| Tag | Content |
|---|
EnhancerAtlas ID | HS089-09493 | Organism | Homo sapiens | Tissue/cell | Hela | Coordinate | chr3:184362180-184363660 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr3:184363275-184363287 | AATTGTTTGTTT | + | 6.22 |
| | | 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 |
| GH03I184645 | chr3 | 184362947 | 184364010 |
| Enhancer Sequence | CCTGCTCCAG AGGATCCAAG ACATCCTCTT ACCTGCTTGA GTCCATGTCC ATGTCCTCTT 60
ACCTGCTTGA GTCCTCCCTC CCCATTAGGT GGCAAACTGA GAGGGGGAGA GTTTGGCCAC 120
CATGACAGAT GCTGCCGAGA GGGGACACTT TTGCTTCCCT TGCCTCTCCC TCCCCACGGA 180
TCTCTGTAAC CCTCAGAACT TCCCTAAGCA GCTCTAAGCT ATCCCCAGGG GAAAGAGCAG 240
GGACTTGAGA ATAAGAGCTC CCCATTTGCC ACTTGCTGGC TGTTTCTCCA GCTACAAGTC 300
TTTGTACTTG TCTGAGACTC AGTTTCATCA ACTGTAAAAT GGGGGTTAAA ATACCTGTCC 360
TGCCTATCTC ACAGGATTAT TGCAGAAATC AAGGGAAATG ATGCATAGGA AAGTAGTTGG 420
ACCTGGTAAA AGTCTATCAA CATGTGCCAG GTATTGTCAT TAAATATTTC TGGGGGCCAG 480
GTGCAGTGGC TCATGCCTGT AGTCCCAGCA CTTTGGGAGG CCGAGGTAGG CGGATCACTT 540
GAGGTCAGCA ATTCAAGACC ACCCTGGCAA ACACGGTAAA ACCCCATCTC TACCAAGAAT 600
ACAAAAAATA GCCAGGTGTG GTGGCGTGTG CCTGTAATCC CACCTACTTG GGAGGCAGGA 660
GAATCACTTG AACCTGGGAG TCGGAGGTTG CAGTGAGTCA AGATCGTGCC ACTGCACTCC 720
AGCCTGGGGG ATAGAGCGAG ACTATGTCTC AAAAATAAAA ATAAATTTCT GGGTTTTCTT 780
TTAACTGACC AACACTATAT CCATTTTAAA GATAGACTGA GCACCCTGGA GAAACTTGAC 840
CCTGTGTTGC TCCCATCTCA GCCCCCAACT ACCCATCTCT CCCTCCTGTC CATTAGCAAA 900
GGAGAGCCCA GGGCTTCCAC CAGGCCTTCC ACCTGCCCCA ACCTGCCTGC TCTGAACATT 960
TTTAAGCATT CTTCAGGCAC CCGCTGCAAG GGCACCTCTT CTGGGGAAAT ACCCCTGATC 1020
CCCAACACAG CTGGAGTCTC CTGCTCCAGG CTTCTGGGCT CACACTTCCT GGCAGCTCTT 1080
ATCAGGCTGC TTGGTAATTG TTTGTTTTTC CAACACTGTT TCACAATTAC TGTGCAATTT 1140
ACAAACTTGA CAACTCAGTG TGATCCAGCT ACTGCAGAGG TGCCACCCAG GTGCTGATTC 1200
CTGCAGGGCC AGCCCTTCCA AGGAAGAAAG CACCACCCCC AGCCCTTACC TGTGCCCACC 1260
CCCACCCCAG GGCCTACACC AGAACCTGGC TGGAGGAGGC CCTTGGTAAA TGTTTATCGA 1320
CTGAAGGAAC ACGTGAATGA GGGATGGAGT GGAGGCTCTG GGAACAAGGC AGAGGGGAAG 1380
AGATGCTTCT TGTTAACATC TCTTCATAAA AGCCAGTGAG TTCCTACATC CAGCTGGTGT 1440
CTGAATTGGG GCCAATCATA AAACCAGGAG GCCCCTGAGG 1480
|
| |
|
|
|
