| Tag | Content |
|---|
EnhancerAtlas ID | HS094-36683 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr6:131211610-131212970 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr6:131211852-131211862 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr6:131211852-131211862 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr6:131211852-131211862 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr6:131211852-131211862 | AACAGCTGTT | - | 6.02 |
|
| | 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 |
| GH06I130890 | chr6 | 131211342 | 131212364 |
|
Enhancer Sequence | GGGAGGAAAA AAAAAAAAAA AGAGAGAGAG AAAGGGGAAG CAAAATTAGA CTTTACGGAA 60
TTTTTTAAAA AAACTTTAAA GCTATGTACT TTCATATCTC ATTTTAAGTA TGATTACTCA 120
AAAACTAAAC TTTCTAAAGA ACATTATTTA TAAACCCTCC TACACACACA GCTTTATGAT 180
GGTGATGAGT AAATCCACAT TCATGTATTC ATGAATAATG TTCTTCTCCA CCTAAGCAAA 240
GAAACAGCTG TTCTCAGTAT ATCAAAGGTT ATTTATTTGT ATTAGCTTAA ATCATTTATA 300
TAAACACATG TCTGAATTTT TGCTTCTAGC TATAAGCGCC AAGTAACAAT CCATTACCAT 360
TAGTAATTCT TAATATTTAT GCCTATTTCT CCTGGGAAGA AAACATCTAA CTCAGGAATC 420
TGTTCCATTA AGTGATTCTT TCCCATGAAG AACATGCCAC ACAGTGGATC TGTAGAGATG 480
GCTAACACCC CTTCTTGCCA GCACAATTCT ACTGCTTAAT CCCTGGGTTC ATAAAGAATG 540
AAATCAAACT TTCTTGATGT CAAATATTTC TAGGCTTATA CAAAAGCATG TTTTTAGCAA 600
ATGGACCAAT CTTTTTGGGA GTTCAACTGA AATTATTTTG CTCTCTTTGA TCAAAAGTTG 660
ACAAATATCT TAACAGAAAC ATAATCTCAG AGCTCTTAAT TTATTAAATA GGAAGACTTT 720
TGTTGACAAC TCAAAAACAT GAAGAATTCC ACCGAAACTT TTCCTATCAT TTACTATGGA 780
AGAGTGATTT CTTAAAGAAC ACTATCATTT CAAGTATTTC TAGACTTTCT GTACAATTTT 840
TTTAGAAATC ATCTTCTGCA ATAAAGAAAA AAAAAAGAAT CCCTGTACAA CACTCAGAAT 900
GGTGACAGGC TCTATTAAAT GCTCCAAGCA AGGGTGTCAG CTTTATTTAT TTATTTATTT 960
ACTTACTTAC TTACTTACTT ACTTATTTAA TTTTTTGAGA AGGAGTCTCG CTCTGTCACC 1020
CAGGCTAGAG TGCAGTGTTG CAATCTCGGC TCACTGCAAC CTCCGCCTCC CGGGTTCGAG 1080
TGATTCTCCT GCCTCAGCCT CCTGAGTAGC TGGGATTACA AAGGTACATG CCACCATGCC 1140
CAGCTAATTT TTGTATTTTT TTAAGTAGAG ACACAGTTTC ACCAGGTCAG GCTGGTCTCA 1200
AACTCCTGAC CTTGTGATCC ACCCGCCTCA GCCTCCCAAT GTGCTGGGAT TACAGGCATG 1260
AGCCACTGTG CCCGGCCATA TCAGTTTTAT TACTACATTC TTATTCCACT AGTATCAATC 1320
TAGCTGATTG GCTATCAATT AATAGATCTG TTTACAGATT 1360
|
