Tag | Content |
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EnhancerAtlas ID | HS141-15353 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr6:220340-221750 |
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) |
NKX2-3 | MA0672.1 | chr6:220544-220554 | ACCACTTGAA | + | 6.02 | ZNF263 | MA0528.1 | chr6:221340-221361 | TGAGCAGTAAGGAGAGGAGGA | + | 6.16 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_32523 | chr6:216889-224055 | GM12878 | SE_58847 | chr6:180087-237324 | Ly3 | SE_61383 | chr6:208326-237283 | HBL1 |
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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 |
GH06I000219 | chr6 | 219489 | 222459 |
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Enhancer Sequence | TATTGTACAT TGATTCATAT AGGTCCTGTA TTTTTGTTAC AGTTATTCCT AAGTATTTTC 60 CCCAATTTTT TTAAATATTT CAAACTCACA AAAAAGATAA AAGAATAGTA CAAAGAACCG 120 CTGTTTGACC TTCACTGTAG ATTGATGAAT TATTAACATT GGCCGTATTT GCACTCTCTC 180 TGCCCCTCTC TCTTTGTTTT AGAAACCACT TGAAAGTAAG TTGCACAGGC CATATTTAAA 240 AATTTCTGGA TGTTTCCTAA CAACAAGGAC ATTCTCCTAC AAAACCACAA TATTATAATC 300 ACACCCAGGA ACTTTAACGT AAGTTTTAAA ATATAGTTTA AAACGGCTTT AATATATAGT 360 TTAAAATAGT TTTAAATATA GTTTGATTCA GAGCAGAATG TGTTGAAGTT TAAAATACAG 420 TTTGATTCAG AGCAGAATGT GTTGAGAGAA ACTGAATGCA CGTAGCTCAG TTCCAGTTGC 480 TGAAGAAATT CAGCCTTCCC CTTCTCTAGC CTGCTTGACT TGAATCAGCA GTCTTGAGTT 540 TGCATTATTG CAAGTCCTAG GCTCTGCCGT CCCCCAGCCC CTCACCTCGG TGCTCTGCAA 600 ATGCTGAATT TCTACGCTGT AGGCACCTAG ACCCTTAAGA AACAAGCCCA AGCCAAGCTA 660 CCTGCTTTCT CGTCTCTGAG GCCAGCCTCT GGCCTCCCCA GGCAATGTCA TGACATTAGA 720 CTAACTTTGG AGAAGTCTGG GAACTGAAGG GAAGCGAGAC AATTCTTGTC ACTCTGAAAA 780 ATATATATAG CTTATTATAT TTCACGGAAG CCTTTTGTTT TGAACTCAAA CGCAAAGCAG 840 ACAGTGGTGC AGGCATATTT TACACATGAG TGCTGTGCAC GGATCTGCTC TATCTCCCCT 900 CCCCGTGTGC CATTTCTAAC TTCATGGGTG CGAGTCATGC TCCTTGTTTC CTGTAAGTGA 960 CCCCACGAGC TCCACTTAGC TCGTTGTGTG AAACTACAGC TGAGCAGTAA GGAGAGGAGG 1020 AGTGATACCA CAAGAAGAGA AAAAGCAGCT TGCCCAGACG GCTGACCATG AAAATGGCCA 1080 CGAACATGAA ACAAGGACCG TTCATTAAGA AAAAGAGACT AGCAACTTTA AAAAAATTAA 1140 ACAAAGTTGC CAAAGACATG AAGAAGTCAT ATGTCGCCAC CTCTAGATTA CTGCTATTCA 1200 AAGATTACTC CTGTCTGTGA ACTTCCATAA AAAGACAGCC ATGGTGAATT CAGAAACCAC 1260 AATACCCTGC CTTTAAGAAT TGGGGTGCTC AAATGGGATT AAGGTGCATT TGAGAGTGGA 1320 CCCTGCAGTC AACAGAGAGC TTTGATGTTT GTGGTATCAA AGTCCTCAAT TTCAGTTATT 1380 TAAATGCAAA GAGTGGCATC TGGGGAGAGA 1410
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