Tag | Content |
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EnhancerAtlas ID | HS179-15007 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr17:76403130-76406050 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr17:76403233-76403243 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr17:76403233-76403243 | GGCACGTGCC | - | 6.02 | NR2C2 | MA0504.1 | chr17:76403352-76403367 | AGAGGTCAGAGGTCA | + | 8.73 | Nr2f6 | MA0677.1 | chr17:76403353-76403367 | GAGGTCAGAGGTCA | + | 7.42 | RREB1 | MA0073.1 | chr17:76403141-76403161 | TGGGTGGTGTTGGGTCGGGG | - | 6.78 | Rxra | MA0512.2 | chr17:76403353-76403367 | GAGGTCAGAGGTCA | + | 6.88 | TCF3 | MA0522.2 | chr17:76405422-76405432 | AGCAGGTGTT | - | 6.02 | ZBTB18 | MA0698.1 | chr17:76404983-76404996 | ACACATCTGGATG | - | 6.78 | ZNF263 | MA0528.1 | chr17:76405178-76405199 | CTCTCTTCATCTTTCTGCTCC | - | 6 |
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| Number of super-enhancer constituents: 18 | ID | Coordinate | Tissue/cell |
SE_00336 | chr17:76403376-76405707 | Adipose_Nuclei | SE_06227 | chr17:76402742-76404378 | Brain_Hippocampus_Middle | SE_09402 | chr17:76402394-76405762 | CD14 | SE_18476 | chr17:76402170-76405866 | CD4p_CD25-_Il17-_PMAstim_Th | SE_24583 | chr17:76402500-76404137 | Colon_Crypt_2 | SE_24583 | chr17:76404346-76406027 | Colon_Crypt_2 | SE_26825 | chr17:76402621-76404160 | Esophagus | SE_26825 | chr17:76404693-76406004 | Esophagus | SE_31461 | chr17:76404354-76405962 | Gastric | SE_36965 | chr17:76401030-76406003 | HSMMtube | SE_42104 | chr17:76403056-76404193 | Lung | SE_42104 | chr17:76404335-76406043 | Lung | SE_45620 | chr17:76403242-76404276 | Osteoblasts | SE_50905 | chr17:76402998-76406411 | Sigmoid_Colon | SE_51088 | chr17:76403004-76406193 | Skeletal_Muscle | SE_51835 | chr17:76403263-76404154 | Skeletal_Muscle_Myoblast | SE_53161 | chr17:76403031-76406409 | Small_Intestine | SE_63627 | chr17:76403263-76404226 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 76403541 | 76404103 | chr17 | 76405329 | 76405828 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I078406 | chr17 | 76402814 | 76406178 |
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Enhancer Sequence | CTGCCCTGGT GTGGGTGGTG TTGGGTCGGG GCGGGGGGTG CCCTGCAACC CAGGAGTGCT 60 GGATGAGTGG GAAATTGGGG ATGATCTTAC AGCTGGATCC CAGGGCACGT GCCCATGTGG 120 GGGATGGGAT TGGGGGAGAG TTGGCAGAGG TGGGTGAGGG ATGGATGGTG TGTGGAGGGG 180 GCTGCTGCTG AGCAGAGGGG CTTCACCCTA AAGCCAGGAA CCAGAGGTCA GAGGTCACTT 240 GATGCTGAAG TGAGAGGCGA GGGTCCTTCC CTGCTCAGTG GTTGTGTCCC CAGTGGGATC 300 TTAAGTCAGC ACCTCTTCAG GCCCATCTTT TGATGGTCAC TTCCTCCAGG GCAGCGTGTG 360 TCAGGTGAGA GATGAGTGGG CAGCCGCAGG GTGCTTGTGG ATTTCGATGG CTGGCCCAGT 420 GGACCATTCA TTTCCTGACT GTCTGCCCTT TGCAAGGCAC TTGCTGGGTA CAGGCTCTGT 480 GCCTCCTTGG GTGTGTCTGT GTTTGGGCCC CAGAAAATTC CTGCCGGTGG CTATGCACTG 540 ATACCTCCAC TCCCTTACTC AGGTCCTGTA GGACAGGCCT GGGCTGATCT CAGCTCCTCC 600 TGCTCCCAGA AGCCCTTGGG CAGAGACAGG TAGCCAGGAC TCTGTGGATT CTAGATCCTT 660 GCCCCTCAGA CAGCACTCTG CTGTCAGCAC AGCACTCTCT GGGAGCCAGG CAACAAGAGG 720 CTTCACGGAG TGACTGTGTT GAACTTGCTG GTGGCCCCAT GAGTGTGGTG ATGCAAGGAA 780 GAGCAGCGTG GGGGGAAGAG GCACCTTCTC ATGTAAAATG ACCCCGTGGC TCAGCAGCTG 840 CCAGTGGATT TCAGTGCAGT CTGGTGACAG AAAATTCAGA GGGCTGGCCT TTATTCTTAA 900 GGGTTTTCTG TGTTGTCAAG TATTGCCAGG ACTGTCTGGC AGTTGCTTAG ATGCCTTGTT 960 GGAAAGATTC TTGTGTGATA ACCATTTGCC GATCGTTCAA CAGCCTGATA CACCTCTTTT 1020 GCATACTATG CTGATTTCTT AACATATTTT ATCTATCAAT CAGTCAATCA GTCTATCATG 1080 TATCTCTATC ACATTTCAAT AAATTGAGCT GTTTCAAAGA ACCAGAGGAA CACTCAACTA 1140 TTTAAAGGCA TGCACTAGAG ACTTCTTTTG CAATATGGTT TATCTATTTC ATTCTTATTT 1200 GGATTTTTGT AAAGGGTGCC TATTCAGAAT ACTCAGGAGA AGCCATGCAA GTGTGATTTG 1260 GCATAGGGAT TACTAGACTT GAAGTCTAGA AGCCTGGTTC TGAGTCCACA TTTACCTGTG 1320 GCCACAGCTG AGGGGCCTGG CTTAACCTCT TTCCTGTGCA GTCGGGGGGA TGGCTCTAGA 1380 TTGTCAGGAG GACACGGGGA ACAGGGCTGA TATTTGACTT TCTATAAAAT AACCGTATGG 1440 TTCCTAGGCC AGGTGAGGCA CCTTGGTGGG GCGCGTGGAG GTTGAAATCA CACTGGGGGC 1500 CGAGGGCTGC TGCGCGTCCC TGAGCGAATA GATTGGCAGA AGGGAGTGGG GTGGGGGCCT 1560 TGGATCCCTT GGTGCCGTGT CTCTGGCCTT GCTCCCTGTA GTTCTGTTGC GCTGATTCGG 1620 TCGTGAAGGA AGGTGCTGCC AGGCCGCTTC ACCTGCATCG CCTTGGCTTT GGGAGGTGGG 1680 GCTGAGTGGG CATCTGGGTT GGATCTCAGG CAGGTGGCAG TTCCTCTGAT TCATGGTTGT 1740 CAGTTTCCTG TTGCCTGGCC CTCGCTCCTC GCCCAGTAGG TGTGGTGGGA CAAGGTTCTG 1800 GGAGCTGGGG TAGAATTTGG ACTCTTAACG GGAAGTGCCT CGTGCTGCCG CAGACACATC 1860 TGGATGGGTG CTGAGCTTTC CTTCCCAAGC CTGGTCCTGA TCGGGGGTGG GGTACAGGCA 1920 GGAGCAGCCC GGCCTTGTCA GCCGTTGAAA GTGTGGTATC TGCTGGGTTG CCAGTAAGCT 1980 CGCTTCGAGG TCTTGAGAGG CAGTGCAGGG GAGGCTGAGT ATGAACCGTG TCAAGCCAGT 2040 TCTTATGTCT CTCTTCATCT TTCTGCTCCA TGGAGGTGAG GGACAGAGTG AGTGGTGCCC 2100 ATCCCATTAT CACATTCAGG CAGGAACCAT GCTGTGCTGA GCCAGGCTGT GTCCATCTGC 2160 TGGGACATGG GCTCTGCCCT CCGGCGTGCA TTTCATGAGG AAGATCAGAA AGTGAGTTTT 2220 AGCATGTTGA CTTCCATTTC TTCTGGACGC AGTATTCTAG CACTAACAAC ACAATGTGGG 2280 TGGCTAGGGC GGAGCAGGTG TTGGATTAAG AGATTTCTGG CTCATGCTGA CAGGGAAATC 2340 TGTTAATGGT TGTGAGAATG TCACTATTTT TATTGCCTTC CTGATAGGCC AATTGGCGTT 2400 CTGCCCAAAG GTGAACTGAT GGTGAGAGGC GGGCAGCCCC ACCCTGTTTG CCTAGGCCAC 2460 ACGTGAGGCG GCTCTCCCCT GGGCACCCAG TGGGTGTGGT AGGGGTGCTG TGCCCGTGCA 2520 AATTGCTTGC TTCAGGCTGA GCACACACAC CAGCCTGTGG GCCCTTACAG TTTCTCAGAG 2580 CTGTACTAAT GTCAGAGCAG GTGAGTGCTT ATCCTGTAAG GATAAGCCTG TGATGTCTTC 2640 TGTCCCCTCC GTGTTTTTAC TGGAGTCTGA GAACCCTGTA AGATTTATTG CAGAATACTG 2700 TGGGAGTGCT TGAGGGAGGA GTATGTGTTC ATGCATGTAC TCTTAAAATG TTCATACACT 2760 TCTGCCTTAG AACTGCAAAG GCCTGGCGTG GTGGCTCACA CCTATAATCC CAGCACTTTG 2820 GGAGGCCAAG GTAGGCGGAT CACCTGAGGC CAGAAGTTTG AGACCAATCT GGCCAACATA 2880 GTGAAACTGT GTCTCTACTA AAAATACAAA AATTAGCCGG 2920
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