Tag | Content |
---|
EnhancerAtlas ID | HS047-17690 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:45244530-45246970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr19:45246334-45246345 | AAGAGGATTAA | + | 6.14 | ESR1 | MA0112.3 | chr19:45246195-45246212 | GGGGTCACAGGGACCTG | + | 6.13 | RREB1 | MA0073.1 | chr19:45245077-45245097 | CCCCCATCCACCCACCCAGG | + | 6.65 |
|
| Number of super-enhancer constituents: 37 | ID | Coordinate | Tissue/cell |
SE_00729 | chr19:45244298-45262300 | Adipose_Nuclei | SE_00795 | chr19:45245366-45245660 | Adipose_Tissue | SE_01042 | chr19:45244433-45246902 | Adrenal_Gland | SE_09606 | chr19:45239082-45248934 | CD14 | SE_23197 | chr19:45244455-45245769 | Colon_Crypt_1 | SE_23197 | chr19:45245798-45246901 | Colon_Crypt_1 | SE_23877 | chr19:45244533-45245299 | Colon_Crypt_2 | SE_23877 | chr19:45245305-45245704 | Colon_Crypt_2 | SE_23877 | chr19:45245814-45246394 | Colon_Crypt_2 | SE_26167 | chr19:45244340-45247135 | Duodenum_Smooth_Muscle | SE_26699 | chr19:45243540-45246867 | Esophagus | SE_27905 | chr19:45244347-45247035 | Fetal_Intestine | SE_28964 | chr19:45244300-45251996 | Fetal_Intestine_Large | SE_30554 | chr19:45244497-45246462 | Fetal_Muscle | SE_31568 | chr19:45243518-45247353 | Gastric | SE_34515 | chr19:45243523-45246769 | HCT-116 | SE_34750 | chr19:45243561-45247412 | HeLa | SE_41147 | chr19:45244406-45246787 | Left_Ventricle | SE_42497 | chr19:45244285-45247426 | Lung | SE_44720 | chr19:45244506-45246805 | NHDF-Ad | SE_45032 | chr19:45244521-45246656 | NHLF | SE_46394 | chr19:45244290-45247033 | Osteoblasts | SE_47531 | chr19:45244489-45245744 | Pancreas | SE_47531 | chr19:45245754-45246401 | Pancreas | SE_48453 | chr19:45244349-45246660 | Psoas_Muscle | SE_48897 | chr19:45244287-45246653 | Right_Atrium | SE_49675 | chr19:45245289-45245710 | Right_Ventricle | SE_50112 | chr19:45244185-45262348 | Sigmoid_Colon | SE_51515 | chr19:45244280-45247217 | Skeletal_Muscle | SE_52390 | chr19:45244342-45253746 | Small_Intestine | SE_53360 | chr19:45244294-45255114 | Spleen | SE_56197 | chr19:45244337-45246861 | u87 | SE_57185 | chr19:45244534-45245709 | VACO_400 | SE_57185 | chr19:45245800-45246557 | VACO_400 | SE_62704 | chr19:45221152-45271677 | Tonsil | SE_65330 | chr19:45243124-45246791 | Pancreatic_islets | SE_67826 | chr19:45244337-45246861 | u87 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAATGTACTT TTTTGTAGAG ACGGGGTCTT GTTCTGTTGC CCAGGCTGGT CTCGAACTCC 60 TGGGCCCAGG TGATTCTCCC ATCCTGGCCT CCCAAAGCAC TGGGATTAGA GGGATGTGCC 120 GCCACACCCA GCCAACAGGT TTTTTCTTGA AGGGGGATGT GAGCTGCCTG TCTCTGTGGC 180 TGCCACTCCC ATACCTATAT GAATAATAAC AATCATTTTA AAATAATATC TTCCATTTAC 240 TGAGACTTTC CTCTGTGCCA GGCCTGTGCT GACGTGTGTG AATTCATTTG ACTCTCACAA 300 CACCGCCGGA AGACATGCAC TGTTTTTACC CTCATTTTAT AGATGAGGAA ACTGGGGCTC 360 AGAGAGGGTA AATAAATCAC CTGCCCAGGG TCACACAGCT GGTAAGTGAC AGAACTGGGA 420 TTGGAACCCA AACAATTAGA CAGGGCCCCA TTCACAGATG AGGACACTAG CCCACTAGTA 480 CCTGGTTGTC TACTGTCACC TCGCTGAGAC CACTGTGACC TTCCTTCCTA TGCCCCGCCT 540 TCCCAGACCC CCATCCACCC ACCCAGGGCA GATGCTGATC TCCACACTCC CCCCACCGAA 600 TCACCCCTCT CTGATCAAGG CAGCTGGCAG GGGCGGCGGA GGGGGTGGGG GGACGAGGGT 660 GTCCAGTCTC CCTGGCCTGC CAAGAGAGGA TGTCGCAATC CTCTGACTCA GCGTCGTGCG 720 TGCAGACCCA GCAAGAGGCA GAAAGGGGAA GATTAAGTCT TGGCTTAGGC CCCAGATGGG 780 CTGATTCTGC TCAATGCCAG GAGCTCCCAG AGCTGCCAAG GCTCCAGGGT GGGGAGGAAC 840 CAGGAGGTGC AGGCCATGCT CCAGGAAGCT GGCCCGCATT CACCCGTGGG GGTGGGGCAG 900 AGCAGCCTCA GGGAGCGGAG CCGTGTGGAC TTCCAGCCCA GGGCCCAGAC TGGAGGCAGC 960 CTGACCTTGG GCATGTCCCT TCCCATCCAG GCCCAGAGTC TCTGTATCCT TCTGTCTGCG 1020 GAATTCACTT GCTCTCCCTG AACCTCTCTG GAGGCTCTAG TGGTTGTTCC TCCTCAAGGG 1080 ACTCTTAAGT CTAACTCTAT TTTTTTTTCT TTTTTGTTTG AGACAGGGTC TTGCTCTGCC 1140 ACCCAGGCTG GAGCGCAGTG GCACGATCTC AGCCCACTGC AACCTCGGCC TCCTGGGTTC 1200 AAGCGATTCT CCTGCCTCAG CCTCCCGTGT AGCTGGCATT ACAGGCGCCC ACCACCACGC 1260 CCGGCTAAGT TTTGTATTTT TAGTAGAGAC GGGGTTTCGC CTTGTTGGCC AGGCTGGTCT 1320 TGAATTCCTG ACCTCAGATG ACCCTCCAGT CTCAGCCTCT CAAAGTGCTG GGATTACAGG 1380 CGTGAGTCAC CATGCCCGGC CCCTTAAGTC TAACTCTATT CCCTCCTGCT GCAATGCCAT 1440 CCTCTCTCCA CGCACGGACC CTCCCCATAC CAGGAGGCAG CAGAGAAGAG TTCCAGGGTG 1500 CGAATCTCCA TGGGTGTCCT CGGACATATG ACTTTCCCTC TCCATGCCTC AGTTTCCCCA 1560 TCTAAACCAT TTCTTCCCAG GGAGAAGGGG CCTAGAATCA AGCTGGAAGG GCACACCTGC 1620 AGTCTCCGAG ACTCATGGCC ACTTCTCCCA GGTCAGAAGC GTGCTGGGGT CACAGGGACC 1680 TGGCTTGAAA TCTCAGCTCT CCCCAGTTCC TCACCGTGTG ACCCGGGCAG TGAGTTCACT 1740 TCTCTGTGCC TGTTTCCTCC TCTATAAAAT TGGGTTTTTA GCTGAATTTT CCTTACAAGG 1800 TGTTAAGAGG ATTAAGTGGG CCAATTCTTA GTTGCAACTC AGCCCGGAGT GAATGTTTCT 1860 GTCTTGTCTC CTCTGTGAGT AGAAAAGGGT GAGAAGGAGG CCCTGGTCTG CTGGATAGGG 1920 TAAGGGTTAA GGCCAGCAGC GTGGAGACAG AAATGAACAT TATTCATTCA TTTATTCCAC 1980 ACACTTTTCT TATTTAATCT GCTCAGTAAG CCTGTGAAAC AGGATCTGTT ATCATCCTGT 2040 TATTATTATT ATTACCATTA TTTTGAGACA GAGTCTCACT CTGTCACCCA GGCTGGAGTT 2100 CAGTGGCATG ATCATAGCTC ACTGCAGCCT TACACCTAAA GCAATCCTCC CACCTTACCC 2160 TCCCAAGTAG CTAGGACTAC AGGTGCCTCC TGAGCCCAGC TAATTTTTAA AAATTTTGTG 2220 TAAGCCTGGT GTGGTGGCTC ACACCTGTAA TCCCAGCACT TTGGGAGGCC GAGGCAGGCG 2280 GATCACAAAG CCAGGAGTTC GAGACCAGTC CAGCCAATAT GGTGAAACCT CGTCTCTACT 2340 AAAAATACAA AAATTAGCTG GGCATGGTGG CACGGGCCTG TAGTCCCAGC TACTCAGGAA 2400 GCTAAGGCAG AAGAATCGCT TGAACCCAGG AGGTGGAGGT 2440
|