Tag | Content |
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EnhancerAtlas ID | HS093-20693 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr22:36741240-36742470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr22:36742311-36742322 | AAAACAAAGAC | + | 6.14 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00116 | chr22:36741927-36743611 | Adipose_Nuclei | SE_01541 | chr22:36741266-36744060 | Aorta | SE_05110 | chr22:36734537-36742108 | Brain_Cingulate_Gyrus | SE_05865 | chr22:36717131-36743101 | Brain_Hippocampus_Middle | SE_06839 | chr22:36722236-36742206 | Brain_Hippocampus_Middle_150 | SE_07886 | chr22:36734649-36742258 | Brain_Inferior_Temporal_Lobe | SE_08803 | chr22:36741657-36741804 | Brain_Mid_Frontal_Lobe | SE_09195 | chr22:36736566-36742350 | CD14 | SE_11020 | chr22:36722390-36744211 | CD20 | SE_17339 | chr22:36719961-36744102 | CD4p_CD25-_CD45RAp_Naive | SE_17788 | chr22:36723586-36741701 | CD4p_CD25-_CD45ROp_Memory | SE_18286 | chr22:36720347-36743699 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19119 | chr22:36737667-36742165 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22328 | chr22:36734799-36741977 | CD8_primiary | SE_26521 | chr22:36741286-36744033 | Esophagus | SE_35739 | chr22:36741281-36743900 | HepG2 | SE_36959 | chr22:36739003-36742325 | HSMMtube | SE_40597 | chr22:36741225-36743740 | Left_Ventricle | SE_42094 | chr22:36741259-36742861 | Lung | SE_45604 | chr22:36739365-36741767 | Osteoblasts | SE_45604 | chr22:36742174-36743331 | Osteoblasts | SE_47169 | chr22:36741730-36743037 | Panc1 | SE_50050 | chr22:36741267-36742026 | Sigmoid_Colon | SE_51217 | chr22:36740405-36741785 | Skeletal_Muscle | SE_52340 | chr22:36741307-36741997 | Small_Intestine | SE_52340 | chr22:36742067-36742912 | Small_Intestine | SE_54489 | chr22:36741203-36743056 | Stomach_Smooth_Muscle | SE_58448 | chr22:36724049-36832686 | Ly1 | SE_62244 | chr22:36719186-36785326 | Tonsil |
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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 |
GH22I036346 | chr22 | 36742241 | 36742390 | GH22I036321 | chr22 | 36717371 | 36741885 |
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Enhancer Sequence | CAGCTACTCG GGAGGCTGAG GCAGGAGAAT GGCGTGAACC CGGGAGGCAG AGGTTGCAGT 60 GAGCCGAGAT CATGCCACTG CACTCCAGCC TGGGCGACAG GGCAAGACTC CGTCTCAAAA 120 AAAAAAAAAA AAAAAAGTTC CCATGGAATC CTCGCAGATG AGGAAGTGAG ACTCCACATA 180 GCCATGTCTC ATGGCCAGTA AGGGGCAGAG CTGGGATTTG AACCAGGTCC TCGAGGCTCC 240 AACTATAGCA CTTAAGGGCT CTGCTTTACT GAGCAGAGGC CATCTCAGCT TAGTGGCACA 300 GCAGAGTGGG TGTGACATAA GCTATAAAGC CTGCCAAGAG GAGCGCCTCC CAATCCCAGA 360 CAGTGAGGCT GCAGCTCCCA TGTCACCCCC ACAGACACAC TGTGCTTCCT TAAAGCACAG 420 TCTGCCATTC ATTTATTTGC AAGTCACTAA TTCTGAATTT CAGTGGTTAA TACTCCTTAG 480 GGACAGGGGC CTTTAATTTG GTCCACATGA TAATCTTATC AAGCAACAGA TGAGACACAA 540 TAGGTCTGAA AATCAGGAAC CCAAGTTCCA GCCTCAGCCT GGCCAACACC TGGCTGTGTG 600 ACCCTGCTTA AGTTCCTTGC TATCTCTGGG CCTCAATTCT TCCCACCTGC CATGTTAGAA 660 GGCTGGGCTG GGGCCGGGCG TGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGACG 720 AGGTGGGCGG ATCATGAGGT CAGGAGTTCC AGACCAGCCT GGCCAATATG GGGAAACCCC 780 GTCTTTACTA AAAATACAAA AATTAGCCGG GCATGCTGGT GGGCACCTGT AGTTGCAGCT 840 ACTCAGGAGG CTGAGGCAGG AGAATCGCTT GAACCCGGGA GGCAGAGGTT GCAATGAGCC 900 AAGATGGCAC CACACCACTG CACGCCAGCC TGGGTGACAA AGTGAGACTC CGTCTCAAAA 960 AAAAAAAAAA AAAGAAGGCT GGGTTGTAAA GGAGACTGTT CCACATATCT ACTTGTTGAT 1020 AGGTCTTTGA TGAGCCAGGT TCATCCCCCA AAGGGTGGGC ATCGATGGCA GAAAACAAAG 1080 ACCTCGTTGT CACAGACTGA TTTAGCAATC AACAAGGAAA TGCAGTCCTA GTCAGGAGTT 1140 CCGGGCAAAT ACAATGGCCC ATGGCTCCCA TTGAAGGCTT TAGCACATTG CAGGGCACTC 1200 AGAAGCATGA GTCTACCTCG TAGAAATGTG 1230
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