Tag | Content |
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EnhancerAtlas ID | HS105-23399 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr13:114199320-114201610 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Sox6 | MA0515.1 | chr13:114201158-114201168 | CCATTGTTTT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 114199368 | 114199421 | chr13 | 114199755 | 114200283 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I113544 | chr13 | 114198350 | 114203270 |
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Enhancer Sequence | TACAGCAAGG ATTTCATCCT CTTCTCATGT TCCCCGCATT CAGAAGCAGG CAGCTGGCTC 60 TGGGACAGTG CTGGGAGCTG CCTTGCTGTT GGGCGTCCCT CCCTGGTGGA TGCAGGTGTG 120 CGCCCCCGCC AGCCTCGCTC ACCTTCACGC CATGGCCTGG TGCCTGTGCA GGCAGCGTCC 180 TTAGCAGCCC TGAACCAGGC ACATACCTCA CATGGCAAAT TTCCTTTACT CAGCCTCCAA 240 ATCCACATTC ACAGATGAGG AAACTGAGGC ACACAGAGAT TGAAACATCG AGCTGGGTCC 300 ACAGTGAATG TGGTGCTCCT GGGTGCTGTG GAGCCGGTGG GGCCCAGGAA CCCAAGACTT 360 GAGCCCAGAG CCCACATAGT TTCTCAGTGC TACACCAAGT ATAGGTTTGA TGTTTGTTTT 420 GAGAATAAAT GACCCTGCAT AGAAAAGTCA GCATAGCTCA TTAAAGAAAT TGAAGGGAGG 480 TTTCCTGTCT CTCATTTTCA TTGCTGTTTC TGGGACTGAC TGGAATGCAT TAGGCTCCAT 540 AATTATTGGC TCACTCCCCC CACCCCCACT CCGCCCCCAG GGCCAGGAAC TCTTAGCTCA 600 GGCAGGGGTG GAGTGAGCCA TGTTCCCAGG GCAGCCCTGC CTTGAAGGAG CTTGCACTGA 660 GCTCAGGCAG GGGTGGAGTG AGCCATGTCC CCAGGGCAGC CCTGCCTTGA AGGAGCTTGC 720 AGCCCAGGGT TGGGTGGGGG GCAGATGCAG GGACACAGCT GTCCAGCTCA GCTGAGAGCA 780 CAGGAGCCTC CGGGGCATCA GCGACTGGCC GGGGTGAGGG ATGCCACCAG GTGCAGAGGT 840 GGAGGCTCAG GGCGTGCTGG GGAGGAAGAG AGGCTTGTGG AAAAGTCCAG AGGTAGGAGA 900 TGGGAAGGAA GCCTGGAATC TCTGGAACAG GACATTCCCA AGCAGGAAGG AAGCCAGTGG 960 GGCTGGAGAT GAAGGGGAGG CTTTCCACCG GGCAGCAGCG GGGAGAAAAC GCAGCCCGGA 1020 ACGCCCAAGG TGGGGAGCCC TGGGTACCTG TGTGGCCGCG ATGTGAGGCC CCCTTTGGGG 1080 AGAGGTGGGA GCGTCCCCTG TGCCATACAC TGTTGTGAGC TTGTCTCAGT TGTGCCGGCG 1140 TGGACATAGG GCCGTGACGG TAGTGACTTC CTAGACACCA GTGTGGCCAA AGGCAGCCTG 1200 GACCGGGCAT TGCAGCAGGG CAGAGGCACA GACATCCTGA GGGGAAGCAG GACTGGGGCC 1260 GGGGCTCAGC TGACAGCTGG GGAGAGAGGG AGGTGGACCC CAGGCCGCCG TGGGGCTGGG 1320 GCTGATGAGG GGGACACAGT GGGGCCAGGC TGGTGGCCGG GGTAGGAGGG GCCGTGGGGA 1380 GCACTGGGAG TGGGCATGGA GGGGGCAGCT CTGAGACCCA GACCCAGGAG GAGGGGCCGT 1440 GGCTAGAAGA CTGGGTGGCC AGAGAAGGCA GCCCTCAAGC GCAAGAGAAC CCCGGGTCGT 1500 GGCAAGAGAA AAAAGGCCAG TGTTTACATT TGTGTTTCTG GGTCAGGTAG AGACAGTGGT 1560 TTGTGAACGG CAGAAAGGTC ATGGGCCTGC TCCGTGCACC TAACCCTGGG GTCTGGGTCC 1620 TTCCGATCAA GAGGAGGCCT CTGGGCTGCC GGGCTTCCTC CGAGGGCTGA CATGCATCAC 1680 TGGGCAGCTC CAGGCTGTGG CTGGAGAGCT GAGCCCAAGC TCAGGTCCAG CCCCAGCACC 1740 GCCGGCCCCT CTGCGTCACT CGGCAGCACA GCAGGACTGA GCAGCCCAGT CCGAGAGTCC 1800 TGAGAGCAGA GAGAAGAAAT ATGTGGAGAC AACGTTTCCC ATTGTTTTTA AAAATGTGTG 1860 AGCCAAATAA AGGAAGGAAA GGAACATTGA CCACAGGCGT CCTGTGAGCG TGGCACTCCT 1920 GGGCACTCCT GGGCACTGTG GGGCTGTGGG CTCTGGGATC ATCTGCACCT CAGCTGGAAT 1980 ATTTCCTGAA GGAGTGCCAG ACCGAGTGCC GCCTCTGTGT GTTTTGCTGT GTCCTCTGCA 2040 GTTGAGGCCT GTTGCAGGGA GTGGAGCTGG GATCCCACCA CATCAGACAG GTCATCCCAG 2100 GGCAGGCTTT TCCCCGGTTC GCTCAGGAAA GGGGCGGCTT TTTAGCATTT GCTGTTGCTT 2160 TCACACGTGC ACTTGGGAGG ATTTAGGATT TTAATTCCTG TATTGAAGCA AGTGACACAC 2220 TGAAGTTGTG AGAAATAGTG TGCGCTGGGG GAGGCTGTCC TGCGGTCGTA ACGTGTCTGT 2280 CCTGTTCCCA 2290
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