Tag | Content |
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EnhancerAtlas ID | HS093-16722 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr2:43439360-43441740 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr2:43439677-43439694 | AGGAACACAATGTTCTT | - | 7.05 | Ar | MA0007.3 | chr2:43439677-43439694 | AGGAACACAATGTTCTT | + | 7.1 | IRF1 | MA0050.2 | chr2:43441415-43441436 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | NR3C1 | MA0113.3 | chr2:43439677-43439694 | AGGAACACAATGTTCTT | - | 6.92 | NR3C1 | MA0113.3 | chr2:43439677-43439694 | AGGAACACAATGTTCTT | + | 7.26 | NR3C2 | MA0727.1 | chr2:43439677-43439694 | AGGAACACAATGTTCTT | - | 6.53 | NR3C2 | MA0727.1 | chr2:43439677-43439694 | AGGAACACAATGTTCTT | + | 7.31 |
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| Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
SE_09435 | chr2:43435994-43442184 | CD14 | SE_13409 | chr2:43439328-43440747 | CD34_Primary_RO01536 | SE_20337 | chr2:43439372-43441120 | CD56 | SE_23724 | chr2:43439967-43440356 | Colon_Crypt_2 | SE_26557 | chr2:43439803-43440723 | Esophagus | SE_27617 | chr2:43439694-43440826 | Fetal_Intestine | SE_28536 | chr2:43439572-43440971 | Fetal_Intestine_Large | SE_30898 | chr2:43439466-43440509 | Fetal_Thymus | SE_42201 | chr2:43439348-43440800 | Lung | SE_49954 | chr2:43439343-43440980 | RPMI-8402 | SE_50052 | chr2:43439292-43440868 | Sigmoid_Colon | SE_51530 | chr2:43439734-43440675 | Skeletal_Muscle | SE_52337 | chr2:43439327-43440880 | Small_Intestine | SE_53288 | chr2:43439337-43441237 | Spleen | SE_55103 | chr2:43439326-43440734 | Thymus | SE_59314 | chr2:43439248-43468696 | Ly3 | SE_61450 | chr2:43354337-43468354 | Toledo | SE_62203 | chr2:43354169-43468733 | Tonsil | SE_65350 | chr2:43439707-43440435 | Pancreatic_islets | SE_68698 | chr2:43441211-43443035 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH02I043212 | chr2 | 43439141 | 43441139 | GH02I043214 | chr2 | 43441444 | 43442310 |
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Enhancer Sequence | TGTCTCAAAA AAAAAAAAAA AAAAAGATAA AAAAGAGGAA AAAATCAACA TGAGGTTCCT 60 TGTACCAAGG AATAGTGCAT CTTTGCCTCT TCTGAATGGC TGGGACACTC CGCCCTCTTT 120 GTGAGGGCCT GGGGCGGCAT CATGGCGCTG CCACTTATGC ACTGGGAGAC CTCAGGCAAG 180 CATCTTTCAT TCTCTGAGCT CCATTTTCCT CATCTGTCCA ATGGGAGCGA ACAGGGCCAG 240 TCTCACAGGG CAGATTGGTT TTGTCGTAGA AACAGTTACT GAAGCCCTTC GAGGAGCCAG 300 GCTTGGGGGC TGCAAGGAGG AACACAATGT TCTTGCTTTG AAGGAACTGA CAGGGTAGAG 360 AGGAAGACAG ACATAACCAG TTGTTGTGGG ATGCTGTGAT ATGTGCTCTG ATAAAGGCCT 420 GGACAGTGCC CCGGTGGGGC CAGGGTTGGG TGGAGAGGCT AGATCTGAGT TTGAGATTCA 480 GCCTGGGCTG ACCGCGGAGG GAAGAGGCGA GGAAGCAGGG GGTCACAAGG GGATGTCCCA 540 GGCAGGGGTG GAAGGAAAGT AAAGGGCCCA GAGTGTGAAC AGCATCTCTA GGAATCCTTG 600 GTGCTCCCGA GCAGCTAAGA AGCAAGGAGC ATAGGCAGAG GAGGGAGGTT TTTCCGGATC 660 CCAGAGCCTC CTTGGACTTG AACAGTGGGT GGTGGGACCC TGTGTAGCGT CCTAGGGCAG 720 AGAAGAGTAT GATCACCCAA GTGCTTTACA ACCTTGCTCT AGAGGAGTGG TGGCCTGGAA 780 GAGGACCAGC CAGGGCTCCT GGTTGACAAG GTGTCTGGGT GAGCGTGGGG CAGGCCTGAG 840 TTGCAGAGGA GCTAGAGACA AAGGGGGCAA AGTCAAGGCC TGGTTAGAAA GCAGAGTCAT 900 GATGGTTGGG CAACCTATGA GGGAAGGGGT AGAGGGAAGT GAGAGAAAAG ACTGGGGAAG 960 CGTGCCAAGT TCTGGCATGG GTTCCTTGAG AGATGTGGTG TCACATGCTT GGGGACAGGG 1020 ACAACTGGAG GGGTTGGTGT GAGGTGCATC TGGGAGGAGG TGGGTCCCAG ACTGCTGAGT 1080 GGGGCTGAGA GATGCCAGCA CGTGTGGGCA GTTAGGCAGA GCTCAGTCCC TTCCCCTCTC 1140 CACTGGCACT TTCAATCTGC CAGGTGGAGC AGTAGTTTGG GAATATTCTG GAGTCTCTTG 1200 GCTTTTGGAA GGAAGGAGAA CCAGCAAGGA CATCATGGGG GTATCCCAGG ACCTGCTGCT 1260 GGAAGCATCT TTCCTTCAGC TGTTGGTATT TTAATAGAAC ATTCTAGACT CACAGTGCTG 1320 TCCAACAGAA CTTTTGTGAT GACAGAAATG TTCTGTGCTG TTTAATGCAG TAGCCCCTAG 1380 CTCCATGTGG CAACTGAATA CTTAAAACGT AGCTATCTAG TATGGCTGAG GAAGTGAGTT 1440 TTACATTTTG CTTACTTTTA ATTAATTTAA ATCTAAATGG CTACACGCAC AGCTACAAAC 1500 CCTGGGAGTT TGGTGGGGGC AAACCATGGG GCCTTCCTGA TGCCCATCAG ATTGGATGCC 1560 TACTGATTAG AAGTGGAAAA ATACCCCAAA ATGGTAATAA CAAACAAACC ATAAATATTG 1620 CACTTTTTTT TTTTGAGACG GAGTTTCACT CTTGTCGCCC AGGCTGGAGT GCAGTGGTGC 1680 AATCTCGGCT CACCGCAACC TCCGCCTCCC AGGTTCAAGC GATTCTCCTG CCTCAGCCCT 1740 CTAGTAGCTG GGATTACAGG CATGCACCAC CATGCCCAGC TAATTTTGTA TTTTTAATAG 1800 GGATGGGGTT TCTCCATGTT GGTCAGGCTG GTCTTTTTTT TTTTTTTTTT TTGAGACAGG 1860 TTCTGGCCCA CATGGCAAAA CCCCGTCTCT ACTGAAATAC AAAAAATTAG CCGGGCATGA 1920 TGGCGGGCGT CTGTAATCCC AGCTACTCGC GAGGCTCAGA CAGGAGAATC ACTTGAACCT 1980 GGGAGGCGGA GGTTGCGGTG AGCCGAGATC ACGCCACTGC ACTGCAGCCT GGGTGACAGA 2040 GCAACACTCT GCGTCAAAAA AAAAAAGAAA GAAAGAAAAG AAAAGAAAAA AGAAAACTGA 2100 AGTTCAGATT TGCTTGAGGT CACGCAGGTA GGAGGCAGCA CTGGGCTGAG ATTTGATTGC 2160 AGTCCAATGG GAGCCCCTGC TTGTAACCCC TTAGGGCCAG GCCCTTCCAC AGCCATGGAG 2220 GTAATGCCTG CCCAAGCTCC CTCCGGTCCC AGCCCCTGCA GCGGCTCTGG ACCTACAGGG 2280 CTATTGTTGG CAAGCTCCTG CCTGTCAGCC CCACAGACTC TCTGGGCCCC CTCTGAGAAG 2340 CCTGCTGGAT GGAACATCCA GGGACCAGCC ATGCTGAGCC 2380
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