| Tag | Content |
|---|
EnhancerAtlas ID | HS127-05172 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr11:16022670-16024150 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr11:16022712-16022724 | AAACAAACATTT | - | 6.27 |
| | | 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 |
| GH11I016001 | chr11 | 16022550 | 16024803 |
| Enhancer Sequence | AAAATGCTGG GATTACAGAC GTGAGCCACT GCTCTCGGCT GGAAACAAAC ATTTCATTAA 60
TCAGAGTACC AAAGTATTTC TTTAAAGAGC AATTTACCTT TTTGATAGAC TAGGCCAGAG 120
GTCAGTTTCT AGGATAGGAA CACCAGCTGT GCTAAGTAAC TTTGCATAAA ATAATATTTA 180
CAAAGTGCTT TCACTGATTA CATTATCTTC ATCCTCATTA CAATCTTTTA AAATGTGTAG 240
GAAGGCAGAT ATCTTTTCAC CCACTTTATG GATGAGGAAA GCAAGACTCA GAGACATGAT 300
AGCACCTTCC TCTGATTAAC CAGTTGCTGG TAATATGAAG CAGAGCCAGT TCTAGAACGT 360
AGATCTTCTG ACTTTCAGCC TAGTACATCA CCCCTTCACC AAAGCTACCC CAATCACTAT 420
TCGGCAATCT GAAATAACTC TGAATTTCAA AGCCCACCAT TTCTTGGCTG GAACATTATT 480
TTCCCACTTT AAGGATGCCA CTTCCCTGCC CAGCTAAGCA CATTAGAAGA GCCCATGACC 540
AGTTATGAAG TTCATGCCAC TGTCTAATTG TTCTCTGAAA TACTGCCCCA CCAAAGATGC 600
AAGGGCATGT CGAGAAAGCA CTAAGGACTA AAATTATAGC TGGGATGAAA ACAATGCTAA 660
ATTAATGCAT TCCTTGGTTA CAGGATTATG AGCAAGTGTT ATTGTGGATA AGACTTCTAT 720
TTTTTTTCTA TTAGAAACTC CATTCTCTTT AAAAGATCAA CAAGAGGAAC CAAAGGGAAT 780
TCCCTAAGGT CAGCTCTGAG GAAACATAAA CCTCTAATTC AATAACTCTG CTACTGCTCT 840
GAAAAAGGGC TTTATTATTG CAACATCCAT ATGGAGCCAA TTGGACATTA ATGACTAATC 900
AATCCCTCCC CTTTCTATTC TACTTAAAGT GTCACAAACT ATGTTTAGAT TAGCCCATTT 960
CCTGCTTAGG ATTGCTCAAG ATGTCTTTTG TTCTTTCAGG ACCAGCCTGA TGGAGGCAGC 1020
TTAAACAAAC ACACGACCGG AGTGGCGCAG GAGTTATAAA GTGCCATATG TGAATGAACA 1080
AAGGGGCTAT ACTAAAGCCT TTTGTGGTAT TTGTTAATGT TTTTCATCTG AGCTTAAAAA 1140
GGCTTAATGA CTTTGTGGTG AGCTGATGCA TGTGGCTCGT GGCTTTGCAA AATGAAGGAA 1200
ATTCTAACCA GTGATATACC AGTCTGTATT TTCAAGAGTC TCTTGCTTTC AGTTTTGATG 1260
CCTGTGTTTA CTTTTTTCAA AATTCTCAAG TTATATTTAC TTTACACAGA TAGCTAAACA 1320
GAGTCCTTTA TCTTATTTCA ACTACAGAAT CCCAGGGCAG CTGGGATAAC TTATATTCTT 1380
TATTTTAATG ACCTGAAGGG AGCATAGAGC ATCAAACATC CCACTTATTA TCTATATGCT 1440
GTATTTATAC ATAGAAGGAG GGCCTACAAG CTGTTGAGCC 1480
|
| |
|
|
|
