| Tag | Content |
|---|
EnhancerAtlas ID | HS062-06761 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr17:7944490-7945680 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:7944865-7944884 | GGCCACCACCTGGTGGCAG | - | 6.35 | | NFYA | MA0060.3 | chr17:7945429-7945440 | TCTGATTGGCC | - | 6.02 | | NFYB | MA0502.1 | chr17:7945430-7945445 | CTGATTGGCCCAGCT | - | 6.42 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CATGGAGACC CAGAGTCAGC CTAGGCCCTG CCAAAACGAG CTGTGAGATC TTAGACCAAT 60
TTTTTCATCT CTTCAATTCT TATTTTCTTC TGTAAAAGAA ACTAAGAATA CCAATCTCGT 120
TTGGGTTAGG AGGAACAAAT GAGAAAATGG TTAAGAATGT AGGTGGTCAG CTGCTAAGTC 180
TTGCACAACT GTGTGCTCTT GCTGTTGTTC CTGTCTTTCA GTTCACTCTG TTCCAACACT 240
CTAGGCTCTT ATAAAACGTA CAGTGAGGTC TCAGATCCAT TGCAACAGCA TTGCCTGGGA 300
GCTTGTTAGA AATCAGAATC TGCATTTAAC CAAGATCTCT ATGTGAGAGG GATTCAAGTC 360
TGAGAGGAAG GGTTTGGCCA CCACCTGGTG GCAGTGTACT TTAATTGCAA ATTTTTCTTT 420
GAAGTTGAAA GCTCAAACCC AAAAGCAAGT TTTGAATGAA TCAAAGAATG AATGAGTGAG 480
AGCATGACTG GCTAGGGGTC ATCAAGTTTG CAGATACATG AATTTACCAT TTCCCTGGAA 540
GGTCTTTGGC TGTGTTGCTT GTTTGAGAAT AGAATTTAGA GATGCCTCGG GCGGCTCCCC 600
CTAAACTATG AAGGCTGAAG TGCCTCTCTA TGGGACACCT ACCAAAGGCA ACTGAAACCT 660
TCTGCGCAGC CCCTGTCCCA GGATAGTCTC GCCTCTACAA GATGCGTCTG TGTTAGTCGG 720
GACTTCTATA GTTGCAAGAA CAAAAGCTAA CTCCAACTAG CAGGCAGAAA AAAAGTTTGT 780
CGGCCAGACA CAGAGGCACT TACAGAAACA CAGGCAGGAA TTGTCCACCC AGTGGAAAAT 840
GGCCATAACT AACAGTCTGT GTTTACTGCT ATAATCTACA TATCCAGAGA GAGACCACCT 900
CTCTGGCTCA GCCCCAATGG CAAATTCCCT GGAAAGGACT CTGATTGGCC CAGCTCTAGT 960
CAGGTGCTCA ACTCTGGACC AATCACCCTT GACCAGGGGA GCCATCTCAC TGTGGGAAAA 1020
TGGCAGCTCC CTTGCAGCCT CCTTGGGTAG AATGGAAGGG CAGCTCCCAG GAGGGCCCTC 1080
TTGGCTGAAG GGGTCTGGCT GTGACCAGGC CCCCCAAGGG GACTGCCACT CCATCTGCCC 1140
TAGCAAAGAG TCTCCCTGAG GCCTCTTGCT GACCACCTTC CCTCTCTACC 1190
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