Tag | Content |
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EnhancerAtlas ID | HS010-01530 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr14:106284020-106285270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIL3 | MA0025.1 | chr14:106284620-106284631 | TTATGTAACAT | + | 6.32 | SPIB | MA0081.2 | chr14:106284633-106284645 | AAAGGGGAAGTG | + | 6.07 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_10471 | chr14:106282350-106287664 | CD19_Primary | SE_11221 | chr14:106281431-106290963 | CD20 |
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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 |
GH14I105816 | chr14 | 106282521 | 106287846 |
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Enhancer Sequence | GAGGTCTTGT CCAAACCAAT GTTTTCTAGA ATAAACTTGG CAGGTATAGA GCCGGCTGTG 60 GCCACAGCCA CAGACATCAG GGCCTCGGCT GGAGAGGAGA GGTGCAGGCC TCTGGAAGTC 120 TCTTTGGGGC TGGAGACTAT GGCCTGATTT CTGTCCAGGT CTTGGGGGGC CTCTGTCCAC 180 AAGTCTAGGG GGGCAGAAAG GGCTCAGACC CTTCCCTCAA AATACCAAGG GAGAGGAGGT 240 CGGCTGGGCC CAGGCAGGTG GCTGGTGGTG AGCGCCCCGA GATCAGGCCA GGCTTGTCAA 300 GCATTGATTT AGGTGTGGGA GGCAGACATG TCCTGTTTGT TACCAGCTGG AAACAGATGT 360 TTCTGCCCCG AGTGCCACCT CAGAGGGTGG CGTCCAGGCC CAGCAGGCTG TGGCGACACG 420 GGTGAGCTGC AGAGCGTGCG GAGGCGAGGG CCCTGGCCCA TGTCAGGAGG CTGAGTTACG 480 ACTGTGGCTT CAGTGCCGGG AAAGCTGTAA ACACATTCCT GTGCGGGGCC CTGGGCCACC 540 TGGGGCATCA CATGCCCCCA GAAGACAGAT TTCTGTAGTC AGTCAGGACT CAATGGACAT 600 TTATGTAACA TGGAAAGGGG AAGTGGTGCT GGAGGGCAGC CCCCTGAATC ACTCTGTTGG 660 AGCAATTCTG TTGGGTGAAG GTGCATGAAA ACAACACAGT GTGGCTGAGG GCCAGGGCTG 720 TAGACATTCG GTCAAGTGCA CAGGCTGTGC TGGAGCAGCC CCGGCACTAG AAACAGGCGC 780 AGGGTGGGGA GTTTGCTGGG GTCAATGTGC ATTGCGTCGT GCATTTTAGG GTATTTCCTA 840 GGTATAATTG CTAGAGAGAA ACAAAGCTCA AATACAGATC ATCTGCCCCA CACCAGGTTC 900 CCACCATCCT CAGGGGAATC ACAGGTTACT GGCTTTGGAG ACCGAGATGT CTTCCCGCCT 960 CCCAGGGGCC TGTGGATGGG ACTCCCTGCG AATTCGACTC CCAGGGGAAA AGCCAAGAGC 1020 TGCCTCCTTG GGACAGCTGG GCAGCAGCTG TGATCGCACA TGGCTCAGGC AGAGGCCTGA 1080 GCGGCTGCCT CCGTTGGCCA GCAGGCTCTG AGAGCACTCG CCCGGCCTGA CTGTTCATCC 1140 ATCCTTTCAC CCGGAGGCCA GCTGTGGCTG TCTGTGCTCT CAGAGGGGAG GCGATGGCAA 1200 GGCGCCTGCC ATGCAGATGG GTGGTGGGAG CGAGCCTGTT ACACTCTGAG 1250
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