Tag | Content |
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EnhancerAtlas ID | HS047-10842 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr14:103046080-103048210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LHX6 | MA0658.1 | chr14:103046331-103046341 | GCTAATTAGT | - | 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 |
chr14 | 103046873 | 103047218 | chr14 | 103047902 | 103048170 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I102579 | chr14 | 103045483 | 103047619 |
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Enhancer Sequence | GCTTGAACCT GGGAGGCGGA GGTTGTGGTG AGCCGGGATT GCGTCATTGC ACTCCAGCCT 60 GGGCAACAAG AGTGAAACTC TTGTCTCCAA AAAAAAAAAA AAAAAAAAAG GAAACTGAGG 120 CCCTGAGAGG TCCAGGGGCT CTCAGGCAGC CAGAGGCAGC ACCTGACCTG GCCCAGGCCC 180 CCTTCCCCGG GAGCACAGAT GCCAGGATGT GTGGATTGGC GCCCTTCTTG GGCTGCTGGG 240 CCCCGTGGTC TGCTAATTAG TCACATCATT TTTGGCATCG CACACAGCCT CGGGAACTGG 300 AGAATGTCAT TGTCAAAGTA TTTTTGAATA TTTGCCTTCT CAGCAAGAAG ATGAGAAAGC 360 TGTGAGGACA CTCAGTCTTC CACGGGGTGG ATACTAACCA AAATCACAAG CAGCTTGAGC 420 TGGAAGGACC TGGGAGCCGG GAGAGATGCC GGAGGAGTCC CGCGCGCTGC CTGTCACAGC 480 TGTGTGACTT CGAGACAGGG CTCTGGCCCC CTGGGCCTCA GTGTCCTCCC CTGGAAAATG 540 GCTCATTCAT TTCTCAGGTG GGCATGAAGT TGCTATGTGC CACGCACTGC TGTAGGCTCT 600 GGGGAGCAAA ACAGGCAAAA ATCTCTGCTC TCACAGGCTG CCATCCCCAG GGGGGCCATA 660 CCATAGAAAT CAAATCAGAT ACACCAGGGG TGACACATAG AAGGGAGAGC CCAGGGGTGG 720 GGCTGTCAGG GATGGCCTTG CTGAGAAGGT GACATGCGAG TGAGAATTTG AAGGGGGCAG 780 GAGGGAGCCC AAGGGGTGTC AGGGGAAGAG CCCTCCAGCA CAGGGAGCGG CAGGCACAAA 840 GGCCCTGCAC TCGGGCAGGA CTGGGTTGTT CCAGGAGCAT CAGGGAGGCC AGGCGGGCTA 900 GAGCAGGTGG TGACTCAGGG AGGCAACATG ACAAGACTGG GTCACAAAAG GCCACTGGAG 960 GCCTGCTTGC TGCTTGTGGA GGGCCTTGTA AACTGCTGGA AAGCCTTTCT TTTCTTTCTA 1020 TTTTTGTTGT TGTTGTTGTT GACAGGGTCT CCCTCTGTCT CCCAGGCTGG AGTGCAGTGG 1080 CTAGAGCTCG CTGTTACTTC AAACTCCTGG GCTCAAGTGT GTGCCACCAT GCTCTGCACC 1140 CAGGCTGGAG TGCAATGGCG CCATCTCTGC TCACTGCAAC CTCCGCCTCC TGGGTTCAAG 1200 CGATTCTCCT GCCTCAGCCT CCTGAGTAGC TGGGATTAAA GCTGCCTGCC ACCTGCACAG 1260 GTAATTTTTT TTGTATTTTT AGTAAAGACA GGATTGCGCT ATGTTGGCCA GGCTCGTCTT 1320 GAGCCCCTGA CCTCAGGTGA TCTGCCCGCC TCCCAAAGTG CTGAGATTAC AGGCGTGAGC 1380 TGCACCTGGC CTTAATTTTT AAATTTAATT TAAAATTTTT GTTTTTGTTG TTGTTGCAGA 1440 AATGGAGTCT CCCTATGTTG TGCAGACAGG TCTTGAACTC ATAGCCTCAA GTGATTTGTC 1500 CGCCTCAGCC TCCCAAAGTA CTGGACTTAC AGGTGTGAGC CATGACACCC AGCCAAACCT 1560 ATGGTTTTTT TTTTTGGTGT TGTTGTTTTG TTTTTTTTTT TTTTGAGATG GAGTCTTGCT 1620 CTGTCGCCTG GACTGGAATT CAGTGGCGCA ATATCTCGGC TCACTGCAAC CTCCGCCTTT 1680 CAGGATCAAG CGATTCTCCT GTCTCTGCCT CCCGAGTAGC TGGGATTACA GGTGCATGCT 1740 GCCATGCCTG GCTAATTTTT TGTATCTTAG TAGAGACGGG GTTTTACCGT TGTTGCCCAG 1800 GCTGGTCTTC AACTCCTGAG CTCAGGCAAT CCACCCGCCT CAGCCTCCCA AAGTGAGCCA 1860 CTGTGCCCGA CCAAGCCTAT GTTTTTGTTC TGGGTGACGG TCTAGAGCAG GACCAGACGT 1920 GATATGGTTT CTGTATTAGC CGTATTCTTC TGTGCCCCAT GCTTCAAAGA TAGAAGCAAG 1980 GAGGCCAGGT GAGATGTGAG GAGGCCTGCC CCATGGTGGG GACAGTGGGG GAACGAGAGA 2040 GGACTGGACT CCAGATGTGT CTGGAGGCAG AGTTGACATT GGGTGTGGAA TTGTAAAAAA 2100 TAATTTGTTG GCCGGGTGTG GTGGCTCACG 2130
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