| Tag | Content |
|---|
EnhancerAtlas ID | HS098-40134 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:135663100-135664580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr3:135663201-135663212 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr3:135663201-135663212 | GACAGCTGCAG | + | 6.14 |
|
| | 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 |
| GH03I135944 | chr3 | 135662929 | 135664573 |
|
Enhancer Sequence | TAGATAGGCA CAGTGGTATA GTCTCCATGC AGCTTCATCA TCTGTGTTCA ATGCCAGCAT 60
TAACTGTTGG AGTCTCAATA GCCTAGGCTG TGGAAGTTTG TGACAGCTGC AGTGATGGTG 120
AAGGTTGTTC ATGTTCTTGG TGTCAAGGGC TTTGGGAGTC TTCCTATGCT CATTTTCCCC 180
ACAATGAGGA TACTTAGTGA ACTACATCCC TCTTGGTGTC ATGTCTGACA TGTCCTATAA 240
GCAGCTACAG CAGTGCTAGG TTCCAGGTGC AGGTGCTCAG AGCAACTGTA GGACCAGAGT 300
CCTAAGCTCA GTCCTAAGCT CAACAGTTTC TCACAAAACT ATTGTTGCAA CTGGGTCTTG 360
GGGTACCATT TGTTTGTTTG TCACAGGTTT GTTCTCTGTC ACAGGTTTGG ATATTGGTTG 420
CCCACAGAGC CAGGATCTGT GCCTCTGAAT CACTCCCTAG AAGCTCAAGC CCAGGGGGCA 480
GGTCATAGCT GTGATTCTAC ACCCAGAGAA CAAAGCACAA AACTGGACTA ACTCCAGAGA 540
AGAAGGGGTG CTCTGCAGGT TTGGGTCCAG AGAGCAGGGT TTGGCTAAAA TTTGAGAACC 600
TGAACCATTA GGGCTCAGTG GCAACTTGGG TCCCAGTGGA TGAGGCACTG TGTAGGTAGT 660
GACTGTGAAC GGTAGGATGG TGGGGTTGGC AGTATCCAAG ACTCTGTGAA GCCAGGTGCA 720
GTGACATCAT GTATCCCAGA ATAGTATAGC GCAGCTGTTG TTTGGGCCCT GGGGATGACA 780
GGGAATAGTA CAGCAATGAC TGTATTCCCC AGAGAGTAGG GTGTCTGAGC AACTCAGACT 840
CTAAAAGTCT AGTTCAGCTC CAGGGAATCA GAGTACTAGA GTTGTTTGGC CTACAGCATA 900
ATGTGTCTCA GCTCACTACT CTGTTTCCCT GGGACTCCAG GTACTATATC AGCTTAGCCC 960
TGGGGTGTGC AGCTTGTCAG CTTGGTCAGG GCACCAGTTC CTAAGGGGAT AATGTGTTGC 1020
TTCAGCTCAG GCCTTGGGGG GATGACTATT CCACATGGCC CAAGGCACCA TTTTCCTAAG 1080
ATGCAGGGCA CTGCTTCAGC TTAGGTAGTG GGGTATATGA CCACTTTGGG TAGCCAAGGC 1140
AGTTTCCTGT GATGTAGACA CTGCTTCAAC TTAGGCGCAG AGAGGTATAA CTACTTTAAG 1200
CAGCCAAAAT ACTATTTTCC CAGGAGGCAA GATATTGCTT CAGCTCCAGC CTGAGAGAAA 1260
AAGGGGAGGA GTAAATAGAG CAGCTCCACC TCCAATTGGT CTCATAGGGA AAGGTCTATG 1320
TAACAGTTGC TTACAGCTTG CCTTGGGGAT GTTAGGCCAC TGACCTGGGT TGATTTCAGC 1380
GGTGACTTAG GGGTGAAGGG GAGCCTTGGC TATTCACCCC CAGGGCAAGG CACACACCAG 1440
GTGTAGTAAG CAGAAGGCAG AGGTTGCAAT GAGCCAAGAT 1480
|
