| Tag | Content |
|---|
EnhancerAtlas ID | HS034-16837 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:100278930-100280090 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU4F2 | MA0683.1 | chr2:100279905-100279921 | ATGCATTATAAATAAG | + | 6.03 |
|
| | 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 |
| GH02I099662 | chr2 | 100278761 | 100280614 |
|
Enhancer Sequence | TTTTGTATGG TCCATTGGGG CAAGGGATTT CCTGGCATTG AAAATTTACT CAAAATATCT 60
GTGGTTAAGT TATCATAACG AATATTACTA ATGTCTAATT CATTAAGACC AACAAGCCAG 120
CATCTTACAT GATGTTTGGT ACTTAGTAGG TATTTGAGAC TATACTCAGT TTTTTGCAAA 180
AACTGTCTAG CTCTTGTTTG CCTACAAATA ACATTGACAA TACAGTTCAT TTCTAATGTA 240
GGAGAAACTT CATTTTGGAG CCTTGCCCCT CAAACCTGGT CCTGATTACT GCTTCAACTC 300
CTGTTTATAT AATTCTACAC AATTTTGGCA GGATTCAAGA GCACATACCA GGGTGTTGGC 360
TTTTATGAAT CTCCTGGGAT GTGAATGTCA CGCTGACTGG ATGAACCCTG GCCACAAATC 420
CCAGACAAGC ACAATGATTC TATTTATTCA GACTTGGCTG CCTGAATGCA GATTGACTCT 480
GTGGGTAATA AATTTTCACA GGCCAAGAGC GTCAGGATCA ACCAAGCTGA TCCTGAGAAG 540
AAAAATGCAA CTAAGGAAGT AGAGTTGGGC TGCAAAAACC TCCTATGTTT TTATTCCATG 600
TCTGCATATC ATTCAGCTAA TTCATTTAGT TACTGATTGA CATGTACTGT CAATGCTTTC 660
AGACATTTTA AAAGCTCTGC TTTGTGTTAT GCAATTGTCA TATTAAAAAG AAACAAGGGA 720
AAAAATGAAG AGCTTCCATT ACAATTGGCA ATCTGCTTTT AAGAGTACAC CCAAAACTGA 780
TGTGAGTCAT CCAGTAATCT CTGTGGTAAA GAGCACAGAA TTGAGATGGG AATGTTTCTT 840
GTGCTGCTCC ATAGGAAACC AAAGGAAACA GCAATAAGAA CTGCAATTTT GTGCTCAGAG 900
CAACCTCACC TACAATCTTG GTATCTTGAT GAAGCAAGGC TTTACATTAT TTCTAAGAGA 960
CACGACTATT ACTCTATGCA TTATAAATAA GAAAATAATT GGCTCTTTAA TTTGCAGATT 1020
TATGTTAATG ATCTAGATAT CTATTAAATT AATTGCATGC TCTCCAAATA TTGATTGGGG 1080
ATTAAAAGGC AGCTTTTCAT TGTGCAAGAA GTAAATTAAC GCCAATGGGG AAATTTCCCT 1140
CTACAGATTA GATCCAATGA 1160
|
