Tag | Content |
---|
EnhancerAtlas ID | HS045-05654 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:223902360-223904190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TP53 | MA0106.3 | chr1:223903596-223903614 | TGCTTGCCAGGGCATGTT | + | 6.17 | TP53 | MA0106.3 | chr1:223903596-223903614 | TGCTTGCCAGGGCATGTT | - | 6.32 |
|
| Number of super-enhancer constituents: 38 | ID | Coordinate | Tissue/cell |
SE_00224 | chr1:223891886-223912166 | Adipose_Nuclei | SE_01908 | chr1:223903739-223904850 | Aorta | SE_02306 | chr1:223899487-223903687 | Astrocytes | SE_04026 | chr1:223903291-223905474 | Brain_Anterior_Caudate | SE_05036 | chr1:223902343-223904766 | Brain_Cingulate_Gyrus | SE_05972 | chr1:223899184-223905867 | Brain_Hippocampus_Middle | SE_09681 | chr1:223899395-223907924 | CD14 | SE_19702 | chr1:223899422-223907008 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23408 | chr1:223902389-223903605 | Colon_Crypt_1 | SE_24051 | chr1:223902436-223903004 | Colon_Crypt_2 | SE_24051 | chr1:223903089-223903543 | Colon_Crypt_2 | SE_24051 | chr1:223903970-223904550 | Colon_Crypt_2 | SE_25230 | chr1:223902434-223903064 | Colon_Crypt_3 | SE_26209 | chr1:223899230-223905388 | Duodenum_Smooth_Muscle | SE_26925 | chr1:223899336-223904834 | Esophagus | SE_31491 | chr1:223898405-223906097 | Gastric | SE_33950 | chr1:223900271-223904290 | HCC1954 | SE_34545 | chr1:223899419-223904575 | HCT-116 | SE_34979 | chr1:223899218-223904777 | HeLa | SE_36294 | chr1:223899426-223904613 | HMEC | SE_37129 | chr1:223899390-223911201 | HSMMtube | SE_38254 | chr1:223899363-223904539 | HUVEC | SE_38957 | chr1:223902403-223904692 | IMR90 | SE_42269 | chr1:223902366-223906841 | Lung | SE_44530 | chr1:223900206-223905349 | NHDF-Ad | SE_44904 | chr1:223902263-223903610 | NHLF | SE_44904 | chr1:223903924-223904809 | NHLF | SE_45872 | chr1:223899383-223910101 | Osteoblasts | SE_50365 | chr1:223899342-223907084 | Sigmoid_Colon | SE_51879 | chr1:223902338-223905051 | Skeletal_Muscle_Myoblast | SE_53249 | chr1:223902420-223905033 | Small_Intestine | SE_55958 | chr1:223898795-223906601 | u87 | SE_63671 | chr1:223902338-223906710 | HSMM | SE_64794 | chr1:223900231-223904926 | NHEK | SE_65644 | chr1:223902687-223903954 | Pancreatic_islets | SE_65644 | chr1:223904002-223904652 | Pancreatic_islets | SE_67677 | chr1:223898795-223906601 | u87 | SE_68376 | chr1:223892363-223922876 | TC32 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr1 | 223903033 | 223903347 | chr1 | 223902428 | 223903910 | chr1 | 223902800 | 223903000 | chr1 | 223903000 | 223903425 |
|
Enhancer Sequence | GAATGTGTTC ACTTTACATT TGCATGGCAC TTTACAGTTT ACATAGTGAG TTCACATACT 60 CATTCACTTA TTCTTTCATT CATTCAGTAA GCATTTCTCG AATACCTACT ATATGCTGGG 120 CACAATGCAT ATGGTTTCTG CTTCTGAAGA CTTACTTCTG AGGCTAGTGA GGGGACAGAG 180 ACAGGTCCCC CAACAGTTGG AAATGCCTGT GGGACTTCCA GATGAGGATG TAGAGGTCTA 240 GAGATGATCT AGCGCCACTG CTTAGGGCAG GCGGGCTGTG CACTGCACAA CTAAGGAAGA 300 GTGTGACTTT TACGATCCCC ATTTGCCAGT TGAAGAAATT GAGGCTTGGG AAGGTTAAAT 360 ACTTGCTCAG AGTCAAGTGG ATATAGGGCA TAGATCCAGG ACTGTGTGTA GTCTGTGCAT 420 GTTGAGCCTA CCCCTTATGG CTGCGCTCTC TGCCTCCTTC CTACCTTCTC AAATGCTGCT 480 GAGGTCAGGC AAGGGGAGCA CAGTTGTTTC CGCTGGATTT GAACACTAGC AAGTCATTGG 540 TGAGTTTAGC AGAGCAATTT CAATGGAAAG GTGAGAGTAG AAGCCAGATT GTTGTAGACT 600 CCAGAGTAAA GGAACTGGAA ATTAAGAACA TGATCAACTT ATTTAAGAAG GACCCCCGGG 660 AAGAGAGGAG AACTGATAGG TAGAGTAGGA CCTGGACTTT GAGAGCCTGT GTTTTTTTCA 720 TATGAGAACA ACTTGAATGT GTCATATGTT GAATCACCAG GAAGAAGGGA TTAAAGATAA 780 AGGCAGGGAG GGGGCAGTGA AACAGGATCC CTGAGGAAGT GAGAATACGG GTTGTGGGCA 840 GGGGAGGGGA GCAGGTTAGC CTTGCAGCAG GAGGAGCTGC TCTTCCTCGG AGAGAGGATT 900 TCACAACACT GGCAAGAGTG GCTCCAGTGC CTGGAGCGGG GATTAAAGCA GTAAGTCCAG 960 TGGGGTCCAA GGGCCATGCA GGGGTACAGT GAGGAGAAAG CAGGTGTGAT CCGGGTGGCA 1020 CATCAGATCC TTCCAGCAAC CAGTCTGTTA GGAGCAAGGG CAGATGTTGT GAGCCCCTAT 1080 GTTTCCCCCA AGAAAATCAA ACCTCTGAGA GGTTTCTCAC TTGCTTATCT TCAGCTGGCC 1140 GAACTCAGCC TCAAACCCAT ATGTCCTGTC TCCAAGTTCA GTGACTGTTA TCATCAACTT 1200 CTTCAACAGT AATAATAATA GATCACATTT ATGGAGTGCT TGCCAGGGCA TGTTTACATC 1260 ATTATCTCAT TTAACACTCA GAACAATCCT CTGTGGTGGG TGTTTTCATC GTTCCCATTT 1320 TGCAGGTGAA AAAACTGAGA CTTCAAAAGG TTAAGTGACT TCCCAGGGTC CTACGACCTA 1380 CATAATAAGT GGCAGAGCCA GGATTCAAAC CTAGGTTATC AGAATAATGC AGCAAAGCCC 1440 AAACCCTCAG CCCCTTTTCA CTGACTGGTA AGACCCATAT TTAATTCGAT GCCCTACATG 1500 CCGTGCACAA GTTTCAGTTT TCTGAAGCAT CGCTTAGATG CTTAGGTGTT TAGCACCACT 1560 CTGAACTCTG ACTTTTCTAG AGAGGCTGCT AAAGGCATTA GAAAGTTTCT GAAGTATAAT 1620 GGAAAAACCC TGCTGGAGTA AGTGCCTGGC ACACTCAGGA TTATCAGTGT GATTCTTTAT 1680 AATAAACAGG CTCCCAGCAC CAAGCCCAAT CTATTCCATC AGCTGGATAA GAGCTCTCTG 1740 GCAGGCCTTG GGCCAAGCTG GCTTCCTTTG CCTCAGCAGA AGAGCATTCT GATTCTCTCT 1800 GCCATCCCCA AAACTGACAG GAGCAGAGAG 1830
|