| Tag | Content |
|---|
EnhancerAtlas ID | HS098-00741 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr1:21148810-21151110 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr1:21150317-21150329 | GTCTGTTTACTT | - | 6.52 | | FOXP2 | MA0593.1 | chr1:21150318-21150329 | TCTGTTTACTT | - | 6.32 |
| | | 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 |
| GH01I020823 | chr1 | 21149682 | 21149798 |
| Enhancer Sequence | CTAGAGGTTT ATCACTTTTA TCTTCTCAAA GAACCAGCTT TTTTTTTTTT TTTTTTTTTT 60
TTTTTGAGAC GGAGTCTCGC CCTTTTGTCC AGGCTGGAGT GCAATGGTGC AATCTTGGCT 120
CACTGCAACC TCCACCTCCT GGAGAACCAG CTTTTGATTT CACTGGTCTT TCTCTAAAAA 180
TTTTTCTATT TCATTGATTT CTGATATAAT GTTTATTATT TCCTTTATTC TATTTGCTTG 240
GAGCTTCATT TGTTCTTATT GTTCTAATTT CTTTTTTTTT TTTTTTTGGT GATAGGGTCT 300
TGCTCTGTTG CCTGGGCTGG TCTCTCAAGC TCCTGGGCTC AAGCAATCTT CCTGCCTTGG 360
CCTCCCAAAG TGTTGGGATT ATAGGCATGA GCCATTGTGT CTGGCCTTAT TTTTCTAATT 420
CTTTAAGGTT GAAGCTGAGG TTATTGACCT TTCTTCTTTT CTAAATATCG ATGATATGTT 480
GTGGTTTTGT TTTCATTCAG TTAAAAATGT TTTTTACTAT CATGTTTGAT TTCTTCTTTG 540
ACCCATGGGT ATTTAGAAGT ATGTTGTTAA GTTTCTCAGT ATGCATTGCC CTAATTCTTA 600
AAGGTTAGTT CAGCTGCACA GGGAATTCTA CATTTACTGC TCGTTTCTCA GCACTCTGAG 660
ATTATTCTAC CATCTTCTGG CTTTCATGGT TGCTACTGCA AAGTCTAATT TTTTGTGTAT 720
TTTTTTTTTG AGGGGGAGGC AGGTAAGTAA TGTGCTTCTT CTTCCCAGCT TCTTTAAAAT 780
CTTTCATCTG TCTTTGGTAT TATGCAGTTT CACTAAAATA TAATTATCCT GTATTGCATA 840
TATGGGCTTT CATTATAGAT TTGTATATTT TATCACTTCT AGAAGTCTCA GCCACTGTCT 900
CTTCAAATAT TGCCTCTTCT CCATTTAGGC TAATTTTCCT TCTGGGACTC CAATTAGATA 960
GGTTAGATGT TCTCTCATTC TTTCCTCCAA ATCTCCTAAC ATATTAACAT ATCTTAGATA 1020
GCTACCTACA GATTTTGGTG TGTGTGTGTG TGGCTTTTGT TTATTTATTT TATTTTTTAT 1080
TTTTGATAGG CTCTCACTTT GTCTCTCAGG TTGGAGTGCA GTGGTGTGAT CGTATCTCAC 1140
TGCAGCCTTA AACTCCCACG CTCTAGTGAT CCTTCTGCCT CAGTCTCTCG AGTAGCTTAC 1200
GACTACAGGT GCACCAATAC ACCTAGCTAT TTTTTTTTAG TAGAGACAGG TCTCACTATG 1260
TTGTTCAGGC TGATCTCCAA CTCCTGGCTT CAAGAGATTC TCTTGCTTCA GCCTCCCAAA 1320
GTGCTAGGAT TATAGGCATG AGCCACTGCA CCCAACCTTT TCTTTTCTTT TCAAATCTCT 1380
TTAACCATTT TGACTAGTCT CTTGTTTGCT CATTTTTGTG ATTCTTTCTT TTACTATAGT 1440
GTTATTTTAT ACTCTGAATG ATAATTCCAT TACCTCAAGT CCATGGGGTC TAAATCTACT 1500
ACTTATTGTC TGTTTACTTT TATCTTTACT TCTTTAATTG TATGTTAAAT GAACACCAAG 1560
TGTCAACTCA TATATTTAAA TAATTTGGAT TTGTAGAAAA TAAGGGGACC TAAGTTGAGG 1620
ATGTTTCTCC AAAGAGCATT TTGATTTGCT GCTTCTGGGA GCCAAGGTAA TACTGAACTG 1680
GGACTAAGTC AACTTTTTCC ATGACATCTG ACAGCATTTG TAATAGTATC TTCCCACTGG 1740
GCTATGTGTC CTTTGGGCAA TATGCCCTTC ACATGTAATT ACTATTCACA GTTCAGGTTT 1800
CATCTCTGGC TTTTCCCCCT CATTAATTCT TTTTGTCCCT TTGAAGGAAA TTACTTCCAC 1860
CTCTTCTAAG TCCAGTAACA CATCAGAAGT TATGCTTCAT GCAGGTTCTT ATTGCTGTGG 1920
CAAGAATGCT CTTCAGTGTT CCAGACTACA ACCAAAAAGA AAGCTAATGT CTGTAGCAAC 1980
CTAATATAAT ATCTTTATCC AGAACAAAAT ACTTATTTTA AAGTCATTTT CAGATTGCAT 2040
TCTTGTTCTC TTTTTACCTA TGGTGATTTT TTTTCTCCTT ATTCCTGATT TTGTTGGCTG 2100
TCTTAGCTTT AGTTTTCCTC ATGAGTTTTA GGATTTTGAT TTTCAGTAAC GTTTTGAGAG 2160
AGTTTTGTTT TCTTTCTGTT ACTTTTCTTG ATCTAATTTG TTTTATGGTT ACCTCAACCT 2220
AACAGCCCAC AAATCCTCCT ATAGGACCAG ATTATACTGA TCATGGGGTC TTCTGTTTTG 2280
TAGATTTCTG GATCTAGTTA 2300
|
| |
|
|
|
