| Tag | Content |
|---|
EnhancerAtlas ID | HS167-00295 |
Organism | Homo sapiens |
Tissue/cell | Retina |
Coordinate | chr1:3648120-3649310 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr1:3648914-3648931 | CAGGTCACGTTAACCCT | - | 6.32 | | ZNF263 | MA0528.1 | chr1:3649165-3649186 | CTCTCCCCCTCCCCCGTCTCC | - | 6.16 | | ZNF263 | MA0528.1 | chr1:3649253-3649274 | CCCCCCTGCTCTCCCTGCTCC | - | 7.65 |
|
| | 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 |
| GH01I003731 | chr1 | 3648465 | 3650502 |
|
Enhancer Sequence | GTAACGCCCG GGTGGACCCC GCTCTGCAGA GGCAGTAGCT GGAGGGGCCC CTGTCCGGAG 60
GGCAAAGAGC CTTCTCTTCC TTGCTCTCGT GGCTGGGAAA CTTGGAAACC CTTTCCCACG 120
GGCAAGCAGA TGCGATGATT TGACTCTTGA GAGCTTAGGC AGATGCAGCC AGGCACGTGG 180
CTGGTGGCGC GGGACACAGG CCCAGGCCTC CGGATGCTGA ACTGGTCATT TGAGCCTTTT 240
TGGACTCCCA GCAGCCAGTG TGCCTTTGAT TTTAGGGGAT GGGCTGTTTC CAAGGCACAA 300
AGAACAGAAG AATGTAAGGC CCCGAGGGAG TCAGTCCAGT TCAGTGCCAT TTACAGAGAG 360
GTCAGCGCCA TTTACACAGA CAGGAAAGGG GACCTAGGGA AGGCAAGCAC CTGGCCCGAG 420
GCCACACAGC TCTTGGCACC CATGGCAGCT GACTGCAGGC ACCATGATTA AACAGCCACG 480
GCTTGTCTTT GGGTTAGAGA CTAGTGGAGT ACAAAGCCTG CTGGTAGCCT AGGACGGTGT 540
GAACCACAGG GCACCGTCAG TCAAGGAAGA GCAAGCCCTC TGGTGGGAAC CTGCCCCCCA 600
GCCAGTGCCG CGGCCCAGGT CCAAGGCCCG TCCCAGACCA TCCCCAGCCT GGGGCTGCAG 660
ACAGAGATGA GGGTCAGTGC GAGCTAGGGC CAGCTGCTCA GCCTAACTGT CCCTCGTGCA 720
GAGAGTGGCC GCGTCTGTGT CCACTAACCG CCCTCCCCGC AACCTGTCCC CAGTGACCCA 780
CGCTGAGCCA GCTCCAGGTC ACGTTAACCC TTGCCTCCCC TGAGTGATGT GTGTGCTTGG 840
TGTGGTGCCC AGAGGGTGTT GGGAGCTCAG GGATGAGCTG GGGGTCCACT CCAGGGGGCA 900
GGGACATGGA GACCAAGGAG GGCCCTGCCC TGAGGCTGGG AGGCAGTTCC TCCCCCAGGG 960
CCAGGTAGAT GCTCAGGGGG CTCCATGTCT AACACTCCCA GGTCAGGGCC CAGGCCCCGC 1020
ACAGGCCAGG AGTGACTCTG GTGGGCTCTC CCCCTCCCCC GTCTCCTGCC TACTCTGGTT 1080
GGGGGTGTAG GGGCCAGGGT GTGGTGTGGC CAGACCTCCA GGCCCAGGGC GACCCCCCCT 1140
GCTCTCCCTG CTCCACTGCC CCCTGCCCCT AATGCGCCGG CCTCTCGCAG 1190
|
