| Tag | Content |
|---|
EnhancerAtlas ID | HS095-21366 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr3:133707370-133708360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F1 | MA0024.3 | chr3:133707956-133707968 | TATGGCGCCAAT | + | 6.07 | | E2F4 | MA0470.2 | chr3:133707955-133707969 | ATATGGCGCCAATT | + | 6.11 | | E2F4 | MA0470.2 | chr3:133707955-133707969 | ATATGGCGCCAATT | - | 6.21 | | RAX | MA0718.1 | chr3:133707773-133707783 | GCCAATTAAC | + | 6.02 |
|
| | 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 |
| GH03I133986 | chr3 | 133705200 | 133709717 |
|
Enhancer Sequence | GGCACATGTT CTCAGGACTT ACTGAGGGCT GTGTCACAGG CCATGGTCAC TCACATTTGT 60
AAAATATTTG AAGAGATGTA TTCGGAGCCA GAGTTTGACT CTTTTTGTCG ACAACAGGAT 120
GCAGGGAGGG AGAGTTCGGG GTACTGAGGA CCATGCTGCT GTTCTCTGAA AGAGGGAGGG 180
GACAGCCATG TGCTGCTGGC TTTAGTCCCT CCCAACCTCT GAAAGTCAAT TTGGCCTCAG 240
GGGACATTCT GCTCTTCTGC TCTCTAGGCC GAGCTGACTG CATACCAGAC AGGTGGGAAC 300
ACGTGAGACA GGAGAACAGA GTCTGGAGAC AAGGAACTTA AGGCCGGTTT GTGCTAACTT 360
CCTAAAAGAG AAAACATCAA GGTCTGGGGG CAGGGAATCT AATGCCAATT AACACAAACT 420
TCCTAAAGCT AAAGCAAAAG GGAAAACCCC ATCTTCCCAC TCTGAGTAAC AAAGGATCAA 480
AGGCTACTCT CCTTGCAACC CTCCCCCTTC CACCACGTCT CAGATGGAAA AGGAGAGTGC 540
CTTAGATTGG CCGGCGGGCC CTGCAGGGAC CTTCCCTTTA TCTGCATATG GCGCCAATTC 600
ACCTCAGCCT TTAATTAGCC ACAAGCCAAA TCCTTCATCC AGATAAAGGG AAGAACCTCA 660
AATGGTTACT TACAGCCCAG AAAACTTTAT AACTGGGCCT TTGAGCTGCT TGCTAGGGCC 720
CACTCCCACC CTGCGGAGTT CTTTCTTGCT TTAATAAATT CCTGTTTTCA CTGCTTCATT 780
CCTGTGTTTC ATTCCTTTGG TACTTTGTTT CTGCATTTTG TTCAGTTCTT TGTTCAAAAT 840
GCCAAGGACC TGGACAACTC ATAGTCAAGA CCCTCCAGTG GTAACACCCC TCTGAGACTT 900
CCCTCTCTTG GGAAGAAGCA TAACTGCACA ACCACACTGA CAACCCCCCT GGATTTGAGC 960
AACACTGGAC AGGCATCCAG TCCTCCCATT 990
|
