Tag | Content |
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EnhancerAtlas ID | HS108-15927 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr16:89048500-89051190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr16:89050709-89050726 | TGGAACATTCTGTTCTC | - | 6.16 | HSF1 | MA0486.2 | chr16:89050701-89050714 | GAACATTCTGGAA | - | 6.54 | HSF1 | MA0486.2 | chr16:89050706-89050719 | TTCTGGAACATTC | + | 6.67 | HSF1 | MA0486.2 | chr16:89050696-89050709 | TTCTAGAACATTC | + | 7.52 | KLF5 | MA0599.1 | chr16:89049046-89049056 | GCCCCGCCCC | + | 6.02 | NR3C1 | MA0113.3 | chr16:89050709-89050726 | TGGAACATTCTGTTCTC | + | 6.14 | NR3C1 | MA0113.3 | chr16:89050709-89050726 | TGGAACATTCTGTTCTC | - | 6.56 | NR3C2 | MA0727.1 | chr16:89050709-89050726 | TGGAACATTCTGTTCTC | + | 6.22 | NR3C2 | MA0727.1 | chr16:89050709-89050726 | TGGAACATTCTGTTCTC | - | 6.64 | TBX20 | MA0689.1 | chr16:89049324-89049335 | CTTCACACCTT | - | 6.32 | TBX21 | MA0690.1 | chr16:89049325-89049335 | TTCACACCTT | - | 6.02 | ZNF263 | MA0528.1 | chr16:89048974-89048995 | TCCCCCACAGCCTCCTCCCCC | - | 6.25 | ZNF263 | MA0528.1 | chr16:89048971-89048992 | TCCTCCCCCACAGCCTCCTCC | - | 7.15 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_15361 | chr16:89048311-89048969 | CD4_Memory_Primary_7pool | SE_31022 | chr16:89048039-89054669 | Fetal_Thymus | SE_39479 | chr16:89047665-89048981 | Jurkat | SE_39479 | chr16:89048985-89050475 | Jurkat | SE_39929 | chr16:89047925-89049875 | K562 | SE_58636 | chr16:89031452-89067045 | Ly1 | SE_58997 | chr16:89033580-89060301 | Ly3 | SE_60491 | chr16:89031523-89060780 | DHL6 | SE_61382 | chr16:89033461-89071390 | HBL1 | SE_61503 | chr16:89031483-89072531 | Toledo | SE_66321 | chr16:89047665-89048981 | Jurkat | SE_66321 | chr16:89048985-89050475 | Jurkat |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 7 | Chromosome | Start | End |
chr16 | 89048691 | 89049270 | chr16 | 89049819 | 89050070 | chr16 | 89050259 | 89050442 | chr16 | 89050571 | 89050973 | chr16 | 89048615 | 89048853 | chr16 | 89049762 | 89050879 | chr16 | 89049132 | 89049661 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I088981 | chr16 | 89047982 | 89051129 |
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Enhancer Sequence | GGGACAGCCG GAACCCCACT GAGGGTCTCG AAGTCACAGG CCCCTGGTTC ACACTCAGCA 60 TTTCCTGTCT GTGCTGGGTA CGCTTGGGCA AATGTCTTGA CCCGTTTCCC CAACTGTAAA 120 GTAAGAAGGT AACAGAGTCA GCTGAATGGG GGTGTGGTGA GGATTTAATA AAACCGTCCA 180 CGTTTGGACT CTCCTATGGT GCCCGTGAAG GTGGGCAAGC ACGGACGGGC AGCTGTGACC 240 CCTGCGAGAT CCCTGAGCCG TGAAGGGGCC AGCCCAGGGG GACAGTGGAA TCCCCACACC 300 GCCTTCTGGC CATGGCCGCC TCCGGGGCAG GCGCGTTGCT GCTAGAAAGC TCTTCCTAAA 360 TTGAGCTCAG GTCGGCATCC CTGCAGATGC GGCCCCTCTC CGGAAGAGTG CTTTGGAAGG 420 GAGAAAGGGC TCTCCCAGCC CCACCGCCGC CCCCTGGAGT CAGCCACAGC CTCCTCCCCC 480 ACAGCCTCCT CCCCCACAGC CCTCCCGCCC CCATGGCAAG AGACCTGCTT CAATTGTGAT 540 GTGGCTGCCC CGCCCCTCCT CTTAAACCTT CAGTGGCTGC CCACCTCCCT CAAGATCAAG 600 GCCAGACCCT GAAGGTGGCT GGGGGCCCCT CCACACTCTG CCCCAACCCT ACATCAGAGC 660 CGCTTCTCCT GAGGGTGTTT CCTCATCTCT GGGCCTTCCC CAGCCCTCCC ATCGAAACTT 720 GCCTCACGTG GCGGGCTCCT ACCCAGCCCT CAGAGCCCAT AGGAAGTGCC CTGTCCTGTC 780 CTGGGCTCCA CACCCCCTGC ACACCTTCCT GGGTTCCACA CCCCCTTCAC ACCTTCCTGG 840 GCTCCATGCC CCCTGCACGC CTCCATCACA GCATTAGCAC CTTGGGTTGC AGTTGCTGTG 900 GGCTGGTTTC CTTGGACCCA CAGGAAAGCA GCCCTGGGCG GGAACCTTGC CTGTCTCCAA 960 GGGCTGTGTT CCCGGCACAA GGCGCAGGGC TCCATGGGTG ATGACTGGCT GGCGGAGTTT 1020 GGCACACCCA CCTCTGGGTC CCCCACACGA CACCTGGAAC TTCTCTAGGC TGAATTCCAC 1080 CTCTCTCGCC CTCAGGACTC CCCTGGGGCT CTGCCCCACA CACATCCCAG GGAACACAGA 1140 GGAAATGGCC GGTCTCCCCA GCTGCTTCCG AAGAGCAGGA TGGGCTGAGA CTCCAGGCCC 1200 GGCCGCCCAG CGCAGCCTTG GGACCCTGGG GCAGCCCCCA AGGCCTAGGG GGCTCAGTGG 1260 CCTTTGCCCG GACAGGAGGG CCTTCCCCAG CTCATCAGCC ACCCCAGGCG GGTAGTGGGT 1320 GTGGGACAGA GAGCTGACGG CAGTCAGAGG CCACAGCCCC ACAGGACCCG CTGTTCCCTT 1380 GGCTGGCATC CTCCTCCCCT CCTGAAGCGC ATGGGGCTGA GCCCAGCAGG GTGGAGTCTG 1440 AACAGAGACA GGAATTTGAG CATCAGGGCA GCAACAGCGT CGCCCCCGCT TCCTGAGCAC 1500 CCTGGACTTG CGGGGGACGC TGGTGACCTG GTGGCATATA TTCGGTGTCT GACAGGACTG 1560 GAGAGGTTAA GCAATTTCCC AGGTCACCAG CGGTGGGATT TGGGACTCAG GCTGGGTCTA 1620 AGCCAGTCCT CTCCCTGAGG CAGAGAGCCT GCTGTGGCTA CACCCACCCA GCTTCCAGGA 1680 CACGGAGCCC TCTGCCCACC GTGGTCTCTG CTCCTCCCCA GCGCCCAGGA GGCATCAAGA 1740 CCCGGCAAGG CTGCCCGTTC TGCAGAACAG GAAACCGAGG CTCCCAGAGG GGAAAGTCCC 1800 AGCCTCCCTG GGGGTCCCAG GGTCCTGGGC TGCTGCACCC CAGCTGCAAA GGGGGAAGCC 1860 CCGTCCGGAG GCCACTTTCC CTGTAAGGAG CCCAGGCGGG GTGAGGGCTG CGACGTGCCG 1920 GTGCCGCCCC GGTTTCCCTC TGACTCAGGC TGAGGCGGCT GCCCCTGTGC TGGTGCCATG 1980 TCTAGTCCGC AGGCCCCACA CCGGTGACCT GCCCTCATCT CATCTCCTGT GAGTCCGCGA 2040 GTCCACGGCT CTGCCGACGG GGGGTGGTGT GTGTGCAGCA GAAGGAATGA ACGAGGGAAC 2100 CCCTGCCCTG TGCTCTTCCT CTCCTCCCCT CCGTCCTGCC TGGGTGTTCA CAGCAGCTTA 2160 AGAGGGAAGA ACGTGGCCCT GGCCTACCCA CCAATGTTCT AGAACATTCT GGAACATTCT 2220 GTTCTCAGCC CGGAGCCTGG GAACTGGGTA AACCTGGGCC ATCGAGCGGC ATCCAACATG 2280 AGGAAAATAC CAAGAGGCTG GTGTGTGGTT CTGTGTGTGT GGCGCGTGGC GCGTGGTGCG 2340 TGGGGAGAGG CAGCCGCCCG CCCTCCAGAG CCAGGGTGCC ACCTCCTGCG TCATAGACAC 2400 CTCCCCCAAG CAGTGCCAAG CTCCTGCCTC CCACCAGTGG CTACTTCGGG CTGCAGTGGG 2460 GCCTGGGGCC ACGGAAGACC CAGCTAGGTC TGGCCAAGAG GCCCAAGGAT ATTCCAGGCA 2520 CCCGGAAGGA TCCGGAAGGA TCTGGGAGTC TTGGGTTAAG AACCATGCAG CCTGACCTGC 2580 TCCAAACGTG GACTTCGTCC CTGAAGAGGC TGCAGGACCC TAACCATTCG CGTCCTGGGC 2640 GATTGTGAGT GTGATGGACG ATCACAGCAC TGTTATTGTA TCTTAGAGCT 2690
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