Tag | Content |
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EnhancerAtlas ID | HS141-16475 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr6:160409580-160410620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr6:160409792-160409803 | TTTGTTTACTT | - | 6.62 | MYC | MA0147.3 | chr6:160410340-160410352 | GGGCACGTGGGG | - | 6.07 | NFE2L1 | MA0089.2 | chr6:160410370-160410385 | TGTGCTGAGTCATTG | - | 6.99 | Nfe2l2 | MA0150.2 | chr6:160410372-160410387 | TGCTGAGTCATTGCC | - | 6.8 | SOX10 | MA0442.2 | chr6:160409853-160409864 | GTCTTTGTTTT | - | 6.14 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_25413 | chr6:160409422-160411292 | DND41 | SE_39766 | chr6:160409533-160410650 | Jurkat | SE_40281 | chr6:160409568-160412134 | K562 | SE_53717 | chr6:160409870-160410870 | Spleen | SE_64757 | chr6:160409420-160411660 | NHEK | SE_66412 | chr6:160409533-160410650 | Jurkat |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 160409611 | 160410525 | chr6 | 160409606 | 160409719 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I159988 | chr6 | 160409584 | 160411846 |
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Enhancer Sequence | ATTTTAGGTA CGTGTGGATC TCTTTAGCGT TGATTCCTAC CAGTTAACTC ATTTTAAATG 60 ACACCCTCAT GCACCAATAT CATATACTTA GGATTGTGAA ATAGTTTAAT GATGCCACTG 120 CCGCTACTTG AAGTTTGTCT CTGTTATCCT GGAGAAACTA GTCATGGCTC CTGAATAAGA 180 GATTAGCATT TTTCCTGAGT AGTAGCCAAG TCTTTGTTTA CTTGTTTATC TTGTATCCTG 240 CAACCTGGAA TATACACTCC GAGAGGGCAG GGCGTCTTTG TTTTGTTCAT TGCTGTACTC 300 TCCTGTGCCT CCCGCAGTAA GTACTTAAGA AATACTTGTG AAACACATGA ATAAAGGTTA 360 ACGAAGGGCA AAGGAAACAA GCCTTTATTG ATGATTTTTC TCTGTGCCCA GTAATACTTG 420 GGTTATTTTC TCATGTCCTT GAGTCATCTT GACTCTAGGA GACACCTCTT AACATGTTCC 480 TGCTGAAAAA GCTGAGCTGA GGAGTCATAC CCCGAGGGTA TCACCCTAAG ATTGGGCACC 540 TGAGTACCCC AGCCTGCTCT TCAGGTCTGT AGCTGCTTAG TGGCTATCAG ACCTTCCAAG 600 TCTCCATGCT TTTGAAGGCC TATGTGTGCG GTTTGGTTTC TTGGCAGGGG GGTTTGATGG 660 GTTCCCAGAC CTAGGAGTTC TTGGCGCCTC GTCTTCCAGT GACCCCACCA GGGCTGCTCT 720 TTCTCCTCCA TTGCTGAAAC TAGTTCAGGG TTGGGGAGGA GGGCACGTGG GGGGGCCTGG 780 TGGTTGGTTT TGTGCTGAGT CATTGCCTTG GTGCACTGTG GAAGGAAGCT CTGGGAGGTG 840 GACGGCTCCT TCTGTGAGGG AGTGCTTCTG TCGTCAAGGG AGTACTGCAT AGGGTGAATA 900 ACACAGTTAT GTAGATATAT ATGGTGGTCT TACCCCCAGG GCCTCCACAA CTCCTGGATG 960 GGCCTAGCCT AAGCAATTCT GATTTAACTT ATTGCCCCTC CTTTTAGCAA TACTGTTGAG 1020 TTAAATAACA GTTTTTGCAT 1040
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