| Tag | Content |
|---|
EnhancerAtlas ID | HS037-07843 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr12:6291000-6292780 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP1 | MA0079.4 | chr12:6291837-6291852 | AGAGGGCGTGGCCTG | - | 6.15 |
|
| | 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 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I006177 | chr12 | 6286985 | 6293820 |
|
Enhancer Sequence | GGTTTTCTGT CTGGGTTGGT TGAAGACTCT TTGTCCCAGA AGGAGTCGCT TGTTTGCTTG 60
TTCATCTTAA GTTTAAATTG AGAGAGGTTA ACGGCTTTTG CCTCAGAAGG CAGGCTGGCC 120
TGGCAGGGTG TGTGTTGTGA GGTGCAGAAA CACATCTTCC CCAGCTGGCC TCACAGGCCA 180
AGAAGCAGAT AATGTCTTCC TTCTGCCAGC TTCCCCGCAG CTTGGTTTTC CTGGGACAGT 240
TCCTCCGCTG GAGGAAGGGA CAGGGGATGG GGACAGGGGA TGGAGGAGGA GTTGGGGAGA 300
CCCTTCAGAG AGTGTGGCAG AAACACGTGT GTACAGGCTG GCACACGAGT CACAGAGGCA 360
ACAGGGTGGC TGCGGGGAGA AATGTGAGCA GAGCTCATGC AATTGTCGTG AGTGAGTGCG 420
CTCTCGCGGC TCTAAGGATT TGGGAAAACA ACTTGCAGAT CCAGGCATGT TTACGTAGGG 480
AGGGGTGCCG TGTGCTGGAC CAGGTCCAGA ACTAAAAATA ACACAGTATT TCTGTGCCCA 540
GCAAGAGCGC TAGCATCTGT GGGGTTTGCG TGGTGGGAAG AGTGTGGTTT CAGCTGAACC 600
AGGCGCAGTG TGACCAGAAC AGTAGGAGGG AAGGCCAGGC CTGGGTGGGA GGCCCCAGGA 660
TGGGCGGGGG AAGGACTGAG GGCGAAGGCC ATCCCAACTC GCAGCAGAAA AAGCCTCCAG 720
GCGGTCACGG GCTGCCCATC TCGTGAGGCC AGATGTGGGT CCTCCTGCAT ATCTGAAACA 780
GCACAGAGCA TTGGGGCAGC CTCCAAACCT CCCCTATAAG GAGCAGTTAA GGGATCCAGA 840
GGGCGTGGCC TGGAGCAGAG AGAAGGGAAG CAACATGTGT GGGGCATTCA CAAGTGCAGG 900
ATGCCTTCTC CGGGCTCCCA TGATGATCCA GACAGGTAGG CGTTTTCCTT CCCTTTTTGC 960
AGATTGTGAA AACAGCGTTC AAAAAAGACT CATGGGCCGG GCGCGGTGGA TCACGCCTGT 1020
AATCCCAGCA CTTTGGGAGG CCAAGGCAGG CAGATCACAA GGCCAGGAGT TGAAGACCAA 1080
CCTGGCCAAC ATGATGAAAC CCTGTCTCTA CTAAAAATAC AAAAATTAGC CGGACGTGAT 1140
GGTGGGCACC TGTAATCCCA GCTACTCAGG AGGCTGAGGC AGGAGAATCG CTTGAAACCG 1200
GAAGGCAGAG GTTGCAGTGA GCCGAGATTG CGCCACTGCA CTCCAGCCTG GTCAATAAGA 1260
GTGAAACTCT GTCTCAAAAA CAAACCAACC AACAAACCAA AAACTCTTGT AACCCTGGGG 1320
CCACCCAGCC ACAAAGAGGC AGGGCTGGGA CAGGCCCCTG CAAGTCTCCT CTGGAAGGCC 1380
AAAGGGCTGC TACTAGGAAG GGGTGGCAGA CTCATCCCAT GTGGCTTCAG AGGGCAGGAC 1440
ATGGACAAAG GTTATGGGAA GGGAGGGAAA CTTTCCAATA ACCAGACTGC ACAAGAGTGG 1500
AGTGGCCTGC CTCAGGAGGG GTAAGCTCAT GCAAAAGCTG GCTGTTGGGG ACATTGGGAG 1560
GGACTCTGAA GGTCACCACC ACTCTGAATC AATGCTGTGT GGGAGGATGC CAGGGTCCAC 1620
TGGACCCATG ACGTGCCTTT AGCGTGGGAA GCAGGGAACC TCAACTTTGG AAAGAGTGAG 1680
GGCACAGTGA TGTCCAGCCA CTCCCAGAAG CCGTCTGTTA ATAGAGCAAC CCCTCGGGCG 1740
GTGTGCAATC CTAATGACCA GCCCCAGGAC ATTGGAAACA 1780
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