Tag | Content |
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EnhancerAtlas ID | HS042-09728 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr12:6289250-6292270 |
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 | TAAAGGATCC CAATCATAGA GGGCTAGGGG CCCACTCTCC TCTAGTCCAA CCTCATTTTA 60 ATTTAACTAA TTCCCTCTGC AGCAACCCTA TCACCAACTA AGTTCACATT CTGAGGCACC 120 GGGGATGAGG ACCTCAACAT AGGAATCTGG GGGGACACAA CACAACAGGT GTGCCGTGAC 180 CGAGACAGAG ATGGGAGGAA CAGAAAAAGC CACCCTGACA GGCAGCATGG GAGGGGTGAT 240 GAGCAAGTTC TTGTTTTGTT GACCCTTAAC CCCTCTGTAC TCCCTACAGG AGCCACTTCC 300 CTGGCGTGCT TCCCCAGCCC GGCTGACTCA CTGGACAGGA AAAGGAAGGG CAGGAATTCA 360 GGCCGATGAG CCAGGGACCC TCACCTCTGG CCGGGCCTGG CACAGCCTCC TGGGGAGCCC 420 CCGCACACCA GCCCTCCCGG CACCACTCGG TGTGTCCTGC CTGGCTGATG GGCAGCCACG 480 TATGCCCCAC CCTCCCCTGA CCGTGCCCAC TTACCCAGGG GCCCAGCTGT CTTGGCTGGC 540 AGGCTTCCAT TGCAAGTCAC TCCTCCATCC ACACAGATCA CTCACGTCCC TCATTCCGTC 600 CCTCGTTCCA CAGAGCGTGT TGACACCCAC TGCGGGGCAG GCCTGGCTGC AGGCCTGGAG 660 ATGCAACAGC AGCAAAAGGA GCAGCCCCTG CCCCAGGAGG CTCCCATTCA AGTGAAGGAG 720 GCAGACGAAA GGCCACAACA GTCGAGTGCA CACTGTCAGA TGGCGATGAG GGCCAAGGAG 780 GCACAGCAGC AGGGGAGGGG ATAGGGAAGG CCCCGGTGGG CTGGGCTGCG TGAGCCACCT 840 CTGACAAGGG TGCCTGGGAG CAGAGGCCCA AAGGATTGGA CAGAACCAGC CATGTGGATC 900 CTGGGGGAGA GGATCCAGGC TGAGGAAGCA GCAAGGGCTC AGGCGAGAGC GGGAGTGCCC 960 CCATCCTTTC CAAGAAACAC CCACGAGTCC AGGGTCTGTG TGTGTGTGTG TGTGTGTGTG 1020 TGTGTGTGTG TGTGTATCTA TATGTGTGTG TCTGTATGAG TATGTGTCTG TATGATGTCT 1080 GTGTGTCTTT ATGTGTGTGT GTCTGTGTAT CTATATGTGT GTGTCTGTAT GTGTATGTGT 1140 CTGTATGATG TCTGTGTGTC TTTATGTGTG TGTCTGTGTG TATCTATGTG TGTATGTGTG 1200 TGTCTGTATG TGTATGTGTC TGTATGATGT CTGTGTGTCT TTATGTGTGT GTGTCTGTGT 1260 GTGTGTCTAT GTTCCTGGGT GTGTGTCTGT ATGTGTGTAC CTATATGTGT GTGTGTGTGT 1320 ATCTATATGT GTATGTGTCT GTATGTGCAT GTGTCTGTAT GATGTGTCTA TGTGTCTCTA 1380 TGTGTGTGTG TCTGTACGTG TGTGTGTATC TATATATGTG TCTGTGTGTC TGTGTGTGTG 1440 TGTGTGTGTG TGTGTGTGTG TGTGTTGGGA AATGGCAGTG GCAGGTGCAC TATATGGTGG 1500 AGACACTGGG TTTTAGGCTT TAATGAGTTT GGGTTTTACC CCCAAGAAAC TGGGGGTAAA 1560 AGAGGGAATA AAAGCAAAAC ATCCCATGCC CTCAAGGAAC GTCTAGTCCA GGATTAGAAG 1620 TGGGGCAGTC CCAGGAAGGA GCCATCTTGA CAGTGAATTC ACGCGGAAGA CGCGTGAACC 1680 CAGCTGGCCT GGAGAGACAG AGGTGCTTTG CAGGGCATGG GGAAGCCAGC AGGTCCCAGT 1740 CGAGAAACCT GGTTTTCTGT CTGGGTTGGT TGAAGACTCT TTGTCCCAGA AGGAGTCGCT 1800 TGTTTGCTTG TTCATCTTAA GTTTAAATTG AGAGAGGTTA ACGGCTTTTG CCTCAGAAGG 1860 CAGGCTGGCC TGGCAGGGTG TGTGTTGTGA GGTGCAGAAA CACATCTTCC CCAGCTGGCC 1920 TCACAGGCCA AGAAGCAGAT AATGTCTTCC TTCTGCCAGC TTCCCCGCAG CTTGGTTTTC 1980 CTGGGACAGT TCCTCCGCTG GAGGAAGGGA CAGGGGATGG GGACAGGGGA TGGAGGAGGA 2040 GTTGGGGAGA CCCTTCAGAG AGTGTGGCAG AAACACGTGT GTACAGGCTG GCACACGAGT 2100 CACAGAGGCA ACAGGGTGGC TGCGGGGAGA AATGTGAGCA GAGCTCATGC AATTGTCGTG 2160 AGTGAGTGCG CTCTCGCGGC TCTAAGGATT TGGGAAAACA ACTTGCAGAT CCAGGCATGT 2220 TTACGTAGGG AGGGGTGCCG TGTGCTGGAC CAGGTCCAGA ACTAAAAATA ACACAGTATT 2280 TCTGTGCCCA GCAAGAGCGC TAGCATCTGT GGGGTTTGCG TGGTGGGAAG AGTGTGGTTT 2340 CAGCTGAACC AGGCGCAGTG TGACCAGAAC AGTAGGAGGG AAGGCCAGGC CTGGGTGGGA 2400 GGCCCCAGGA TGGGCGGGGG AAGGACTGAG GGCGAAGGCC ATCCCAACTC GCAGCAGAAA 2460 AAGCCTCCAG GCGGTCACGG GCTGCCCATC TCGTGAGGCC AGATGTGGGT CCTCCTGCAT 2520 ATCTGAAACA GCACAGAGCA TTGGGGCAGC CTCCAAACCT CCCCTATAAG GAGCAGTTAA 2580 GGGATCCAGA GGGCGTGGCC TGGAGCAGAG AGAAGGGAAG CAACATGTGT GGGGCATTCA 2640 CAAGTGCAGG ATGCCTTCTC CGGGCTCCCA TGATGATCCA GACAGGTAGG CGTTTTCCTT 2700 CCCTTTTTGC AGATTGTGAA AACAGCGTTC AAAAAAGACT CATGGGCCGG GCGCGGTGGA 2760 TCACGCCTGT AATCCCAGCA CTTTGGGAGG CCAAGGCAGG CAGATCACAA GGCCAGGAGT 2820 TGAAGACCAA CCTGGCCAAC ATGATGAAAC CCTGTCTCTA CTAAAAATAC AAAAATTAGC 2880 CGGACGTGAT GGTGGGCACC TGTAATCCCA GCTACTCAGG AGGCTGAGGC AGGAGAATCG 2940 CTTGAAACCG GAAGGCAGAG GTTGCAGTGA GCCGAGATTG CGCCACTGCA CTCCAGCCTG 3000 GTCAATAAGA GTGAAACTCT 3020
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