| Tag | Content |
|---|
EnhancerAtlas ID | HS052-10061 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr12:132487920-132488940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr12:132488923-132488934 | GATTTAATTAA | + | 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 |
| GH12I132003 | chr12 | 132487932 | 132489100 |
|
Enhancer Sequence | TTACGTGCAA ATATACATTA CTTTATATAA GGGACTTGAG CATCCTTGGA TTTTGGTATC 60
GAAAGGGGCC TTGGAACCAC CTTCTCAGGG ATACTGAGGG ACGACTGTAT TTAATTTTCT 120
GTCTAAACAG GTTTTTTTTT CTTCGATTTC ATTTTCTAAC TCATTTCCAT ATGTGGAGGC 180
TGATTTCTGT GTATTGTTTG TTCTGAGACA CCTTACAGAA TTATCTTCTT ACTGGAAGTT 240
TCCAGTGGTT TGGCTTGTTT TTCCTACTTA CATATAGCAT CATATGCTGT AGTGGTGCAT 300
CCCAGCATTT CGCTCTGGAA GCATCAGACA GACAGGAAAG GTGAAGAACC TTGTTAGGAA 360
CATCATGGAC ACACCACCTG AATTCCACAG CCAACACTTA CTTTCACTGG GCTCCATTAG 420
GTCTATGTCC ATCAAGCCAG TGTGGCAAAT ATTTAACATC CTGAGCAAAT GAATTCAAAA 480
AGTGTTTTGC TAGTCCCAAG TGGACAGTGC CTTTAACATG GTCCTTGTAG GGTGCTTGTC 540
CATGGCATTT GTTGTTTTGG CTCAACAGTC TTTGACATAA AATACAGATG CAAACAAGCT 600
CACATATCAC AAGTACACAG CCCAACTAAA GGGTTTTCCC CTGTTAGATC TACCACTGTG 660
TGAACATTCT TTGAACAGAA ATCTGGGTTC ACATTTCTGT CATTCCTCTG GATAGACTCA 720
CTAAAAGGGG AAATGATGAG GTTGAGGGCA TTGGATTCCA AAGCCCTTCA GCTTTCCGTG 780
TTGATTTCCA GAAAAATCCA GCCAGTTTAT GCCATTATCA GCAGCATGTG GGAGTATCTA 840
ATTCATAATA ATTTCCCAGT GTTATGATTT TAAGGTGGTT GATAATTTGG TACTTAACAA 900
ATTGTGCACT GATTTCCAGG GATGATTAAT GAAAAAACAT TTTATTGCCC TTTACACTTT 960
TATGTATGTA ACAGCTTCAT ATCCTTTGCC CACTGTTATT GGGGATTTAA TTAATGTGTG 1020
|
