Tag | Content |
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EnhancerAtlas ID | HS047-11822 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr15:75952430-75954500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr15:75954298-75954311 | GGTGACAGCTGCA | - | 6.5 | Myog | MA0500.1 | chr15:75954301-75954312 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr15:75954301-75954312 | GACAGCTGCAG | + | 6.14 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00448 | chr15:75950549-75956919 | Adipose_Nuclei | SE_01620 | chr15:75949399-75957459 | Aorta | SE_02426 | chr15:75952557-75954556 | Astrocytes | SE_03062 | chr15:75953622-75954438 | Bladder | SE_24007 | chr15:75952770-75953200 | Colon_Crypt_2 | SE_25223 | chr15:75953125-75954151 | Colon_Crypt_3 | SE_26310 | chr15:75951695-75954782 | Duodenum_Smooth_Muscle | SE_26676 | chr15:75950618-75960618 | Esophagus | SE_30075 | chr15:75952287-75954521 | Fetal_Muscle | SE_31932 | chr15:75951252-75954515 | Gastric | SE_34597 | chr15:75952501-75954488 | HCT-116 | SE_36093 | chr15:75952406-75954880 | HMEC | SE_37864 | chr15:75951836-75955030 | HSMMtube | SE_41356 | chr15:75952281-75954601 | Left_Ventricle | SE_42347 | chr15:75950358-75957604 | Lung | SE_44203 | chr15:75951679-75957628 | NHDF-Ad | SE_44859 | chr15:75952132-75954746 | NHLF | SE_45931 | chr15:75952243-75954914 | Osteoblasts | SE_46892 | chr15:75952424-75952725 | Ovary | SE_46892 | chr15:75952820-75954363 | Ovary | SE_47752 | chr15:75953278-75953909 | Pancreas | SE_48850 | chr15:75951340-75954548 | Right_Atrium | SE_50411 | chr15:75951368-75957615 | Sigmoid_Colon | SE_52931 | chr15:75952661-75954579 | Small_Intestine | SE_53820 | chr15:75951189-75954605 | Spleen | SE_56214 | chr15:75952763-75956620 | u87 | SE_64409 | chr15:75952140-75954652 | NHEK | SE_65676 | chr15:75951303-75952771 | Pancreatic_islets | SE_65676 | chr15:75952976-75954759 | 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 |
GH15I075658 | chr15 | 75951061 | 75963062 |
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Enhancer Sequence | CTGGACCCAG CTGCCTCGTT TCCTCCCTTA CTTTGCTCTG AGGGGGTGGA AAACAAGGCT 60 TCTCTTTCTG CCCTGGACAG CTACCAGCAC CCGGGGTAGG GGATCCCCTG GTCACCAGTC 120 TTGGCCCAGT ACAGGAAAAG GAATCCGCTT TGTGGCCACA GATGGGGGCT GGGGATGGAA 180 GCAGACCTCA GATCCTGCAT CTCTTCACCC GCTGGACACA GGAGGGCTAT GAACCACTGT 240 GCCGTGGCTG CACCACTGGC TGGAGCAGAG CCAGGCCTGG GAGAGGCAGG TGGCCCCATC 300 GGCCCCTGCT CTGCACCACC CCTCCCAGAT GACAGAGCCA TATGTCTTCC ACGTGTCTAC 360 ACACTCACAG ACTCACGAAT GTAATCGCTC AGTCTCACAA CAAGCACACG CAGTCACACA 420 CCTGCCCACA GGCACATACG CCACATAAGC ATGCCTGTAT GCTCACACAG TCATACTGCC 480 ACACGCTATT ACACATTCAC AGCCACAGCC ACACATGCCT TGCCATCCAT TCAAAGCACC 540 AGTGGCTACT TTGTCAGACA CAGCCACACC ACAGTCCTAT GCACATGGTC ATAGCCTCAC 600 ACAGTGACAC ATACTCGGGC ACACACCGCC ACAAAGCCAT GCTTGCACAG AGCAAAGGTG 660 TCATAAGCAT CTCTGTGCCT GGACTGCACC TGCATGACCT CCCAGGGTCC CCACCTCATC 720 AGAGATTAAG GAGAGCTTTG CTTGGAGACA CCACCCCTGG AGGGGGTGTC TCCAAGGGGG 780 AGTAGAGCCA GTCACAAGCA CCACATACAG GCACACAGCC TGAGGTCTAG GGATGCAATT 840 GGGATGACTG GATACCACCA AGTTCAGCTC CTTATTGAAC AGATGGGCGC CTGAGGCCCA 900 GGGAGCAGTG GTGGCTGGCC TTATCACCCA GCAGGGCAGG GGATACTCTG GGGCCAGAGC 960 CTGGCTCTGG GCAGACTCTG TTTCCTGGCC CTGCCCTCCC CTGGGCCAAT CCTCTGGGCC 1020 AGGCTGCCTC TGAAGGCCCC TGGCTGAACC GATCCAGCAG AGCTCCAGGC AGCTCCCTTC 1080 TCAAGCTAGA GCTGAGCTGC AGTGGCCACG GGAGCCGGAG CCAGGATGCG GTGGGCAGGG 1140 CCTAGGCCTG GGCGGGAGGA ACATTCCTGC ACCATCTCCT CCCCAAGCAT GTGAGGACCC 1200 AGCCCGCCCT GCCCGCCTGC CCGCTGACTC AGGCCTCCAG GAGCCAAGCC TGCTCAGCTC 1260 CCCCACCCAC CCTAACCTGC TTCCCCACTA GTTCGGCTCT GGTTCCCCTC TCCACTGGCT 1320 GGGGCAGGAG AAGACGGTGA GCCCTGGTAG GAAGACCATG GGGAAAAATC AAACCTCACC 1380 ACCCCCCGAC ATAGCTCAGA AGGGCTGATT GTGAAACCCA GCTCTGTTCA ACATAGTTGA 1440 ACACAAACTT TTTTTTTCTT TTGGTTTGGT TTTGTTTTGT TGGTCAAACC CCAGTGCAGT 1500 GCAGTCTGTT TAAGAAGTAG TGTCGCATAG CTGTGGCCTG GATCTGCTCA GCAGCCCCAG 1560 TAGGCAGCAT TTATTCCCTT TCGCAACAAA GAGACTGAGA CTTGGCCAGA GGGAAGATGG 1620 GACCTGCCTA GGTTCACACA GGGAATCTCT GGCGGGGCTG GACTCAAACC CAGCTCCCTG 1680 CCATCACTCC TTAGAGTCAC ACTGATGAAC TCATTTAGGG CCAAAGGAAG AAGGGGAGGC 1740 AGATTTCCCC TCTAGATGAG TGAAGGGATA GGAGGCTGGT GAACCCAACG GCTGAAATGT 1800 GAAGGGTGAG AGGGTAGGGT GAGTCCCCCC AGCCCTGAGG GATGAAGGGT CTGAAGATGG 1860 CACTGCACGG TGACAGCTGC AGTGACTCAG GAGCTCCGTT TACAAAGGAA CATGAGTGAG 1920 GAACATAACT TAATTTTTTT TTATATCTGA CCTGAATTTC TGTTTTCCTC CCCCATTCCC 1980 CACATGGTAG AAGTGTAATC TCACATCAAT TTGGGGACCC TTTCTTTCCC CAGGGATGTG 2040 TAGAACTTTT GGGGATGGCA CATTTGAAGA 2070
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