| Tag | Content |
|---|
EnhancerAtlas ID | HS127-11829 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr16:29695270-29696630 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr16:29696493-29696506 | AAATTAATTATTT | + | 6.78 | | Nr2f6(var.2) | MA0728.1 | chr16:29696575-29696590 | GAGGTCAAGAGTTCA | + | 7.64 | | RARA | MA0729.1 | chr16:29696575-29696593 | GAGGTCAAGAGTTCAAGA | + | 6.45 | | ZNF263 | MA0528.1 | chr16:29696276-29696297 | CCCTCCTGCTGTCCCACCTCC | - | 6.13 | | Zfx | MA0146.2 | chr16:29695911-29695925 | CCCGCCTCGGCCTC | + | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGGCACAAAA ACCGCTCTGG CACAGGCCTC ACAGTTGCTA AGTGCAGAGC CCCATCCTCA 60
GTCTTCCTTC TATTTACTTC TGCTCACCTC CCAAAACCCT CTTCTCCTTC CCAGGTACCC 120
ACTCCTGATG ATGCTTCTCT TTTTGTTGGA CATGCCCTGT GGGTTCTTTA TCTTATTATT 180
TTATTTTAGA GACCGTGGCT TGCTCTGTCA CCCAGGCTGG AGTGCAGTGG TGCAATCACA 240
GGTCACTGCA GCCTCCAACT CCTGGACTCA AGCCGCAGCC TCCCGAGTAG CTGGCGAGTA 300
GCTGGGACTA CAGGCGTGCA CCCCCATGCC CAGCTAACTT TTTCTTTTTT TCTTTTGTTT 360
TTTGAGACGG AGTTTTGCTC TTGTTGCCCA GGCTGGAGAG CAATGGCACT ATCTCGGCTT 420
ACTGCAACCT CTGCCTCCCA GGTTCAAGCG ATTCTCCTGC CTCAGCCTCC TGAGTAGCTG 480
GGATCACAGG CGCCCACCAC CACGCCTGGC TAATTTTTGT ATTTTTAGTA GAGACGGGGT 540
TTTGCTATGT TGGCCCCGGA GTTCAATTTT TGTATTTTTA GTAGAGACGG GGTTTCACCG 600
TTTTCACCAG GATGGTCTTG ATCTCCTGAC CTCGTGATCC TCCCGCCTCG GCCTCCCAAA 660
GCGCTGGGAT TACAGGCGTG AGCCACCGCG CCTGGCCACG GCAGCATCTC TTCTGAACTC 720
CAGAGCCATT CCCTACCACC CTCTGGGCAC CACCATCCAC ATCTCCTGCT GCCGCCTCAG 780
CCTTAACCTC TGCAAAACCA AATCCGTTCT TTCTCTCGAG CTCTGCAGAA GCTAAGCTGT 840
TTCACCAGGC CACGATTCAG GAAACGCTTT GGGATTCAGC TTCTGTTCTT GTGAAATGGG 900
AAGAATCCCT GTGGTGAGCT CCAGATGAGA GCACAAAGGG GAACAGGGGT GCCCGCGGCT 960
GGCACGCCAT GGCTGGCACG CCATGGCACT CAGTGGGGTC ACCGCCCCCT CCTGCTGTCC 1020
CACCTCCACC CTGCCTGCTC TTCTCCTGGA ATGACTCCTT CTGCCAGCTC TCAGCTACCC 1080
AGGCCAGAGG CCCAAGGCTC CCACATCTCT TTAGCTACTA ATTCTGGTAG ATCCCCTTTT 1140
GGAAATAGCC CTCAAATCTA CCCCAGAGCT ACTGTCAAAG TTCAGGGCTC CATCTCTTTT 1200
GGTTTTTTTG AAAATATTTT TTCAAATTAA TTATTTGTTG GCCGGGCGCA GTGGCTCACA 1260
CCTGTAATCC CAGCACTTTG GAAGGCCGAG GCAGGTGGAT CACCTGAGGT CAAGAGTTCA 1320
AGAACCAGCC TGACCAACAT GGTGAAACCC CATCTCTACA 1360
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