| Tag | Content |
|---|
EnhancerAtlas ID | HS131-00238 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chr1:33190570-33191570 |
Target genes | |
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 | GTCTCTTTAC ATCACTCCCT CCTGTGTGCC CAGAGCATAG GACGGGGACA CCAATGCACC 60
AGCGCGCCAA ATCTGCGTGA CCTCGTGCAA GCCACTTAGT CTCCTCACCT GTGAATTGGA 120
GGTGATCGGC CCTACTTCCC AGGGCTGTTC GGAGCATTAA AGGCAATCAC AGAAGTGAAG 180
CACCCCAGCT GGAGTGGGCG AGGCAGTCCA GCAAAGGCTA GTTGTTACAG TGGCAGAGGC 240
GCTCCTCTCC CAGACTGCCC CACACAGCTG GCAATGGTGG GGACTGGCCA GGAGAGCTTG 300
TGGGGAGGAG CCCTCTTCCT TCCTGCCCCT TCCAGCTGGG TATCAAGATC TGAGACCAGA 360
TGTGTTGGTG AGTGACTCAG CGCTTTCCTG CCTGGAAACT CCTCCCTGCC TGTCTCACCA 420
GGCTGGGCCA GGGAGGGTGA GACAGCAGAC TGGGGGTGGG AGTGGCTGGT TCCGAAAAAC 480
CTCAGGGGAG CCATGGGGGC AGGAAGGGAG AGGGAAGGAG GGATGAGAAT AGTGTGCCTT 540
GGCCTGCAAG ATGGGGATGG GATGAAGGAA GTGGGACACT TCCGAGACTG TCAAGGAAGA 600
GCTAGGTTGA GGGTGTCCTT GTCTGTCTAG TCAACCTAAA ATGACCAGGT GGGAGGAGGA 660
AAGCTCACCC CTTCCTCTTC CCACCTGCAT ACATCCTAGC CCCAGTATTT CCAGGCCAGC 720
CCAAACCCAT TTGTCTTGCC CTCCTGGGCT GCATACCCAC ATGACGCTCC CTTCCTTCCC 780
TTTCCTCTCC TCCTCTTCCC AGCCAACCAC CTCCACTTCC CCATCTCCCA CTCCACTGGA 840
TCTGTTACTA ACTCCTTGGT GCCCACTCTC TCTGGAAGGT TGTCCTCTAT TGCCTAATCC 900
CTCACCCTGA CAGCTTAAGC TGTCAGGGAC AGTAAGCATG GTTGACCTGG TCCTTCTGGA 960
CCTTCATGGA GCTTTTGTTT TTGAGACGGA GGCTCTCTCT 1000
|
