| Tag | Content |
|---|
EnhancerAtlas ID | HS139-49031 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr6:154768870-154770650 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr6:154769409-154769427 | CCTTCCTGCCTCTCTTAC | - | 6.29 |
| | | 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 |
| GH06I154447 | chr6 | 154768283 | 154771176 |
| Enhancer Sequence | TCTATCATAA AATCAACATC CACTAAACTA AGTTTACATA GAAACCTCTT TTATAACACC 60
AAGGCCAACT GCATTTACAC ATTAACTGCC CTGGAGATGT TCTGTTCAAA GCATCACCAA 120
TTTATATATC CAAAGATCTA TATGCTATAA ATGGATTAAA AAGACAGTAT AATTAGTATA 180
TGAATTATAA TAAGAATATT CAAAAAGGAG ATTATATCCA GACTAAAGAC ATTTTAGTAA 240
AACTCACTAA AATAATCCAC ACTCTTTTGT GAACCCCTAA GTGACCCCCC CTGTCCAATG 300
TAGTCACTGG CACAGAGCAG GTCCAGAATG AGTCTGAGGT CAAAGCTTGG TCTACAAAGG 360
AAATTAGAAG GAAATTGTAG GAGATAAAAC ACAGCTTTAG GTTCTGGCAT TTGTCCAGCT 420
TTGTTCATTT TAGCCTAATG CTCTAAGAGG TAGAGAAGAG GAAAAAGCAA AGAGAATGCC 480
CAGAGGCAGC TGTTACGTTT ATCATCCCAC TTGATGCATG TGATGCGTCT CTAGCTGACC 540
CTTCCTGCCT CTCTTACTTT GGATTTCCAA GTAAATTTAC CTGTCCTCAA AGTATTACTG 600
CAAAGTGAAA GAGACAATTT GCAAAACATC AAGCAGAAAA GACGGAAAAG CCATGTTCCC 660
AGAAAGTATA ATAAAAGTAA ACTCAAACAC GTTTGTACAA AAAAAAAAAA AAAAGAAAAT 720
ACAGTTTCGG TAATAAACAG GATGCTTAGA TGTCTGGGCA GTGCAAAACA CACAATAGTA 780
CACAGCCACA TCTAAGGTGA GCGTTACTGT ACAGATGGGA AAAACAGACA TCACCATTTC 840
CCCAGAGGTC ACAGAGGGAG TAGCATGTAG CAGAGCCAGG ATTAGAATGC AAATTCCTGC 900
TTCCCAGACC CGTGCTCAGA CTACTTGGCC ATAGCGTCTC CCAGGCGGCA GCTCATTTAT 960
CAACTACAAA TAATTTCCCC ATTACTTTCC TAAACAAGAG CAGCACATCT CAGAGCAGAA 1020
GACAAGGCTC TGTCCATTTT AAGAAGAAGA ATACACACAA TGCAGCAAGT GTTATATAAT 1080
CAACAGTACG CAGACCAGCG ACGGCAAAAT CATCAGCAGC ACATTCTTTC CCACCATTCT 1140
CAGTGATGTA ATTGTATATA CCCCTGGCTG GGGTTCAGGG CATTACTAAC CCAGCCTGAA 1200
TGCTGTCGAG TTTGTCCAAA TCCTGACAGT TAAGTAAACT GCATCTTTAG CCTGGCACCG 1260
GGACAGGCAG ACTTGAATCC CACCCACACT AACCAATTTA TAAACAAAAT GTCCTTACAG 1320
GTGTTTTTGG CCCACACCTA ACGAAGCTAC CCATGTGATT CTAGTGTCAG GACCCAGCAG 1380
GATTTTACTC ATTCATGTTA AAGCCAAAAC CCATCATCTA CAAAATGTAA TGAAGGCCAC 1440
ATTTTTTTCC CATTTTATAG GTCATGTCAA GTGCAAATAT CAGTTATTTA AATATCACAA 1500
ATATCTGTGA AACTCAACCG CTTTTTATAG TAACAAAATC AGACATGAAA ATCAGAACCT 1560
ATTTCTCACT TCAATTTAGA AGATGACATT TTCTTTTCTT TTTTGAGACA GGTTCTCACT 1620
CTGTCACCCA GGCTAGAGTG CAGTGGTGCG ATCTCTGCTC ACTGCAGCCT CCACCTCCCA 1680
GGCTCAGGTG ATTCTCTGAC CTCAGCCTCC TGAATATCTG CGACTATAGG TGCGTGCTAG 1740
CCACACCTGG CTAACTTTTG GTATTTCTAA TAGAGACAGG 1780
|
| |
|
|
|
