Tag | Content |
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EnhancerAtlas ID | HS191-36659 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr8:27223260-27225050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr8:27224377-27224388 | AGAGGGTGTGG | - | 6.02 | ZNF263 | MA0528.1 | chr8:27223781-27223802 | CCTTCCATCTCTTCATCCCCC | - | 6.59 | mix-a | MA0621.1 | chr8:27223975-27223986 | CCTAATTAATT | - | 6.32 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_09156 | chr8:27216720-27239058 | CD14 | SE_10267 | chr8:27216807-27227080 | CD19_Primary | SE_10868 | chr8:27181046-27285079 | CD20 | SE_12034 | chr8:27222241-27227040 | CD3 | SE_13758 | chr8:27218532-27227087 | CD34_Primary_RO01536 | SE_14795 | chr8:27222640-27227221 | CD4_Memory_Primary_7pool | SE_16778 | chr8:27223029-27226240 | CD4_Naive_Primary_8pool | SE_17600 | chr8:27217455-27229236 | CD4p_CD25-_CD45RAp_Naive | SE_18325 | chr8:27216741-27229078 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19392 | chr8:27222414-27227035 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20066 | chr8:27216778-27230915 | CD56 | SE_21397 | chr8:27222826-27226673 | CD8_Memory_7pool | SE_22414 | chr8:27216753-27229136 | CD8_primiary | SE_27921 | chr8:27222457-27225133 | Fetal_Intestine | SE_28623 | chr8:27222072-27225298 | Fetal_Intestine_Large | SE_31168 | chr8:27218925-27226604 | Fetal_Thymus | SE_32488 | chr8:27216612-27229104 | GM12878 | SE_40108 | chr8:27217492-27224812 | K562 | SE_41696 | chr8:27223062-27225285 | LNCaP | SE_43522 | chr8:27216759-27225361 | MM1S | SE_50221 | chr8:27218813-27227034 | Sigmoid_Colon | SE_52630 | chr8:27218810-27227024 | Small_Intestine | SE_53591 | chr8:27223100-27227044 | Spleen | SE_55148 | chr8:27223214-27226976 | Thymus | SE_59882 | chr8:27206325-27247753 | Ly4 | SE_60867 | chr8:27217627-27263346 | DHL6 | SE_62276 | chr8:27181124-27271753 | Tonsil | SE_66769 | chr8:27223351-27225091 | Jurkat | SE_67171 | chr8:27216759-27225361 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr8 | 27223294 | 27224773 | chr8 | 27223741 | 27224600 | chr8 | 27223958 | 27224492 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I027359 | chr8 | 27216947 | 27230373 |
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Enhancer Sequence | AGCCTGTGCT CCCTCCTAGA GGGCAAAATG CACAACCTTA AAGCTAGGAG GGCCTGAGAT 60 GACCCTGGTG ATGGGGACTG TTCCAGCCAG ACATTGCTGG TAATTTGCCT TCCTTTCAAG 120 GGCTGTAAAA CTGCTCCTCA GTTATGAAAT GAACCAATTA AGGACTTCGG ACTTAGCCAG 180 TCCTGACAGA AGCATTTCAA ACAGAACCAC TAATCATACC TGATGTTTTT ATTGTTTTCT 240 GTTGACACTG CCCCAGAAAC ATGAGGCTTC TGGCAGCCAG CCCTGGCACA CCTGCCTCAT 300 CTCTTCATGA CACCATGTTT CAAAGAAGCT TCCTTGTCAA ATAGGAGAAG GACCCACCTG 360 TGCTACTTCC TGTGATTGAC AGGAAGTTCT GAAACCCAAA GAAGCAAATC ATGGCTCTTG 420 GGTCTTGGGG TGGCACAAGT CACTAGAAAA TCTCACTCCA TTGCTGATCC TAGAATTAGT 480 TCAGGCTCCC TGAGGACAGA TCCACCCCAG TACCTCCCAC CCCTTCCATC TCTTCATCCC 540 CCAGGGGGAG GCTGTCTACT TCTTTTGGGG CTTTGGACTA ATCCCCCCAG TTCCCATCTT 600 CTGAGGTTTT GTGCTAATCT TGTTTGTCTC CTATGTGTAC AAAGCAATCA CCCAGGCGAC 660 ATCCAGCTTC TAGATTTGGG TGCCCAGGGT TCATGTGGTG CCATGTTGGC CTTTGCCTAA 720 TTAATTTTAG GAAGTCTTTC CACCAGCCAG ATCATGGTCT TCCAAAAATC CTATGGAGTC 780 AGTTCTAGGC AGAAGCTGAG CAGGCATCTG GGCATGGCAA CAACTTCTAG CCTCTTCCTC 840 TTACCACTTG GCGTCTAGCT CCCAGGCAGG TATTTCCTGA GCCAGGGTTC CTGTGCAGGT 900 CAGTCTTTAC AATATGCAAA TTTCTTGTGA CCCAGCCCAT TTCCCCCCGA GGGAGGCAGG 960 AAGTCCCTTT TGAAATTTCT GAGCACACAC AACAGAGGCT AGGAGAGGAC CAGCTCTGAG 1020 ACTCCCACTC AAGCATGTCA AGGGGTGTTT GTGGCTGTGT GGCTGTGTGT GGAGAGCAGA 1080 GGGCAATGCT GGGCTGGGGC AGGGGAGGGT GCAGAGGAGA GGGTGTGGGG GAGGGAGGAG 1140 CTGCAGCCTC AGACACAGAA TTGGACTGAG AAAACAGGAT GCAGCAGAGG AGGAGGCTGA 1200 GTGTGGTGGC TCGGCTGGCA CTGGAATGCT CAATGTGAGG AGGTAGAAGG TGCCTGAGAC 1260 CAGGGTCTCT GGAGTTCTAG AAAAGCCTGG GCCTCTTCCA TGTTTGGAGT CTCTCTGGAT 1320 TAAGAAAGAA GAAGAAGAGA CAGAAATAGC CAAATAGGAC AGCAAACATT ATGATGTTGT 1380 TTAAATGTTT ACTTTCACCA ATTAATAGTT TTAAACACAC ACGCACACAT GCCACACACA 1440 CACTGACTAC ATGAATGGAC TCATTTGGAA ATAATGTCAA GGGCTCTTTG TCCTGTGAGG 1500 CCTGGGCCCA GTGGCCATCC TGGTTTTGGG AGCAGCTCTG CCTGAGAGAC CCTCCTGTGG 1560 GCATGGTGGC AGCTGGAGGG TGTTCTGGGC TGTTGAACAA AAAGTCCAGA AAGTCCATCT 1620 GGACTGGTCC TGCTGGGGAT GGTGAGGGAC TGAACAGCCC AGGTGCGGGG TGTCTGGGCT 1680 TGCCCACCTG TCCATGTTTA GCCAAGTGTC CATTTCAACA AGGAGGAAGG TGACAGGCCC 1740 CCAGGACGAT GGCCTCTCTC CTCAGTCACC CCAGGTCAGT CCCCAGCAAA 1790
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