| Tag | Content |
|---|
EnhancerAtlas ID | HS127-24289 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr5:448260-449840 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 448604 | 448795 | | chr5 | 448605 | 448866 |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH05I000449 | chr5 | 448605 | 448866 | | GH05I000448 | chr5 | 448928 | 449328 |
| Enhancer Sequence | CAGATCCCAG AGCAGAAGGG TTGAGGCGAG CAGCAGCTCC CAGGCAGGAG GAGAAGCGTG 60
TGTGCACAGG CCAGGGCAGA GGCGGGGCTG AGCGCCGTGG GGGAGTGACC CTTTCAGTCT 120
TCTCCCTGAA TGCCTCAGTT AGAAGGATGC CAAGGGCCCT GTAACCTGTC CCTGAACGGT 180
GCCAGCTGGC CCTGGGTGGT GGCTCCCAGC ATTTGTGTTC ACAGTCTCCT CCTGCTTGCT 240
GTGACAGGAG CTGCTTCCAC AGCCTCATCC CTCCCCTTGG TCCCCGCTCT GTGTCAAGGT 300
CAGCAGCATC CTTCCAGTCC CCAACTCAGA AGCCTTGGCA GGGTCTGATT CCTTCCCTTT 360
CTTTGTTCCT GTCTCTGGCC TCTTGGCAAG TTCTTCCTGT TCCTCTACCA GACGTCTCTG 420
CCCTGATGTC TGTATGACAC TTCCCCATCC CCAGCCGTCA CGTGCCCCAG CTCACCCTTC 480
ACAGTGGCTG TGCTGCATCA TCTGTGACGC TGCTCGGCTC CTGAGGCCAC GTGTGAATTG 540
GCGCGGTTCT CCCCAGCTGC CCACAGCGCA CCTTGGTAAT CCGTGTCCCG TCCACCCTGT 600
CCTCTCTGCC CTCCTCTCGT GCTTGCGGCT GCAGCATTGC CGAGCACCTT GTCCCGTTGC 660
TTTGTGTGTG CCCTTCTTCC AGGGCATGAT CCGTAGGGTC ACATGTGTGG CTGCAGTCCG 720
TGTCTCTTTG TGCATGCCCA ACACGAACGC CACTGTGCTG CCAACTCAGA AAGCAGCTCT 780
TCTTGGTGAC TGTGGGCCGC CTGGAACAGG AATAAAGTCC TCTCGACGGA GTCTCCTTGG 840
TGATGCTCAG CTGGCAGCTT TCTAGTTAAT TTCCTCTTAT TTCGTATTGG CTGGCTACAT 900
TTCCTTCCGG TCTTTTAAAC TAATGCCTGA TGACCAAAAA GGTGCATTAC TGGAATTAGT 960
TTATCCACAG CAGTTGAAAA TAATTTCCTT TCCTTGGTGA ACAAATGAGC CTGCGTGGTA 1020
TGCATGTTTT TTGTTACGGA TAAATTTTCA TTGAGAAGAT TGGTTTGGTT GCCTTCAGAC 1080
TTGTCTCATT GCCTATAACT CAGCAATGCT GTGTACACAG CTCCCCTCCC CCATTTTTTC 1140
TTCTTCTAAA ATGCATATGT ACAGTTTGCC GTCTTAACCA TTTTTAAGTG TACAGTTGGG 1200
GACTATTAAG AACATTCATA TTGTTGTGCA ACCATTGCCA CATCCGTCTT CAGAACTCTT 1260
TTCATCTTGC AGACATGAAA ATCTGTACCC ATTAAACACT GACTTCGCAC CCTCTGCCCC 1320
AGCTCCTGGT CACCACCATT CTGCCTTCTG TCTCTGTGAA TTGGATGACT CTGAAGACCT 1380
CATAGAAGTG GCATCACACA TTATCTGTCT TTCTGTGACA TGCTTATTTC ACTCAGCATG 1440
ATGTCCTCAG GGGTCTTCTA TGCTGTGGTA TTGTAGAATT TCCTTCACTT TTAAGGCTGA 1500
ATAATATTCC ATTGTATGGA TGGACCACAT TTTGCTTATC CGTTTGTCTG TTGGTGGACA 1560
TTTGAATTGC TTCCACGTTT 1580
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