| Tag | Content |
|---|
EnhancerAtlas ID | HS056-02306 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr11:14258360-14259830 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:14258970-14258991 | AGAGAAGGATGGAGAAGAAGG | + | 6.03 | | ZNF263 | MA0528.1 | chr11:14258965-14258986 | GGAGGAGAGAAGGATGGAGAA | + | 6.43 | | ZNF263 | MA0528.1 | chr11:14258958-14258979 | GGGGGAGGGAGGAGAGAAGGA | + | 8.16 |
|
| | 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 |
| GH11I014237 | chr11 | 14258747 | 14259643 |
|
Enhancer Sequence | AGGGGTCACA AGAGCTGAGA GCTGGGCACT GACTTTGGCT TTGGCACGGA GAGGTCACTG 60
GTGACCTTGA CGGGAGCAGT GAGTCTGCTG TCAGAGGAGA GGTGAGTCTC AGTTGCCTCA 120
CCTGAGAAAT GGGGACACCC TCCTGCCTTC CTCAGAGAGC AGCAGTGCAG ACCATGGGCA 180
AACTGCAAAG TGCCACCAAA TATGAGCTGT TTTATTTATG ACCTGAGAAG CCCAGAGGCT 240
GTTGAAATGA GGGGAGGCTA CTGTTGGGCA CAATTGGTTT TAAAGATGCT TACAGCCCCG 300
TTATCACCTC ATAAAATGGC TCATTTCTTG CTACTCATCA CCAGAACACT CACCCAGGCA 360
TGAAAAAGTT ACCTTCAGAG GTAGAAGCTG TCAGGATGGA TATTTTTTGT GCATGGCAAC 420
TGGGAAAGAG AAAAAGCAAA TAATGGGGCC AAATAGTGCT CACCGGGGTC TCCACGCAAG 480
ATTCCAGACA CTGCTCTCCC AGAGGGAACC CCAGTGATCC TGTGCCTCAA AGCAAGGGCT 540
CCTTGGAGAA AGCCACCAAC CAGGGTCAGC TGTGCTCTCA CTGCAAAATG AGCAACATGG 600
GGGAGGGAGG AGAGAAGGAT GGAGAAGAAG GACAGTCAGG GAAAGTGGAA AGAATGTGAG 660
TTTGGAGTCA GATACACATG CGTTGGAATC GTGGTTCCTG TGTGGTCAGC AAATGACCTG 720
ACTCCTCTGA GCCACAGCTT CCTCATCTGC AGTGGACAGC GTGATAGCTA TTTCCAAAGC 780
TTTCTGTAAG AAACAAGCTG TTGAATGGGG GAATGCACAC TGTGTGTGTG GCTGCGTATC 840
ACTGCATTTG CAATTAGTGG CACTGGGTTT TCCCCTGTTT AGTAGCAGAC AGTTTTTCTT 900
CAGCCCAAGG AGCCTGTGCC TTCCCGGCTT CATCAAACCG GTCGTCAGAA CAGCAGTAAC 960
TTTCAGTGTT GTGAACATGG TCTGATATTC TTCCACGTGT GGCTGTGATA TGCAGAACTG 1020
AAAGTAGGCT AGGACATGCC CTTAAGAGCA GCAGAAGTAG GAGGGGTGGG CCTGGTTCTC 1080
CTGGGCCACA GTGTGCACTT TCAGGCCCCA TCTGCCTGGG TTCATGGTGG CAACGGGTGT 1140
GGCCTCTAGA ATCAGACTGA GGTCTAAACT CTAGCTCAGC CAGTTAACTA ACTGTGAAAC 1200
TAATTTGGCC AAATAAATGT GTTTCTGAGG ATTAAAACGT ATATATCCAC CTTGCAAATG 1260
TGTTGTAAGG ATTAAATCAG ATGCTGTCTA TTAGGCAATT TGCAAGGTTA GCAAGATGCT 1320
TAGCACATAA AAAATAAATA ATTATTGTTT TATTATTGTT GCTGTTTCCA CCTGTTTCTA 1380
TTCCTTTCCC TCTCTGATCA TGGATTGCAT CCCATTTCTC TTCCTGTGGG GAGGAGAGAT 1440
GGTAGGGGCA TCAGGCAAGT TGGCCAGGCT 1470
|
