| Tag | Content |
|---|
EnhancerAtlas ID | HS127-16051 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr2:9277080-9278160 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr2:9277573-9277586 | GAACTTTCTAGAA | - | 6.41 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 9277400 | 9278000 | | chr2 | 9277097 | 9277807 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I009136 | chr2 | 9276801 | 9278718 |
| Enhancer Sequence | ATACTAAAAT TAATATGGTG TTTTCCTTTA AAAAGACTTG AGGCTTGTTT GAGGAAGTGG 60
GCGTTGGGGT TGTGAGCTGG GTGATCTGGA ATTGGGGGGG CATTCTAGCA CCAGAGCTGG 120
ATGGATGTGG ATGTGACTCC TAACACACCC TGTGAACGGA GGGCTGGAGG GTGCATGGGT 180
GGGGTTGTGT GTTCCTAGGG TGTGTGCGAG GGTGGGGTTG TGTGTTCCTA GGGTGCGTGC 240
ACGGGTGTGG TTGTGTGTTC CTAGGTTCTG GTCAGCCAGG TGCCATTCTC TGCATTCGCC 300
TGGTGTTTCT GAGGACAAAA TTGTGCAGAG CGAATGTGAA CTTTGAAACT CACGTTATGC 360
TCCAATTGTT CCCTACTCTA GCAATTGGGA ATTGCTATTG GAGCAATTGG AGCAATTTCA 420
TTTTCAAAAC AAGCCGTACA GCGGAACTGA AAGTATCACA TCCCTTGAGG ACTCCGGACA 480
TGTTGGGGAA GGGGAACTTT CTAGAAGGTG GCATCTGCAG ATGTCAACAT CGGCGGCGGT 540
GCCAAGAGGG GCTTTGCAGG GCCACAGGGC AGCAGCTCCA TGCAGCTGGC CCCATCCCAG 600
GCCTGGTGAG CTCTCCTGGC TGTGTACTCA GCCCTGAGCC TGATGACCAA CACCAGATGC 660
ACAGCCTGCT GTTTACCAAG CCCTCCCACC CACACCAGGG TGCCTCCTGA CAGCCTCACG 720
GGGACAAAGT GCAGGCATCA TTCGTCCACA TTTGACAGAG ATGGAAGGGG GGCTCAGAGA 780
AGCTGATTAC TTACCCGAAG ACACACAGCC TGCAAAGGGA GGTGGCACTT CCACATCCCA 840
CGCTCTGGCT GACCCTCTGC CTGTCCTCCT GTGCAGTATG TGGGGTCTCG TCACCAAGCG 900
CTGGGATAAA CTCGAGGGGC CAGGCTCAAG GCCACGCGTC CAGAGGCAAA TGCTGCAAGA 960
AGAGAGGTGC AGGAAACCCA GGTAACCGAA AGGCACCTGC CTCGAGTGAG CTCCCTCCAG 1020
CCCTGACACC TGTTCCTTCT TTCAGTGGAA AGGACAAGCC GCCGTCCACA CTGCGCCTTT 1080
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