Tag | Content |
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EnhancerAtlas ID | HS044-13271 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr9:38045650-38048870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr9:38046525-38046540 | CATCTTGGGTGGTCA | - | 6.13 | Nr2f6(var.2) | MA0728.1 | chr9:38046007-38046022 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr9:38048102-38048123 | ACCTTCTCATCCCCCTCCTCA | - | 6.25 |
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| Number of super-enhancer constituents: 39 | ID | Coordinate | Tissue/cell |
SE_00446 | chr9:38045747-38049347 | Adipose_Nuclei | SE_01843 | chr9:38046152-38049346 | Aorta | SE_02310 | chr9:38046305-38049227 | Astrocytes | SE_04803 | chr9:38046770-38048376 | Brain_Cingulate_Gyrus | SE_05785 | chr9:38046345-38048668 | Brain_Hippocampus_Middle | SE_23246 | chr9:38046063-38049111 | Colon_Crypt_1 | SE_24298 | chr9:38046599-38048217 | Colon_Crypt_2 | SE_24298 | chr9:38048224-38048921 | Colon_Crypt_2 | SE_26555 | chr9:38045401-38049172 | Esophagus | SE_27864 | chr9:38045888-38049329 | Fetal_Intestine | SE_28791 | chr9:38045859-38049065 | Fetal_Intestine_Large | SE_31580 | chr9:38045924-38049491 | Gastric | SE_33929 | chr9:38045505-38049339 | HCC1954 | SE_34811 | chr9:38045382-38049638 | HeLa | SE_36884 | chr9:38046003-38048334 | HMEC | SE_38030 | chr9:38045868-38049525 | HUVEC | SE_38998 | chr9:38046222-38048950 | IMR90 | SE_40993 | chr9:38046204-38048239 | Left_Ventricle | SE_40993 | chr9:38048259-38049182 | Left_Ventricle | SE_41666 | chr9:38046198-38048280 | LNCaP | SE_42283 | chr9:38045806-38049314 | Lung | SE_44329 | chr9:38046297-38049224 | NHDF-Ad | SE_44779 | chr9:38046563-38049370 | NHLF | SE_45758 | chr9:38045918-38049671 | Osteoblasts | SE_47196 | chr9:38029911-38057164 | Panc1 | SE_47459 | chr9:38046113-38048759 | Pancreas | SE_48861 | chr9:38046201-38048278 | Right_Atrium | SE_51847 | chr9:38046298-38048909 | Skeletal_Muscle_Myoblast | SE_52833 | chr9:38045965-38049401 | Small_Intestine | SE_55662 | chr9:38045991-38049449 | u87 | SE_57367 | chr9:38046058-38048166 | VACO_503 | SE_57367 | chr9:38048192-38049021 | VACO_503 | SE_57926 | chr9:38046119-38048165 | VACO_9m | SE_57926 | chr9:38048223-38048625 | VACO_9m | SE_63571 | chr9:38046244-38049004 | HSMM | SE_64986 | chr9:38046170-38049325 | NHEK | SE_65279 | chr9:38044665-38046524 | Pancreatic_islets | SE_67542 | chr9:38045991-38049449 | u87 | SE_69063 | chr9:38047228-38048255 | H9 |
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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 |
GH09I038045 | chr9 | 38045447 | 38049805 |
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Enhancer Sequence | CAATTTCCTA CCACTTTGTA ATGAACCTGA CTATACAACG TGAGATCCTA CACAGCACAA 60 CACAGGTACA ATAAAAACGG TGCATTTTAA AAAGACGTAT GTTTTTTGAC ATGAGAACGT 120 GGGCAACTTC TGTGCAATGT AAAGATTGAT TAAAGATCTT CTAGCGTGTC TAGGCCAGAG 180 ACAGCTTGAA AGAAACCAAG AGGGAGTGGG GTCAAAACAA TCAGGTCAAA ATGGGTATGT 240 ATAAAACACA GAGATTACAA GTTAACATGG GTCATGATTA TGAAAAGAGG CACCAGGCAC 300 AGGTGGCTCA CGCCTGTAAT CCTAGCACTT TGGGAGGCAG AGGAGGGCGG ATCACCTGAG 360 GTCAGGAGTT CAAGACCAGC CTGGCCAACA TGATGAAACC CTGTGTCTAC TAAAAATACG 420 AAAATTAGCC AGGCGTGGTG GTGTGTGCCT GTAATCCCAG CTATTCAGGA GGCTGAGGTG 480 GGAGAATCGC TCAAAACCGG GAGGCGGAAG TTGCAGTGAG CCGAGATAAG AAAAAAAAAG 540 AAAAGAGGCA CCTAATGTTT TCAGCCAGGG TTGGGCAAAG CTTCACTTCT GTAAGTAAAG 600 CATTGCTGAA CGTGGCCAGG CCTGCTCATT TATATATTGT CTGTGGCTCC CTGAAGAAGT 660 GAACAGAGGC AACAGAAACC GTGTTGCTGC AAAGCCTGAA ATACTATTTG GCCCTTTACA 720 GAAAAAGTTT GTGACCTCTG TGTTAGACAC ATAAGAATTG AATACAGGCA AACAAGAACA 780 AGCAGTTGCC CTGAGGGCAA TATACTGATG CTCGAAGCCC CCCCGGGTCC TCCTTCTCCG 840 AGTAGGGCCC TCAGGAGACA CCACATTCCT CTGAACATCT TGGGTGGTCA ATCTTCCATA 900 CTCTGGAGTG GATTTAATTT CTAGAAACTG CCCACGGCTT TTCCAAACCA ATTTAGGTGA 960 AAAGGTGGGT GATCACGCCA AGCAATGAAA CATACAAACT TGCCAGGGGC AGGACGCAAG 1020 CCTCTAACAC GGAAGGAATT GAAATCGCAA TGAGATGTGG CTTCATTGTA AAGTTGCACA 1080 ACTTGGTTTC TTGTGTCTCA TTAATTGGGG ACAACAGTCA TATAATGTTT GGGCCTCGGC 1140 CTGACAGGCC TGACAGTAAA AATCCCTTCG TCGCTTGTGG CTTATGACTA CCTCTTACAA 1200 GACAAACCAC ATTCCACAGG AACCTGCGGT CTGGAGAGGG CTGTTAAGGG CTGTCCTGGG 1260 AAGTTTTTGG AAAAGATGGG GCCTGGTGAG AGAAAAGAAC ACCTGGCCTT TTTACAAATG 1320 CAGACACTGT GGCCCAGGGA GGGGAGGGGC CTTGCCAACA TCACCTAGCC ATGGCACCTC 1380 AAGGTTCAAC GTACCCAAAG TGGCCAGTGT TTCAGGTTCA GTGCCAGCTG TGGGGGATGA 1440 GTGAAAAATG AGTTCATGTT CTCCAAGAGT CCAGTCCCTG GTATCCAGAT AACACAGGAA 1500 TGTCAATAAA AACAGAGAAG TTTGGCAGGC CTTGGGTATG TCCCCTGACC TCTCCAAGTC 1560 TGCTTACTTG TATGAAAAAT AGTATCTTCC TTACACAATT CCTGTGAGGA CTCCAATGAG 1620 AGATGTACCT GAAGCACCCA GCAGAGTATA GCATACAGTA AGTGCTCAAC TGAAAGCAGC 1680 TAATCACTTC AGGCACAAGG CTGAGCTATT TTCTAGTTGC AGCGGTCCAA TCTTCTTACC 1740 CACAAGTGTG TACACACACC TCCCCTTCGG TGCAGAAAAC TGGAGACTGC AAGGCTTCAC 1800 TGAGCACCTG TCCTGTGTGA GGAATGGCCC TGCCTGCCTC CAACAGGGAA GTTAACAGAG 1860 GGGAAAACTG CAATCTGGCT CTGGAACTGC AACATTCCTA CCCCTCTTGG CTAATGCCTT 1920 CAGCAGGACC ACAATTATAA ACACAGAACT AACAGGAACT GAGAAACAGC AGCAGATCAA 1980 AAAGCAGGTT GCTCTTGCTT TTGGAGGATG TGAGACAGAT TTCTTCCAAA GAGGCAAGGG 2040 AAAATCCCCC ATCTTTACAG GTCAGGAATA GCGCCAGTAA ATCCCTCCAC TTTGTCCTTT 2100 CTCCTTTCAT GGAATAGCCC AATGCGCCAG TGGGTGTTAA GCAAACAAGG GTGTGAGTTG 2160 CAGCTTCCTG TGCCTGACTA TGCAGTTCCC GCACAGGTCC TTGCCCGAGC TAACGCTGTG 2220 GCCCCGGACA CAGACAGATA AAGTCCCGAT CGAACACTAA GGGCCAAAGC TGGCACCAAT 2280 GAGCAAGCCT GGTGAGCTTA TATAACAAAG GGCTTGTCAC CACTTCCTGT GATCCTCATC 2340 GCCAGCATTC CAACACAATG AGACACTCAG CGGCTTTGAA GTTCAACAAC TCATTCAGAT 2400 GGCCCCAGCA AAAACTCTGC TGGGAGGTGG AGAGCCTGTG CTCCCTTACC TCACCTTCTC 2460 ATCCCCCTCC TCACGTTGTG CTTGCAATGT TACCACTTCA AAAAAATTTC CAATAGTAAT 2520 TAAATGATTT GCATTTGTTT TTAAAAACTG TAAAATATTC CAACCTTCCA GCGATAACCA 2580 GTGTATACAT TTTGGTCGAT TTCCTTCCAG TCTTTTTTCT ACATATGTCG GTGGGAATGC 2640 AGTAATTGGA AAAGAATACA AATATTCATC ATTTTTTATA TCCTGCGTTT AAAAAAGTAT 2700 TACTTCTGGC CAGTTGCAGC AGCTCATGCC AGTAATCCTA GCACTTTGGG AACTGAGGTG 2760 GGAGGATCAC TTGAGTTTGA GATCAGCCTG GGCAGCACAG TGAGAGCCTG ACTCTACATA 2820 AAATTTTTAA ATTAGCTGGG CATGGTGGTG AGTGCCTGTA GTCCCAGCTA CGTGGGAGGC 2880 TGAGTCTGGA GGATCTCTTC AGCCCTTGAG GTGGAGGTTG CTGTGAGCTA TGATGGCACT 2940 GTTGCACTCT AGCCTGGGTG ACATAGCAAG GCCCTGCCTC AAAATAATAA TGATAAATAC 3000 ACATACAAAA AATGAAAAAG TATTACATTG TTGAGTGTTT TCCATCTTAA CGATATTGCA 3060 GTGGAGTTAC TCAACTCAGC TTTTGTTGGC TGTATTCCCT CTCACTTTAG GCCACACGTT 3120 AGCCACTTCC CATGGCTGGA TATTTAGGTA ATTTCCAGTT TTTGGTTTTG CCAAATGTTT 3180 TAGGTGCTTT TCCCTAGGAG GGCACCACTG GGTTCCCAGG 3220
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