| Tag | Content |
|---|
EnhancerAtlas ID | HS010-01501 | Organism | Homo sapiens | Tissue/cell | B_cell_blood | Coordinate | chr14:90186670-90187740 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr14:90187515-90187526 | AAAACAAAGAA | + | 6.62 |
| | | 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 |
| GH14I089718 | chr14 | 90185172 | 90189541 |
| Enhancer Sequence | CCCATTCTGG GGTAGTGTCT TTGCAGCAAT GTGAGAACGG ACTAATACAA TGGGGAAATT 60
AAGAAATGTA CCCAAGGTCA CATCTGGTAA AGGAAGAATG GGGCTTTGCA CTCAAGCAGT 120
TTCTTAACCA GTCGTGAAGA TTCTTGTTAG TGGGGCACTT ATGATGTGCC ACATGCTTTA 180
CGTGAATTAT CTCCTTTAAC TTTCACAGTG GCCCAACAAT ACAGTGCCTA TTATCATCCT 240
TGCTTCATGA AGAAGAACAC GAGGTTTAGG AGGGTTCACC CTCTCAGTCA AAGTCCCTGA 300
AGTGCAGAAC TTGGCCAACC CCACAGTGGA CTGGCTTCTG CTAGGCAGTT GGGAGCCACT 360
GCCATCTCCA AACAGCAGGA AGAGATGCTC AAAGCTGTGC TTTTGAAAAA TCAATCTGGC 420
AGTAGTGGAG AAGATACACT GTCTTTTCTC AGCTCAGCAT ACCAGTTGGA AGGCCTAACC 480
ACAGAGCCAG CAGGCGGCAG AGCTGGGGGT TAGATCCCAC ATCTACCTGA TTCCAGCACC 540
CTTGCTCGAA TCCCCCAAAC CTAGCTGCTT GAGGCCAGAT GAAGGCTTCC GGCTTCACAA 600
GTGCCCTTCC CTCACTGCGG GTGCATTGGC ACCTCACTTC CTTGCCACAC TTCCTCTTGT 660
TTTGAACCAC TATATTGGCT CATCTCAGCA GCAGACAGTT CCTCTGAATA GAGTATGCCC 720
TGAAAAGTCA AAATCTACCA CCAGCTGGAG CTGGTAAGGC TGCAGTACTT CCTGTTGAAT 780
CGGGTCTTGG GGCCAGAAAC CACATTGTTA TTTATACCCG AAGCTCTTTA TTCACGGTGC 840
TTTACAAAAC AAAGAAGGGG CAGCCCCCTG TCTTATGGAG CCAGCAGACC CCAGAGATAC 900
AGAAGACAAC AGACAATAAT AAGCCCTCTC CCCTCTCCTT AAGCTGTAAC TTCCATCCTG 960
CCTGACCAGT CCCTGCCACT GCCCCTTTGT TTCTTCTATT ACCTTCCTCT GAGCAGTCTT 1020
ATTATGGAAA TAGACTCCTA ATTAACACAT CAGGTTTCCG CTTTTCCAAA 1070
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