| Tag | Content |
|---|
EnhancerAtlas ID | HS060-27499 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr5:68520680-68522130 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr5:68520766-68520776 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr5:68520766-68520776 | GGCACGTGCC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr5:68521626-68521641 | TGAACTCCTGACCTC | - | 6.22 |
|
| | 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 |
| GH05I069225 | chr5 | 68521366 | 68522415 |
|
Enhancer Sequence | CATGAGGTCA GGAGATTGAG ACCACCTTGG CTAACACGGT GAAACCCCGT CTCTACTAAA 60
AGTGAAAAAA ACTAGCCGGG CGTGGTGGCA CGTGCCTATA GTCCCAGCTA CTCGGGAGGC 120
TGGGGCAGGA GAATCGCTTG AACACAGGAG GTGGAGGTTC CAGTGAGCTG AGATCGTGCC 180
GCTGCACTCC AGCCTGGGCG ACAGAGTGAG ACTCCGTCTG AAAAAAGAAA AAAAAAAAAA 240
AGGCAGTAAA TTTCCAGTGT TTTTTCTTTG AGATGGGGTC TCACTCTGTT GCCCAGGCTG 300
GAGTGCAGTG GCAAGATCTG AGCTCACTGC AACCTCTGCC TCCTTGGTTC AAGTGATCCT 360
CCCACCTCAG CCTCCCAAGT AGCTGGAACT ACAGGCACAT AGCACCACAT TTTTTTTTTT 420
TTTTTTTTTG AGACGGAGTC TCGCTCTGTG GTCAGACTGA AGTATGGTGG CACTATCTCT 480
GCTCACTGCA ACCTCTGCCT CCTGCGTTCA AGCGATTCTC CTGCCTCAGC CTCCTGAGTA 540
GCTGGGATTA CAGGTGTGCA CTACCACCAT GCCCTGCTAA TTTTTGTATT TTTAGTAGAT 600
ACGAGGTTTC ACCCTGTTGG TCAGGCTGCT CTCGAACTCC TGACCTCGTG ATCCACCTGC 660
CTCAGCCTTC CAAAGTGCTG GGATTACAGG TGTGAGCCAC CATGCTCAGC CACCTTTTTT 720
TTTTTTTTTT TTTTTAAGAT GGAGTCTCAC TCTGTAGCCC AGGCTAGAGT GCAGTGGCAC 780
GATCTCAGCT CACTGCAACC TCTGCCTCCG GAGTCCCGGT TGGTTCAAGC AGTTCTCCTG 840
CCTCAGCCTC CCAAGTAGCT AGGATTACAG GCACGCATCA CCATGCCCAA CTAATTTTTG 900
TATTTTTAGT AGAGATGGGG TTTCACCATG TTGGCCAGGC TGGTCTTGAA CTCCTGACCT 960
CGTGATCCGT CCGCCTCGGC CTCCCAAAGT GTTGGGATTA TAGGCGTGAG CCATCACACT 1020
GGGCCTTGTT TTTCTTTTTG TTTTTGTTTT AATTTTTGGT AGAGACGGGG TTTCACCATG 1080
TTGCCCAGGC TGGTCTCAAA CTCCTGCACT CACGCAATCT GCCTGTCTGG GCCTCCCAAA 1140
ATGTTGGGAT TACAGGCATA AGCCACTGCA CCCAGCCAGC TTTCATTCTT ACCAATCTAT 1200
AAGTCATGCA ACATAAACTC TACATCATCT CCTCCATTGG GTTGCTTTGA AGTGAAGTAC 1260
ACCTTCGATA GTACAATGAA GTCTTGTGAT ATATAAAGTA CAAAGTTGTG TTTACCGGGT 1320
AGACAAGTTA ATAATTCATA GACCAGCTTT CCTGGTTGGG GAAGAGTATA ATTTAAAGTT 1380
GCTGTAAAAT AGTAATTTTA ACAAACGTAT CTACTTATGA GGTTTAGTAG ATCATTTCTT 1440
TTAGTTAATG 1450
|
