| Tag | Content |
|---|
EnhancerAtlas ID | HS184-14455 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:81021400-81023500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr17:81021745-81021759 | AACCACGCCCCCTC | + | 6.29 | | KLF16 | MA0741.1 | chr17:81021746-81021757 | ACCACGCCCCC | + | 6.14 | | SP1 | MA0079.4 | chr17:81021743-81021758 | CCAACCACGCCCCCT | + | 6.03 | | SP3 | MA0746.2 | chr17:81021745-81021758 | AACCACGCCCCCT | + | 6.09 | | SP4 | MA0685.1 | chr17:81021743-81021760 | CCAACCACGCCCCCTCC | + | 6.24 | | SP8 | MA0747.1 | chr17:81021746-81021758 | ACCACGCCCCCT | + | 6.52 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_23159 | chr17:81022316-81022753 | Colon_Crypt_1 | | SE_24692 | chr17:81021999-81023366 | Colon_Crypt_3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 81021529 | 81021683 | | chr17 | 81022417 | 81022626 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I083064 | chr17 | 81022000 | 81023366 |
|
Enhancer Sequence | GCTGTGCACC GTGCAGGGCG GCGGCCAGCA CAGCTTGGTG CCCAGGAACT GCTGACGGAC 60
CGAAGGAGGA GCGCCTGAGA CAGTGCCAGC GAATAGGCCC CTGCAGCAAA CATTACGACT 120
GCGCTTACAC CTACATCTAG TTAGATACGG ATTCTATTAC TGAAGTAACT CAAACTTTCC 180
AAAATGCTTA AGTGAATTTC ACAGGTGGGT GTGGAATTGC CAAACGCCAG GTGTACACTG 240
CTGGTTTGGA TTATCTGGTC ATTTTGATCT GTGAAGTCAG GTAATATTCA GGCCCTCCCA 300
GAGTTTCCAT TGTCCTGTTC TATGGTCAAG GCGGGGCTGC AAACCAACCA CGCCCCCTCC 360
CCGCATCCCC GGATGCCTGT GGGGGCTGCA GAGTGATCGA AATGTCAGGT AATTCCACAA 420
AAATCCACAT TTGGATTTCG GGCTTCTCTT GGAACTGACC ATCTGTAACT CCGGCTCACG 480
CTGTCCTGCC GGCACCTGGC TGGGGCTCAG CGGGAGCTGT TCTCTCACTC CTTCCCAAGC 540
CCCGTTGTCC CCCTGGACAA ATGGGTGGAA TTCTATTAAG GCTGTGAACT TAAGAGAGCT 600
CCGGAGCTGA GAGAGGTGCC GGCCGTGCCG CTGGTGCCTT TGAGAAGCTC CTGGCTGCCG 660
TCCATCCAGG CCTGGCCTCA GACCTGGATC CCTGTTCACC CTGGGAGTGG CCCACCTGTG 720
GAGGGAGGTG CTCCCCACCA CAGCCCCCAG CCCTGCAGCC CCTGCACCAT CTGTCCCCAG 780
GGCAGCTGCC TCTGCAGCCA GGTCCAGGCC TGGGGAGCTG GAGGGCACCA AGCGGACCGC 840
AGGTGAGGGG CCCGCAGGTC AGCACAGGTG GGTCAGGTCC TAGCCCGCTT GTCATACAGG 900
TCATATGGGA CTTAGCCTAC TTTCCCTTCT GTTTAATATC TGCACCCCTG AATAGTGCAA 960
ATGCCCAGAG GGAGGGATCG GAGGCTGGGA GATCCATGGG GGATTCAGGG GGCAGCTTGG 1020
GGGACAACCG TTGCAGCCGT GCCCTGATGT CAGACACAAG GATACCACTA GGCCCTCGCC 1080
CAGGCGTCCA GAGAGAAAAG TCAGCTGGCG GCAAAGGCCT TGTTCTCAGG GCCACATGCT 1140
GATATTTTAA CCAGTTCTAG CTCACCTTGG AAATGCTGAT GCCAGCAGGA CGACACCAGG 1200
TACAGGGTGC AGGTGGGTGC TGGACCCCCC AGGTGGCAAA TGAAAGCGCC TGCGGGGGAC 1260
TCGGTCAGAG GGAGCCTCAC AGAACGTTCT GGGCTAAATC TGGTCATCAG ACTCGGGGCT 1320
GGCGTCTTCC CGACACGTGA ATTTGGAGGG TGTGTGAGTC AGGATTCCTG GCTGAACTGG 1380
TTTGCACTGG TTTGAAGTCA GGCAGGTTGG CTGGTTGCCC GTGTCACAGG AAGGTGGACA 1440
GGACATAGGT GCCGCTGTCA GGAACAAAGC CCCAGCCTCT GCCTGTGACG CCCCTCTGAG 1500
GGGGCATGGG TCTCCCTCCC CCGGAGGCCC GGACAGCGGC CAGGAGCAAC TGAGCTTCCT 1560
GCCAACCTGG TGACCCCAAA GGTCGGAGGG TGAACTCCCT CCAGCTTCAG CAGAACCAGT 1620
GTTGATCAAC TCATCCCAGT TGGCCTGGAA CTCAGAACCG ATGTTGATCA ACTCATCCCA 1680
GTCGGCCTGG GACTTTCCTG ATGTTAGCAG GGAGGGTTCT GAGTCCCAAG AAGCGCTCAG 1740
TCCCCAGCAT GCCCTGCGCG TCGGTCACGG AGCCCCAGGA GGAGCGTGCA GCCCGCAGCC 1800
TGGGCCTGGG CACAGCCGGC TTTATCAGCA GCTCCATCCC AGCCCCACAG ACAGGGGAAG 1860
AAAAGGTTGG GGGCTGGGCA GACAAGACCA TCCAGGGCCC CGGCTGGTCA CCCAGGCTGA 1920
AACGGAACAC ATCTGTTTCT CTACACTCTA AACACTTTGC ACCAAATGTG CGGGATTTTC 1980
ACACCAAGCA ACTTTCCAGT TCTCAGTGGA CACCAACGGG GTGTCCCACG ATTCAGTTCG 2040
ACTCTCACAC TACCTGCAGG TAGCGCAGAC CCCGCAGGCT GGGGCTCCGT CCCACAAGCT 2100
|
