| Tag | Content |
|---|
EnhancerAtlas ID | HS076-04416 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:166875260-166876700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr1:166876485-166876495 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr1:166876485-166876495 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr1:166876485-166876495 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr1:166876485-166876495 | 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 |
| GH01I166904 | chr1 | 166873677 | 166876767 |
|
Enhancer Sequence | GTGACTGAGA TCATTTGTAC TGGCTGAGAT GTGACCTGGA TGTAAAAGTG TTTGCGCTTA 60
TTCAACCTGC ATGGGAGTGA CTGCTCCGCA GCCTTCCTGA GGTCAGAGCT CTCAGGATAT 120
CATAAAATGA TCTCATTTTG GTTTAGTTAA GCTCACACTA CAAGACCTAC TGCATGCCAC 180
ATACCACAGT GGTATGAAGG ATACCAAGAA AAAGAATACT TTCAAAGAAC TTGCATTCCA 240
GTGGGCAACC AGACACAAAA ATAGATCATT TTGTGTTTAT GCATTGAACA TGGTGACAGG 300
GCGAACACTG CAGAGGAAGC ATGGACCTGG GGCTCTTAGC TCAGCCTGGT GGGAGTGGGG 360
CTTCCTAAAA GATGCAACAT CCAAGCTGAA TCTTAAAATG TATGTAAGAA AGTGCTCAGA 420
GAGGGGAAGG AAGGTATTCT GGAATAAAGG AACAGAGGTA TAGAACAACA CAGTGTAGTC 480
AAGCTCTACA AATGTTTCTG CATATTACAG CATAGCAAAG ACGTAGAAAA GAAGTAGAGG 540
TAGAGACTGG CAATGAAGCT GTGATGGCAG AAAAGGGTGG GATCACAAAG AGCTTTGTGT 600
GTTCTAAGGC ACTTGACAAT ATGTGAAAAA GACTATGGAG AGCCAGAAGG GTTTTAAGCA 660
GAAAGTGGCA AAGTCAGACT TCAGTCTTGC CAGGTATCTT AATTTCAACT GAACCACTTG 720
TTATTTGAGT TTTCTGCTTA GGAAACATTT GGAGGTCTGG AATTTCATGA CTGAGAGTCC 780
TTATCAAGAT ATGACGTGGC TGTATGTGAG AGTTCAGATG TACCCTCAGG CTCACCCTCA 840
CGAATAAACT GTGTGATGCT CTAGGGTTTC GCCTGGACCT AGGGGGCCCA GCCACCCATC 900
AGTTCAGGGC CTCCATGGCA TGCAGCCCAG TGCCCCATTG CCCCTGTCCT CTGTGCAGGT 960
CAGCACTGCC CACTGCCAGA CTGCCCTCTA CCAAAAACCA GGGTTAAGTA GCTCCCTTTC 1020
ACCACTTACA ATTCTTACAG CGCAAGTCTT TAGGTCAATT TTTTCTTTCT GATACTGTGA 1080
GGATAATTTG GCAGCATTAT CAAAGCTGCT GGTCTCCTTA AGTCAAGAAT TTAAATCATT 1140
CCATTTAGTT CTGAACTTCC TTGAGAGAGA GAAAAAAAAA TGTGTTGATG AGTTCCTTGG 1200
AATGAGAAAT ATATTTGCTG TGATGAACAG CTGTTTGCCA GTTCTTCAAG ACGTTTCTCT 1260
CTGAAGCAAT GAAAATATAC ACAATAGCCC TCAAGTGTCT GGAGAAGAGG TTTCCTTTTG 1320
AAAATTCCCC ATGGCCTACT GTGACTGACT TGAGTATGGA TCACTGTGAA AATCCACCTT 1380
CATGTGAGAG AGTTATTTAC GTCTCAGGAA TCGCCATGGA ACAATGAGCA CTCTCCAAGT 1440
|
