| Tag | Content |
|---|
EnhancerAtlas ID | HS052-03426 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:212260960-212262450 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr1:212262429-212262440 | AAAACAAAGAA | + | 6.62 |
| | | 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 |
| GH01I212087 | chr1 | 212261281 | 212262542 |
| Enhancer Sequence | GATTACTCCA TTTCTGGGTG ATGCTAGGGT TACTCTGAAG AGCACTACGA AGCAACAACC 60
TGACACGGGT TTTCAAAGGC TGGCACACTG ACCATTCGAC TCTCTAAGCC AGCTTCCAGC 120
CACAGATTTG CTGCTTCTAA TCACATTGCC ATCTTGAAAA TCATGTTCCC CTGCTTTCCC 180
AAGCTTCTAA TTGCCACGCC AACCTTTCAT TGCTGTCCTG GGCTGCTTAT CTTCACTTCT 240
GGCCCTGGCT TGTAAACCCC CTCAGTTAAC ACATTAATTG GAAGGGTTTA AGTGCTAAGA 300
CATAGCCTCT TTTTCTCCTG CCCTACCTTT CCCAGCCGGC ACCTGCTTCA TTGCTTACCA 360
CTCTTTCCCT ATGTTTTAGC CAGAGATCTC ATAGCACTGT TGAAACCAAT AGTCCTCAAT 420
CTTGGCTATG CATCATAGCT ACTTGGGGAG CTTTTCAAGT CCGTGTATCC CCAGTGATTG 480
ATTCAATGGG ACTGGACCTG TATTTTTACA AAGCTCCAAG GAGGTCTGTT ATGTAGCGAG 540
GATTGAGAAC CTCTGGTTTA GGCATTATTG AGTGATAAAG TTGATTATCC TTATCCTAAA 600
GAGAAGGAAA CCCTACCTAT TCTGCCTCAG TTGCTTGCTG CAGTCTCACA AGTCAGCAGG 660
ATAATTATAG AGTCAATTTT CTGATCCCTA GAACCTCACC TGTATCCTTG TCAGCAGTAA 720
TGAAACTTAA CAAACATTGT TTAATAATTC CTTACTACGC ACTATAGGGG CACTGGGCCT 780
AAAGATGAGT AAACCATTAT TAGCTGCCCT CGAGGCTCAC AGTCTAGTCT AGGAGGCAGA 840
TTCAAAAACT ATAGCACACA GCCATTAGCT GTGTAAACAA GGGGCTCTGA GAACCTACTT 900
CCCCTGTGAG AGGAGAGCTC TGTGGGAGAA GAGGAAAGAA GTTGTGAATT CTTCACAGTG 960
GAGTTAACAT TGTCATCAGA GCCTTGAAAC ATGAGAAGAA TTTCTGCCTG GCAAAGGAGG 1020
AGCTGACTTG GCAAGAAAAC CACATGAACA AAGAAATGTG ACAGTACACA GCTTGTTCAG 1080
GAAGCAACTA GTAGTGTCCT GTAACGTGAT CCTAGAATAG CAAAGTACAT GATAAGACTG 1140
AAAAGGCAGG CTGAGGCCAG ATGGCAAACT CATATAGAAA GAAGCTGGCT GGGCACGGTG 1200
GCTCACGCCT GTAATCCCAA TACTTTGGGA GGCCGAGGCA GGCGCATCAC CTGAGGTCAG 1260
GAGTTCGGGA CTAGTCTTGC CAACATGGCA AAACCCCATC TCTACTAAAA ATACAAAATT 1320
AGCTAGGCAT GGTGGCACAC GCCTGTAATC CCAGCTACTC GGGAGGCTGA GGCAGGAGAA 1380
TTGTTTGAAT CCAGGAGGCA AAGGTTGCAG TGAGCCGAGA TCATGCCACT GCACTCCAGC 1440
CTGGGCGACA AGACAAGACT CCGTCTCAAA AAACAAAGAA AGAAGCTGCA 1490
|
| |
|
|
|
