| Tag | Content |
|---|
EnhancerAtlas ID | HS165-14965 | Organism | Homo sapiens | Tissue/cell | Ramos | Coordinate | chr8:28299610-28301140 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr8:28299772-28299783 | TGCTTTGTTTT | - | 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 |
| GH08I028442 | chr8 | 28300301 | 28300533 |
| Enhancer Sequence | CCACCATGCC TAATTTTTGT ATTTTTAGTA GAGACAGGGT TTCACCACGT TGGCCAGGCC 60
GGTCTCAAAC TCCTGACTTC GTGATCTGCC CTCCTCGGCC TCCCAAAATG TTGGGATTAC 120
AGGCGTGAGC CACTGTGCCC GGCCGGAATT TGTATTTTTA ATTGCTTTGT TTTATATGGA 180
ATCTTGTTCT CATAACTAAT TGTAATGGGA GTGTCTTGAC ATTTACATAA TTTTCATAAG 240
GAGCCTTCAA AACTGTAAAG GATTAGCAAT CAGGTCTAAG CTTTATTCCC ATCTTTTTTC 300
TTCTTTTTGA GACAGAGTCT TGCTCTGTCG CCCAGGCTGG AGCGCAATGG TGCGATCTCA 360
AGCCACTGTA ACCTCTGCTT CCTGGGTTCA AGTGATTCTC TTACCCCAGT CTCCCAAGTA 420
GCTAAGATTA CAGGTGCCCG CCACCACACT TGGCTAATTT TTGTATTTTT AGTAGAGATG 480
GGGTTTCACC ATGTTGGCCA GGCTAGTCTC AAACTCCTGA CCTCAGGTGA TCCGCCTGCC 540
TCAGCCTCCC AAAGTGCTGG GATTACAGGT GTGAGCCACC TCGCCCAGCC CATCTTTCAT 600
CAATCATTCA CCCTAAAAAG TGGTTAGACT AAGTGGTTCT GACTAAGGCA GCACTTGGGG 660
TCCGCTTTAG AATCAAAAGC AGAAGAGCAA ATCAGGCACA CTTTCAAGGT GGCGGGTTTT 720
GAAACCTCAA ACTCATCAAA TAATAGGAAA CATGACAAGC TCACCGCAAC ATGTGCAAGA 780
TGTGAAACCG TTTCCCCAAG TATGGTTCTG TTTTTGGAGA CAGCGCTCAC ATCTGAAGGC 840
TCTAAGTAAT GACAGGCAAA AAGGGAGGCT GGTGTCAGTG ATCTGACAGC CACATCCCCA 900
GAGAGATGGA CTAAGGAATA TTACTTGTAC TTTTTTTTTT TTTTAGGTAG GGTCTCGCTC 960
TGTCACCCAG GCTGGACTGC AGTGGTGAGA TCATGGCTCA CTACAGCTTC AAACTCCCGG 1020
GCTCAAGTGA TCCTCCCACC TCAGCCTCCA GAGTAGCTGG AACTACAGGT GCATGCCCCT 1080
GCCATGCCCA GCTAATTAAA AAATGTTTTA TTGTAGAGAT GGGATTTTGC TGTGTTGCCC 1140
AGGCTAGTCT CAAACTCCTG GCCTCAATTA TTCTCTCATC TCAGCCTCCC AAAGTGCTGG 1200
GATGACAGGT ATGAGCCACT GCCCCCTGGC CATGTGTCCT CTTTTATTCT CCCATTATCT 1260
TCTCTCTTCC TGCCCTCTCC ATTTAACAAA GCCTCTTTCC TGATATTAGG CGTGAGGAAT 1320
CTTCAAGTGT TCAGGTCTCA GGTAACCTCC TAGGTTTGGG GGTCAGGGTT TGGGGGTATG 1380
TCACTTTCAT CTTTGCCTTT AGAAGGTGCT CCCCTAAGTT TGTCCTGCTC ACCTGCTTCT 1440
CTAGGTCCTC CTGAAATCTT CCTCCATAAA CCTGTCCAAA TGATGGGGGA ACTTTCTGTC 1500
AGAGGTGTTT GAACCAGGGC AACTCCATCT 1530
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