Tag | Content |
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EnhancerAtlas ID | HS047-00340 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:16275470-16277750 |
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) |
MITF | MA0620.2 | chr1:16276939-16276957 | AAAGGTCACGTGAGCACA | + | 6.13 | MITF | MA0620.2 | chr1:16276939-16276957 | AAAGGTCACGTGAGCACA | - | 6.13 | MSC | MA0665.1 | chr1:16276484-16276494 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr1:16276484-16276494 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr1:16276484-16276494 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr1:16276484-16276494 | AACAGCTGTT | - | 6.02 | RREB1 | MA0073.1 | chr1:16277529-16277549 | CCACATACCACCACCCGCCA | + | 6.33 | SP1 | MA0079.4 | chr1:16276264-16276279 | GAAGCCACGCCCCTC | + | 6.67 | SP4 | MA0685.1 | chr1:16276264-16276281 | GAAGCCACGCCCCTCAC | + | 6.35 | TFAP2C | MA0524.2 | chr1:16277366-16277378 | TGCCCTGGGGCT | - | 6.11 | ZNF263 | MA0528.1 | chr1:16276035-16276056 | TTCTCTGCCTACTCCTCCTCT | - | 6.37 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_01097 | chr1:16275403-16279590 | Adrenal_Gland | SE_01987 | chr1:16272432-16279631 | Aorta | SE_02709 | chr1:16274610-16280662 | Astrocytes | SE_03452 | chr1:16275260-16277700 | Brain_Angular_Gyrus | SE_04408 | chr1:16274061-16278759 | Brain_Anterior_Caudate | SE_05249 | chr1:16273948-16279656 | Brain_Cingulate_Gyrus | SE_06124 | chr1:16270812-16279644 | Brain_Hippocampus_Middle | SE_07342 | chr1:16272948-16278751 | Brain_Hippocampus_Middle_150 | SE_08131 | chr1:16272535-16279679 | Brain_Inferior_Temporal_Lobe | SE_18522 | chr1:16273733-16281386 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19255 | chr1:16273419-16281362 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_27189 | chr1:16274173-16281550 | Esophagus | SE_36664 | chr1:16274460-16277822 | HMEC | SE_38820 | chr1:16274752-16281466 | HUVEC | SE_40080 | chr1:16274659-16281418 | K562 | SE_45001 | chr1:16274543-16280813 | NHLF | SE_45986 | chr1:16274066-16281079 | Osteoblasts | SE_47059 | chr1:16275327-16277770 | Ovary | SE_55849 | chr1:16274274-16283539 | u87 | SE_61132 | chr1:16274043-16303645 | HBL1 | SE_64852 | chr1:16274416-16281190 | NHEK | SE_67570 | chr1:16274274-16283539 | u87 |
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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 |
GH01I015947 | chr1 | 16274011 | 16281336 |
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Enhancer Sequence | GACAGGTGAA GACAAGACGG TGTTTCATCA GCCAGTGTTG CAGAACTCGG CCCCTCTCAG 60 GCTCTGCACG TACCCCATCC CCCGACAAAG CCTAGCTCTC CCTCTCTTTC TGATTCATGG 120 GAACTACCTA GAGTTGCGGA GTCTTCTGAC TCCAGAAACC TGTGTCCTGG TGGCCATCCC 180 AGGAGAAACA ACTTTGATCC TGACCCCAAG AGCTGCTGAC CTGGCCACAA CTTCTCTGTC 240 AAGGGCCTCA CTTAATGCCT GGAAATCCCA CAAGTGAAAA TGCTCAGGAA AATTCCATGG 300 CCCAGTGCCG AGCAGTCTTG AACCGCACAA GCCGTGACTA AGTAACTATC TAAAACAGCT 360 CTCCCTCCCG CCCCAACACC ACCCAGAGTG GGCGTCAACA TCAGCAATTG TCTAGGGAAA 420 ATAAGCGGGC CCTCTTTTCT AGAAAGAACC CATTTCAGAA TGTTTGAAGA GAAAAATCAA 480 CACCCACTGT CTGGGGCCAC ATTAGACAGA TTCAACTGGG CACGGCTGTC ACGCCCTGGC 540 CCAGGATCTG CTAAGGGGTA GTGAGTTCTC TGCCTACTCC TCCTCTTCTC TGAGGCCTGA 600 GTCTGCACGG GGCTGGCTCC CCGGCTTCTG GGCAGGTGAG AGGGACACTT TGGGGCTCTC 660 CGCCCCCAGT TTCGGCAGCT CTGCCCCGGC TCAGGCACTC CCCTGTGACA TCAGCATCTT 720 GGGGGGTGAA TCACTGCCGC AGCTCTGAAG CTGCTGTGGC CATGCATGGC TGTCGGGCTG 780 TGATGAGTCC GGAGGAAGCC ACGCCCCTCA CACCAGCACA GGTCGGCCTT GAAGGGCGCC 840 AAGGCCTCCC ACCACGTGAT GTCTGGAAAC TTTTCACAAG TGGGGGTATC TGCTGAGCGG 900 GGGGAAGTGA CGCAACAAAT AACGGGGAGC ATGGCAGTGG CAACAGGCAT GAGCCACAGC 960 GCACCAGCCT CCGAGCCACA AGTTCAGCGT TGCTGCTGCT GCCAGAGGCC CAGAAACAGC 1020 TGTTCCCTCC CCCTACACAT CCCCGCGCAG GCTTTGGCTC TCTCAATGAC ATTCCTAAAT 1080 GGCTGTGGCT AGAGCCCTAA GTGTAAGCAC TGGAGAGCCA GGGCCAGCCC CGAAATCAGG 1140 AGGTAAGGCC CTGGGGCAGC TGGCCCCGCA CCAAGTGCAC CAAGTGGCTG GCAGCAGCAC 1200 ACGGCCACCT GGAGCAAAGC ACAGAGGCCT TTCTCTCCTG TCCTCAGTCC CTGGAAGCAG 1260 CAGGTTCCTA TCTGTGACCT GAAGGAACGC AAGGGAGAAT CGTGGCTGCG CTGCTCCTAT 1320 GCACTGGACA TGGGGAGGCA CCAATGTCCA GCTTGTGGAT CAAGACCTGA AGGGCACAAA 1380 GGGCAAGGTG GGTGCAGAAG GAACCAAAGG CAGGGGCGAG GTGGGCCCAG GCCACGGCAA 1440 CCCTAGAGCT GTCTTCTCCT GGCTGTGGAA AAGGTCACGT GAGCACACAG GTGTGTGGGT 1500 GGCAAGCCCT GGGCCTCAAT TGCTAGTCAC CCCCTACATA CCCAGGAGCC CCAAGTGCAG 1560 AAGAGGGGAA TACCAGGGCC CACACAGGGC AAAATCCTCA ACTGGCTTCA GAAGCAGCCC 1620 ATCTGGAACT TGCAAGTGAG GCCCAACCCT TCTCTCCAGG CTGTGTGCCT GGCTTCCTCA 1680 CCTTCCCCAG GAGCCAACCC GAAACTTGAG CCACCCAGGT GCTAAAACAA CCTGGGGAGC 1740 ATCAGCTGAA CCCCCAGAGG TACAAAGAAC CCTCTAGCAG GAAAACCATC TGACTTGCCG 1800 GGAAGAGACA TGTGAGGAGA CTCCTAGCCA AGGGGAGGGA CAGGATCAAT CCCCTTGTGT 1860 GGGCCCAAGG CTGGGATGAG CCTCCCTGTG GCCATGTGCC CTGGGGCTTC CTGGCAAGCG 1920 CAGCCCCGCC CAGCCATACA GCTGTCCTGG GACTGGATGG ATGGATGGAT GGGTAAGCTA 1980 GATAGATTAG ATAAGACACA TTCGCTAGAT AATAAAATAG TAAAGGCCCC AAGGACAGGG 2040 TGGGTGGTGG CCCAGCCCCC CACATACCAC CACCCGCCAA GAGAGCAGCT GTGTGCCCAT 2100 GAGCAACATT TTCCACCGTG CTGACTGCAC TTTTCCAATG CAAGATGCCC GCCCAGAAGT 2160 GGGCTCCTCC CACACACGGG TGTTAGGAGG AGAAACAGAG GCGTCTATAA TCCTCTGAGG 2220 CTGCCCCAGC AGAGAAACGC ACCAAAAGGG AAGAAAACAG GAGAAATGAT AAGAAGGGGG 2280
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