| Tag | Content |
|---|
EnhancerAtlas ID | HS139-52223 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr7:150541890-150544060 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF3 | MA0522.2 | chr7:150543944-150543954 | AGCAGGTGTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGTGGTCCC GGCTACTTTG GGGGCTGAAG TGGGAGGATC GCTTGAGCCC CAGAGGCGGA 60
GGTGGCAGTG AGCTGAGATC ACGCCATGCA CCTCACTTCA GCCTAGATAC AGAGTGAGAT 120
GCTGTCTCAA ACAAAAAAAA AAAAGAACAA AAAGTAGGGG AACAAAGATA AAGAGAAAGT 180
CTTTATTAGT GTTCTTTTTG CTTTTTAGTT TGCTTGTTTA TGCAAGTAGT GTTAAGTTGT 240
TATCAACTTA ATAGATTGTA AGAGTATTTG CAAGCCCTGT GGTAATCTCA AATCAAAAAA 300
CATACAACAG ATGCACAAAA ATTAAAAAGC AAGAAATCAA ATCATACCAC CAGAGAAAAT 360
CACCGTCTCT AAAAGGAAAA GTTAACCGCT TTTCCCACAT AACATCCAAC TAAAAGAAGT 420
AGAACCTGGA TTCAAACTCA GGCCTTCTGG CTCTATATCC TGTACCAGTA ACCATGCTGC 480
TATATTTCCT TCCAAAATTG TGCTCAGCAA AGGGCTGCAC AGAGGCAGTG ACTGTTCTGG 540
TGATTTCTGA AGTCCTACAT GCTACCTCCA ATATGCACCT GGAATGTCAT AGTCACCAAA 600
ATGGTTTAAC ACAAATACAT CCCTGCACCA CACAAGGTCA CATGTCTACC AACACAAATT 660
CTTTATTTCA AAGATCAGCA ACATATTTTA ACTTCTGCTT CCTGATTTTC TGGCCTCTTG 720
ATTTTTTTCT TCTTTAAGAA TCCAATGCAC ATTTCGTGAG GTAGCTACTA AAGAGAGCCA 780
GGAGGAAGGA AGAATTCTGC TGTGTCTACT GCCCAGCCCC GGCTGCCAGA CACAGCTGCA 840
GCTGGAGGGA GGAATGTGGG ATTTGACGGG GAAGCTGTCA GCTGGCCAGC ACTGCCAGGC 900
ATGGTCAGTG AAGATACAAA GAGCGCCTGG AGGACCCAGC CCTGGTCTCT GACTCCTCAC 960
AAAGGTCTCC TTGGGGCTCC CTCCACCCTT GCCCCTCATG TGCCTTGGGA TCCAGCATCA 1020
AAGTCCAGAA GTGGGCTCAG CCAGCAGCCA GCCATGCTCA CACACTGAAG CATCCTGACT 1080
CAGCTCCTGG CTGCCCCAGC AGAGCAGAAC CTCTGCCCGA ACTTGGGGTC ACCTGGCTCT 1140
TCTCTCTGGA GTCTCATATC CCAGCCCTCA GCAAATCTCC CCCAGCCTCC CTTCCAGCTA 1200
CATCCAGAAT GTGGCCACTT CTCATCACTT CCACCCCTGC AACCCTGACC TGGCAACCAG 1260
CCTTGCCCCC CAAGACTATT GCAACCACCC CCCGGCCTGC TCTCTGCTCC TGCCATCATT 1320
GCAGCCTTCA CTCTTTTGCA TTCTGTCTCC CCCAGCACCT CCAGATAGCA CTTGCTAGAG 1380
GCAGGTCAGT TTTGGCCTCT GCACGAACCT GACAGAGGCT TCCCAAGTGG CTCAGAGTAA 1440
AATCCCAGTG ACAGCCTTGG AGGCGAGGGC GTTTGGTCAC TCTCTGAATC CACCTGCCAC 1500
CACTTGCCCC TGGCGACAGC AGTCCCCTCA CTCTGCATCA GGGACTTTGC ATTCCTTGCT 1560
CCTTCAGCCT GAAATGCCCC CGCCACCAGG CATCCTTGTG GCCCACTCCT TCACCACATT 1620
GAGGAGAAGA GGAGTCCCCT TTCTGAAAGG TCAGGCCCTG CCCCCACCAC ATGCCCCTGC 1680
TCTGTTTTCC CCTGAGCATG TGCCCCACTG GAACACACTG GGTCACCACT TGCCGCCAAC 1740
GCCTGCAGGA CACCTCTCTG AACACCCGTG ACACCTCATG GCACCTCTGC TGTCAGAGCT 1800
TCACTAGGAC TCACCAGACT AAGCAGACAG TTATACCCAC GGCCAACACA CAGCAAGGAC 1860
ACAGCGGGGT CTGGAGGGGT CAGGGCACAG ACTCGCTGAG CTCTCCCTCC CATGAAGGCT 1920
GCACAGAGCA TACCCTGCGC CCTGCATCTC CCCAGGGAAG TAGAAGCTCA GAGCTGGGGC 1980
AGAGGTTGGG GCTGGTCACG TAGGCACACT CTCTGCCCAC CACAACTAAC AAGATTCCAG 2040
ATTCCCAATA GGAAAGCAGG TGTTCACTAA TCACATTGTC TGTAAAAACA GTCAGCAGGC 2100
CGGCACAGCG GGGCAGGATC CTGAAAGTTA AGTTCCCAGA TGCCAGCCCA GGGCCAGCCC 2160
CTGTCATCAG 2170
|
