| Tag | Content |
|---|
EnhancerAtlas ID | HS098-40498 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr3:149901330-149902780 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr3:149901697-149901710 | ACGATGATGTAAT | + | 6.09 |
| | | 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 |
| GH03I150183 | chr3 | 149901483 | 149902787 |
| Enhancer Sequence | CCACAAACAT TGAGCACCCA ATATGTGCCT AGGACTATTC CAGAGCATGA GGACCATGCC 60
TGGAACTAGA TAGACAAAGT CCATGGGAAC TCACAATCTA ATGGAGTGAC AGACAATAAA 120
TAACTGAACA GATAAATACA TGAGAAAAAT AAAGCAGAGG ATATGGTGAT GAATGGAGGC 180
TCTGCTTGAG AATGAATGGT TGCCTTGCAG AGGCAACACT GAAGCCGAGA CTATTCTCAT 240
TAGGAATTTA CTATCAGCTT TGTGGGGGTG GAGGTGTAGG TTGGTCAGGA GCAGAGTGAC 300
CCCAGTACAT GTGGATTACA GACCAATCAT TTACTCATTT CTCCTGCTAA TTCTCTTCCT 360
TTTCCCTACG ATGATGTAAT GTTATTTTTT CAGTAAACAA TAAAAAATGT ATTGAGTCCT 420
TCTTTGTATG CTAGGGGGAG ATAGTTGCTA CTCAGAAGGT TATAATCAAG GTTGTCGCTG 480
AAGTGGGAGT TCATGGATTC CGCTTCCCTC CCGTCTCTAA GGAAAAGGCA GTGAACTGTA 540
GGTTCGAAAT CATTTGATCT CACGCTTGCC TAGAAGCAGA AGAATGAAGC TGACTAGAAC 600
ACCCCTTAAG CCTCTTAGCT GTCCTGAGGG AAAGGAGCAC TGCACCCTCC CCCAGAGTAA 660
AGACATCGCG AATTAATTCC TGGGTGGTGG ACGGCGACGT CCTTGTCCTG CGGGAAGTGC 720
AAGGGCACCC GCTCAGGGTT GTGAGAAACT GCGGGGCCCA CGCTGCTGGC GAGAGTCAAG 780
AAGGAACGAA AAGAAGGAGC TCCATCTAGC GTTGTTACGA AACAAGACCA GCGGCATCCT 840
GAACAGTTAG CTCCTTTCTG AAGGGCGAGT ACCAAATGAA AAACGCACCT TATCTTCCGC 900
CTAAAAATTT TACCGAAAAA GCCAGAGCCG CTGGGCTGTG GGAATTTAGC GCACAGTACA 960
AGCCTGACAT CACCTTTGTC TGGGAATGAA CCCAGGAACG GAAAGAAGAC TAAATTATCT 1020
TAAGGTCTTG CTTATCAGTA ACTACACATG AAATGTTTCC TCCTAGGACA GGAGCGCAGG 1080
CTTCTTTGTT GTTATAAAAT CATGATCTGG GGACTTGACA ACGTCCAGAG CAATCTGGGG 1140
AGGCCCATAA ATGGGATCCT GTATATTATG ACTTTGGGGA CATTTGTGCA AGTATTTGTA 1200
ATTGATGGGT CATAGGGTTC ACATACCTTC AACTTCAGTA AACAATGACT AACTGCTTTC 1260
CAAGGGAAAT ATAACAGTTT ACACTCTCAT CAAGACTATG AGGGTTCCCT TTGCTCCTTA 1320
TCATCTGCAA AAGTTAGTAT TGTCAGCCAG TTTCATTTTT GTCATTCTGA TGGGTGGGGT 1380
CAGGATACTT CATGGTGTTT TAGTTGGCAT TTTCTTAGTT ACTAGTGAAG TCAAGCACTT 1440
CCCATATGTT 1450
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