| Tag | Content |
|---|
EnhancerAtlas ID | HS175-17956 | Organism | Homo sapiens | Tissue/cell | SK-N-MC | Coordinate | chr21:44435990-44437010 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr21:44436974-44436991 | CGTTTTCTAGTAATTCC | + | 6.27 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGATTTTTT TGGTTGTTTT TCTGTTTTCA GTTTCATTGA TTTCACCTTG ATCTTTATTA 60
TTTCCTTTCT TCTGCTTTCG GTTCATGATG TTCCTCTTTT TCTAAGATCT TAAGGTGGAA 120
GCTGGGATGA TTGATTTGAC TAGCTTAACT TTTATTACAG CCTAATTAAT GTGGCAGGCT 180
TTAAGCGTAG CCACTAAGCT TACACATTCC GCTCGATGAT GGCCCACAGA ATCACCGCCT 240
TGGGGTGGCG TCCCCTTATG CTATGTAACT GCTCACATGT CAGGGCACAT GAGTGTGCCA 300
GGCCCGGCAC TGGAGGCTCC TCTCCCCTGC CAGCTGCCCA CCCAGGCGTC ACAGTCAGTG 360
GATAAAGTGG CCCATGTGGA TCTAACCCCA GATGCATAGA GTCCTCCATG GGGCATGTAG 420
AAACATTTGC ATGGGGCTCG CTGTAGGCCG GGCACAGTTC CAAGCACTGT ACAAGCAAGA 480
ACACTGGGGA AAGCCAAGAT CACACTTAGT CCGTGCCGGG GTCAAGAGTC AAGGTGGGTG 540
CCAGGGGCTG ACTCCCCAGC ACAGCTTGGA ATACCTCAGC CCTGGTCACT TCTAGTGCCT 600
CCCAGGCCTG TGCTATAATC TCTTGAATGC TCTTATCGGT CAGGGAGAGC TTGGTTCATG 660
GAAAACTCAA GAGTCCACCA AGCCAAGTCT AATGAAAAAG ATGTGTGATC AGAAAGCAGG 720
GTCTTCCTCG ATATACTCCT GGGCTGTAAG GCACGTGGAA TATGGCAGTG AGATGAAGAT 780
AATCTTTTGG AAGCCACAGT GCAGGCTGAC GTTGCAGGCT GGCTTGTTGT GTTTAATACA 840
CAGTTGAACA TCTCTTGCTT TCCGTGTGTG CTGCGTGCAT TCTGAAGCCG CGTCATCTGA 900
GGATGTTCTT TCCCTCAAGC TTCTCTTTCC TTTTTTAATG GTGTCATTAT GCTACTTATG 960
TTAAAGTTTT AAACATGGGT TTTCCGTTTT CTAGTAATTC CTTCAACATG TGTGTTCTGA 1020
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