| Tag | Content |
|---|
EnhancerAtlas ID | HS053-08708 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr12:7175840-7176820 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYB | MA0100.3 | chr12:7176059-7176069 | GACAGTTGGT | - | 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 |
| GH12I007068 | chr12 | 7175430 | 7177082 |
|
Enhancer Sequence | AGGGCTGAGG CTTGGGGAGA GATGATAGCC ATGGGTGACT GGGAGTCACC TTCTGAAAGC 60
AACTGTAATC CTCTTGGGAA AGGACTGAAC AGTGACCTGC CAGAGTCCAG CTCAGTGAGG 120
TGGCAGTATC ACTGTGCCGT GGGCTGCCAG GGCCGTGGGG AACCTCCTCA GCCGCACTGA 180
AGCCAGGCCA ACTGGAAGGA AATAGAAACG TCAGCCAGCG ACAGTTGGTG TCTGGTAATG 240
TAGCTGCAGT GAGAAGATAC AGAACTGCTA AAAACAGGGC CTGAAAGCTG AGAGTGTGTG 300
AGTAATCAAC ACTCAGAAAC AAGTCTAGCT AAATAGCCTA GTTATTATAT TAAAAGTTTA 360
TAGGGCAGCA AGATATAGAG GAATTCAAAG AATGAGGAAG ATAAGAGTTG GGTAGCAGAA 420
GGCTGAGGCA AATCCAATAG GATAATAACC ATCCTGGGTG GTACTGAAAG CTGAAGACTG 480
AGCTGATTTG TTGCATTTAT TATCTCATTC GTGTCCGTAT AACAGCCCTG TGAGCTAGGT 540
GTCATTGGTC TTATCTGACC AATGTCAAAT GTGAATGGGT GGGGTGCAAG TTCACAGAGT 600
TAGCAAGTGG CAAAGGCAGG CTTTGAGCCC AGGTCTGTCT AAGTTCACAG CCCATTGTGC 660
TCAACTTGGA GTCCCTCCAG GCTGTCTAGT AAGGGATTTA AGTAAGCAGC TTCACTTGAA 720
TTCAGTTATT AGTATAACTG AATGGTAATG GCACCAGTCA CTGGGAGTGA GAGGTCAGGG 780
CCAAAGAAGG GACCCCTCTC TACTTCCTAG GCTGACCTGT GGTTTACTAG GAGGGACTCA 840
GGTGCAACTA GGACTCCAGT AAAGAAGGTG ATTAAAGTTT GATCTGGGCA TCTGAAGAAG 900
GCAGAAATCT TTCCTCCTCC ACCATCTGTG TGAGAAAAGG GTTTCCAGCA CTGGCTCTTG 960
ATTGGGCACC GGCCTCATGT 980
|
