Tag | Content |
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EnhancerAtlas ID | HS023-13252 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr19:44256030-44258800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr19:44257542-44257554 | TTCTGTTTACTG | - | 6.02 | JUN(var.2) | MA0489.1 | chr19:44257365-44257379 | GGAAAATGACTCAT | + | 6.76 | KLF16 | MA0741.1 | chr19:44258732-44258743 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr19:44258733-44258743 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr19:44258731-44258746 | CGGGGGCGGGGCCTG | - | 6.11 | SP4 | MA0685.1 | chr19:44258729-44258746 | GGCGGGGGCGGGGCCTG | - | 6.26 | Zfx | MA0146.2 | chr19:44258732-44258746 | GGGGGCGGGGCCTG | + | 6.19 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_02767 | chr19:44256100-44260167 | Astrocytes | SE_09619 | chr19:44255368-44262466 | CD14 | SE_10575 | chr19:44256833-44260060 | CD19_Primary | SE_11483 | chr19:44255253-44262275 | CD20 | SE_13735 | chr19:44255931-44257680 | CD34_Primary_RO01536 | SE_13735 | chr19:44257681-44261073 | CD34_Primary_RO01536 | SE_14657 | chr19:44256014-44261046 | CD4_Memory_Primary_7pool | SE_18182 | chr19:44255605-44260321 | CD4p_CD25-_CD45ROp_Memory | SE_18680 | chr19:44255276-44260362 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19217 | chr19:44256242-44260273 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20985 | chr19:44256876-44261109 | CD8_Memory_7pool | SE_23510 | chr19:44257834-44261164 | Colon_Crypt_1 | SE_23897 | chr19:44258182-44260089 | Colon_Crypt_2 | SE_27247 | chr19:44256975-44262719 | Esophagus | SE_31804 | chr19:44257590-44260338 | Gastric | SE_32542 | chr19:44255365-44264271 | GM12878 | SE_33868 | chr19:44256868-44261203 | HCC1954 | SE_34298 | chr19:44255426-44256716 | HCT-116 | SE_34298 | chr19:44256799-44272203 | HCT-116 | SE_34813 | chr19:44256968-44262677 | HeLa | SE_36558 | chr19:44255760-44264581 | HMEC | SE_37675 | chr19:44254852-44262981 | HSMMtube | SE_39921 | chr19:44256960-44261248 | K562 | SE_50403 | chr19:44256946-44260066 | Sigmoid_Colon | SE_53073 | chr19:44256976-44257621 | Small_Intestine | SE_53073 | chr19:44257665-44260035 | Small_Intestine | SE_53761 | chr19:44256508-44260208 | Spleen | SE_56117 | chr19:44257406-44262941 | u87 | SE_59025 | chr19:44248893-44290143 | Ly3 | SE_60730 | chr19:44257018-44289948 | DHL6 | SE_62525 | chr19:44242576-44303622 | Tonsil | SE_64692 | chr19:44256932-44264220 | NHEK |
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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 | ACTTGCAGCC AAAACTATTC CCAACTATTA AAATGCTCCA ACATAAATAA ACTCACAGGG 60 GCAAGTTCAC ATAAAAATAG GATATTCTCC TTACCAAAAT GCAGCAAGGC ATTTGCTTAC 120 AAACCAGCAA TGTGATCCTC AGTCCAACAG CTACTCTTGA TTAGTCATTA CTAGTGTATG 180 TCATGGTGGG GCTCCAGCCA CTTACTAGTG TATGTCATGG TGAGGTTCCA ACACTCAAGG 240 GCCTATTTTC ACCTGGTATC CCACTACATT TCAGTGTCTG TCTGTCTTCC GTTCCTGACG 300 GTCTGCCTTC CCTCACAGTG AATTTCATTT CAAGGTGTCT CCAGTGTTTA TTCTATTTGA 360 GATGTTATAT AATGTCTGGC TACCTATGCA ACCCACTCTC CACCATTTCA GTATCTGTTT 420 ACAGGTCCTT AGAGAGTTTT CCCAGCTGTT CACACATCAG TCTAGGGTGG TATTTGACTA 480 CTTAACTGTT TGTAGAACTC AGTGGGGCTA TCTGCTCAAG CTCAGAAGTC AGGTTGACAA 540 AGTGTGGCCT AGGGGCCAAA TCTGGTCTGC TTTCTGTTTT TGTAAATAGA AAGTTTTATC 600 GGAACATGGC CACATCCATC AATTTAGAAA CTGTCTGTGG CTGCCTTCTT GATGCAATGG 660 CAGAGCTGAG ACAGACAATA CAGTCTGCAG GGCCTAAAAT AATTATTCTC TGGCCTTAAC 720 AGAAAGTTTT ACTGAATGGC CGAGTATGGT GGCTCACACC TGTAATCCCG ACACTTTGGG 780 AGGCCGAGAC AGGAGGACTG CTTCAGCCCA GGAGTTCGAG ACCAGCTTGG GCAACATAGC 840 AAGATCCTGT CTCTATATAA CATTTAAAAA AGAAAAAAGT AGCTGGGCGT GGTGACATGC 900 ACCTGTAGTC CCAGCTACTT GGGAGGCTGA GGTGGTGGGA TCACTTGAGC CTGGGAGGTC 960 AAGGCTGCCA TGATCATGCT GCACCACTGC ACTCTAGCCT GGGTAACAAA GCAAGACCCT 1020 GTCTAAAAAA AAAAAAAAGC AGAACCCTGT CTCAAAAAAA CAGTTTGCTG ACCCTTGCTT 1080 AGCTTGGAAG TATCTGTTAA ATCCCTCCAT GAATCCTCCC CTGCCCCACC TCATAATGAC 1140 ATAAACAGGT CCCTCCGAGA CTCTCCAGAA TGGAAGGGTC TGTTTACAAG ATGCAGTCAT 1200 AATTTTGCTA GCCAGACAAG TGGCTTGTCT AGCTCCTCTC CTACTGTGCT ACATGACCTC 1260 TCCCAGAGCC ACAAGCCAGG CTGAAGACTG CTTTCCTAGA CAGAGGAGGA CAAGGGCCTG 1320 TTTACAGCTG CTTAGGGAAA ATGACTCATT CCATACCGAA ATGACTGCTT AGTCTGGGAT 1380 GGAGATTCTC CCCAGAATCT GAGACTCCTC CCTCACTTGC AATTAAGTGT CTTTACACAT 1440 TATTCTGAAA TCTACCCAGT GCTTAAGTAC TTGTCTTCAT GCCTCAATTG GGATACTGCC 1500 CAGCCCTGAG GTTTCTGTTT ACTGGCCTAT GAGGATGCCC TTTCCTGTGC AAAGTAAGCG 1560 CCCCTGTGTG AATGCTTTTC TTTTTTTTTT TTTTTTTTTT TTGAGACGGT CTTGCTCTGT 1620 TGCCCAGGCT GGAGTGCAGT GGCACGATCT CAGCTGGCTG CGGCCTCTGC CTCCCGGGTT 1680 CAGGCAATTC TCCTGCCTCA GCCTCCCAAG TAGGTGGGAT TACAGGTGCA TACCACCAGG 1740 CCGGGCTAAG TTTTGCATTT TCAGTAGAGA CGGGGTTTCG CCATGTTGGC CAGGCTGGTA 1800 TCGAACTCCT GGCCTCAAGT GATTCGCCAG CCTCGGTCTC CCAAAGTGAT CGGATTCCCC 1860 GGGTAAGCCA CCGCACCTGG CCTCCCTGTG CCCTTTATTC TGGGAGCTTC CACAGTATCT 1920 GAATGTGGGG AGTTCCTTGG AACTTAAAAG CCCACCTAAA CCAGGTGTGG AGGATACAGT 1980 GAGCCGAGAT CGTGCCACTG CACTCCAGCC TGGGCGACAG AGCGAGACTC TTGTCTCAAA 2040 GAAAAAAAAA AAAAACCCCA CCCACATGCA AGCTGGGGAC TTCCAATGCT GTTTCCGGGC 2100 TCCTTTGGGG ATTACCCCCA AACTTAGGAA AGCTGGTCTA TTTAAGTGTC TGCTGATGGA 2160 CTTCTAGGGT GACTTCCCGA AAATTAACAA ATCGAATTTA CATATTTTTG GGGAGTGTCT 2220 CCTCAGTATT TAGGCATCGC TTCACACACT CCCTTCGGGG ATCTCCCAGA ACCTCACTAT 2280 TTGCAAATAT TTGGGGAGAC TCTCCCGATT CCTGAGTATG TAAGCCCACT TCGTGGGGCA 2340 CTCCCCAGCC CAGAACTGTA GTCGATTTGC ACATTTTCCT AAGGACTCCC TAGGATTTAA 2400 ACTTCTCTCT ACGGGGTTCT AGAAGGGAGC CTCCCCCGGA TTTAGGCATT GCTTTACAAA 2460 GCTTCCCTCG GGGAACCCAA CTCAAGTTTC TCGTTACACG TTATTGGGGC GGCCTCCCCA 2520 GTACTTGACG GGCAGTTTGC AGGCTGTACT TGGATCTCGC AGAGCATAAG TTTCTCATTT 2580 ACACGTTATT TCCGTCCCCC GCCCCCATTC CTGCCAACCC AGTATCGAAT TGACGGTCGC 2640 CGGCCCCCTA CTCAGTGCCG CACCCCCGCC GGACGTCCCA GCGACCTTTC AATGGCCAAG 2700 GCGGGGGCGG GGCCTGCCGG AGCGCCCCGC CCGCCGCCGG TGCGCTAGCC TCGCGCGGGC 2760 TCGCGGCCCC 2770
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