| Tag | Content |
|---|
EnhancerAtlas ID | HS187-00732 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr1:42446520-42448000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr1:42447810-42447821 | GTTTTAATTAA | + | 6.14 | | Myod1 | MA0499.1 | chr1:42447547-42447560 | GGGGACAGCTGCT | - | 7.04 | | Myog | MA0500.1 | chr1:42447550-42447561 | GACAGCTGCTG | + | 6.14 | | Tcf12 | MA0521.1 | chr1:42447550-42447561 | GACAGCTGCTG | + | 6.02 | | ZNF263 | MA0528.1 | chr1:42447456-42447477 | GGTGAAGGAAGAGAAGGGAAA | + | 6.23 | | ZNF263 | MA0528.1 | chr1:42447098-42447119 | GAGGGAGGAAGTGGTGGGGAG | + | 6.41 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCCTTGACAG ACAATTCAGA GGAACAGTCT CCTTGGAGCA GAGGTTCTGC TGCCAAGCAA 60
ATACTCCATG AGGAATGTTA GGAGGATGGG CCTGCTGGTG TCTGGGCCAG CAGGAGAGAA 120
AGCAAGGCAA GACCAGTGCA AACCGTGCCC AGCAGGGCTA AAGTGGGTAT CGTTGCACAG 180
CTGGGCAAGC TTGAGAGAGG CCTGGCTCAG AAGCACACAT CAGGATTCGC TTCTGCAAGG 240
TGTGGGTGAG CTCTGGCAAG CTGGGCCCAG AGGCAAGGAG AGAAGCAAAG TCCTCCCCTT 300
GTGAGAACAG TGAGGGTGGA AAGCAAACAA CAAGAGGAAG AAGGTACGTG TCTCCAAAGG 360
GAGCAAGCTC TTACAGGGAG CTTGGCAACA TTTGCATCAG CCTGGTAAAA CATCGAAATA 420
ACAACACCTA AAATAGCCCT ATAGGAACCT TGTCAGAAAA TAAAGGCAAG ATTCCTGAAG 480
GACTCTGCCT TCATCCCCAC GGAGCTGGGA AGCAAACGGG GAAATGCAAA CCCCATTTAT 540
AGGGTCACAT TTGGAGGAGC CGGCTCCGTC GGGGGCAGGA GGGAGGAAGT GGTGGGGAGG 600
CTCAGGGTGT GTCAGATCCA GCCTCCCCAC CTCTGCTGAG CTGGCGGCTG GACTCAAGGC 660
CTGCCACGTC TTCCTGCTCT GCAGTGCACT AGCTGTGTGA CCTTCTGCAA ACTGGGTAAC 720
CACACTGCCT CCCCACCCCA TCTCCTCCAA GGTAAAGTGG AGATTTTACC TGCTGCAAAA 780
AGTTGGGTGA GGACTGATGA GAGAATGAGG GTTGATAAGA GAAGGTAAGG CATTAAAGGT 840
AAAGGAAATT GCGTTTTGTT ATATATATAA ACAGCTTCTC ACTGCTTTCG CTGGATTCAT 900
CATTCTGGGA CTTTCTGTCT TCTACATACT TTTAAAGGTG AAGGAAGAGA AGGGAAAATG 960
TGAAAGACAA TATTCCAGTC TCCACTGAAT GTGTGGGCAC TTCAGTCTCG TGGCAAGTTC 1020
AGGCCAAGGG GACAGCTGCT GAAATGTGGG GGTCCAGGGG CTGCAGAGGG GTTCTGCTGC 1080
CTAGCATTTA AAAGAAGAGG GAAGTAAATA TTTCTGAGGT GAGTCAGTAA AAGTAAAGAA 1140
ATGCTTACTT CTTGTAAATG AGAAGGTGGC AGATGAACAC ATGAGGGAAT GGGCATATAT 1200
TCATCCCACT TGTAAAACAT ACTTCAAAGG AGGTAGTTCC AACATCAATT TCTTTATCGT 1260
GGTACTTTAT AAGATTTCCT TGTTTGCTTG GTTTTAATTA ACAGCAACCA TACAGCATTG 1320
AAAGCGAAGC CTTATCCATC ATCCACGTCA AAGGGGCTGG AAAGGTCCGA ATCCACCTGA 1380
ATGACAACTA AAGTTTCGAG AATGGGAATG CAAAAGGGGA TTCAAAGGTA ACAAAATCCT 1440
TGTCCTTCCA TTTTCTTCTT CCGCACAAAC AAAAGCAGTT 1480
|
| |
|
|
|
