Tag | Content |
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EnhancerAtlas ID | HS098-31319 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:120994730-120995510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr2:120995484-120995505 | CCCTCCCCTCTCCTCTCCTTT | - | 6.33 | ZNF263 | MA0528.1 | chr2:120995462-120995483 | TCCCCTCCCCTCCCCTCCCTT | - | 6.47 | ZNF263 | MA0528.1 | chr2:120995472-120995493 | TCCCCTCCCTTCCCCTCCCCT | - | 6.9 | ZNF263 | MA0528.1 | chr2:120995466-120995487 | CTCCCCTCCCCTCCCTTCCCC | - | 7.03 | ZNF263 | MA0528.1 | chr2:120995479-120995500 | CCTTCCCCTCCCCTCTCCTCT | - | 7.08 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27989 | chr2:120995243-120998525 | Fetal_Intestine | SE_28776 | chr2:120995138-120998740 | Fetal_Intestine_Large |
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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 |
GH02I120237 | chr2 | 120994937 | 120998381 |
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Enhancer Sequence | GCCAAATCTC CCCTCTGATC ATTTTGGACC AAGTGCAGTG AGCATGAGTT GGAGGTGTCC 60 TCAAATTGCA ATCCTCTGGG GTCTTCCTCT GTCTCTTCTT TTCGGGTGAG TTTGGCAGCG 120 GATGTGAGGA AGGTGCTCTT CATCAGTCGC TGGGTTCATG AATGGTCCTC ATTTCCTGAA 180 TCCTTCTGGA TCATTCTCTG AATTCAGCAG GGGCATGTCT CCCTGGGCTG ACGGGTGGGG 240 CTCCAGGTGC ATCTGGCTGC AGCACTCTGG GAGGGGGCCC GAGGTGCATG CAGATCTTGA 300 GTGGGTCTCA GAGAAAGAGA CACACAGGCC CCACATGCGT GTGCACACGC ACACATGGGC 360 ATGAATGTGG GTACGAGGCA TGTGTGCTCC ACACGCTGAC TTCACTGGGA ACACTGACCC 420 CAGCTGCAGA GAGACCGGAG CAAGGGCTGA GGGAGGCAGA GTGAAGGAGC GCTCATCCCT 480 GGGAGGGCGC CTGGGAGGAG AAGTGAGTCA TTGACCAGTG GTCATGGTGA GTTTGCCTTA 540 CGGAGCCATC TCTGGAGCCT GAGGTCACAG GGTCTCTGGA ACTGGCCCTT CAAGTTCCTG 600 GGAAGGGTTT TGACAGGGAA GTCGTCCACA AGGGCTTTCC CCCACTGGAA CACTGCCTAG 660 CCTTCTCAGA AACGCCCCAT GTCTGTGGCA GGCTTGGTGT TCCTCCTGCC ATTCCAGGCT 720 TTCTGCTGCC CCTCCCCTCC CCTCCCCTCC CTTCCCCTCC CCTCTCCTCT CCTTTCCTTT 780
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