Tag | Content |
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EnhancerAtlas ID | HS047-10767 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr14:100415800-100417350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx3-2 | MA0122.3 | chr14:100417267-100417280 | TTAACCACTTATA | + | 6.11 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr14 | 100415802 | 100415907 | chr14 | 100415963 | 100416188 | chr14 | 100416614 | 100416963 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I099949 | chr14 | 100415478 | 100415881 |
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Enhancer Sequence | ATCCAGCCAC CTCCCGTCAG GCCCCACCTC CAACACTGGG GATTCCCATT CAACATGAGA 60 CTTAGCAGGA GCACATAGCC AGTGTATCAG AGGGTTAGAG AGACTGAGGT ACTTGCCCCA 120 GGTCACTCAG TAAGTTGGTA ACAGAGCTAA GGGTGGAACT CCCAGTTCTC ACAGCTACAT 180 TCTGTGCTGG CGTTCTCAGC CTGGTGTCTT CAGAGCATTA TTAGAGTGGG TGCTGCTAGA 240 GTTTCAAATA ATTTGAGACT GTGCTGCACA CTGCACATGA CAGAGAGAGA TGTGAGCGCC 300 AGTTGCCTCT GAAAGGCATA GGAAGGTTAT ACATTTGGGC ATTTCCCCAT CTCGAGCATC 360 AGACACCTTT GCTCCTAAGG CATTAGTGAT TGGCCCAGGG ATCAATGTTC CACACATCCA 420 TCTTGGGAAA TGCTGTGGGA GAAGGTTAAT CATACAGAGG TGGCCCGGCA TGGTGGCTCA 480 TGCCTGGAAT CCCAGCACTT TGGGAGGCGG AGGCAGGCGG ATCACCTGAG GTCAGGAGTT 540 CGAGAGCAGC CTGGCCAACA TGGTGAAACC CCATCTCTAC TAAAAATACA AAAATTAGCC 600 GAGCGTGGTG GCGGGTGCCT GTAATCCCAG ATACTTGGGA GGTTGAGGCA GGTGAATCGC 660 TTGAACCCGG GAGGCGGACG TTGCAGGGAG CCCAGACTGC ATCACTGCAC TCCAGGCTGG 720 GTGACAGAGT GAGACTCCAT CCCTGCCCCG CACCCCCCAA CCCCCGCAAA AAAAGAATGT 780 GGTTATAACA TTTCAGCTTA TAACATTGGG ACGATTCCTC CCTCCTTACC AGGACCGAAC 840 TAGGAAATGG CCAGACTTCC TGTCATGGTA AGACTGATGT CACATGCTCA GTGACATTTC 900 TGAGATTCTT TTGGCCAAAT GGGCTTCAGA ATCACTTAGG TTCTCCCAGG CCCTCAGACT 960 GTGGCGACTG AAAATAGAAT GGACTGTGAT CACCACCACA CTGCCCAGCT GCCCCTTGAC 1020 GCCCATGGGG TTCCTCTGCA CGGGGTTCCC CTGTTTTCAT GTGGCTTATT TTACTCTGAT 1080 TCACACAGAG GAGGCAGGTT TAGAAACACA GCATCCGTTT GTCTGCATTT AAAACAATCC 1140 TTGGGAGAAG CAGGCAGCAG CCCTGTAGTC CTGGCCACAG TGGCAGCTGA GGTAGCCCCT 1200 CCTCACCTTC AATCACTGCT CCTCCATTTG AAAGCATTCT CAGAAACTGA TGCTACAGGA 1260 AAGGCCTCTA CCTTGTTCTG GCAAGTTCCC TCCTGCACTT CTTTCCCAGG CTGAGGCAGC 1320 TCCAGGGCTC AGACGTCAGC CAGAAGTAGG GGAGGGAGAG GACTCAGCCA GACATAGGGA 1380 TCTGGGGTCC AGAGGGCAGC CGCACAGCCA CCACGCTCGT CTGCCATGCT CGTGATACCT 1440 GCCCACCCCA TAGCAGAGAT GTTTCTGTTA ACCACTTATA GAATGGTGGG GCTGCAGTGA 1500 CGCTCAGGGG TCGTCTTGGG GGAGCATCTC CCAAAGTATG TTCTGTGAAA 1550
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