Tag | Content |
---|
EnhancerAtlas ID | HS060-18016 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:44256020-44258800 |
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 |
|
| 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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCTATCTCTT ACTTGCAGCC AAAACTATTC CCAACTATTA AAATGCTCCA ACATAAATAA 60 ACTCACAGGG GCAAGTTCAC ATAAAAATAG GATATTCTCC TTACCAAAAT GCAGCAAGGC 120 ATTTGCTTAC AAACCAGCAA TGTGATCCTC AGTCCAACAG CTACTCTTGA TTAGTCATTA 180 CTAGTGTATG TCATGGTGGG GCTCCAGCCA CTTACTAGTG TATGTCATGG TGAGGTTCCA 240 ACACTCAAGG GCCTATTTTC ACCTGGTATC CCACTACATT TCAGTGTCTG TCTGTCTTCC 300 GTTCCTGACG GTCTGCCTTC CCTCACAGTG AATTTCATTT CAAGGTGTCT CCAGTGTTTA 360 TTCTATTTGA GATGTTATAT AATGTCTGGC TACCTATGCA ACCCACTCTC CACCATTTCA 420 GTATCTGTTT ACAGGTCCTT AGAGAGTTTT CCCAGCTGTT CACACATCAG TCTAGGGTGG 480 TATTTGACTA CTTAACTGTT TGTAGAACTC AGTGGGGCTA TCTGCTCAAG CTCAGAAGTC 540 AGGTTGACAA AGTGTGGCCT AGGGGCCAAA TCTGGTCTGC TTTCTGTTTT TGTAAATAGA 600 AAGTTTTATC GGAACATGGC CACATCCATC AATTTAGAAA CTGTCTGTGG CTGCCTTCTT 660 GATGCAATGG CAGAGCTGAG ACAGACAATA CAGTCTGCAG GGCCTAAAAT AATTATTCTC 720 TGGCCTTAAC AGAAAGTTTT ACTGAATGGC CGAGTATGGT GGCTCACACC TGTAATCCCG 780 ACACTTTGGG AGGCCGAGAC AGGAGGACTG CTTCAGCCCA GGAGTTCGAG ACCAGCTTGG 840 GCAACATAGC AAGATCCTGT CTCTATATAA CATTTAAAAA AGAAAAAAGT AGCTGGGCGT 900 GGTGACATGC ACCTGTAGTC CCAGCTACTT GGGAGGCTGA GGTGGTGGGA TCACTTGAGC 960 CTGGGAGGTC AAGGCTGCCA TGATCATGCT GCACCACTGC ACTCTAGCCT GGGTAACAAA 1020 GCAAGACCCT GTCTAAAAAA AAAAAAAAGC AGAACCCTGT CTCAAAAAAA CAGTTTGCTG 1080 ACCCTTGCTT AGCTTGGAAG TATCTGTTAA ATCCCTCCAT GAATCCTCCC CTGCCCCACC 1140 TCATAATGAC ATAAACAGGT CCCTCCGAGA CTCTCCAGAA TGGAAGGGTC TGTTTACAAG 1200 ATGCAGTCAT AATTTTGCTA GCCAGACAAG TGGCTTGTCT AGCTCCTCTC CTACTGTGCT 1260 ACATGACCTC TCCCAGAGCC ACAAGCCAGG CTGAAGACTG CTTTCCTAGA CAGAGGAGGA 1320 CAAGGGCCTG TTTACAGCTG CTTAGGGAAA ATGACTCATT CCATACCGAA ATGACTGCTT 1380 AGTCTGGGAT GGAGATTCTC CCCAGAATCT GAGACTCCTC CCTCACTTGC AATTAAGTGT 1440 CTTTACACAT TATTCTGAAA TCTACCCAGT GCTTAAGTAC TTGTCTTCAT GCCTCAATTG 1500 GGATACTGCC CAGCCCTGAG GTTTCTGTTT ACTGGCCTAT GAGGATGCCC TTTCCTGTGC 1560 AAAGTAAGCG CCCCTGTGTG AATGCTTTTC TTTTTTTTTT TTTTTTTTTT TTGAGACGGT 1620 CTTGCTCTGT TGCCCAGGCT GGAGTGCAGT GGCACGATCT CAGCTGGCTG CGGCCTCTGC 1680 CTCCCGGGTT CAGGCAATTC TCCTGCCTCA GCCTCCCAAG TAGGTGGGAT TACAGGTGCA 1740 TACCACCAGG CCGGGCTAAG TTTTGCATTT TCAGTAGAGA CGGGGTTTCG CCATGTTGGC 1800 CAGGCTGGTA TCGAACTCCT GGCCTCAAGT GATTCGCCAG CCTCGGTCTC CCAAAGTGAT 1860 CGGATTCCCC GGGTAAGCCA CCGCACCTGG CCTCCCTGTG CCCTTTATTC TGGGAGCTTC 1920 CACAGTATCT GAATGTGGGG AGTTCCTTGG AACTTAAAAG CCCACCTAAA CCAGGTGTGG 1980 AGGATACAGT GAGCCGAGAT CGTGCCACTG CACTCCAGCC TGGGCGACAG AGCGAGACTC 2040 TTGTCTCAAA GAAAAAAAAA AAAAACCCCA CCCACATGCA AGCTGGGGAC TTCCAATGCT 2100 GTTTCCGGGC TCCTTTGGGG ATTACCCCCA AACTTAGGAA AGCTGGTCTA TTTAAGTGTC 2160 TGCTGATGGA CTTCTAGGGT GACTTCCCGA AAATTAACAA ATCGAATTTA CATATTTTTG 2220 GGGAGTGTCT CCTCAGTATT TAGGCATCGC TTCACACACT CCCTTCGGGG ATCTCCCAGA 2280 ACCTCACTAT TTGCAAATAT TTGGGGAGAC TCTCCCGATT CCTGAGTATG TAAGCCCACT 2340 TCGTGGGGCA CTCCCCAGCC CAGAACTGTA GTCGATTTGC ACATTTTCCT AAGGACTCCC 2400 TAGGATTTAA ACTTCTCTCT ACGGGGTTCT AGAAGGGAGC CTCCCCCGGA TTTAGGCATT 2460 GCTTTACAAA GCTTCCCTCG GGGAACCCAA CTCAAGTTTC TCGTTACACG TTATTGGGGC 2520 GGCCTCCCCA GTACTTGACG GGCAGTTTGC AGGCTGTACT TGGATCTCGC AGAGCATAAG 2580 TTTCTCATTT ACACGTTATT TCCGTCCCCC GCCCCCATTC CTGCCAACCC AGTATCGAAT 2640 TGACGGTCGC CGGCCCCCTA CTCAGTGCCG CACCCCCGCC GGACGTCCCA GCGACCTTTC 2700 AATGGCCAAG GCGGGGGCGG GGCCTGCCGG AGCGCCCCGC CCGCCGCCGG TGCGCTAGCC 2760 TCGCGCGGGC TCGCGGCCCC 2780
|