| Tag | Content |
|---|
EnhancerAtlas ID | HS127-08694 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr13:45940890-45942360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr13:45941085-45941097 | AAACAAACAAAC | - | 6.32 | | HES2 | MA0616.2 | chr13:45941300-45941310 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr13:45941300-45941310 | GGCACGTGCC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr13:45942203-45942218 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr13:45941218-45941233 | GAGGTCAAGAGTTCG | + | 6.24 |
|
| | 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 |
| GH13I045366 | chr13 | 45940916 | 45943622 |
|
Enhancer Sequence | CCAACATGGT GAAACCCCGT CTATACTAAA AATACAAAAA GACTGGCGTG GTGGTGGGCG 60
CCTGTAATCA CAGCTACTTG GGAGGCTGAG GCAGGAGAAT CGCTCGAACC CAGGAGGCGA 120
AGGTTGCGGT GAGCCAACAT TGCACCACTG CACTCCAGCC TGGGCGACAC AGCAAGACTC 180
TGCCTCAAAA TAAATAAACA AACAAACAAA AATATCTGGC AGCAATTTTC AAGCATTCAA 240
AAGAGATGTG AAGGAAAAAA ATTTGGCCGG GAGCAGTGGC TCACGCCTGT AATCCCAGCA 300
CTCTGGGAGG CCAAGGTGTG CGGATCACGA GGTCAAGAGT TCGAGACCAG CCTGACCAAC 360
ATGGTCAAAC CTGGTCTCTA CTAAAAATAC AAAAATTAGC TGGGCATGGT GGCACGTGCC 420
TGTAATCCCA GCTACTCAGG AGTCTGAGGC AGGAGAATCG CTTGAACCTG GGAGGCAGAG 480
GTTTCAGGGA GCCGAGATCA CACCACTGCA CTCCAGCCTG GGCAACAGAG GGAGACTGTC 540
TCAAAAAAAA AAAAAAATAA ATAAATCAGC ATAGTAATTG ATGAGGACAA GGACATTTTA 600
TTATCATGGG ATTATGGGGA CAAATGATTG CTGAAATCAT AATTAGCTTT CTGGCGGGGG 660
AAGATAGTAA GGTAGAAAGA GGAGAAATGG GTGTAATCAA AGGAAGTGGC AGAGAGAGAT 720
TAAAAAAAAA AAACAGGAAA TGAGAACAAG AATATGACTA ACAATGCCTG AGCCCCACCC 780
ACCCATCCTC AGAGTGGACT CCCTCTCTCA AAGGCTTGTG GGCACCTGCC CCCGAGCTGA 840
CTCACCCTGT TCAGTCATCA CAGCTCACTG CAGTGATGAA GGCTCAGGTG ATCCTTTCAC 900
ATCAGCCTCT CCAGTAGCTG GGACTAAAGG CATGTGCCAC CATACCTGGC TAATTTTTTG 960
TTTTTGTTTT TGTTTTGAGA TGGAGTCTTG CTCTGTCACC CAGGCTGCAG TGCAGTGGCA 1020
TGATCTAGGC TCACTGCAAC CTCCACCACC TGGATTCAAG CAATTCTCTG CCTCAGCTTC 1080
CTGAGTAGCT GGGACTACAG GTGCCTGCCA TGACGCCCAG CTAATTTTTT TGTGTATTTA 1140
GTAGAGATGG GGTTTCACCA TGTTAGCCAG GATGGTCTCG ATCTCCTGAT CTCGTGATCC 1200
ACCTGCCTCA GCCTCCCAAA GTACTGGGAT TACAGGTGTG AGCCACCGTG CCCGGCCGTA 1260
TTTTTTGTAT TTTTAGTAGA GACAGGGTTT CACTATCTTG GCTAGGCTGG TCTTGAACTC 1320
CTGACCTCAA GTGATCCACC CACCTCGGCC TCCCAAAGTT CTGGGATTAC AGGCATGAGC 1380
CACTGTGCCC AGCCACCCGT CACCTGCTAG TGTAGACAAA TGAATAAACT TAGACAAGCA 1440
CATGGGCTCC CTCTATACCA GCCTAGACTT 1470
|
