Tag | Content |
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EnhancerAtlas ID | HS047-03520 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr10:132980-135290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mecom | MA0029.1 | chr10:135054-135068 | AAGATAAGATAACC | + | 7.28 | NFYA | MA0060.3 | chr10:135011-135022 | GGCCAATCAGA | + | 6.02 |
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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: 2 | ID | Chromosome | Start | End |
GH10I000087 | chr10 | 132975 | 133673 | GH10I000088 | chr10 | 134361 | 134510 |
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Enhancer Sequence | TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACTGCTCCT GGCCTCTATG CATTCTCTCT 60 CCCTTTTGTC TTCTTAAATA AAGACCCATC CCAGGATTTT ACCCCAGGAA GGTGGACAAG 120 AGTGGCAGCA AGGTATCCAT GCAACAGATG GCACTTCCTT AACTCTGTTG CACCCCTGTT 180 CCAAGGTGCC TCCAAAGGAC AGCACCACCA GAAGGGCAAA GCCCCCCATG CTGGAGTATG 240 AGCCTGAGTC CCAGGATCCC TGGAGGAGCC AGAGGTTGGC TGGAGATAAG GCGCTCGGTG 300 TCAGGAAGCT CTTGTGTGTG GGAAAGCTGC TGACGCCCTA TCACCCCGTT TGCAGCTCCA 360 CTGATACACC CATAACCCGT AGGCAGGAAG CAGGGCCAAC CTGGTTACAC AAGACTGATT 420 AGTGATAAGG AGGAGAAAAA AACCAGACAT GCACCCAGAC TACAGCATAC ACGCAGACTA 480 CAGCACGCGC ACCCTTAAGG AACCCACACA CCCTCAACGG GCAGCAGGCA CTACTCTAAC 540 CCCACTCCAC CCTACTCCTG GCAGCCTATC CAGGTACCCA CTGGACAGTC CCCTGTTAAG 600 ACCGATGATC AGGAATCCTC ACTCTTCCCC AGAATGGAGC GTGCAGCCTG GCCCCAACAG 660 CCGCAGCATG AAACGCCGTG GCAAGTTCTC TGCAGCAGGG TCTGTCCCTT CTTGCAGCAG 720 CTACTGGAAA GGTGGGAATG GGGAAGACAG TCAGCCTGCT CTTGGGATAT CTGAGGGCAG 780 GGTTGGAGTC ACCACCAGGA CCTGGGGGAA GCACAGGCAC AATGGCCACA GCTGAGAGCT 840 GACCCAGGCC CCAGGATGGC CGACCGCTGC CCCAGCAGTG GAGAAACGCC CACGTCGGTG 900 TAGAATCAGG CCAGGCCAGC CACAGGCTAA CCCAGGAGCA GATGGCTTGA GAGCAGGGAG 960 TGGGGCAGCT CCAAGCTCAG CAGGCCTCAT TTCTAGACAG GGAGAGGGGA TGGTAGGCCA 1020 GGACCCACAT GTGACACCTG AGAGCTACAA AGGAGGAGGC CAGGACACCC CCTGGGGGAG 1080 CACTGGAGTG TTGGGTACAG CAACAAGGCA ATATGGCCGT CTGAGGGGAA GGTCTCTGCT 1140 TTTCCTCTGC ACTGAAAACT TACATCTGTA CCTGGTAAGC TGAGCAGGGC AGGGTTACCA 1200 CCCTCCTGCA GATGAGGAAA CTGAGGCTCA GAGACCTGGG ACCTGCCCAA TACCTGGCTG 1260 CTGACACCTC TGTTCTTAGC ACATTCCTAC CAGCTTCTAC ACAAGCCAGT GAACTTCCTG 1320 AGGGCAGTGC CTGCGAGGCA CCACTCAGCA CATGCCCCAG CAGAAGGCAC CACAGTGCTT 1380 TATAAAGGGG GTGGAGCTGC AGGCAGAGCT GCCTTCCCCC ATCCTTGACC ACAGGGCCAG 1440 GCAGTCAGGG CACGTGCACA CACCCAGACC TGCAGGCTCC CTGCTCGTGG ATGTCACTAG 1500 GAGGCAGAGG TTGCAATGAA CTGAGATGGT GAGATGATGC CACTGCACTC AAGCCTGGGT 1560 GACGAGCAGG ACCCCTGCCA AAAAACAAAG CCAGCAGGTC TGGGCTAACC TTTAATTTCT 1620 TCTTCTATGA AGTGAGATAA TTGGACAAGA CATCTTTTAC AGGCAGCTCT AAAAGATTAC 1680 AATGCTGGGA TAATTGGGAA AGACCTACAC TCTAAGAATC TGCCTTAGAG TGTAAGACCT 1740 ACACTCTTTC CAGGGACAGC CCTGAGGTAG ACAGGCTCTC TAGAAGATGG ACAGGCTCTC 1800 TAGAAGGTGG ACAGTCTCTC TAGAAGGTAG ACAGGCTCTC TAGAAGGTAG ACAGGCTCTC 1860 TAGAGGGTGG ACAGGCTCTC TAGAAGGTGG ACAGGCTCTC TAGAGGGTGG ACAGGCTCTC 1920 TAGAAGGTGG ACAGGCTCTC TAGAAGGTAG ACAGGCTCTC TAGAAGGTGG ACAGGCTCTC 1980 TAGAAGGTAG ACAGGCTCTC TAGAAGGTGG CCAGAAGGGG CTGTTCTTCC TGGCCAATCA 2040 GAACTGATCA CTGGTGTTTC TGGATTTGCC TCCCAAGATA AGATAACCCC AGAGCAAAGA 2100 ACATTATAAA GCTTTACAGT AAATTATTCT ACAACTAGCT CAATTTCTCA TTATTCATCA 2160 CCAACTTGAA ACAAAATCCC AACCTTGGGA AAACACACAT TCACTCACAT ACACACACAC 2220 ACACACACAC ACACACACAC ACACCCCTGC TGGGAGATGG GTGGCATAGG GTTTTTCTTA 2280 AACAACTAAA CAGTAGCAGG CCATTTGTGT 2310
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