Tag | Content |
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EnhancerAtlas ID | HS030-00276 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:16275520-16277780 |
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 | CCCCTCTCAG GCTCTGCACG TACCCCATCC CCCGACAAAG CCTAGCTCTC CCTCTCTTTC 60 TGATTCATGG GAACTACCTA GAGTTGCGGA GTCTTCTGAC TCCAGAAACC TGTGTCCTGG 120 TGGCCATCCC AGGAGAAACA ACTTTGATCC TGACCCCAAG AGCTGCTGAC CTGGCCACAA 180 CTTCTCTGTC AAGGGCCTCA CTTAATGCCT GGAAATCCCA CAAGTGAAAA TGCTCAGGAA 240 AATTCCATGG CCCAGTGCCG AGCAGTCTTG AACCGCACAA GCCGTGACTA AGTAACTATC 300 TAAAACAGCT CTCCCTCCCG CCCCAACACC ACCCAGAGTG GGCGTCAACA TCAGCAATTG 360 TCTAGGGAAA ATAAGCGGGC CCTCTTTTCT AGAAAGAACC CATTTCAGAA TGTTTGAAGA 420 GAAAAATCAA CACCCACTGT CTGGGGCCAC ATTAGACAGA TTCAACTGGG CACGGCTGTC 480 ACGCCCTGGC CCAGGATCTG CTAAGGGGTA GTGAGTTCTC TGCCTACTCC TCCTCTTCTC 540 TGAGGCCTGA GTCTGCACGG GGCTGGCTCC CCGGCTTCTG GGCAGGTGAG AGGGACACTT 600 TGGGGCTCTC CGCCCCCAGT TTCGGCAGCT CTGCCCCGGC TCAGGCACTC CCCTGTGACA 660 TCAGCATCTT GGGGGGTGAA TCACTGCCGC AGCTCTGAAG CTGCTGTGGC CATGCATGGC 720 TGTCGGGCTG TGATGAGTCC GGAGGAAGCC ACGCCCCTCA CACCAGCACA GGTCGGCCTT 780 GAAGGGCGCC AAGGCCTCCC ACCACGTGAT GTCTGGAAAC TTTTCACAAG TGGGGGTATC 840 TGCTGAGCGG GGGGAAGTGA CGCAACAAAT AACGGGGAGC ATGGCAGTGG CAACAGGCAT 900 GAGCCACAGC GCACCAGCCT CCGAGCCACA AGTTCAGCGT TGCTGCTGCT GCCAGAGGCC 960 CAGAAACAGC TGTTCCCTCC CCCTACACAT CCCCGCGCAG GCTTTGGCTC TCTCAATGAC 1020 ATTCCTAAAT GGCTGTGGCT AGAGCCCTAA GTGTAAGCAC TGGAGAGCCA GGGCCAGCCC 1080 CGAAATCAGG AGGTAAGGCC CTGGGGCAGC TGGCCCCGCA CCAAGTGCAC CAAGTGGCTG 1140 GCAGCAGCAC ACGGCCACCT GGAGCAAAGC ACAGAGGCCT TTCTCTCCTG TCCTCAGTCC 1200 CTGGAAGCAG CAGGTTCCTA TCTGTGACCT GAAGGAACGC AAGGGAGAAT CGTGGCTGCG 1260 CTGCTCCTAT GCACTGGACA TGGGGAGGCA CCAATGTCCA GCTTGTGGAT CAAGACCTGA 1320 AGGGCACAAA GGGCAAGGTG GGTGCAGAAG GAACCAAAGG CAGGGGCGAG GTGGGCCCAG 1380 GCCACGGCAA CCCTAGAGCT GTCTTCTCCT GGCTGTGGAA AAGGTCACGT GAGCACACAG 1440 GTGTGTGGGT GGCAAGCCCT GGGCCTCAAT TGCTAGTCAC CCCCTACATA CCCAGGAGCC 1500 CCAAGTGCAG AAGAGGGGAA TACCAGGGCC CACACAGGGC AAAATCCTCA ACTGGCTTCA 1560 GAAGCAGCCC ATCTGGAACT TGCAAGTGAG GCCCAACCCT TCTCTCCAGG CTGTGTGCCT 1620 GGCTTCCTCA CCTTCCCCAG GAGCCAACCC GAAACTTGAG CCACCCAGGT GCTAAAACAA 1680 CCTGGGGAGC ATCAGCTGAA CCCCCAGAGG TACAAAGAAC CCTCTAGCAG GAAAACCATC 1740 TGACTTGCCG GGAAGAGACA TGTGAGGAGA CTCCTAGCCA AGGGGAGGGA CAGGATCAAT 1800 CCCCTTGTGT GGGCCCAAGG CTGGGATGAG CCTCCCTGTG GCCATGTGCC CTGGGGCTTC 1860 CTGGCAAGCG CAGCCCCGCC CAGCCATACA GCTGTCCTGG GACTGGATGG ATGGATGGAT 1920 GGGTAAGCTA GATAGATTAG ATAAGACACA TTCGCTAGAT AATAAAATAG TAAAGGCCCC 1980 AAGGACAGGG TGGGTGGTGG CCCAGCCCCC CACATACCAC CACCCGCCAA GAGAGCAGCT 2040 GTGTGCCCAT GAGCAACATT TTCCACCGTG CTGACTGCAC TTTTCCAATG CAAGATGCCC 2100 GCCCAGAAGT GGGCTCCTCC CACACACGGG TGTTAGGAGG AGAAACAGAG GCGTCTATAA 2160 TCCTCTGAGG CTGCCCCAGC AGAGAAACGC ACCAAAAGGG AAGAAAACAG GAGAAATGAT 2220 AAGAAGGGGG GAGGAAGAAG TGAAGATGGG CAAAGTAAGG 2260
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