Tag | Content |
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EnhancerAtlas ID | HS178-01688 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr1:156065480-156068060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr1:156066188-156066199 | TGTTGTGCAAT | - | 6.14 | CTCF | MA0139.1 | chr1:156066570-156066589 | GGGCCAGCAGGTGGCGCCA | + | 7.82 | NR2C2 | MA0504.1 | chr1:156065864-156065879 | TGACCTCTGACCCAA | - | 6.32 | NR2C2 | MA0504.1 | chr1:156065510-156065525 | GGGGGTTAGAGGTCA | + | 6.51 | NR2F1 | MA0017.2 | chr1:156065860-156065873 | CTTTTGACCTCTG | - | 6.59 | Nr2f6 | MA0677.1 | chr1:156065864-156065878 | TGACCTCTGACCCA | - | 6.37 | RFX1 | MA0509.2 | chr1:156066986-156067002 | GGTTTCCATGACAACG | - | 6.89 | RFX1 | MA0509.2 | chr1:156066986-156067002 | GGTTTCCATGACAACG | + | 6.91 | RFX2 | MA0600.2 | chr1:156066986-156067002 | GGTTTCCATGACAACG | - | 6.76 | RFX2 | MA0600.2 | chr1:156066986-156067002 | GGTTTCCATGACAACG | + | 6.88 | RFX5 | MA0510.2 | chr1:156066986-156067002 | GGTTTCCATGACAACG | - | 6.22 | RFX5 | MA0510.2 | chr1:156066986-156067002 | GGTTTCCATGACAACG | + | 6.3 | RREB1 | MA0073.1 | chr1:156067775-156067795 | CCACCCACCACCATCACCCC | + | 6.09 | Rxra | MA0512.2 | chr1:156065511-156065525 | GGGGTTAGAGGTCA | + | 6.09 | Rxra | MA0512.2 | chr1:156065864-156065878 | TGACCTCTGACCCA | - | 6.12 | TBX21 | MA0690.1 | chr1:156068038-156068048 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr1:156068038-156068049 | AAGGTGTGAAA | + | 6.62 |
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| Number of super-enhancer constituents: 45 | ID | Coordinate | Tissue/cell |
SE_00096 | chr1:156065452-156068563 | Adipose_Nuclei | SE_01581 | chr1:156065560-156068296 | Aorta | SE_02264 | chr1:156065996-156067725 | Astrocytes | SE_04119 | chr1:156066419-156067747 | Brain_Anterior_Caudate | SE_05125 | chr1:156065563-156067404 | Brain_Cingulate_Gyrus | SE_05929 | chr1:156065385-156069202 | Brain_Hippocampus_Middle | SE_08091 | chr1:156066374-156068302 | Brain_Inferior_Temporal_Lobe | SE_12411 | chr1:156066236-156067919 | CD3 | SE_13990 | chr1:156066343-156067150 | CD34_Primary_RO01536 | SE_14505 | chr1:156065871-156068273 | CD4_Memory_Primary_7pool | SE_16807 | chr1:156065659-156067859 | CD4_Naive_Primary_8pool | SE_17218 | chr1:156065550-156068458 | CD4p_CD225int_CD127p_Tmem | SE_17950 | chr1:156065300-156069187 | CD4p_CD25-_CD45ROp_Memory | SE_19616 | chr1:156065431-156069425 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20836 | chr1:156065575-156067852 | CD8_Memory_7pool | SE_23093 | chr1:156065378-156066171 | Colon_Crypt_1 | SE_25840 | chr1:156065674-156068547 | Duodenum_Smooth_Muscle | SE_26548 | chr1:156065336-156068204 | Esophagus | SE_27785 | chr1:156066105-156067222 | Fetal_Intestine | SE_28870 | chr1:156066270-156067179 | Fetal_Intestine_Large | SE_29555 | chr1:156065372-156068015 | Fetal_Muscle | SE_31480 | chr1:156066184-156067846 | Gastric | SE_34290 | chr1:156065319-156067522 | HCT-116 | SE_34622 | chr1:156065156-156067691 | HeLa | SE_35870 | chr1:156065471-156067456 | HMEC | SE_36976 | chr1:156065737-156067519 | HSMMtube | SE_37998 | chr1:156065282-156068432 | HUVEC | SE_40679 | chr1:156065452-156067998 | Left_Ventricle | SE_42123 | chr1:156065499-156068113 | Lung | SE_44150 | chr1:156065487-156068218 | NHDF-Ad | SE_44752 | chr1:156066014-156067478 | NHLF | SE_45674 | chr1:156065383-156068099 | Osteoblasts | SE_46650 | chr1:156066459-156067742 | Ovary | SE_47353 | chr1:156066082-156067442 | Panc1 | SE_48596 | chr1:156065694-156067966 | Right_Atrium | SE_50099 | chr1:156065286-156067986 | Sigmoid_Colon | SE_51113 | chr1:156065341-156068292 | Skeletal_Muscle | SE_52395 | chr1:156066354-156068063 | Small_Intestine | SE_53563 | chr1:156065686-156068198 | Spleen | SE_54528 | chr1:156065632-156069193 | Stomach_Smooth_Muscle | SE_55941 | chr1:156065931-156068449 | u87 | SE_63596 | chr1:156066572-156067180 | HSMM | SE_64308 | chr1:156065447-156067140 | NHEK | SE_65290 | chr1:156066034-156067742 | Pancreatic_islets | SE_67798 | chr1:156065931-156068449 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 156065683 | 156067549 | chr1 | 156066868 | 156067143 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I156095 | chr1 | 156065334 | 156069110 |
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Enhancer Sequence | TAGGCCCTCT TCCAGCTCCC CCAGGAGTCT GGGGGTTAGA GGTCAGGCTG CTCCCCACTC 60 TATTACCTCC CCACACTTCT AATTAATTCT TGTGTTCAGT CCCAGAACCT GGAGAGTTAC 120 ACTCAGGCTG CCTGGTCCTG CTTATTGCCC ATATCCTAGA GGCACTTGCA TGCCCTTCCA 180 GGCGGGTAAC TGTACATGTC TCTCCCAGGC AGCCTTCACA GACTACTCAG GGGTATGGAT 240 TGGCTCCAGC TCTGACACTC AGACCTGAGC AGAGGCGTGA TCTACTCTGG CCTCCTGTGT 300 TTCTGTGCCC CACCTTCCCA CACTGCCCAG GGCTCCCTGA GAGTGATGCT GAGTCTAGTC 360 TCAGCTTTTA TGTTGCTTTG CTTTTGACCT CTGACCCAAC ACATGCCTCC TTTCCCTCTG 420 AAGTCTTGAT TTTCTCCCTG GCTTTTCTCC ACCTTCTGGG TGTTCCTTTT TGGCCTTCTT 480 TGCCCATCTC TCCTCCTCTG TCTACACAGC CAGGGGCTCC CCCTTCCGTT TCCTCTGCCT 540 GGAACACACT TGCTTCTCCC TTTCTGACTG GCTATTCAAG CAGGATCCTG TAGGTGGGTG 600 GCAGTGCACT GTGTATTACC TGTGAGCCCT ATGCAAATTA CCGCACATCT CTGAACCTGT 660 TTTCCCATCT ATAAAGTGAA GCTAATAGTA GCAATTACCT CATGGGATTG TTGTGCAATT 720 AGTGGGAAGA GGCATGTAAA GTACTGACAT ACTGTCTAGT ACACAGAAAG TGCTTAATAA 780 ATGTTGGTGA TTATTATCCA GGACTCAGCT TAATCATCCC TTCCTCAGGC AGGCCTGCCA 840 CACAACCGCA GACCGGGTTA GGTGCCGGGT TTTCTGCTCC CCAGCGTTTG GAGGCACTCA 900 TCACACATTA ATTACTTTAT CCATGAAGAT GAAAGCTGTC TTTGGCACCC AGATGGTACT 960 GAGTAAATAT CTGTGAATGA ATGAATGATG TGGAATGTCT CCTCTGGAAG GACACAGTCA 1020 GGGCCTCCTG CCACTCAGGA CTAGCCTGGA TGCACCCACA GGGAAGGAGA AGGTGGGGCT 1080 GGTCTCCGCT GGGCCAGCAG GTGGCGCCAG GGCCTGTCGG TCTCTCCCCT TGGCCACCTC 1140 CCTTGCGCTT GCTCATCTCA TGCCCAGGCG CTGAGGGTTC TCAGCTGGGG CAGGAGAGAT 1200 GGGGTCCTGA GGCCTGGGTG AAGTTCCAAG CCCTGGGGCT CGGGGGCAGA CTCTCGCTCA 1260 CCCCTCCCAG AAAGATGTTT TCCTAGGGGA TGTCCAGCCT AACACGGCAG GGAAGGAAGT 1320 GGTGGTCACC TGGGAAAGGG GCCAACCTGA GAGGTTGGGG GTCCTGATGA GGCTGCTATT 1380 CTCTTGAGGA CATGAAATGA GAGGCGGTGA AGTCAGTCAG TGAGTCAAAA GCTGAGATCT 1440 AGGAACCAGA CACAATGTGG GAGAAGCTGC GGTGAAATCA ATCAGTGAGA GAGGAAGGGG 1500 AGGCCCGGTT TCCATGACAA CGGTAGTGTT TGTGGCAAGC TGGGGACTCC TGGGTCCCCA 1560 GGGCCCGCAA GCAGTGATTC ACCACAGGAA AGGGAAGGCT GCAGAGTGAC CTGGTGCTGG 1620 GGACCGGATG CCTTGTGGCT CCTTCTCACT GCTGAGCATG CATTCCCCCA GCCCAGGCCT 1680 TGGATCTCTG CTCTGCCAGC TACTGGCAGG GAAACTGAGG GATGGCAGAA CTGAGCCCCA 1740 ATAAGGGGCA GGCGCTTTGC TCCACGCCGT ACATGCACAT ATCACTTATA TCACTTATTG 1800 CTCACAACAG TCCTATGGAA TTACCGTTAT CCCTGTTTTA TCAAAGAGGA AACTCTCAGC 1860 CTGGCCCACG GTGCCATGGG CAGGACATGA GTGGCAGAGC CAGGATTGGA ACCCAGGCTA 1920 GCCTGACTCT TTACCATGCT TGGGAAGGCC CAGAAAGCAG AAAAGGAAGA GCAGGAGCAT 1980 GAGAGTTAGA GGATGGTTCA GACCCCAGAG GAGATGGACC CCAAGGCCCC TAGCCTCCCT 2040 GCCTGCCCTG CCCTATGCGA GCCCAACACT GATACGGAGG AAAGCTGGCC AACTGCATGG 2100 CCTAATGTGG GCCAGAACCT GGGCAGCCAG CCTACCTCTC ACTCTCCTCC AAGCCCAAGA 2160 GAGTAGGCCC CAGTTCCAGT CCATCCAACT GGATGGTAGC TCCCCCACCG TTTTCTCTCT 2220 GCCCTGGTCC TAGGGGCAGG GGTGCGTGTG CGTGTGTGCG TGCGTGTGTG TGTGTGTGTG 2280 ATCATCATGT CTACACCACC CACCACCATC ACCCCTATCC TCCAGCTTCT GCTATAGCCT 2340 GGGAGTTCCC AGCCTTTTAG TCCCTGTCAG GATAGTTTCA TTCTTGTTCA GCTTTGGGGC 2400 CCACACAATT TCAGTACAAA AGGGGTATGC CCATCTCACC CTGGGCCTTG ATAGCATGCA 2460 AGAGCATAGT TCAGGCCCTC ATCATCTATT CCCTTGTAGT AGAAGGGATG GAGGTTGGAA 2520 AGACCTTAGA AATCTTCCAG TCTGGTTCTC TTGTTTTGAA GGTGTGAAAG CTGAGGCTCA 2580
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