| Tag | Content |
|---|
EnhancerAtlas ID | HS176-05443 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr10:75610450-75611590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr10:75610751-75610772 | CCCTATAGCTCTCCCTCCTCC | - | 6.01 | | ZNF740 | MA0753.2 | chr10:75611506-75611519 | GTGGGGGGGGGGA | - | 6.3 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_01737 | chr10:75607913-75616643 | Aorta | | SE_06416 | chr10:75607594-75615799 | Brain_Hippocampus_Middle | | SE_08120 | chr10:75607927-75614049 | Brain_Inferior_Temporal_Lobe | | SE_26988 | chr10:75608341-75611646 | Esophagus | | SE_52779 | chr10:75609869-75610743 | Small_Intestine | | SE_54678 | chr10:75607583-75621499 | Stomach_Smooth_Muscle | | SE_65905 | chr10:75610741-75611438 | 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 |
| GH10I073850 | chr10 | 75609982 | 75611483 |
|
Enhancer Sequence | GGGGCTGGGT GGCCTGGACT TACTATTCCT AAAATCTGAT GCTGGGGATG CCACAAGAAC 60
CAAGGGGTCG TACTGGGTCC CTGGGGGCTG AAACTCGGGC CTCCCCATAG GACACAGCCC 120
AAGAGTGGGC CACAGAAACT TTAAGACTGA GCTATAGAGG CGAGTCTCCA CAGAGATGTA 180
TAATTAGAAC AGAGCCGGGC TAGCAGGGAG CGCCTTCTGG CCAAAAATGG CAAAAGTGCG 240
AAGTGTCCCA GCAGAGCCAG GCCAAGCCCA CTGGTACAGT CACCCCCCCT CAGGGCCCCC 300
TCCCTATAGC TCTCCCTCCT CCCCGCAGGC TCCCTGAGCC ATCACTGCCT CCTCCGTCCC 360
AGAGCCTCGT CCTCCCCTGC TGGCACTGGA ATTCATCTCC CCACTTGAGA ATTCTTCCCG 420
AGGCTGAAGC ATCTGAAGTT GATCAGCAAA CATTGGCCTC TCAAGGTTGA GAAATTCGTG 480
AGGAAGCTGC ACTCCCCCAC TCTCCAGAAG CAGCCAGAGC TGCCACATAA GCCAGATAAG 540
CTGCAGGCAG GATGATCAAA ACCAGGTTGT AGGGACATCA CCCTCGAGAA AAGCAAGGCT 600
GGGGGAAGAG CCAAGGCGGG AAAGGCAGGC TGAACAGGCG CCTGAGAGCG TGGGTGAGGG 660
AGGCACCAGG GATTCCAGGG AGGGCAGAGG CTGAGGCATG TGGCCGGGGA ACGGTCCTCA 720
AGTTGGAGGA GCCCCACGGC AAGGCTGGTC ATGGTGGTCT AGGGACAAGG TGACAGAGGC 780
TGAAAGCTCC CGGGGCTCTA TGGTTGGATT ATCAGCCCAG AACTCTCCAC TCCCTCAGGA 840
CAGAAACCAT GTCTTCTGCA CCTCTGGATC ATGCCAGAGC CTCAGCACAG TGGCTTGAGC 900
ACACCAGAAT TTGTCAAAGG AAAGAAAAGG GCAGAGGGGG ACATTGGGCA TGGTGGCGAG 960
TACATGGTAG TGCAAAAAAA AAGTATTTCT GGGGTCACAG GGTAAAGGAG ACTTGGAAAA 1020
GCTTTGTAAA ACATTCATTT GGAAGTGATT TTTTTTGTGG GGGGGGGGAG GGGGACATAG 1080
TCTCGCTCTG TTACGCAGGC TGGAGTGCAG TGGCATGATC TTGGCTCACT GCAACCTTCG 1140
|
