Tag | Content |
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EnhancerAtlas ID | HS092-23850 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:42327820-42330250 |
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 | TCTTCTCATG CCTCCACTCC CCAGTATAGT GTAAAGCGGC CTCCTCACTC AGGCCCAGGT 60 CAAGACTGAC CTCAGTGCCA CCCTCCCGGC TCTGCCTCTA AACTTCACCC ACCACAATGC 120 AGCCAACAAT CTCACAAGGG GCCGGCCTCT CTCTCAGGGC AAGCCTCATC CCCTAGAAGC 180 CGACTCCGCC TGGCCCACCA TGCCTGCAGC AGAAAGGCCT GAGGCTGGGC CTAGAACACT 240 GAGGACGTCA GTGGCCAGGA CTTTCCAAAG CTGAAACTGG GACCTGCGGA GGCCTCACTG 300 TCCGGAGCAG CGTCCAGGTC CTCAGCATCC TCTTCGCTGG GCCCCACGCG TGTCGTGCGC 360 CACCCCAGAA GGCAGGGCCT GATTCGGATC AGCAGGGGCT GCAGGGCCGC TCTGCAGGTG 420 GGTGACTCAG GCCCCTCTTG AACCCTTAGG CCTGAGGCAG AGACTGGGCA GGAGGCTGGG 480 CGTGGCCGGG GAGCCCCTTC ACGTGCTCCC CTTCTCGAGG GTTCACGGGG CTCTGGAGGC 540 CCAGATGCTG GCAAAGTGGC GGGAGCGCTC CAGGGACGAG GACTCAGGTC GGGGCGCCCC 600 CGCCAGCGCC AGGATCCCCG CTCACCCTCC GCCGCGCCCC GCCCCCGCCC CGACACACTG 660 GGGGAGCCCC GCCCTCCCCG AGGCCCGCGC GGCGCCGCAG GAGGAATCCC AGCCATTTCC 720 TCCACGCTGC GCGGTATGTG GCCTGCCCGC CGCCAACCGC AGCGCGAGCC GGTCCCCAGC 780 CGCGCCTGGC AGCTGCCCCG GCTCCGCCGT GCTGCTCGGG ATTCCGGGAA GGCCGCCCCC 840 TCGTCCCGGG CCACCAGACC GGCCTTTCCA GCGGCTCCAG GCCCGTGCAG TCCCGCCGGA 900 CGCCGGCTAC ACCACGCGCC GCTGCTGGAA CCTCTCCCAG CCCCGCGTGG CCGCCCCCGG 960 CCCAGGCACC CCCTCCCCGG AACGCCCCCG ACGGCCCCTC GCGTCCGAGC TGGAAACTGA 1020 AGTTGACGCT TGCTCCGTCA CCCTGGGGCA AATTGCTTTG CCTAAGCCTC AGTTTCTCCA 1080 TCTGTGAAAT GGGGACGTTG GCAGGAGTGC CTGTCTCGTT GTGCTGCCCG AGGGGTGAAT 1140 GAGAAAAGGA AAGCGTTGGA CTACTGTCAA CGCGATTTTC ATTTCCCTAG GTACCACGAG 1200 GGTCCTGGCT TTTCGCACAG GATCTTAGCA CCCACCCTGC CCCTCGCCTC TCCTCCAGCC 1260 CAGTTGCCGG TGGAGCAAGC AGGCCGGGCT TTGCGAGTGG GCAGAGGAGA GGGCTGGGGC 1320 CTGCCCAAGA CTGCGCCCTG CACAGATTAA ACAATGCCTG AAGGTCCCAC GACACAGCCT 1380 TCCTCGAGAT TCACCGTTGC CCTCTCCTCA ATCACTAGGT TCTTGAAAGA CCCAAAGGAC 1440 AGTTATTTAC ATTTTTTTTA AATGATGTCA TCGCAGTCTG AGAGCAGCCA GACACGTAGT 1500 GATCAGGGAA AGTCGAAAGT GCAGATGGGT TCGCAAACGT GGACTCTCTA GTTTTGGGTC 1560 TGCAGATGGG GCCGGCCACC ACGTGCTCTC TGAGTTCTCT TTCCAAGTAC AGATCCCTCC 1620 GGAGACGGAA CATTGTTCCG CCTTTAATTC TTCCCAGGAG CTGCGGAGGA AGGCGTGAGA 1680 ACCGGAGCCC GGGGTGACTT GCGGGGGAGG GGATCGCTTC CCCGTCGCCC ACACCTGCCT 1740 AACCCACGCC CACGGCGGCC GCAAAGGCGA CACCGCGTGA ATCTGGAAAG CCCCGAGTTT 1800 CAACAGGCCC AACCATCGGC GGCTTTGCAG GCGCAGCACC AAGTGCTGCT CTGCCTGTGT 1860 TCCCCCAGAC AGCCCCTGGT TGTGATTTGT CGTTTCCAGT CCAGCTAGAG TCCCAAGGCC 1920 AAGAACTAGA CCCTTGCAGC GAGATCCGCG CCCCCCCCCA CCCCACCCCG CCTCATTCTC 1980 CACAGGCGCC ACAGCCACAG GCCGCATAAA TAAATCCAGG TGGAGGCAGA CCCAGAAACC 2040 CAGGTGCTAT AAATATCCCA GCCCAGCCGG GAGACTGACC TCCCAGGCAG CCCCTCGCCC 2100 CCACCCGCCC TAGACCAGCA CTTCCGGCCA CCACAGCGCT GAGGGCGGAT CTCCCCGCGG 2160 TGGGAGGAGC GGGCTCCACC AGGATGCAGG CCTGGCTTCC CTTTCTTTCT TCTCCTGGGA 2220 GCCTCTGGCG GCCCAACCTG AGGGCTTGCC CTCTTCTCTG GAACCACCTC CCTAACTCTC 2280 AATCGCATAC CTCTCCCTCC CTCCCCCTGG TATTTTTAGA GAGGCCTTCT CTCAGGGACC 2340 CCATACTGCG ACCAGACTTC AAGAAATGCT GACTTCTCTT TCTAGATGAA TAAGCATAGT 2400 TGGAAGGCAA CAACCTCAAT CAGAGTTTAC 2430
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