| Tag | Content |
|---|
EnhancerAtlas ID | HS056-05378 | Organism | Homo sapiens | Tissue/cell | GC_B_cell | Coordinate | chr16:8984910-8985950 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr16:8985208-8985223 | TGAACTCCTGACCTC | - | 6.22 |
| | | 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 |
| GH16I008890 | chr16 | 8984638 | 8988331 |
| Enhancer Sequence | TCTGACCCTA GCCTAAGCCC AAACCACAAG AGAGATGTCT TACTTACACA CCTCACCTTA 60
GTAATTCAAG GAACCTTCAG GTGCTATGGC TTTGAGACGG AGTCTCCCTC ACGCTGTCAC 120
CCAGGCTGGA GTGCAGTGGC ACGATCTCAG CTCACTGCAA CCTCTGCCTC CTGGGTTCAA 180
GTGATTCTCT GGCCTCAGCC TCCCGAGCAG CTGGGACTGC AGGTGTCTAC CACCATGCCC 240
GGCTAATTTT TGCGTTTTCA GTAGAGACAA GGTTTCACCA TGCTGGCCAA GCTGGTCTTG 300
AACTCCTGAC CTCAAGTGAT CCACCGATCT CAAGCCTCCC AAAGTGCTGG GATTACAGGT 360
GTGAGCCACC GCATCCGGCC CAGGTGCTAT AGGTTTTATC GCATTTGCTT TAACTGTGAA 420
GGTGGTTTCA GAGTTAAGAC TTTAAACTAC TCACAATTTC CATCCCTGGC ACCATAAACA 480
TTTGCCTCAC AGCAAATGAG TGATGTTATG TATGACGCCA AATGTCCTTG CCGTCTGGTG 540
AAAGAGAAGC TGGGTCAGGG CCTCCATCAG GAAGCGATGG TGTCTAGACG TGGCTTCTCG 600
CCCTGTCAAG GCACCCACGT TGCAGGGGAC TCTGCCAGGT CCCATAGTGT CTCCCTTGGG 660
CTTTGCTCAC AGCACGAGCC ACCGCGCCTG GCTGCTCTTC TCATTTTGAA ACAAGACTGC 720
TTCAGCTCGC TGCTCTTGTG TGTGAGGGCG TGGGAAGGGC CACTGTGACC GCAGGCCCTT 780
GCTGTCACGC AGTGGTTTTC AGGGCTCCCC GCTGTGAAGA CTCCGAATGC TGTCAACAGA 840
TGGCATCCAC ACCCCACAGA GGGAGAGGAC ACAATAGTCC CAGGGGTTAC AGTGAGGCCG 900
GAGAAGGGGA GTTCATTTTT CTTTCTTTAA AATTTCAGCT TGTCTCCCCA GAACCAGTTT 960
AACAAACTCA AACTCCTGAC ACTGTAACTG CGAGTGAGTG GAAAAGGGAA CGCGGCAGAT 1020
GACGGAAACA TTACAACACG 1040
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