Tag | Content |
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EnhancerAtlas ID | HS044-05055 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr16:11198310-11199530 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr16:11198475-11198496 | GAGGGAGGAAGGAGAGGTGGG | + | 7.29 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_15354 | chr16:11193626-11201871 | CD4_Memory_Primary_7pool | SE_25367 | chr16:11198153-11202755 | DND41 | SE_31322 | chr16:11198298-11200072 | Fetal_Thymus | SE_33447 | chr16:11190194-11200351 | H2171 | SE_38883 | chr16:11192300-11200250 | IMR90 | SE_45167 | chr16:11198198-11199828 | NHLF | SE_55273 | chr16:11198426-11199968 | Thymus | SE_62880 | chr16:11169251-11234543 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I011098 | chr16 | 11192262 | 11200196 |
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Enhancer Sequence | AGACTATGTC CTCTGCCTGG GGACCTCACC CCCTAAGGAA GGAGAATACC CTGGGCCAGG 60 ATCTGCTCTC TGGAATACCC TTGTGTACTT TTCTGATGAG GTGCCTTACA GAGGAAATCC 120 AAGGGAAAGA GAAGATGTAG CCCCATCTTC AAGAACTTCT CTCCAGAGGG AGGAAGGAGA 180 GGTGGGCCCA TACCACGAAG GTGGAGAAAA ATCACAAGCC CTCTCTGCAC CCCAGCTTAC 240 TTGTTCCCAA CAGCATTCCT ACAAAGTAGG GGTGTCCTCA TTTTTCAGAT AAGGAAACAG 300 CCTCTGAAGG GTCACCCAGT GTAAGGATGC ATCTGCCTTC TTCATCCCTG TAGCCCAGTA 360 CCCGACACAC AGTAGCCCCA TAGCCCTAGG CACAAATGGG GTAGAGAGAC CCTGACCACA 420 TCCTGTGGAA GGTCCAGAGC AGAGCCATCA CAGAGGGCTT CCGAAGACCA GGATACCCTT 480 GTTCCTGGGC TGCTGGGCTG CTGAACAGCG GGGAAGAGGA GCTGTGTGAA CCTAGATTCC 540 ATGTGACTTT ATCTGGCTGC ATAATGAGCT TAAGTATTCA GATCTTTTCT TGGAAATCTC 600 AAGTATTCCA TTTGGCTGCC TCACAGAGTT AGGCAATTTT ATTTACTCAT GCTAAACAGG 660 GCCATTTTCA GAGAGGAAAT TATGCAATGT ACTATGCAAA TGTGGCATTC CGAGAGCAGA 720 GATAAGTGTG GTCACCGATG CATTGTAAGA TGAGATCGTG TCTCTGGCAG CTGGGTGTCA 780 CTTGATAAGG GGATATGCCA GACTGTACTT GGAACTGCTG CTCCCTTGGA CTCGGTTTCT 840 GGTAATTGTG TTTTCACCAA GTTGTCAAGC TGTGAACTGC ACGTATTGAA GAAGAGGAAC 900 AAGGAGTGAA GCTTTTGCAA GTTGCTCATC CTTAAGTAGA CTTCAGCAGT CAGAGAGGCT 960 GCCCCCATAC ATGTTCTGGA CACATGGGAA CAAGGAGGGT AAAATTCTCA TCCTCCATTC 1020 TCCCAAGAAG AGTCTTAAAA TTTGACACGG GGGAAAGATG AAGACACACA ACTGGTTTTC 1080 CTGGCCACTG TGAAAACCAG TCACCTCATT TTACTAGACA TGGCATGTGC CTTTCATACT 1140 GAGAGAAAGG AAGTAGCTGT GGAAAACCCC ACCTTTGGAA GCAGACAGAG CTGAGCCCAA 1200 AGCTAGCACT TCCCCCAGCC 1220
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