| Tag | Content |
|---|
EnhancerAtlas ID | HS153-00229 |
Organism | Homo sapiens |
Tissue/cell | Osteobl |
Coordinate | chr1:33190450-33191600 |
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 | GAGTGGGGCA GGAAGGATGG CCCTCTCTCC ACTGGGACTT TGAGAAGGGG CCATTTTGGC 60
AGGAGGATGG GCGCAGTCTG CCTACTGGTA TGCTTGAGCC CCTGGACAAC TTCATTCACT 120
GTCTCTTTAC ATCACTCCCT CCTGTGTGCC CAGAGCATAG GACGGGGACA CCAATGCACC 180
AGCGCGCCAA ATCTGCGTGA CCTCGTGCAA GCCACTTAGT CTCCTCACCT GTGAATTGGA 240
GGTGATCGGC CCTACTTCCC AGGGCTGTTC GGAGCATTAA AGGCAATCAC AGAAGTGAAG 300
CACCCCAGCT GGAGTGGGCG AGGCAGTCCA GCAAAGGCTA GTTGTTACAG TGGCAGAGGC 360
GCTCCTCTCC CAGACTGCCC CACACAGCTG GCAATGGTGG GGACTGGCCA GGAGAGCTTG 420
TGGGGAGGAG CCCTCTTCCT TCCTGCCCCT TCCAGCTGGG TATCAAGATC TGAGACCAGA 480
TGTGTTGGTG AGTGACTCAG CGCTTTCCTG CCTGGAAACT CCTCCCTGCC TGTCTCACCA 540
GGCTGGGCCA GGGAGGGTGA GACAGCAGAC TGGGGGTGGG AGTGGCTGGT TCCGAAAAAC 600
CTCAGGGGAG CCATGGGGGC AGGAAGGGAG AGGGAAGGAG GGATGAGAAT AGTGTGCCTT 660
GGCCTGCAAG ATGGGGATGG GATGAAGGAA GTGGGACACT TCCGAGACTG TCAAGGAAGA 720
GCTAGGTTGA GGGTGTCCTT GTCTGTCTAG TCAACCTAAA ATGACCAGGT GGGAGGAGGA 780
AAGCTCACCC CTTCCTCTTC CCACCTGCAT ACATCCTAGC CCCAGTATTT CCAGGCCAGC 840
CCAAACCCAT TTGTCTTGCC CTCCTGGGCT GCATACCCAC ATGACGCTCC CTTCCTTCCC 900
TTTCCTCTCC TCCTCTTCCC AGCCAACCAC CTCCACTTCC CCATCTCCCA CTCCACTGGA 960
TCTGTTACTA ACTCCTTGGT GCCCACTCTC TCTGGAAGGT TGTCCTCTAT TGCCTAATCC 1020
CTCACCCTGA CAGCTTAAGC TGTCAGGGAC AGTAAGCATG GTTGACCTGG TCCTTCTGGA 1080
CCTTCATGGA GCTTTTGTTT TTGAGACGGA GGCTCTCTCT GTCGCCCAGG TTGGAGTGCA 1140
ATGGTGTGAT 1150
|
