| Tag | Content |
|---|
EnhancerAtlas ID | HS095-00756 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:33189860-33191630 |
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: 2 | Chromosome | Start | End |
| chr1 | 33190298 | 33191276 | | chr1 | 33191365 | 33191490 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I032724 | chr1 | 33190202 | 33191737 |
|
Enhancer Sequence | TCAAGACCAG CCTGGCCAAG GTGGTGAAAT CCCATCTCTA TTAAAAACAC AAAAATTAGC 60
TGGGCGTGGT GGCAGGCTCC TGTAATCCTA GCTCTCGGGA GGCTGAGGCA GAGAATTGCT 120
TGAACCCAGG AGGCGGAGGT TGTAGTGAGC CAAGATCACG CCACTGCACT CCAGCCTGGG 180
TGACAGAGTG AGACTCCGTC TCAAAAAAAA AAAAAAATTA CTATTGGGGC TAGTCTGGCC 240
TAGAGAAGAA CAGTGATTTG CACGCTCTCC TGTATGATGT ATGTGCAATA ACCCATCCTG 300
TGGGGAGTGA AGTGACTTGC CCAATGTCAC ACTGCATGTT GTATAAAAAA CCAGCCTGGG 360
CCCCAAGAAG GCTGCTTTGC AGCCTGGGAA GAGGTGACAG GCCCTGGCAT GATCTGCCCT 420
GCCCTCTCAG GACCTGAATG CCCCTCTCCA CTCAGGACAA TGGGAACGCC TCCTGCCAAA 480
GCCACTGCTA TTCCTCTCAG TGGGGAGGAG GGAGAAGACA ATGAAAGAGG CTGGGGAATG 540
AGGGGTGTGG GGGACTCCAA ACAGAGCCAG CAACAAATGG GCAGGGCACA GAGTGGGGCA 600
GGAAGGATGG CCCTCTCTCC ACTGGGACTT TGAGAAGGGG CCATTTTGGC AGGAGGATGG 660
GCGCAGTCTG CCTACTGGTA TGCTTGAGCC CCTGGACAAC TTCATTCACT GTCTCTTTAC 720
ATCACTCCCT CCTGTGTGCC CAGAGCATAG GACGGGGACA CCAATGCACC AGCGCGCCAA 780
ATCTGCGTGA CCTCGTGCAA GCCACTTAGT CTCCTCACCT GTGAATTGGA GGTGATCGGC 840
CCTACTTCCC AGGGCTGTTC GGAGCATTAA AGGCAATCAC AGAAGTGAAG CACCCCAGCT 900
GGAGTGGGCG AGGCAGTCCA GCAAAGGCTA GTTGTTACAG TGGCAGAGGC GCTCCTCTCC 960
CAGACTGCCC CACACAGCTG GCAATGGTGG GGACTGGCCA GGAGAGCTTG TGGGGAGGAG 1020
CCCTCTTCCT TCCTGCCCCT TCCAGCTGGG TATCAAGATC TGAGACCAGA TGTGTTGGTG 1080
AGTGACTCAG CGCTTTCCTG CCTGGAAACT CCTCCCTGCC TGTCTCACCA GGCTGGGCCA 1140
GGGAGGGTGA GACAGCAGAC TGGGGGTGGG AGTGGCTGGT TCCGAAAAAC CTCAGGGGAG 1200
CCATGGGGGC AGGAAGGGAG AGGGAAGGAG GGATGAGAAT AGTGTGCCTT GGCCTGCAAG 1260
ATGGGGATGG GATGAAGGAA GTGGGACACT TCCGAGACTG TCAAGGAAGA GCTAGGTTGA 1320
GGGTGTCCTT GTCTGTCTAG TCAACCTAAA ATGACCAGGT GGGAGGAGGA AAGCTCACCC 1380
CTTCCTCTTC CCACCTGCAT ACATCCTAGC CCCAGTATTT CCAGGCCAGC CCAAACCCAT 1440
TTGTCTTGCC CTCCTGGGCT GCATACCCAC ATGACGCTCC CTTCCTTCCC TTTCCTCTCC 1500
TCCTCTTCCC AGCCAACCAC CTCCACTTCC CCATCTCCCA CTCCACTGGA TCTGTTACTA 1560
ACTCCTTGGT GCCCACTCTC TCTGGAAGGT TGTCCTCTAT TGCCTAATCC CTCACCCTGA 1620
CAGCTTAAGC TGTCAGGGAC AGTAAGCATG GTTGACCTGG TCCTTCTGGA CCTTCATGGA 1680
GCTTTTGTTT TTGAGACGGA GGCTCTCTCT GTCGCCCAGG TTGGAGTGCA ATGGTGTGAT 1740
CTCGGCTCAC TGCAACCTCT GCCTCCCAGG 1770
|
