| Tag | Content |
|---|
EnhancerAtlas ID | HS064-04087 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr13:99129950-99131020 |
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 | ATTAGAGTCG GGTCCCATCT CCCATCTCCT CCTTCACCAA GTCTGTGCCC AAGCCGACGA 60
TCAATACCTG TGGTTAGATC TGGACTTAAC CACCTCCCTT CCATTACCAA GTCTCCCAAA 120
AGCAACGGCA GAGCGGCCTG CTGTCATTCC CAAAGGGCGC TAAGAGGAAG AGGTGAGGAA 180
CACTCATGGA AAATCCTCCC CTGGATAATT AAGGGCTGGC TCTGTGATGA CTGTCTGCAT 240
GGTTCTGCCC TTTTAAATCT GCCCTGAACA CCATCCATCA TTGACTTATA TGCCCATGGG 300
GAACGAGGAG GAAGGGGAGA AAAAGAGATA AAACTCTCCT TACTTGGGGG GAAATCCTTT 360
CTGCGTCAAA ATTCACTATA AAGGGTATTC GGCTGCTGTC TACCCCCCAG AGTGCCTCAT 420
GAGCAGCTCG GACCAGGCCA AGCTCTCCAA GTCAGCAGCT GGTGTTCGCC ATTGCGACCA 480
TGCTCTCCAT CATTCAGGCA CTTGCAGACT CTTCAAATAG GACCCAGGAA AAAAACCTAG 540
ACCACATCCC ACCTCTGTGT GACTTCTAAC TCCCCCTCCC CGAGCCTGTC CTCCCCTGCT 600
TCGAAGCTCT GTAACAGGGA CTATTGGCCG GGGCACTCAG CCACAACAAG AAACCACATT 660
TCCCAGACTC TGAGCAGCAG CCTGTGGTCA GGTGACTAAG ACCTCGCCAG TGGGTCAGAC 720
AGGAGCAAAT GTGCCCCATG CCCCTGCTTG GTCTTGGCCC TGAAGCACTG GCAGTGGGAG 780
AGGACAATGG CTGAAGACCA AGGGAAGCCT GGGGCTCCAG ATGCTGAAGC CACCCACCAG 840
CACAGACCGT GACGGTATGG ACCAGAGCCA CTGACCCCAT GTGCAGGGGG AGAAATAAAT 900
TTCTATCTTT TGTGAGACAC TGTTTTAGAG CTGCTATGAT GGCAACTTGG CCTAAACATT 960
AATGAATATG CCATCTCATT TCTTAAAACC CATGTCGTGT ACTCATTTTT TAAGTCCGTC 1020
AAACATCTCT GCCTGATTAA GTGACTGGTT TATGTAGCAT TGTCCCTTTG 1070
|
