| Tag | Content |
|---|
EnhancerAtlas ID | HS139-49408 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr6:170404500-170406110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA(var.2) | MA0072.1 | chr6:170405066-170405080 | TTGACCTAATTTTA | - | 7.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 170405400 | 170405579 | | chr6 | 170404880 | 170405014 | | chr6 | 170404800 | 170405400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I170086 | chr6 | 170401808 | 170405516 |
|
Enhancer Sequence | TCCTGCTGCT GGCTTCCCCT GGGGACTCAC TGAGCCAGGG TCTCCATGCA TCACGGCATC 60
GGTGGCAAAA TCTCACCAGC ACTCAGGCAA AGCAAAGCTC ACCTCCTCCC TCCTGAGCTG 120
GCTGCACACG CCTCTGCTTC CATTTCCTGT AGGTTTTATT CAGCAGGAGT ATTTCTAAAC 180
TGCAACATAC AAAGTATCTA AAAACAGATT TTTATTCTTC TCCACCTTCT TTTTTTTTTA 240
AACAAAGCTA ACTTACATCT TCCCTTAATG ATAATTGGTT TGAATGTCAT TTTCAGAGAG 300
TGACTTTTAA AAAGTACTTG TCATTTTAAA TGAGTCTCTG CATAATTGCA CTGGATTCTC 360
TTGAGAACGT GGCTTTGACT CAGCCTTGGT TGCCCACGGC CAGGAGCCCA TGGGCCTGGC 420
TCTTTCCGAG ACAGAGCTGA TTTCCGGAAC GCTCTTATCG GCCTTCTGCG GTCTGGGCCT 480
GAGCTTTGTG GTCTGGCGGG GCCTTGGCCA GGCCGTCCCC ACTTCCTACC ACGCTCCCGC 540
CTTCGCCCCT GGCTCTAGTC TTTCCTTTGA CCTAATTTTA ATGTCACTGC ATGGCCACCT 600
GTGCTCCAGA TTCACACACA GCCACTCCCC TGCTTTTTAT TCCCTTAGAT TTTGCCCGAA 660
CCCAATCTTA CTGTTAAAAC ACACATACAG ACACACAACA GACAAAAGCT CACATCCCTT 720
GTGACACCAC CCAGTGCTCC CCTGACACTG TGACCGGTGC GTTTGTGCCT TCCTGCGTGT 780
GGCCTGCATG TCTTCGTCTG CCATGCCCAC GCTGTGATGT GCCCAAGTGC TCCCCACAGC 840
TGCAGCCTTG CTCCCCCACG TCCTGCGGGT GGGCACTCCC TCTGCTCCCA GGGGATCTCT 900
GGCATGACCT CTGTCATGAC GTCTGCCATG GTCTCTGACA TGGCCTCCAC TGTGGTCTCT 960
GACGTGGCCT CTGCCGTGGT CTCTGCCTTG CCAATGTTTC AGCTGCTTCC CTGCTCATCA 1020
TCCCCTGCTC ATCGTCCATT CTTCCCTAGG GTAAATGCTG AGAAAAGAAA CTGATGCATC 1080
ACAGAGTCAG TGCAATTTTA ATGTAATCAA TTTGATGAAT TTATTTTGAG ATGACGAATT 1140
CTGACTTTTT AAAAAACCAT TTATGCACCA ATTTCCTCTA ATGTTTGACA TTAAACGTTT 1200
TCATTTCTTC TAATCTAATG GGAAAAAAAT CAGACTGTTT TCCATTGCAG TTCCCTGATC 1260
TGTTGTGAGA TTGTGCAGCT TTTAAATGCT TCTTGGTAAT TTGCATTTCT GCTTTTGTAA 1320
GTTTTGCTCA TATTTCTTTG GCCATTTTCT TCACAGCTGT GTGTTCTCCC CACAGCGGAG 1380
GAATTGTCTT CTCGCACCTG TGAAGTGCTA TTGGATTCAC CCACTGTGCC AGCCCCTTCC 1440
TACGAACAGT CGGTCTCACT CTGCTACTCG TGTCTCGAGG CTTCTCTACA CGCCCATCAT 1500
ATTGATGCTG TCGTACTCAT GGTTCTTTTC TTTTGTGCCA GTTTTTCTGT TATATGCAAG 1560
AAGATGCTCT CTGCCCGCAG GACCATACGG ACACTCTTCT TTCTCCCGTC 1610
|
