| Tag | Content |
|---|
EnhancerAtlas ID | HS184-15954 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:16152600-16153650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr2:16152633-16152645 | AAACAAACAAAC | - | 6.32 | | Gfi1b | MA0483.1 | chr2:16153420-16153431 | TGCTGAGATTT | - | 6.32 |
|
| | 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 |
| GH02I016012 | chr2 | 16152381 | 16154316 |
|
Enhancer Sequence | AGCCTGGGAG ACAGAGTGAG ATCCTGTCTT AAAAAACAAA CAAACAACAA CAACTACAAC 60
AAAAAGGCGC CTTGGGAGAG GAAGCTCATT CCCAGCAGAC CTGTGACACA GCCTGTCTCC 120
CCAGCGAACC CAGACCATTT CCCACTCTGT GGGCAGATTG ACCAAGCAAC AGCACTTTTC 180
TGTCTTCATC TGGAGTCCCT GGCAGAGGCC ACCTCACTGA GGTTCAAGGC AATCCAGACT 240
CTTGGGTAGA GCACACTCTG ATGGTGGCAC TACATCAGCT TGCACGAGCA TGTGGCACAG 300
GGGCCAGGCA GGAGCTGGTG TCTGCAAGGA GCCGGGAAGG GAGGGGCTCC TAGGCTTGCC 360
ACGGCTGCAG TCTCCAGGAA TGAAAACCTG TCCTGCCAGT TGCATATGTA GCAATTTTGA 420
ATGCAAATAG CCACTTCCCA GATTTTTTTT TCTTTCTTCC CAGCAAAACA CCCACATCAT 480
TTCCTTCCTT TGTTGGGCCC TTCCTGAGAC CACTGGCTGG GGGCACATAG TAGGCACTCA 540
ATAAATATTT GCCGAGTGCG TGAATGGGTG GTAATCCAGC ACTAATCCCC CTCTCTTCAG 600
CTCCCCACCC CCAGGAAGAA ATAAAAGATG TCCATTTGTG GCTTGGCCAC ATTCAGGCAA 660
ACTTCCATAT TGCTGCCAAG TCCTGCCATC TGCCACCTCC GAGGTGCAGG TGCTGGGCAC 720
CCACAAAGCC CGGCCGTGGG CACAAAGGCC CGATGTGCAC TGATAATTGC CGAGTGCACA 780
GCCCGCCAGG CCGGCCAGGC TGATGCAAGT TTGCTGGGTC TGCTGAGATT TGCATACAGA 840
TGGCCAGTCG GGGCGCAGGG CCGCCGCCAC CGCGACAACG CCGCCCGCGC CCCGGGTAGA 900
CCGGCCGCAG CCCCTTTAGA AGTGCGGGAG GCTTTGACTG CAGCCGAGCC CCAGAGAGGC 960
CTCATTCTGC CTGTCCTGAA TAGTCCGTCA TTCAAAGCAA CGCTTTGAAA TTTGAAAAAG 1020
AGAGAGAGGA AAAGAGAGAG AGGAGAGACT 1050
|
