| Tag | Content |
|---|
EnhancerAtlas ID | HS037-24295 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr3:23077200-23078550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr3:23078037-23078052 | TATTAATCATTAAAT | + | 6.28 | | HNF1A | MA0046.2 | chr3:23078280-23078295 | AGTTATTCATTAATT | - | 6.29 | | REL | MA0101.1 | chr3:23077851-23077861 | GGAAATCCCC | - | 6.02 |
|
| | 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 |
| GH03I023035 | chr3 | 23077257 | 23079183 |
|
Enhancer Sequence | GTTTGCCTGG ATATCACCAG CAGAAGCTGC AGAACAGCCA ATATTGCAGA AGGGCAAATA 60
TTGCTGCCTG ATCCTTCCTC TGGAAGCTTC ATCCCAGAAG GGCTCCTGCC TATATGAGTT 120
GTCTGTCGGC CCCTACTGGG AGCTGTCTCC CAGTTAGGCT ACACGGGGGT CAGGGACCCA 180
CTTGAGGAGG CAGTCTGTCC ATTCTCATTC TCAGAGCTCA ACCACTGCTC TGGGAGAACA 240
ACTGCTCTCT TCAAGCTGTC AGACAGGGAC GTTTAAGTCT GCAGAAGCTG TCTGCTGCCT 300
TTTGTTCAAA TATGACCTGC CCACAGAGGT GGAGTCTATA GAGGCAGTAA GCTGTGCTGA 360
GCTGTGGTGG GCTCCACCCA GTTCAAGCTT CCTGGCCTCT TTGTTTACCT ATTCAAGCCT 420
CAGCAATGGT GGACGCCCCT CCCCCATCCA GGCTGCCACC TCGAAGTTTG ATCTCAGACT 480
GCTGCAATAG CAGTGAGCAA GGCTCCATGG GCGTGGGACC TGCCAAGCCA GGCATAAGGG 540
AGAATCTCCT TGTCTGCCAG TTGCTAAGAC CTTGGGAAAA GTGCATTATT CAGGCAGGAG 600
TGTCCCGTTT TTCCAGGTAC AGCCTGTCCT GGCTTCCCTT GGCTAGGAAA GGGAAATCCC 660
CCAACCCCTT GCACTTCCTG GGTGAGACGA CACCCCACCC TGCTTCGGCT CATGCTCCAT 720
GGGCTGTACA CACTGTCCAA ACTGGTTGGA CCCATCTTCT GCATCAATCA CGCTGGGAGC 780
TGCAGACTGG AGCTGTTCCT ATTCGGCCAT CTTGGAATGG ATCCCTTCCC TCTACTATAT 840
TAATCATTAA ATTTTCTTCT TCACATTTTA ACACTTCCAT GGAATTTTTT TTTAATTTTC 900
ATAGAGTACT CTTCCCCTTG TCTGACTTCT CTCAAGAATA CTAAGGTGAA GTCTATATTT 960
ATAAGAATTA TGCCCAGTAT TTCTACCATA CTATTTTTTT CTAAATACAG TATTTTTTTT 1020
ATTTTGTGCT ATATCAATGG ATTAATTACG ACTTAAGTCA CTATCTCTAA GTCCCAGATG 1080
AGTTATTCAT TAATTTCCTT AAATACCCAA CGAAACTCTT TGACATCTCT CTGATCTAGA 1140
CTCTCCCTTA ATGACTCTGT TCTCCACTTC TTACTTACTT TCCGTTTTTC TTATGTCACT 1200
TCTATAATTA GAAAGAACAC TGGGGCTACA AAATGTGGTC TTTAAACACC CAAAGGGCAA 1260
AAGCAAACAT TCCATGAGAG TCAAAGAGAA ACTGAAGCAC CAAAAAAAGA ACGATGACTT 1320
AGCCAAATTA ACTCCCCCAG GAAATTATTT 1350
|
