACCATGCCCA GCTAATTTTT TTTGTATTTT GTTTTCTCTG TCTTCTTTTG TAGAGACAGG 2220 GTTTCACCAC GTTGCCCAAG CTGGTCTCAA ACTTCTGAGC TCATGCGATC CACCTATGTC 2280 AGCCTTCCAA AGTGTCTTTG CTTTTTTTTT TTTTCTTTTC CTCTCTCTCT CTCTCTCTCT 2340 CTCTCTCTCT CTTTCAGATG GGGTCTTGCA ATGTTGCCCA GTCTGTAACC TCTCTCTTTA 2400 GCCACTGTGT TAGATACTTT GGGCGGACAG TTGTATGCCC ATATCAAATT CAGAATAGAG 2460 GTATCAGAAG TCATTTTACG CAGTTACTTC TTTTACAAAT GGGAAGACCA AAAACAAGAT 2520 CTCACTGGAG AAAGAGCTAA CTGGCTCTTT CCTTTGGTCT TTTTCTTCTT TTATTCATTT 2580 AACCAACAAC TACTGAGTAT CTACCATGTG CTGAACATTG TTACAGGTGC TATAAGGGAA 2640 GATGCCAGGA AAACAGAATG TTATCATCTA ATGATATTTT TAGGGGGCAA GGAGTGCCAG 2700 GGCAGTATGG GAACACAGGA AAGGACCACT TAGGTTAGTT TATGGGGCAT GGGTGTATGT 2760 GATAACATGT TTGGGGAGGT CAAGCTGACT TTGAGGTGGT 2800
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