| Tag | Content |
|---|
EnhancerAtlas ID | HS176-20734 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:62889520-62890980 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr2:62890410-62890421 | TTTGTTTACAT | - | 6.14 | | Lhx3 | MA0135.1 | chr2:62890876-62890889 | GAATAATTAATTT | - | 7.34 | | Tcf12 | MA0521.1 | chr2:62889867-62889878 | CAGCAGCTGTT | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 62889776 | 62889941 | | chr2 | 62890111 | 62890469 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I062659 | chr2 | 62886726 | 62892801 |
|
Enhancer Sequence | ACCTGCTAGA GATTTGTAAG AAATCATTTA AAAGAGACTG GAAATACATT ATTTGCCTGT 60
TGAACACCTC AGTTCTTCCT TTCCATGCTG CTATTTGCAT GAAAATTTGC TGCTTAGGTC 120
AGGGCTTATG ATAGGTTAGA AAAGTTTCCA ATAGCCGAAC ACAAACCCAG GAATCAAAGT 180
CCCCCAAATA TACACAAAGG AAAAAACACA CACACAACCT ACCTAATCTG TAGCTAGAGT 240
GCTTCTGGGC CATGGAACCA CCCCATTGTG CCTTGGCCAC TCCAGCTCAG AAACCAGAGT 300
GTTGCCATGG TGGCAGGGAC CCAACCGTGA GGGCTGGTTT CAATACCCAG CAGCTGTTCA 360
CTTCAGAAAA AGCAGGATGG CAGCCCACTT CTGAATGCGC ATTTTTCTCT AGGCTTTGAC 420
CTGACCTGAA TATTGTTTCT CATTGAATTT CCTTTTATTT ATTTCTTTTT AGATATCAAC 480
TTTCCTTGAA CTTTTCCTGT CATTTGTGTT GCAGTTGGCA GAACTACAGA ACTTCTCCCT 540
TCTGCAAAAA ATGTGTTTTT TTTCTTTAAC CATTTCTAAG TTTTTCCCTG TGTTGTCTTT 600
ATCTCCCCCA CTTCTATATT TTACACACAC ACCTGTGCCT CATTATATGA CGACCCAGGA 660
CAAATTCATC AGGTTTGTTT ATTCCAAGAA GTGTGAAGGC CTCAGGTAGC CCCCTAAAAA 720
ATCCCTCCAT GACTCACCTG ACAGCAGAAA TTTGTCCTAT GAAACTTTGG AGCTGGATTA 780
GAAAATATGA CCCTTTACTC TCTTCATTCT GGCCATGGTC ATAGAATCTG TGTTTAATCC 840
TAAACACATT CTCAATTCAC ACTTGATTCA TAACCTGCTT TTTTCTTCTC TTTGTTTACA 900
TGTTGGCAAA ACATAAGGAA TGTAAAAATA TAAAAACTAT TATGAATTAT GAGCCCTGCT 960
CACAAGGATT GTAGAAAAAC TGTTCTTGAT GCAAAAAGGA GCTGCACTAT ATTTAAGGTG 1020
AATTTATCCC TCTCCAGCTC TAAAGGAGTT TGGAATAATT TATAAATGAG GTTGTACTGC 1080
TGTTGAATAT TTTTTTTAAC TAGAAACAGT TTGTTTACAA GTTGTTACTA AAGACTGTCA 1140
GAAAAAAATG CTTGTGGACA TGGTATCCAA AAGGCTGACA GAACCCAGAA CTTGCTTGGT 1200
ATTCATTTGA GAGCTCATCC AACATTATCC TGCACAGTGT ATAATTACTT GCATGTTGGG 1260
AGCCAAAAAA GGGAATGTAA CCCTGTGAGT GTGTGTTTAT ACTGAAAAGT TGGAGAAGCA 1320
AAACAATTCA GCAGCATTCT TCATCCCAAC ATCTGGGAAT AATTAATTTG CTAGCTATGA 1380
TGTATAACAT GAAGTTGATA AAGTTGCCTG AAGCTCTGCA TTTAGACCAT TTGCCTTATT 1440
TAAAGCTTTC TGCTTTAGGG 1460
|
