| Tag | Content |
|---|
EnhancerAtlas ID | HS184-27916 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr7:43847460-43848570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr7:43848478-43848493 | TGCCCCTTGACCTCT | - | 6.49 | | NR2F1 | MA0017.2 | chr7:43848481-43848494 | CCCTTGACCTCTT | - | 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 |
| GH07I043808 | chr7 | 43847714 | 43849035 |
|
Enhancer Sequence | ATAGAGTCAC CGCCCTTCTG CTCTCGTGTT CTCAGCTGCC CTATCTACCC TGCAGGTTGC 60
TGCTGCTGCT GGAGCCCACG CAGGTCATGT GCCACTGTGG CATTTCCTAA ACACTCCTGC 120
CTCTGAAGGT GGCACCCCAT GCCCCAGTCA CAATTCTTTC AGAGTGTCAC AGAAGGAAAG 180
AATCCACATG TATTCCTCAG CAGTCTGTCC CTCTGTCCAA TTTGAAGAAA AAAAAAGCCC 240
TTAATCCCGC TGTACTAATG CTCCTAAGTG TTGAGGGGTC CTTCAGGAGG GCCTTGTGTC 300
TCCAGGCAAG AGTGACCACA GAGGTGCCCT TTGCCCCTCA GCCCCTCTCC CTGTGGCAGC 360
AGTGACCTGC CTGTCTGGTG AAGCTGGAAA AGGGACTAAA CACATGACAC CCAGCCACCT 420
TCTCCCTCTG AACCGACATC CTTAGGATGC ACCCAAGCTT GTCCACGTGG CAGGTGACTA 480
AAGCAGACTC TTCCTCTGCA AGTAGGTGAC CTGCAGCTGT GATGAAGAAT TGAGTTACCC 540
TAAGACAGGG CAGTTACCCT AAGACAGAGC CTAAGACAGT TACCCTAAGA CAGAGCCTAA 600
GAGTTACCCT AAGAGTTTAA GAGCCTAAGA CAGAGTTACC CTAAGGTGGA GCCTAAGAGT 660
TATCCTAAGA CAGAGTTACC CTGCAGGGAG CCAAAGGCCC GCGGGACGTG ACCAACTCAG 720
CATTCCGCTG GAGGCTATAT GATCAAACAG CGAACTGTTT ATCATGAATG CAGGATGTGG 780
GCAAACTCAC ACTGCCTTGC CACCAAAATG TTTGCTGAGG GACATCATGC CCTGGCGCCG 840
GGCTCCTGGA AGTTATCTAT TGAGAAATCT AGCGCCTATT GTTCACAAGC CCGCTGTGAA 900
CCAAACGGCT GACTGACAAT TACCCGACAA CCATCCTCCC ACTTTCTTGC TGTCTCTTTC 960
ACCTAATAAA TACAGAGGGC TGTGTAAAGC TCACGGCCCT TGTCCACTAG AGGCAAGATG 1020
CCCCTTGACC TCTTCTTCCA AATATACTCT TTTGTGTCTT GTCTTTTATT CCCACATTCG 1080
CCCCCCTTTG TTCAGTCCCC CGAGGTCCAT 1110
|
