Tag | Content |
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EnhancerAtlas ID | HS176-11866 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr13:99094050-99096300 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr13:99096131-99096149 | GGAAGGAGGGAAGGGACA | + | 6.04 | IRF1 | MA0050.2 | chr13:99095387-99095408 | AATGGGTTTCACTTTTTTTTA | + | 6.21 | TBX20 | MA0689.1 | chr13:99094866-99094877 | CTTCACACCTC | - | 6.02 | TBX21 | MA0690.1 | chr13:99094251-99094261 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr13:99094251-99094262 | AAGGTGTGAAA | + | 6.62 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_32401 | chr13:99095360-99096258 | Gastric | SE_37511 | chr13:99094873-99096932 | HSMMtube | SE_45616 | chr13:99094612-99099363 | Osteoblasts | SE_65772 | chr13:99095332-99096284 | Pancreatic_islets |
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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 |
GH13I098442 | chr13 | 99095039 | 99098865 |
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Enhancer Sequence | GAGGCAGGAG GTGGGCAGGG AAGCCTGGCT TCTGAACCTT TCACTTCAGG GTATTGTTTT 60 CTGAGCCCAC CACCTGAAAG TTGGCTTTGA AGATGCATCT CTCCCAGATC TTGAATCCTT 120 CCAGACCCTT CCAAATGCCC ATTCCCTAAG CATTCTTCAG TCCAGGCCCA TAGCTGTGTT 180 TCAGAACACT TCAAGCCCGT GAAGGTGTGA AACAGGAAAG CTTTCTTCAT CTCTCACTGG 240 CAGTGGAAGC TGCCCTGAGC TGGGGCGAGG CCATTCATCA TTGTGATTGT GTTTTATGTG 300 AATGCTCACG TTTCACCGCA GAATCTCTGC CCCCGCGCCC TCTGCGGGGC TGCTGCAGTC 360 GAGGCAGGAC TCCCTTCCAA ACGCAGAAAG GGCCAGTTCC CACACAGGCC TGGTCCAAAG 420 AGTGTCACAT AAGAGACTCA GGCCAGGACA GGAGTTTGCT GGCTCTTGGA ACCAACAGCA 480 GCAGGAATGA GCCAGCAGTG CTTCATGGAG GGTCTCGAGA GAGTCTCGGA ATTTATTCTC 540 GGGAAACGAC CTTCCCCGTT GCTCAGACCT GCCTTTATTG AGTTTCCTGC TACAAGCCGC 600 TTGTTTCTAA GCCCAGGCCT GCTTCTGAAG ACATCCTCAA GGGGACACAT CCGAGGTGCA 660 GGCCCTGGCT CCCCCACGGG CACAGCCTTT CTTCCCAGCT GTCCCCACAT ACGAGGCTCT 720 GTCCCATGGG GTTCCCCTGA GTGTGCAGGT GTGAATATTC CCTCCCCGGG CCTCCTGACA 780 GCCCAGGTGT GAAGAGCACT AAACATTCTT CCCCAGCTTC ACACCTCCAC CAGGCCTGTG 840 CGCAAAGCTT GCGGGTCTGA GACTTCTCCC AGGGGATGGG GATTATGATA GCAGGAAAGG 900 AGACCCCCGA AGCGGAGGAG CAGGGAAGAA CCCGTGATAG GCTCATGGGA AACGAGGCCT 960 CATCAGATCT CACCTGTGGG CGTGTGTCTG AAACGAAGCC AGTCGATGTG TGGCGCCGCC 1020 ACTGGGGAGG AACCGTCTTG GCCTTGCTTC GTCCTGACCT CAGCAATGTG TGAATTACGA 1080 CTCTCAAGGC TGGGGTTTGT CATAGGCCTC AAAGCTTTTT ACATACCTGG AGGCACCCAG 1140 GCCATTCAAC GAGGCAGCAA ATACCCAAGT GGGGTCCAGG TGGCCCAGAG CCACCTGCAG 1200 CCCAGCTTTT TTGGATAACA AATCTACACG GTCGCAGCCT TCCGTGTGCA TGATCAGGTC 1260 AAGGCACTGA GTCAGGGGCA CGCTGGCCCC CAGCCAGATC TAGCCCCGGC CTGGTGGCTT 1320 ACAGCCTGCG AACCAAGAAT GGGTTTCACT TTTTTTTAAT GGCTGCTACA TAATGTCTTC 1380 AGTTTTGCCC CTTGGCCTGC AAAGCCTGAA ATATCTGCCG TCTGCCTTTT GAGGAAAAGT 1440 TTGCTGACCC TAGTAGAGAG CAGGAGAGTG AGCCACTGGC CAGTGGGGTT TGAAGGTGGC 1500 AGTGACCACC TAGTACAGTC AGGGACCTGG GCTGCTCTAT CACTTTGCAG ATGTCCCTCC 1560 TTGCCAGAAA GCCCCCTCCC AAGGCACGTG GCATCAATCT TGTGTCGGTG GCAGGCAGCC 1620 CTCATGTGCC AGACGCCAAA TGCTCGCTGA CTCGCAGATG AGCCATCCCC AGGGCCTCCT 1680 CCCTGCATGA CAGGACAAAG CAGCTCCATC TCCTCCTGAC TCAACAGCCT CCTCTCCCCA 1740 GTCCCGTGCC CAGCCTCTCC CAGTTCCCAC TCCCGTCTGA CTCGTGTAGG CACACTTGAG 1800 GAAGGGGCGT ATCTGGGGAC CGTGTGGCCT CACTGGCCTC TGCTAAAAGT TGTGGGCAAG 1860 CCGGCAGGCC TGGGGGCTCC CACTAGAGGT GGGGTCAGAT GTTGGGATGG CCAGAGGGCT 1920 GCCCAGCCTG TGGGCACTAG AGCCAGTGAA GGGCCAGAGG CAAAGCAATG CAAGTTGTCT 1980 TTTAAGGCTG GAGTGGCGAG ACGGGACAGC AGGGAAGTTG TTCAGCAGAC AGAGCGCAGA 2040 CAGGACTGGG AGGAGGGAAG GGACGGGGTG CAGACAGGAC CGGAAGGAGG GAAGGGACAG 2100 TGAGGCCAGG GAGTGGCGGG CACGGGGGTT ATATTTGTTC CCCGTGGCGT CACTCGGCAC 2160 CAACCTCAGA CTGGGTGAGG CCACAGAAAC ATCTCCCACA GTGCGGGAAG CCGGAAGTCC 2220 AAAATCAAGC TGCTGGCAGG TGGGTTCCTT 2250
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