Tag | Content |
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EnhancerAtlas ID | HS118-18170 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr8:27218210-27220940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RORA(var.2) | MA0072.1 | chr8:27219169-27219183 | TAAAATTAGGTCAT | + | 6.06 | SREBF1 | MA0595.1 | chr8:27218434-27218444 | GTGGGGTGAT | - | 6.02 |
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| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_08208 | chr8:27218876-27220303 | Brain_Inferior_Temporal_Lobe | SE_09156 | chr8:27216720-27239058 | CD14 | SE_10267 | chr8:27216807-27227080 | CD19_Primary | SE_10868 | chr8:27181046-27285079 | CD20 | SE_12034 | chr8:27217227-27222204 | CD3 | SE_13758 | chr8:27218532-27227087 | CD34_Primary_RO01536 | SE_14795 | chr8:27217610-27222557 | CD4_Memory_Primary_7pool | SE_16778 | chr8:27218837-27221619 | 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 | chr8:27216824-27222187 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20066 | chr8:27216778-27230915 | CD56 | SE_21397 | chr8:27217312-27222271 | CD8_Memory_7pool | SE_22414 | chr8:27216753-27229136 | CD8_primiary | SE_27921 | chr8:27218674-27221105 | Fetal_Intestine | SE_28623 | chr8:27217934-27222042 | Fetal_Intestine_Large | SE_31168 | chr8:27217705-27218580 | Fetal_Thymus | SE_31168 | chr8:27218925-27226604 | Fetal_Thymus | SE_32488 | chr8:27216612-27229104 | GM12878 | SE_40108 | chr8:27217492-27224812 | K562 | SE_41696 | chr8:27218982-27220305 | LNCaP | SE_43522 | chr8:27216759-27225361 | MM1S | SE_50221 | chr8:27217559-27218746 | Sigmoid_Colon | SE_50221 | chr8:27218813-27227034 | Sigmoid_Colon | SE_52630 | chr8:27217169-27218561 | Small_Intestine | SE_52630 | chr8:27218810-27227024 | Small_Intestine | SE_53591 | chr8:27217074-27218682 | Spleen | SE_53591 | chr8:27218861-27222787 | Spleen | SE_55148 | chr8:27219032-27220487 | Thymus | SE_55148 | chr8:27220567-27220878 | Thymus | SE_59882 | chr8:27206325-27247753 | Ly4 | SE_60867 | chr8:27217627-27263346 | DHL6 | SE_62276 | chr8:27181124-27271753 | Tonsil | 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 | 27219196 | 27220432 | chr8 | 27219305 | 27219672 | chr8 | 27219743 | 27220043 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I027359 | chr8 | 27216947 | 27230373 |
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Enhancer Sequence | ATGACACGTA TATTCTGTGA ACTTTCAAAA AAGGATGTGA AAGACTTCTG TGCAAACATT 60 TCACCTGGGA TCTTTTCACT AGCAAGATGG GGAGAAAAAG CCAAAACTGC ATTTCTCTCG 120 CCCTCTGGGT CTAGATGTGG GGATTTCTTC TCCTTCCAGA TGACAACCAG GAAGGGCCCC 180 CAATTATTCT CGAAATAAAA CGTGTCGGTC TTTCGAAATG GTCAGTGGGG TGATGTCTGG 240 GTCCCAGGAA AGAAAGAAAC ATAGGATTTG TGCTTTTTGT TGATATGAAG TTAAGGGGTA 300 CAAGTGAGAG TGATTTTGTT ACATGGGATA CATTGCATAG TAGTAAAGTC TGGGCTTGTA 360 GTGCAACCAT CACCCGAATA CTGTTTATTG TACCCATTAA ATAATTTCCT ATCCCTCACC 420 CCCTTCCCAC CCTCCTGAGT CTCCAATGTC TATTATTCCA CACTCTATGT CCATATGTAC 480 AAATTATTTA GCTCCAGATT TAGCTTTTTA TTTCTTTTTT GTTTCCTTTT TGTTTGTTTA 540 TTTGATATAG GGTCTTGCTC TGTTGCCCAG GCTGGAGTGC AGTGGTGCAA TCATAGCTCA 600 CTACAGCCTC GAACTCCTGG GCTCAGGTGA TCCTCCCATC TTAGCCTCCC GAGTAGCTGG 660 GACCACAGGC ATGCACCACC ATGCCTGGCT AATTTTTTAT TTTACTTTTT GTACAGATGG 720 GGGTCTCACT TTGTTGCTCC AGCTGTTCTT GAACTCCTGG CCTCAAGCGA TGCTCCCACT 780 TTAGCCTCCC AAAGTGCTGG GATTACAGGC ATGAGCCACC GCAGCCGGCC TGGATTTGGC 840 TCTTTAAAGG AAAGAGCGAG CCCTGGACTG GGCAGGGTGG GAAAATGGCC CCAGCTCTCC 900 CTCTGACTTC AGGGAGGGAC CTTGGATAGG GGGCTTATGG GCTCCAGGCA CCTTCTCTGT 960 AAAATTAGGT CATACTAAGG GAGCTGGAGG GCCCTTCTCT TTCTGGTATC CCAGGTGGTC 1020 TCCCCAGGGG TGGTGGTTGT GGCTGAGGCC CACTGCCTGC TTTTCTGGTG CTCTCAATGA 1080 AGTACAGTCC TGGGGTCCTC TGTATGTGGA TGGACTAGGC TGTGAAGTCT ATCCGCCCCC 1140 CTGCTCCGCT CCACACCCAC ACACTGCTCT TCACTGATAA CCCCGATGAT GCAGACAGCC 1200 TCCCTCAGGA ATTTTTCTCA TCCTCCTAGT CATCATTTCA GTCAGCCCTG CCCCGTGTGC 1260 CAGACAAGCA CACTCTATGT GTTCAAAGGT GATGCACCGA TCGTGCCCTG TCTGATGTTT 1320 ACTAACCAAC CTGACTGGGT CTGTGGGTGA CAAGGGCAGG CCCTGTTTCC CTTGGATCTT 1380 CCTTTTATGG ACACAAATCG CTGACCTGTC TGGGCAGGCC TGCTCTAATC CAGGTCTGGC 1440 CCTGAGCCTC CTGTCATTTT GCTGACCCAG TTCATCATCC TGGAGGCAGG GCTTGAGTTG 1500 AAAAGTTAGA GCCTCAGGGC AGCACCAGGA GCCTGCACTT TCCGGGGCCT CCCCTTCTCT 1560 CTCCCCTAGG CTGACCTGTC CTCCCCTCTC CACTTCCTGG GCGTGACTCA CAGGCAGGCC 1620 CTATCGGCAT GGCAGGTATG TGTCATTTCC TTATGCTGGT GAGACCCAGA GTTTCAGTGT 1680 TAGCACCCCC ACACTGTGGC TCTTCTAGCC CAATGGAGAA GGGCTAAGGG TTTCTAAAGT 1740 CGTTGACCTA GGGATTTACT GTTGGGATGA ATTTCTCACC TAGGGGAGGT GTTCTGTTTT 1800 TGCTGAGAGA TGACTGTGGG GAGCAGGGTT CTCTGCTCCT CTGACACTAC TCATCCTCCT 1860 TCCCAACACC TGTGGGCCTT TAGCAAAGCA ACACCCCACC CCCACCTTCA CCCTGACCCC 1920 AGCAGTGTTT TCTTTCCCCC CACCAAGACT TCCTTGGGGC CCTCTGGCCT TGCCAAACCC 1980 CCTTTGTAGC AGCCTCCCCT TCCAGCAGTG ACAGGAGGGA CCCAGCCTCG GGAGCCTGTC 2040 TCTGAGAGAC AGATGCAGGC AAAGAGCCGT TACCATGCAA AATCTAGAAC TGTTCCCACG 2100 TGAAATCTAG AACTTCTCCC ACACGAAATC TAGAACTGCT CCCACACGAA ATCTAGAACT 2160 GCTCCCATGC GAAATCTAGA ACCACTCCCA TGCGAAATCT TGAACCGCTG GGTGGAAATG 2220 AGGTTCAGTA GGTGCGGCAG TGTCACCTCT CTGGAGCATC TTCCCAAGTC TTTATGACAA 2280 ACAGGGATAC CCTCATGGCC AGAGTCAGCT GGGAATTTTT GTGGAAGCAG CTCCTTGGAT 2340 AGCATCACTC CTGTTCTCGT CATGGTGGAA AATGACTAAA AACTCAGGAT ATCCCACTGG 2400 CCCTGGGCAA ATTCCCTCAT TGGAGTAGGG ACTAGGACAA GGGCCAGCCC ATCCTGTCAG 2460 GCCAGAGCAC TTCTGTGGTC TTCAGCCCAG TTCTGAGGGC CCCTCTTGAA CCAGCTTTTG 2520 GGAAGCTTTG AGGGAGAGAG GGGAGCCAGA GAGGACGTCT CGTGAGAAGT GTTTGGAGGA 2580 ACTGAGGCAG GTCCAGGGAA GGCCTGGGAG AGCAGAGGAG CTGTTTTCCA CTAGTGAAAG 2640 GTCAGGAGGT GGAAGTGAGA TGGGTTTTGT TCTGTGCATC TCCATGAGCA GGCCCAGGAA 2700 GTTACAGAAA AGTAGATTTG GGATGAATAT 2730
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