Tag | Content |
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EnhancerAtlas ID | HS017-21266 | Organism | Homo sapiens | Tissue/cell | CD14+_monocyte | Coordinate | chr21:35365350-35366870 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr21:35366345-35366366 | TTTCTCTGCCCTTCCTCCTCT | - | 6.68 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH21I033993 | chr21 | 35365859 | 35366586 |
| Enhancer Sequence | TGCCTTGTTG GCCAGGCTGG TCTCAAACTC CTGGGCTTGA GTAATCCTCC TGTCTTAGCC 60 TCCCAAAGTG CTGGCATCAT AGGTGTGAGC CACCACACCC AGCCTCACTT GTGTTATCTG 120 GACCCCTATT TTAGATGTAA GTAGTCCTGG GAAGGCAGTG CTGCTCTAGA CTTTCCATGG 180 CTGTTTTGCC AGACATGCAG CAGAACTGGT GTGCCTGTCT GGGGTAGGGA GATGGGGCCC 240 AGGGTGGGCT CTGAAAGAAG GCTCTGGAAG GAGTTTGGAG CATGACAGCA TTGGGTGCCC 300 TCAGGGGGCA AAACAGCAGA GGACAAGGTA CAGAAAGATC TAGGTGGTAG GAGAGGCTTC 360 CAGAAGAGAG GCAGTAGGGA CCTGGGTCTC GGCTATGCAG GCCCACGCCC TTGGACCTCA 420 GGCACGCTTA TCTCCAGCTT CTCCCCTTCC CTGCTGTGGG TGGGGCATGC CCACCTGCTG 480 AGGAAATACC TGGAAAGAAA CCATGGGACA ACAATCTAAC CGGTACTTTT CCACTCCATA 540 TGGATCTAGA ACTCCTGGCA CATACTCCTG TGTGATCTTG TGGAACACTG GGCTTCTCTG 600 GAGGAGTCAT TAAGTGCTGG CTGCACCCTG AAACGGTGGC CCTGTGACTC TGCAGAGGTC 660 ACCACAGAAG TTCTTTCACT CTGGGTCATC CCCCATCTTT AGCTCCCCTC CCCTTGGTCT 720 TGTGTTGCTT ATCTTCATTA ATTTGTGATG AGGAGATATG TTTTTATCAC TGAGGCCTCA 780 GCCTGCCACC TGCCTCCCCG TTTTCCTTTT GCCTTCAGAA ACTAGTTATT TTTACAAAGG 840 AGGGAGGAGT GCTCCTCCCT CCAATTCCAT TTAAAACAAA CATGGTTTTG GCACAACAAG 900 CCTGCCTCCT CGAAGTAATG GCCGCTCCCC CGTGCCAGTT GCTATTCTGC CCTCATGAGA 960 GTGGAGCGTG TGTTTCCTCC CCTAGTTCCT CTTTGTTTCT CTGCCCTTCC TCCTCTGAGG 1020 GCACAGGGGC AGACAGGACA TCCTCCCACC AGGGGCTGCC TAGTGACTGG CCGAAGATTC 1080 TGATCATTTC AGGCCTCCCT TCACATTCTC CAGCGGCATT TTAAGGTCTT TGCTGTAAGG 1140 CAAAAGCTGG TTTTTCATCC TTCCTCCTTA TCCAGGTCTT CTGTTTCTGG GGTCAGTCTG 1200 GTGCGTAGAC AGTTCCACAC ATACTCTGTA TTAGGGATCC TGAAAGAGAG AAAGCTAAAA 1260 GGGACTTCTT CCATTTCAAG AAGAGACTTA AACAAGATAG AATTCCCTTT CCTTCTTATG 1320 AGACTGAGAA TAAGCACTCT AGCAGCCCTT AGTATCAGGG TCCCAGGCTC CCTCTGCCAT 1380 ATTGTTTTGC CATCTATAGG GTGTTGCTGC CTTTTACGGG ACTCACAGTG GGTCACAATC 1440 ATTTATTGAT CCAGGTAGTA GGATGCCCTT TAAGGGCCTG ATTCAGAAGT TGTACATATC 1500 ACTGCCACTC ACATCCCATT 1520
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