| Tag | Content |
|---|
EnhancerAtlas ID | HS176-21497 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:120994900-120995890 |
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 |
|
| | 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 |
|
| | 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 |
| GH02I120237 | chr2 | 120994937 | 120998381 |
|
Enhancer Sequence | ATTTCCTGAA TCCTTCTGGA TCATTCTCTG AATTCAGCAG GGGCATGTCT CCCTGGGCTG 60
ACGGGTGGGG CTCCAGGTGC ATCTGGCTGC AGCACTCTGG GAGGGGGCCC GAGGTGCATG 120
CAGATCTTGA GTGGGTCTCA GAGAAAGAGA CACACAGGCC CCACATGCGT GTGCACACGC 180
ACACATGGGC ATGAATGTGG GTACGAGGCA TGTGTGCTCC ACACGCTGAC TTCACTGGGA 240
ACACTGACCC CAGCTGCAGA GAGACCGGAG CAAGGGCTGA GGGAGGCAGA GTGAAGGAGC 300
GCTCATCCCT GGGAGGGCGC CTGGGAGGAG AAGTGAGTCA TTGACCAGTG GTCATGGTGA 360
GTTTGCCTTA CGGAGCCATC TCTGGAGCCT GAGGTCACAG GGTCTCTGGA ACTGGCCCTT 420
CAAGTTCCTG GGAAGGGTTT TGACAGGGAA GTCGTCCACA AGGGCTTTCC CCCACTGGAA 480
CACTGCCTAG CCTTCTCAGA AACGCCCCAT GTCTGTGGCA GGCTTGGTGT TCCTCCTGCC 540
ATTCCAGGCT TTCTGCTGCC CCTCCCCTCC CCTCCCCTCC CTTCCCCTCC CCTCTCCTCT 600
CCTTTCCTTT CCTTTTTTTA AATAGAGATG GGGTCTCCTC ATGTTTTCCA AACTGGTCGC 660
AAACTCCTGG GCTCAAGCAG TCCTCCCACC TTGGCCTCCC AAAGTGCTGG GATTACAGGT 720
GTGAGTCACC TTGCCCAGTA ATTTGTGTAA GCATATACCT TGGATTCTCT ACTAAACCGC 780
CTAGTCTTGC CAGTCACTTC CTAGTCTTTC CTGCCTCCTG GCCTTCCTTT ATCTCAGTCC 840
CCTGCTGCCT GGAATGCTCT AATTCTCTCT CTTTCTCTCC CTCTTTTGTG TTTGTCAGAA 900
TCCTCATTGT TTTTTAAGCC CACTCAAGCC TCAAGCTCCA CCTCTCCCAG GAAACATGGG 960
GGCCTACTTT AGTCGAAGAA GACTCTTAGC 990
|
