| Tag | Content |
|---|
EnhancerAtlas ID | HS098-14893 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:124520690-124521840 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:124521319-124521338 | CAGCCACAAGGGGGCACCT | + | 6.51 | | HSF1 | MA0486.2 | chr12:124521713-124521726 | GAAGGTTCTGGAA | - | 6.3 | | LHX2 | MA0700.1 | chr12:124521242-124521252 | ACTAATTAAC | + | 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 |
| GH12I124036 | chr12 | 124521019 | 124521548 |
|
Enhancer Sequence | ATAAATAGCA TGGTGCCCTT GTGTAAGGCT GCTTTCACAT GGCATAATGC TTTTGTTATG 60
TACCCATGTC GTGTGTGTCA CAATAGCCTG TGATTTTTAT TGTTATGGAG TAGCCTGTCA 120
CATGATGTGT CCACCATTTA CTCATCCATC ACTTGTTGAG GGACATTTAG GCTGAATCTT 180
CCATTTGGCG ATGATGAGTA AAGCTGCTAT GAACATTTTC ATGTACAGGT TTTTTTGTGG 240
ACTCTCGCAA ACGTCTCCTA CTGCTGGTTT ATTTTAACCA TGATGCAATC AAGGTCCCAC 300
CCTGCAGCCG ATTGTTGTGC TTCTGACGTT TCCTTTAATT AAGTTGAAGG GGCCCAGTCA 360
AACCCCCTGT TGTAGCCACA GCTCCGGTTA CCTGCCAGGC ATACAAAGGA GCTGAGTTCT 420
CAGAGTAACA ACAGCTACTG AGCTGCTTGT GTAGACCTTA GGCTTGTGAT TGGAATGGTT 480
TCGTTGTACA CCCGCCGGTT GTTACAGGGA AGAAAGACTC CAGGCTGGAC ATCTCAGAAC 540
TAAACTAATT GAACTAATTA ACCTAATCTC TCCCTCTTTC TCATACTCTG GGAGTCAGCC 600
ATTTTTGTTG GTGATGCTGC ACTGTTTCGC AGCCACAAGG GGGCACCTGT GTGCTTTGTA 660
TGATTTAAAA TTTTCATTTG GCAATTAAAA AAAGTTCTCC CAGAAAATCA GTATTTTAAG 720
ATGCTTTCCC TGTTTCCCAG TCTATTGAAT TCAATGGTGA CTTTTGTTCA ATTGTTCAAT 780
ACGTATTTAC CGAATACCCA CCATGACTAA TGCATTGTGC TACGCACTGT GGGTGGTGAA 840
GAAATAAAAT AGTTCCTACC CTTGGGACTC TTCTGACCCA CAGGGAGGAG AGAGAACCAC 900
AGTACAGCTC GGCATGTGTT TGAAGTCAGA AGAATGGGGC GAAACTGTGG AGATTCAGGT 960
GGGTGGGAGC TGGCATCGCG ATATTCCGGG AGGCCATGAT GTCAAGAGCA AGTGAAGAGA 1020
CCAGAAGGTT CTGGAACCCA GGATCTGTTA GGGATGCTGG AAGGGATTCG ATGGTCCAGA 1080
GCTAGGGAAT TTGGAACTTA TTCATGATGT TGAATGACAC GGGGGAGTTT TCAGTGGGGA 1140
AGTGACTGGT 1150
|
