Tag | Content |
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EnhancerAtlas ID | HS122-00891 |
Organism | Homo sapiens |
Tissue/cell | LoVo |
Coordinate | chr1:156064890-156067660 |
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 | JUN(var.2) | MA0489.1 | chr1:156065195-156065209 | ATGAGTCACTCCCC | - | 6.13 | 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(var.2) | MA0728.1 | chr1:156064938-156064953 | TGAACTCCTGACCTC | - | 6.22 | 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 | Rxra | MA0512.2 | chr1:156065511-156065525 | GGGGTTAGAGGTCA | + | 6.09 | Rxra | MA0512.2 | chr1:156065864-156065878 | TGACCTCTGACCCA | - | 6.12 | Zfx | MA0146.2 | chr1:156065391-156065405 | CCCGCCTCGGCCTC | + | 6.01 |
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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 | TGTATTTTTA TTAGAGATGT GGTTGCACCA TGTTGGCCAG GCTGGTCTTG AACTCCTGAC 60 CTCAGGTGAT CTGTCCTCCT CAGCCTCCCA AAGTGATGGG ATTACAGGCG TTAGCCACTG 120 CACCCGGCCA ACTCCCAGTG CTTTCAAAGC CAGTTTGTGT GTTCATGTTA CTCGGACTGA 180 TCGCTCTCCA TGAATAAGGG ATGTGTCTCT CCAAAACCTA GCATATAGGA GGCATTCAAT 240 AAAAATTTAT TGAGTAAATG ATTGATTGAA TGAATGAAAG GAATAAAATG ACCATGTGAT 300 ACTGAATGAG TCACTCCCCA TCTCAGTTTC CTCTTCTCAA GTGATTCTCC TGCCTTAGCC 360 TCCTGAGTAG CTAGGATTAC AGGCACCTGC CACCACACCC AGCTAATGCT TTTTTTTTTT 420 TTCTTTTTTG TATTTTTAGT AGAGACGGGG TTTCACCAGG TTGGGCAGGC TGGTCTCGAA 480 CTCCTGACCT CAGGTGATCC ACCCGCCTCG GCCTCTCAAA GTGCTGGGAT TACAGGCGTG 540 AGCCACTGCG CCCGGTGTCC AAGACACTTC TAACGCCAAC ATCCTTGTAC TAGGCCCTCT 600 TCCAGCTCCC CCAGGAGTCT GGGGGTTAGA GGTCAGGCTG CTCCCCACTC TATTACCTCC 660 CCACACTTCT AATTAATTCT TGTGTTCAGT CCCAGAACCT GGAGAGTTAC ACTCAGGCTG 720 CCTGGTCCTG CTTATTGCCC ATATCCTAGA GGCACTTGCA TGCCCTTCCA GGCGGGTAAC 780 TGTACATGTC TCTCCCAGGC AGCCTTCACA GACTACTCAG GGGTATGGAT TGGCTCCAGC 840 TCTGACACTC AGACCTGAGC AGAGGCGTGA TCTACTCTGG CCTCCTGTGT TTCTGTGCCC 900 CACCTTCCCA CACTGCCCAG GGCTCCCTGA GAGTGATGCT GAGTCTAGTC TCAGCTTTTA 960 TGTTGCTTTG CTTTTGACCT CTGACCCAAC ACATGCCTCC TTTCCCTCTG AAGTCTTGAT 1020 TTTCTCCCTG GCTTTTCTCC ACCTTCTGGG TGTTCCTTTT TGGCCTTCTT TGCCCATCTC 1080 TCCTCCTCTG TCTACACAGC CAGGGGCTCC CCCTTCCGTT TCCTCTGCCT GGAACACACT 1140 TGCTTCTCCC TTTCTGACTG GCTATTCAAG CAGGATCCTG TAGGTGGGTG GCAGTGCACT 1200 GTGTATTACC TGTGAGCCCT ATGCAAATTA CCGCACATCT CTGAACCTGT TTTCCCATCT 1260 ATAAAGTGAA GCTAATAGTA GCAATTACCT CATGGGATTG TTGTGCAATT AGTGGGAAGA 1320 GGCATGTAAA GTACTGACAT ACTGTCTAGT ACACAGAAAG TGCTTAATAA ATGTTGGTGA 1380 TTATTATCCA GGACTCAGCT TAATCATCCC TTCCTCAGGC AGGCCTGCCA CACAACCGCA 1440 GACCGGGTTA GGTGCCGGGT TTTCTGCTCC CCAGCGTTTG GAGGCACTCA TCACACATTA 1500 ATTACTTTAT CCATGAAGAT GAAAGCTGTC TTTGGCACCC AGATGGTACT GAGTAAATAT 1560 CTGTGAATGA ATGAATGATG TGGAATGTCT CCTCTGGAAG GACACAGTCA GGGCCTCCTG 1620 CCACTCAGGA CTAGCCTGGA TGCACCCACA GGGAAGGAGA AGGTGGGGCT GGTCTCCGCT 1680 GGGCCAGCAG GTGGCGCCAG GGCCTGTCGG TCTCTCCCCT TGGCCACCTC CCTTGCGCTT 1740 GCTCATCTCA TGCCCAGGCG CTGAGGGTTC TCAGCTGGGG CAGGAGAGAT GGGGTCCTGA 1800 GGCCTGGGTG AAGTTCCAAG CCCTGGGGCT CGGGGGCAGA CTCTCGCTCA CCCCTCCCAG 1860 AAAGATGTTT TCCTAGGGGA TGTCCAGCCT AACACGGCAG GGAAGGAAGT GGTGGTCACC 1920 TGGGAAAGGG GCCAACCTGA GAGGTTGGGG GTCCTGATGA GGCTGCTATT CTCTTGAGGA 1980 CATGAAATGA GAGGCGGTGA AGTCAGTCAG TGAGTCAAAA GCTGAGATCT AGGAACCAGA 2040 CACAATGTGG GAGAAGCTGC GGTGAAATCA ATCAGTGAGA GAGGAAGGGG AGGCCCGGTT 2100 TCCATGACAA CGGTAGTGTT TGTGGCAAGC TGGGGACTCC TGGGTCCCCA GGGCCCGCAA 2160 GCAGTGATTC ACCACAGGAA AGGGAAGGCT GCAGAGTGAC CTGGTGCTGG GGACCGGATG 2220 CCTTGTGGCT CCTTCTCACT GCTGAGCATG CATTCCCCCA GCCCAGGCCT TGGATCTCTG 2280 CTCTGCCAGC TACTGGCAGG GAAACTGAGG GATGGCAGAA CTGAGCCCCA ATAAGGGGCA 2340 GGCGCTTTGC TCCACGCCGT ACATGCACAT ATCACTTATA TCACTTATTG CTCACAACAG 2400 TCCTATGGAA TTACCGTTAT CCCTGTTTTA TCAAAGAGGA AACTCTCAGC CTGGCCCACG 2460 GTGCCATGGG CAGGACATGA GTGGCAGAGC CAGGATTGGA ACCCAGGCTA GCCTGACTCT 2520 TTACCATGCT TGGGAAGGCC CAGAAAGCAG AAAAGGAAGA GCAGGAGCAT GAGAGTTAGA 2580 GGATGGTTCA GACCCCAGAG GAGATGGACC CCAAGGCCCC TAGCCTCCCT GCCTGCCCTG 2640 CCCTATGCGA GCCCAACACT GATACGGAGG AAAGCTGGCC AACTGCATGG CCTAATGTGG 2700 GCCAGAACCT GGGCAGCCAG CCTACCTCTC ACTCTCCTCC AAGCCCAAGA GAGTAGGCCC 2760 CAGTTCCAGT 2770
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