Tag | Content |
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EnhancerAtlas ID | HS032-00259 |
Organism | Homo sapiens |
Tissue/cell | DLD1 |
Coordinate | chr12:6290770-6293190 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP1 | MA0079.4 | chr12:6291837-6291852 | AGAGGGCGTGGCCTG | - | 6.15 |
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| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_00985 | chr12:6290507-6292062 | Adrenal_Gland | SE_00985 | chr12:6292206-6292982 | Adrenal_Gland | SE_01613 | chr12:6290594-6292119 | Aorta | SE_01613 | chr12:6292178-6293897 | Aorta | SE_03988 | chr12:6290792-6291792 | Brain_Anterior_Caudate | SE_04905 | chr12:6289324-6293306 | Brain_Cingulate_Gyrus | SE_05857 | chr12:6287388-6293430 | Brain_Hippocampus_Middle | SE_07876 | chr12:6289745-6293464 | Brain_Inferior_Temporal_Lobe | SE_23086 | chr12:6290753-6292057 | Colon_Crypt_1 | SE_23086 | chr12:6292201-6293938 | Colon_Crypt_1 | SE_23760 | chr12:6290811-6292000 | Colon_Crypt_2 | SE_23760 | chr12:6292242-6293084 | Colon_Crypt_2 | SE_24754 | chr12:6291005-6292084 | Colon_Crypt_3 | SE_24754 | chr12:6292220-6293863 | Colon_Crypt_3 | SE_25881 | chr12:6290586-6291938 | Duodenum_Smooth_Muscle | SE_25881 | chr12:6292265-6293935 | Duodenum_Smooth_Muscle | SE_26531 | chr12:6290619-6292172 | Esophagus | SE_26531 | chr12:6292175-6293815 | Esophagus | SE_27879 | chr12:6290695-6293924 | Fetal_Intestine | SE_28805 | chr12:6290511-6293953 | Fetal_Intestine_Large | SE_30052 | chr12:6290681-6292144 | Fetal_Muscle | SE_31631 | chr12:6290651-6293026 | Gastric | SE_34881 | chr12:6288010-6291925 | HeLa | SE_37709 | chr12:6286475-6292578 | HSMMtube | SE_37940 | chr12:6286549-6293824 | HUVEC | SE_41013 | chr12:6288021-6292951 | Left_Ventricle | SE_42122 | chr12:6287877-6292200 | Lung | SE_42122 | chr12:6292204-6293894 | Lung | SE_48662 | chr12:6287969-6292096 | Right_Atrium | SE_50072 | chr12:6290476-6292094 | Sigmoid_Colon | SE_50072 | chr12:6292172-6294061 | Sigmoid_Colon | SE_52457 | chr12:6287948-6292107 | Small_Intestine | SE_52457 | chr12:6292166-6294018 | Small_Intestine | SE_53862 | chr12:6287321-6293849 | Spleen | SE_54512 | chr12:6288437-6293993 | Stomach_Smooth_Muscle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 6292247 | 6292800 | chr12 | 6291358 | 6291755 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I006177 | chr12 | 6286985 | 6293820 |
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Enhancer Sequence | TAATGAGTTT GGGTTTTACC CCCAAGAAAC TGGGGGTAAA AGAGGGAATA AAAGCAAAAC 60 ATCCCATGCC CTCAAGGAAC GTCTAGTCCA GGATTAGAAG TGGGGCAGTC CCAGGAAGGA 120 GCCATCTTGA CAGTGAATTC ACGCGGAAGA CGCGTGAACC CAGCTGGCCT GGAGAGACAG 180 AGGTGCTTTG CAGGGCATGG GGAAGCCAGC AGGTCCCAGT CGAGAAACCT GGTTTTCTGT 240 CTGGGTTGGT TGAAGACTCT TTGTCCCAGA AGGAGTCGCT TGTTTGCTTG TTCATCTTAA 300 GTTTAAATTG AGAGAGGTTA ACGGCTTTTG CCTCAGAAGG CAGGCTGGCC TGGCAGGGTG 360 TGTGTTGTGA GGTGCAGAAA CACATCTTCC CCAGCTGGCC TCACAGGCCA AGAAGCAGAT 420 AATGTCTTCC TTCTGCCAGC TTCCCCGCAG CTTGGTTTTC CTGGGACAGT TCCTCCGCTG 480 GAGGAAGGGA CAGGGGATGG GGACAGGGGA TGGAGGAGGA GTTGGGGAGA CCCTTCAGAG 540 AGTGTGGCAG AAACACGTGT GTACAGGCTG GCACACGAGT CACAGAGGCA ACAGGGTGGC 600 TGCGGGGAGA AATGTGAGCA GAGCTCATGC AATTGTCGTG AGTGAGTGCG CTCTCGCGGC 660 TCTAAGGATT TGGGAAAACA ACTTGCAGAT CCAGGCATGT TTACGTAGGG AGGGGTGCCG 720 TGTGCTGGAC CAGGTCCAGA ACTAAAAATA ACACAGTATT TCTGTGCCCA GCAAGAGCGC 780 TAGCATCTGT GGGGTTTGCG TGGTGGGAAG AGTGTGGTTT CAGCTGAACC AGGCGCAGTG 840 TGACCAGAAC AGTAGGAGGG AAGGCCAGGC CTGGGTGGGA GGCCCCAGGA TGGGCGGGGG 900 AAGGACTGAG GGCGAAGGCC ATCCCAACTC GCAGCAGAAA AAGCCTCCAG GCGGTCACGG 960 GCTGCCCATC TCGTGAGGCC AGATGTGGGT CCTCCTGCAT ATCTGAAACA GCACAGAGCA 1020 TTGGGGCAGC CTCCAAACCT CCCCTATAAG GAGCAGTTAA GGGATCCAGA GGGCGTGGCC 1080 TGGAGCAGAG AGAAGGGAAG CAACATGTGT GGGGCATTCA CAAGTGCAGG ATGCCTTCTC 1140 CGGGCTCCCA TGATGATCCA GACAGGTAGG CGTTTTCCTT CCCTTTTTGC AGATTGTGAA 1200 AACAGCGTTC AAAAAAGACT CATGGGCCGG GCGCGGTGGA TCACGCCTGT AATCCCAGCA 1260 CTTTGGGAGG CCAAGGCAGG CAGATCACAA GGCCAGGAGT TGAAGACCAA CCTGGCCAAC 1320 ATGATGAAAC CCTGTCTCTA CTAAAAATAC AAAAATTAGC CGGACGTGAT GGTGGGCACC 1380 TGTAATCCCA GCTACTCAGG AGGCTGAGGC AGGAGAATCG CTTGAAACCG GAAGGCAGAG 1440 GTTGCAGTGA GCCGAGATTG CGCCACTGCA CTCCAGCCTG GTCAATAAGA GTGAAACTCT 1500 GTCTCAAAAA CAAACCAACC AACAAACCAA AAACTCTTGT AACCCTGGGG CCACCCAGCC 1560 ACAAAGAGGC AGGGCTGGGA CAGGCCCCTG CAAGTCTCCT CTGGAAGGCC AAAGGGCTGC 1620 TACTAGGAAG GGGTGGCAGA CTCATCCCAT GTGGCTTCAG AGGGCAGGAC ATGGACAAAG 1680 GTTATGGGAA GGGAGGGAAA CTTTCCAATA ACCAGACTGC ACAAGAGTGG AGTGGCCTGC 1740 CTCAGGAGGG GTAAGCTCAT GCAAAAGCTG GCTGTTGGGG ACATTGGGAG GGACTCTGAA 1800 GGTCACCACC ACTCTGAATC AATGCTGTGT GGGAGGATGC CAGGGTCCAC TGGACCCATG 1860 ACGTGCCTTT AGCGTGGGAA GCAGGGAACC TCAACTTTGG AAAGAGTGAG GGCACAGTGA 1920 TGTCCAGCCA CTCCCAGAAG CCGTCTGTTA ATAGAGCAAC CCCTCGGGCG GTGTGCAATC 1980 CTAATGACCA GCCCCAGGAC ATTGGAAACA GGGTCCTGCT GACCACAGTC TAGGAGACAG 2040 GGCTGCACAC AGACGGAACC AAGCACACAA GACGAGAGAG GGTGTGTACC GCAGAAACCA 2100 AGGGCTCATT TATGTGCTGC GTTCTCAGTC TGCAAGGAGT CAGAAGAGAG GACAGTGAGG 2160 CCAGGAGAAC TCAGGGAACA CTCCTTGTTG TAATCATCAC AGTTATGTAA CTCATATTAC 2220 CAGCTGTTCT TTCGTGAGCA TTCTCTATGT GCCAGGCTAA GTGTTTTGTA TGCACTGTAT 2280 GATTTAATCC TAGAACAACA CTATGAAGCA GGAGCTCTTA GTATTCCCCT TTTACAGATG 2340 AGGAGGCAGG CTCAGAGAGG TGATGTAACT TGCCCAGAAT TATATAACTA GTGTGTGGCA 2400 GAGCCTGGAC TCAAGCCCAG 2420
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