Tag | Content |
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EnhancerAtlas ID | HS104-04553 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:180008590-180009780 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr1:180009584-180009594 | TCTAATTAAA | + | 6.02 | ESR2 | MA0258.2 | chr1:180009434-180009449 | GGGCCATCCTGACCT | - | 6.11 | IRF1 | MA0050.2 | chr1:180009171-180009192 | TTTCAGTTTCCTTTTCCATTT | + | 6.4 | IRF1 | MA0050.2 | chr1:180009165-180009186 | TTTTTTTTTCAGTTTCCTTTT | + | 6.69 | NFAT5 | MA0606.1 | chr1:180008737-180008747 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:180008737-180008747 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:180008737-180008747 | ATTTTCCATT | + | 6.02 | Nr5a2 | MA0505.1 | chr1:180009441-180009456 | CCTGACCTTGAAATC | - | 6.91 | ZBTB18 | MA0698.1 | chr1:180009342-180009355 | TTTCCAGATGTTG | + | 6.25 |
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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 |
GH01I180039 | chr1 | 180008708 | 180009757 |
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Enhancer Sequence | TGATGTGAGG AAGAGAGTCA AAGTTTCTTT TTCTCTAGTA TGGATATTCA ATTGTTCCAG 60 CACCATTTTA TTAAAAAGAC TTAAATTACC TTGGTGCCTT TATCAATGAT TAAGTGATCA 120 ATTATGTGTA GATCTATTTC TAGACTCATT TTCCATTAAT CTATTCATCT ATCTGTAATG 180 TCAGTACCAT ATTGTCTTTA TTACTATGGC TTTTTAGTGA GTTTTGAAAT CAAGACATAA 240 TTCCTCCAAC TTTGTTTCTT TTTTTCAAAG ATGATTTTGG CTATTCTAGG TTTTTTGCAT 300 TTCCGTGTAA CTTTTAGAAT CAGTTTGTTA GTTTCAACAA CAACAACAAC AAAAAGCCTG 360 GTAGGATTTT CATTAGAATG GTATTGAATC TGTAGGTTAG TCAGTCTGGG GAGAATTCAC 420 ATCTTAACAG TGTTGCCTTT TCTAATTCAT GAACATGATA TATTTTTCTA TTTATTTAAA 480 TCTTTGAATA TTTCTCTCAT TAGTATTTCA TTGTAGAGGT CTTATACATT TTAAAATTTA 540 TTCCCAAATG TTTTATGGTT TTTGATGCTA AAATTTTTTT TTTTCAGTTT CCTTTTCCAT 600 TTGTTCTTCC CAAAAGACCC GTCAGACAGT TCTTGGTGTG GGACTGTTCC CATACTTTGC 660 AGAGATCCCA TCATTCCTGC CCTCCCCCCG CCACTGCCCG ACTAAATAAC AGTAGTGTTG 720 TCCAGTCATT GTGACAGCAG AAACTCTGGA CATTTCCAGA TGTTGCCTGG TAGAGGGTGG 780 GGAGGGACTA ATGCCAACTT TGTTGATAGT CATTTTATTG AGGAAATGAC TCCATTGTAG 840 TGGAGGGCCA TCCTGACCTT GAAATCTGAG TCAGCACTGA GGTTTTCTGC CACTTTAGAA 900 ATACATTATA ATTCTGGGTT TCCAGATTTG GGCAGAGCAT TACCACAGCC TTACATACAG 960 CCTTACCACC ATTTTTTGTT TTCTTTTGTT TTGTTCTAAT TAAAAAAAAA ATAGAGGTGG 1020 GGGGGTCTCA CTCTGTTGAC CAGGCTGATC TTGAACTCCT GGCCTCAAGT GATCCTCCCA 1080 TCTTGGCCTC CCAAAGTGCT GGGATTGCAG ACATGAGCCA TTGTGCCCAG CCCTTACCAC 1140 CTTTTGAAAA CCTCTATTAT TTAGCAGTAT TTCAAAGGAG ATGAAAAAAA 1190
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