Tag | Content |
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EnhancerAtlas ID | HS146-09068 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr2:241312800-241314770 |
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) |
SPIB | MA0081.2 | chr2:241314704-241314716 | CACTTCCCCATT | - | 6.18 | ZNF263 | MA0528.1 | chr2:241313763-241313784 | AGAGAAGGAGGATGGGGAGGA | + | 6.85 | ZNF263 | MA0528.1 | chr2:241313766-241313787 | GAAGGAGGATGGGGAGGAGGC | + | 7.95 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_37774 | chr2:241311909-241315234 | HSMMtube | SE_52304 | chr2:241312770-241314688 | Skeletal_Muscle_Myoblast | SE_64063 | chr2:241312770-241314688 | HSMM |
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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 |
GH02I240368 | chr2 | 241307753 | 241314834 |
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Enhancer Sequence | ATACTCCCCA TGGACAGGCC ACGCTTCTTG CCTCAGCTTG GATCTTCTAG GCCAATGCAG 60 GTCCCAGCCC AGCAGCCTCA GCGGACCGAG TCTCGGGGGC CGGCAGGGGT CTGTACCTGC 120 TTCCCCGGCC CCTTTACCGC CCACCACTCT GCTCAGGTCT CTGGACCTGT GGGCTTTCCA 180 GGCTCCTTAG ACCAAAGCCC ACCAGCCCGA GCCCAGCATC TGCGCAGGTG CTGTGGGGAC 240 CAGGACATGG GTGCTGGGGT GCACGGCCTC TGTGATAATC CGGGACACAG CACTCGGACG 300 GAGCCTGCAC TGTTTCTTAA ACACACACAA GGTGGCCTGG ACACAGATGC TGGAGTGCGC 360 GGCCTCTGTG ACAATCCGGG ACACAGCACT CAGAGGCTGC ACCATTTCTT ACACGCACGG 420 GTGGTAGCCC CTTCGATGGA CAGTACTCAT TCTCAGACTC TGGCTGGGCC CCTGGGGTGC 480 TGGAACCAAG ATGAGGAATC AAAAACAAGG GTCTGGGAAG TAGCCCAGGC TGAGGCTCCT 540 AGGAGGGAGG GCGAGAAGTA CCCGAGTACT AGGGCTAGCT GGACGTGTTG ACCCTGCTTG 600 GCCTCCCCTC CCAAACCCTG GACCTCAGTG AGCCTGGGTA CTGGGGCTAG CTGGACGTGC 660 TGACCCTTCC TGGCCTCCCC TCCCAACCCC TGGACCCAGG TGGACTGGGG TACCAGGGCA 720 AGCTGGGCAT GCTGACCCTG CCTGGCCTTT CTGGTCTCAT TGTGACTCAG GCCTGGGGGT 780 TCCCGAGGCT CCCAGCTTAG AGGCGGACAT GGCTGTGAGG CCCTCGCCCT TTCCCACTCA 840 GCAGGGATGA GTTCAGGGAT GGCCAGGCCC CAGTGATGTC ACCAAGTTGA GCTTCTGAGC 900 TTCTGGTGCC TGTGTGGGAG CTGCAGCCCT CAGGAAGAAG TGTCCTCCCC TCCTCAAGGG 960 ACCAGAGAAG GAGGATGGGG AGGAGGCCTG GCCCGAGGTC GTCTGATGCC AGCCTGGGGC 1020 CTGGAGCAGC CTGGAGCCAG CATGCGTTCC AAGGGGAATT CCTGGGGAAT GATGCAGCCG 1080 GCCTCGCTAT CACAAGCTGT CATTTGAGGG AGAGCCGCAC TCGGAACGCC TCCCAGCCCC 1140 AGTGCAGGAA TCCATCTGGC AAGTCTGCCC TCGGACACTC ACAGGACACT CTTCCAGGAT 1200 CCCTGGGCCT CGGGGTGGGG CCAGGGTCTC AGGGGAGGAA GTGCCCAGAT TCCTGGACGC 1260 TGGCCCCGAG GAGGGTCTGG TGGCAGCCAC CTCGGTCAGG ACGAGGACAG AGCGTCCAGC 1320 CCCGTGCCAG CTCAGTGGCC TCAGAATACC ACAGCCACGT CCCTCCTGTC CAAGGCCCAG 1380 CAGTCCCCGG GACACTCCAA GAGCCATCCA CTTTCTAGAT TTGGGCTTCC CCTCCTCAGT 1440 GACCCCAGCT CCTCCCCAGA GAGCAAACCC TGAAGCAGCT CCTCTGGGGG TCTTTAAGAG 1500 GAGAATAGGA CTCGTGCTAT GCTCGGGGTG GACTGAAATC ATGCTCATCA CACTAAAGCA 1560 TACTGCAACA TAAAGCCAGG TGTTTGCAAA TGAAATGCAA ACAGTCACAC AGAGCCAGCA 1620 AAGCTACCCT TCACCTCACT TGCCGAATGA GGCTGTTCGG CTGAAACTCA GTGTCACCGG 1680 GCCCTGAGTC TGCACACTCA CGCTCTCAGC TGCTACAGAA TGATGACTCG GTTTCCCCAC 1740 CGCTCTTTGG ATTCAAGCTG CTGCAAAGCC CTCCCCAGCC TGGGTGTCGA GAAGTTGCTT 1800 GGCCCAGTCG CATGGCACGC CCAGGCAGTG GGGCCCGCAG ACAGCGTGGG CACCGTTTAC 1860 GGATGAATCG ACGAGCCCCT CTTCGCCTCC ATCCCTACGC GATGCACTTC CCCATTCTCC 1920 TGACACCGCA TGGGCTGTTT CTGACTTCCA GCTACCAGGA GCAAGGCTGC 1970
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