Tag | Content |
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EnhancerAtlas ID | HS051-11095 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr17:1775820-1777280 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DMRT3 | MA0610.1 | chr17:1776318-1776329 | ATTGATACATT | - | 6.62 | FOXP2 | MA0593.1 | chr17:1776627-1776638 | TTTGTTTACTT | - | 6.62 | MEF2A | MA0052.3 | chr17:1776713-1776725 | TTTATTTTTAGA | - | 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 |
GH17I001869 | chr17 | 1773276 | 1776198 |
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Enhancer Sequence | GTGAGATGCC TCACGGGGCG TGCGCTGACC AGGGGTGTCA GACTTCGGAA TCATGTTTTG 60 AAGTTGAATC TGGGACTAAA GGGAGTTTTC CAAATGCCAT TCATTACAGG GTTGTGTCTT 120 GGAAAGAATA ATTCTGATTC ATATTTTAGA GTATGTGATT GAAAAAATAA TTAAAGATTG 180 TCTTTTTTTT TTTTTTTTTT TTTGGAAGTA GGGTCTTGCT CTGTCAGCGG GGCTGGAGTG 240 CAGTGGAAGC ATCACAGCTC GTTGCAGCCT TAACCTCCCA AGTAGCTGGT ACTATGGGCG 300 CATGCCACCA TGCCTGGCTA ATTTTTTTGT AGAAATGGTG TCTTACTATG TTGCCCTGGC 360 TGGTCTCAAA CTGCCCTGGC CTCAAGCAGT CCTCCGTCCT TGGCCTCCCA AAGTGCTGGG 420 ATTATAAGTG TGAGCCAGGG TGTCCAGCCA AAGATAATCT TAAAGATACT TAACAGCCAG 480 ACTTTTAAAA AAGATCAAAT TGATACATTC TTCTCTGTTA GTAGTTGACC AAGTAGTTTC 540 TTCGTTTCCC ACATCATCAG GTTTTACACC CTCTGACTTT GCATTCCTTT TAAGTTCTTG 600 CCTTTTAACT ATCCAGGACC CACTTACTAA GTTTGGCTCA TCTCTCTCCG AGTTTCCTAT 660 TTTGGGCCTC GTGGGTGTTT ATCGTTTGCT TGAAGACAGT ATTACTTATA TTGGTCATAG 720 GTTCTCCTTC TCAATTTCAT GGATGAGAAA TGGTTTCTTC ATTTACTTTT CTCTGCAGCA 780 GGTCCTAAGA GGCATTAATG GAATCATTTT GTTTACTTTC TGGCCTTTAC TTTAGGAACC 840 TCTTGATCTG GGAAGTCACC GTTGAAAATT TGGATTTGTA GAATGTGGTT GGATTTATTT 900 TTAGAGGTCC TTTTTTCTGT CACGGCTTCA CATACACCTC CTCTCCTCCC CTCAACTATT 960 AGTTTCTATT TTTCAGTGCT AAGATTCTGA GAAAAGCAAG GTTAAGATGT CACTGATGTT 1020 TCTGTGAAAC TCTCAGGACT TTCCCCCTTG CCCTTTGTTG TTTTTAATCT ACCTTGCACG 1080 ATCCGTCTAC CTCTCTCGCT CTTGCACGTT CTCTCTCTTG CTCTGTCTCT CCTTTTATAA 1140 GAGGATCTAT TTATACACAA CTCAAAAATT ACATGCTGTT GGCCAGGCTT GGTGGCTCAC 1200 GCTTATAATC CCAGCACTCT GGGAGGCCGA GGTGGACGGA TCACTTGAGG TCAGGAGTTC 1260 GAGACTAGCT AGCCTGGCCA ACATGGTGAA AACCCATCTC TACTAAAAGT ACAAAAATTA 1320 ATCGGGCATG GTGGTGTGCA CCTGTAGTCC CAGCTACTCG AGAGGCTGAG GCATGAGAAT 1380 CATTTGAACC CAGGAGGCGT AGGTTGCAGT GAGCCAAGTT TGCGCCAGTG CCCTCTAGCC 1440 TGGACAACAA AGTGAGACTC 1460
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