| Tag | Content |
|---|
EnhancerAtlas ID | HS006-00017 |
Organism | Homo sapiens |
Tissue/cell | Astrocyte |
Coordinate | chr1:993410-996440 |
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 | TGAGCCGCGA TTGCACCACT GCACTCCAGC GTGGGCGACA GAGCGCGACT CCGTTTCAAA 60
AAAAAAATGA AAAGATAATA CCCACAAGCT CCACACCCAG GAGGTCCCAT GCGTCTGAGT 120
GTTTGCTTTC TGGGCTTTTC ATCACCTGGT CCTCTGGGGA TATGCTGACC GACCCTGTGT 180
GCCTGGCAGG TGTCAGGCAC TGGGGGTCGG GGAGGAGAGA GTCCAGGAGC GGTGGCCACA 240
CACAGGTCGC TGACGGTGGG GGGCCAGGGT GGGGGCAGAC TAACTTTGGT TTTCAGGAAA 300
GGTCCAGAGA AAACACGCCC AAACCCAGAC CCGAAGCATG AGCAGGGGGA GGGCAGGTGA 360
GGAGGCCAGA GGCGGGGCAT GTGGTGTGGG TCCATTGGAC GGTGTGCAGG GCCCTGTGGC 420
TTGACAAAGG GATCTTTCAG CAGGAAGCGG AGGCGTAGGA GCGGCCAGAG GCCAGCGTGC 480
AGGACAGAGG CCACAGGTCA GAGCAGCAGA GGCTGGACAG AGATGGGCAG GGCAGGTCCA 540
GTGGGGCTGC GTGGGCCTGG GGAAGAGAGC TGGGGGTGCT GCCTGAGGAG CTGTGGGAGG 600
CTCCTGGAGG GCTCCAAGCA GGAGGCCACC AGATTTCATG AAGACGCCCC TGGCTAGGAC 660
AGGGTGCTAG GCTGCAGGGG GAGCAGAGGG AGGGATTTGG GGGAGAATGG GCGGGTCGAG 720
GGGGGTGAGA AGAGGCGCTC AGGGACGTGG AGATGGAGCT GGAGGCACCG GAGCTTTGGG 780
TGGATTCGCC CTGATGCGTC TGGAGGGATG GCTGGGCTGG GGAAGCTGGG GTTCCCTGAG 840
TGGGGTCCAG GGGGCCGAGG GGTGCCAGGC AGGGAGAGGC TGGGCTGAAG CCTGAGGCAG 900
GTGCTCCTGC TGGGTGTTGC CTAGGAGAGG AGAAAAAGCC CCGACGCCAG AAATGGAGGA 960
GGGAGGAGGA CCTCGGAGGG GAGGAGGAGG GTGCGCAGAA CCAGGAGAGG CAGTTTGGGG 1020
AGCAACCGCT GCGGAGCGCG CAGGACCCAG AGGACTCAAA GGGGACCTGG AGGGTGACGA 1080
GGCCTTCCGT GGCCGGGGGT GAGGAGGAGG GAAGCCGCGC GGGCGGAGAG GCGCTGGTGG 1140
GTCCCAGGTT GGAGGCTGTG GGTCTGAGAG GCGAAGCCCA GGGGAGCCCG GGGCCACCGC 1200
TGAAAAGGAT GGCAGCTGAG CGCAGGCGAG GGAGAGGCGC GCGTGTCCGG GACAGACCGC 1260
GGTGGGAGCT CGACTCCGGA AACCGGCGGG CCTGGGGCTG GGACCTACAG GGAGGCGGAC 1320
GCGGCACAGC CAGGGAGGTC GGTCCCGCGG GCCCCGCCCC GCCCCCCAGC CTGGAGCGCC 1380
CCCCTCCGGC CCCGGTCCGC AGTGGAGGCG GCCCCGGAAA AGCCAGAGGG TCTTGGAATG 1440
GAGGGCGGGA CGGAGCCGCC TGCAACGCCC GCGACCCGCG ACCCGGCTGC CCGCGGGACC 1500
CCCGGCTCTG AAGCGGGGAC GGCCGGAGCT TCCGCCTGCA GCCCAAACTC CCAGGCGCCC 1560
GGCAAGAGTG GCGGGCGCGG ACCCTTTAAG AAGGCCGGGG GGCGTGGCCT CGGGGCGTGG 1620
CCCGGGGCGT GGCATCGGGG CGAGGCTTCG GGGGCGGAGC CCAGGCAGCG CCTTCGCGGA 1680
GTTGCCGGAG GGTGCGGCCG CCCAGAGCGC ACCCCGAGCG CCGGCGAGCG GCGCGGTGAG 1740
ACCCTCGTGC AGGTGAGCCC GGCGCACGGC GGCCCAGAAT CCTGGACCCC AGGAGAAGCG 1800
TCTACGGCCC CGACAGGTGG GCGTGGCGAA ATGCCACCCG GGCCCTCCTC GCGCTCCCAG 1860
CTGGGTCACG CCTCAGACCC GGGGTCCTGG ACGCCTGCCC CCCTCCACCC GCAGGCCCTG 1920
CCAGGACACT TTGGTCCCTG GCCCGCCAGG CCTGGCCTCA CTCAGGCTTG GCTGTGGGGT 1980
CAGAGTCGGG CAGAACGGAA CCAACAGTCC TGGCAGGCCC AGGCGGTTGG AGGAGAAGTG 2040
GTCGGCTCTG GACACCTTTG TTGTTTTTTG TTTTTTGTTT TTGAGATGGC GTCTCACTGT 2100
GTCACCCAGG CTGGAGTGCA CTGGCGCGGT CTTGGCTCAC TGCAACCTCC ACCTCCCGGG 2160
TTTATGCAAT TCTCCTGCCT CAGCCTCCGG AGTAGCTGGG ATTACAGGTG TATGCCACCA 2220
TGCCTGGCTA ATTTTTGTAT TTTTAGTAGA GACGGAGTTT CACCATGTTG GCCAGGATGG 2280
TCTTCAACTT CTAACTTCGT GATCCACGCT GCTGGGATTA CAGGTGTGAG CCACCGCGTG 2340
TGGCCTCTGG GCACCTTTTG AAGGTAGGAT GAGAGGAACT CATGGATCGG AGCCGGCAGG 2400
GAGCGCCGAG GGGGGCCGGG GGCAGGGCGG CCACCCTTGC CTGTGTGGGG AAGATGAAGA 2460
AGAGGGTGTG GGCCGCGGGG GCAAGATCAG GAGCTTTGGG TTTTGAAGAT GTTAGGAAAG 2520
ACGTGCTGCT GACTTTGCAA ACGGAGGTGC TGAAACCGGG TGTCTGGAGC TCAGAGAAGA 2580
GGTGGCGCTG GACTGGCCTA GACTCTGTGC AGACACAGAA GAGCCAGGGC CTGGGGCTCC 2640
CATCGAGGAG GAGGACAAAG GGCCCTGGCC AGGGCAAGGT GGGAAGCCGG GAAGTGCAGC 2700
CTCCACAGAG CCTCGCAGAG AAGGCGCCAC TGGAAGAAGG CGGCACTGAC GGCCTCGGAG 2760
GCTGCTGAGG ACCGGCTGGG CCCCGACGTC CGTGGCAACC CTGACAGCCA AGTCCTCCGT 2820
GGGCTTGGAG GGCGGGACAC GGCTCTGGAG ATGAGGGAGA GGACGGGCCG TGCCGACCGG 2880
CACCGCGGTG TTCCTGAGCA GTGGCACCGT GGCTGTTGCT GAATTTTATT ATTGTTAATT 2940
AATTTATTTA TTTTTATTTT TGATACTGAG TTTTTCTCTT GTTGCCCAGG CTGGAGTGCA 3000
GTGGCGAGAT CTCGGCTCAC CGCAACCTCC 3030
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