Tag | Content |
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EnhancerAtlas ID | HS112-09104 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr21:47546710-47548810 |
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) |
BHLHE41 | MA0636.1 | chr21:47547742-47547752 | GTCACGTGAC | + | 6.02 | BHLHE41 | MA0636.1 | chr21:47547742-47547752 | GTCACGTGAC | - | 6.02 | MITF | MA0620.2 | chr21:47547738-47547756 | GGATGTCACGTGACCTTT | + | 7.42 | MITF | MA0620.2 | chr21:47547738-47547756 | GGATGTCACGTGACCTTT | - | 7.42 | USF1 | MA0093.2 | chr21:47547742-47547753 | GTCACGTGACC | + | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_54792 | chr21:47547628-47549365 | Stomach_Smooth_Muscle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 47547200 | 47547409 | chr21 | 47546732 | 47547136 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I046127 | chr21 | 47547655 | 47549150 |
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Enhancer Sequence | CTCGGCATGT GGCCACTGGT CTTGAAGGCC CACCATGGGC CTTGCAGTCT CCCTCAGCTG 60 CCGCCCAGCT CCCATGGGCT GGCCGTGCAT GTGCCACTCG GAGGAAGCCC TGGATTCAGT 120 GAGTGAAACC ATCCCGGGGT GGAAGCACTG ACACCCCCCA GCACCAGCAG GTCTTGCTCC 180 AACCCTGGCC TGCCTCGGAG CTGCAGCTGC GGCTCTCACA TCTCTGGGAG TGGGGGAGCC 240 CATGTCCCGG ATGTGGCCCA CGTGGGTGTG AAGCTGGAGC TGGGGGTGCC GTCCAGGCTC 300 TGCTGGACGT GGTGCTGCCC CCATGGTGCA CTGCTGCACC GTACCTGGGC CCACAGGAGG 360 TCCCCGGGGG CGTTAGGAGC TGAGTCCCCC TCAGTGAGCC GTCCCCTCCA GGAGTGTGAG 420 GGTAGGGATG CCATGGAGAC AGGGTGGGAG GGTCCGACCT GGAGGACCAC AGGGAGGAAA 480 CCTCAGGGTC TGCGGTACGA AGTCAGCGCT TCCTCAGCAC GCGGGTCGCG GTGTGCGTTC 540 GGGCGTTCCA TGGGGAGCTC CCGGTGGGTG AGCTGGGCCA CTGAGCACAT TCACAGGCCC 600 TGAGGCTGCC CCAGGGGAGG AGCCGTGGAC TCAGAGCCGA GGTTCCCCAT ACGTGCTGCG 660 ACAGAGAACC TAGGGCTTGC ACCTGGGTCT GGCTGCCCTT CAGCAGGCGG GCAGCCTCTG 720 GCCCCACAAC AGTGGGCTGT GCTTCTGCCG CCAAGGTGCA GGCGTCCTCC CCCAGGGTCC 780 ACATCAGCAG CAGGGGCACC TGGACCCTGA GGGCAGGAAC CAGACCTTGG CTCCTCCACC 840 CACCCCCTCG TTCCTGATGG GGCAGGGAAG TCTCGGGACC CCATGATGGG CGACATGGCG 900 ATGGTCACTG TGGGTGCTTT GCTATCAGGT GGGGGGCCTT CCTCTCCACT CTGGGTCCAG 960 TGTGAGTGGC CGCTATGGCT TCCCCTCCAC TCCAGGTTCT ATCGTGAGTG GGTGGGTGCT 1020 GCGTCTGTGG ATGTCACGTG ACCTTTCCTC TTTAGCCTAT CATTGTAGTT GGGAGTTAGT 1080 TAGCCCGTTG AGCGTCATTG AATTTCCAGT GTTGAGCCAG CCCTGCGTGC CCGGGATAAA 1140 CCCACCTGGC CGTGGTGTGT GGCCCTGTTT ATGCACGTGG GCCCTGATTC GCTGATGCCT 1200 GCCTGAGGGT TTGCGCTTAT CGGCGACATC AGCCTGCACT TTTCTTTTCT CGTGATCTCT 1260 CTGGTTCTGG CCTCAGGGTG ACGTGGGCCT CGTAGGGTCC TGTGGTGGCT CCTCCCCAGA 1320 CGGTGACATG GAGTGAGCCC ATTCTCCCTC CTGGGAGTGG GTCACTCAGG CCACCAGAGC 1380 ACCACAGGGA AAGCAGCCAG GGAGGACACG GAGGCCCTTG AAGCTCTGGC CTCTTCTGAG 1440 GCCTCCAGGA CCTGACAGTG AGTGGGAGCA GCCCTGGCAG AACCCCTCCC CTCCTCTCGG 1500 CCGCCCTGAC ACCTCATCCC CGACACTCAG AGCTCATCCT CCTTCCCAGC TGTTTCCAAT 1560 TTCAAAGTGA ACTCGACCTT GTGGCTCCAG GAGATGCAGC AGGGACAGTG TTAAATCGGC 1620 TTTCACCAGC CCACACGGCC AGGCATCCTC CTCGGCCCTC CTGGGCACTG GGTGGACACC 1680 ACTGGCTGTG GCCTGGCCCT GGCCTTCTCC AGACAGCCCT GTCCACCCCA AAGCCCAGCC 1740 ACCCTGGGCC TGCAGCAGGC CTGTGGAGTT CTCAGTTGCG TGGGGACCAG AGGGTGCTGG 1800 AGAAACAAAC CAGACGCAGC TGAAGGCAGT CAGGGCAGGG CGCAATCAGC GATAAGAGCT 1860 GCATAGGGGC CACAGCGTAA CCTGAGCTCC AGTCGGTGGA AAGAAAAGGC AGAGACGTTG 1920 CAGAGGCCAG GTCTGCTCAG GGGAAGACAG TTCTGGGTGT AGAGGACTCA CATCCCAGAG 1980 AGGCTGAGGA AGGGTTTACC ACCGCAAGCT TTCTCAGGCG GGCTCTTGAG GGGTGGCTGG 2040 GGTCTTCCTG GCGACGGGCC TGCGGCACTG GAAGCCCTAC TGGAGTTTGG CCTGTCTCCG 2100
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