| Tag | Content |
|---|
EnhancerAtlas ID | HS105-28336 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr15:76442260-76444910 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr15:76443560-76443570 | TCTAATTAAA | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr15 | 76442351 | 76444484 | | chr15 | 76444640 | 76444698 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH15I076149 | chr15 | 76442265 | 76444603 |
| Enhancer Sequence | TAATCATCTG GAATAAATAT AGTAAAGTGG GACCCAGGGG TTTTGCTGAC CAACAAAACC 60
ATTGGCAAAG TCAGCTGTGA CACCCAGGAC ACAGGTGTTC AGCATCATAG AACTGGCACG 120
AGTGGAGCTA GGCGGGGCCC CAAATTACCC AATCCTGGGG CTTTAACCTG GAGCCTGGGT 180
ATCCTTAGAT TATCCGTCAG TGAGATTCAA GGAGTCCGTG CACTCCCTGG AATGTTATGC 240
ACAGTGCTGT AGTTTTGTGC ATTTGGGGGG TGTAAGGGCA TAGCTTGTAT CCACTGCTGG 300
AGAGCTCTGC AGTCCAGAAA GCTTTTGAGC CCTTGTCTAG CAGAGCCTTC CTGAAGGCAG 360
AGTGACAGCA GCTGGGGAAG CCCAGGGCCC CAGGCTTCGA TCTGGCTCCT GCTACCAGGC 420
AGCTTCCAGT CTCATTTTGA TCACCTCCCT CAGCTCCTTC CTTGAGAACT TGAAGGATGA 480
AAATCTCAAA GTAGGGCCGA CAGGGTTAGC TAGTTTGGCT GCCTTCAGGG AGATGGGCTG 540
ATGCCGTGAC TCTCCACTGC CTGTGAGCCC CTTTTAGGAC ACCTTGAGGG TCTCCACGGT 600
CCCCCTGCTC TAGCCACTCC CCAGCTTGCA CCTCAGGAGA TTCAGTGCAG TCACTCCCCT 660
CTCTGCCACC ACGTGTCCTC CCAGCCACAG ACAGCCTGGC AGCCACTGCA GACCAATTGC 720
ATAGTGGATT GTGGGGTGGG AGAGGCCAGG CCCCACAGAA GCAAGCACAG CCCTCCCCAT 780
CCTGGCGCCA CACGGCTCTA CTTCCCCTTC CAGATTGGGG CTGTTTCAGT GCCAGGCTTG 840
GGAACGCTGC CTGACAGAGC AGTGGCTTGA GCCAGCTCCT TCCAGGTCAC CCCTGTGGCT 900
TTATCGCATA TAAAGCCTCT GCCGGAAGTT TGTCAGTTCA TTTTCATATT CTAGAATTTA 960
TTCTTTGAAT TTTTTATGCA AACACCTAAG ACTATGAAGC AGAAGCAGTG AAGGTACTCA 1020
GCCTCCCCTC CCACCCCAGG ATTTCTCTGA GGCCTCAAGA GTGACTACCT TATGGTAGAA 1080
TACTCGCCCA CCTGCCAGGA CATGCCATCT GCTTGTTGGT ATTTGCAGAC TCTGGCAGCC 1140
CAAGCCGGGC CCCTGGAGCT GTACCCTCCC TACAGCAGCA CCAAGACAGG ACATTGGGAA 1200
ACGCCTGCCC TCTCGTGGCA ATTCTGGGGA TAACACCACC CTGAGAACCA GCCCTGGGGC 1260
CTTGATGGGC CGACGCTGAA GACAGAAGGA AAGCACCTTC TCTAATTAAA CAGTCAACGC 1320
TGATTTCCCC TTTGGCCCAC TAAGCCCCTT GAGTCATTAC TGAACCACTC AGGAATCTTT 1380
TGAAACTGGT CACATTCTAT TTCACTGCTA AAACACAGTC TTCTAGGAAT GTCCGAGTCA 1440
TCTGAATTTC AGATGAAATT TTATTGGCAG CTTGGGATTT TCAAACACTG GTCAACCAAA 1500
AGCCTGCGGC TTCAGCCCAG CCTCCCAGCC CCCAACCCAC CCTCCAGGGC CCTGTTCTGG 1560
AGCCCTGGGG TCTGTGGTCT TGCAGTCTAG TGCAGCCCTG CCCTGTGTTT CTGCTCTTCA 1620
GGAAGGAGCC CAGAACCTAC CTGAACACTC TTGCCCCACC CCACACACAT AGCCTGCCTG 1680
CACTATTTCC TTGATGCTCC AGGGCTGCTT GACCCTGGCT TGCCTTCTTT GTCTCATCTC 1740
TCCTACTCCC AAACTCCCTT TGCCATACCC CCTTTACCTT TCTGAGATAC CTGTTACCTC 1800
TTAGTAGGCC GCCAGAAGCA TTTGTTCTCA CCCAAAGCAC CTGGGATCTC ATTGAAATGC 1860
AGACTCAAAT TCAGCAAGCA CGGGGAAGGG CTGAGACGCC GCATTCCTAA CAAGCGCCAG 1920
GTGATGCTGC TGCTGCTGCT CTGTAGATTC CACTGAGTAT CGAGGACCTG GAACAGCGGT 1980
TTTCCATCCA CCTTGATTGC ACACTGGAGT CATCTGAGGA GGCCTGGGTC CTCCCGCAGA 2040
GGTTGTTGTT CAGGAGGTCT GGTGTGCAGC CTGGGCATTG GAGTTCTTAA GAGCTCTGTT 2100
GGGTGCTCTA GTGTGCAGCT GGGCTGAGAT CCACTGACCT GGAGGCAGAT CCCACCCCCA 2160
GTCTCCATGG CTCCCTGCTC CAAGGCAGCC AGGCCTCACC AGCCACTGTA TCCCCTGGGT 2220
ACCATCTTTT CCTTGACAGT GGTCTTCTGT CCTTCCACTT CCGTCGAGTC ACCCCCATGT 2280
GCCTTGCCCT GGGGTTACCA AGAGGAGGGG GTGCACAGAG CAAGATGCAA GTGGTACCCC 2340
CAACAAGGAG ACCTGCACGA ACTCACTCCC AGACTGGCAC AGTGGAGGGG TGGGTCGCTG 2400
AGGGCAGAGT GTGGGCAGGG GACAACTGAG CTGGCGTGAG AATGAAAGGA CAGGCCCAGA 2460
GCAGCGTGGC ACAGGCCTGA TTGTGCAGCT GCCTCGGGTT TCTTGGGTGC TGTGTGTTGG 2520
CTGTGCCAAG GGCTGTGGCT GCACCAGCAG CATCTGCCCT AGCTGGTGGT GGGTGGTGAG 2580
CTATACCCCC TGCTGAAGGG GGAAGCCCTA TCCTCCTCCC GGTCCAGCTC CTGGCTCCCA 2640
TCACCCTGGT 2650
|
| |
|
|
|
