| Tag | Content |
|---|
EnhancerAtlas ID | HS088-00031 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:993460-996460 |
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: 2 | Chromosome | Start | End |
| chr1 | 993716 | 993800 | | chr1 | 993800 | 994951 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I001059 | chr1 | 993741 | 993890 | | GH01I001060 | chr1 | 995969 | 996344 |
|
Enhancer Sequence | CCGTTTCAAA AAAAAAATGA AAAGATAATA CCCACAAGCT CCACACCCAG GAGGTCCCAT 60
GCGTCTGAGT GTTTGCTTTC TGGGCTTTTC ATCACCTGGT CCTCTGGGGA TATGCTGACC 120
GACCCTGTGT GCCTGGCAGG TGTCAGGCAC TGGGGGTCGG GGAGGAGAGA GTCCAGGAGC 180
GGTGGCCACA CACAGGTCGC TGACGGTGGG GGGCCAGGGT GGGGGCAGAC TAACTTTGGT 240
TTTCAGGAAA GGTCCAGAGA AAACACGCCC AAACCCAGAC CCGAAGCATG AGCAGGGGGA 300
GGGCAGGTGA GGAGGCCAGA GGCGGGGCAT GTGGTGTGGG TCCATTGGAC GGTGTGCAGG 360
GCCCTGTGGC TTGACAAAGG GATCTTTCAG CAGGAAGCGG AGGCGTAGGA GCGGCCAGAG 420
GCCAGCGTGC AGGACAGAGG CCACAGGTCA GAGCAGCAGA GGCTGGACAG AGATGGGCAG 480
GGCAGGTCCA GTGGGGCTGC GTGGGCCTGG GGAAGAGAGC TGGGGGTGCT GCCTGAGGAG 540
CTGTGGGAGG CTCCTGGAGG GCTCCAAGCA GGAGGCCACC AGATTTCATG AAGACGCCCC 600
TGGCTAGGAC AGGGTGCTAG GCTGCAGGGG GAGCAGAGGG AGGGATTTGG GGGAGAATGG 660
GCGGGTCGAG GGGGGTGAGA AGAGGCGCTC AGGGACGTGG AGATGGAGCT GGAGGCACCG 720
GAGCTTTGGG TGGATTCGCC CTGATGCGTC TGGAGGGATG GCTGGGCTGG GGAAGCTGGG 780
GTTCCCTGAG TGGGGTCCAG GGGGCCGAGG GGTGCCAGGC AGGGAGAGGC TGGGCTGAAG 840
CCTGAGGCAG GTGCTCCTGC TGGGTGTTGC CTAGGAGAGG AGAAAAAGCC CCGACGCCAG 900
AAATGGAGGA GGGAGGAGGA CCTCGGAGGG GAGGAGGAGG GTGCGCAGAA CCAGGAGAGG 960
CAGTTTGGGG AGCAACCGCT GCGGAGCGCG CAGGACCCAG AGGACTCAAA GGGGACCTGG 1020
AGGGTGACGA GGCCTTCCGT GGCCGGGGGT GAGGAGGAGG GAAGCCGCGC GGGCGGAGAG 1080
GCGCTGGTGG GTCCCAGGTT GGAGGCTGTG GGTCTGAGAG GCGAAGCCCA GGGGAGCCCG 1140
GGGCCACCGC TGAAAAGGAT GGCAGCTGAG CGCAGGCGAG GGAGAGGCGC GCGTGTCCGG 1200
GACAGACCGC GGTGGGAGCT CGACTCCGGA AACCGGCGGG CCTGGGGCTG GGACCTACAG 1260
GGAGGCGGAC GCGGCACAGC CAGGGAGGTC GGTCCCGCGG GCCCCGCCCC GCCCCCCAGC 1320
CTGGAGCGCC CCCCTCCGGC CCCGGTCCGC AGTGGAGGCG GCCCCGGAAA AGCCAGAGGG 1380
TCTTGGAATG GAGGGCGGGA CGGAGCCGCC TGCAACGCCC GCGACCCGCG ACCCGGCTGC 1440
CCGCGGGACC CCCGGCTCTG AAGCGGGGAC GGCCGGAGCT TCCGCCTGCA GCCCAAACTC 1500
CCAGGCGCCC GGCAAGAGTG GCGGGCGCGG ACCCTTTAAG AAGGCCGGGG GGCGTGGCCT 1560
CGGGGCGTGG CCCGGGGCGT GGCATCGGGG CGAGGCTTCG GGGGCGGAGC CCAGGCAGCG 1620
CCTTCGCGGA GTTGCCGGAG GGTGCGGCCG CCCAGAGCGC ACCCCGAGCG CCGGCGAGCG 1680
GCGCGGTGAG ACCCTCGTGC AGGTGAGCCC GGCGCACGGC GGCCCAGAAT CCTGGACCCC 1740
AGGAGAAGCG TCTACGGCCC CGACAGGTGG GCGTGGCGAA ATGCCACCCG GGCCCTCCTC 1800
GCGCTCCCAG CTGGGTCACG CCTCAGACCC GGGGTCCTGG ACGCCTGCCC CCCTCCACCC 1860
GCAGGCCCTG CCAGGACACT TTGGTCCCTG GCCCGCCAGG CCTGGCCTCA CTCAGGCTTG 1920
GCTGTGGGGT CAGAGTCGGG CAGAACGGAA CCAACAGTCC TGGCAGGCCC AGGCGGTTGG 1980
AGGAGAAGTG GTCGGCTCTG GACACCTTTG TTGTTTTTTG TTTTTTGTTT TTGAGATGGC 2040
GTCTCACTGT GTCACCCAGG CTGGAGTGCA CTGGCGCGGT CTTGGCTCAC TGCAACCTCC 2100
ACCTCCCGGG TTTATGCAAT TCTCCTGCCT CAGCCTCCGG AGTAGCTGGG ATTACAGGTG 2160
TATGCCACCA TGCCTGGCTA ATTTTTGTAT TTTTAGTAGA GACGGAGTTT CACCATGTTG 2220
GCCAGGATGG TCTTCAACTT CTAACTTCGT GATCCACGCT GCTGGGATTA CAGGTGTGAG 2280
CCACCGCGTG TGGCCTCTGG GCACCTTTTG AAGGTAGGAT GAGAGGAACT CATGGATCGG 2340
AGCCGGCAGG GAGCGCCGAG GGGGGCCGGG GGCAGGGCGG CCACCCTTGC CTGTGTGGGG 2400
AAGATGAAGA AGAGGGTGTG GGCCGCGGGG GCAAGATCAG GAGCTTTGGG TTTTGAAGAT 2460
GTTAGGAAAG ACGTGCTGCT GACTTTGCAA ACGGAGGTGC TGAAACCGGG TGTCTGGAGC 2520
TCAGAGAAGA GGTGGCGCTG GACTGGCCTA GACTCTGTGC AGACACAGAA GAGCCAGGGC 2580
CTGGGGCTCC CATCGAGGAG GAGGACAAAG GGCCCTGGCC AGGGCAAGGT GGGAAGCCGG 2640
GAAGTGCAGC CTCCACAGAG CCTCGCAGAG AAGGCGCCAC TGGAAGAAGG CGGCACTGAC 2700
GGCCTCGGAG GCTGCTGAGG ACCGGCTGGG CCCCGACGTC CGTGGCAACC CTGACAGCCA 2760
AGTCCTCCGT GGGCTTGGAG GGCGGGACAC GGCTCTGGAG ATGAGGGAGA GGACGGGCCG 2820
TGCCGACCGG CACCGCGGTG TTCCTGAGCA GTGGCACCGT GGCTGTTGCT GAATTTTATT 2880
ATTGTTAATT AATTTATTTA TTTTTATTTT TGATACTGAG TTTTTCTCTT GTTGCCCAGG 2940
CTGGAGTGCA GTGGCGAGAT CTCGGCTCAC CGCAACCTCC GCCTCCCGGG TTCAAGCGAT 3000
|
