| Tag | Content |
|---|
EnhancerAtlas ID | HS052-02595 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:157059650-157060970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:157060096-157060115 | TGGCCACCAGAGGGCACTC | + | 8.8 | | ZBTB18 | MA0698.1 | chr1:157060174-157060187 | GAACATCTGGATT | - | 7.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 157059687 | 157059816 | | chr1 | 157059853 | 157060623 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I157089 | chr1 | 157059561 | 157060966 |
|
Enhancer Sequence | GGTGTGTATC TGCACGTGCC TTTGGTACGG TGGAGCCGAG TGCCCAGGAG CAGGGCTGGC 60
AGGTGAGCTG ACTCTGCTGT GTCTCGGCCC GGTGTCCACT GTCCTGGAAG AAGACTGAGC 120
ATCCACAGCA TTCTATCCCC AGATGAGGCT GACAGTCACA GTCACAGATG GCCAGAGGAT 180
GTGCTGTCAC CTGGTTGCAC CAGAAACAAA CAGGCTGCAG AGTGTGTTGC TACGTTAGAC 240
CTATACGCCT TTGGTGGATA GTCCATGATT TGCTAAGGGG GTTTGAAATG GGAAGGTTCT 300
CACAAAATGC TTTTATTCTG CAACTCTCTT CCTCCTCTCA GAGGATTCCA AGGTGGGCAT 360
CACCCCTTCA CCTCAGAGTC GGCTGTGGGC TCTGCACCCA GCCTAGGCCG GGGCTCTGAG 420
CTCCTCTCGA CCGCCGGTAC TGACTCTGGC CACCAGAGGG CACTCTTGCC TTGTGGAGAC 480
CAACAGTCTT CTGAGTCCGA GGAACCTGGT TCCCATCTTT GCCAGAACAT CTGGATTTGC 540
TGAAGCCTTT CTCTACTTAA GTGGTTCTCC ACTGGGAGCA GTTTCTCCCC TCTCCCCAGG 600
AGACATTTAC CAATGTCTGG AGACAGTCTG GTTGTCCTAA CCGGGTGGGG GAGGGTGCTC 660
CTGGAATCTA CTGAGTAGGG GCCCCAGATG CTGCTAAACG CCCAGGAATG CACAGGACAG 720
CCGCCCACAA CAAAGAATTA TGCAGCCGAA AATATCAACA GTGCCAAGGT TGAAAAAGTC 780
TGCTCCACTC GAATCTATTG CCTAGACGCA GAGTGCACCA TCTGGAAATG TAAGTCCTCC 840
GGGGCTGAGC TTTTAGTCTC CCAGTTTCAC CTACTCCAAA GAGAAATTTT AGAAGAGTGA 900
CCTCGAGGCA TTTCCCATTG CCTGAGACGT GAGGGTCACA GATACCACAA AGCACTGAAG 960
AGGCAGTGGG GTCTGGCAGA GGGGCATGTG AAGATCCCCA TGAAGGAGAA CAATTCTGTC 1020
CCAGGAGCTG GTCTCTCTGA ACAGGGCCCA AACCCCATGA CAAAACCATC CAGTTCCTTA 1080
TGCTGGAGCA GACAACACTA GCTCTTTGTC TCCCAAAACT GGGCAGGGTG ATGGGAAAGC 1140
CCCTGGGAGC TCGTCCTTCC TGCAGGGCCA GGGATGGGCC TGTGGCTTTG GGGGCAAGTG 1200
AGAAGCAGTT TTCATTGTAG CGCTGGGAAC TCTCAGGAGA GAAACTCTGT GGTCCCCACT 1260
TTCTTGGCAT CTGACATGAA GGAGGGAGAC TGAGATGAAG AACTCTCATA GATCCTTTCT 1320
|
