Tag | Content |
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EnhancerAtlas ID | HS146-00768 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr1:110469420-110471200 |
Target genes | |
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) |
GFI1 | MA0038.2 | chr1:110470377-110470389 | TGCTGTGATTTG | - | 6.52 | Gfi1b | MA0483.1 | chr1:110470377-110470388 | TGCTGTGATTT | - | 6.62 | RELA | MA0107.1 | chr1:110470914-110470924 | GGGAATTTCC | + | 6.02 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_00603 | chr1:110467604-110475254 | Adipose_Nuclei | SE_04393 | chr1:110469347-110472853 | Brain_Anterior_Caudate | SE_06043 | chr1:110464238-110474855 | Brain_Hippocampus_Middle | SE_32320 | chr1:110469375-110474485 | Gastric | SE_47194 | chr1:110462831-110479044 | Panc1 | SE_50838 | chr1:110468044-110473482 | Sigmoid_Colon | SE_53269 | chr1:110469281-110473349 | Small_Intestine | SE_53713 | chr1:110465215-110474535 | Spleen |
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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 |
GH01I109925 | chr1 | 110467674 | 110475106 |
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Enhancer Sequence | CCACATCCCT AAGATTGTAA GCCCCTTGAG GGCAGGGACT GTCTTCCACT TTTTTTTGTG 60 TTTCTTTTTC CATCCTGGGT TCTACTAAGA GAGGGCCTCT CCACATTTGC CAAACATGCA 120 ATAAATGTTG ACTGACTGGC TTCAGGGCTG ACTCACGGAC TGACCCTGGC CAGCTGTCTC 180 TAACTGACCA GCCTCTAGCT GACCAGTTAA CCAGCTAACT GACTGACTCT GACTGACTGG 240 CTGACCAGCT GGCTGGGTGA ATGACTAACC AACCAACTAT CTTGGTAACT GCCTAACTGA 300 CCAGCTGTTG CTTGGGGAGC CCATTGAGCA ACTGACTAGC TGATTGCCTG ACTAATTGGC 360 TGGTTGGCTG ACTAGCTGGG GTGACCCAGT CAAGTTTCCA GTCACATCCT TTACCAAGTG 420 CAAGCCAGTG CCGCAGGGCT CTCCCATGTG TGGAGTGACA GGTCTGGGCC CCTTCTAGAG 480 AGATAGGGAA TTTGGCAAAT GCTCAAAACC AGGGGAACCT ATTTAGACAA GAACCAGCAG 540 TAACAACATA TCTGGAATCC TGGGGTCTAC CTTGTCAGTG GGGTGGGCTA AGATGGGTGA 600 GTGGGTCAGC TGGGGCACTG GCAAGACTGT GAAATGACCC AGGCCTCCTC AGAACTGGTT 660 GCTGGTGGCT CAGTGCCACA ACACCCTTCC CACGGGTCGT CTGTCCCCAA ACCCCTCGCC 720 GTGGTCTTGG CCCTCTGTCC CACCCCTCTA CACGCCCACC CTCCTTTCCC CACTTGCTTA 780 TTCTCAGGCC CGTCCCAAGC TTTCCTCTTC CCCCTCAAGA TTTCACTTGG AGAGGGAATC 840 CAGGGCAGGG GCTACATCCA GATCCCACTT GGCCCGGCAG GTCCAGCCCT AAGGTGGTCT 900 CCAGGCCAGG CACCAGTGGC CTTGGAGAGA TTGAGTGCCA GCCCCTAGAG TGACTGCTGC 960 TGTGATTTGA GAAGTGAGAG AGAGAAACAT AGAGGCAGAG ACTGAGATAG GGACTCAGAG 1020 CCACAGAAAA TGCAGACACC AGCACCTCAG CCCTAAGCAG CTAGAAGATG GGGCAGCAGG 1080 CTGGAACTCG CTCACTGGGT CCTTCTCCCC TCCTGGGCCC TAGCTGGGCC TGTGGCCTGG 1140 CTGTACCCAG CATGGCTCAT GTCCAGTTTA TGGTTCCCCT TCTTTCCCTC TAGAGCATGG 1200 GAATGGGCAG GGAGCCAGAG GCTGTGGTTC CATCTTCCCT CCTTACCCAG TAGGGCCTAT 1260 GGATGTTAGG GAGGGAGGCT CCACACAAGG TCCAAAGTCA AACTGTTGGA TGGGGTCCAG 1320 GGGATTTCTG CTCTGGGAAC AAAGCGTCCT GAGGATGCTG GGCAAGAGGA CAAGGATGGG 1380 GGTGGAAGGC GAGAGGACAA GGCCCTGACT CCCATGGATG ATGCGGGAGG CAAGGCCCTC 1440 GGCCCATCCA GGAGGGGCTG GGTTGCTTAG GGGTCGCGTG CCAAATGACA GTGTGGGAAT 1500 TTCCTTGTCC TGGCACTGCC TCTAGACTTT TCCTCTCTGG CCCAAGTTGT TCCTCTTCAG 1560 CTAGCTCTGC CCTACTGTCT TGAACATCAT ATGTGATGCC CCTCTGATGA AATGAAAGAT 1620 TCTTCTTTGC TAGTGTTAGC AGGAATCACC CTTTGTTCAC TGGACCAAGG CCAATGAGAT 1680 GACCTCGCCT GAGGAGGGGT CCAAAGACAT TCAAGTGCCC GCTTCGCTCC TTGTCAGAGC 1740 CCTCTGCTTG AGCAGTAACC CCTCTTCCCA GCCCTGCCCA 1780
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