Tag | Content |
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EnhancerAtlas ID | HS093-15571 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr19:39179120-39180260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr19:39179695-39179710 | ATATGACTCAGCAAT | + | 7.68 | OLIG2 | MA0678.1 | chr19:39179966-39179976 | ACCATATGGT | + | 6.02 | OLIG2 | MA0678.1 | chr19:39179966-39179976 | ACCATATGGT | - | 6.02 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00117 | chr19:39172768-39180290 | Adipose_Nuclei | SE_09404 | chr19:39164511-39180526 | CD14 | SE_13490 | chr19:39179003-39180338 | CD34_Primary_RO01536 | SE_14624 | chr19:39179374-39180514 | CD4_Memory_Primary_7pool | SE_25779 | chr19:39179417-39180269 | Duodenum_Smooth_Muscle | SE_26525 | chr19:39179021-39179809 | Esophagus | SE_26525 | chr19:39179873-39180389 | Esophagus | SE_27614 | chr19:39164407-39180553 | Fetal_Intestine | SE_28533 | chr19:39164445-39201888 | Fetal_Intestine_Large | SE_34681 | chr19:39170836-39180506 | HeLa | SE_35812 | chr19:39168616-39191950 | HMEC | SE_36926 | chr19:39172838-39186932 | HSMMtube | SE_40018 | chr19:39179218-39180516 | K562 | SE_40594 | chr19:39179201-39180442 | Left_Ventricle | SE_42097 | chr19:39179722-39180563 | Lung | SE_44161 | chr19:39179045-39180304 | NHDF-Ad | SE_44797 | chr19:39179102-39179721 | NHLF | SE_45660 | chr19:39172827-39180503 | Osteoblasts | SE_47114 | chr19:39164477-39226374 | Panc1 | SE_51136 | chr19:39179021-39180428 | Skeletal_Muscle | SE_51705 | chr19:39179204-39179729 | Skeletal_Muscle_Myoblast | SE_51705 | chr19:39179740-39180298 | Skeletal_Muscle_Myoblast | SE_53291 | chr19:39179735-39180329 | Spleen | SE_56725 | chr19:39179083-39180391 | VACO_400 | SE_58038 | chr19:39179862-39180220 | VACO_9m | SE_62811 | chr19:39125155-39186863 | Tonsil | SE_63494 | chr19:39179071-39179729 | HSMM | SE_63494 | chr19:39179752-39180316 | HSMM | SE_64225 | chr19:39179057-39180305 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 39179451 | 39180013 | chr19 | 39179503 | 39179787 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I038673 | chr19 | 39164536 | 39206516 |
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Enhancer Sequence | GAATCGCTTG AACCTGGGTG GGAGAGGTTG CATTGAGCCG AGATCACGCC ATTGCACTCC 60 AGCCTGGGCA ACAGGGTGAG ACCCTGTCTC TAAATAATAA TAAAAATGAG AAATTGGCCA 120 GGTGTAGTAG CATATTCCTG GGAGGCTGAG GTGGGCAGAT TGCTTGAGCC CAGGAGTTCA 180 AGGCTGCAGT GAGCTATGAT GACACCACTG TACTCCAGCC TGGGCAACAG AGTAAGACCC 240 CAACCCTAAA ACAAAAAAAA ACAGAAAACC ACAATGAGAT ACCACTGCAC ACCCACCATG 300 ATGGCTATAA TCAGAAAGTC AGATAATAAG TATTGACTAG GATGGGAGAA ATCAGAACCC 360 TCACATTGCT GGTCAAAGTG TAATGTGGTG CAGCTTCTTG GGAAAACAGT CTGGCAGTTC 420 CTCAAAATTT AAACATGTTT TGTATTTTTA GTAGAGACGG GGTTTCACCA TGTCACCCAG 480 GCTGGTCTTG TCTCAGCCTC CCAAAGTGTT GGAATTACAG GCATGAGCCA CCACGCCCAG 540 CCAAGTTCCT CAAATTTTTA AATATAAGAG GTATCATATG ACTCAGCAAT TTTACTCCTA 600 GGTATATGCC CAAGGCAGTT GAAAACATGT CCACATAAAA CTTGTACATG AATATTCACG 660 GTGGTGCTAA TATCCAAAAG ATAGAAGCAA CACAAATAAT GCCCATCAGC CAATGAATTG 720 ATAAATAAAA TGTGGTATAT CCATACAATG GAATGTTATT CAGACAGGAA CGAAGTACTG 780 GTACATGCTA CAACATGGCT GAACCTTGAA AACATGCTAA GGAGAAGCCA AACTCAAAGA 840 TCATATACCA TATGGTTCCA CTTATATGAA ATGCCCAGAA TAGGTAAATT GCAAGAGACG 900 AAAGAAAGGT AGGTTAGTGG TTGCCAGGGG CTGGGGGCTG GGTAGGAGGG AAGTGGGGTT 960 GGAGAGTAAC TGTACCAGTT TTGCGGTGGT AGACATGTTC CTTGTATTTT TGGTTTTTTG 1020 TTTTGTTTTG TTGTTTTGAG ATAAGGTCTC ACTGTCGCCC AGGCTAGAGT GCAGTGGCGC 1080 TGTCATAGCT CACTGTAGCC TCGAATTCCC AGGCTTAAGT GTTCCTCCCA CCTCAGCCTT 1140
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