| Tag | Content |
|---|
EnhancerAtlas ID | HS105-15350 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:77595000-77596200 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr11:77595636-77595647 | TATGTAAATAT | + | 6.62 | | HES2 | MA0616.2 | chr11:77595942-77595952 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr11:77595942-77595952 | GGCACGTGCC | - | 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 |
| GH11I077883 | chr11 | 77594553 | 77596081 |
|
Enhancer Sequence | AAAGGGTGAC AGAAATGAGA AAAAGGCAGA AGCGAGAGGA GCATTTAACA AAATGGATGA 60
TGACATCTGT TGTGAACCTC AAAACACAAG AAGAAACATG ACACCAACTT TACTAAGATT 120
GAGCCTTGGG GGTAGGTCAA CACTGTAGAC ATCTCTATTC CCCTAATCCA GCATGAAGCA 180
GTGTTCAGTA AACATTTCCT GAATTCATGG TGAATAAGTA ATATGAACAG AGTGTCTCTA 240
TTAAGCGCAA AGACAGGTAA GAATATTAAT TCTTATTATG AAAAGTGTTC TCAGGCACCT 300
TCACCAGAAG AGCACTCCCT CCCTGGCTCT GAATCATACC ATGGCCCAGC ATCCATCACC 360
AACCACCAGT ATTTGGAGTT ATTTTGTAAT TGCATTCTTT CCACTACATT GCAAGCAGCT 420
AGGAAGTCAT TTATCTCTCT CTCTACGGAG AGACGGCTCA ATGAAGAGTC CACTCAAATC 480
ACTGGCCAGT TCTTTAAGGC TCATAAACTG CAACAGAGTT CTTTCCTCAG CATCCTGGGG 540
GACCTCCCAG CTCCCTGTGT AGACAGCCTA CTATACTGCA GCGCACAAAG GAACTAGAGG 600
AACAAATGAA GCTTATCCTA GGACTAGGAC CTGCTCTATG TAAATATACT TATGAAGGCA 660
GAGTAGGGAA CCACACAGGT CTTCCAATGT TGAAACTGTG GTCAATGTTG AAACTGCGGA 720
AGGCATGTCT CACCCACTTG CCCTATAATC CTTCATCTCT CCTCAGGTCA TGGGGCCTCC 780
CCCTGATTCT ACACTTCTTT CTTTCTTTTT TTTTCTTTAA AACAGGGTCT TACTCTGCCA 840
CCCAGGCTGG AGTGCAGTGG CACGATCATA ACTCACTGAA GCCTCAAACT CCTGGGCGCA 900
AGTGATCTTC CTGCCTCAGC CTCCTGAGGA GTGGGGATTA CAGGCACGTG CCACCACGCC 960
AGGTAATTTT CTTTTTAAAT TTTTTTGTAG AGACAAGATC TTGCTATGTT GCCCAGGCTA 1020
GTCTCCAACT CTTGACCTCA AGTGATCCTC CTGCCTCAGA CTCCCATAGT GTTGGAATTA 1080
CTGGCATGAG CAATTGTGCC CAGCCTACCC TTATTTCTTT TTCTTTTTCT TTTTTCTTTT 1140
CTTGAGATAG TCTCACTCTG TCACACAAGC TGAACTGCAG TGGCATGATC TCGGCTCACT 1200
|
