| Tag | Content |
|---|
EnhancerAtlas ID | HS139-28499 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:39846920-39848310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr2:39847532-39847543 | GTTTTATTGGC | - | 6.14 | | ZNF143 | MA0088.2 | chr2:39847222-39847238 | TTCCCATAATACACTG | + | 7.02 |
|
| | 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 |
| GH02I039620 | chr2 | 39847141 | 39847740 |
|
Enhancer Sequence | CCCAAATCCT CGGAGCTTAA TATTATTATG ATGCCCTCTT TACCAGTAAG GAAATTAAAG 60
TTTAGCAATG TTAAAGTATT TGTTTGAAGA TATTATCTTA AATCTCTGGA CTTTCAGTCC 120
AGCACTTTCT CTACTACTCA ATTAAACTTC ACTCTTTTTT GTTTGTGCAA TTGAAATGTA 180
GTTAAAAATA CTTTCCAGAC TAGGATTATC TTTTAAAAAA ATTTATGAGA AAATACATAC 240
ATGGTATTTA GCACCAATAC TTGATTTCCT ATATTCCTCA TAGCCTGTAT CAAAAGTATA 300
TCTTCCCATA ATACACTGCT TTGTGTTATT GTCTAGTTTG TGTTTACATG GTTTGTCTTG 360
TCTGAGCAAA AACTTTTTCC CTGCTCAAAA TCTAGTAAAT TTTCTCTCTC ACCCCTTCTT 420
TGCAACTTCC CTTAAGTTCA CCGCCTGCCT ATGGCAGACT GCCAGATTTC ATTTGTCATG 480
CCGGTGGCTG TGGTTATCAG ACATTGCAGC AGGATTTTGG CAAAAATCTC ATAAATAGTG 540
TGCAGCAATG TCAGCGGTCT CTGCTGCTAA TACCTTCCTT CTCTTCCTTT TAAAATCATG 600
CTTCGACGTC TTGTTTTATT GGCGGACCAT TTCACCTTTC TCACATGTGG CAGAGAAGCT 660
CTTCTCATTT AGTAGAAGCA GATCCTGAAC TTTTCATAGT CAAAGGTACT TCCCTTCTTC 720
AGTAATTTCG TCTTGTTACT CCCTAAATCC CTTGCTCCTT TAGTTTCCAT TAGGAACTCT 780
TAACGGAGAT GTGCAGTGTT GAATACTGGT CATAGGCTTC AGATTTAGGG TCCTGTCTTC 840
AAATCCTGGC CCCATCACTG TCTGGTTGGG TCATCTTAGG CAAACTTCTC TGAGCCTCAT 900
CTGTAAAATG AGATCACGTT GTACATACCT ACCTGGTAGA ATTGAGAAGA TGGAATTAGA 960
AGAGAAATTA AATTGCCTAG GATAGTGCTA GGCACATTAT AATGGCTACT AGGAAAAAAA 1020
TGTTAATTTC CACATGTACT ATTCCTGTAA ATAACTCTTC CGCTGAAGTT TCTCTTTGCT 1080
GCCATGCCAA CCACTCAGTT GGAGGTCACA AAATCACCAA TGCCCTCTCA CTTTTGAAAC 1140
ATTCTAAGTC AGCTATTTTG TTTCTTTTTA CTTAACTTGT ATATTTCTTG AGCACCTTGA 1200
TTCACCTATA TCTCTTTTTA AACATTTTTG CTCATTCTTT TCCTGAAGAG TTTTTAGGAC 1260
CTCCAACTCT CTGGCATTTT AGATTGGAGC AAATATTCCC TCTGGGCCAT TCCTCTGACA 1320
TTTTTAGTCA TGTCCTAGTT TCATAGTAGT TTGCTAACTC CACATGTAGT CTGATAAACT 1380
AATTTCCAAA 1390
|
