Tag | Content |
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EnhancerAtlas ID | HS047-26499 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr4:186886550-186888160 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr4:186886730-186886745 | AGGTCAGAGAGACCT | + | 6.44 | JUN | MA0488.1 | chr4:186887057-186887070 | GAAATGATGTAAT | + | 6.07 |
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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 |
GH04I185965 | chr4 | 186886548 | 186887754 |
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Enhancer Sequence | CAGGGGTGTT GATGGACTTC GGTCTTTCTT CCTGTGATAT GAGTGCAGTT AATGAAACTC 60 AGGGAAGGCA GTTGTGTTCT TTTGGCCAGT CTGGTTTCTA GGAAGATAAA GGATCCTCAG 120 AGAACAACTT CATTCTGTTC CTTGGGAGAG ACAAAACATT GAGAAATGGG GGTGAGGGGT 180 AGGTCAGAGA GACCTTGGGA TCGCTTCTTC AATCCAGCAT GTCAAAGGGC CATATGTTGG 240 AGTTCAGGTT TCTGAGACAC AACACTTCCT GTTGTAGCAG CAGAAAAGGA GTGATCCGTT 300 TCCTCCCTGT CATAGGGGTC AAAACGGACA CCTCTGAAAC AAAGACAGAT TAACAAGAGA 360 AAAGCCCAAC AAATATATTC GACCACAGCT TTACAATACA CAGGAGCCTT CGGAATGAAG 420 ACCCAAAGGT ACCGGGGAAA CTCTCTGATT GTGTGCCCAG GTTTCAGGGA GCAGGGACAG 480 TCATGCAGAA ATGTGACCGG ACAGAAGGAA ATGATGTAAT GGTAACAGGC TAACTAGGGA 540 CACTCGGTGA GGCCTGTCTG TTCAGATCTT GCTCAGCCTC TCTGTGTAGC TTTCCTTCCT 600 CGCAGGTATC CGGCAGGACC CTTTCTGTAA TGGGGGGCCT ATTACCTACC ATTAAATAAG 660 ATAGGTCAGA AAATTTTTTC TGGCCAATTC TTACACAGAA AAACAGCCAA AAGTGAAAGT 720 GCCTTTAGGC TACACGTTGG CTTTGGGGAA AAGGAACTCT GGTTTCTGTG ACACTCGTTG 780 GGGCAGAGAG ATTCTAGTTC CTGCGACTGG CCTCAGGGGA GAATGGGGCT GAGAGACAGG 840 AGGGTGAGAG AAGGTCACAG GGAAACTTCG CTTCTGAGGC TGCTTCTGCC GTCTTCACTT 900 TGAAGCATCA TTTTTCTGAG CCTCAACATT CTTCAGTCTG AAACTTCCCC CCAGTAGTTT 960 TTTTGTTTGT TTGTTCATTT GTTTTGAGAC AGAGTCTCAC TCTGTCGCCA GGCTGGAGTG 1020 CAGTGGGGCG ATCTCGGCTC ACTGCAACCT CTGCCTCCCT GGTTCAAGCG ATTCTCCTGC 1080 CTCAGCCTCC CGAGTAGCTG GGATGACAGG CACCCACCAC CACACTGGGC TTATTTTTGT 1140 ATTTTTAGTA GAGACGGGGT TTCACCATGT TGGCCAGGCT GGTCTTGAAC TCCTAACCTC 1200 AGGTGATTCA CCCACCTCGG CCTCCCAAAG TGCTGGGATT ACAGGTTTGA GCCACCACGC 1260 CCGGCCCCCA TAGGTAGTTT GACAGTCCAC GGATCGGGTT GGTGGATTGT CTCCCAGGCT 1320 GTTCCCAGGC TCTCAGTCCT GAGAAGAGGC CTTTCAGCTA ATCAGTTGAC AGTTGTGTCT 1380 CATTTCAGCA GCAGTGTTGC AGACTGGCTT CCACCGAAGT CAGGCCCCAA ATAGTGTGAA 1440 CAGTCATGTA CGTAGCAAAG GGCATTTCTA GGGAAAGAAA AGAAAACAAA CCTTTGGGTC 1500 TAGAGGGCAG CCAGTCAAGA TTTTCAGATG TTAGACTTGA AGCATCTTCA TATGGAGTGA 1560 GAGCAGACAG TGGCAATCTG GGATTTTTCC GGTTCGCAGT TTGCATCCGG 1610
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