Tag | Content |
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EnhancerAtlas ID | HS176-14076 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr15:67442190-67443360 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr15:67443036-67443048 | AATTGTTTGTTT | + | 6.22 | SP2 | MA0516.2 | chr15:67442662-67442679 | CCAACCCCCGCCCCCAG | + | 6.12 | STAT1 | MA0137.3 | chr15:67442805-67442816 | TTTCCAGGAAA | + | 6.62 | Stat4 | MA0518.1 | chr15:67442805-67442819 | TTTCCAGGAAAAAA | + | 6.02 |
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| Number of super-enhancer constituents: 42 | ID | Coordinate | Tissue/cell |
SE_00035 | chr15:67436757-67445463 | Adipose_Nuclei | SE_02258 | chr15:67434429-67443726 | Astrocytes | SE_02918 | chr15:67441987-67442963 | Bladder | SE_09181 | chr15:67436431-67443849 | CD14 | SE_10875 | chr15:67436777-67443225 | CD20 | SE_14469 | chr15:67441694-67443321 | CD4_Memory_Primary_7pool | SE_17822 | chr15:67438131-67443611 | CD4p_CD25-_CD45ROp_Memory | SE_18371 | chr15:67441444-67443356 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19163 | chr15:67438237-67443338 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20091 | chr15:67441765-67443150 | CD56 | SE_23212 | chr15:67438436-67443079 | Colon_Crypt_1 | SE_25827 | chr15:67440940-67443576 | Duodenum_Smooth_Muscle | SE_26536 | chr15:67436749-67443276 | Esophagus | SE_28551 | chr15:67441761-67443508 | Fetal_Intestine_Large | SE_31411 | chr15:67440403-67443154 | Gastric | SE_35122 | chr15:67438336-67444036 | HeLa | SE_35858 | chr15:67437440-67443735 | HMEC | SE_36917 | chr15:67432472-67444892 | HSMMtube | SE_37941 | chr15:67424014-67445333 | HUVEC | SE_38858 | chr15:67432374-67443213 | IMR90 | SE_40854 | chr15:67440475-67443283 | Left_Ventricle | SE_42172 | chr15:67436843-67443113 | Lung | SE_44149 | chr15:67433529-67443310 | NHDF-Ad | SE_44749 | chr15:67432338-67443689 | NHLF | SE_45534 | chr15:67405577-67448068 | Osteoblasts | SE_47100 | chr15:67357928-67475420 | Panc1 | SE_47566 | chr15:67442362-67443080 | Pancreas | SE_48052 | chr15:67436792-67443191 | Psoas_Muscle | SE_48704 | chr15:67440533-67443140 | Right_Atrium | SE_50064 | chr15:67436770-67443203 | Sigmoid_Colon | SE_51081 | chr15:67436595-67443592 | Skeletal_Muscle | SE_51859 | chr15:67436149-67443786 | Skeletal_Muscle_Myoblast | SE_52344 | chr15:67436796-67443154 | Small_Intestine | SE_53518 | chr15:67441740-67443198 | Spleen | SE_55348 | chr15:67442328-67442692 | Thymus | SE_55686 | chr15:67433900-67443259 | u87 | SE_58377 | chr15:67342858-67447290 | Ly1 | SE_62286 | chr15:67356723-67443338 | Tonsil | SE_63642 | chr15:67434343-67443975 | HSMM | SE_64236 | chr15:67438078-67443807 | NHEK | SE_65752 | chr15:67442449-67443748 | Pancreatic_islets | SE_67502 | chr15:67433900-67443259 | u87 |
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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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Enhancer Sequence | ATTGCTGTCA TGCAAATGCT GCATTTTTTG CATGTAAAGG TACCTCTTTA CCTCCATGGT 60 CCTTAAACTA ACTTTTTCAA GAAACATGGT CATTTCCCAC CCTTCCTTTA CTTCCAGCTC 120 CCCATTCATA CCCAACAGTG GCTAACTGAA AGGTTTGCAA ATCCTGAAGG CTTTGGGGCT 180 TCTTTTAAAA AGAAGAGACT GAGTTGTAAA TGTCATAAGA CTGAGATGGT TGTAAATGTC 240 CCAACCATAC TGTGTGACAT TTGCTAGGAA TTGTTGTAAA ATCACTGGAG TGAGCGCTTG 300 TCCTGAGGCA CTGCCTCTCC GCGTGAATGT CACTGAGTCG CCCGGTTGAC CCGTTGCATG 360 TTATGCAGCA CTTGTGACAT TGTTTTATCT CTCTAGCCGG TGACTCATAA TTAAGGAAGT 420 CAAAACTGTG CAATTAACAC AAAACCTCCT CATTTGCCCT CTTCACCTCT CCCCAACCCC 480 CGCCCCCAGT CAGGAATGCC CGCCTGACAT TTTCTCTAAG TCTTTGGAAA CTTTAAGATT 540 TGTTTTGATA GAACAAGGCC GCCAGTTATC ATCGCCTGGT TCCACTTGTT TTACCCCAAA 600 AGTCTGTGAG AATCTTTTCC AGGAAAAAAA AGAAAGAAAG AAAGAAAGTA AATCCCACCC 660 CCAAGCGTGC AGTCTGCCCA CAGGAAGTGA TTCATGGTGC TCCGATTCGG GCAGACCTGA 720 CTGCAGGAGG CGGGAGGCTG GGAACCAGGT CTGGGAAAAG AGGGCAGAGA GAGGATACCC 780 AGACCTAATG GCTTCTGCTC TGTGGAAGAA AGTGAAAAAC AGAATGACTA AGAGTCCTGT 840 AATAAGAATT GTTTGTTTTG TGAAGTTGAA CTAATAGTGA GGTTTGCCGG CAGATAAGAC 900 TTGAGAAATT GCAGTTGTCA GGGGAGGGGA CTTTTCCATG TCCTGCTTTT TTTTTTTTTT 960 TTTTTTTATT AAGAGAGCAA AGCTATTTCT CAGTCTTTTT TTTTTTTTTT TTTTTTTTTT 1020 TGAGATGGAG TCTCTCTCTG TCGCCCAGGC TAGAGTGCAG TGGCACAATC TCGGCTCACT 1080 GCAACCTCCA CCTCCCAGGT TCAAGTGATT CTCTTGCCTC AGCCTCCCCA GTAGCTGGGA 1140 TTACAGGTGC CCACCACCAT GCCTGGCTAA 1170
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