| Tag | Content |
|---|
EnhancerAtlas ID | HS006-29433 |
Organism | Homo sapiens |
Tissue/cell | Astrocyte |
Coordinate | chr4:6326310-6327780 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr4:6327479-6327492 | TTCCAGAAGGTTC | + | 6.15 | | KLF4 | MA0039.3 | chr4:6327181-6327192 | CCACACCCTCC | + | 6.32 | | Klf1 | MA0493.1 | chr4:6327179-6327190 | GGCCACACCCT | + | 6.32 | | ZNF263 | MA0528.1 | chr4:6326440-6326461 | TTTCTCTGCTCTCCCTGCTCC | - | 6.26 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr4 | 6326343 | 6327574 | | chr4 | 6326548 | 6327555 | | chr4 | 6327616 | 6327666 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I006325 | chr4 | 6326728 | 6327327 |
|
Enhancer Sequence | CCAGGGGCCC GCCTGTCCCG AGGACTCGGG CGAATAAACA AACATGCATC GCCATGAGGG 60
TCGGGGCGAG CAGTGCTGAC GTGCAGGGGC TCGCTGCCCT CACCGTCCCG CTAAAGAGAA 120
TTCCACACCA TTTCTCTGCT CTCCCTGCTC CTAAGGAGAA GGGGTTCCTG CCGGTGGGAG 180
GAAGGGTAAG TTCATCCACA TAGTAAGAGG CAGGAGAGAA AGCACAGTTC TGTGGGCCTG 240
CGCCCAGAGG GAGGGTTTTG GGGTTTGGCC TCTGCAGGGC CCTGGAGCAG CTGTGAGGTG 300
CAAGGTAACT GGGGAGGAAG AGGATGTTAC GAAAAGCGAC CATAAAGAAG TTGTCCTGCT 360
GAAGGCTCTT CAGGGAGGAA ATCCTGTTTC CTTTTGGAAG CTGAGCTGGG CTTCCTGAGG 420
GTGACACTGC TCTGTGACAG AACCAGGTGG ATCCCTGGGT CTCCAGGGGT TATGCACAGA 480
GGACAAAAGC TCACACGTGA GCTCCGGCAC TGCAGTCAGG GGCTTGGGCT CTGGCCAGTC 540
CGCCTGGGTC CGGATCCCAG CTCTGCCCTA CCCTGACATG CGCACTCTCT TAGTTTTCTA 600
TAAGAACTGG GATCAACAAG GGAACGCAGC CCCTGGTGAG CGTGAATCAG GGGACATAGG 660
CTGAACACCC CGCACAGTGC TGGGCTTGAG GCACTTTGCT TCTTGTTATT TACCAGGTAC 720
TCCTCGATCC TAATCGTCCA TGTGACCAAA GCCGCACCCG CTTTATATGT GACTCAGAGC 780
CTGGGACAAG GGAAGCAGCA TGCGAGGGGG GCCGGGTGAA CGAGTCCCAC AGAAGGGCCC 840
TGCCCAGGCG CCACAGGCTG ACTGGGGGAG GCCACACCCT CCCCGCGCCA GCACAGTGGG 900
GAGGCAGCCC CCTTTGTTCT TCAGGGAACA GTTCACAGAA TGAACCTGGG TGATTTCACA 960
CAATGCTGGT TCTTCTGATC CATTTAGTGG AAGGAGAGCG ACATAATTAA AGTCATTTGC 1020
AACCCACACA GTTCCTGATC CTCCCCCTGT TCGGGTGTGG AATTCAGCTG ACACGTGCTC 1080
TGGGGGAGAG GGAGGGGCCC CTCTCATCCT AGAGCACCAG GCCGCACCAC CATGAGAGCC 1140
ATTCCTCACA TTCAGGCAGG TTTCTTAAAT TCCAGAAGGT TCCCTTAACA GGGAAAAGGG 1200
CAGGGGAGCT GCTTCACCTC TCCTAGCCTC ATCTGCATGT GGGACCACAA CGCCGGCTGC 1260
TTTCAGCCCC AGTGCTCCGC TCCTCTTTCC TTTGGGGAAA GAAAGGCTCC TGCCCTCGCC 1320
ACCCGTGGCG CCTGTAATCC CAGCTACTTG GGAGGCTGCG GCAGGAGAAG TGTTTGACTC 1380
CAGGAGGCGG AGGTTGCAGC GAGCCGAGAT GGCGCCACTG CACTCCCTAT CCCTGTGAGC 1440
GGTCAATCAC AGTGCTCTCC TCGCCCCTTG 1470
|
