| Tag | Content |
|---|
EnhancerAtlas ID | HS056-16432 | Organism | Homo sapiens | Tissue/cell | GC_B_cell | Coordinate | chrX:135332450-135333440 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HINFP | MA0131.2 | chrX:135333167-135333179 | CCGCGTCCGCGG | + | 6.04 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCAATTAAAA TTAATAAAAT CGTTTTATTC GCGCTCATAG CAGAGGGAAC TAGTCTAACA 60
GGCTAAAAGC AACCTCCTGA AAGGAAGAAA TCCTATCTCA GGTAGTGGAG CAGTCTCCTG 120
GACCAAGCAA TGTGCTGTCA AATTGTATAA GATTAACGGT TTTCGAGGAG GGAAAAACGT 180
TTTGGCGATG GGACTAGTTG AGGAAAAAGC ACTCTGAAGT GCTGATTCCC GTTCAGTTCA 240
GCCTAGAGAC TGCAAGATGT CCCACAGAAG ATGACATCTT GTTGAAGTCA TGTGCTACAG 300
CAGGCAAATC AGGAGATGCA AAGAGCCAAG TTTCATCCCA ACTTTTAAAG CAACTTTTAA 360
GCATCCCCAC CCTCACCCAG CTTCCTCCCT GGACCTTGAC CGGGAGGGTG CAGGAGGTAA 420
GCCTTTGGGA GAGGCAAGGA CTGCGACAGT AAAAGCGCCT AAACTCGCCC ACGACCCGGG 480
CTGGGGGATA ACTCAAACTT TCCGTGCCTG GAAAGGCTGC CTGGCGGCGG AGGCGGCGCC 540
GGCGCGCGGA GTCCCTGCGG GCGCCCGCAC ATCCCAGGCA GCTGTGCGTT CGTTGGGGCG 600
GTTGCGCGGG CGGCCACCGC CCCCCAAGGG CAGATGGGGC ACGGGGCGGT CCGCGGGGTC 660
CGGCTTCCAG CCGCCCCCGC CCCGCCCGTC GAAGCAGAGC CCGTGAGTTG CCTCGCGCCG 720
CGTCCGCGGG GCTCAGACCG TTGGCAGCGG CAGTTCGACC GTTGGCGGCG GGACTCAGGC 780
GGCTCGCGGC GTCGGCTGAC AATTTCAACC CCCCGCCCCC GCCCCTGTCC CATCCCAGGG 840
CACTCCGGCG GGGGTGAGGG GAGGACCAGA TAGCACGAGG CGACTCCAGG GAAAAGTTTT 900
GTGGCGCCCG CTGCGCCGCT CCGACGGCCC GGGGACTGCG GGAACCCTGC CTCCCACGCG 960
GGCCCGAACC ACCCCCGGGA GCCACCCGCC 990
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