| Tag | Content |
|---|
EnhancerAtlas ID | HS095-26021 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr6:37624950-37626020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr6:37625467-37625478 | GGATGACTCAG | + | 6.32 | | JUNB | MA0490.1 | chr6:37625467-37625478 | GGATGACTCAG | + | 6.14 |
|
| | 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 |
| GH06I037657 | chr6 | 37625139 | 37626050 |
|
Enhancer Sequence | AAGCTTAAGA AAGAATCGAT ATTTGGCCCC ACCCCTGATC AATTACATCA GAATCTCTGG 60
AAGGAAGCCC CAGGCATCCG TTTTTTTAAA GGGTCCCCTA GAGAGCTTAA TGTATGGCTG 120
TGAGTCACAG GCATTGACAG TACACATTCC AACATCTTGC AACGAATGTT CCAGCAGCCC 180
ATCATTCTGC CCCTTCCACA GCCTACTGGG ATAGAAGTCA CCACCATGGC CATGAGAGGA 240
GGTGGGCATT GGTGGGGTCC AGGCTATGCC TGCCAGCCTC TTCCAGGGCC AATAACCTAA 300
GAAATGGCCC TCAGCTCCAG GGTTTGGCAG GACCCTGGCT AGCTGATGAG GGACAGAAGA 360
GAGGTCTGGG GTGTCAGTGT TCATCACTCT ACTGAGTCCC ACTTAGGGAG TGTGAGGATG 420
TATAGCTAAT AGGTAGGTTC ATTATAAGCC TTAAAATGGT GCCAGACAGG CTCCTGGGCC 480
TGGGCCAACA GTTTCTGGGT ACCTGACTCA GCCTGACGGA TGACTCAGGA AAACAGGCTC 540
CTCGGGCTAA AGGATTACCC GTGGAGAGCA GGTAGGGACT GGCAGCTTCT CATGCAGCTA 600
GCAGCTAGGA CCTGGGGAGT GGGGCTTGGT CCTATATGTA ATGTAGTAAG GAGGGAAATC 660
TCAGAGCTGC AGCAGGACAA AAGCAGAGAC ATGAGGTACT GTGGGAAGGG CAGCGGACAA 720
TGGGGAAGAG ATCTGTGTCT TCCTCTCAGC TCTGAGGCTA CCCCGCTCCA TGCCTGTGGG 780
CAAATCACAT GGGACCTCAG TTTTCTCATC TGCAGAAGGA GTGTAAATCA ACCCATCCTG 840
CCCTCCCTGC TCACCTCAAG GGAAGTTGCA AGGTTCATAT GAGATTACAG GTGCGAAGGT 900
GTAGATGGTA GAGGGTGGTA CACACCGCCT GGTACCTCTT AGGCTCCTCC ACCAAGGTCA 960
GCTTCTCCGT TCCACCCCAT GCCCACTTCC CCACCTCACC TCATCCCTGG GGCGCCCTCT 1020
GGCCCGGGCT GGGCTGTCAG GGCCCGGGGA GAGAGGGGGC CTCAACTCAC 1070
|
