| Tag | Content |
|---|
EnhancerAtlas ID | HS194-03181 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr2:120994990-120995900 |
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 | AGCACTCTGG GAGGGGGCCC GAGGTGCATG CAGATCTTGA GTGGGTCTCA GAGAAAGAGA 60
CACACAGGCC CCACATGCGT GTGCACACGC ACACATGGGC ATGAATGTGG GTACGAGGCA 120
TGTGTGCTCC ACACGCTGAC TTCACTGGGA ACACTGACCC CAGCTGCAGA GAGACCGGAG 180
CAAGGGCTGA GGGAGGCAGA GTGAAGGAGC GCTCATCCCT GGGAGGGCGC CTGGGAGGAG 240
AAGTGAGTCA TTGACCAGTG GTCATGGTGA GTTTGCCTTA CGGAGCCATC TCTGGAGCCT 300
GAGGTCACAG GGTCTCTGGA ACTGGCCCTT CAAGTTCCTG GGAAGGGTTT TGACAGGGAA 360
GTCGTCCACA AGGGCTTTCC CCCACTGGAA CACTGCCTAG CCTTCTCAGA AACGCCCCAT 420
GTCTGTGGCA GGCTTGGTGT TCCTCCTGCC ATTCCAGGCT TTCTGCTGCC CCTCCCCTCC 480
CCTCCCCTCC CTTCCCCTCC CCTCTCCTCT CCTTTCCTTT CCTTTTTTTA AATAGAGATG 540
GGGTCTCCTC ATGTTTTCCA AACTGGTCGC AAACTCCTGG GCTCAAGCAG TCCTCCCACC 600
TTGGCCTCCC AAAGTGCTGG GATTACAGGT GTGAGTCACC TTGCCCAGTA ATTTGTGTAA 660
GCATATACCT TGGATTCTCT ACTAAACCGC CTAGTCTTGC CAGTCACTTC CTAGTCTTTC 720
CTGCCTCCTG GCCTTCCTTT ATCTCAGTCC CCTGCTGCCT GGAATGCTCT AATTCTCTCT 780
CTTTCTCTCC CTCTTTTGTG TTTGTCAGAA TCCTCATTGT TTTTTAAGCC CACTCAAGCC 840
TCAAGCTCCA CCTCTCCCAG GAAACATGGG GGCCTACTTT AGTCGAAGAA GACTCTTAGC 900
TCTGAAGTTC 910
|
