| Tag | Content |
|---|
EnhancerAtlas ID | HS073-03807 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr13:99129900-99130920 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr13:99129967-99129988 | TCTCCCATCTCCTCCTTCACC | - | 6.03 | | ZNF263 | MA0528.1 | chr13:99130247-99130268 | GGGGAACGAGGAGGAAGGGGA | + | 6.13 | | ZNF263 | MA0528.1 | chr13:99129964-99129985 | CCATCTCCCATCTCCTCCTTC | - | 6.24 | | ZNF263 | MA0528.1 | chr13:99130256-99130277 | GGAGGAAGGGGAGAAAAAGAG | + | 6.78 | | ZNF263 | MA0528.1 | chr13:99130253-99130274 | CGAGGAGGAAGGGGAGAAAAA | + | 6.7 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_11626 | chr13:99127788-99131320 | CD20 | | SE_27318 | chr13:99129890-99130939 | Esophagus | | SE_32245 | chr13:99130242-99130932 | Gastric | | SE_37511 | chr13:99127619-99131417 | HSMMtube | | SE_38638 | chr13:99127244-99131850 | HUVEC | | SE_45616 | chr13:99127310-99132615 | Osteoblasts | | SE_65772 | chr13:99126270-99131228 | 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 |
| GH13I098475 | chr13 | 99127656 | 99131531 |
|
Enhancer Sequence | CCTGGGTGAC AGAGCAAGAT TCCGTCTCAA AAAAAAAAAA AAAAAGTCAC ATTAGAGTCG 60
GGTCCCATCT CCCATCTCCT CCTTCACCAA GTCTGTGCCC AAGCCGACGA TCAATACCTG 120
TGGTTAGATC TGGACTTAAC CACCTCCCTT CCATTACCAA GTCTCCCAAA AGCAACGGCA 180
GAGCGGCCTG CTGTCATTCC CAAAGGGCGC TAAGAGGAAG AGGTGAGGAA CACTCATGGA 240
AAATCCTCCC CTGGATAATT AAGGGCTGGC TCTGTGATGA CTGTCTGCAT GGTTCTGCCC 300
TTTTAAATCT GCCCTGAACA CCATCCATCA TTGACTTATA TGCCCATGGG GAACGAGGAG 360
GAAGGGGAGA AAAAGAGATA AAACTCTCCT TACTTGGGGG GAAATCCTTT CTGCGTCAAA 420
ATTCACTATA AAGGGTATTC GGCTGCTGTC TACCCCCCAG AGTGCCTCAT GAGCAGCTCG 480
GACCAGGCCA AGCTCTCCAA GTCAGCAGCT GGTGTTCGCC ATTGCGACCA TGCTCTCCAT 540
CATTCAGGCA CTTGCAGACT CTTCAAATAG GACCCAGGAA AAAAACCTAG ACCACATCCC 600
ACCTCTGTGT GACTTCTAAC TCCCCCTCCC CGAGCCTGTC CTCCCCTGCT TCGAAGCTCT 660
GTAACAGGGA CTATTGGCCG GGGCACTCAG CCACAACAAG AAACCACATT TCCCAGACTC 720
TGAGCAGCAG CCTGTGGTCA GGTGACTAAG ACCTCGCCAG TGGGTCAGAC AGGAGCAAAT 780
GTGCCCCATG CCCCTGCTTG GTCTTGGCCC TGAAGCACTG GCAGTGGGAG AGGACAATGG 840
CTGAAGACCA AGGGAAGCCT GGGGCTCCAG ATGCTGAAGC CACCCACCAG CACAGACCGT 900
GACGGTATGG ACCAGAGCCA CTGACCCCAT GTGCAGGGGG AGAAATAAAT TTCTATCTTT 960
TGTGAGACAC TGTTTTAGAG CTGCTATGAT GGCAACTTGG CCTAAACATT AATGAATATG 1020
|
