| Tag | Content |
|---|
EnhancerAtlas ID | HS073-10234 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr3:46870880-46871890 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr3:46871446-46871457 | GATGAGTCACT | - | 6.02 | | JUND | MA0491.1 | chr3:46871446-46871457 | GATGAGTCACT | - | 6.32 |
|
| | 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 |
| GH03I046829 | chr3 | 46871093 | 46872080 |
|
Enhancer Sequence | CTGTCTAAAA CCATCCATCC AACTCACAAC TGGGCAGGCA GAGACTTCCT CTCTCACTCT 60
TTAGTTTAAA AAGAATCATC AACATCTTCC TAAGCTTAAT GTGAGGTAAG TTGTCTTCAG 120
TGTCCCCAAT AACCAGGCCA GTAGACATGG AGAACATAGG AGACTCTCCA AACATTTATT 180
TAGTTGATTT CTGAAAACTC TGCACTCCAT AACTGCCTCA ATACAACTTG TAGTGTCTCT 240
GAAAGTGGCC ACTAGGGCAC TGAGGAAGGG GGTGCCAAGA ATGGGTAGCC CCAAGAGAGT 300
TAGTGTGGCA GAGGCTGTCC ACTCACAGAT GGATCCACAC TGGGCTGCAG GGGAACTTCT 360
CCCAGCCCCA GACAACTGAG CCTAGAGTGG AAGTCCCAGG CCTCACACCT CTGCAGGGAC 420
CTGGTAACGC CTCCTTCACG CTGAGCAATC ACCCAGCTGG CTGGTTTCAC AAAGTCTTAG 480
GTGGGAGCCC TGAAACCAGA ACCACATCTA ACACTTGCTT CACTGTTGAT GATGTCTCTT 540
CTTTGATAGA TGTTCCCCCA GATACTGATG AGTCACTGTG GCCCACCTGG CAGGGAGGCT 600
GGTCCTCTAG CTGGAATTAG TTCACCCCCT CCTTCCCACT AGCCAGAGCA CAGCCCTGGT 660
GCAGGCATGG CTGAGGCAGG TGACCAGAGC ACCAGGCAGG GGCACTTTCC AGGCCCCAGT 720
CTCCCTGCTG TGCTCTATTG TATGGATCTC CAGAGGGCCC GTGGATTCCA ACTGGGATTT 780
TCAGAAACGG CATTGAGAAG GAGTGGGAGG TTGGAGGAGA GGCCTAGTAT GAGACTCAGA 840
AACAAAAGGG GAGTGGGCTG GGGTGATCAC TGGGCCACCA GGATGCCCAG GGGCAGCACC 900
AAATGCAGGA CTAAGATGAG GAACACTGCT GGATACAAAC AGGTAGCCTG ATCCACCACT 960
GCAATCAGCC ACTTACTGTA GACACCAATT TCTGTATAAA CTCCAGGCAA 1010
|
