Tag | Content |
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EnhancerAtlas ID | HS085-01785 |
Organism | Homo sapiens |
Tissue/cell | Heart |
Coordinate | chr2:42328050-42330220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELK4 | MA0076.2 | chr2:42329937-42329948 | GCACTTCCGGC | + | 6.14 | FOSL2 | MA0478.1 | chr2:42328239-42328250 | GGGTGACTCAG | + | 6.02 | JUN | MA0488.1 | chr2:42329278-42329291 | TAAATGATGTCAT | + | 6.67 | JUNB | MA0490.1 | chr2:42328239-42328250 | GGGTGACTCAG | + | 6.02 | JUND(var.2) | MA0492.1 | chr2:42329277-42329292 | TTAAATGATGTCATC | + | 7.09 | KLF16 | MA0741.1 | chr2:42328455-42328466 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr2:42328455-42328465 | GCCCCGCCCC | + | 6.02 | Klf12 | MA0742.1 | chr2:42328292-42328307 | AGGCTGGGCGTGGCC | - | 6.01 | MAX | MA0058.3 | chr2:42329397-42329407 | ACCACGTGCT | + | 6.02 | PLAG1 | MA0163.1 | chr2:42328804-42328818 | CCCCCGACGGCCCC | - | 6.33 | RREB1 | MA0073.1 | chr2:42329770-42329790 | CCCCCCCCCACCCCACCCCG | + | 6.95 | RREB1 | MA0073.1 | chr2:42329775-42329795 | CCCCACCCCACCCCGCCTCA | + | 6 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00451 | chr2:42323824-42331106 | Adipose_Nuclei | SE_10312 | chr2:42325221-42336343 | CD19_Primary | SE_11146 | chr2:42323572-42336874 | CD20 | SE_11946 | chr2:42327841-42337002 | CD3 | SE_14693 | chr2:42327772-42338606 | CD4_Memory_Primary_7pool | SE_16102 | chr2:42328229-42330615 | CD4_Naive_Primary_7pool | SE_16740 | chr2:42328038-42330759 | CD4_Naive_Primary_8pool | SE_16987 | chr2:42327433-42336274 | CD4p_CD225int_CD127p_Tmem | SE_17444 | chr2:42325062-42338640 | CD4p_CD25-_CD45RAp_Naive | SE_17811 | chr2:42325303-42338643 | CD4p_CD25-_CD45ROp_Memory | SE_18685 | chr2:42325197-42338156 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19964 | chr2:42327606-42335969 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20190 | chr2:42327806-42336196 | CD56 | SE_21801 | chr2:42328127-42336332 | CD8_Naive_7pool | SE_22420 | chr2:42327613-42337810 | CD8_primiary | SE_30543 | chr2:42327857-42328518 | Fetal_Muscle | SE_30543 | chr2:42328585-42330631 | Fetal_Muscle | SE_43599 | chr2:42327765-42335085 | MM1S | SE_50137 | chr2:42325319-42330465 | Sigmoid_Colon | SE_53105 | chr2:42327856-42330509 | Small_Intestine | SE_53609 | chr2:42323895-42330707 | Spleen | SE_55583 | chr2:42328464-42330317 | Thymus | SE_62313 | chr2:42323195-42370065 | Tonsil | SE_67366 | chr2:42327765-42335085 | MM1S |
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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: 1 | ID | Chromosome | Start | End |
GH02I042097 | chr2 | 42324141 | 42336955 |
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Enhancer Sequence | CTAGAACACT GAGGACGTCA GTGGCCAGGA CTTTCCAAAG CTGAAACTGG GACCTGCGGA 60 GGCCTCACTG TCCGGAGCAG CGTCCAGGTC CTCAGCATCC TCTTCGCTGG GCCCCACGCG 120 TGTCGTGCGC CACCCCAGAA GGCAGGGCCT GATTCGGATC AGCAGGGGCT GCAGGGCCGC 180 TCTGCAGGTG GGTGACTCAG GCCCCTCTTG AACCCTTAGG CCTGAGGCAG AGACTGGGCA 240 GGAGGCTGGG CGTGGCCGGG GAGCCCCTTC ACGTGCTCCC CTTCTCGAGG GTTCACGGGG 300 CTCTGGAGGC CCAGATGCTG GCAAAGTGGC GGGAGCGCTC CAGGGACGAG GACTCAGGTC 360 GGGGCGCCCC CGCCAGCGCC AGGATCCCCG CTCACCCTCC GCCGCGCCCC GCCCCCGCCC 420 CGACACACTG GGGGAGCCCC GCCCTCCCCG AGGCCCGCGC GGCGCCGCAG GAGGAATCCC 480 AGCCATTTCC TCCACGCTGC GCGGTATGTG GCCTGCCCGC CGCCAACCGC AGCGCGAGCC 540 GGTCCCCAGC CGCGCCTGGC AGCTGCCCCG GCTCCGCCGT GCTGCTCGGG ATTCCGGGAA 600 GGCCGCCCCC TCGTCCCGGG CCACCAGACC GGCCTTTCCA GCGGCTCCAG GCCCGTGCAG 660 TCCCGCCGGA CGCCGGCTAC ACCACGCGCC GCTGCTGGAA CCTCTCCCAG CCCCGCGTGG 720 CCGCCCCCGG CCCAGGCACC CCCTCCCCGG AACGCCCCCG ACGGCCCCTC GCGTCCGAGC 780 TGGAAACTGA AGTTGACGCT TGCTCCGTCA CCCTGGGGCA AATTGCTTTG CCTAAGCCTC 840 AGTTTCTCCA TCTGTGAAAT GGGGACGTTG GCAGGAGTGC CTGTCTCGTT GTGCTGCCCG 900 AGGGGTGAAT GAGAAAAGGA AAGCGTTGGA CTACTGTCAA CGCGATTTTC ATTTCCCTAG 960 GTACCACGAG GGTCCTGGCT TTTCGCACAG GATCTTAGCA CCCACCCTGC CCCTCGCCTC 1020 TCCTCCAGCC CAGTTGCCGG TGGAGCAAGC AGGCCGGGCT TTGCGAGTGG GCAGAGGAGA 1080 GGGCTGGGGC CTGCCCAAGA CTGCGCCCTG CACAGATTAA ACAATGCCTG AAGGTCCCAC 1140 GACACAGCCT TCCTCGAGAT TCACCGTTGC CCTCTCCTCA ATCACTAGGT TCTTGAAAGA 1200 CCCAAAGGAC AGTTATTTAC ATTTTTTTTA AATGATGTCA TCGCAGTCTG AGAGCAGCCA 1260 GACACGTAGT GATCAGGGAA AGTCGAAAGT GCAGATGGGT TCGCAAACGT GGACTCTCTA 1320 GTTTTGGGTC TGCAGATGGG GCCGGCCACC ACGTGCTCTC TGAGTTCTCT TTCCAAGTAC 1380 AGATCCCTCC GGAGACGGAA CATTGTTCCG CCTTTAATTC TTCCCAGGAG CTGCGGAGGA 1440 AGGCGTGAGA ACCGGAGCCC GGGGTGACTT GCGGGGGAGG GGATCGCTTC CCCGTCGCCC 1500 ACACCTGCCT AACCCACGCC CACGGCGGCC GCAAAGGCGA CACCGCGTGA ATCTGGAAAG 1560 CCCCGAGTTT CAACAGGCCC AACCATCGGC GGCTTTGCAG GCGCAGCACC AAGTGCTGCT 1620 CTGCCTGTGT TCCCCCAGAC AGCCCCTGGT TGTGATTTGT CGTTTCCAGT CCAGCTAGAG 1680 TCCCAAGGCC AAGAACTAGA CCCTTGCAGC GAGATCCGCG CCCCCCCCCA CCCCACCCCG 1740 CCTCATTCTC CACAGGCGCC ACAGCCACAG GCCGCATAAA TAAATCCAGG TGGAGGCAGA 1800 CCCAGAAACC CAGGTGCTAT AAATATCCCA GCCCAGCCGG GAGACTGACC TCCCAGGCAG 1860 CCCCTCGCCC CCACCCGCCC TAGACCAGCA CTTCCGGCCA CCACAGCGCT GAGGGCGGAT 1920 CTCCCCGCGG TGGGAGGAGC GGGCTCCACC AGGATGCAGG CCTGGCTTCC CTTTCTTTCT 1980 TCTCCTGGGA GCCTCTGGCG GCCCAACCTG AGGGCTTGCC CTCTTCTCTG GAACCACCTC 2040 CCTAACTCTC AATCGCATAC CTCTCCCTCC CTCCCCCTGG TATTTTTAGA GAGGCCTTCT 2100 CTCAGGGACC CCATACTGCG ACCAGACTTC AAGAAATGCT GACTTCTCTT TCTAGATGAA 2160 TAAGCATAGT 2170
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