Tag | Content |
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EnhancerAtlas ID | HS108-39366 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:66934400-66935470 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYB | MA0502.1 | chr8:66935114-66935129 | CTCATTGGCCCAGTT | - | 6.36 | Nkx3-2 | MA0122.3 | chr8:66935085-66935098 | ATAACCACTTAAG | + | 6.78 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_58369 | chr8:66892495-66954790 | Ly1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 66935129 | 66935374 | chr8 | 66934931 | 66935375 |
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Enhancer Sequence | ACAGCTCTGC TGGAACATAT ACCGGACCCC CCACCCCGCC CCCAGCAACT CCTGCCAGTG 60 AAATCATTGC TGGGGATGCG GACAGTTCTG TTTTCTTTAC CTTGCCTTGG GGTTTTGGCT 120 TCTACAATAC TTGTTTCTTC CTGGAGTCTT GGGGCCCTGA GAGGCTCTGA GTGACGGCAA 180 AGAACTGTTC TGTTTACCAG TGGGGCGGAG CATGGGGCCA GCGCCAGGCC CTGACTCATC 240 CCCATGTGGA CTCCCTTGGG TCTTAGCACA CTGCGACCCC GGAGTTGGAG CACAGGACAG 300 CTCAGGCAGG CACGCTGAGC TCTGCCTGCA AGGTCAGAGT TGATGGCGAT GCTCCCTCAG 360 TGGGAGTAAG AGTCCATGTT CTGACAGGTA GGTCAGTTAC CCACAGGGGA CCCCAACAGC 420 CATCGACAAG AAGAGGAGGA GATGGATTCT CTATCCACAG GACACAACTC TAACTCTCCT 480 TGGCCTCCAA CACATCACGA ATAAATATAT CACAGCAGTA AGGTCAATAC TCTCACACTC 540 TATGAAAGTA GTAATAGTCC CCAAAGCATG TAAAACTGAG AGATCCAGAT AAAAGCAAAA 600 TATACTTGCA CATAAACTTC ATAGCACACA TTCAACTTCT GTACAGAAGT CACTGTGATT 660 TTCACAATTA GGTTATGATC TAATCATAAC CACTTAAGAC TTGAACATTA AAATCTCATT 720 GGCCCAGTTT TTAGGCTTCC TTCATTGATA GCCATTGAAA ACTAAGTTTA AGCTGAACCT 780 CAGATAATAC CCACAAAACA CAGAATGTCC TAACTCATCT CCATTTGCAT TTGTTGACTG 840 TAACGTTCCC TGATCCTTGT GTTAGTCACA TGCTGCTGCA GCCTGTCGCA TACTGCAGAA 900 TTTTAGAGTC GGAGGGGAAC TAGAAGATCA TCCATTCCAC AGCTTCGTTT CCAGGAGAAA 960 CCACACAGAG AAGTGTCTCA GCTAAGGGTA TCAAGCTAGT TAGTGCTGGG GACTAAAGTT 1020 TAAGCCCCCT CACTCTTAGC CTGGTGGCCT CTCCAATACA CTCTGCCCCA 1070
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