| Tag | Content |
|---|
EnhancerAtlas ID | HS177-00073 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr1:7728110-7729230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BARHL2 | MA0635.1 | chr1:7728270-7728280 | GCTAAACGGT | + | 6.02 | | RFX1 | MA0509.2 | chr1:7728729-7728745 | TGTTGCCATGGGAACC | + | 6.37 | | RFX1 | MA0509.2 | chr1:7728729-7728745 | TGTTGCCATGGGAACC | - | 6.4 | | RFX2 | MA0600.2 | chr1:7728729-7728745 | TGTTGCCATGGGAACC | + | 6.78 | | RFX2 | MA0600.2 | chr1:7728729-7728745 | TGTTGCCATGGGAACC | - | 6.7 | | RFX5 | MA0510.2 | chr1:7728729-7728745 | TGTTGCCATGGGAACC | + | 7.02 | | RFX5 | MA0510.2 | chr1:7728729-7728745 | TGTTGCCATGGGAACC | - | 7.04 | | RREB1 | MA0073.1 | chr1:7728443-7728463 | CACCAACACACACACACACA | + | 6.14 | | TFAP2A | MA0003.3 | chr1:7728682-7728693 | AGCCTCAGGCA | + | 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 |
| GH01I007667 | chr1 | 7727681 | 7731218 |
|
Enhancer Sequence | CCCTTTGTCT GGCCCTCGTC CTGTCCCCTC CCTGCCAGCC TGTCTGTGCA CTGACTGCAT 60
CAGGAGTCCA ATCTGGCCAG GTTCTGCCAA GCTCAGGGAG GGCTCTACAG GCAGGCTCGT 120
CGGCCTGGGC CCTACTTCCC AGTCTGCAAA ATGGGGTTTG GCTAAACGGT TACTCAGCAC 180
CCCCACCCAG CTCTAAACCT CAATGCATCT ACCTAGCAGG AATGCGATGG CCGGGGCCAT 240
CCTGCTGTCT CTTCTCTGAG TGGCCCTCCC TCCCACAGGC TGCTCCCATT TCTCCTATCT 300
CTGTCCACCC CTTCACCTCC AGCTGCAGCT GGTCACCAAC ACACACACAC ACACACACAC 360
ACACACACAC ACACACACAC ACCCACCACA CACCCCAGAG GCGTCCCCCT ATGCCCCAGC 420
ATCTGCCCTG GCTGCATCAG ACATGGGCCC TTTATCTCAG GACTCAGAGA CCTCAGATGG 480
CATTTCGTGC CCCCTCCCCA CCCCCAAAAC CCTCCTGCGT CATCTCCCAC CACTGACACT 540
CCTGCTGCAG CAGCAGAAGA GCCTGCAATT ACAGCCTCAG GCACGCGCGT CACCACCAGT 600
TCAGCGCAGC CAGGCGGGCT GTTGCCATGG GAACCATCCC TTGAATGGAT GGATGCTGAG 660
CTGTCCTGCG GCGGTTTCCA TGGAGAAGGT CCTGATGTTC TCCAGTAATT TCTGCAGTTC 720
TTTGTTCCCG GCAGCAGCCC CAGCCTCATG CTAGCAGCTG TTGATTGCGG TTATTATTTT 780
TTCCCTTTTT CTCACATGGT AACTGTCTGT GGCCTTTTGA AGTCACTGCT CTTCCACTTC 840
CCAGGATCCT GGGGGATGGT GCCCTGAGCT GGCCTTCTGG TGCTTCCAGA CATCCCAAAG 900
TCAGGCTCCA CCTGTCCGCC GGCACTCTTC TCAGCCAGGC ACCCACTCCC CCCAATGCCC 960
CGCCACTTCC ACGGAGCTGC AAATATCCCT GGGCATCAGA ACAAGGGATG CTGTGGTCAG 1020
AAGGGCCCCT AGCAAGGAGA TGCCACCCAG AGAGGCTGGG CCACTTGCCT GAGGACACAC 1080
AGCTACTGAG GCGCAGGAGC AGGCCTCCTG CTTTTGTTTC 1120
|
