| Tag | Content |
|---|
EnhancerAtlas ID | HS053-00838 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:28567870-28569190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:28569074-28569089 | GAGGTCAAGAGATCG | + | 6 | | TP53 | MA0106.3 | chr1:28568543-28568561 | AGCATGTCTATGCATGCC | + | 6.01 | | TP53 | MA0106.3 | chr1:28568543-28568561 | AGCATGTCTATGCATGCC | - | 6 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_29182 | chr1:28567909-28569014 | Fetal_Intestine_Large | | SE_64750 | chr1:28567934-28569130 | NHEK |
|
| | 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 |
| GH01I028241 | chr1 | 28567986 | 28569000 |
|
Enhancer Sequence | CGGACGGATC ACTTGATCCC AGGAGCTTGA GACCAGCCTG GGTAACATGA CCAAACCCCA 60
TTTCTGCAGA AAATACAAAA TAATAATAAT AATAATAATA ATGGCGGTAC AGGCCTGCAG 120
TCCCAGCTAC CTGGGAGGCT GAGGTTGAAG TGAGCTGTGA TCATGGCACT GTACTCCAGC 180
CTAGGCAACA GAGTGAGACC CTGTTTCCAA AAAAAAAAAG AATCATTGGG GTGCTTTTTT 240
TTATATATTT GAAAGAGTTC TATAGAATTT TATGCAGTGA AGTTATTTAA CAATCGCAGA 300
ATTAATGGAG CACTTTAAAA TTATTTGCTC ATTAAATCTC ATATTTTTAG CAAATAGATC 360
CATTCCATTA GTTTAATTTT ATAACCATAG TAACCGAAGC AGGGAATTGT GAAGTAACTT 420
TCACAAGGTC ACATGATCAG GTTTGTGCTG ATCAAGGTCT TCACTTCAGA ACTCTTGCTC 480
CCACAACCTT GAGTTGCAGT TCCAATCCAG TGCTTCAGTT GCCTATTAGC TAGCTCCCTC 540
CTCAATCTGG GGGAGTGGGA GGTACATGGG TAGCGGGGTA TGGGTGGTAA AGGCAAGGGC 600
TCCTGGAAGT AAATATAGAA GTGCCAGCGG TTGGTGTTGG CATTAGCTTT TTGGCTGTAA 660
CATAAACCCC GTCAGCATGT CTATGCATGC CTATATGATG CAAACACATG TTTGCAATAG 720
AGGCTAGTTT GAGATTTTCA CAACAGTAAG TCTAAAGTTG TAGTTCTCAG GCCGGGCGCA 780
ATGCCTCACA TGTGTAATAC CAGCACTTTG GGAGACCGAG GCAGGCGGAT CACCTGAGGT 840
CAGGAGTTTG AGACCAACCT AGCCAATGTG GTGAAACCCC GTCTCTACTA AAAATACAAA 900
AATTAGTCAG GCATGGTGGC GCACACCTGT CCAGCTACTT GGGAGACTGA GGCAAGAGAA 960
TCACTTGAAC CCAGGAGGCG GAGGTTGCAG TGAGCCGAGA TTGCACCACT GCATTCCAGC 1020
TTGGGCGACA GAGCCAGACT CCAACTCAAA AACAAGTAAA ATAAAATAAA ATAATAAAGT 1080
TGTAGTTCTT AGCACAGGTG GCACACTGAA ATATGTGGAG AGCTTTAAAA TCTCTTCCGC 1140
AGCTGGGCGT GGTGGCTCAC GCCTGTAATC CCAGCACTTA GGGAGGCTGA GGCGGACGGA 1200
TCACGAGGTC AAGAGATCGA GACCATCCTG GCTAACATGG TGAAACCCCG TCTCTATTAA 1260
AAATACAAAA ATTAGCCACG CATGGTGGCA CGCGCCTGTA GTCCCAGCTA CTCGGGAGGC 1320
|
