| Tag | Content |
|---|
EnhancerAtlas ID | HS182-08496 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr16:70494480-70495940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| USF1 | MA0093.2 | chr16:70495748-70495759 | ACCACGTGACC | + | 6.32 | | USF2 | MA0526.2 | chr16:70495746-70495762 | TGACCACGTGACCCAG | - | 7.16 | | ZNF263 | MA0528.1 | chr16:70495204-70495225 | GGTGGAGGGAGGAAATGGGGG | + | 6.69 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_28634 | chr16:70494462-70495286 | Fetal_Intestine_Large |
|
| | 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 |
| GH16I070460 | chr16 | 70494704 | 70495303 |
|
Enhancer Sequence | TATTTTTATT AGAGACGGGG TTTCACCATA TTGGCCAGGC TGGTCTCAAA CTCCTGACCT 60
CGTGATCTGC CCGCCTTGGC CTCCCAAAGT GCTGGGATTA CAGATGTGAG CCACTGCGCC 120
CAGGTGGCAG TGCAGTTCTA AGCTGCCTGC CAGAGGAGTC TGGAATTTCA CAGGAATAGG 180
TCTGTTTCAG TGTCCCAGCT GTGCTCAGTC ACTGGTTGTG AGAAGGTTCG TTCAAAGCGT 240
GGCCTCCATG TAAACAAGGT GGGAGATTCA GATCGTAGCA GCTGGGGGCG TCTGTTAGTT 300
ACACTCCCTG CTGCAGCTGA CCTGAGGGTT AGACGTGCCT ACGGCCATAC AGTAAATTGG 360
TGGCAAAGTT GGAGGGAGGG CTTGGTGGGC ATCCTGGGAG GAGCCTTCAC CCTCAAGTGC 420
CTGGCTGGGA TCTCTAGCTG GAATTTCCCC TCTGGATTTC CCTGCTGGGC TGAGTAGGGA 480
ATGGAGCAAT TTCTGACAGA GGCTTTTCCT GAAGGCGTGG GTGTTGCTGA GTGGTGGTGT 540
CCTGTCAGCC TCTTCTCTTC TGGTGGCAGC AGAGCCTGGC ACTGGAATAG CCTGTGGCTG 600
AGCTTCAGGT TTCCTGTCAC TTTGGCTGGG GTGTGGGCTG ACCACCAGAT GTGTGCTCAG 660
GGCGCAGCTC AGCCAGTGGT GAGCAGCTTA CTTGCATGGG CTTTTCCCAT GCTGAGTTTT 720
GAGGGGTGGA GGGAGGAAAT GGGGGTGCTG CTTTGTGGGA CAGCAGTGGG AGCCCTGCCA 780
GAGGTGAATG TGTGGGTACT CCTGGGGGAC TCGGTCTCGG GGAGGCCAGG GGCTCAGGAG 840
TCAGATTGGT TTTCCATCTG GCAGGAGTGC TGGCAGGTTG GGGGAGACAG GGGTGGGGGT 900
GAAGCCAAAT CTTTGGCCTT GCTTTCCCCC TACTTGCTGA GAGTGCCCTG GAGGAAGATG 960
GCGGGCAGGT AGGGCTGCAG CCCCCGCTGG GCTGGCTGAG ACCCCTGGGA AGGGAGGTCT 1020
CCAAGTGCCT GCTCCTGCAG CTCTGAGTGC ATATGCGCTC CCCACAGCTG CCCCCTTCTC 1080
CGGGGAACCC CCATCAGCTT GAGGAGCCTG GGGGGTGGGG TTAGGCATTT GCTCTCGCCT 1140
TCCTTTCCCC CTTGCTTTGG GTGGCCCCAA CTCTTACCCC ATCCTGCTGC CCTCCCTTCC 1200
TCCTTCCTGG GCACACTCCC TGGGGAAATC ACACCCATCC ACATTTTGGA ATGTCAGCAG 1260
ACATGCTGAC CACGTGACCC AGCCATCCGC CTTGGTGTCC ACCTGGGGAG ATGAAATCTT 1320
CTGTTCACAC GAACCTATCT CCGGAGGTTC ATAGCAGGAC TATTCACATC TGCCAAAAAC 1380
TGGAGATGGC CCAGATGCTC TTCAGTGGGT AAATGGAGAA ACAGATGCGG CCCATCCATG 1440
CGAGGGATCA CTGCTCCTCC 1460
|
