Tag | Content |
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EnhancerAtlas ID | HS187-16917 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:35337130-35338480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE40 | MA0464.2 | chr3:35337580-35337590 | ATCACGTGAC | + | 6.02 | Foxq1 | MA0040.1 | chr3:35337841-35337852 | AATTGTTTATT | + | 6.02 | MITF | MA0620.2 | chr3:35337576-35337594 | TTTGATCACGTGACCCTA | + | 6.38 | MITF | MA0620.2 | chr3:35337576-35337594 | TTTGATCACGTGACCCTA | - | 6.38 | MNX1 | MA0707.1 | chr3:35337475-35337485 | TTTAATTACC | - | 6.02 | TFEB | MA0692.1 | chr3:35337580-35337590 | ATCACGTGAC | + | 6.02 | USF2 | MA0526.2 | chr3:35337578-35337594 | TGATCACGTGACCCTA | - | 6.52 |
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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 |
GH03I035296 | chr3 | 35338035 | 35338359 |
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Enhancer Sequence | TTTGAACATA CATTAGTTGG TCTTGAGCCC TATACTTCTT TTCTCACATT TCTGGGAGTC 60 GCTTACTGGC ATTCCCCTGA GGCCTGATCT CACTGGGCAG GTATTGCTGA TAATAATAAA 120 TGATGACAGG GCCATGCTTT GCAGCTTGGA GTAGTCCCGT TTGTATTCGA TTTCTGCACT 180 ATCCTAGGAA TTTAGATAAC TAAGGCAGAG TTCCCTTTTT TTCCCACTTT CCCCATTACC 240 AAAAAGTTCT TATGCTCAGG TTCTTTTGAT CCTGGCATCT TCATTGCCAT CAAAATTAGT 300 TATTCTGTGA CTCTTGTCAT CTTGGAACTG TCTAGGAATA TCATATTTAA TTACCACTTT 360 GCCAAGCTGT GAGTCCTTGC ATCAGTCACC CACCCTCTTT GATTCTATTT CCTCATCTGT 420 TTAATCAGAC AAGATGATCT CGAACCTTTG ATCACGTGAC CCTAAATCAG TCTTTCTCAA 480 CCCCAGCACT ACTGACATTT TGAGCAAAAT AACTCATTGT TGTGAGGAGC TGTCCTGTGT 540 GTAATAGAAT ATTTAGCAGC ACCTCTGACC TCTATACAAG ATACCAGTAG TAAATAAGAC 600 CCCTTCCTAG TTATGACCAT CAAAGATATC TCTAGACATT GCTGAATATT CCCTGGGTAG 660 GGGCAAAATC ACCCACAGTG GTGAACCATC ATTCTAGACC CATATCAAGA AAATTGTTTA 720 TTTTTACAAA ATACTAAGAT AGGTGCCATG CAGTTGTCTA AAAAAAATTT TTAAGCATAG 780 ACTATCCTAA AATATAAATC TCATATTCAG TAGAATTCCA CTGTCTCCCT TACCATTCCC 840 ACAAAATTAC ATGTTCTTTT TCTTCTCTTT CTGCCCTGTT TAAATGCTGG TTCTGCACCA 900 CCAGATGTGG TCTGATCAAG GCTCTCCTGA CAGTGTGCCT CTGACCCATG CAATCTACCA 960 CAGCTGGTGC TGCTACGTTC AGTTACATCA CTTTTTCTGT TATTGCAAGT GGGCCTGTTT 1020 CAGTCTCAGT CTTTGTGACA TCTGGTTGTT CTCTCCTTTC TAAAATCCTG TTTGCACAGC 1080 CACTTTCATC CCACTCTGTT CCCACAAGAG AAAGAGGTTC ACACTTTCTT TTTTGTGGTT 1140 GACCCTATTG TGAGAACTGG TGACTGTTGC GGTGAGCCAT ATCAACGAAG AACTGTTTCT 1200 TCATGTGGGC TTGTCTGAAA GCAACTACAG TGTTGTCTTC TCTCAATGTG CACGTCTCTG 1260 CACTGGGCTA GTTAAAGAAG TTGTAGAAAT AATAATCAAT TTATATGCAT TCTGATGCAA 1320 TGAAATTAGT ATTTGAAAAT TTATGTTTTG 1350
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