| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08203 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:93531410-93532300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr12:93531997-93532008 | AATGAGTCACA | - | 6.62 | | RUNX1 | MA0002.2 | chr12:93531822-93531833 | AAACCACAGAG | - | 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 |
| GH12I093137 | chr12 | 93531204 | 93533775 |
|
Enhancer Sequence | AAGAAAAAAG ACAATATTGT AATGGCATCA TTATTAAATG GTTTTCTGAA TAGGCTGCCT 60
CTGCTATGAG ACAAATAGCT GAGATTCTCA CAGATTTCCA GTTTCCATAC TAGCAGGCAT 120
TGAGATCCAG GCAAAAGGAG GTTAATAGTG AAACACAAGC CAGAGAGAAA TTCCTCCCCT 180
TCATCTCTGG TGCCAACATC ATCAAATACC AGTCACTGGC CAAACCTGTG TTTATTCCAT 240
GCCCTGTGGC CTAATGAGAG GGGATGGGAC AAGAAGCAGC TCTGCTAATA ACTGTCATGA 300
AAATAATAAT ATCACTTGGC TGTATGCGGC AACTTTCATT GGAAGCTCTT GAATCAATTT 360
TTTCCTCTTG CATAACTATT ATTTCCATTT TATTTCCACT AAAGGAGAAG CCAAACCACA 420
GAGTGGTTGT GACTTGCCCA AGGTCATGGA GCAAATCAGA AGAGCAGTTT TTAAAAGCTG 480
AGAAGGATAT CAGGGGATGT AAAATCCAGT TGCCTTCCCA GCCTAGAATG GGCTGGGTTC 540
ATGACTCAGT AAGACACATG GCGTTACCTA AGCTCAGTGT CTCTGAAAAT GAGTCACACT 600
AAGGGAGACT CAGGGCCTGA GGGGCTGTGT CAGACATACG TTTTCAGTAG TCACTCATTG 660
TCCCTGCCCA TCAGATTTTA ACGTCTGTCA CCGAAGCCCA TCACAGACAG GGCCTCTTGG 720
GAGGTTTAGC CTATGGAACT GGGAAGGTCT GCCTTGGGGG TGTCTGTCTT TTCTGGATGT 780
TTACCCAGCT GTCAGTTCCT ATGAAGCCCA GGTCTCCCCA TTCCATTATC CATCAGGAGC 840
CCATGGCTGG GGTAGCTGTG GCTTCCACTC GGTCCATGAT GATTCTGGTG 890
|
