Tag | Content |
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EnhancerAtlas ID | HS154-04142 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr11:75022430-75024010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SREBF2 | MA0596.1 | chr11:75023777-75023787 | ATGGGGTGAT | + | 6.02 | TFAP2C | MA0524.2 | chr11:75022753-75022765 | AGCCCCAGGGCA | + | 6.11 | ZNF263 | MA0528.1 | chr11:75023176-75023197 | CCTCTCCCTTCTCCTTCCTCC | - | 6.86 | ZNF263 | MA0528.1 | chr11:75023179-75023200 | CTCCCTTCTCCTTCCTCCACC | - | 7.29 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00135 | chr11:75016201-75027347 | Adipose_Nuclei | SE_03287 | chr11:75022298-75024209 | Brain_Angular_Gyrus | SE_04031 | chr11:75020093-75025864 | Brain_Anterior_Caudate | SE_04951 | chr11:75011977-75027109 | Brain_Cingulate_Gyrus | SE_05927 | chr11:75011975-75026931 | Brain_Hippocampus_Middle | SE_07122 | chr11:75020120-75026037 | Brain_Hippocampus_Middle_150 | SE_07907 | chr11:75011958-75027094 | Brain_Inferior_Temporal_Lobe | SE_13386 | chr11:75022344-75023722 | CD34_Primary_RO01536 | SE_23271 | chr11:75022374-75023957 | Colon_Crypt_1 | SE_24003 | chr11:75022650-75023773 | Colon_Crypt_2 | SE_25192 | chr11:75022381-75023965 | Colon_Crypt_3 | SE_25898 | chr11:75021122-75025829 | Duodenum_Smooth_Muscle | SE_26962 | chr11:75022396-75025702 | Esophagus | SE_28109 | chr11:75022444-75023821 | Fetal_Intestine | SE_29208 | chr11:75022428-75023853 | Fetal_Intestine_Large | SE_31429 | chr11:75022250-75025778 | Gastric | SE_42220 | chr11:75019878-75027219 | Lung | SE_46889 | chr11:75022715-75023607 | Ovary | SE_47208 | chr11:75022351-75024084 | Panc1 | SE_50175 | chr11:75022398-75024164 | Sigmoid_Colon | SE_52494 | chr11:75022371-75025749 | Small_Intestine | SE_53599 | chr11:75022306-75025821 | Spleen | SE_54712 | chr11:75022246-75025882 | Stomach_Smooth_Muscle | SE_65484 | chr11:75021917-75025888 | Pancreatic_islets |
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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 |
GH11I075311 | chr11 | 75022321 | 75025870 |
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Enhancer Sequence | AGGAGCAGCT CCATTCTTTC TGGGATGGGC AGGGGGCTGT TGAGAAAGTT GCAGAGAGCA 60 GGTGACATCT GAGCTGGACT TGAAGCACAA TGAAGAGTTT GTCAGATTGT CAAATTGCAG 120 AAGAGAACGT TAAAGGAACA GGCTATGCAT GGAATGCACA TCCTTACATA GCAGACTGCA 180 CATTTCAAAA ATCAGTTCAA AATCACAATC TCGTTTCACC CTCTCAAATC CCATAATGGT 240 GTTATTAACT GCCTCTCCCA CGGCCCTCCA CCTGCCACAC ACAGGCAAAC AAAAAAAGTA 300 AGGTCCAGTG AAGGCAGATG GTGAGCCCCA GGGCAAACAA ACGGTGACTG ATTTCTGAGT 360 AGAGGGAAGT GAGGGGTGGA CTCTGGCTGA AATGGTCCTC TTCTCACTGA AGTGGGGGAT 420 TCCTGAATTC CTGTCCGGCG GCAGCACCCC ACTTCGGCCC CTGCTGGCCT GTGACACCCT 480 CCTCTCATCC CCAGCATACA CACACACTCC TCCGGCCACC AGGGCCTGTC AGAAGGGGCT 540 GGCTGAGAGG GGACGGCCGG CAGAGGAACC AAGCAGCAGG GCCTGGGCCG AGGGGCTGGG 600 AAAAAGCTGA CCGTTCTCGA AGGCCCAGAT CGGAGGCCCT GCCCAGCCTC TTCCCCTCCT 660 CTAAGTGCTG ATCACCTCAG CCTCTCCCGC TGCAAGTCTC CTTCCATGGC CTCTCCTCTC 720 CCATCTCTTG CAGTGGCTGC TGCTGGCCTC TCCCTTCTCC TTCCTCCACC CTCGCCCTCC 780 CCGGGGAGTG GTGAGCTCAG CCTTTCCCAG CAGCCGTCCC TAGGAATGAT GGGAAATGCA 840 CCGCCAGGAA CTGAGAACAG GCCTGCCCCT GGGAAGGAGT GGGAGAAGAG GCGTCAGGGA 900 CAGGGCTCAA GTCTGCCACT TCCTAGGACC CCTGACCGCC GAAGGGACAG TCTGCCTGTG 960 TGTACTGCAC GCTGGAAGGA CATGGGCTCA GACTGTGTGG ACTGCCAGGG ACCTTGTCTT 1020 ACAGATGGGG AGACAAAGGC CCCAGGAGAG GAGAAAGGGG ACTGACTGCC TGTCCCAGGC 1080 ATTGGGAGCC TTTCATTGTC TCATGTCATC CTCACAACTG CTCTGCAAGG TGTGTGTGGT 1140 AGGCTGAGTA ACAGCCCCCC GAGATGCCCA CATCCTAATC ACCAGAGCTG TGGCTGTGTT 1200 GGGTCATGTG GTAGAAGAGA TTCTGCAGAT GTGATTTTGT TCAGGGCCTT GAGATGGAGA 1260 GATTATCCTG CATGACCTGG GTGGGCCCAA TGTCATCACA AGGGTCCTGA CAAGAGGGAG 1320 GCAGGAGGGT CAGAGAGAGT AAAGGCAATG GGGTGATGGA AGCATTGAAA GACAGACGAA 1380 AATCTACACT GCTGGCTTCA AAGCTGGAGG ATGGGGCTGG GAGCCAAGGC ATGCAGACAG 1440 CTTCTGGAAG CCAGCAGAGG CAAGGGAATG GATCCCCGCT AGAGTTTCCA GAGGACACAG 1500 CCCTGACAAC CCATTTCAGG ACTTTGGACC TCCAGAAGTG TAAAGAATAT ATTTGTGTTG 1560 TTTTAAGCCA CTAAATATAT 1580
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