Tag | Content |
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EnhancerAtlas ID | HS047-29087 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr6:44040160-44041300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr6:44040656-44040670 | ACTCCCTTGGGAGT | - | 6.16 | IRF2 | MA0051.1 | chr6:44040814-44040832 | CAAAAGTGAAACTATATG | + | 6.04 | SOX10 | MA0442.2 | chr6:44040703-44040714 | TCCTTTGTTTT | - | 6.32 | Sox3 | MA0514.1 | chr6:44040704-44040714 | CCTTTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr6:44041262-44041283 | GTGGGAGGGGGAGGAGGAGGG | + | 6.08 | ZNF263 | MA0528.1 | chr6:44041265-44041286 | GGAGGGGGAGGAGGAGGGGAG | + | 6.64 | ZNF263 | MA0528.1 | chr6:44041274-44041295 | GGAGGAGGGGAGGGGGAGGCG | + | 6.75 | ZNF263 | MA0528.1 | chr6:44041268-44041289 | GGGGGAGGAGGAGGGGAGGGG | + | 8.45 | ZNF263 | MA0528.1 | chr6:44041271-44041292 | GGAGGAGGAGGGGAGGGGGAG | + | 9.2 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_09949 | chr6:44040205-44042136 | CD14 | SE_14577 | chr6:44038642-44046904 | CD4_Memory_Primary_7pool | SE_20856 | chr6:44038769-44047024 | CD8_Memory_7pool | SE_27491 | chr6:44039968-44045075 | Esophagus | SE_30421 | chr6:44038832-44043203 | Fetal_Muscle | SE_33566 | chr6:44038829-44047590 | H2171 | SE_33766 | chr6:44040091-44041089 | HCC1954 | SE_34623 | chr6:44039653-44043982 | HeLa | SE_36098 | chr6:44038743-44043034 | HMEC | SE_38995 | chr6:44038963-44043058 | IMR90 | SE_39876 | chr6:44039122-44041224 | K562 | SE_44621 | chr6:44038810-44043059 | NHDF-Ad | SE_44869 | chr6:44038682-44043014 | NHLF | SE_45608 | chr6:44038165-44043196 | Osteoblasts | SE_48946 | chr6:44040061-44045010 | Right_Atrium | SE_55652 | chr6:44037278-44047598 | u87 | SE_56954 | chr6:44040118-44043720 | VACO_400 | SE_58482 | chr6:44031130-44055866 | Ly1 | SE_59912 | chr6:44034777-44059300 | Ly4 | SE_60555 | chr6:44039716-44047737 | DHL6 | SE_61065 | chr6:44025790-44055630 | HBL1 | SE_61568 | chr6:44025185-44065830 | Toledo | SE_67450 | chr6:44037278-44047598 | u87 | SE_68990 | chr6:44039895-44045800 | H9 |
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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 | GACCAGTCCC CTTCAGTTCA CTCCCACAGG GAGGTTCAAA ACACCACCGA CCCTATTCAG 60 ACATCCCTTT GCAAGGCCCT GTCACCTGTC TTGCCCAATG CCCACCTAGC CAGGAGAGCC 120 AGGATGCACA GTGAGGAAGG TGGAATGAGG TGCCAACGTA GCCCATCCAG GGAAGGAAGA 180 CAGCCCCCCC CCCCCGGCCA CCCACTTGCC AGTGGCCCAG GTGGCAGGCC AGCCACTTGC 240 CAATCCCCTT CCTGATCAGG GATTCAGGAA GTGAAGAGAG TGCCCCTGGA AGTCAGGAGA 300 CACCTCCAAG ATGAAGGCCC TGCCTGCCAT AGCCTGACAC AGCCTCCCTG TACTCCCTGG 360 GTTGTCCCAG GACGCAGACT CTGTGCTTAC CATACCACAC CTTTGTCAGT GGTGTGGGCA 420 GGGCCCAGCA GAGTCCTGGA CACCCCAGGG AGTAGGAGCT GTGCAGGTAA CATAGGAGGG 480 GGTGAAAGGG AAATGAACTC CCTTGGGAGT TCCCCATCCC AGAGGAAATA AAAGTCAAAG 540 CACTCCTTTG TTTTTTCTTC CCAAGCCCTT ATAAGGGGCT TTATGGGGCT TGCCTAGGTT 600 TGAGGTGCAG CAGAGGCAGG CGGGTGAGGG CCTCCAGGCT GAGAGATCCT GGGGCAAAAG 660 TGAAACTATA TGGTCATGAA CACGGGCATG TTCTGAACTC TGTGAAACCC TAGCCCAGGA 720 CCTGGCTGAC TGTACAATCC GTCACCCGGC ACACCGTAAC AGAAGACCCT ACTACGCGCA 780 GAGGACAGTA CTATTGGGGT GGCAACTGAA AAGGGTCCTG GCTGGAGGCG GGGTTTGCTG 840 GAGGGGTAAC AGAGCGTGCG CGGAGTGGAG AGGGTACGGA GGCTCACCGC CCAGCATCCC 900 CAACCCCGGC GCTCAGAAGA GCAGCGCGCT CCGGAGCTCG GCGCGCGCGA TCAAAGCCGG 960 CGCCGCACGC GCACGCGCGC CCGCAGCCGC TCCCCCGCCC GCGCCGCTCC GGCTCCCGCG 1020 CGCGCGCACT TGAGGCCTCC CTTGTGCGTC TCCTCCATTC GCTACGTGCA GAATGGTCCG 1080 TCGGCAGCAG CTGCAGCGCT GGGTGGGAGG GGGAGGAGGA GGGGAGGGGG AGGCGGCGCC 1140
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