Tag | Content |
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EnhancerAtlas ID | HS108-39993 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:125900100-125901670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYB | MA0100.3 | chr8:125901271-125901281 | ACCAACTGTC | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 125901034 | 125901439 | chr8 | 125900200 | 125900990 |
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| Number: 2 | ID | Chromosome | Start | End |
GH08I124889 | chr8 | 125900581 | 125900750 | GH08I124888 | chr8 | 125901061 | 125901250 |
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Enhancer Sequence | CTTCTCAGAA ATACCAGCAC CCTAACACCA GAGCATTTCT TAGTACTTTG CTAGATAGAG 60 TTTCCTCTCT GCAGGAGGTT TTCAGGCCTT AAAAGTATAT CCATTCTAGC ATGTCCTCTT 120 CTCGGATATT TTGACTCCTT CCAAATCTGC CACCATGACC TGGCATTCTG TCACCTGGTG 180 TTGGCTAGGC TTTCTCAGAG CTTCCCAGGA CCATTCTAGC AGTATGGCAG CACCATCTTT 240 CACAGTCCTT GCCACGATGT TAAATCCCAC ATTATGATAG AGTGCCCCAG TGCTGATAAG 300 CACTACCTCA GCCAGCTTGA CATTCTGATC CTCTGGACCC AGCACTCTCA AGATCCAGTC 360 CTATTCCTTC TTGCTTCTGA CTGTACGTGC AGACTGTGCA GACCATGTCC CACACCCAGC 420 TCACTTGGTG GATAATGCTA TTCCTTCCTT GCTGGACCCA GGACTTCCCT GTCTGAGTTA 480 CATTGTGACA AACCTCGTAG CTCCTGATCT AGTGCCAGGA GGGAGGTGGA GGAAAGTCCT 540 GGGGAGAGAG AGTTACAAGG TAGAGGCCTC TGAGTCATCT TGTGAGCGTG GGGAGGAGAA 600 CCTGGAACAG GGAGCTGTGG GCTGCGTCTG CAGGCCCTGA GGGCTCCGAG TTATCTAGAG 660 ACATTGGCAT AGATATCCCC ACTGCATCTC AGGGCCCCAT TTTTTCTCAT TAGATCCTGA 720 CTTTGCCGCA GCAGTTCTGC TCTATTCGGG AATGTAAACT TCTTGAGAAT CTGGCTACTT 780 TTATGATTAA TCCTGGTCCT TATCCTCAGC TCTATCTTCT CTCCTGGCTT CAAGAGTTTC 840 TTGTATGCTG ACAAGAGGCC CTCTGGCTTT CACATTTAGC CTTTAATTGC TGATAAAACA 900 CCTTCAGCCT CTTATCATTG AGGGTCTTTT TTTTTTTTTT TTCCTGTTCA AAAGGATCTG 960 TTTTCTCCAA CAACAGCCAT CCAATTCTAT TGTGTCTATA CTACTCTGTC CACAAGCTTA 1020 GCCTGATCTA TTGCTCCCAC CTGGTGTACT ATCCCAGTTC ACCACTGGGG ACAGTGTCAA 1080 TTGCATTGGT GCACATGACA GGGACTGCTG TTGCTCTACC TGCCACCAGT GATGGAGTTC 1140 TCAGAGTCTC TTTCCTAAGG TCATTCCTGG CACCAACTGT CACAGGTTAG GTTTCTGGGG 1200 AAACGGACGT CGAGATGGAA ACTCACTGGG GGAAGGGGGG AATCTCAAGA TGAACAACCT 1260 CAGAAGGGAA AGAAGCAGGA CTGGGCAGAG GGAGAAGGTG GCCTGTGTTA CAGTTGCAAC 1320 AAAGGCTGTC AGTGGATCCC ACAGGGATCT CTGGAGCTGG GATGGCCCTG CCTTGCAGCA 1380 AAGGGAAACA AGCATTTATA CCCCTTCATT GACCAGTCAC TGAATGCAAG GTGCCCCAGG 1440 AAAGGAGCAT AACCTTTAGC CAGGTAGCTC TCTTTGTGGG GTAGGGGTGG GGACACACGA 1500 CACTCCCAGC ATCTCTGGGC ATGAGGGCCT CCGTCCCAAA GAGGAAATTT GGATAATGCA 1560 TCCCAGCCTT 1570
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