| Tag | Content |
|---|
EnhancerAtlas ID | HS060-13782 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr16:89800450-89802680 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr16:89800489-89800499 | GCACGTGACC | - | 6.02 | | Foxd3 | MA0041.1 | chr16:89802298-89802310 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr16:89802302-89802314 | GTTTGTTTGTTT | + | 6.32 | | MEF2A | MA0052.3 | chr16:89802604-89802616 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr16:89802604-89802616 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr16:89802603-89802618 | TTCTATTTTTAGTAG | - | 6.57 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr16 | 89801553 | 89801622 | | chr16 | 89801074 | 89801159 | | chr16 | 89801875 | 89801925 | | chr16 | 89801424 | 89801474 |
| Enhancer Sequence | GCCTATCGCC AGTGTCGCCC ACGCGGGTGA CAGCCAGGGG CACGTGACCT GCTTTCCAGT 60
CTTCCTCATA CCCATCCCCG CCCCAAGAGT TGGGGGTGCG TGAAGGTGGC TCATGGGGTC 120
TTTGGTACTC AGTCACGTTG GTAGATGAAG GCTAGAGTAG GGCGTCAGTG TGAATCTGCC 180
CTTCCCTGTG ATGGAAGGAA TTCCTGACTT CCCCAGGATC TAGGCAGTTT GTCAAAACTA 240
ATAGCCAAGC AATCTTGGTG TCCTTTTGCA AATTGGTCAT TTTATTTTTT AATTTTTTTT 300
TGAGACGGAG TCCTGCTCTG TTGCCCAGGC TGGAGTGCAG TGGCACCATC TTGGCTCACC 360
ACAACCTCTG CCTCCCAGGT TCAATCAATT CTCCCGCCTC AGCCTCCCAA GTAGCTGGGA 420
TTACAGGCAC CCGCAACCAT GCCTGGCTAA TTTTTGTAAT TTTTGGTAGA GACGGGGTTT 480
CACCATGTTG GCCAGGGTGA TCTCTAACTC CTGACCTCAA GTGATCTCAG CCTTCCAAAG 540
TGCAGAGATT ACAGGTGTGA GCACTGCACC TGGCCCAAAC AAGTGTATCT TAAAAGGCAA 600
GGCAGAAGGC ATGAAGGCAC ACCAGCTCTG GGGAGCTGCC CACGTGGACA GGCGGGAGGC 660
ACGTGTGGTT CTGCCTTTTC ACATGTGTGT AGGTCGTGTC ATTAAGACCG GAGGCGGATG 720
GGGGAATTAT GACTGAGGGT GCTGTCTCTG TGCCCGTCTT ATTTTTCACA ATTTCTATAA 780
TGCACAAGTT ACTTTTATAA TCCAACAAGG ATATGTTTTC AAAATGACAA ACTTGGCCGG 840
GCGTGGTGGC TCACACCTGT AATCCCAGCA CTTTGGGAGG CTGAGGTGGG TGGATCACCT 900
GAGGTCAGCA GTTCAAGACC AGCCTGGCCA ACATGGTAAA ACCTGGTCTC TACTAAAAAT 960
ACAAAAATTA TCTGGGTGTG GTGGCACACG CCTGTAGGCA CAGCTACTTG GGAGGCGGAG 1020
GTGGAGGTTG CAGTGAGCCG AGATCACACC ACTGCACTCC AGCCTGGGCA ACAGTGAGAC 1080
ACTGTCTCAA AAAAAAAACT TGTTTGAACC ACGTGGACCC ACATATCCAT GGTCAGGGAC 1140
TCGAATCCCT GGTATTCAGA GGGCTGCCTT TTCCTAAGTG CAGGTTCTGT AGGGTCTTTG 1200
CAGGGCTAAC TTCGGGACTT CAGTATGAGC AGATTTTGGT AAGGGGTGGG GGGGGGCCTG 1260
GAACCAGCTG AGGACAACTG TATATTGATC CTTACACACA CAGTTTTCCT TGGTTTTGAA 1320
CTTATTACAG AATAAGAATT ATTTATTCTT ACTTGAATTT ACTGAAGTAT TTTTTCATTA 1380
GGATTGCTTT TCACTGCTGG GTCATCTCCC GACATGCGGG TTGTTATTTT TTGGGTTCTC 1440
CGACATCTCT CCTGATGGCA GCACTTCCTT GGGTTTGGTC CTTCAGACTC TGCATCTGTC 1500
CGGTCACTGA TGGTCACAAC CAGCAGTTCC TTAAAAACCT GAAATTGGGC CGGGTGCAGT 1560
GGCTCATGCC TGTAATCGCA GCACTTTGGA GGCTAAGGCA GTAGGATTGC TTGAGGCCAG 1620
GATTTTGACA CCAGCCTGGG CAACATAGTG AGGCCGTCTT TACCAAAAAC TTTTTTTTTA 1680
ATTTATTGAT GGAAACAGTC TCACTCTTAT CACCATGGCT GGAGTGCAGT GGCGCGATCT 1740
TGGCTCACTG TAACCTCCAC CTCCCTAGTT CAAGCAATTC TCCTGTCTCA GCCTCCTGAG 1800
TAGCTGGGAT TACAGGCATC TGCCACCACG CCGGGGGTGT TTTTTTTTGT TTGTTTGTTT 1860
GTTTTTTTGA CTGAGTCTTG CTCTTGTCGC CCAGGCTGGG GTGCAGTGGC ACAATCTCAG 1920
CTCACTGCAA GCTCCTCTTC CTGGGGTAAA GCCATTCTCC TGCCTCAGCC TCCCAAATAG 1980
CTGGGACTAC AGGTGCTGGC CACCACACCC AACTAATTTT TCGTATTTTC AGTACAGACG 2040
GGGTTTCACC ACGTTAGTGA GGCTGGTCTC AATCTCCTGA CCTTGTGATC CACCTGCCTC 2100
GGCCTCCCGA AGTGCTGGGA TTATAAGCGT GAGCCATGAC GCCTGGGTAA TTTTTCTATT 2160
TTTAGTAGAG AGGCAGGTTT TGCTATGTTG GCCAGGCTGG TCTCGAGTTC CTGACCTCAG 2220
GTGATTTGCC 2230
|
| |
|
|
|
