| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05277 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:34195790-34197360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr11:34196044-34196063 | GTGCCACCAGGGGACGCCA | + | 6.4 | | IRF1 | MA0050.2 | chr11:34195886-34195907 | AAAAAAAAAAAGAAAGAAAAA | - | 6.59 | | Zfx | MA0146.2 | chr11:34196097-34196111 | CAGGCCGCGCCCGC | - | 6.42 |
|
| | 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 |
| GH11I034174 | chr11 | 34195548 | 34196704 |
|
Enhancer Sequence | GAACCCGGGA GGCGGAGCTT GCAGTGAGCT GAGATCGCGC CACTGCCCTC CAGCCTGGGC 60
GACAGGGCGA GACTCCGTCT CAAAAAAAAA AAAAAAAAAA AAAAAAAGAA AGAAAAAGAG 120
TAGCGGCTTC AAGTCCCACA GGGAGGAATG GTCCTAGCGG GTCCGAGTAT CACTAAGAGC 180
CCACAAAAGC AGGGAAAGGC GGCGGCAGGC TTAGAGCTGC AAACTCCCGG GGCGCCGCTC 240
ATGAGGCCCG CTCTGTGCCA CCAGGGGACG CCATGTGCAC AGCCTGTGCT GGGCCCTGAC 300
TGCGGCTCAG GCCGCGCCCG CCCCTGCCCT CGGCGAGCGG CTCAGATTCA GCTGGGGGGC 360
GGGGACGCGT TTCTGTCCTC TGCCAGCTCT GGCAAGGCTC CGTGTTGGAG CCCCCTCAGG 420
AGACCACTTC GCCGTCCAAC AGACCTCCCC GCCACCGAGG GGCCCGGATG GCAGCCTGTG 480
GCTTCATGAC TTCGTGGGAC ACCCACCTGC TCTGCCCAGA ATGGACGGAG CTCTTTCCCT 540
GCTCCATCAC AGGAACAAGG CAGCCCTGGA GCCCTGTCCC TCACTCATGC TGTTCTCTCT 600
GATGACAGCC CAAAAGTCAG CCTCCCGGCT CCTGCCTGTT CCCAGCCCTT CCCGATGCCA 660
CTCTTGTCCT TCCTTACAAA TTAAGCCAGG GAGCGGGCAG GCAGCCAGGG GCAGGCGGCC 720
AGGCCTCCAG CCACCCCAAC TCCCTCGGGG CTCTTGGAGC GTCCCGCCTG TGCGGTCACT 780
GTGGTCTCTC CCCTTGACAT GCAGCTAAGT GCTCCCGCCA GGGAAAAGAT GTCCATTCTC 840
TCTCCTTGGC TAGGAAGTAA GCCACCTCCA GGGAGTCAGC CTGGGCTGCC CTCGGAACCC 900
CTATCTCAGG TCTCCAAAAG CTCGGGTCAT CTCCAGAGTT CTAAAAGTTT CTTCTCTCCT 960
TGAGGGCAAA GAATGCTTTT ATTTTAAAAA GTGGCAAACA AATATAAATG CTCCTTGACT 1020
TAGGATGGGG TTACATACCA ATAAACCCAT AGTAAGTTGA AAATATCCTA AGCGAAAACG 1080
CATTGAATAC ACCTCACCTA CTGAATAGCC TACCTTAAAC ATGCTCAGAA CACCTACATT 1140
AGCCTACAGT TAGGCAAGAT TATATAAGCC AAAACCTGTT TTATAATAAT GTTGAACATC 1200
AGTGTAACTT ACTGAATACT GTATGAAAGT GAAACAGAAT TGTTGTGTGG GTACTCGAAG 1260
TAGTTTCTAC TAAATGCATA TCGCTTTCAC ACCACTGTAA AGCTGAAAAA TTGTAAGTTG 1320
CACCATCATA AGTTAGGGAT TTTCTGTAAT CAGAAGTGAT CTTAAAGGTC TTTCCTTTGG 1380
GAAGGTATTC TGATGTTCTG GTTCTGTCAT TTCCAATATT CCTGGGTTTG AACCACTTAA 1440
CTGGTCCACT GAGCATACCA ATCTGTATGA AGGGGAGGGC CACAGGCCAG TAAAGCCTCA 1500
CTATCTCTGG CCCTCAAGGA CTCCCAGAAC CTCACCTCAC CCTATCTCCT GCCGTGACTC 1560
ACCCCTGTTA 1570
|
