| Tag | Content |
|---|
EnhancerAtlas ID | HS184-25716 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr6:10403570-10404740 |
Target genes | |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr6:10404706-10404716 | GGGGCGGGGC | - | 6.02 | | SP2 | MA0516.2 | chr6:10404600-10404617 | CTTCTCCCCGCCCCCTT | + | 6.01 | | ZNF263 | MA0528.1 | chr6:10404450-10404471 | GGAGGAGGGCGGAGCGGAGGA | + | 7.74 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_34695 | chr6:10401774-10421419 | HeLa | | SE_35866 | chr6:10398835-10421638 | HMEC | | SE_47200 | chr6:10398261-10421381 | Panc1 | | SE_64242 | chr6:10398566-10421509 | NHEK | | SE_68277 | chr6:10400415-10427887 | TC32 | | SE_68580 | chr6:10401874-10435207 | TC71 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 10403800 | 10404334 | | chr6 | 10403752 | 10404250 |
|
Enhancer Sequence | TAAACAGTCT CCAATATTGG GGATGGGGGA AGGGAAGGAA AAAGCAGAGG GCAAGGAAAA 60
GATCTGTGTC AGTGAAAGAC TACAAAGGGA AAGCAAAATG ACTGTGCAGG AGGAAGAAAA 120
GACTAGAATG GTTGATGTTA AACCCTTCCA AAAAATGATC TTTATAGGCT TTGTGCGGGA 180
TATAGCCACT AGAAAGGAAC TGTGGGTCTA TCAACACATA AGTAAATGAA TAACAGTCAA 240
AACAATGAAG TTCTCAGTAT TATTAAAGAA GAGAAGAAAC ATTATCCGGG TAAGTTCAAC 300
ACAAGCCCCA CAACTCACAA CGTGCAGTGG AATCCTAGGG GTAGGAAGCC CACAGCAGGG 360
AGAAAACTGC CCTAAGGGAA GGTGCTTTAC CTTGCTGACC CTTATAAAAT CTTATCTACT 420
AAATGAATCA CTCAAACCTC GCAGGGGTGA GGTAAGAATC CCTGGCTATG TATGTAACAG 480
ATGCATTCCT TGGTAGTGAC TACACACAAT GCACGTAAAC ATGCTCGCAC GCAGCCTGGC 540
ACACATCAGG GCCTCAGTAA ATTGGGAATC ATCATCATAT GCAAACGCCT ATAGTATGGG 600
GGTCTGGAGA TGACAGCGAC CGGAAAGCAT GGCGTGCGGA CTCAAGAGGA CAACCATTCT 660
CTTCCTTTAG TTAAAAGCCA TTCTATTAAA ACCCTATACA AGGCACGACC GGTTACCCTC 720
GGAGACCCTA CTCAGAGAGG TAAGGCAAAG CGAGGAGCCT GAGAGGAACT TTTCCTGGGC 780
TTGCAAGGTG TGCGCGAAGA GGGAAAAGGT GGCTGTACGG CGCCCCGCGG CTGCAGTGGC 840
CGGGATTGAG CCCGCGGCGG AGCGAGCTGC GCTTGCGCGA GGAGGAGGGC GGAGCGGAGG 900
ACTCCGCGAG CGCGCGGCAG CGAACGAAGC GCGCACCAGA ACTCGCTCGC GGGAAAGCAG 960
CGGAGAGCGC AGGCGCGCGC CGCATCGCCC GCTCCCCCGC CCCCAGATCC CGCCCACTTG 1020
GCTCTACGCT CTTCTCCCCG CCCCCTTTCC TTTCCCGCGT AGGGAGGGCC GCGGCGCGAG 1080
GCCTGTTTGC GTCGCCGCCA CCGCCCCGGC GCAAGCGCAG TGGTTCCCCC GGCCGCGGGG 1140
CGGGGCGGGC GGGGCCGTGC CGGGCCTCAC 1170
|
