| Tag | Content |
|---|
EnhancerAtlas ID | HS019-10687 | Organism | Homo sapiens | Tissue/cell | CD20+ | Coordinate | chr21:41425630-41427100 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF3 | MA0522.2 | chr21:41426397-41426407 | AGCAGGTGTT | - | 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 |
| GH21I040054 | chr21 | 41426441 | 41426610 |
| Enhancer Sequence | AGGGCTCTTG CTGATACATG ATCCTGCATG GACTGGGATG GATCTCTGGC GAACGGTCAT 60
ATTTACAAAT GGAAATGACT GGCAGGCTTC CTCTGGTGTT AAGCCCCCCA GTGACCAGCT 120
CTTGGAAGGC CATAGACCAC TCATGGCATC TGCCTAGCTA TCTATTTTCA TAGCCATATG 180
TAGGATTATT GTCTAGTGAG ACGCATTTAG CAAATATTGT AACGTGTTAT ATAACCATGG 240
TGACCTCCAC AAACTATGTA ACCTCTCTGT GTCTCAGTTA CAAAAGAAAC TTTTCCTATG 300
TTGGCTGGAA GGGTTAAATT AAATAATGCA TATAAATGGC TTATAAAATT ATATGGTCAA 360
AGGAATTACA TTCTAATTTT TGAAATTTTT TCAAAGGAAA TTTTCAGTTT TAATGCCCAA 420
TCTACTGGGT GAAACAAAAG AGATTCCAGG TATACCTTCC CCTTTCCCAA AAAAAGATAA 480
TCAAAAGCAA AACATAGTAG CTTATCCCTT GTCCTGATAC AAGCAAGCTA ATAAAATCTT 540
GTGTACTTTA GGGCAGGTAG TGCCACCTCA CATACATGGT TTAACTGAAG TGTTTCACTG 600
AAGTTAGCTG ATCAAGAGCC ACTTTGCACT TGACCAATCT TTAAGTGCTG CTATGCCTGG 660
ACCAAATGTG ACTTCAGCCA GGAGAACCCA GGCCTTAGAA TTTAGGAGCC ATTAGGTCAA 720
GATGTCTCCA GTGGTGGGTG GGGCAGCAGA AGGGTGATGG TTGATGGAGC AGGTGTTCTG 780
CCCACCTGGT CTCTTACCAC TGCCTTCCCG GCAGGAGGCA GCTGGGCTAT GTGCTGAGAG 840
TCAGGCAGTT TATCCAGACC ACAAGAAAGG GTTGTCCTGG GACTCATGCC AGCAAACACC 900
TTCCAAAACA AACATAGCCA GGTTTGAAAA GAGGCAGCCT CGGAGCCTGC CTCAGGGTGT 960
TTCCATGGGC ACTCAAAAGC TTGGATAACT TCTGGTTGAG GGTTTCTTGG AAGCAGCCTG 1020
TTGGTGTGGA AGCAGGTGGC CTGCTGCTGT GCTAGCTGTC ATTGGAGACA GACAGCATGG 1080
CGGTGAGTGT GGCCAGGTGG GGAACCTGGT TCTGCGCCTG TCTCTGTGAC CTTGGAAAGC 1140
TACACAGACC TCTCTACATC TTGGTTACAA AAGCAAGACT TCTTTCATAT GTTGGTTGAA 1200
AGGTTAAATT AAGTAATGCA CACGAAGTGC TTATAAAAAC TATGTGACAT TTACAGAATT 1260
CTCAATACAT GTTAGCTATT CTTCTCATTA TTACTGGAAA GGAAATATAA GGTATTTCAC 1320
TCCGGAATAA ATAGAATAAT CGAGGCAGGC AGTGTGGGGT AATGGACTTC AGGTGGAAAG 1380
AGGCTGGGAA GAGTGAAGAT ACCTGGGTTC TGGTTGAACA AGCCAGAAAA CCTCAGGGTG 1440
GCTGTTCTGA AACCCTAAAA CTAGGGCCCT 1470
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