| Tag | Content |
|---|
EnhancerAtlas ID | HS056-07085 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr18:46518790-46519900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPIC | MA0687.1 | chr18:46519286-46519300 | TACTTCCCCATTCT | - | 6.45 | | ZNF263 | MA0528.1 | chr18:46518868-46518889 | CCCTCCTCTGCCTCCTGCCTC | - | 6.24 | | ZNF263 | MA0528.1 | chr18:46519563-46519584 | TCATCTTTTCCCTCCTCCACC | - | 6.53 | | ZNF263 | MA0528.1 | chr18:46519560-46519581 | CCCTCATCTTTTCCCTCCTCC | - | 7.93 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_35081 | chr18:46516237-46521361 | HeLa | | SE_46295 | chr18:46518915-46525824 | Osteoblasts | | SE_52478 | chr18:46519747-46521087 | Small_Intestine | | SE_53633 | chr18:46518612-46521698 | Spleen |
|
| | 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 |
| GH18I048987 | chr18 | 46514328 | 46525924 |
|
Enhancer Sequence | GGCCTCCAGC CTCATTTGCT GTCATCCAGT GGCCGCTTTT CAGGCCCTCT CTGGGTGATG 60
TTGATGCCAT GGACCGTCCC CTCCTCTGCC TCCTGCCTCA TCTTCTAGAA CACTCCCCAC 120
TCCCCCAACT GTCCTCTCAG TGGACTCCTC AGTCTCCCCT GCCACTTGCC CCAAATGTGG 180
GTCCCCTGGG GACTGGCCTC AGTACTGTCC TCGCTCCACA TTCTCCAAGG AGTGACTTCA 240
CCCAAACCAC GGTTTCAAAT GCTATCTGTG CCCAAGGCCT CTCGAGCCCG GACCTCCTTT 300
CTGAATTCCG GACCCCTCAC CCAGCTGCGT GTAGACCCTC TCTCCAGGCA CAGCCCCAGC 360
CTGGCCACAC TCAGTCTGCT CCTGCTCTGG TTTTCCCAAT GCACAAATGA CAGCGTCATC 420
CGACAGATTT CCTCAACCTT GTCCTTGACT CCTTCCTGCC CCCACCCCTA CTAACTTCAT 480
GGCTGATTTC AGCACTTACT TCCCCATTCT GTCTACTGCT CTCCACCTCC CTCCACCAGC 540
CTGGGCCAGG CATTGTCATT TGTCACCAAA CCACTGCAGC CATCTGTTAA CTTAATGTCA 600
CACTGCCACG CTCATCCACC TTCAAGCCTT CATACCCCGC CTTGGGAAGT CTGAAACAGG 660
GGAGCCTGGG TGTGCCACAT TCCTGCCTAA CTCCTCCCAT CGCTTCCCAC TGCTCTAGGA 720
CAGAGTCCTC TGGAAGGAGG CTGACCTTCC TTCGTCCTCG CTCCCATCTG CCCTCATCTT 780
TTCCCTCCTC CACCCACATT CCAGCCATTA TTCCCTGTCT GCTCAGAGTT TCCCAACATG 840
TTGGGATTGA TCCCTCTGAG ATGTCCACCT GCTCTAGAAT GCCCTGCCTC CTTCCTCCAG 900
CAAACTCCTA TTCATTCCTC AAAACATCAT TCGTGTGCTA CCTCCCCTGG GAAGCCTTCC 960
AGGACTTCTC AGTCTTTGTG TGGTAGGGAC TTAGAACGGG TCTTGGTGTT TCACAGTGCA 1020
GAACACAGTT TCTGCTTGAG CTTTCAAGGC AACGACTTTT TCAGTTGCCG TGACCATGGG 1080
GAATTCACAG CCCTGCGGGG GACCAGAGAA 1110
|
