Tag | Content |
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EnhancerAtlas ID | HS047-18415 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:16120460-16121500 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr2:16120585-16120596 | ACAGGGTGTGG | - | 6.14 | Stat6 | MA0520.1 | chr2:16121404-16121419 | ATTTCTGAGGAAATG | - | 7.85 |
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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 |
GH02I015979 | chr2 | 16119952 | 16121482 |
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Enhancer Sequence | ACCAGAGCAC AGAGAGGTTA AGTCTTTCAC TAAAAGTCAC ACAGCTAGTA GACTTTGGGG 60 CCAGGATTCA AATACAGGCA AACCACAGGT CTTGACCCCT ATGCATGTGG CTTGCCCTGA 120 TCACCACAGG GTGTGGGATG CCTTTATCCG CTAGCACTTT CAAAGGTCAT TTTCAAATGG 180 CCTTTAGCAC TTTCTGCCTT GTATGAAGCC TCGGTATCTG GGATTTCACC TTCTCGGGGT 240 CAACCATTCC AAAGCCCCAC TGGAAGTCCC AGCCCTGTGG ACGTGGTATT TGGTGGCGAT 300 AGCCGATCTG AATTGTGAGC CGGCCCAGCC CAGCGCAACA TTTGCATCTC AAAGAAGCTC 360 TGTGATTTTC TCGAGATTCC AAACACAGTA ACTGCGGGGA GGGCCCCATG GTATTTGCAA 420 GGTTGAGAGT TTGCAAATGC CTGGAGGCTG ACCCCTGGAT CTCCTTCACC CCGGAGACCG 480 ACCAGCACAC CATCTAACTC AGTGCCTTTC ACATCGTATT CAGTCTGAGA AACAGTTTTG 540 GTGTTTTGTT TTTTCCTACC GTGTGCAAGA CAACAGATGT TTGGTGACTG CATGAAAGAA 600 AAATTTTTTT CTTTTCTTTC ATTTTATTTA TTTATTTATT ATTGTTATTA TTTGAGACAG 660 AGTCTTGCTC TGTTGCCCAG GCTGGAGCGC AGTGGCACGA ACTCGGCTCA CAGTAACCTC 720 TGCCTCCCAG GTTCAAGTGA TTCTCCTGCC TCAGCCTCCC GAGTAGCTGG GATTACAGGC 780 ACACACAACC ACGCCCAGCT AATTTTTTAT TTTTAGTAGA GATGGGGTTT CACCATGTAG 840 GCCAGGCTGG TCTCAAGCTC CTGACCTCAG GTGATCCACC CACCTTGGCC TCCCAAAGTG 900 CTGAGATTAC AAGTGTGAGC CACCACGCGC GGCCAGAAAA TTTCATTTCT GAGGAAATGA 960 CATATTGGAC CTTATTGGCT CTCAAAGACA GAAAAGATGT CCAGTTCTTT TGTTTTGTTT 1020 TGTTTTGTTT TGTTTTTCAG 1040
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