Tag | Content |
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EnhancerAtlas ID | HS105-39364 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:16694230-16696830 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr19:16695079-16695100 | AAAAAAAAACCGAAACCCAAA | - | 6.42 | IRF9 | MA0653.1 | chr19:16695081-16695096 | AAAAAAACCGAAACC | + | 6.02 | REL | MA0101.1 | chr19:16696774-16696784 | GGGGATTTCC | + | 6.02 | RREB1 | MA0073.1 | chr19:16694303-16694323 | GCAAGGGTGTTGGGTGGGGG | - | 6.02 | RREB1 | MA0073.1 | chr19:16694310-16694330 | TGTTGGGTGGGGGTGGGGGG | - | 6.06 | RREB1 | MA0073.1 | chr19:16694313-16694333 | TGGGTGGGGGTGGGGGGTGT | - | 6.88 | RUNX1 | MA0002.2 | chr19:16696082-16696093 | AAACCACAGAG | - | 6.14 | SPIB | MA0081.2 | chr19:16695724-16695736 | AAAGGGGAAGTG | + | 6.07 |
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| Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
SE_09556 | chr19:16689941-16700289 | CD14 | SE_10322 | chr19:16693911-16700445 | CD19_Primary | SE_11025 | chr19:16689881-16701279 | CD20 | SE_15319 | chr19:16691347-16700340 | CD4_Memory_Primary_7pool | SE_19879 | chr19:16693803-16700556 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_41644 | chr19:16691491-16695023 | LNCaP | SE_41644 | chr19:16695151-16695629 | LNCaP | SE_41644 | chr19:16695682-16696627 | LNCaP | SE_42812 | chr19:16694113-16700278 | Lung | SE_43691 | chr19:16693975-16701621 | MM1S | SE_47925 | chr19:16695127-16695622 | Pancreas | SE_47925 | chr19:16695910-16696283 | Pancreas | SE_50580 | chr19:16693677-16700293 | Sigmoid_Colon | SE_55639 | chr19:16694186-16694995 | Thymus | SE_55639 | chr19:16695217-16696705 | Thymus | SE_58924 | chr19:16691452-16706437 | Ly3 | SE_60472 | chr19:16691717-16741782 | DHL6 | SE_62862 | chr19:16692050-16720109 | Tonsil | SE_65774 | chr19:16691062-16701216 | Pancreatic_islets | SE_67326 | chr19:16693975-16701621 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 16696208 | 16696379 | chr19 | 16694400 | 16696526 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I016579 | chr19 | 16690318 | 16701250 |
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Enhancer Sequence | ACACTGACCG CCCCTGCCCA CTTAATTTGC TTCAGTTTGG CCTCTTCATT GCTGCGGGAA 60 GTGCCTGTGA AGGGCAAGGG TGTTGGGTGG GGGTGGGGGG TGTCGACAGC AGAACCTCCA 120 TGCAGCTACT AGGAGAAGCA GGGGTAAATG CAGCAAGGAG CACTCTGGAA GCAGGTGGGA 180 CCTCCCTGGG GTGCCTGCTC CAAAGGCAGG CAGGGCAGGA AGTTAGCAGG TGGGACCAGG 240 TGTGGCACAG GTATACATGC AGGTCCAGCC CAGCCGCCTG GTACATGAAT GTTGATGGAA 300 CTGACTCCAC TGTCACACCG AACACTTTCA GGTCTTAGAA TGGAAATCCA TGAGGCATGA 360 TCAGGTACAC ATGGGCCAAT AGGAATGTGA ACATTAATCT CGTCCTTCTG GAATCTCAGA 420 AAAACCAAGC AGGGAGGCCT GGTCTCAGGT CATAGGCATC ACAGCTAGCA TAGATACTGA 480 GGAAGAACAG TTTGCATCCA GGCAGAGGGT GAACTGGGGC CACCAGCACA ACCCTCAGCA 540 CACAGGTGCC CCACACTTCA GGGATGCCCC AGGAACACAC GCATGGGGGC ATGGAGGGGA 600 CAACTTCTCG CCCAAGACCA CAAGAGGTCT GGCTGTCCCA GGGCTCTTTT GTGGTCATCC 660 TTCCACATGA GAACTTAAAA AGGCTTCCAC GGGCGCGGTG GTGTGCACCT GTAATCCCAG 720 CTACTCGGGA GGCTGAGGCA GGAGAATCGC TCAAACCTGG GAGGCGGAGG TTGCAATGAG 780 CTGAGATCAC GCCACTGCAC TCCAGCCTCG GTGACAGAGC AAGACTCCGT CTCAAAAAAA 840 AGAAAAAGAA AAAAAAAACC GAAACCCAAA CACTGCCCCC CCCCGCCCCG CCAAAAAAAA 900 ACAAAAAACA AAACAAAAAA AAGAAAGGCT TCCGGAAAGG CTGGCACCTT TGTCCCCAGA 960 GAGCCCCATA GCCTGTGCTA AGCCACAATT CCAGCCAGCC TAACTGGTGA CATGTGCTGT 1020 TCAGCTCACA GGAAATGTGA GGAAGGAGGC GGGGCTGGAC ACGCACAGAG ACAGCCTGAG 1080 GGAGGGGCCA GCACCCCTCA GAAGCAGCCT GGGTCAGGCG CCTGGAGCTG CGTGAGACAC 1140 CTCATTCTCC CACACCCTGG GAGCAGTGGG GAACCCTGTA TGCGACTTCA CAGCACACCA 1200 CGCTCCGTGT GAGCTATTAA AGACCCACCA CGCATCCTCG TCTTTCAGTG ACACTTTCCT 1260 GAAGAAATAA TACAATCTGG AATTTGCTAC AGAATCATCC CCTAGGGTGA GTGACAGGAG 1320 GGGGATGGGT GAAACAAAGT CACATGGCTG TAAGCAGCTA TCTACTGAAG CAGGATGGTT 1380 ACCTTTCTCT ACTTTTATGC TTGAAATTTC TCACAAATAA AGATGAGAAA ATACATCTAT 1440 TTCCTAGCAT TTGTTTGGGA GAGTTCACTG ATCTAGAAGG ACTGGCAGCC ATCTAAAGGG 1500 GAAGTGAGCA AATAGCTGTT TCCAACTCCT CATAGTGGCT TCACTGTCCA CCATCTGGCC 1560 CCTGAGTGGG GCAGCAAGGG CCGAGGGCTG GGTAGGATGC CACCTCCCTC CACGTGAGCC 1620 TGTCTCAAGT CTCAGGCCTC CTAACTGATT TGAACTGCAC AACACCATCT ATCTGGTGAG 1680 ACCCCAGGAG CCCCTCACCA AGCTCCCCTA CTCTGGTACT GGGCTGCTGC TTAACAGACC 1740 TGGTGCAGAA ACAGCAGGCA CCCCTGGGGC TGGAGAGGGG AGCTCTGAGT ACCCATGCCA 1800 GCTGTCCATC CCGGTCCGAC TCTCAGGTGT CCTCACGCCT CTCTTCTAAA GGAAACCACA 1860 GAGAGCCCGA ACCAGGGGCA CACGCTAGGT CGACAGTTCC TTCCTGCAGG GAGAGGCCTG 1920 ACCTGTACCA GGAAGGAGCC CAGGACAGCC ACCACCACAG AGAGGACAGG CCCTCAAGTG 1980 GCCCAGACCA GGAGGGAGGA CTTGGCAAGA AGGGGTGGGG GCTAGGTCAC TCTCTTCCAG 2040 AAGGGGAGAA ACATAACAAT GAGCCAGCAG TAACCCAGGG AAGGGACAGC CGTCACTCCA 2100 GGACCTGCCC AGCCCCAGTC AGCACCACCT CCCTCCCATC TGCGATCCAC ATCCTATGGC 2160 TCTGGGCACA GCTGAGCCAC AGGACACAGC CACTCAGAAC TTTCTTTCCA GGTTTCCCTC 2220 AAAGGCCAGC CAGCAGCACT CCTCTGTGGC CCTGTGAAAC CCAGTGACAC CTCTGACCCC 2280 TCCGGAGTCC GGAAGACTAG ACTCTTCTGA AAACCCACCT ACGACAGGGT GCGTGGAATC 2340 ACCTTTCAAA CCAAACTCCT GTCGGCAAAT ATTTTAATTG GGCCACGGCA TGTGTCCGAG 2400 TTTTTCTTCT GTGAAGAGGA TCACTGGGTC TGAGTGCAAA GCTGGGGCCT GTTCAGTGGA 2460 GTGGACCCGC TACTGGCCAA CCTCTTCCTC GCTTTATTAC AGGGGTGTGT AAGTAAAACC 2520 CTCAGGCCCT GAGTAATTAC TGCTGGGGAT TTCCAGCCCT GGTCTGAAAC AAGGAACTGA 2580 GACTGAGTTT TGAGTCCCAG 2600
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