| Tag | Content |
|---|
EnhancerAtlas ID | HS007-09153 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr2:100278850-100280430 |
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 | GCAAGACTAA AAAGAAAAAC GAACATACAG TATTCTTTTT TTCTGTGTTG CTATGAGGTT 60
TAATATATTT AATATATACT TTTTGTATGG TCCATTGGGG CAAGGGATTT CCTGGCATTG 120
AAAATTTACT CAAAATATCT GTGGTTAAGT TATCATAACG AATATTACTA ATGTCTAATT 180
CATTAAGACC AACAAGCCAG CATCTTACAT GATGTTTGGT ACTTAGTAGG TATTTGAGAC 240
TATACTCAGT TTTTTGCAAA AACTGTCTAG CTCTTGTTTG CCTACAAATA ACATTGACAA 300
TACAGTTCAT TTCTAATGTA GGAGAAACTT CATTTTGGAG CCTTGCCCCT CAAACCTGGT 360
CCTGATTACT GCTTCAACTC CTGTTTATAT AATTCTACAC AATTTTGGCA GGATTCAAGA 420
GCACATACCA GGGTGTTGGC TTTTATGAAT CTCCTGGGAT GTGAATGTCA CGCTGACTGG 480
ATGAACCCTG GCCACAAATC CCAGACAAGC ACAATGATTC TATTTATTCA GACTTGGCTG 540
CCTGAATGCA GATTGACTCT GTGGGTAATA AATTTTCACA GGCCAAGAGC GTCAGGATCA 600
ACCAAGCTGA TCCTGAGAAG AAAAATGCAA CTAAGGAAGT AGAGTTGGGC TGCAAAAACC 660
TCCTATGTTT TTATTCCATG TCTGCATATC ATTCAGCTAA TTCATTTAGT TACTGATTGA 720
CATGTACTGT CAATGCTTTC AGACATTTTA AAAGCTCTGC TTTGTGTTAT GCAATTGTCA 780
TATTAAAAAG AAACAAGGGA AAAAATGAAG AGCTTCCATT ACAATTGGCA ATCTGCTTTT 840
AAGAGTACAC CCAAAACTGA TGTGAGTCAT CCAGTAATCT CTGTGGTAAA GAGCACAGAA 900
TTGAGATGGG AATGTTTCTT GTGCTGCTCC ATAGGAAACC AAAGGAAACA GCAATAAGAA 960
CTGCAATTTT GTGCTCAGAG CAACCTCACC TACAATCTTG GTATCTTGAT GAAGCAAGGC 1020
TTTACATTAT TTCTAAGAGA CACGACTATT ACTCTATGCA TTATAAATAA GAAAATAATT 1080
GGCTCTTTAA TTTGCAGATT TATGTTAATG ATCTAGATAT CTATTAAATT AATTGCATGC 1140
TCTCCAAATA TTGATTGGGG ATTAAAAGGC AGCTTTTCAT TGTGCAAGAA GTAAATTAAC 1200
GCCAATGGGG AAATTTCCCT CTACAGATTA GATCCAATGA TTGTTGTCTG TAAAATTAAA 1260
ATAGTCAGTT AAAGGGGATA AACCATGTTC ATTTAAAGAG AAAAATGTGG CAACAGAGTT 1320
AAAATAAAAA GACTGCCCAA TATGTTTGGA TAACGTAATT ACTGGAAGCT GCAGGCATGT 1380
ACATAGCCAT TCAATTTAGA TCCCTGGTCC CTTCCTCTCC CTAAGCTATG TATTTGTCAT 1440
CTCCGAAACA CTTGTCTGCA GTTGACACTA TCTCAGCTGC TCCTTGCTGA AAGTCTTAAT 1500
CATGTGTCCC TGTCCTCATG CCTTAGCTAT AGTAATGCCA TCTACTTATT TGCTTGTGTC 1560
CAACCTCCCA AGCTTACCCT 1580
|
