| Tag | Content |
|---|
EnhancerAtlas ID | HS184-09450 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr13:111207990-111208960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr13:111208338-111208352 | TACTTCCTCATTCT | - | 6.18 | | SPIC | MA0687.1 | chr13:111208338-111208352 | TACTTCCTCATTCT | - | 6.87 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_00969 | chr13:111207016-111208874 | Adrenal_Gland | | SE_23291 | chr13:111207550-111208943 | Colon_Crypt_1 | | SE_23995 | chr13:111207728-111208823 | Colon_Crypt_2 | | SE_31501 | chr13:111206501-111210796 | Gastric | | SE_42567 | chr13:111206455-111208888 | Lung | | SE_47578 | chr13:111206982-111208816 | Pancreas | | SE_50368 | chr13:111207657-111210845 | Sigmoid_Colon | | SE_65594 | chr13:111206143-111209027 | Pancreatic_islets |
|
| | 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 |
| GH13I110554 | chr13 | 111206554 | 111210722 |
|
Enhancer Sequence | GAAGCGCAAA CGTGAATCAG CCTGTGCCTT CTGCGGGTGA AACCAGTCAT CAGCCGGCCC 60
CCTGCTCGAC TCCAAACAGC AAAGGAAGAA ATTCAATATG GCCAGGTCTC CCAGGTTGCT 120
GAGCCCTTGG GTGGCAGATG GCGACTTTTA TTCTCACTCT TTACCACGGC CACCGCGAGT 180
GCCCCCAGCC TTCCCTCCTC TCGCCGTGGC CTCCCCATTT ATTAGAGACT TGTTTGCTAG 240
GGGCCCAGCT GAGCCTCCCT CCTCCCTTTG TAACATGCCT GCTGGTGTAA CCTCAGTGAC 300
AGGCACCCAA GGCCAGGAGA CAATGTTTGT TTAGCAAAAC TCACATGGTA CTTCCTCATT 360
CTGGCCACTG TTCTGAGAAC CTTGCCAGTG TTAACTGGCT GACTCCTAAC AAAGCTCAGA 420
CAGGTGCCCC TTTCTTCCCT TATTACACAG GAGGAGCCTG ATGCAAAAGG AGGTGACACA 480
GCCACAGCCA CAGCTGTGGT CGGCAGATGC CCTGATCTCC AGAACCTGTG CCCTCATCAC 540
ATGGGTGAGG GACGCTGAGC CTGCCAGTCA ACCACCCTGA AAACAAGGGC CAGGATGGAT 600
CCCACAAAAT CACAGGGGTC CTTTAAACCC TTAGAAGAGG GAAGCAGAGG GGCTGGTTCA 660
GAGGGATGCT GTGTAGGACA GACCTGACCT GACTGCCTTT TCGGAGAGAG GATAAAACCA 720
GGAAATCAGG CAGGCTCCAG AAGCTAGGAA AGTCTAAGAA ACAGGTTCCT CCCTTCAGCC 780
TCCAGAAAGG AATGCAATCC TGCAAGCTTT GACTTTAGCC CAGTGAGAGA CTCATTTGGG 840
ACTTCTGACC TCCAGACTAC TTAAAGACAA TATATCTATG GTTTTAATTT TTATTTATTT 900
ATTCATTTGA GACAGGGTCT TACTCTGTTG CCCAGGCTGG AGTGCAGTGG TATGATCATG 960
GCTCACTGCA 970
|
