Tag | Content |
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EnhancerAtlas ID | HS051-12843 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr18:10213310-10214190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr18:10214144-10214155 | TTAATTAAATT | - | 6.32 | Lhx3 | MA0135.1 | chr18:10214150-10214163 | AAATTAATTATTT | + | 6.78 | PHOX2A | MA0713.1 | chr18:10214145-10214156 | TAATTAAATTA | - | 6.62 | PROP1 | MA0715.1 | chr18:10214145-10214156 | TAATTAAATTA | + | 6.32 | PROP1 | MA0715.1 | chr18:10214145-10214156 | TAATTAAATTA | - | 6.62 | Phox2b | MA0681.1 | chr18:10214145-10214156 | TAATTAAATTA | - | 6.62 | RREB1 | MA0073.1 | chr18:10213630-10213650 | CCACAAACCACACCCCTCAG | + | 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 |
GH18I010213 | chr18 | 10213311 | 10214121 |
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Enhancer Sequence | ATTTTGAGAA TACTATGGAG TATTAACACA GATAAACTCA TTTCAATGGA TACGAATTAA 60 TCAAAGGTTT GTCTGGACTA TTTTCATGTC CTCCCAGGAA TTCTACAGTA ATGGTAATTT 120 TTTTGTTCCT TGCAATGAAT AATTCAACTT TCTCAGTTAC TATATCTTTA ATAGTCATTC 180 AGAAATAATT TAAGATTATG TGGCATTTGT CAAACAAAGG AAGACTGATA AAACCAAGAA 240 AGGTAGTGAT CTGAGTTAAT TATTTTTCTG TTTGCTCTAA AGAAAAGCAA ACTCTTTAAA 300 TTCTTACAGA TATCACTCAG CCACAAACCA CACCCCTCAG AAAACACACA AGAAATCCAT 360 AGCCACTTAA AAACACAAAA CCAACGTGAA GCAATCCTGA TGCTTAAGAG GCAAAGCTGC 420 TTGGTTCCAC TTCCTGTTTC TAACTGTTGT TGACAGAGTA CGTGACATGT GATTTCTGGC 480 TCAGTATACT ACAACAAGGG AATCATAGCC TACAGAAGAC CCTTGAGAAA CACAAAACGG 540 TGTGGTTGCC CTGTGGAGTT TATTCACCTG GGGTTTGTCC TCAGCACCTG GGAAGCATCA 600 GGAATACACC AGCTTCTCAG AGGCAGGGGA TAAAAACAGT CTTGTGAAAT ATTCTCCTTC 660 TCCTTCCCAA AAAAGTACCT GTGGAAGCTT AAAATAATAA TTAAAATAAT CTCAGAAACC 720 TTGAGCTAAG GCTGGATTCA GAAAATTGTG TACACTCCTA CATGTACACA GAACTTAGAG 780 ACATCTTTCT CATCTCCTTC CCAAGAGAAA TAGATCTGTG GCTATCAGCA CTCATTAATT 840 AAATTAATTA TTTATCATAC CTTCAACAGA ATCAATTGTC 880
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