| Tag | Content |
|---|
EnhancerAtlas ID | HS173-01202 |
Organism | Homo sapiens |
Tissue/cell | SH-SY5Y |
Coordinate | chr1:209975390-209976780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:209976578-209976599 | GGAGCAAGAGAAGGAAAAAGA | + | 6.09 | | ZNF263 | MA0528.1 | chr1:209976575-209976596 | GATGGAGCAAGAGAAGGAAAA | + | 6.19 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27309 | chr1:209975849-209977189 | Esophagus | | SE_27823 | chr1:209974553-209977405 | Fetal_Intestine | | SE_35823 | chr1:209974126-209984775 | HMEC | | SE_64223 | chr1:209974556-209984573 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTATGGAGAA AAGGAGGGGT CTCAGCTGGC TATCCATACA ACAATCCAGT GTCTGGGAGA 60
AGGCTTGGGA ACACTGGCGA CAAAGGCTGA GAACACGTCT CCACTACTGA GTCTGGTAAA 120
GCTCAGAAGC CCTAGAATAA CCAAATACTA AAGTACTAAG AGTACTTAGA GTACTAAAAG 180
CAGTCATGAG ACAAGCTTTG CATGGCTAGG ACAGCCTCCT CCCTTGGGTC TGTTTATCTC 240
CCAGTGAAGG CTGGAGTGAA CCAATTGGTT GCAGGAGCCA GCATGGGTAA AGTCTGCAAT 300
TGATTCTTGT AAAAATACAT GGGCATAGCA GATAACATTC AAGAGCAGCT GGCACTCACA 360
GCAGAAAACA AAAGCCTTCC CAGATTGGGT GACTGATAAA AAAACAGTCA CTGGAGAATT 420
GTTTGTCTGA GATGTTGTGT TTGGATTTTT TGGTGTTCTT ATTTTGTTTT TACTTAAGAT 480
GAGAATGAGA TGCCTGGAAA AAGAACACTC ATTCAACAAA TATTTGTTCA TCAGCTACTG 540
TGTGCCAAGC ACGGTGTTAG TTACTAAACA CTGACGCTCC ATGTTCCTTC TTGAGAAACT 600
CCACACTGGA ACTTCTCAAG CCCCACAATG GCCTGAGAAG GAGGGGAAGA TAAATAGGTC 660
ACCTTCATAC CCAGAAAGAT CCCTACCTGG ACCACAGTTC TGAAACCAAA CAACCTTACA 720
GCAAAGCAGC TAAATATGGG AATAAACTGT GCCAGGTGGG AAAGAAAAGA GGTTAAAAGG 780
GTCAGCTGAA GGCTCCTACT CAGAAGAGCT TAGCTGACGG GGTGGCCCAT AACACCACTT 840
CTCTCCCCAG CCAGACTCCC AACAAATGTG AAAAACCCAA ACCCAACTCA GCGTCTGGCA 900
CTTTAAGAGC AAGGCAAGAC CTGCTCTCAC CTGAGCTTTC TGACCCAATT ACCAAGTCCT 960
GCAACTGAAA CCTTCCCCCT GGGAGCATAG TGGGTAGGTC AGGTTGGCAC GCAGTGTTCA 1020
AGTACCCCCA TGTAGTTGGC CTTGAATTAC GGTGTTTTGT AGGGCAGCAT GTGAAACCAT 1080
CAAACCATGG AGTGCATTAT AAGCCTTATA AGGAGGAGGG GATGCATATT CTCTCAACGG 1140
CTAGTTCTAC CTTCTGCTCC CCAGTCCTAT CACTACTGAA AGGGGGATGG AGCAAGAGAA 1200
GGAAAAAGAG GATAGGGAAA TAGGCACCAA ACCAGTCAAT CTAGTAAAGA GCTTTTGAGA 1260
ATTTCCATTG CAATACTGGT AAGTGCTGTG TTTGGGCCTG TCAGACATTA AAATCCAACT 1320
CTTGACTGAT AGTGGACTGG AAGAAAAGTC CAAAAGGACT TATTGTAGTT GATCCAAATC 1380
CCACCATGCA 1390
|
