| Tag | Content |
|---|
EnhancerAtlas ID | HS138-35251 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr6:31480820-31481960 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr6:31481474-31481485 | AGTGACTCATG | + | 6.14 | | Myod1 | MA0499.1 | chr6:31481826-31481839 | AGCAGCTGTTTCT | + | 6.28 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 31481232 | 31481578 | | chr6 | 31481697 | 31481858 |
|
Enhancer Sequence | AAAATAAATA AATAAATAAA GTGGAGCACT TGACGGCCAT GGGAGAGAAT CGGCTATGAC 60
CACACACAGC AAGATGATGA GCCCAGCAAA GATGATGAGC CCAACTACAT GAAAACAACT 120
TCTAATTTCA TTCAATCAGA ACCAACAGAA CTCATCTACA GTGTTAAAAA TCAAGACAGT 180
GGCTACTCTA GGGTGGGGGA GGCTGGTTTA TGACTCAACG GTGTTTCTTG GAGGGTGAAA 240
ATGATGTTGC TTGATGAAGG TGTTGTTTAT CCGAGTTTTT ACTTGGGCAA AATCCACTGC 300
CCACCTGTGA TTTGTCCACC TTTCTCCATG CATGTTGTCC TTCATTCAAG TTTACATTTC 360
TGGTGTTTTG AAACAATTCT CTCTAAGCTA ATATAGAATT TCTCCTACTC CAAGTCCTTA 420
GAAATGCTGC ATTGAAAATA CCAGTGAATT TTTTTTTAAT TCCAGGAAAT AAATGCCCAT 480
GACTCAGATA TAAAAAGGAG AATCTACAAG AGCAGTAGGC TTGGGAGCTG ACACCAGAAC 540
AGCTTTGGAA AGGGCTGTCG AGCCAGGAAC TAGGAATCAA AACCCAAACA AGACCACAGG 600
AGGTAGAGGG TAGAAATTAT GCCCCAGTAG TGCATGAATG AATGAATCAA GGGCAGTGAC 660
TCATGGGTTG CCTGGCCAGT CTGGAACTTG GGGAAAATAA AGTTGGAAAA TTGGCGGATG 720
GAAGAGAGAA GTGTGCACTG ACCACTTTCC ATGGGAAGAG CATGTGAAGA TAGAGGTTGC 780
ATATGGATGC CTGCCAGAGG GTCTCCAAGG GGCTGGGGCT CCCTGTAACC AGGTGAGCGA 840
GATGGCTTGA TGGATGATGC CACTCAGCCG CACAAGGCTT GCTCATGAGT CCCTGCACAA 900
AGTGGCCGTG GTGGCTGGGA TGGACACTGC ATGGACAGAG CAATTGAGTC ACCACTCACC 960
AAGGCTGACC TGGCAGCTGC CACTGCTGAG GACCCAGCCT GCCAAAAGCA GCTGTTTCTT 1020
TGAACAGAGA AAAAAAACAG ACAATGTTAA TTAAGAGCAA GACAGTGTTA TGACAGATAA 1080
ATATGCCACT GCAGCTATAG TAGAGATGTA AACAATCTTG AAATTATAAA AAAAAAATGT 1140
|
