Tag | Content |
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EnhancerAtlas ID | HS045-14206 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr12:6289400-6292040 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Rxra | MA0512.2 | chr12:6289509-6289523 | TGACCCTTAACCCC | - | 6.23 | 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 | chr12:6289433-6290385 | Adrenal_Gland | SE_00985 | chr12:6290507-6292062 | Adrenal_Gland | SE_01613 | chr12:6287777-6290458 | Aorta | SE_01613 | chr12:6290594-6292119 | Aorta | SE_03988 | chr12:6287691-6290093 | Brain_Anterior_Caudate | 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 | chr12:6289496-6290357 | Colon_Crypt_1 | SE_23086 | chr12:6290753-6292057 | Colon_Crypt_1 | SE_23760 | chr12:6289538-6290171 | Colon_Crypt_2 | SE_23760 | chr12:6290811-6292000 | Colon_Crypt_2 | SE_24754 | chr12:6289387-6290267 | Colon_Crypt_3 | SE_24754 | chr12:6291005-6292084 | Colon_Crypt_3 | SE_25881 | chr12:6290586-6291938 | Duodenum_Smooth_Muscle | SE_26531 | chr12:6287925-6290403 | Esophagus | SE_26531 | chr12:6290619-6292172 | Esophagus | SE_27879 | chr12:6290695-6293924 | Fetal_Intestine | SE_28805 | chr12:6290511-6293953 | Fetal_Intestine_Large | SE_30052 | chr12:6288016-6290605 | Fetal_Muscle | SE_30052 | chr12:6290681-6292144 | Fetal_Muscle | SE_31631 | chr12:6289050-6290342 | Gastric | 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_48662 | chr12:6287969-6292096 | Right_Atrium | SE_50072 | chr12:6287999-6290419 | Sigmoid_Colon | SE_50072 | chr12:6290476-6292094 | Sigmoid_Colon | SE_52457 | chr12:6287948-6292107 | 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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I006177 | chr12 | 6286985 | 6293820 |
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Enhancer Sequence | GGGGACACAA CACAACAGGT GTGCCGTGAC CGAGACAGAG ATGGGAGGAA CAGAAAAAGC 60 CACCCTGACA GGCAGCATGG GAGGGGTGAT GAGCAAGTTC TTGTTTTGTT GACCCTTAAC 120 CCCTCTGTAC TCCCTACAGG AGCCACTTCC CTGGCGTGCT TCCCCAGCCC GGCTGACTCA 180 CTGGACAGGA AAAGGAAGGG CAGGAATTCA GGCCGATGAG CCAGGGACCC TCACCTCTGG 240 CCGGGCCTGG CACAGCCTCC TGGGGAGCCC CCGCACACCA GCCCTCCCGG CACCACTCGG 300 TGTGTCCTGC CTGGCTGATG GGCAGCCACG TATGCCCCAC CCTCCCCTGA CCGTGCCCAC 360 TTACCCAGGG GCCCAGCTGT CTTGGCTGGC AGGCTTCCAT TGCAAGTCAC TCCTCCATCC 420 ACACAGATCA CTCACGTCCC TCATTCCGTC CCTCGTTCCA CAGAGCGTGT TGACACCCAC 480 TGCGGGGCAG GCCTGGCTGC AGGCCTGGAG ATGCAACAGC AGCAAAAGGA GCAGCCCCTG 540 CCCCAGGAGG CTCCCATTCA AGTGAAGGAG GCAGACGAAA GGCCACAACA GTCGAGTGCA 600 CACTGTCAGA TGGCGATGAG GGCCAAGGAG GCACAGCAGC AGGGGAGGGG ATAGGGAAGG 660 CCCCGGTGGG CTGGGCTGCG TGAGCCACCT CTGACAAGGG TGCCTGGGAG CAGAGGCCCA 720 AAGGATTGGA CAGAACCAGC CATGTGGATC CTGGGGGAGA GGATCCAGGC TGAGGAAGCA 780 GCAAGGGCTC AGGCGAGAGC GGGAGTGCCC CCATCCTTTC CAAGAAACAC CCACGAGTCC 840 AGGGTCTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTATCTA TATGTGTGTG 900 TCTGTATGAG TATGTGTCTG TATGATGTCT GTGTGTCTTT ATGTGTGTGT GTCTGTGTAT 960 CTATATGTGT GTGTCTGTAT GTGTATGTGT CTGTATGATG TCTGTGTGTC TTTATGTGTG 1020 TGTCTGTGTG TATCTATGTG TGTATGTGTG TGTCTGTATG TGTATGTGTC TGTATGATGT 1080 CTGTGTGTCT TTATGTGTGT GTGTCTGTGT GTGTGTCTAT GTTCCTGGGT GTGTGTCTGT 1140 ATGTGTGTAC CTATATGTGT GTGTGTGTGT ATCTATATGT GTATGTGTCT GTATGTGCAT 1200 GTGTCTGTAT GATGTGTCTA TGTGTCTCTA TGTGTGTGTG TCTGTACGTG TGTGTGTATC 1260 TATATATGTG TCTGTGTGTC TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTTGGGA 1320 AATGGCAGTG GCAGGTGCAC TATATGGTGG AGACACTGGG TTTTAGGCTT TAATGAGTTT 1380 GGGTTTTACC CCCAAGAAAC TGGGGGTAAA AGAGGGAATA AAAGCAAAAC ATCCCATGCC 1440 CTCAAGGAAC GTCTAGTCCA GGATTAGAAG TGGGGCAGTC CCAGGAAGGA GCCATCTTGA 1500 CAGTGAATTC ACGCGGAAGA CGCGTGAACC CAGCTGGCCT GGAGAGACAG AGGTGCTTTG 1560 CAGGGCATGG GGAAGCCAGC AGGTCCCAGT CGAGAAACCT GGTTTTCTGT CTGGGTTGGT 1620 TGAAGACTCT TTGTCCCAGA AGGAGTCGCT TGTTTGCTTG TTCATCTTAA GTTTAAATTG 1680 AGAGAGGTTA ACGGCTTTTG CCTCAGAAGG CAGGCTGGCC TGGCAGGGTG TGTGTTGTGA 1740 GGTGCAGAAA CACATCTTCC CCAGCTGGCC TCACAGGCCA AGAAGCAGAT AATGTCTTCC 1800 TTCTGCCAGC TTCCCCGCAG CTTGGTTTTC CTGGGACAGT TCCTCCGCTG GAGGAAGGGA 1860 CAGGGGATGG GGACAGGGGA TGGAGGAGGA GTTGGGGAGA CCCTTCAGAG AGTGTGGCAG 1920 AAACACGTGT GTACAGGCTG GCACACGAGT CACAGAGGCA ACAGGGTGGC TGCGGGGAGA 1980 AATGTGAGCA GAGCTCATGC AATTGTCGTG AGTGAGTGCG CTCTCGCGGC TCTAAGGATT 2040 TGGGAAAACA ACTTGCAGAT CCAGGCATGT TTACGTAGGG AGGGGTGCCG TGTGCTGGAC 2100 CAGGTCCAGA ACTAAAAATA ACACAGTATT TCTGTGCCCA GCAAGAGCGC TAGCATCTGT 2160 GGGGTTTGCG TGGTGGGAAG AGTGTGGTTT CAGCTGAACC AGGCGCAGTG TGACCAGAAC 2220 AGTAGGAGGG AAGGCCAGGC CTGGGTGGGA GGCCCCAGGA TGGGCGGGGG AAGGACTGAG 2280 GGCGAAGGCC ATCCCAACTC GCAGCAGAAA AAGCCTCCAG GCGGTCACGG GCTGCCCATC 2340 TCGTGAGGCC AGATGTGGGT CCTCCTGCAT ATCTGAAACA GCACAGAGCA TTGGGGCAGC 2400 CTCCAAACCT CCCCTATAAG GAGCAGTTAA GGGATCCAGA GGGCGTGGCC TGGAGCAGAG 2460 AGAAGGGAAG CAACATGTGT GGGGCATTCA CAAGTGCAGG ATGCCTTCTC CGGGCTCCCA 2520 TGATGATCCA GACAGGTAGG CGTTTTCCTT CCCTTTTTGC AGATTGTGAA AACAGCGTTC 2580 AAAAAAGACT CATGGGCCGG GCGCGGTGGA TCACGCCTGT AATCCCAGCA CTTTGGGAGG 2640
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