| Tag | Content |
|---|
EnhancerAtlas ID | HS184-09498 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr14:21316760-21317880 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA(var.2) | MA0730.1 | chr14:21317637-21317654 | TGAACTTTCACTGACCT | - | 6.12 |
| | | 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 |
| GH14I020848 | chr14 | 21316514 | 21317829 |
| Enhancer Sequence | AGTTTTTGAC TGGGCAGGAA AGATAGACTG ACAGTTCCCT CATTCTATCT TTATATAGAA 60
CTGGAGAGCA GCACAGAAGG AGGGGGACAT GTCAAGGAAT ACCAGGCGGG CAGAGCCTGC 120
TTTAAGGCAT CTTCCAAAGG TTATGAGTCA CTGCAGACAC ACTGAGAGTC ACACTGGGGG 180
AAGGTGCAGC AGACAGGGAG AAGTTCAAAG TGGTGTTTCT GAGAGACTTG GGGCACTGTG 240
TACAATTAAT CATCTCTCCA CATGGGTGAC TGTGGGAGCC ACAGCAGTGC CTGAGTCTTC 300
CAGGGGAAAC ACTGAACATG GAAATTTGTG GAAAGGAAAC GAAGGAGGTG GATGAAAGCT 360
GGAGGAACAA GTGTTTAAAC AATGCAGCTT TTCTTGCCCT GGAAGGTTCT TTGGGTACTA 420
ACCTTCTGTG TGGTAGACAG AGGGCGGCCG GGGAGAGGAA GGAAACTACC AAGAGAGAGC 480
AGCAGCAGTC TTGCCTGTGC TCCCCTGTGG TGCCCTTTCT TTTGAACTCT TTCTTGAACC 540
CTTAATCCCT GTCAGGCTCC TGGAGGAGCC TCACTGGGCA GCCTCAAATC TCCCCAGTTT 600
GCCCTGTCCT CAGAAAAGCA GACCATTGAA ATTGCTATTT CAGAGCTGGA AGCTGGTCAG 660
CCAGCTCAGA TGACCGGAGT TGCAGCTCTT ATTTGCCTGA ATAATAAAAT CATTATTGAC 720
TTAAGTTCTC AGCAAACAGT GGGGTATTTG TTTCACATTT CTGAGCTGCT GCTCAAGTTC 780
CAAAAAATGT CCCCTTCCAA AGAAAAGTAT TTAAAATTGG ATTGAGAGCG AAGAGTAGGT 840
GGAATAGGCT ATTGTGGGGG AGGTCCTGGA TTTGCAGTGA ACTTTCACTG ACCTTTCAGC 900
TCCTTAGGGC ATGCTCCTTG TCATCTGTCC ATCATGCCCA ATGGCCAGCC TAAGGGGAGA 960
AAATAGAGTG CTCTCTCCAT GATGGCCAAA ACTACCTGCC TGGCTGGCTG TCCGTCCGTT 1020
ATCATCTCAG TCTCTAACCC ACTTCTTGCT GCTCCTGATT CTATGCCCAC TTAACTTGTC 1080
AACTGTGACT TTGTGGAACA TAATATAACA AAAAAAGGCA 1120
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