Tag | Content |
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EnhancerAtlas ID | HS047-23026 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr22:42695520-42696900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:42696059-42696077 | CGTTCCTTCGTTCCTTCG | - | 6.54 | EWSR1-FLI1 | MA0149.1 | chr22:42696055-42696073 | CTTTCGTTCCTTCGTTCC | - | 6.95 | ZNF263 | MA0528.1 | chr22:42695935-42695956 | GAGGAAGAAAGGAGAGGAGGG | + | 6.03 | ZNF263 | MA0528.1 | chr22:42695830-42695851 | AGAGAAGGGGGAGAAGGAAGC | + | 6.08 | ZNF263 | MA0528.1 | chr22:42695944-42695965 | AGGAGAGGAGGGGAAGGAAGG | + | 6.1 | ZNF263 | MA0528.1 | chr22:42695810-42695831 | TGGGGATGGGGGAGGGGAAGA | + | 6.23 | ZNF263 | MA0528.1 | chr22:42695953-42695974 | GGGGAAGGAAGGGCGGGGAGG | + | 6.26 | ZNF263 | MA0528.1 | chr22:42695956-42695977 | GAAGGAAGGGCGGGGAGGGGG | + | 6.33 | ZNF263 | MA0528.1 | chr22:42695938-42695959 | GAAGAAAGGAGAGGAGGGGAA | + | 6.36 | ZNF263 | MA0528.1 | chr22:42695947-42695968 | AGAGGAGGGGAAGGAAGGGCG | + | 6.4 | ZNF263 | MA0528.1 | chr22:42695796-42695817 | GGAGGAGGAAGTGGTGGGGAT | + | 6.58 | ZNF263 | MA0528.1 | chr22:42695839-42695860 | GGAGAAGGAAGCGGAGGGGAG | + | 6.69 | ZNF263 | MA0528.1 | chr22:42695836-42695857 | GGGGGAGAAGGAAGCGGAGGG | + | 6.79 | ZNF263 | MA0528.1 | chr22:42695853-42695874 | AGGGGAGGAGGGAGGAGGGAA | + | 6.84 | ZNF263 | MA0528.1 | chr22:42695793-42695814 | AGAGGAGGAGGAAGTGGTGGG | + | 6.93 | ZNF263 | MA0528.1 | chr22:42695966-42695987 | CGGGGAGGGGGAGGGGGAGGG | + | 7.01 | ZNF263 | MA0528.1 | chr22:42695817-42695838 | GGGGGAGGGGAAGAGAGAAGG | + | 7.11 | ZNF263 | MA0528.1 | chr22:42695914-42695935 | GGAGGAGGGGGAAAGGGAGCA | + | 7.5 | ZNF263 | MA0528.1 | chr22:42695856-42695877 | GGAGGAGGGAGGAGGGAAAAG | + | 7.69 | ZNF263 | MA0528.1 | chr22:42695908-42695929 | GGTGGAGGAGGAGGGGGAAAG | + | 8.08 | ZNF263 | MA0528.1 | chr22:42695911-42695932 | GGAGGAGGAGGGGGAAAGGGA | + | 9.32 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_23330 | chr22:42695863-42698813 | Colon_Crypt_1 | SE_23842 | chr22:42695766-42696384 | Colon_Crypt_2 | SE_23842 | chr22:42696407-42698797 | Colon_Crypt_2 | SE_25072 | chr22:42694701-42695817 | Colon_Crypt_3 | SE_25072 | chr22:42695921-42698957 | Colon_Crypt_3 | SE_50938 | chr22:42695852-42698100 | Sigmoid_Colon | SE_56829 | chr22:42695891-42696837 | VACO_400 | SE_65474 | chr22:42695910-42696986 | Pancreatic_islets |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH22I042298 | chr22 | 42694880 | 42697851 |
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Enhancer Sequence | TGGTGGGTCA CCCAGGAACC CCGAGGAACT GGAATGGGGG TGGAGGGGAA TCACATGTCC 60 CACTGGTCAC CAGTCCCTCT TGCCTTTCTG TCCCAGCTAG CAGCTCTCCA ACCTCTGTAC 120 CTCTCCCCGA ACGCAGGCCC CCCTGCCCGC ACCCCAACAC TTCAAGACCT CCTAGGAGTG 180 ACCTGGCTGG GGTCTCTCTA GGTCAGGTAA TTAATAGCAG GAGGGAAGTG CAATTAGCAG 240 GTACCTGGAG TGGGGTCGGT AAGAGAGAAT AGCAGAGGAG GAGGAAGTGG TGGGGATGGG 300 GGAGGGGAAG AGAGAAGGGG GAGAAGGAAG CGGAGGGGAG GAGGGAGGAG GGAAAAGACA 360 GAAAGGGGTA GAAGGGAAGC TTGGAGCGGG TGGAGGAGGA GGGGGAAAGG GAGCAGAGGA 420 AGAAAGGAGA GGAGGGGAAG GAAGGGCGGG GAGGGGGAGG GGGAGGGGCG CGCTGAAATC 480 ACCCGCAACA TCAAAGCCTT CCCCAGCCGC AAAGCAGTCA CGTGCAGCCT GGTTCCTTTC 540 GTTCCTTCGT TCCTTCGCTG GTAGAAGCCG CTGGGCCTGG GGCTGCTGAA GGAATTTTAA 600 AACGAGGCAG ATTGTCTGGA ATATCAGGGG GTTAGGGGAA TGCGGTTTTA TCTCAAGGCA 660 GGGTAAGGGG AGGCAGGTTT TGAAACCTGT TCCCCCAAGG AGAGCGGCAG GGCTTTGGGG 720 CCTCTGCTAG GAGGCTGGGC AGGTGGCCAA GAGTGAAGAC CACCCAGCTA CTCCTGCCGG 780 TGAGAGCTCG TGGCTGGGCC AGCCCAGATA TCAACAGAAG CCAGAAATCT AGATTTGTAT 840 GTGAAAACTT CCCTGTTTTA ATTTTGGCTC AAACTAAAAA AAAAAAGAAA AAAAGCGCCA 900 CATGGGCCAA ATAGAGCATG TCCTGACTGG GGCCCAGAAC CTCGGTCACC TCCCACTTCT 960 GATGGTGGGC AGCAACGCTT TTGTTTCCCA GGGGGCACTG AGGCCCAGGA AGGGAAAGGC 1020 ACTTGTTCAG GGACACACAC AGTGAGTGCT CAAGGGGTGC GGGCTAAGAC TTGGGGTCTC 1080 AGGACTCCCA TGCCTGAAGC CTCCTGCGGT CAGCAGCCCA AGGGGCAGGG CTGTGGCTGC 1140 TGGGAAAGGG AAGTATAGGG AGGTTAGTGG CAGGGGAGGG TCTCAGAAAA CCCCTCGTCC 1200 AGCCCAGGGC CAACACACTC AGCCCCACTC ATCACCCTGA TGACTAACCC AGGCCTGCCT 1260 CTCTGCCTTT GCCTCTGCTC AGCCCATCCT CCCTATCCAC TCCTGACATT CCCTCCTCCC 1320 CCTGCCAAGA CCTGGGCAGC TTCCCCTCCC CCGAGCCCCA CCTGCAGAAT GCACCATGCA 1380
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