| Tag | Content |
|---|
EnhancerAtlas ID | HS094-00659 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr1:33189870-33191680 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
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 | CCTGGCCAAG GTGGTGAAAT CCCATCTCTA TTAAAAACAC AAAAATTAGC TGGGCGTGGT 60
GGCAGGCTCC TGTAATCCTA GCTCTCGGGA GGCTGAGGCA GAGAATTGCT TGAACCCAGG 120
AGGCGGAGGT TGTAGTGAGC CAAGATCACG CCACTGCACT CCAGCCTGGG TGACAGAGTG 180
AGACTCCGTC TCAAAAAAAA AAAAAAATTA CTATTGGGGC TAGTCTGGCC TAGAGAAGAA 240
CAGTGATTTG CACGCTCTCC TGTATGATGT ATGTGCAATA ACCCATCCTG TGGGGAGTGA 300
AGTGACTTGC CCAATGTCAC ACTGCATGTT GTATAAAAAA CCAGCCTGGG CCCCAAGAAG 360
GCTGCTTTGC AGCCTGGGAA GAGGTGACAG GCCCTGGCAT GATCTGCCCT GCCCTCTCAG 420
GACCTGAATG CCCCTCTCCA CTCAGGACAA TGGGAACGCC TCCTGCCAAA GCCACTGCTA 480
TTCCTCTCAG TGGGGAGGAG GGAGAAGACA ATGAAAGAGG CTGGGGAATG AGGGGTGTGG 540
GGGACTCCAA ACAGAGCCAG CAACAAATGG GCAGGGCACA GAGTGGGGCA GGAAGGATGG 600
CCCTCTCTCC ACTGGGACTT TGAGAAGGGG CCATTTTGGC AGGAGGATGG GCGCAGTCTG 660
CCTACTGGTA TGCTTGAGCC CCTGGACAAC TTCATTCACT GTCTCTTTAC ATCACTCCCT 720
CCTGTGTGCC CAGAGCATAG GACGGGGACA CCAATGCACC AGCGCGCCAA ATCTGCGTGA 780
CCTCGTGCAA GCCACTTAGT CTCCTCACCT GTGAATTGGA GGTGATCGGC CCTACTTCCC 840
AGGGCTGTTC GGAGCATTAA AGGCAATCAC AGAAGTGAAG CACCCCAGCT GGAGTGGGCG 900
AGGCAGTCCA GCAAAGGCTA GTTGTTACAG TGGCAGAGGC GCTCCTCTCC CAGACTGCCC 960
CACACAGCTG GCAATGGTGG GGACTGGCCA GGAGAGCTTG TGGGGAGGAG CCCTCTTCCT 1020
TCCTGCCCCT TCCAGCTGGG TATCAAGATC TGAGACCAGA TGTGTTGGTG AGTGACTCAG 1080
CGCTTTCCTG CCTGGAAACT CCTCCCTGCC TGTCTCACCA GGCTGGGCCA GGGAGGGTGA 1140
GACAGCAGAC TGGGGGTGGG AGTGGCTGGT TCCGAAAAAC CTCAGGGGAG CCATGGGGGC 1200
AGGAAGGGAG AGGGAAGGAG GGATGAGAAT AGTGTGCCTT GGCCTGCAAG ATGGGGATGG 1260
GATGAAGGAA GTGGGACACT TCCGAGACTG TCAAGGAAGA GCTAGGTTGA GGGTGTCCTT 1320
GTCTGTCTAG TCAACCTAAA ATGACCAGGT GGGAGGAGGA AAGCTCACCC CTTCCTCTTC 1380
CCACCTGCAT ACATCCTAGC CCCAGTATTT CCAGGCCAGC CCAAACCCAT TTGTCTTGCC 1440
CTCCTGGGCT GCATACCCAC ATGACGCTCC CTTCCTTCCC TTTCCTCTCC TCCTCTTCCC 1500
AGCCAACCAC CTCCACTTCC CCATCTCCCA CTCCACTGGA TCTGTTACTA ACTCCTTGGT 1560
GCCCACTCTC TCTGGAAGGT TGTCCTCTAT TGCCTAATCC CTCACCCTGA CAGCTTAAGC 1620
TGTCAGGGAC AGTAAGCATG GTTGACCTGG TCCTTCTGGA CCTTCATGGA GCTTTTGTTT 1680
TTGAGACGGA GGCTCTCTCT GTCGCCCAGG TTGGAGTGCA ATGGTGTGAT CTCGGCTCAC 1740
TGCAACCTCT GCCTCCCAGG TTCAAGCGAT TCTCCTGCTT CAGCCTCCCA AGTAGCTGGG 1800
ATCACAGGTG 1810
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