Tag | Content |
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EnhancerAtlas ID | HS105-25674 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr14:95948700-95951140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arid3b | MA0601.1 | chr14:95948780-95948791 | TTAATTAATAT | - | 6.62 | FOS | MA0476.1 | chr14:95949719-95949730 | TGTGACTCATT | + | 6.62 | Lhx3 | MA0135.1 | chr14:95948777-95948790 | TAATTAATTAATA | + | 6.25 | Lhx3 | MA0135.1 | chr14:95948774-95948787 | AATTAATTAATTA | - | 6.78 | Lhx3 | MA0135.1 | chr14:95948773-95948786 | AAATTAATTAATT | + | 6.92 | POU6F1 | MA0628.1 | chr14:95948775-95948785 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr14:95948779-95948789 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr14:95948775-95948785 | ATTAATTAAT | - | 6.02 | POU6F1 | MA0628.1 | chr14:95948779-95948789 | ATTAATTAAT | - | 6.02 | ZNF143 | MA0088.2 | chr14:95949843-95949859 | CAATGGATTCTGGGAA | - | 6.05 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_00648 | chr14:95942213-95958964 | Adipose_Nuclei | SE_01178 | chr14:95949063-95949732 | Adrenal_Gland | SE_01178 | chr14:95949842-95950512 | Adrenal_Gland | SE_02016 | chr14:95948732-95951037 | Aorta | SE_05018 | chr14:95948717-95950188 | Brain_Cingulate_Gyrus | SE_05914 | chr14:95945570-95953183 | Brain_Hippocampus_Middle | SE_07492 | chr14:95948854-95950445 | Brain_Hippocampus_Middle_150 | SE_08083 | chr14:95948735-95950654 | Brain_Inferior_Temporal_Lobe | SE_09499 | chr14:95948665-95954411 | CD14 | SE_19409 | chr14:95948879-95950655 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19409 | chr14:95950667-95951851 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_24540 | chr14:95949214-95949718 | Colon_Crypt_2 | SE_24540 | chr14:95949980-95950257 | Colon_Crypt_2 | SE_50603 | chr14:95948779-95951045 | Sigmoid_Colon | SE_54167 | chr14:95949011-95950606 | Spleen | SE_59423 | chr14:95945702-95991197 | Ly3 | SE_62638 | chr14:95923241-95991137 | 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: 1 | ID | Chromosome | Start | End |
GH14I095479 | chr14 | 95945829 | 95951039 |
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Enhancer Sequence | GCAGAGGTTG CACTGAGAAG AGATTGCGCC ACTGCACTCC AGCCTGGGTG ACAGCGAGAC 60 ACCATCTCAA AATAAATTAA TTAATTAATA TTATCTGGGA ATTTGAAAAC ACTAATTCTT 120 GTCATTCAGT GATCCAGAGG CTCCAAGAAT CCTGCTCAGG TCCTAACCCA ATCTCGTTAG 180 CGAACTCCCC TGAAACATGA GAGCAAGCCC CTCCCGAGCA AAGAAAGCGG CAACGTCAGT 240 TTCAGGGAGT GACTGTCATG TGGCGGGCAT TATTTGTCCC ATTTTACAAA GAGGGAAACT 300 GAGACTCGGA GACACAAACA GTCTGCTGAA AAGTGGTGGA CCCAGGTCCA CCAATGACAG 360 TAAAAGCCGA CATTTACCCG GTGTTCTGCA GGTGCCTGAC TGTATGACAA AAGGTTTGTA 420 GGTATTAACT CACTTATCCT ACATAGGCCC AGTGACACAT TCACATTATC CCTACTTTAC 480 AGCTGAGAAA ACAGGTTTAA TGATACTAAC AACGCTGCCC AAAGTCACCG GGATGCTAAG 540 TAGCAGAGGC AAGACTTGAA CCAAGGATGA CTTGAGTCTA AACTCTTTGC TATTAAATCC 600 CCTGGTGCCA CACAGCTTCC ACGGCCCTCT CTGTCCCTCC CAGAACCCCA CTGGTAACTG 660 CCGAGTTCCA GGAAGGTAAC TCCAGGGCAG GAATCTATCT TGAGCTGCAG CTCAAGAATC 720 TAGAGTTCAG GGAAACCAAC TGAGCCCCCC AGCTGCCAGG CAGCCTCCGT CACACTGTGC 780 CCGCTCACTC CAGCCCTGTG CCAACCCAGC TGCCCACTGA CATTCTGCTC TGGAACTCAG 840 AAGGCGTTGG GATTCAGACC CAGGTAAACC CAGGTAAAAC CCCAGCTCCC ATGGCAGGCC 900 CCATTAGCGA TTACAGCCTG GTGCCCCTGC TCTGTCAAGC TGGCCGGGGC CGCCCACCAC 960 AAGCTGACCC AGAGTTCTGG CATGGGCGTG CTCGCTTGCC GTGACTCACT CGGCTGTCCT 1020 GTGACTCATT CCTGCCCTGC CACACACATT CCCACCCTTA TCCTCTCTTT CCCACTGCTC 1080 TCTTATGCTT GGATGTTATT TCAGGAACTG AGTTACAGCT GGTCTTAATC CCAAAGCTTT 1140 TTCCAATGGA TTCTGGGAAC ACAATTTTGT TTATTTATCA CAGAGGAGGT TGCACCAAGA 1200 GGATAGACCT TGGCAATCTT CTCCTCTGTG GCACTGGCAG AAGGTGATTC TCAGAACAAA 1260 GTGTGTGAAA GGAGGGATAG GAACTCAACG GTAGCGCCCA TGCATTATCT CATTTAATCT 1320 CACAACAACC CTGCCAGGCA GCTAATCCAA AGTGAGGAGC AATTACTGGG CTTCATTCCG 1380 CCTTAGAGGT GAGCAGACAG AGGCTTGGCA GGTTAAGGGA CTGCACCAAA GCCATGCGGG 1440 CTGCAGGGCC ACGCCACCCT CTGTCCACCA GCTAGGCATG GTTACACAAG AAGTCCCACC 1500 TTGGAAAGGG TTGTGAGGTC TACTCTACAA TTACAGCCAC AAAGGACACT GGCCAGGGAC 1560 TGCTTTGGAG GCAAGCGGTC CCGAAGCCAT TTTAAGTCAG TCCCACTGTC ACAGACCGGT 1620 GGTGTCTGGT AGGGAAAGCC AGCTGCTCTC TGATGCACCT GCTTCTCCAG ATACGCCAAC 1680 CATAAAACCC ATTTCCAGTC TCTCTTCAAT GAATGAAACC CAAGTTCCCT AGGCATAGTC 1740 TGGAGGATGC CAGGATTTCC ACCTGGGAAG TGCTGGCCTT GGCAACACAC AAATACAGGT 1800 GTTTGAGAGG GAGAGAAGAC ACCAGGGCAG CTAAGAGGGA AATGGGACAG AGTGGAGGGG 1860 GCAGAGTGTA TGCAAGGTAA AAAGAGGTCC CCAGCCGTGG TAGGGATGAA GGCCAGGCTG 1920 CTGCAGAGAT ATGTTCCTAG GGCAGGGTGG GTGGCTCCAA GGGGTGGGGC CTTAGCTCTT 1980 GGGACCAGGT GTGATCGTCT CAGGCTCCAA TTGGACACTT TGAAGGGGAG GGCTCCCAGG 2040 AGGTTCAAGG GGGCTCCTGA GGGGAACCCT GGCCACGGAG TAACAGGGGC TGCTGGCAGT 2100 GTGGGCGGAG CCGGTCAGAG GGCAGGCAGG CAGGGCACTG GCCATCTGCT GCAGGTCAGA 2160 GAGCACTGAG CAGGGTACCA GGGCACAGGT ACCAGCCTGG CTGGAACATT GAGTGCCATG 2220 GGCCACTGGT GTGTGGACAA GCCAGTCAAT GCAGCGGGGT TGGTACTGGC TTTTCACACT 2280 GGGAGTGTGA CTTATGCATG GGTTGTGAAA TCTACTCAGG GGTCTTGATC AAAAGTGCTT 2340 TGTAAGGAAA GAAGATAGAA TAGAATGAAA AATATCACAG TGCCTCTCAT GGATGAAGGA 2400 TAAATACTGT TTCATGAGAC TGTTGCTTGT TTGATGGATG 2440
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