| Tag | Content |
|---|
EnhancerAtlas ID | HS167-06592 |
Organism | Homo sapiens |
Tissue/cell | Retina |
Coordinate | chr7:72824320-72825770 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr7:72825087-72825098 | GGGCGGGAAGG | + | 6.62 | | EWSR1-FLI1 | MA0149.1 | chr7:72825695-72825713 | CCTTCATTCCTTGGTTCC | - | 6.49 | | IRF1 | MA0050.2 | chr7:72824320-72824341 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 |
|
| | 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 |
| GH07I073410 | chr7 | 72824530 | 72825543 |
|
Enhancer Sequence | AAAAAAAAAA AGAAAGAAAG AAAGCCTGAG TCACAGGGAG AGGCTTCTCC CCAGCCCCTG 60
GGAAGCCGAA GAAGCCCTGG CCAGGCCGGC TCCCAAACTC ACGGGTCCTG CTAGGCACCT 120
GCTGTCACTC TCACTACCGA CCTGGGAGAA GGCAATGGCC CATTTATGAC ACTGGAGGCG 180
AGGGCCATGC ACCCCCTAAG CAGGCAGCAC CTCTGGAGCC ATTCTGCAGC TGGAGGTTCA 240
TTTCCTTCCT GATGTCATAG TGCTCCAAGG TGGCACAGCC AGGACGGGAG CCTAGGGAAT 300
TGTCATCCAC CCTGGAGCAC TTTCCGTCTC TCAGCGGCTG TCCCAGCCCT GCACTCAGGC 360
AATTCCTGCG GGAATCGGTG GCCCCTGGGC GTCCTGGATG GGGAACCACA GCCCCTGAGG 420
CAGAGCGGCA CAAACCCTCC AGTGGATCCC GTTCTCTTCT CCCAGGGATC AATGAAGCCC 480
AGGGTGTGGG GGCTCAGCCT TGGTGTCCCG GCCCCTGTGG TCACACAGCA GCTATTGCTA 540
TGGGGTTGGG ATGCAGGGAG GAAAAGCCCA GCGTCCCCCT TTCCACCCCA GGCCCCAACT 600
TCTCTGTATT TGTTTATTTA CCTTGGAAAA AGCCCCACAG CCCAGGCAGG AAATGGGCCA 660
ATTCCAGGAG GCCGGGCCGG GGAACAAGGA GCTACATTGT GCTCGGGCGG TGGCTCCCCA 720
CCCGGGCCTG CCAGGAGCCC AGAGGTGGGG GGGTCTGCAT GGGGACCGGG CGGGAAGGAG 780
GCGTGGGGCT GAGGGGCTGC CAGTACTCCC AACCAGCCAG CGTGTGAAAA GGCTTCTGTG 840
CAGGGGGTGG GATGGGGGCT GTGGCTCCCC GTCCCACCTG GGAATGAACA GAGGCTGGGC 900
AGTGGGGGAG GCAGACGCTG GGCTGGGGCT GGACCCCGGT CTTGACCCAG GGCCCACCTG 960
GCACTGATCT GCCTGCCCAA GGCAGACCCT GGCCTGGGAA CCCCATCTCC TTGGGCTGAG 1020
ATCCCACCCT GTGGCTGGAG AATGTTCCCG CCCTCGGCCT CCCTTCTGGG GTCTCAACTC 1080
CTGCCAGGCA GCTGGCCTGA CCTCAGACTG CCCCTAGCCC AAGGCTGGGG GCTGGAGAGC 1140
CCTGTGGTCA GAGCCCTCCC CTCCATGCCC AAGCCCAGGC TGGCACTGGG GCTGATGTCA 1200
TCATGGGGGC GGCTTGAGGA GGGCTGAGCT CTCCCTGACC CTAGACTCTT CTTTACTAAC 1260
AGGCTAGTGT CCATATGGAT GGATCATTCA TTCACTCATT CGTTTATTTA ATACACTCCC 1320
TGTCTGTTCG ACGCACACTC CCCTTCTCTC CACTTCTGGC CCCGTTTCCT CTAATCCTTC 1380
ATTCCTTGGT TCCCAGAGGG TTAAATGTAG ATCGATATGT CACCTCTGGC TCCAAAGGTC 1440
TCTGAAGGGC 1450
|
