| Tag | Content |
|---|
EnhancerAtlas ID | HS184-16591 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:100278990-100280590 |
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 | GTGGTTAAGT TATCATAACG AATATTACTA ATGTCTAATT CATTAAGACC AACAAGCCAG 60
CATCTTACAT GATGTTTGGT ACTTAGTAGG TATTTGAGAC TATACTCAGT TTTTTGCAAA 120
AACTGTCTAG CTCTTGTTTG CCTACAAATA ACATTGACAA TACAGTTCAT TTCTAATGTA 180
GGAGAAACTT CATTTTGGAG CCTTGCCCCT CAAACCTGGT CCTGATTACT GCTTCAACTC 240
CTGTTTATAT AATTCTACAC AATTTTGGCA GGATTCAAGA GCACATACCA GGGTGTTGGC 300
TTTTATGAAT CTCCTGGGAT GTGAATGTCA CGCTGACTGG ATGAACCCTG GCCACAAATC 360
CCAGACAAGC ACAATGATTC TATTTATTCA GACTTGGCTG CCTGAATGCA GATTGACTCT 420
GTGGGTAATA AATTTTCACA GGCCAAGAGC GTCAGGATCA ACCAAGCTGA TCCTGAGAAG 480
AAAAATGCAA CTAAGGAAGT AGAGTTGGGC TGCAAAAACC TCCTATGTTT TTATTCCATG 540
TCTGCATATC ATTCAGCTAA TTCATTTAGT TACTGATTGA CATGTACTGT CAATGCTTTC 600
AGACATTTTA AAAGCTCTGC TTTGTGTTAT GCAATTGTCA TATTAAAAAG AAACAAGGGA 660
AAAAATGAAG AGCTTCCATT ACAATTGGCA ATCTGCTTTT AAGAGTACAC CCAAAACTGA 720
TGTGAGTCAT CCAGTAATCT CTGTGGTAAA GAGCACAGAA TTGAGATGGG AATGTTTCTT 780
GTGCTGCTCC ATAGGAAACC AAAGGAAACA GCAATAAGAA CTGCAATTTT GTGCTCAGAG 840
CAACCTCACC TACAATCTTG GTATCTTGAT GAAGCAAGGC TTTACATTAT TTCTAAGAGA 900
CACGACTATT ACTCTATGCA TTATAAATAA GAAAATAATT GGCTCTTTAA TTTGCAGATT 960
TATGTTAATG ATCTAGATAT CTATTAAATT AATTGCATGC TCTCCAAATA TTGATTGGGG 1020
ATTAAAAGGC AGCTTTTCAT TGTGCAAGAA GTAAATTAAC GCCAATGGGG AAATTTCCCT 1080
CTACAGATTA GATCCAATGA TTGTTGTCTG TAAAATTAAA ATAGTCAGTT AAAGGGGATA 1140
AACCATGTTC ATTTAAAGAG AAAAATGTGG CAACAGAGTT AAAATAAAAA GACTGCCCAA 1200
TATGTTTGGA TAACGTAATT ACTGGAAGCT GCAGGCATGT ACATAGCCAT TCAATTTAGA 1260
TCCCTGGTCC CTTCCTCTCC CTAAGCTATG TATTTGTCAT CTCCGAAACA CTTGTCTGCA 1320
GTTGACACTA TCTCAGCTGC TCCTTGCTGA AAGTCTTAAT CATGTGTCCC TGTCCTCATG 1380
CCTTAGCTAT AGTAATGCCA TCTACTTATT TGCTTGTGTC CAACCTCCCA AGCTTACCCT 1440
GACTTGAGAG GCAGAGCTCA TCTTTTTGCC AAATGGGAAG ACATGCAATA TAATTAATCA 1500
GTCCCTTCCT AATCTATTAA ATTTTTTTAA TACTTACTGT CTTAAGTCTT CTAATTCCTT 1560
CACATTGTTT CACAAAAACA TTGGTCTTTG GAATTGTTAA 1600
|
