| Tag | Content |
|---|
EnhancerAtlas ID | HS113-00792 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:33189910-33191710 |
Target genes | | Number: 12 | 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 | AAAAATTAGC TGGGCGTGGT GGCAGGCTCC TGTAATCCTA GCTCTCGGGA GGCTGAGGCA 60
GAGAATTGCT TGAACCCAGG AGGCGGAGGT TGTAGTGAGC CAAGATCACG CCACTGCACT 120
CCAGCCTGGG TGACAGAGTG AGACTCCGTC TCAAAAAAAA AAAAAAATTA CTATTGGGGC 180
TAGTCTGGCC TAGAGAAGAA CAGTGATTTG CACGCTCTCC TGTATGATGT ATGTGCAATA 240
ACCCATCCTG TGGGGAGTGA AGTGACTTGC CCAATGTCAC ACTGCATGTT GTATAAAAAA 300
CCAGCCTGGG CCCCAAGAAG GCTGCTTTGC AGCCTGGGAA GAGGTGACAG GCCCTGGCAT 360
GATCTGCCCT GCCCTCTCAG GACCTGAATG CCCCTCTCCA CTCAGGACAA TGGGAACGCC 420
TCCTGCCAAA GCCACTGCTA TTCCTCTCAG TGGGGAGGAG GGAGAAGACA ATGAAAGAGG 480
CTGGGGAATG AGGGGTGTGG GGGACTCCAA ACAGAGCCAG CAACAAATGG GCAGGGCACA 540
GAGTGGGGCA GGAAGGATGG CCCTCTCTCC ACTGGGACTT TGAGAAGGGG CCATTTTGGC 600
AGGAGGATGG GCGCAGTCTG CCTACTGGTA TGCTTGAGCC CCTGGACAAC TTCATTCACT 660
GTCTCTTTAC ATCACTCCCT CCTGTGTGCC CAGAGCATAG GACGGGGACA CCAATGCACC 720
AGCGCGCCAA ATCTGCGTGA CCTCGTGCAA GCCACTTAGT CTCCTCACCT GTGAATTGGA 780
GGTGATCGGC CCTACTTCCC AGGGCTGTTC GGAGCATTAA AGGCAATCAC AGAAGTGAAG 840
CACCCCAGCT GGAGTGGGCG AGGCAGTCCA GCAAAGGCTA GTTGTTACAG TGGCAGAGGC 900
GCTCCTCTCC CAGACTGCCC CACACAGCTG GCAATGGTGG GGACTGGCCA GGAGAGCTTG 960
TGGGGAGGAG CCCTCTTCCT TCCTGCCCCT TCCAGCTGGG TATCAAGATC TGAGACCAGA 1020
TGTGTTGGTG AGTGACTCAG CGCTTTCCTG CCTGGAAACT CCTCCCTGCC TGTCTCACCA 1080
GGCTGGGCCA GGGAGGGTGA GACAGCAGAC TGGGGGTGGG AGTGGCTGGT TCCGAAAAAC 1140
CTCAGGGGAG CCATGGGGGC AGGAAGGGAG AGGGAAGGAG GGATGAGAAT AGTGTGCCTT 1200
GGCCTGCAAG ATGGGGATGG GATGAAGGAA GTGGGACACT TCCGAGACTG TCAAGGAAGA 1260
GCTAGGTTGA GGGTGTCCTT GTCTGTCTAG TCAACCTAAA ATGACCAGGT GGGAGGAGGA 1320
AAGCTCACCC CTTCCTCTTC CCACCTGCAT ACATCCTAGC CCCAGTATTT CCAGGCCAGC 1380
CCAAACCCAT TTGTCTTGCC CTCCTGGGCT GCATACCCAC ATGACGCTCC CTTCCTTCCC 1440
TTTCCTCTCC TCCTCTTCCC AGCCAACCAC CTCCACTTCC CCATCTCCCA CTCCACTGGA 1500
TCTGTTACTA ACTCCTTGGT GCCCACTCTC TCTGGAAGGT TGTCCTCTAT TGCCTAATCC 1560
CTCACCCTGA CAGCTTAAGC TGTCAGGGAC AGTAAGCATG GTTGACCTGG TCCTTCTGGA 1620
CCTTCATGGA GCTTTTGTTT TTGAGACGGA GGCTCTCTCT GTCGCCCAGG TTGGAGTGCA 1680
ATGGTGTGAT CTCGGCTCAC TGCAACCTCT GCCTCCCAGG TTCAAGCGAT TCTCCTGCTT 1740
CAGCCTCCCA AGTAGCTGGG ATCACAGGTG CGCACCACTT GGCTAATTTT TAAATTTTTA 1800
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