Tag | Content |
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EnhancerAtlas ID | HS087-04789 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr12:6290510-6293390 |
SNPs | Number: 2 | 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 | GTGTGTCTAT GTTCCTGGGT GTGTGTCTGT ATGTGTGTAC CTATATGTGT GTGTGTGTGT 60 ATCTATATGT GTATGTGTCT GTATGTGCAT GTGTCTGTAT GATGTGTCTA TGTGTCTCTA 120 TGTGTGTGTG TCTGTACGTG TGTGTGTATC TATATATGTG TCTGTGTGTC TGTGTGTGTG 180 TGTGTGTGTG TGTGTGTGTG TGTGTTGGGA AATGGCAGTG GCAGGTGCAC TATATGGTGG 240 AGACACTGGG TTTTAGGCTT TAATGAGTTT GGGTTTTACC CCCAAGAAAC TGGGGGTAAA 300 AGAGGGAATA AAAGCAAAAC ATCCCATGCC CTCAAGGAAC GTCTAGTCCA GGATTAGAAG 360 TGGGGCAGTC CCAGGAAGGA GCCATCTTGA CAGTGAATTC ACGCGGAAGA CGCGTGAACC 420 CAGCTGGCCT GGAGAGACAG AGGTGCTTTG CAGGGCATGG GGAAGCCAGC AGGTCCCAGT 480 CGAGAAACCT GGTTTTCTGT CTGGGTTGGT TGAAGACTCT TTGTCCCAGA AGGAGTCGCT 540 TGTTTGCTTG TTCATCTTAA GTTTAAATTG AGAGAGGTTA ACGGCTTTTG CCTCAGAAGG 600 CAGGCTGGCC TGGCAGGGTG TGTGTTGTGA GGTGCAGAAA CACATCTTCC CCAGCTGGCC 660 TCACAGGCCA AGAAGCAGAT AATGTCTTCC TTCTGCCAGC TTCCCCGCAG CTTGGTTTTC 720 CTGGGACAGT TCCTCCGCTG GAGGAAGGGA CAGGGGATGG GGACAGGGGA TGGAGGAGGA 780 GTTGGGGAGA CCCTTCAGAG AGTGTGGCAG AAACACGTGT GTACAGGCTG GCACACGAGT 840 CACAGAGGCA ACAGGGTGGC TGCGGGGAGA AATGTGAGCA GAGCTCATGC AATTGTCGTG 900 AGTGAGTGCG CTCTCGCGGC TCTAAGGATT TGGGAAAACA ACTTGCAGAT CCAGGCATGT 960 TTACGTAGGG AGGGGTGCCG TGTGCTGGAC CAGGTCCAGA ACTAAAAATA ACACAGTATT 1020 TCTGTGCCCA GCAAGAGCGC TAGCATCTGT GGGGTTTGCG TGGTGGGAAG AGTGTGGTTT 1080 CAGCTGAACC AGGCGCAGTG TGACCAGAAC AGTAGGAGGG AAGGCCAGGC CTGGGTGGGA 1140 GGCCCCAGGA TGGGCGGGGG AAGGACTGAG GGCGAAGGCC ATCCCAACTC GCAGCAGAAA 1200 AAGCCTCCAG GCGGTCACGG GCTGCCCATC TCGTGAGGCC AGATGTGGGT CCTCCTGCAT 1260 ATCTGAAACA GCACAGAGCA TTGGGGCAGC CTCCAAACCT CCCCTATAAG GAGCAGTTAA 1320 GGGATCCAGA GGGCGTGGCC TGGAGCAGAG AGAAGGGAAG CAACATGTGT GGGGCATTCA 1380 CAAGTGCAGG ATGCCTTCTC CGGGCTCCCA TGATGATCCA GACAGGTAGG CGTTTTCCTT 1440 CCCTTTTTGC AGATTGTGAA AACAGCGTTC AAAAAAGACT CATGGGCCGG GCGCGGTGGA 1500 TCACGCCTGT AATCCCAGCA CTTTGGGAGG CCAAGGCAGG CAGATCACAA GGCCAGGAGT 1560 TGAAGACCAA CCTGGCCAAC ATGATGAAAC CCTGTCTCTA CTAAAAATAC AAAAATTAGC 1620 CGGACGTGAT GGTGGGCACC TGTAATCCCA GCTACTCAGG AGGCTGAGGC AGGAGAATCG 1680 CTTGAAACCG GAAGGCAGAG GTTGCAGTGA GCCGAGATTG CGCCACTGCA CTCCAGCCTG 1740 GTCAATAAGA GTGAAACTCT GTCTCAAAAA CAAACCAACC AACAAACCAA AAACTCTTGT 1800 AACCCTGGGG CCACCCAGCC ACAAAGAGGC AGGGCTGGGA CAGGCCCCTG CAAGTCTCCT 1860 CTGGAAGGCC AAAGGGCTGC TACTAGGAAG GGGTGGCAGA CTCATCCCAT GTGGCTTCAG 1920 AGGGCAGGAC ATGGACAAAG GTTATGGGAA GGGAGGGAAA CTTTCCAATA ACCAGACTGC 1980 ACAAGAGTGG AGTGGCCTGC CTCAGGAGGG GTAAGCTCAT GCAAAAGCTG GCTGTTGGGG 2040 ACATTGGGAG GGACTCTGAA GGTCACCACC ACTCTGAATC AATGCTGTGT GGGAGGATGC 2100 CAGGGTCCAC TGGACCCATG ACGTGCCTTT AGCGTGGGAA GCAGGGAACC TCAACTTTGG 2160 AAAGAGTGAG GGCACAGTGA TGTCCAGCCA CTCCCAGAAG CCGTCTGTTA ATAGAGCAAC 2220 CCCTCGGGCG GTGTGCAATC CTAATGACCA GCCCCAGGAC ATTGGAAACA GGGTCCTGCT 2280 GACCACAGTC TAGGAGACAG GGCTGCACAC AGACGGAACC AAGCACACAA GACGAGAGAG 2340 GGTGTGTACC GCAGAAACCA AGGGCTCATT TATGTGCTGC GTTCTCAGTC TGCAAGGAGT 2400 CAGAAGAGAG GACAGTGAGG CCAGGAGAAC TCAGGGAACA CTCCTTGTTG TAATCATCAC 2460 AGTTATGTAA CTCATATTAC CAGCTGTTCT TTCGTGAGCA TTCTCTATGT GCCAGGCTAA 2520 GTGTTTTGTA TGCACTGTAT GATTTAATCC TAGAACAACA CTATGAAGCA GGAGCTCTTA 2580 GTATTCCCCT TTTACAGATG AGGAGGCAGG CTCAGAGAGG TGATGTAACT TGCCCAGAAT 2640 TATATAACTA GTGTGTGGCA GAGCCTGGAC TCAAGCCCAG ATCTGTTGGA CTCCAGACCC 2700 CGTGTAGAAC CATAAGGAAC TGATGCTGCT TCAATTTCTG CACTGATACG GAAATCTCTC 2760 CGAGATATCA TGCCGTTGTT TTCTATTGTT GCTATAGCAT ATTATCACAA GTTTAACACA 2820 TATTTATTGC ACACTTCTGG AGGTCAGCAG TCTGACATGT GGGTCTCACT GGGCTAAAAT 2880
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