Tag | Content |
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EnhancerAtlas ID | HS095-15308 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr19:44256000-44258800 |
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 | CAGTGAAAAA CAAATACACA TCTATCTCTT ACTTGCAGCC AAAACTATTC CCAACTATTA 60 AAATGCTCCA ACATAAATAA ACTCACAGGG GCAAGTTCAC ATAAAAATAG GATATTCTCC 120 TTACCAAAAT GCAGCAAGGC ATTTGCTTAC AAACCAGCAA TGTGATCCTC AGTCCAACAG 180 CTACTCTTGA TTAGTCATTA CTAGTGTATG TCATGGTGGG GCTCCAGCCA CTTACTAGTG 240 TATGTCATGG TGAGGTTCCA ACACTCAAGG GCCTATTTTC ACCTGGTATC CCACTACATT 300 TCAGTGTCTG TCTGTCTTCC GTTCCTGACG GTCTGCCTTC CCTCACAGTG AATTTCATTT 360 CAAGGTGTCT CCAGTGTTTA TTCTATTTGA GATGTTATAT AATGTCTGGC TACCTATGCA 420 ACCCACTCTC CACCATTTCA GTATCTGTTT ACAGGTCCTT AGAGAGTTTT CCCAGCTGTT 480 CACACATCAG TCTAGGGTGG TATTTGACTA CTTAACTGTT TGTAGAACTC AGTGGGGCTA 540 TCTGCTCAAG CTCAGAAGTC AGGTTGACAA AGTGTGGCCT AGGGGCCAAA TCTGGTCTGC 600 TTTCTGTTTT TGTAAATAGA AAGTTTTATC GGAACATGGC CACATCCATC AATTTAGAAA 660 CTGTCTGTGG CTGCCTTCTT GATGCAATGG CAGAGCTGAG ACAGACAATA CAGTCTGCAG 720 GGCCTAAAAT AATTATTCTC TGGCCTTAAC AGAAAGTTTT ACTGAATGGC CGAGTATGGT 780 GGCTCACACC TGTAATCCCG ACACTTTGGG AGGCCGAGAC AGGAGGACTG CTTCAGCCCA 840 GGAGTTCGAG ACCAGCTTGG GCAACATAGC AAGATCCTGT CTCTATATAA CATTTAAAAA 900 AGAAAAAAGT AGCTGGGCGT GGTGACATGC ACCTGTAGTC CCAGCTACTT GGGAGGCTGA 960 GGTGGTGGGA TCACTTGAGC CTGGGAGGTC AAGGCTGCCA TGATCATGCT GCACCACTGC 1020 ACTCTAGCCT GGGTAACAAA GCAAGACCCT GTCTAAAAAA AAAAAAAAGC AGAACCCTGT 1080 CTCAAAAAAA CAGTTTGCTG ACCCTTGCTT AGCTTGGAAG TATCTGTTAA ATCCCTCCAT 1140 GAATCCTCCC CTGCCCCACC TCATAATGAC ATAAACAGGT CCCTCCGAGA CTCTCCAGAA 1200 TGGAAGGGTC TGTTTACAAG ATGCAGTCAT AATTTTGCTA GCCAGACAAG TGGCTTGTCT 1260 AGCTCCTCTC CTACTGTGCT ACATGACCTC TCCCAGAGCC ACAAGCCAGG CTGAAGACTG 1320 CTTTCCTAGA CAGAGGAGGA CAAGGGCCTG TTTACAGCTG CTTAGGGAAA ATGACTCATT 1380 CCATACCGAA ATGACTGCTT AGTCTGGGAT GGAGATTCTC CCCAGAATCT GAGACTCCTC 1440 CCTCACTTGC AATTAAGTGT CTTTACACAT TATTCTGAAA TCTACCCAGT GCTTAAGTAC 1500 TTGTCTTCAT GCCTCAATTG GGATACTGCC CAGCCCTGAG GTTTCTGTTT ACTGGCCTAT 1560 GAGGATGCCC TTTCCTGTGC AAAGTAAGCG CCCCTGTGTG AATGCTTTTC TTTTTTTTTT 1620 TTTTTTTTTT TTGAGACGGT CTTGCTCTGT TGCCCAGGCT GGAGTGCAGT GGCACGATCT 1680 CAGCTGGCTG CGGCCTCTGC CTCCCGGGTT CAGGCAATTC TCCTGCCTCA GCCTCCCAAG 1740 TAGGTGGGAT TACAGGTGCA TACCACCAGG CCGGGCTAAG TTTTGCATTT TCAGTAGAGA 1800 CGGGGTTTCG CCATGTTGGC CAGGCTGGTA TCGAACTCCT GGCCTCAAGT GATTCGCCAG 1860 CCTCGGTCTC CCAAAGTGAT CGGATTCCCC GGGTAAGCCA CCGCACCTGG CCTCCCTGTG 1920 CCCTTTATTC TGGGAGCTTC CACAGTATCT GAATGTGGGG AGTTCCTTGG AACTTAAAAG 1980 CCCACCTAAA CCAGGTGTGG AGGATACAGT GAGCCGAGAT CGTGCCACTG CACTCCAGCC 2040 TGGGCGACAG AGCGAGACTC TTGTCTCAAA GAAAAAAAAA AAAAACCCCA CCCACATGCA 2100 AGCTGGGGAC TTCCAATGCT GTTTCCGGGC TCCTTTGGGG ATTACCCCCA AACTTAGGAA 2160 AGCTGGTCTA TTTAAGTGTC TGCTGATGGA CTTCTAGGGT GACTTCCCGA AAATTAACAA 2220 ATCGAATTTA CATATTTTTG GGGAGTGTCT CCTCAGTATT TAGGCATCGC TTCACACACT 2280 CCCTTCGGGG ATCTCCCAGA ACCTCACTAT TTGCAAATAT TTGGGGAGAC TCTCCCGATT 2340 CCTGAGTATG TAAGCCCACT TCGTGGGGCA CTCCCCAGCC CAGAACTGTA GTCGATTTGC 2400 ACATTTTCCT AAGGACTCCC TAGGATTTAA ACTTCTCTCT ACGGGGTTCT AGAAGGGAGC 2460 CTCCCCCGGA TTTAGGCATT GCTTTACAAA GCTTCCCTCG GGGAACCCAA CTCAAGTTTC 2520 TCGTTACACG TTATTGGGGC GGCCTCCCCA GTACTTGACG GGCAGTTTGC AGGCTGTACT 2580 TGGATCTCGC AGAGCATAAG TTTCTCATTT ACACGTTATT TCCGTCCCCC GCCCCCATTC 2640 CTGCCAACCC AGTATCGAAT TGACGGTCGC CGGCCCCCTA CTCAGTGCCG CACCCCCGCC 2700 GGACGTCCCA GCGACCTTTC AATGGCCAAG GCGGGGGCGG GGCCTGCCGG AGCGCCCCGC 2760 CCGCCGCCGG TGCGCTAGCC TCGCGCGGGC TCGCGGCCCC 2800
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