Tag | Content |
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EnhancerAtlas ID | HS049-06572 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr6:27720070-27721390 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr6:27720876-27720893 | TGGATTCCAAGAAAGCC | - | 6.18 | Mafb | MA0117.2 | chr6:27720348-27720360 | AAAATGCTGACT | + | 7.22 | ZNF263 | MA0528.1 | chr6:27721308-27721329 | TTTCCCTCCACCCCCACCTCC | - | 6.63 | ZNF263 | MA0528.1 | chr6:27720985-27721006 | AAAGGAGGATGAGGGTGAGGG | + | 6.85 | ZNF263 | MA0528.1 | chr6:27721302-27721323 | TCCCCCTTTCCCTCCACCCCC | - | 6.9 | ZNF263 | MA0528.1 | chr6:27721299-27721320 | TTCTCCCCCTTTCCCTCCACC | - | 7.38 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I027751 | chr6 | 27719661 | 27722579 |
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Enhancer Sequence | AGGAGGTTCC CCCAAAGTAC TGCTGGCCAC CATGCACTGC AGGAGGTTCC TACTAGGTAA 60 ACTGCTCAGG CTGTGGGAGC CAGGCCACTG TGCACAGTAA CGCCAAGAGA TTATTTCCTC 120 CAGCAATGTC TCTCCATCGC CCTCTATTGA CAAAATTTAA TATTGAGCTA AACTGCGACA 180 GAAAATATTT AAAGGGCCCA GCTCCGTTCC ATTGTTATGG AGCAAGGAAA AGTGATTTTG 240 CTGCTGAGAG GTAATAAATA GATAACCGGA CAGAAGAGAA AATGCTGACT TTCTTTGGAC 300 TGGTTCGAAT TCAAACACAC TTTTATATCC TTGTCCAAGT GCACAATCCA TGGTGAAAGT 360 TTAAGAGCTG TCAAAAAGTT TGTTTTGGCC GGGCGCGGAG GCTCACGCCT GTAATCCCAG 420 CACTGTGGGA GGCCGAAGCG GGTGGGTTAC CTGAGGTCAG GAGTTCGAGA CAAGCCTGGC 480 CAACATGGCG AAACCCCATC TCTACTAAAA ATACAAAAAT TAGCGGAGCG TGGTGGTAAT 540 CCCACCTACT CGGGAGGCTG AGGGAGGAGA ATCGCTTGAA CCCGGGAGGC GGGGGTTGCA 600 GTGAGCCGAG ATCGTGCCAC TGCACTCCAG CCTGGCAACA ACAGCGAAAC TCTGTCTCAA 660 AAAAAAAAAA AAAAAAAAGT GTTTCCTCTC TGTGCTTCAG CAAAAAAAGA GCAAATCCAA 720 TTCCCCGAAG GGCTCAAAGC GAAGCGCTCT TCCTTAGAAA TCCCCGAGGA AACCCCCTCC 780 ACGAAAAACC CGCAAGTGCT GCTCTCTGGA TTCCAAGAAA GCCTGTCTCA CCTGCGAGGT 840 GCAGGCGGGT GGAGTTCTGG GACTCCGGTG CCTATTGGGA TTGACACCAC CGGGGTCACT 900 CAGACGGAGA TCAGAAAAGG AGGATGAGGG TGAGGGTTCG GCGTGGGGTA GAGAAAGGTG 960 TGACGCGGGA TTCAGCGCCA CGTCGCTGGG TGACGGAAGG AGTACAGAAG TTGAGGGTTC 1020 ACGTGCTCGG CAAAAAGCAA AGATTCTATT GGTTCAAATG AAAATACTCA AAAACAGAAT 1080 TAGCGATAGA AAAAAAAGCG ACTCTCTTTG TTTCCGCCCG GTTTCGAACC GGGGACCTTT 1140 CGCGTGTTAG GCGAACGTGA TAACCACTAC ACTACGGAAA CCAACGGTTA CAAAGCTTCT 1200 TCTTTTTGAC CTAAAAGACT AGTCCTGAAT TCTCCCCCTT TCCCTCCACC CCCACCTCCG 1260 ATTTTTTTTT GATTATGGTG AATTACACAC TTTCACATTT ACTATTTATA ATATAAAAAC 1320
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