| Tag | Content |
|---|
EnhancerAtlas ID | HS167-06081 |
Organism | Homo sapiens |
Tissue/cell | Retina |
Coordinate | chr6:116550070-116551220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | - | 7.21 | | RFX1 | MA0509.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | + | 7.24 | | RFX2 | MA0600.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | + | 6.93 | | RFX2 | MA0600.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | - | 7 | | RFX5 | MA0510.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | + | 6.55 | | RFX5 | MA0510.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | - | 6.82 |
|
| | 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 |
| GH06I116228 | chr6 | 116550108 | 116551187 |
|
Enhancer Sequence | TACCACTGGG AAGCTTTTAA CTATCATCTA TATACTGATG GTTGACATTT CCTTGTCTCT 60
GGGCTTCACA TTTCTCTGAC CTTCAGAAGC CCATTTCTAT CTGTCTTCTA AAATCTTCAC 120
ATCCCACAGC CCCAGGGTGG CAGGAAAGTT GATGTGCTTG CAACAGCTCA TTAAATCCCC 180
ATCCCATTTT AGCATGCCCC TCTTCCCATA TTCCATAATT ACATTTTAGT TACTTTTCCA 240
AGCACAGACT TTAACCAAGC TAGTAAGCAA AAACCACAAT TACTTTTGCA CTAACCTAAA 300
AAATCAGTCA TCCTCATTTC TTCCCTCCCT TTTAAGTTGT CCTTCTGTTT TCTCAGGTTT 360
GTCCTCACTA CATTCCCACC ACTGCCCGCA TCATCCCTTG TGTGAAATGG CACAATATTT 420
AAGTCATTGC TCCAAATGGT TAAAGTAAAG TTAATGCAAC TGAGCTGGCT GGGATGGAAG 480
GCACAGCGAG CCAATCACGA AACACAGCAT GGCCTTAGCG AGTCGCACAG GTTTGACGTC 540
AGCGGTTGTC ATGGTAACAG GGGCAAAGAT GCTGATGCCA GTGTCAGTCA GGACTGAGCT 600
CCTCCCTCCA GTCTGATTCC TGCCAGTGCT TAAGGATGTA TGGAGGGGAG AAGCGTCTTC 660
CAAGCAAAAT CTTCATCCTC TGTTCTCTAT CACGTGCAGT GCGTCACCAG ATCCTCGCCA 720
GTGCTGAGGG TGGGGATACG GGGGAATCTC TGACTTGCAA GATTAAATTA TCATTGGAGA 780
GGGAACGTGT CAGCCTTGTT CACCGCAGTG TCGCCAATGC TGCTAGCTCA GTTCCTGCCC 840
CTGCCCACCA TTGGGAGAAT CATGAGCCAA CTCTCTCTGT CTCTCCTCTC TCTCTCTCTG 900
TCTCGTCCCT TGGCCTTAGC TGTCACCAAT ACACTGACTC TGACTCCCAA ATCTTTCCCT 960
GAGACCTGTT TTCCTGAGTC TCATACGCAG TTCCTCCTCC ACACTAGGCA GCTCCACTCA 1020
GTGTTCTGAT ATCAAGCTTG AGATTCTCCT TCCGCCTAGA AACCAAAAAC AACCAAACAT 1080
GCCGGTCACC TTGTGTGTAT TCTTTACTTA ACCATCCATT AGAATTCTCC AGCTAATAAC 1140
CTCCGTTGTC 1150
|
