| Tag | Content |
|---|
EnhancerAtlas ID | HS052-01676 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:68734630-68736040 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr1:68735093-68735108 | TTCTATTTTTGTATT | - | 6.44 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 68734714 | 68735078 | | chr1 | 68735429 | 68735584 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I068269 | chr1 | 68735284 | 68735683 |
| Enhancer Sequence | TAACATGCTG TACAGGTTCA TAACCTAGGA GCAATAGACT ATACCTTATA CCTGAGGTGT 60
TAGCAGGCTA TACCATCTAG TTCTGTGTAA GTTCCCTCTA TGATGTTTGA ATAACAGCAA 120
AATTGCCCAA GGATGCATTT CTCAGACGGT ATCCCCATCA TTAAGCAATA CATGACTGTA 180
GTTACATTTT GGTGAAAAGC TTGTGGCTTA CTTTCTTTTC CTTGATATTA ACGTATTTGT 240
TGTACAATAT ATTAAAATTG GGAATACAAA AGGTGTGTTT GTGTGTGTGT TAATCTTTTT 300
AATCACTTTC TATGGGAAGC GAGATTGCAT TTCATGTGCA CGTGCCAATC TCTCACTGTT 360
GCTCACTGGG AATGACTAAT ATCATTTTTC TTCCTTCTGG CCTAATGCAA ACAAGCCACT 420
GTGACATCCA ATTTCTGATT TTTGGTCAAT AGAAGGCTCA GATTTCTATT TTTGTATTGC 480
CAAACAATTT GCAGCTTTAA ATATTATTTT TGTTTAGTAT TCACACATGA TAATTTTTTT 540
GGAGGTATCA GTCAAAGGCC AAAGCCTTTT CCACACAATA CCACTGACCT TCCTTCAAAA 600
TCCATGGATG CAAAAGGACA GATAGTGGAG TGATAATTGG TGAAATAAAG AGGGAGTTGC 660
TCCAGACAGG AGACGAAAGT TGCTGCTATT GAGACCAAGA AATGAAACCA AACTGTTTAT 720
CTATTACTGT ATAAAAAGCT AACCCAAAAG GTAGTGGTTT AAAACAGCCA TATTTTTGCC 780
CATAATTCTC CAATTTGGGC AGAGCATGGT GGTGGCAGCT TATCCCTGCT GTGTGGTGCT 840
GGACAGGGTG ACTCACCTGG GCTGGAGAGT CTATGGTGAC TTCACTCACA CGTCTGGGGC 900
TCCAATGGGG GTGGCTGGAA TGTGAGGTAT GGCTGGGCTT GTTTCTCTTT ATACAGCCTC 960
TCTGTGCATC ATGGTCAATG AACTCTTTAT CAAACAGCAT CCTATTAAAT CATTTGATTC 1020
TCACATTAAT CTCTAAGGTT GTATCTTAAG AACTGAAAAA GAAACGGAGC CCTTTTACTT 1080
AGTCTTGTTT TCCCACTCAA CCTGTATTTT TCTTGGAACT TATATGTATT TACATATTTC 1140
TGTATGCAAT TTATTTACTT TAGTTTATTG TAGGTATTCT TATAAACTGT CCTAATTCTG 1200
CAGTACAGAT ACAAAGATAA ATATGTGGTT TGTTACATAA ATATGTTACT ATTTATCTAT 1260
CTTAAATCAG GCTCAGGGAG GTTTAGTGAC TTGATCAAGG TTACATGCCT AACGCATGAC 1320
AGAGCCTAAC TTGGTACTCA GCTTTTCTGA ACCTGTGAGA GCTAAATAAT AAAATCCTAA 1380
TCATATTATC TATTTTAGAT TTTCTTAAAC 1410
|
| |
|
|
|
