Tag | Content |
---|
EnhancerAtlas ID | HS184-16447 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:72011750-72012750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr2:72012295-72012306 | GATGAGTCACT | - | 6.02 | JUND | MA0491.1 | chr2:72012295-72012306 | GATGAGTCACT | - | 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 |
GH02I071785 | chr2 | 72012181 | 72012330 |
|
Enhancer Sequence | GAGGGAGGCA CAGAACTTTT GGGGGGCCCA GGAGATATTG CAGAGTTCAC GGTTTACAGC 60 AGGGAGGTGC TGAGGGCCTG GAGACAGGTT CTCAGTACCC TAAGGTGAAG CCTTTGATCA 120 GGAAAACATC TCTTCCCAAG GCCAAAGTCC TTGGGCTGTC TATGGCACAC ACATGCGGAA 180 GGCCAGGGCA CATTTGCCTC AGCTCAAAAC ATACAACTCA CTACATGAAC AGCTCAACTG 240 AACTAGGCCC TTTGATTTAT GTGTTTACAT TCCCAAAGGG AAACTTTCTT TACCTGAGGG 300 ACTCTTGGCT GGGTTCCTTT CATGATGAGA ACAGGACATG AAACTTTGTT TATGGAGAGG 360 TAGTACTCCA AGCCGGGGTG GAAGCCGGCC CTTAAAGTTT GGGGCTGGGC AGCCCTGATA 420 ACCACCAGGT GGGGAATTTT GTCTCTGAGC TTTCTGTCCC TGATGTCTCA GCCTGGGCAC 480 CCAGCAGGAC TCCCTGGTGT CAGCAACATG AGTGACAGAT GAATCATTCA TTCCTGAGGC 540 GCTCAGATGA GTCACTGGAG AAGCAGTGTC ACCTTTCCAA AATTTAACTT TCCAGCAACT 600 TCAGGAATTC AGCAGTCGTG TAGAGAGAGG GATGCCTGCA GTTCGATTTT TGTCCCTTCC 660 CACCACCCTT TTCACCTGCT TGATGGTGCA GGGTGGGGAG GACGGGCAGG ACACTGCAAA 720 CAGCTTTTAG CTGGGTGAAG ATGAAGGAGA ACTTTCTTGC TTATGGCCAC CCAAAATAGA 780 TCCAAATGCA GTTCTTTCTC TCCCCAGCAG AAGGGAGTGA GGCTAGACTT TGGGGAGTAC 840 TGATCTGTAG AGGAAGAGCA GTGGAGCGGC TCCCCTCAGT CTTCCAGGCT GAACCTTGTC 900 AGGGTTGAGA AGGTAGGTCA GATGCCGCTG GGGCCCCACT GGAGAAGGTG ACAGCTGGTG 960 GCAGAGGGCC GGGCTACCCA GGGCTGTGTC AGTGCTGGAA 1000
|