| Tag | Content |
|---|
EnhancerAtlas ID | HS098-01600 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:41784800-41786590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr1:41785278-41785296 | GTTAGGCTTTCACATTCC | - | 6.41 | | Myod1 | MA0499.1 | chr1:41786255-41786268 | AGTAACAGCTGCA | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 41784887 | 41785136 | | chr1 | 41785169 | 41785326 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I041318 | chr1 | 41784592 | 41786704 |
|
Enhancer Sequence | TCACTGCTGT GGCCCCACTC TTGTCTCCCT GCTTCTGCCT TTGTCTTCAT CTCCCCTCAA 60
CAGCCTCAGA TTGGAGGCTC TGCCACTTGC CCTGTTCTCA CCTGCCGTGC CAGCCACAGA 120
CTGACGGTCT TGGCCCAGTG CTTTTCCCTT TCTCCTGGGT CAGCCCTGAC CTCTCATTCC 180
CATAGGCCTG GCTCCTGTTC CTACAACACT AGACCTCCTG ATGGTGACAT CAGCTCAGAA 240
GTGACACAGA CAACTCTTCT GTTCCTACCC ATGCTATCTC TTCTATCTGT CCTCTGTCAC 300
TGCAGATCCA GTATTTTTGT GTCCACACTT AGTAGTCCTG AGGAAAAAAA AAAAAAAAAA 360
AAAAAAACAG CCAGGCCTAA ATCTCTAGGC CCTTGGCCAA TATCTGGGGC TCAAGAGCCT 420
GCCAGGAGCT GAAGGTCATG GGGCTGGGGA TGCCAAGAGG GTGGGGTATT TCTTTTCTGT 480
TAGGCTTTCA CATTCCCTGT CTCCTTTAAT TTCCCCCAGA TCCCTGTGAG GCAGGAATAA 540
TTTCCCCTCC TGTGGGTGAG GGGAAGGAGA AAAGAGAACT CACTTGACCA CAGCTGCACA 600
GTTAGTTGGG ATCAGAACCT GAGCCACCTG GCCCCATGCT CCTGAAGCTT TGACCTCCAT 660
GGTCATTAAA GACCAAGTCA TATTCCTCCC ACCCTTCATA CCTCCCCCTC CTCATTTTTC 720
ATTTACAGAA GAGGTCACTG AAATCCAGAG GTGGGGAGGG CCTTTCCCAA AGTCACAGAG 780
TGGCTCAGTG ACTGGGCCTG AAGGAGTCCC AGGCCTCCAG GCACTGCTGT TCCCCAGTGG 840
CCCAGAGGCA GGACGGGCAC ACACCCCAAG GCCGGCCCTC CCCCCACATG GCTCAGTTCC 900
TGCCTCCCAG ACTGAGGTCT GGAGCCCTAA ATAGAACAAG CACCACCGTC TCCCTTCTCA 960
GGGAGGGGAA GCCAGCTGTG GCAGTTGTGG CAGGCGGAGA GAAATTTTCC CTTTCTGTAG 1020
ATTGGATCAG TCACTCTCAG AATTGATGGC AACGGCTTCA TCACAAAGAT CTAATGCTTT 1080
AATTATGTTG TGACATGACC TGACATGGGG GTGGCATTTG ATGGATTCTC TGGTGTCATC 1140
AGCATGGCCC TGACATAGGA AAGTGGCAGA AGGCAGGGGG TGGGGAAGAG GAAGGGCTCT 1200
CAGTGGGAGA CGTGTCCTTC CAGGGCCCCC TACCTTCCCC TGCTCTCTGT CTTCCAAGGC 1260
AGTCCTGCAG TAGTGGAGAC TCAGGAGAGG AGGGGGAGCA GCCCCTGTGC AGGGGAGGGT 1320
GGCTGCGCCC TTCCGGGATG GACTGGATCC TGGGGGCCCC GTAGGAGTGC ATGTGTGTGT 1380
GTACCTGTGT GCATGTGCCT AGATACACAG GGACATGTCG GAGCGGGTGA GAGGGATTCA 1440
GACCCATGTG GTAGAAGTAA CAGCTGCACT GCTGTCTGGC CTGCAGAGGA CTAGGAGGTG 1500
GAGGCCAGGG CAGGACACCT GGCTGGTCTG CATGTCCTGG GCTGTCGTGA GCAGAAGGAG 1560
CAGATGTACT CAGGCAGCCT GGGAGCAGGC TTAGCTCAGC AGAGAGAGGG CTCCCTGGCC 1620
AGGGAATGCA CAGCTTTAAA AGGCACTGAG CAAATGTCTC TGGGAAGGAC TGAGGGGTTG 1680
CTACAGAGCA GATCTTTTCC CTTGGTGGGC ACTTGGTGAC TCCCTACCTC TGGGGCTAGG 1740
ATTGCATGTA TCTGTGGGTG AAGGGGTTTG CCTCCCTCTT TTCCTCCCAC 1790
|
