| Tag | Content |
|---|
EnhancerAtlas ID | HS187-18920 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr4:123610480-123611630 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr4:123610620-123610631 | TGCTTTGTTTT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGTGTGAATA TATATGTAGA TTTTTGAATT CAAAAATCAC TACTCAATAT ATTGATTATG 60
TGTTTGAAGA TATAAGAAGA GAGTACTGTT ATTAATGTCA CTTTCTGCCA ATGTCTATAA 120
TTGCTACTTG CGGGTAAGGT TGCTTTGTTT TGTTTTGTTT TTCCTTCTGG TCTTGGAGTG 180
TCATGGAAGG AGTGGGGTTT TATTTGTTTC ATAAGAATCC TCTATCAGTA TTATCAGTTT 240
CTTGGGTGAG TGGGAAAAAC AGACACCTCT CCCTTACTCC TGTATCCTTC CATGTGGAGA 300
GAGTACCTTT CCCCTCGCAC GCTACCCCTT TACTCATCTG TCCATTAGAG GAAGATGGGC 360
TTTGTGGAAG ATTGTTTGCA AAGGCGATCA CAATAATTCC TCCCTCCCCA GGACCTTTAC 420
AATGTGGATT TGGCACTCCT CCCATCAAGA GGTGAAATTA ATTTCTCCAC CCTTTCCATC 480
TGGCTGGTAC TGTGACTTGC TTTCACCCAC AGTATGTGTG CAAGTGATGG GCTGTCGCTT 540
CAGAACCTCT CAGCCTCCAG CGGCCTTGCA GCTTCTGCTC TCAACCTTGT GTGCTGCTTC 600
TACGTAAAGA AGCGCAGACT AGACTTCTTA ATGATGAGAG GCTGCATGAG AAAGGGTCCA 660
GCTAACAGCC AAAACCAATA GCCATATGTG GGCTTCTACC TACTTTCTAC CCTCCAGCCC 720
CAGGTGAGCT GCAGATGACT GCAGCTACAT GTGTGCCCCA GACAAGACCA GCAGAATGGC 780
CTCCCAAATG GGCCCAGTGA AAACTGCTGA CATTGTGAAC AGAGAGAATG GTGGTTGTTT 840
GAAACCACTA AGTTTTCAGG TGGTTTTTAA GCAGCAGTAG ATAATGGATA CAGACTTAAT 900
CTGATTGGTG ATCAGAAAGA GAATGAGGGT GCACAGCCCA ACCCCTTTCT CTCACTCTCT 960
GTTTGACAGG AGGCAGCCCA CTGAAAATCC AAGTTCTCTC TTCCTCCCCC AGACCATAAT 1020
CTTACAGTGC ATCACTACTG ATGCACTGAT ATATATATTT TGCCAAGTGC TAAAGGGCTG 1080
GAAATTAAAG TCAATATTTG ACTGAAGCCA AGGCCAAAAC CGAATATTGC CATTAAAAAC 1140
TTCTAGGAAT 1150
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