Tag | Content |
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EnhancerAtlas ID | HS102-21606 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr8:27223290-27225530 |
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 | CACAACCTTA AAGCTAGGAG GGCCTGAGAT GACCCTGGTG ATGGGGACTG TTCCAGCCAG 60 ACATTGCTGG TAATTTGCCT TCCTTTCAAG GGCTGTAAAA CTGCTCCTCA GTTATGAAAT 120 GAACCAATTA AGGACTTCGG ACTTAGCCAG TCCTGACAGA AGCATTTCAA ACAGAACCAC 180 TAATCATACC TGATGTTTTT ATTGTTTTCT GTTGACACTG CCCCAGAAAC ATGAGGCTTC 240 TGGCAGCCAG CCCTGGCACA CCTGCCTCAT CTCTTCATGA CACCATGTTT CAAAGAAGCT 300 TCCTTGTCAA ATAGGAGAAG GACCCACCTG TGCTACTTCC TGTGATTGAC AGGAAGTTCT 360 GAAACCCAAA GAAGCAAATC ATGGCTCTTG GGTCTTGGGG TGGCACAAGT CACTAGAAAA 420 TCTCACTCCA TTGCTGATCC TAGAATTAGT TCAGGCTCCC TGAGGACAGA TCCACCCCAG 480 TACCTCCCAC CCCTTCCATC TCTTCATCCC CCAGGGGGAG GCTGTCTACT TCTTTTGGGG 540 CTTTGGACTA ATCCCCCCAG TTCCCATCTT CTGAGGTTTT GTGCTAATCT TGTTTGTCTC 600 CTATGTGTAC AAAGCAATCA CCCAGGCGAC ATCCAGCTTC TAGATTTGGG TGCCCAGGGT 660 TCATGTGGTG CCATGTTGGC CTTTGCCTAA TTAATTTTAG GAAGTCTTTC CACCAGCCAG 720 ATCATGGTCT TCCAAAAATC CTATGGAGTC AGTTCTAGGC AGAAGCTGAG CAGGCATCTG 780 GGCATGGCAA CAACTTCTAG CCTCTTCCTC TTACCACTTG GCGTCTAGCT CCCAGGCAGG 840 TATTTCCTGA GCCAGGGTTC CTGTGCAGGT CAGTCTTTAC AATATGCAAA TTTCTTGTGA 900 CCCAGCCCAT TTCCCCCCGA GGGAGGCAGG AAGTCCCTTT TGAAATTTCT GAGCACACAC 960 AACAGAGGCT AGGAGAGGAC CAGCTCTGAG ACTCCCACTC AAGCATGTCA AGGGGTGTTT 1020 GTGGCTGTGT GGCTGTGTGT GGAGAGCAGA GGGCAATGCT GGGCTGGGGC AGGGGAGGGT 1080 GCAGAGGAGA GGGTGTGGGG GAGGGAGGAG CTGCAGCCTC AGACACAGAA TTGGACTGAG 1140 AAAACAGGAT GCAGCAGAGG AGGAGGCTGA GTGTGGTGGC TCGGCTGGCA CTGGAATGCT 1200 CAATGTGAGG AGGTAGAAGG TGCCTGAGAC CAGGGTCTCT GGAGTTCTAG AAAAGCCTGG 1260 GCCTCTTCCA TGTTTGGAGT CTCTCTGGAT TAAGAAAGAA GAAGAAGAGA CAGAAATAGC 1320 CAAATAGGAC AGCAAACATT ATGATGTTGT TTAAATGTTT ACTTTCACCA ATTAATAGTT 1380 TTAAACACAC ACGCACACAT GCCACACACA CACTGACTAC ATGAATGGAC TCATTTGGAA 1440 ATAATGTCAA GGGCTCTTTG TCCTGTGAGG CCTGGGCCCA GTGGCCATCC TGGTTTTGGG 1500 AGCAGCTCTG CCTGAGAGAC CCTCCTGTGG GCATGGTGGC AGCTGGAGGG TGTTCTGGGC 1560 TGTTGAACAA AAAGTCCAGA AAGTCCATCT GGACTGGTCC TGCTGGGGAT GGTGAGGGAC 1620 TGAACAGCCC AGGTGCGGGG TGTCTGGGCT TGCCCACCTG TCCATGTTTA GCCAAGTGTC 1680 CATTTCAACA AGGAGGAAGG TGACAGGCCC CCAGGACGAT GGCCTCTCTC CTCAGTCACC 1740 CCAGGTCAGT CCCCAGCAAA TGCAGTGGGG CCTTGATGGG GAAAGTCCTT TCAGGGTTTG 1800 TATCAATTTC TTTGCATTGT TGTAGCAGAA TATCAGAGGC TGGGTAATTC ATAAAGAAAA 1860 GAGGCTTAAT TGGCTCATGG TTCTGCAGGC TGTGCAAGCA TGGCACCAAC ATCAGCTTGG 1920 CTTCTGGTGA GGCCTCAGGA AGCTTCCAAT CATGGCAGAA GGGAAGAGGA GCTGGCATCT 1980 CAAATGGCAA GATAGAAGCA GGGGAGGTGC CAGCCTCCTT TTTAAACAAT CAGATCTCAC 2040 ATGAACTCAT TAAACTCATT ACATGGGGAA GGCACCATGC CATTCATAAA GGATCCACCA 2100 CATGACCCAA ACACCTCCCA CCAGGCCCCA CCTCCCACAC TGGGAATCAC ATTTCAACAT 2160 AAAATTGGAG GGAACAAACA TCTAAACCGT ATCAGGGTCT CTGATTCCAC AAGAGCCAGG 2220 GGACAAAGCA GGCCCCACGG 2240
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