| Tag | Content |
|---|
EnhancerAtlas ID | HS052-14716 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr16:70510120-70511650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROD2 | MA0668.1 | chr16:70510375-70510385 | GCCATATGGT | + | 6.02 | | NR2C2 | MA0504.1 | chr16:70511593-70511608 | GAGGGGCAGAGGTCA | + | 6.52 | | Nr2f6(var.2) | MA0728.1 | chr16:70511305-70511320 | TGAACTCCTGACCTC | - | 6.22 | | Zfx | MA0146.2 | chr16:70510149-70510163 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 70510201 | 70510773 | | chr16 | 70511298 | 70511640 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I070474 | chr16 | 70508755 | 70511590 |
|
Enhancer Sequence | TGGTCTCGAT CTCCTGACCT CGTGATCCGC CCGCCTCGGC CTCCCAAAGT GCTGGGATTA 60
CAGGCGTGAG CCACCGCGCC CGGCCTGTGC TGTGCCTCTC ATGCTTGTTG GAACCAGGTG 120
CTGTGCTTCG TGACTGTGCC TTTCCAGGGC TGTGCTGGGG TAGGGCTGGG CAGAGCTGCT 180
TTGGACCTTC CGCCTGTCCT GGCATCGTGC CCTTACTTGA GATATGATCA CCTGTGCCCC 240
CGCCCCCACC CCCTGGCCAT ATGGTGGGAC AGCAAGAGCC CAACAATGAC TATGATCTAA 300
TGAATGTCAC CAGCGCCAGG CTTCTCACTC CTCCTGGCCA CCGAGCCCCC TGGAACCCAT 360
GGCCAGTGTA GAGCAGCTAC AGCTTGTCTG GTTTCAGGTC CACCTCAGGG TGTCAGGTCC 420
CGTCTCCAGC ACACCCCTGG AAAGAAACTG CTGCAAAGGC CTACTGAAGC CTGACTGTGG 480
TGTTTTCTGT CACTCTGCAG CTCAAGCCTC ACATTTCACT GTAGTGACTC ATATCCCATA 540
ATCGGTAGTC ATTAGCAAAA GGAGCAGATG GGGAAGCATT TTCAGTTTTC TTTTGAGGTG 600
TACCATTCAA GTTCTACATT TGGCCAACGG AAAACTATTT GTTGAGAACC CACTCTGTGG 660
GGCCCCAGGG ATAAAATGAG CAAAAATGGG GTCCCTGCCC TCAAAAGTCC TGTGGTCTCC 720
TGGAGACAGA CATTAATCAA TAACTACTCA GGTGCATGTG TATTACAAAC TGTGCCAAGT 780
GCTTTGAAGC AGAGGGGCAC AGTTAAGTCT TGACATTTCA AGACTTAGCC ACTTTGCAAC 840
TACCAGGTTT TGGCTGCAAA GTTCCAGATG GCTTCTGTCT TTTGCATTTC ATACTTTAAA 900
CCCTTGCAGG CCCTTCCCTA ACTATCAAGG GCCTGTCCCA GAAGCAACTC AAGTTTTGTT 960
ATTTTTAATT TTTTTTTATT TTTGAGATGG AGTCTAGCTC TGTCACCCAG ATTGGAGTGC 1020
AGTGGTGCGA TCTCAGCCCA CTGCAACCTC TACCTCCCGG GTTCAAGAGA TTCTCCTGCC 1080
TCAGCCTCCC AGGTAGCTGG GATTACAGGT GCCTGCCACC ATGCCCAGCT AATTTTTTGT 1140
ATTTTTAGTA GAGATGGGGT TTCACTGTGT TGGCCAGGCT CGTCTTGAAC TCCTGACCTC 1200
ATGATCCGCC TGCCTTGGCC TCCCAAAGTG CTGGGATTAC AAGCGTGAGC CACCATGCCC 1260
GGACTAGTTT TGTTATTTTT ATGCAGCTAC AAGGAGGAAA ATGATACATA CCTTTCATTA 1320
CTGAAGATGG AAAGATGTGT AAGTTAGATA AGAGAAAAAC AGATCCTGAT GACCTTCCTT 1380
CCAACATAAA CCACCTGTCA GAAGACGGTG CAGGGAGACT CAGGCCAAAG GGAAGGTATC 1440
TGTCAGCCTC TCCTCTGACT AAAACTCCCC TAGGAGGGGC AGAGGTCAGT GTAAAATATG 1500
TATTTTTTGA GACAGAGTCT CACATTGTCA 1530
|
