Tag | Content |
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EnhancerAtlas ID | HS024-04340 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr13:102969840-102972460 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr13:102971465-102971477 | GCTATAAATAGC | + | 6.32 | MEF2B | MA0660.1 | chr13:102971465-102971477 | GCTATAAATAGC | + | 7.22 | MEF2C | MA0497.1 | chr13:102971463-102971478 | GTGCTATAAATAGCA | + | 6.04 | POU2F2 | MA0507.1 | chr13:102971607-102971620 | ATATGCAAATGAT | - | 6.78 | REST | MA0138.2 | chr13:102970003-102970024 | CTGAGAACCAAGGAGAGCAGC | + | 6.21 | STAT1 | MA0137.3 | chr13:102971747-102971758 | TTTCCCAGAAA | - | 6.02 | STAT3 | MA0144.2 | chr13:102971747-102971758 | TTTCCCAGAAA | - | 6.32 | Sox3 | MA0514.1 | chr13:102969930-102969940 | CCTTTGTTTT | + | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I102317 | chr13 | 102969601 | 102970757 |
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Enhancer Sequence | TTCTGCTTCT GTCTCTGTTA TAAATTATAT CACTTAAATA TAAATGAATG AATTTTTACT 60 CTATAGCTTT GAGACATTCT GGTTTTTAAA CCTTTGTTTT TTTTCTAAAC ACTTTCCAAA 120 ATATAGGACC AAATTTTTAA CATACTTGAG AGGCTTGAGT AAGCTGAGAA CCAAGGAGAG 180 CAGCAGATCC CTCAGTCCTG GACAGGACCC GCCCCTCCCT TCACTACTGG GGAGGAAACA 240 TCCCACCCCT TCTGGCTTCT ACCAAATGTG ACAACTTGCC TGCTTGGCCT TCTGTTAAGA 300 GCTGGATTTC CTGTCCCCCT CCCACACACT GGGCAGCAGC CAGACTGCAA AAGTCCAGTT 360 TGACCATGTG GAAACCTTTG CTTGGTTCCT GCCAGAGCCT TTCAGTAAGC TGCCCTATTT 420 AGAGTCCAGC TCAGATAAAT CCTCCCCTTC CACAATCTGG CCTACTACAA CAATTGCAAG 480 ACCATAGACA TCGGCCCCAG TCATGCTTGA TTTTTAATTT TTGTTTGCTT AGACTAGGGT 540 TTATTCATCA TGTTACCATC ATGTCTGAAA AAACTGATAA TGGTATCTGG CATTTTCAGT 600 AAATGGAGGG AGTTGGAGGC CCCAGCCACC TGGGTCTTTC CCAAGTATCT TGAAAGCTGA 660 GAGGATCAAC ACCTCAGCAC ACCTGCAGAC ATTTAGGGCC AAGCAGTGGG AAGATCTAAA 720 CCCCTGGAAG GAGCCAGAAT TCAGTTTGAA ATCTACTCAC ATAGGGAGTG CCCTGGGTGC 780 CATAGGAGCT GCTGGCAGCA GGGGGTCCCA ACTGCGTATC CTCAGCCTTA GAGCACCCAC 840 CCTACCCAAA CTGGGCACTC AGATGTATTT GTGTCCTAGG CTGCTGTAAC AAGGCACCAT 900 CAGCTGCGTG GCCTAAACAA CAGACATGTA TTGTCTCACA GCTCTGGAGG CTGGAAGTCT 960 GAGATCAAGG TATTGGCAGA GTGGACTCTT TCTGAGAACT GGGAGGGAGA CTCTGGTCCA 1020 CGCCTTTTCC AAGCTGCTAG TGGTTTTTCT GCCTGTCTTC AGCTTTCCTT GGCTTGTAGA 1080 AGTATCACCC TGATCTGTGT CTTCTTCTTC GACTGGCATT CTCCGAGTCC CTATCTGTGT 1140 ATAAATTTCC CCTTTGTGTA AGGACACAGT CATATTCAAC GAAGGGTCTG CCCTACTCTA 1200 GCATGACCTT ATCATGACTA ATTACATCTG CAACAACAGA ATTTCCAAGT AAGGTCATAT 1260 TCTGAGGTTC TGGGGATTAG GACTTCAGCA CATAAATTTG AGGGGGGCAC GTTTCAACCC 1320 ATAACTCCAG GAATGACATT GATGGCTACC TGTAGATCAT CTGAGACAGG GTTTGGCACA 1380 CAGTAGGTTG GTACTCAATA CACATGTGAG TTAAATAAAC GAATGCATGA GTGAATCATC 1440 CTTTCTGAGT GCCAGTGAAG AAGTCTTTAA CTTGGGGTGT CGTGATTTTC ATGATCACCA 1500 TTGAGCATTG AAGACTATTG AGGAGAGAAG CCGTTGCTGC GAGCTTTCTG AGGCTGCTTG 1560 CTGAAAGACG AAGGCACTCC TTGCTGTCTG ATCACAGCAG AAGGCTCTGA ATTTGAAGTT 1620 GGAGTGCTAT AAATAGCAGT TAGTCTTATC CTTCAAAATG TCATGTGTAC TTTTTAAAAA 1680 GATTTTAGTG TCATATGAGA GTCCCTGAGT AATTCAATTT ATAGGAAAGG GAGATCAGAA 1740 AGAACTAACC ATATTATAAT TAATTACATA TGCAAATGAT GGACTACATC TAGATGCATG 1800 AATCCATGTC TAATCATAGT TGGCAAAGGT TGGCAACTGC ACACCTGGAC TGGGGAACAC 1860 ACCCCCTGCT CTGCTTAGAT ACAGACGCCA TCAACAACCT CTGAAAATTT CCCAGAAAAC 1920 CTGGAAATTC AGTCCTGTAA GTGCCAAGCC TCCTGCCTTC CCCCATCCCT CTCTGGGGCT 1980 TGCCCCCACC AGCACACAGC AGTGCAGACA CCATACAGCA TGGCTGCGCT ATGGTGAGGC 2040 ATGGCCAGTG GGAGGAAGGC CACCAATTGC ATACAATAAC AACTTTGTTG TCACTGCTAG 2100 GAGCCGAACC AGCTGCGATG CCTTACAATT GCTACTTAAA TGTAAGCAGT GTCAGGAAAG 2160 TCTGAATGTA AAGAAGTTTC TCAGTTCTTG AGCCAAATGA CCGGTTGCTT GTGTTCTTCT 2220 ATTAACTCTA AAACAATTAA CTCTATCAGC TTATGCTGAT AGCCACTGTG CATTTTTTGG 2280 AGCACCTGGG CACTAGCTAA GGATAGTGAC TGATATGTGG ATGATGAAAT ATATAATAGA 2340 GATGATATAG ACATAGATGT GCCAAATGCT ATATATACAT GTATGTATGT ATATATTCAT 2400 ATATATGCAC ATGCATACTG ATGAAAGCCA CTTTGCTGAT ATCCCCAAAT AACCACTGAA 2460 CTACAGATTC CAGATTTATA GAGCATATTG TTGGTGTTGT TTCTGAGAGT ACCTACCATA 2520 GTATTCCTGT GGAAAGATAC ACACCTATAT AGTTTCCATT TTCAAAATGC ATGCATGTGC 2580 CTCTGTGTGC GTGTGTGTGC TCCCAAAGCA GCAGTTGTAG 2620
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