Tag | Content |
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EnhancerAtlas ID | HS092-05488 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr10:3889810-3891330 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr10:3890801-3890812 | ATTGCACAATA | + | 6.62 | EWSR1-FLI1 | MA0149.1 | chr10:3891263-3891281 | GCTGCCTTCCTTCTCTCC | - | 6.33 | EWSR1-FLI1 | MA0149.1 | chr10:3891267-3891285 | CCTTCCTTCTCTCCCTCC | - | 6.94 | GFI1 | MA0038.2 | chr10:3890643-3890655 | TGCTGTGATTTA | - | 6.27 | Gfi1b | MA0483.1 | chr10:3890643-3890654 | TGCTGTGATTT | - | 6.62 | MEF2A | MA0052.3 | chr10:3890873-3890885 | TCTATTTTTAGC | - | 6.92 | MEF2B | MA0660.1 | chr10:3890873-3890885 | TCTATTTTTAGC | - | 6.44 | MEF2C | MA0497.1 | chr10:3890872-3890887 | TTCTATTTTTAGCTT | - | 8.73 | Pou2f3 | MA0627.1 | chr10:3891178-3891194 | TTTTATGCTAATTCAG | + | 6 | ZNF263 | MA0528.1 | chr10:3891304-3891325 | TCCCCCCTCCCCTCCCCCTTC | - | 6.11 | ZNF263 | MA0528.1 | chr10:3891272-3891293 | CTTCTCTCCCTCCCCTCCCCT | - | 6.18 | ZNF263 | MA0528.1 | chr10:3891277-3891298 | CTCCCTCCCCTCCCCTCCCCT | - | 6.37 | ZNF263 | MA0528.1 | chr10:3891296-3891317 | CTCCCCCTTCCCCCCTCCCCT | - | 6.61 | ZNF263 | MA0528.1 | chr10:3891308-3891329 | CCCTCCCCTCCCCCTTCCCCT | - | 6.64 | ZNF263 | MA0528.1 | chr10:3891288-3891309 | CCCCTCCCCTCCCCCTTCCCC | - | 6.7 | ZNF263 | MA0528.1 | chr10:3891307-3891328 | CCCCTCCCCTCCCCCTTCCCC | - | 6.7 | ZNF263 | MA0528.1 | chr10:3891267-3891288 | CCTTCCTTCTCTCCCTCCCCT | - | 7.51 | ZNF263 | MA0528.1 | chr10:3891289-3891310 | CCCTCCCCTCCCCCTTCCCCC | - | 7.5 | ZNF263 | MA0528.1 | chr10:3891282-3891303 | TCCCCTCCCCTCCCCTCCCCC | - | 7.81 | ZNF263 | MA0528.1 | chr10:3891301-3891322 | CCTTCCCCCCTCCCCTCCCCC | - | 8.18 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_18564 | chr10:3890099-3891121 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19317 | chr10:3889825-3890957 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_45602 | chr10:3889603-3896249 | Osteoblasts | SE_47115 | chr10:3890056-3891285 | Panc1 | SE_55908 | chr10:3889824-3896295 | u87 | SE_64931 | chr10:3889898-3892472 | NHEK |
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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 |
GH10I003847 | chr10 | 3889830 | 3896611 |
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Enhancer Sequence | CCCGAGTAGC TGGTATTACA GGTACACGCC ACCATACCCA GTTATTTTGT GTGTGTGTGT 60 GTGTGTGTTT TTACTAGAGA TGGGGTTTCA CCATGTTGGC CAGGATGGTC TCGATCTTAT 120 GACCTCATGA TCTGCCTGCT TTGGTCTCCC AAAGTGCTGG GATAGAGGTG TGAGCCACCG 180 CACCCGGCCT ATTTTCTTCT TTTTAAGAGT TAATTCCTCA GACAACAAAG AATCTGAAGT 240 TTAGAGCTAC ACCTTAAGCA TGGAATATTA AATTGTTTTA AGACACCAGC AAGTATTAAA 300 ATTCTTCAGC AATGTGATGG TAACCTAACT AGATGTAGTC ATTAGGAATG ATTAAATATC 360 AAATACATTT TCCTTTTTAA AAAATCAGTT AGAAATGGGA CACAGTGAGA GTGTTATCTT 420 CAACATCAGC TAATAATGTT TAAAGGCAGT CTCATGCCTG TGATAAGTGT GTCTGTTTCA 480 TAGATGTCAT TGGTGCTCTG ATAAGTCTAC CTCACATACT GTGTGGGTTA ATATCAATAT 540 TTGTAATCCT TCTAAGAGAC TATGATTTCG TAAGCAAGCA AGGCAGAGCA AAGCATACCT 600 TTTGTGATTT GACTTTTTGT AACTTGTGAG TGATTCACAA ATTCTGATCG TGTCCTTGGA 660 ACATGAAATT GCACACATAT ACTACTGTGT AGATACCTGA AGACACTAAT TGTTCCCTAA 720 TTTGCTTATT ATTTCAGCCT GGGCTCTAAC TGATAGAAAA CTTACGGGCC TTTGATATAT 780 GGGATCCATG TGCTTCAAAA GACAAGAAAC CTACAGTCTT GTCCAGAATC CACTGCTGTG 840 ATTTAAGAAT GGGATGACCA GATAGAAGTC AGCCTTCTAC GAGGCTCTGA AATTGGATTA 900 CTGCCTTTCA GCAGCTTTGT TGGATGTTGA TGTTGAGACA TTTGGAAGGA GATCAATAAT 960 CATCAGATGT CTCAAATTCA CTGAAAAAAT AATTGCACAA TATTTAACTA GTGTCACGGC 1020 ATGACAGAAT GGTCTTTCTT CAAACATAGA ATAGCGTTAT ACTTCTATTT TTAGCTTAAG 1080 ATAGTTTATA AAAAGCCTAC TTCTTTCTCT CTCTCTATAT ATACACACAT ACACTATATT 1140 TATAACTCTA TATGTAGCTA TATATAGTTT ATATATCTAT ACACACATGT ATAGATATAT 1200 ATATATATAA CTGTTCTCTG TTTCATACTA AATGAGACAA TGATAAAAGC ATGAAGCAGC 1260 CTGACTCAGA GTTGCCATGG ACATTTGAGG TGATTTCACT CTGATTCAAC CCATTTTCTA 1320 ATAAGTAAAA ATGAACTGAA TCATATCAGT AGCTTTTTTG GCAGTGACTT TTATGCTAAT 1380 TCAGTTTTTG GAGAATGTGT CAATTAGCAT TACCAGTAGG GGTTAATATC TCTTTTTACT 1440 TCTTTGGAAG ATTGCTGCCT TCCTTCTCTC CCTCCCCTCC CCTCCCCTCC CCCTTCCCCC 1500 CTCCCCTCCC CCTTCCCCTT 1520
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