| Tag | Content |
|---|
EnhancerAtlas ID | HS184-03704 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:51542650-51543740 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX2 | MA0688.1 | chr10:51543398-51543409 | TTTCACACCTC | - | 6.14 |
|
| | 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 |
| GH10I046051 | chr10 | 51541952 | 51544286 |
|
Enhancer Sequence | TCCAGCTCCC TTCCCACCTC TCAGCCCTCC ACCCTGGGGT GGTTCTGGAA GGCACTGCTC 60
ATGGTAAGGA CAGAAGGTTG CTGGCTGGCG TTCTTCTGTC TGATTCAGTG GCTGCATTTA 120
CTTAGCATGT GCTCTATGAG GAGAATAAGG GCCTGTGATG CTGGTATAGA TCAGTTCAGA 180
TATACTGGTG GGTACGTGGC TGCTGCCCAA CACTCCTGAG TGCCCCCACT CAGCATGTTG 240
GATCCTGGCC CCTCCAGACC TCAACATCAT CCAGAAACAG AAGGAATAGA GCCTCGCACA 300
GTAGGGTCCC CCAGACTGAC TTCTGGCAGC TGAACTGAAG GGTCAGTGGT TGAGCCATAC 360
TGGTTGTTCA ACACTTTGAA TACCACATCC AGAAAGAAAA TACAAGCTCC CTGTCACGGT 420
AGCCTCCTTG TGACTGTGTT ACATTCAACA CAAGACAAAC ATCAGCTTCA CAAAAGGGAG 480
CAGTCTCTGG GACAATCCAT TGAAAGCGTG AGAGGCAGGT AGTTCCTGGG TTCTGTGCAT 540
AGTTGCTTTA AGCTGTAAAC ACACAATCCT TGACCAAATA CCCTTTAATC CACTTGACAA 600
ACAAGAAGCT TCCGGGCCTC CAAGGGGATG CCCAAGTCTC CCTTTTCTCT GGGACAAAAC 660
CTGGTTTTGT TTCTTAGGTT TCTCAGCGGC TAATCTGGAA CATGTTTGCT TTTGCCCCGT 720
TTCTTTGTCC CAGTGTTTTT TCTGCTGTTT TCACACCTCT CTGGATAAGC TTTCCAAGTT 780
CCTTACAGAA AACCAGAAAG ATTATTCACC AGCAGTCTTC CTGGTCCCTG GCTTGTCAGC 840
CTCAATGCAT TCCAGTGCAC TCTTGTGACA CTGTATCCAG AGTAGCTGTG GCTCACAGCA 900
TTTACAGTGT TCTTTCTCGC TATTCTATTA GTGGCTTCCT TTTCCAACCC AGTTCTTTGC 960
CTGGATATCC AGGATCTCTA TCCCACCGTC ACCCTCACTC CATATAGGGG GTTCATCCTA 1020
CAGCATTTCT GTTGCTGTAA AAAGACCCTC TACTGCATCC TTTGGCATGG AGAATTTGTC 1080
TTATTGTATT 1090
|
