Tag | Content |
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EnhancerAtlas ID | HS038-15318 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr3:184513000-184514430 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr3:184513925-184513946 | TATTTCTTTTTCTTTCCTTTT | + | 6.14 | ZNF263 | MA0528.1 | chr3:184513434-184513455 | CTCCCTCCCTCCCCCTCCCCC | - | 7.84 |
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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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Enhancer Sequence | GTGTTTGAAC ACGTTTGTGG ATGGTAGGGG TCCTAGGGAG TTAGAGGATT GCTGGGGTTG 60 ATACAGGAAG GCCCCACATG TTGGCTTGGC TCTGAGGTGT CAGACCTCTA GAGGTGGCAC 120 AAACCACACA ATAGCTGTGG TTCCTGCTGT CCTGGGACTT TTAACAATGA CACAAGCCAC 180 ATCAAGCTGC TTGAACAAGA ACATGTGCAT AATGTTCTTG TTTCCACCCC ATACACCCAT 240 GAAGTCAGGT GCAGGGGCAA AAGCCCAGGG TGTGGTCTGA GTTGGATTTG GCTTCTGGGT 300 TTGGGGCAGG GCCCGGGGGA TTCAAATCTC CTCTGTCCTG CACACAGCAT CATGGTGACT 360 TGGGGATGGA GGCTGCACAG TCAGCCTGGC TGTTTGCAGC CTCTCTGCTC CTCCCTCCCT 420 TCTCTGCTCT GCTGCTCCCT CCCTCCCCCT CCCCCTCACT GTCTCCAGCC CTGCAATCCA 480 TCACAGCTCT GTGTCCCTGC CCTCTGTGAC CGCGTCTCTC TGCACCACTA CTTTTGCATT 540 TTGATGTTAA AACAATATTT TACCCAATAT ATGACAGCAC TTGGAGCCTT TGCAAAGGCC 600 TTTCACATCT GTTATTTCAT TTGATCCTCA CCAGGTTGCT GTCAGGTAGG CAGGGAAGGT 660 ATTATTAGTG AGGGTGGTAG TCAAAATATT TAACAGCCCA TATATGATGG GCTCAACCAT 720 CAGAGTGGAT GCAGGTCTAG TGCTGGAGAG GGCCCTGGAG GCATCTTCTC TTAGTTATTG 780 GAGCAAGGTC TGGGGGAGGG GGCACTGGCG TGGGGACCTG GAAGTCTGGG GCAGTCCAGT 840 GTGGGTGGGG GCAGACATGA AGGATTCAGG GAAGTGGCTT TTTGCCAAGC AGTCTGGAAG 900 CATTTCTGTT TTTTCCTTTT CTTTTTATTT CTTTTTCTTT CCTTTTTTTT TTTTTTTTTT 960 TTTTTGAGAC AGAGTTTCGC TCTTATTGCC CAGGCTGGAG TGCAATGGCG CAATATCTCA 1020 GCTCACCACA ACCTCCGCCT CCCGAATTCA AGCAGTTTTC CTGCCTCAGC TTCCCAAGTA 1080 GCTGGGATTA CAGTCATGCA CCACAACGCC TGGTTAATTT TGTATTTTTA GCAGAGACAG 1140 GGTTTTCCCA TGTTGGTCTG TCTGGTCTTG AACTCCCGAC CTCCGGTGAT CTGCCTGCCT 1200 CAGCCTCCCA AAGTGCTGGG ATTACAGGCA TGAACCACTG CGCCCAGCCT CTGTTCTTTT 1260 TGTTTTTTGT TTTGTTGTTT GTTTTTTAGC AGGATTGAAC TGTACTAGTG CTTACCATGG 1320 TCTGTAATTA TCTGTCCAAT TGTGGTAATG TGGGAACCGA GGTCCAGAGA GGTGAGTAAC 1380 TTGCCCAGGG TGCAGGATGA AAAGAGGGCC GGCGGTGAGG TCGCTGGACT 1430
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