| Tag | Content |
|---|
EnhancerAtlas ID | HS056-03952 | Organism | Homo sapiens | Tissue/cell | GC_B_cell | Coordinate | chr13:31340910-31341880 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr13:31341858-31341873 | 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 |
| GH13I030766 | chr13 | 31340980 | 31342117 |
| Enhancer Sequence | CAATAAAAGC CATTATTATT ATTTTATTAC ACTAGTTTTC AATTCCTGCA TAGCAAATTC 60
TTGCAAATGT AGGGACTCAA AACAATATAA ATTTATTATC TGACAGTTTT TCTGGGTCAG 120
AGGTCTTACT AGGCTGTAAT CAGAGGGCAA CCAAAGCTGT GATCTCAGCT GAAGCTCAGG 180
ATTCTCTTCC AAGCTCACTG GTTGTTGGCA GAATTCAGTT CTTTCCAGTT GGAAGACTAA 240
AGCCTACAGT CTTCAGTCTC TAGAAGCCTT TTCTCTGGCA CAGGTTTCTC TACAACATGG 300
CCATTTATGT CTTTAAGGCC AATAGGAGAA CATGATTAGC ATATTTTTTT TAAGTGAACT 360
TTAGACCCTT TTTTAAAGGC CTATCTGATT AGGCCAGGCC CAAGTGAGCT TTAAGTCAAC 420
TGATTAGAGA TCTTAATTAC ATCTGCAAAG TCCCTTCATG TTTACCGTAT AACATAACTT 480
AGTGAAAGGA GTGAAATTGC AACCAGGTTC TGCCTGCACT CCACGGAAGG GGATTCTGCA 540
GAAGTGTGGG TCACGGGGGG GTTATTTTGG GATTCTGCCT ACGTCACTGA GTCAAAAGAA 600
GCTGAATGGT TGTGATGCTG AGGTTTTTGG GCAGCAGCAG TGTGTGTGTG TGAGTGAATT 660
CATACGTATG ACCACCTGGG AAGAAAGGAG GCTGTGGTTT CCTCCACCTC CTGGCAGACA 720
GAGAAATTTC TTTTTTTTTT TGAGACAGGG TCTGGCTCTG TTACCCAGGC TGGAGTGCAG 780
TGGCTTGATC TCTGCTCACT GGCTCACTGC AGCCTCTGCC TCCCAGGTTC AAGTAATTCT 840
TGTGCCTCAA CTCCAAGTAG CTGGGATTAC AGACACACAC TGCCACGCCT GGCTAATTTT 900
TGTATTTTTA GTAGAGACGA GGTTTTGCCA TGTTGGCCAG GCTGGTCTTG AACTCCTGAC 960
CTCAAGTGAT 970
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