Tag | Content |
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EnhancerAtlas ID | HS196-11202 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr16:70641650-70642980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr16:70642250-70642265 | TGAACTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_29256 | chr16:70641988-70643157 | Fetal_Intestine_Large | SE_54230 | chr16:70642379-70642888 | 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 |
GH16I070608 | chr16 | 70641989 | 70643157 |
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Enhancer Sequence | TTCTTTTTTT TTTTAATTTT AATTTTTAAT TTTTTGAGAC AGAGTCTTGC TCTGTTACCT 60 AGGCTGGAGT GCAGTGGCGT GATCTCGGCT CACTGTAACC TCTGCCTCCT GGGTTCAAGC 120 AATTTTCCTC CTGCCTCAGC CTCCCTAGTT GTTGGGATTA CAGGCGAGGG TCACCATGCC 180 TGGCTAATTT TTGTATTTTT AGTAGAGACG GGGTTTTGCC ATGTTGGCCA GGCTGGTCCC 240 GAACTCCTGA CCTTAGGTGA TCTGCCGGCC TCGGCTTCCC AAAGTGCTGG GATTACAGGC 300 GTGAGCCACC TTGCCCGGCC GGTTTTTCTT TTTTTAGTTT GTTAACATGG TGAATTATGA 360 TGATTGATTT TCTTTTTTCT TTTTTTTTTT TTTTTTTTTG AGATAGAGTC TTGCTCTGTT 420 GCCCAGGCTG GAGGGCAGTG GTGTGCTCTC GGCTCACTGC AACCTCTGAC TCCCGGGTTT 480 AAGCCATTCT CCTGCCTTAG CCTCATTTGT AGCTGGGATT ACAGGCATGC ACCACCATGC 540 CCAGCTAATT TTTGTATTTT TAGTAGGGTC AGTGTTTCAC CATGTTGGCA AGGCTGGTCT 600 TGAACTCCTG ACCTCAGCTG ATCCACCCGC CTTGGCCTCC CAAAGTGCTG GGATTATGGC 660 TTGAGCCACC ACGACCGGCC TTGATTTTCA AATATTAAAC TAATTTTTCG TTCCTGAAAT 720 TGCATATGGG ATTAGGAGAT TAGGATACAG GGATCTAGGT GCCCCCAGCA CATGGTGGGT 780 CTGGTTCCCC AGTAAAACCC AGTTTTGGGC CTGGTCATCT GGTAGAGGGA GGGAGGAGGC 840 ACAGATCAAG GGTGGGGAGA GGGCTGACCT CCAGACACTA TAGCCTCTGC CGCCAACTCT 900 GAGCAGCACA GGTGAGTCAG CCCAGGTGAG CCTTAGGCCA AGGCCGTGCA GGCGACTGCT 960 TCCCACAGCA GGTTCAGGTG GGGCAGGCTC TGCTGCCTCT CTCTCTTGCC TGGAGAGGCA 1020 CCTGGGGCTC ATCATGGGTT CAGTGTGCAG ACTTGCACCT CAGCCTCACG CCTCAGTCTC 1080 TGCATCTGGG AAGCTGGGAA GCAGAGCTGG CCCCAGGGAA AGCTCAGGCA GCGAGGAAGG 1140 CGGGGTGTGG GGGCGGGTGT TGCCACTCAG ACCTGGTTCC AATTGTGCTT CCCTTCTCTG 1200 TAAAATGGGG GTAATCATGC CTTCCTTCCA TGTGATATGA GCTGATGGTG ACAAGCCACT 1260 TAAATACATG AGAGGAAAGC ATAATTCTTT TATTTTTTAT TTTTATTTAT TTTTTAAAAA 1320 TTATGTTTAT 1330
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