| Tag | Content |
|---|
EnhancerAtlas ID | HS153-00015 |
Organism | Homo sapiens |
Tissue/cell | Osteobl |
Coordinate | chr1:993320-996360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr1:995224-995238 | AGGTGGGCGTGGCG | - | 6.25 | | KLF14 | MA0740.1 | chr1:995005-995019 | CGGGGGGCGTGGCC | - | 6.32 | | KLF16 | MA0741.1 | chr1:994765-994776 | GCCCCGCCCCC | + | 6.02 | | KLF16 | MA0741.1 | chr1:995007-995018 | GGGGGCGTGGC | - | 6.62 | | KLF4 | MA0039.3 | chr1:995870-995881 | AGAGGGTGTGG | - | 6.02 | | KLF5 | MA0599.1 | chr1:994760-994770 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr1:994765-994775 | GCCCCGCCCC | + | 6.02 | | Lhx3 | MA0135.1 | chr1:996342-996355 | TGTTAATTAATTT | - | 6.19 | | SP1 | MA0079.4 | chr1:995225-995240 | GGTGGGCGTGGCGAA | - | 6.2 | | SP1 | MA0079.4 | chr1:995006-995021 | GGGGGGCGTGGCCTC | - | 7.17 | | SP3 | MA0746.2 | chr1:994764-994777 | CGCCCCGCCCCCC | + | 6.11 | | SP3 | MA0746.2 | chr1:995006-995019 | GGGGGGCGTGGCC | - | 7.22 | | SP3 | MA0746.2 | chr1:995225-995238 | GGTGGGCGTGGCG | - | 7.52 | | SP4 | MA0685.1 | chr1:995223-995240 | CAGGTGGGCGTGGCGAA | - | 6.13 | | SP4 | MA0685.1 | chr1:995004-995021 | CCGGGGGGCGTGGCCTC | - | 6.26 | | SP8 | MA0747.1 | chr1:995006-995018 | GGGGGGCGTGGC | - | 6.44 | | SP8 | MA0747.1 | chr1:995225-995237 | GGTGGGCGTGGC | - | 6.62 | | ZNF263 | MA0528.1 | chr1:993742-993763 | GAAGCATGAGCAGGGGGAGGG | + | 6.18 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_24070 | chr1:995142-995502 | Colon_Crypt_2 | | SE_24817 | chr1:994228-995515 | Colon_Crypt_3 | | SE_24817 | chr1:995968-996344 | Colon_Crypt_3 | | SE_34539 | chr1:993520-995869 | HCT-116 | | SE_65935 | chr1:993812-995036 | Pancreatic_islets | | SE_65935 | chr1:995102-996141 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 993716 | 993800 | | chr1 | 993400 | 993707 | | chr1 | 993800 | 994951 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I001059 | chr1 | 993741 | 993890 | | GH01I001060 | chr1 | 995969 | 996344 |
|
Enhancer Sequence | ATCTGGGCGT GGTGGCAGGT ATCTGTAATC CCAGTTACTC GGGAGGCTGA GGCACGAGAA 60
TCGCTTGAAC CCGGGAGGCG GAGGTTGCAG TGAGCCGCGA TTGCACCACT GCACTCCAGC 120
GTGGGCGACA GAGCGCGACT CCGTTTCAAA AAAAAAATGA AAAGATAATA CCCACAAGCT 180
CCACACCCAG GAGGTCCCAT GCGTCTGAGT GTTTGCTTTC TGGGCTTTTC ATCACCTGGT 240
CCTCTGGGGA TATGCTGACC GACCCTGTGT GCCTGGCAGG TGTCAGGCAC TGGGGGTCGG 300
GGAGGAGAGA GTCCAGGAGC GGTGGCCACA CACAGGTCGC TGACGGTGGG GGGCCAGGGT 360
GGGGGCAGAC TAACTTTGGT TTTCAGGAAA GGTCCAGAGA AAACACGCCC AAACCCAGAC 420
CCGAAGCATG AGCAGGGGGA GGGCAGGTGA GGAGGCCAGA GGCGGGGCAT GTGGTGTGGG 480
TCCATTGGAC GGTGTGCAGG GCCCTGTGGC TTGACAAAGG GATCTTTCAG CAGGAAGCGG 540
AGGCGTAGGA GCGGCCAGAG GCCAGCGTGC AGGACAGAGG CCACAGGTCA GAGCAGCAGA 600
GGCTGGACAG AGATGGGCAG GGCAGGTCCA GTGGGGCTGC GTGGGCCTGG GGAAGAGAGC 660
TGGGGGTGCT GCCTGAGGAG CTGTGGGAGG CTCCTGGAGG GCTCCAAGCA GGAGGCCACC 720
AGATTTCATG AAGACGCCCC TGGCTAGGAC AGGGTGCTAG GCTGCAGGGG GAGCAGAGGG 780
AGGGATTTGG GGGAGAATGG GCGGGTCGAG GGGGGTGAGA AGAGGCGCTC AGGGACGTGG 840
AGATGGAGCT GGAGGCACCG GAGCTTTGGG TGGATTCGCC CTGATGCGTC TGGAGGGATG 900
GCTGGGCTGG GGAAGCTGGG GTTCCCTGAG TGGGGTCCAG GGGGCCGAGG GGTGCCAGGC 960
AGGGAGAGGC TGGGCTGAAG CCTGAGGCAG GTGCTCCTGC TGGGTGTTGC CTAGGAGAGG 1020
AGAAAAAGCC CCGACGCCAG AAATGGAGGA GGGAGGAGGA CCTCGGAGGG GAGGAGGAGG 1080
GTGCGCAGAA CCAGGAGAGG CAGTTTGGGG AGCAACCGCT GCGGAGCGCG CAGGACCCAG 1140
AGGACTCAAA GGGGACCTGG AGGGTGACGA GGCCTTCCGT GGCCGGGGGT GAGGAGGAGG 1200
GAAGCCGCGC GGGCGGAGAG GCGCTGGTGG GTCCCAGGTT GGAGGCTGTG GGTCTGAGAG 1260
GCGAAGCCCA GGGGAGCCCG GGGCCACCGC TGAAAAGGAT GGCAGCTGAG CGCAGGCGAG 1320
GGAGAGGCGC GCGTGTCCGG GACAGACCGC GGTGGGAGCT CGACTCCGGA AACCGGCGGG 1380
CCTGGGGCTG GGACCTACAG GGAGGCGGAC GCGGCACAGC CAGGGAGGTC GGTCCCGCGG 1440
GCCCCGCCCC GCCCCCCAGC CTGGAGCGCC CCCCTCCGGC CCCGGTCCGC AGTGGAGGCG 1500
GCCCCGGAAA AGCCAGAGGG TCTTGGAATG GAGGGCGGGA CGGAGCCGCC TGCAACGCCC 1560
GCGACCCGCG ACCCGGCTGC CCGCGGGACC CCCGGCTCTG AAGCGGGGAC GGCCGGAGCT 1620
TCCGCCTGCA GCCCAAACTC CCAGGCGCCC GGCAAGAGTG GCGGGCGCGG ACCCTTTAAG 1680
AAGGCCGGGG GGCGTGGCCT CGGGGCGTGG CCCGGGGCGT GGCATCGGGG CGAGGCTTCG 1740
GGGGCGGAGC CCAGGCAGCG CCTTCGCGGA GTTGCCGGAG GGTGCGGCCG CCCAGAGCGC 1800
ACCCCGAGCG CCGGCGAGCG GCGCGGTGAG ACCCTCGTGC AGGTGAGCCC GGCGCACGGC 1860
GGCCCAGAAT CCTGGACCCC AGGAGAAGCG TCTACGGCCC CGACAGGTGG GCGTGGCGAA 1920
ATGCCACCCG GGCCCTCCTC GCGCTCCCAG CTGGGTCACG CCTCAGACCC GGGGTCCTGG 1980
ACGCCTGCCC CCCTCCACCC GCAGGCCCTG CCAGGACACT TTGGTCCCTG GCCCGCCAGG 2040
CCTGGCCTCA CTCAGGCTTG GCTGTGGGGT CAGAGTCGGG CAGAACGGAA CCAACAGTCC 2100
TGGCAGGCCC AGGCGGTTGG AGGAGAAGTG GTCGGCTCTG GACACCTTTG TTGTTTTTTG 2160
TTTTTTGTTT TTGAGATGGC GTCTCACTGT GTCACCCAGG CTGGAGTGCA CTGGCGCGGT 2220
CTTGGCTCAC TGCAACCTCC ACCTCCCGGG TTTATGCAAT TCTCCTGCCT CAGCCTCCGG 2280
AGTAGCTGGG ATTACAGGTG TATGCCACCA TGCCTGGCTA ATTTTTGTAT TTTTAGTAGA 2340
GACGGAGTTT CACCATGTTG GCCAGGATGG TCTTCAACTT CTAACTTCGT GATCCACGCT 2400
GCTGGGATTA CAGGTGTGAG CCACCGCGTG TGGCCTCTGG GCACCTTTTG AAGGTAGGAT 2460
GAGAGGAACT CATGGATCGG AGCCGGCAGG GAGCGCCGAG GGGGGCCGGG GGCAGGGCGG 2520
CCACCCTTGC CTGTGTGGGG AAGATGAAGA AGAGGGTGTG GGCCGCGGGG GCAAGATCAG 2580
GAGCTTTGGG TTTTGAAGAT GTTAGGAAAG ACGTGCTGCT GACTTTGCAA ACGGAGGTGC 2640
TGAAACCGGG TGTCTGGAGC TCAGAGAAGA GGTGGCGCTG GACTGGCCTA GACTCTGTGC 2700
AGACACAGAA GAGCCAGGGC CTGGGGCTCC CATCGAGGAG GAGGACAAAG GGCCCTGGCC 2760
AGGGCAAGGT GGGAAGCCGG GAAGTGCAGC CTCCACAGAG CCTCGCAGAG AAGGCGCCAC 2820
TGGAAGAAGG CGGCACTGAC GGCCTCGGAG GCTGCTGAGG ACCGGCTGGG CCCCGACGTC 2880
CGTGGCAACC CTGACAGCCA AGTCCTCCGT GGGCTTGGAG GGCGGGACAC GGCTCTGGAG 2940
ATGAGGGAGA GGACGGGCCG TGCCGACCGG CACCGCGGTG TTCCTGAGCA GTGGCACCGT 3000
GGCTGTTGCT GAATTTTATT ATTGTTAATT AATTTATTTA 3040
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