| Tag | Content |
|---|
EnhancerAtlas ID | HS041-00599 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:22675850-22677430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr1:22677408-22677419 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr1:22677408-22677418 | GCCCCGCCCC | + | 6.02 | | SP1 | MA0079.4 | chr1:22677405-22677420 | CTAGCCCCGCCCCCC | + | 6.67 | | SP2 | MA0516.2 | chr1:22677404-22677421 | CCTAGCCCCGCCCCCCT | + | 7.39 | | SP4 | MA0685.1 | chr1:22677405-22677422 | CTAGCCCCGCCCCCCTC | + | 7.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 22677022 | 22677200 | | chr1 | 22677200 | 22677422 | | chr1 | 22676281 | 22676600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I022349 | chr1 | 22675891 | 22678331 |
|
Enhancer Sequence | GCATTCTGGG TATAGATGAG CCATGCCCTT CACCCTAAGT GGCAGTCCTA ATGCTCCTTG 60
CTGGGTCCTG GATTTCAACC CTGTGTCTCA CATGTACATG CAAACGTGTG TGCAGACAGA 120
TGTGTGCACA GTGTGTTTCC TGAGGCTGGG CATGCTGCCA GCTGATGCCA AAATAGGGGT 180
GGGGACAGTA ATCTCTAATC CAGAGACGAG AATGATCTTT GATATGAGAG CTGGTTCTTA 240
AAGCTGCTTC TCTTGTTCCA GGCAAATAGA CTAATTGGGA TTGCCTCCCC GTCATTTTCC 300
CACCCTACTC CAAACACGCA CTCACACACC CAAGAGACAC ACATGCGAAT ATACAGATTC 360
TTAACAGCTA GGCATGGCTT CTTTTTGCTG GGAGAAAAAC AGAGACAAAA GGATTAAAAA 420
CATACATGTG GTGACCTCGA GTGTGTCTGC ACAATCTCCA CCGGGAGTGC TCCAGCAGGC 480
GCACCCACGT GCACGTGCAC ACACACACAC ACACAAACAC ACACACGGCA TGCTCCCAAG 540
GACACAGCAT CTGTGTGTGC TTTGGGGGGT ACACACATGT GCCCACACAT CTGGGCAGCG 600
TGGTCCTGTG AAAAGAGACA GGTCCGTGTC CAGTTTGCTG CTTATTAATT TTGTGAATTT 660
AAGCAAGTGT GGCCTCTGGA AGCCGTTGTT TCTTCCTCTG GGCAGTGGGA GGGCAGGTGT 720
GGACGTGCTT TATGCATTGT AAACTGCCAT CTACATTAGG GAGCCCACCG TTGTTAGATA 780
TGCACGGGCT CATATTTATA AAAACCATAG GAAGCAGTGT TGGTAGACTC TCCCTCTCCC 840
CGCCTCTGCC TTCCGCACTG GGATGCTGTT CTCATGGCCT CCCTTCTGCT CTGCTCGGCT 900
CACTGCTGTC ATCTCCGCCT GCATCACGTT AATTACAAAT CTTGGCGCTT TCAGATCTAG 960
CTCGGGAAAG GATCTCAGAA GTTACCCAGT CAGAGAGGCA TGCGCTGTTT CTGTCCCAGA 1020
GAGGTATAAC CCAGGTCTCA GCAGAACCTG GCATACACTC TGGATGTGGC TTCAGCCCTC 1080
TCAGGGAGGG CACCACTCCT GGATGACTGA GCCAGGGCGC GAGCCCCAGG GAAAGGGGGA 1140
TCAACAGACC CAGGAACTCG CACTAGCTCA CCCCAGCAAG GGGAGGGGCT GGCCCAGGGG 1200
CCCTGCTGGC AGAGCCGGCC AGGCTGGGAT TTATGGGCCC CTTTTGGACA CGTTAAAGAT 1260
CACATTAAGT GCAATAAATG TAGATCACGC TCCTAAATAA GCTGAGATTT ATCCCCGGAT 1320
CCTCTCCGCA GGGGCCAGCT CCATAAATCC TGCGCGACCC TGTCCCCTGG CCAAGGGATG 1380
GGGGAGGGGA GGCCAGAGTG GGGAGGGGCG AGGTGTAGCA GGGCAGTTCC AGGTACAGAA 1440
GGATGGAGCT GAGCAGGGGC TGCAACAGGG GCCAAGAAAG GGGGCAACAG TGGGCCCAGG 1500
CGGCCTGCCC CTGACCTCCC GCTCACTTGC CCAAGCTCCT TACCCCAGCC CTCTCCTAGC 1560
CCCGCCCCCC TCGCATCCTT 1580
|
