Tag | Content |
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EnhancerAtlas ID | HS051-13462 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr19:4296000-4297710 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HEY2 | MA0649.1 | chr19:4296701-4296711 | GGCACGTGTC | - | 6.02 | LBX2 | MA0699.1 | chr19:4296624-4296634 | GCTAATTGGC | - | 6.02 | Npas2 | MA0626.1 | chr19:4296701-4296711 | GGCACGTGTC | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr19:4297635-4297650 | GAGGTCAAGAGATCG | + | 6 |
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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 | CAACTCCTGG GCTCAAGTGA TCCTCCCGCC TCAACCTCTC AAGTAGCTGG GACTATGGGT 60 ATATGCCACC ATGCCTGGCT AATTTTAGAA TTTCTTGTAG AGATGAGGTC TTGCTGTGTT 120 GGCCAAGCTG GTCTCGACCT CCTGGCCTCA AACAATCCTC CCACCTTGGC CTCCCAAAGT 180 GCTGGGATAT CAGGCGTGAG CCACTGCACT TGGATTATAG CAAGCACTTT GGCTATAACT 240 GCTCTAAAGT CACCCGACCT GATGAGGAAA AACTATTCAC TGTATTTTGA CAGCAGAGGG 300 AACTGGCACA GAGAGGTCAA GTCACTTGCT CAAGGTCACA CAGCAAGTAA ATGAAACAGA 360 GGATTGAATC CAGGTTGTAT AATTTACAGG AACCCCAGCT AAAGGCTGTG AATGCCGCAA 420 TTAAGATAAG GTCCAGCACC CCAACCCCCT TCTTTTGCAG CCTCTGAGGT TGGCAGGGGA 480 TCCCTGGGGA CTGCCAAGCT GCTGTTCAGG ATTGGTGGGG TGTGGGGAAG CCAGCTGTGT 540 GGGGTTGGAC CCGCGCCCAC TCCCTGCTCT CTCACAGCTG CCAACGCACA GCCTGGCGCC 600 TCCACCACCC CGCCTCCTCT AATTGCTAAT TGGCCCCTTT GACATCAGAG GGGTGGGAAG 660 AGGTGGGTAA CACAGCCATA ACACACCCCT CCCTTGAGGC AGGCACGTGT CCCCCGCCAG 720 CAGGCTGGTC CTACCAGCTG GAGAGGAACA GGCATCTCTA GGGGCTGAGA GCTGGGTGCT 780 TCATTCTGCC AGAGGGGGCT GGACAGAGGC CCGGGGCCCA CAGGCACCTC TCACAGAGCA 840 GGAGGCAAAG CCTGCATCCC CTTGGGTTTC CCGATTCTGC CCAGGATGGG TCCATAAGTG 900 GGGGACATGG CAAAGGGGAC AGTGCATAGG GTGCACCCCT GCCTGGTGCA TAACGCTAGA 960 TATGTCTTGG CCCTCTCTGG TTCACCTGGC TCATCTGTAA AGTGAGGCAG CTGGCGTTGC 1020 TGACCTGGAA AGCTATCTGG AGGGTTTCTT CCAACTTTGA GAGTCTGTGG CTTTTTTTTT 1080 TTTTTTTTTT TGAGACAGAG TCTTGCTCTG TAGCCCAGGC TGGAGTGCAG TGGTACAATC 1140 TGAGCTCACT GCAACCTCCC CCTCCCGGAT TCTCCTGCCT CAGCCTCCTG AGTAGCTGGA 1200 ATTACAGGCT CACACCACCA TGCCCAGCTA CTTTTTGTAT TTTTAGTAGA GAGGGGGTTT 1260 TCATCATGTT GGCCAGGCTG GTCTCGAACC CCTGACCTCA GGTGATCCAC CCACCTTGGC 1320 CTTCCAAAGT GCTAGGATTA CAGGGATGAG CTACCGCGCC CAGCTGATGG CTTTATTTTA 1380 TTTAGAGACA GGGTCTCGCT CTGTCGCCCA GGCTGGAGTG CAGTGGTGCA CTCATAGCTC 1440 ACTGCAGCCT CCAGCTCCTG GGCTCAGGTG ATCCTCTTGC CTTAGCCTCC CAAAATGCTG 1500 GGATTACAAG CATCAGCCAC TATGCCTGGC TGATGACTTT CAATTTTGTA TCCTAAAATT 1560 CTTGGATTAT GGGCCGGGCA TGGTGGCTCA GGCCTGTAAT CCCAGTACTT TGGGAGGCTG 1620 AGGCAGGCAG ATCACGAGGT CAAGAGATCG AGACTATCCT GGCCAACATG GTGAAACCTC 1680 GTCTCTACTA AAAATACAAA AATTAGCTGG 1710
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