Tag | Content |
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EnhancerAtlas ID | HS080-30200 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr6:10591050-10592410 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr6:10591100-10591111 | TTTTATGGCTT | - | 6.62 | ESR1 | MA0112.3 | chr6:10592126-10592143 | AAGGTCACTGGGACCTT | + | 6.44 | ESR1 | MA0112.3 | chr6:10592126-10592143 | AAGGTCACTGGGACCTT | - | 6.66 | Klf1 | MA0493.1 | chr6:10592148-10592159 | TGGGTGTGGCT | - | 6.14 |
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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 |
GH06I010591 | chr6 | 10592093 | 10592386 |
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Enhancer Sequence | CTGGGATTAC AGGCATGAGC CACCGCGCCC GGCCTAATTT TGACCTATCT TTTTATGGCT 60 TTTTAATGAC ATCCTCTCAT AAAGAATGTC CTTCGTGTTT GATGCCCTTC CTGTCTAACT 120 CTTCATCCTT TATGTCTAAC TCTGTCTAAC TCTTCATCCT ATATGGCCCA CCTTGGAAGT 180 CACTTCCTCT GGATGCCATG TCTGATCACC TTCCTCCCAG ATCGTGTTTC AACTCTGGGT 240 TCTCCTGGAC CTAATGCCAC TGCTGCCAGC ATTGAATTGT AGTCACCTAT TAACTGAATA 300 GCTCTTCTAC CAGACCTCCT CAGTATTTGA GCTCCTTAAG CATAAGAAAA GTGACATCTG 360 TCTTTGTGTT CTCCACCACT ACTCCTACGC TGCATGCATC ACTATGCACC TGCCTGATCT 420 GATGATATGC AGGGTGCTAG ATGGATGTGG AAGGGTCGGG AGGGGCAGGA ATGTGCTGGA 480 GAGTTCTGAG AAGATGGGCA GAACCTATGA AAGTGTACCC TGTACCTAGG ATGGGGGATA 540 ATTTTTGGTA GTAGGGATTG GAGAAACAGT AGGTAAAACT CCACAATGGC CAGGCCAACA 600 AATGATATCA GTAAATATGA GAGAGTCCTG AAAGAATTAG CGAGCCCCAC TTTATTCCAG 660 ATAAAATGTT AATGGGATAG AGTCTTTCCT TAGAAAATGT GGCTCCCACA CAGCCAACCT 720 GGGCCCATGA TGCAGTCGGA TTCTGATGCC AAGAGAAAGT CACAGCAGGC GGCGTATGCA 780 GACGCCTCCA CTTAGTTTCT GCCTTCCTTG CACCTGGTGT GAGTTTCTTC CACACCTGCC 840 ACCCACTCCC TCCTCCTGCT AGTACCACTC CCGGGCTACT CACATTCATG CACTGGGCTT 900 CTTCTCACTT AATTTAATGT AGACTTCTCC TGAATTGTTG GCTTAGGAAA AAAACCAAGA 960 CTATAAGAAT ATGAGAGGCT AAGAAGAGAC AACAATAGAA AGAAACTCAA AACGTCTCTC 1020 CAGCTCTCAA CAACTGTAAA CACTGAGCTA TTTAGAAGGT ATATGTTCTC TGCAGGAAGG 1080 TCACTGGGAC CTTACGTCTG GGTGTGGCTG AATCAGTCCC AGTCTTTTTC AAAGTATGCA 1140 TTGTGTTCTC TCTACATCAG CCCAGACTTT GAATTCAGTT TCTAGGACCA CAAAGGATTC 1200 ATTCACTCAT GCTGATTGGA CCCGTGACTG AGAATTAATT ACAAACGTTG AATGATGGGG 1260 TAGAATCATG TCTTAACAAA CGTCACCAGG ACGTTCGAGT CTAAAATAAC GCTACTTGGG 1320 GGGGCTGGAG GACAATCCAC ACTGACATTT GTCTTGTCAA 1360
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