| Tag | Content |
|---|
EnhancerAtlas ID | HS136-00245 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr1:25466600-25467680 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:25467070-25467088 | GGAAGGAAGCCCGGCAGG | + | 6.35 |
|
| | 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 |
| GH01I025140 | chr1 | 25466725 | 25467101 |
|
Enhancer Sequence | CCATCTCAGT TAAGCACACA CCACCCCACG GGCAGGCAGC TGCTATCATT ATCCCTTTCT 60
CATGGTGGGG AAGTGAAGAT CAGAAAGGCT GAATAACTTG CTCAAGATCA CAAGTCTGGA 120
CTTGACTGCA GGCCTGGCTG ATCCCAGAGC CCAGATCAAG AGTCTCCCCT GGTGCCTCTC 180
CCCTAAAACC ACCTCAGAAA CCCCCTGGTG TGTAACTCTA AACCATGCCT GCGGCAAACT 240
CAGCCCATTT CCTCTTCTCG CATCTTAAGC CCAGATGGGG TCTGAGTGAC ACTTATCTCA 300
TACCCTGTCA TAGAGCTGGA GCCCCACAGG AATGTGGAAC TCCCCATGGA CAGAGGGCAG 360
GAGGAAGTGA CCGCCGGCCC GAAGGGGGCT TGGTCCACTG GGTCCAAAGG TGCCGTCTGG 420
CCCTGGCTGC CACATGCCTC GTGTCCACAA AGCAGAAGTC ACAGGGACAG GGAAGGAAGC 480
CCGGCAGGCA GACTGTCATC ACAGGTGGTG TGTCCTCCTA TCCAGGGACA AGCAGAACTA 540
GCCAAGATTG CCTTCTCCAC GCAGCCTCTC CTGATTCCAC ACTTGTGACT TCATGTTCCC 600
AGAGCGCTGT GCTGGCACGT GTGCTATGAT CTTGACTCTG TATGCACCCC GACGCCCAGC 660
TACAAGCAGC TCTACCCTTA CCTAACCTTT AAATTGCTCG ATTGCCTCAT CTGTAAAAAC 720
AGGGATGTTA ATAGCACCTG TTTCACGGGG TTATTGGAAG GTGTGTGTAC ATACACACAC 780
ACACACACAC TCATCAATAT AGATGAGTAT AGATTGTGTG TATGTATACA TGCTTAGAAC 840
AATTCCTGGC ATATAGTAAG TGCTTAATGA ACATTACCTA TTCTTATTCA TGTTAAGTGG 900
CTATGACAAT GTGCCAGGGA AGGACATCAC TTGTAATGAC GGGGGATAAC ACCTCTTACA 960
AAATCAAGTT GAGGTTCCCC AAAACTGGTC TGTGAAACAG CCTCCAGGGG GCTGTTTGTT 1020
AAAGAGACAG ATTCTGTGGT CCCACTCCTA GATCTAATGA TTTTAAGTCT CTGAGATGGA 1080
|
