Tag | Content |
---|
EnhancerAtlas ID | HS184-02336 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:207126480-207127750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:207126556-207126577 | GGAGAAGCGGAAGGAGGAAGA | + | 6.68 |
|
| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23166 | chr1:207124137-207129767 | Colon_Crypt_1 | SE_24017 | chr1:207126364-207126794 | Colon_Crypt_2 | SE_24017 | chr1:207126818-207128113 | Colon_Crypt_2 | SE_26377 | chr1:207126349-207129958 | Duodenum_Smooth_Muscle | SE_29373 | chr1:207124093-207129896 | Fetal_Intestine_Large | SE_33978 | chr1:207124836-207130412 | HCC1954 | SE_58988 | chr1:207121014-207154864 | Ly3 |
|
| 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 |
GH01I206951 | chr1 | 207124381 | 207129677 |
|
Enhancer Sequence | AGGGACATAT GAGCAAACCT TTTTTGAGGT TACCCAACCA TTGTCCTATG TGCTGTTACC 60 TCCACACCCT GGCTAGGGAG AAGCGGAAGG AGGAAGATTT TTGGAGTAGA CATCCAAAGT 120 CAATAGGTGG AGTGTCAGGT GACTGGGCCC AGCCCCTCTC ATAAGCCACT GGGGTCCTGC 180 TGAAGACTTG CTGTTTCCTT GTTCCTGGTC TGAGCCTGGC TCTCGGCCCA AGGCTTGCCT 240 GACAGGCAGC GATTGGAAAA ATAGCCCCTG TAATCCCCTG CAGCCTGTGT TCATCTGAGC 300 CTCAATGTTC CCATCTCTAG AATGGGAGTA TGTTTCTTTT TGGTGATGTA TATTGTAATT 360 AATTTGTAGT TGTCTGTACT CCACTGGCAG AGGTAGGGAA GGAAAGTGCT GGCCCCATAA 420 AATGTTTAGA TTAGTTGCAT TTGCTAATCA GTCTGATCTT CCCATGCCAG GCCCTAAAGA 480 AGCCACAGTC TGAATTCTTT TTCTTGAACT CTTGTCTGAA ATGAAACACA GTATCTTCAG 540 ACAAATTAGA GCATTCTGAA AACACCTTTG GACACAGTAG TCCTAGCTTT CTTCCTCTTC 600 TCTAAAGTAC TCAAGGTTAG GAAGCCAGAA GTTTGCCACT CAGGGAAAGA AGTAGCCTTT 660 GTTTGACCCT CTATGCTCAC AGCAGAACTG GTAGATCTGG ATAGAGGTAG CAAGTAAGTG 720 AGCAGTGGGA ACAAGGCCAG AGGTGGCAGA GGCAGAACAT AGAAGAGTTC AGATCCTACT 780 CAGTAAATGT GTGTCTTTTT GTTGTTGTTG TTTGTAGAGA TGAGGTCTCA CTATGTTGCC 840 CAGGCTGGTC TCAAGCGCCT GGCATCAAGT GATCCTCCTG CCTCACGCTC CCACAGTGCT 900 GGGTTTACAG GCATGAGCCA CGGTGCCTGG CTTCAATCAA TGTCTTTGAT GCAATGCATC 960 CAGGAGGCAA ACAGTGGTCT GCAGGCCAGG GGCATTGGCA CTGGTGATCA CCACATGCCT 1020 GTAGAGGTGC AGCATGGGGT TCTCTCCTAA GGCTGCCGCT TCTCTGCTGC CCACATGGGT 1080 TTCAGCTGGC CCCTTAGAGA GTAGGCAGTA GGATGACAGC TCATCATACT GCTGACAGTG 1140 AAGGGAGCAG GCTGGCCCGG GAAGGCCAGC ACCTGTAAAC CAAGCTGTGT CACTGTATGA 1200 AAAATGAAGA GCTTGGTGGT GCTGGACCCT GAATGCAGGG TTTGTTTCTT TCTGAGTAGA 1260 ATCTCCATTC 1270
|