| Tag | Content |
|---|
EnhancerAtlas ID | HS109-00449 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr1:33190330-33191500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:33191065-33191086 | GGGGCAGGAAGGGAGAGGGAA | + | 6.43 | | ZNF263 | MA0528.1 | chr1:33191348-33191369 | CCTTTCCTCTCCTCCTCTTCC | - | 6.64 | | ZNF263 | MA0528.1 | chr1:33191342-33191363 | TCCTTCCCTTTCCTCTCCTCC | - | 6.98 | | ZNF263 | MA0528.1 | chr1:33191345-33191366 | TTCCCTTTCCTCTCCTCCTCT | - | 7.24 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_00938 | chr1:33190447-33191596 | Adrenal_Gland | | SE_23116 | chr1:33190582-33191538 | Colon_Crypt_1 | | SE_26629 | chr1:33189838-33191609 | Esophagus | | SE_41588 | chr1:33190432-33191573 | LNCaP | | SE_65538 | chr1:33190156-33191692 | Pancreatic_islets |
|
| | 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 |
| GH01I032724 | chr1 | 33190202 | 33191737 |
|
Enhancer Sequence | TCCTGCCAAA GCCACTGCTA TTCCTCTCAG TGGGGAGGAG GGAGAAGACA ATGAAAGAGG 60
CTGGGGAATG AGGGGTGTGG GGGACTCCAA ACAGAGCCAG CAACAAATGG GCAGGGCACA 120
GAGTGGGGCA GGAAGGATGG CCCTCTCTCC ACTGGGACTT TGAGAAGGGG CCATTTTGGC 180
AGGAGGATGG GCGCAGTCTG CCTACTGGTA TGCTTGAGCC CCTGGACAAC TTCATTCACT 240
GTCTCTTTAC ATCACTCCCT CCTGTGTGCC CAGAGCATAG GACGGGGACA CCAATGCACC 300
AGCGCGCCAA ATCTGCGTGA CCTCGTGCAA GCCACTTAGT CTCCTCACCT GTGAATTGGA 360
GGTGATCGGC CCTACTTCCC AGGGCTGTTC GGAGCATTAA AGGCAATCAC AGAAGTGAAG 420
CACCCCAGCT GGAGTGGGCG AGGCAGTCCA GCAAAGGCTA GTTGTTACAG TGGCAGAGGC 480
GCTCCTCTCC CAGACTGCCC CACACAGCTG GCAATGGTGG GGACTGGCCA GGAGAGCTTG 540
TGGGGAGGAG CCCTCTTCCT TCCTGCCCCT TCCAGCTGGG TATCAAGATC TGAGACCAGA 600
TGTGTTGGTG AGTGACTCAG CGCTTTCCTG CCTGGAAACT CCTCCCTGCC TGTCTCACCA 660
GGCTGGGCCA GGGAGGGTGA GACAGCAGAC TGGGGGTGGG AGTGGCTGGT TCCGAAAAAC 720
CTCAGGGGAG CCATGGGGGC AGGAAGGGAG AGGGAAGGAG GGATGAGAAT AGTGTGCCTT 780
GGCCTGCAAG ATGGGGATGG GATGAAGGAA GTGGGACACT TCCGAGACTG TCAAGGAAGA 840
GCTAGGTTGA GGGTGTCCTT GTCTGTCTAG TCAACCTAAA ATGACCAGGT GGGAGGAGGA 900
AAGCTCACCC CTTCCTCTTC CCACCTGCAT ACATCCTAGC CCCAGTATTT CCAGGCCAGC 960
CCAAACCCAT TTGTCTTGCC CTCCTGGGCT GCATACCCAC ATGACGCTCC CTTCCTTCCC 1020
TTTCCTCTCC TCCTCTTCCC AGCCAACCAC CTCCACTTCC CCATCTCCCA CTCCACTGGA 1080
TCTGTTACTA ACTCCTTGGT GCCCACTCTC TCTGGAAGGT TGTCCTCTAT TGCCTAATCC 1140
CTCACCCTGA CAGCTTAAGC TGTCAGGGAC 1170
|
