| Tag | Content |
|---|
EnhancerAtlas ID | HS073-10243 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr3:47181670-47183100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr3:47182134-47182149 | GAGGTCAGGAGTTCA | + | 6.22 | | Pou2f3 | MA0627.1 | chr3:47182923-47182939 | TTTCATGCAAATTAGC | + | 6.25 | | RREB1 | MA0073.1 | chr3:47182572-47182592 | ACACCACCCACCCCCGCCCC | + | 6.54 | | RREB1 | MA0073.1 | chr3:47182568-47182588 | CCTCACACCACCCACCCCCG | + | 6.85 |
|
| | 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 |
| GH03I047140 | chr3 | 47182091 | 47183890 |
|
Enhancer Sequence | AGGTTAAGAC TATAATCCCA AATGTTAACA ACTGTATTTA TGCCTGAAAT GTTTCTCTAC 60
TTGTCTGCCA AATAGATACA CAAGAATACC TACCTAAAGT GAATGATATT CACCTGTTAA 120
AGCCATCTGC TTTTTCCAAA ACCCATAAGT TGGAACGTTG GGTGACCTAA CCTGAACATT 180
TTAGAGCCCA GTGTTGAAGA CTATTGTATT CAATTGAATT CCAGTAATTT TACTCATTAC 240
TCTGAGTTAA TCTTTTCAAT TATCCATTTG TTTTCCTCAT TAGCAAAAAG TGAGAGAGGA 300
AAACCTCCAA TACCAAATAA GCCTCAAAAG ATAAATATGC ATAAATGCTG AAATTCATCT 360
TTAGTACAAG CCAGTGAATC ACACAGAAAG AGTTGACTGG CCAGGTGCAG TGGCTCACGC 420
CTGTAATCTC AGCACTTTGG GAGGCCAAGG CGGGTGGATC ACTTGAGGTC AGGAGTTCAA 480
GATCAGCCTG GCCAACATGG TGAAATCCTG TCTCTACTAA AAATACAAAA ATTAGCCAGG 540
CATGGTGGCA GTCATCTGTA ATCCCAGCTA CTCGGGAGGC TAAGGCACAA GAATTACTTG 600
AATCCCAGTG GGGTGGAGGT TGCAGTGAGC TGAGATTGCG CCATTGCACT CCAGCCTGGG 660
TGACACAGCG AGACTCTGTC TCAAATAAAA AATTAAAATT AAAATTAAAA ATTCTAAGTA 720
TCGAATACGA AGAAAGACAT GAGATAGGTT TCTGAGGGAG ATGGCTTGTT ATAATTAGAC 780
TATTATAATT AGACTGTAGA CTCTAAGCTC GCTTGGTTAA TATTGTTTTT TTGTGAGACA 840
GGATCTCACT GCCCTCACCC AGGCTGGAGT GCAGTGTCAT GATCTTGGTT CACTGCAACC 900
TCACACCACC CACCCCCGCC CCATTCTAGT GATCCTCCCA CCTCAGCCTC CCAAGTAGCT 960
AGGATTATAG GCACACACCA CCATGCCTGG CTAATTTTTG AATTTTTAGT AGGGATGGGG 1020
TTTCACCATG TTGCCCAGGC TGGTCTCAAA CTCCTGGGCT CAAGCGATCT GCCTGCCTCA 1080
GCCTCCCAAA GTGCTGGGAT TACAAGCATG AGCCACTGCA CCCAGTTGGT TAATGTTTAA 1140
ACTGTACCTA TCTTGTATTG TACCAGACTA AGTACTTATG TCAGCCTTCC TGTCCTACTC 1200
TTGCTTAACC ACATTAAATG AGAATACAAA AACAGCTCTT TCAAGTTACA GCCTTTCATG 1260
CAAATTAGCT CTGAAAAACC CACCTTCTAA ATAAAAACAC AGAAATAAAA CCTGTGATGT 1320
GATTAAATGG AAAGACATGA GAAAGACAAG GTCTCTCTTT TTATACATAT TTCAGATCTC 1380
TTTCCATCAT AAATAACTGC TTACTTTCAT CTTAATACTA AAAATGCTTC 1430
|
