| Tag | Content |
|---|
EnhancerAtlas ID | HS010-03731 | Organism | Homo sapiens | Tissue/cell | B_cell_blood | Coordinate | chr6:710470-711720 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr6:711502-711523 | ACTTGCTTTCTGTTTCACTTC | + | 7.26 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 711154 | 711526 | | chr6 | 710742 | 711015 |
| Enhancer Sequence | TCTGATTTGT CTTTTGCTTT TCACAGCAAC TGAGCACATC ACTGTGTTTT CCCCTTTTCC 60
CTGAAGAAGT AAACTTGTCT TTTTAGTCTC ATGACAAAAG CAGGCAACTC TGGTGGCTTA 120
TATTTAGTTA CAATTTATAA AGGCAGGACT GCGAGTCAAA CCCGGGACGT TTTTTTCTGT 180
TGTGTGTTTG CGTGCTGACG GGGACTGGCT TTTCTTCTTC TTCTTGTAGT TTGAAATGGA 240
AACGCTGCAC TGCTGAGAAA ATACCACGGA AATAGAACCC ACTGCATTCC AGGAAAATAA 300
ATAAGCAAGG CCACCCAAAT TTTCAATGAG TGCTCCTGCA GAATGCAGGA AATGGCAGGA 360
GATCCGTCCG AGGCACCCCA GGCCGGGTCG TGGGTAGAGA GCAGGGACGA GGGCTGGGAG 420
GGGACGCAGG CACAGGGTGA GGGTGGCCCG TCTCCAGGGA GAACTGCGCG CTCACAGGCG 480
GGGCCGGCTT CCCGCATCAG CCCGGCCGGG CTGCAGGTTC TGAGCGAGGG GGCGGCCGTG 540
CCTCACTCTG GGCGGGACGC GGCCTGGTGC AGGGACGCTC ACTTCCAGTG GCATTTCCCG 600
TCTTACACGA TGAGCTTCAT CCACGTTCTC CATAACCCCC TCCCCGCCAC GGGAAGCGTC 660
AGCCACCTGG AACAGCCCTA TTCTGCTCGG TTGTAAAAAG CGTCAGGCGC TTTTGATTTG 720
AAAAGCGTTA GGCCTGGGAA TCGCTGTTGC TCCCTCGGTG GGCACGCCCT GCTGACACGC 780
CCTAGCCCAC CGGGGAAGCC ACTGGCCACG AGGGAGCGAG GCGCACGGGT GTCTTCCCTC 840
CCCAGAGTGA GTGTCAGGGA GGAAGCCAGG TCTTCCAGGG CGCTGACAAG GCAGGGCCGG 900
GCTCCTTCCC TCCGTTGTGT TTCTCTGAAA TGTTCGAATC ACTGGTGTGA CGGGAGCACT 960
TAAAGCCGAA AAAGGAAAGA CGAAAGCAAA GGATTCTTCA GGGCACATGT GTACAGACTC 1020
CTGCTTCCCC TCACTTGCTT TCTGTTTCAC TTCTCAGATC ATCACTACAG CGTTTGCAGC 1080
TTTCCAGCTC ATCATGCTGA ACTGAAGACA AGACGAGGGG AAAATCAAGG GTGGGTTTTT 1140
CCGCAGCACC GTGGTGTCCC GGCTTGGGAT ACGTTTTATC TGTTGTGAGC CTAAACCTTT 1200
TTTACTTCTC AAGCCAGGCC AAATTTTTGG ATCCCCTTCA GGTTGCATTG 1250
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