| Tag | Content |
|---|
EnhancerAtlas ID | HS053-27909 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr3:127813180-127815050 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:127814152-127814171 | TCCCCAGCAGGGGGCACCA | + | 7 | | Nr5a2 | MA0505.1 | chr3:127814005-127814020 | GAGATCAAGGCCACC | + | 6.05 | | ZNF263 | MA0528.1 | chr3:127813587-127813608 | CCTTCCCCCTCTCTTTCCTTC | - | 6.61 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_41754 | chr3:127813076-127813728 | LNCaP | | SE_41754 | chr3:127813796-127815422 | LNCaP |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr3 | 127813400 | 127814038 | | chr3 | 127813773 | 127813849 | | chr3 | 127814011 | 127814530 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I128094 | chr3 | 127813601 | 127815262 |
|
Enhancer Sequence | GGTGAGCGGC AAGAAGCCGA GAGGGAGCGT ACACTACCTG GGAAAGAACA CTCCTAGGAG 60
GCTGCATTTT CACGGCAATC TGTTGTCAGC ATCCAACAGT TCCCCACTGC CACCTCCAGG 120
CAGCACCCCG TCAAAGCTCC ATCCCCGCTC ACAGCCCAGG GTCCACTGGG AAGCGGTGTG 180
GGAGAGCAGT GAGAGCATGG AGTTTGGACC CAGACGTTCC TCTGGGCTCA GGTTCCAGTG 240
GCAACACTTT CTAGCCTATG GCCTGGGCAG GTAACCTCCC ATTTGAGTCT GGAGATAACC 300
TCAACTGCTC ACAGGGTTGT CAGGGTGTCC TGGGAGGACA TGAGATGGCC CATGTAGAGT 360
GCTCTGTATA GTTTCTGACA CACAGGAAGC CCTCAGTTAG TCACCTCCCT TCCCCCTCTC 420
TTTCCTTCGG AGCTCTAGAG ATCAGATGTG GTTCTGGGGG GTAAGGAAGC CCTGTAGTTC 480
CCCTCTAGGG GTGGAGTCTG TGGGAAGCAT ATCAGATGGC TATTATTGTT GGCTATTACT 540
TTTTTCATTA CCATGTTGAC ATTATTATCA CCACTACAAC AAATTTCCTA CTAGAACATA 600
GTGCCAAAAT TCTCTTCCAA AGCAAACAAC CGAATCTGCG TTACCTGAGC CGACCTGCCT 660
AAAAATCCAT GTTCTGAGTG TCTTCCTTCC ACTTGAGTAA CTACAGTCTA GCAAGGAGTC 720
TCCACAACCT CTAGCAGCCC TTGATCAAAT CAGCCCAGAT GGGGCTGGGG CCAAATCTCC 780
CGGGTCTCAG GCTGACCAGA GCTTTGTCTC CACTGAGCAG GTTCTGAGAT CAAGGCCACC 840
TTTCTGTGCA CCTTAGTCCT GAGTGGGATG GGACTGAGAG ACCTTACTTC TGAGACGAGA 900
GATGCCAGGC TCTGCAGGTA TGGGCTGGGC TGGGTTCCCT ACTGTGGAGG GAGGGAAGCC 960
TATTAGCAGA GCTCCCCAGC AGGGGGCACC ATCTGTCCAA GGCTGAGCCC TTTCACCAAC 1020
TGCACTGTCA GGCTTCAGCC TGGCCTAGCC AAGGCTAAGC AAGTCCAGAC AGCCACAGGC 1080
ATGCCAGGCA TACCAGCCAT AAGGCCCACA TGCATCTGTC TCCAGAAGCT GCCCAAGTAG 1140
CCATGCTGGA TCTGGCACAC ACTTTCTCTC CAAGACTTAG GAAGCACTTA TGACAGTGGT 1200
CTTGTCTAGA GAGCATCACG GACGGGGATT CAGAGTAGCT ACAAGATGCT GCCACATGGA 1260
CTTGAATCAC GCATTCGATT CCTAATTGCA AGTGAAAGAA ACCGCCTGAG GGGGAAGGGC 1320
TGTTGCTATA CTGCAGTGCT CACAGCACTA CAGAACCCCC ATTGTGGGGC TTACCCAGAG 1380
CCAGCAACAC CAGAGTTTGC ATGTTTTGTT TTTTTTTAAT TATTTTTAGA GATGAGGTCT 1440
CACTGTTGTC CAGGTGGGAG TGCGATAGCT ATTCACAGGT GCAATCATTG CACACTACAA 1500
CCTTAAACTC CTAGCCTCAA GCAATCTTCC CGCCTCAGCC TCCCAGAGAG TACACTACAG 1560
GTGCATACCA CTGTGCCCAG CTTGGACAGT CTTAATAATA AAGCTTCTCT ATTAAAAGCA 1620
AACTAAAATC TTAGATAGGG CCCACCATCA TTCAGAGCTG AGTTAGGCAA ATCAGCAGTT 1680
TTTATTTCAA ACTCAGTTTG GCTCCAGCTG TGTCCTGAGA TACTCATGGG CCACAGGGTG 1740
TCTTTCTAAC TCCCACTGCC TCCACTGCCC TGAGCATGCA GCCTCAGGGA CTTTGTCCCC 1800
ACACTACTCT ATTGCAGGCT TGAAAACAGG CCCCTCATCA CCCACCTTTG TGCCCCCAGC 1860
ACTGCAGAGA 1870
|
