| Tag | Content |
|---|
EnhancerAtlas ID | HS182-11254 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:35157310-35158540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr19:35158394-35158404 | GCTAATTGGG | - | 6.02 | | FOXA1 | MA0148.4 | chr19:35158422-35158438 | CTTTATTTACATAGGG | - | 7.15 | | SP1 | MA0079.4 | chr19:35157509-35157524 | CAAGCCACGCCCACC | + | 7.91 | | SP3 | MA0746.2 | chr19:35157511-35157524 | AGCCACGCCCACC | + | 6.78 | | SP4 | MA0685.1 | chr19:35157509-35157526 | CAAGCCACGCCCACCGG | + | 6.51 | | SP8 | MA0747.1 | chr19:35157512-35157524 | GCCACGCCCACC | + | 6.62 | | STAT3 | MA0144.2 | chr19:35158184-35158195 | CTTCCCAGAAG | - | 6.14 | | ZNF263 | MA0528.1 | chr19:35158167-35158188 | ACCCCATCCTATCCCTCCTTC | - | 6.27 |
|
| | 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 |
| GH19I034666 | chr19 | 35157763 | 35158955 |
|
Enhancer Sequence | CCAAGCCTCT CGCCCCACAT ACAATGTGAC AGGCCACTGG GCCACCTGCG GGTCCCAGTG 60
CACATGGATG CCTGCAGTGC ACAGCCACCT AGATCCTGCA CCACCGGACA GGAAGGGGGC 120
GGGTACCTGG CAGATGCCAC CTGCTGCGCC CACTGGGCCA CCAGAAACTC CACCTCTCCC 180
CGACTCTCCA GGTCCCAGCC AAGCCACGCC CACCGGGCCT GCCCCCAGGA CCCTGAGTTT 240
AAAGACCCCA TCTCCCCAAA TGCCAGAGGG AGAGGATTCC GCACCACCCC AAGTGTAACC 300
CACACCCTAG TCGGCCCTGA CCCCGCACTG CATGGCGCCC ACCTGAGCCC TGGCGTTGCT 360
GGGCCTCCTG CTGCTGCTGT TGCTCGTGGG TAGGCCCTGC CAGGAGACCC TGGGCTGCGC 420
TGCAGCCCTG GGGTACCCAC CCCTCCCTGC TCACGTGCTC CTACTCTCCC TGCAGATCCC 480
AAGAAACTAT GCCCGCAGCT CGTGACCGTC ATGAACCAGT TTCTGACCGA GGACAAGGAC 540
ACCTACATGG ATTCTGTCAA CAGATATCAT CCCACGGAGC TGGAAAGAAA CACACCCTCC 600
AAACTCAAGG ACATGGTGAC CAACACCACG ACCCCCGAGG AGGGACAGGC CGTCATGCAG 660
CAGGCCCGGC CACCAGCGCC TCCTCACAGC CCTTGACCTC CTTTGAGATC AGGGACTCTG 720
TTCCCTGAGA GCCTCTCTCT CCACCCAAAC ACTTCCCCAC CTCTCACCAA GCAATGTCCC 780
TGCAGACGGG CAGCTGCCCA GGGAAAAGAC CTCAGGGCGC TGGGTCTCCG CCCTCTGATA 840
CTCAACCTCT GCTGTCAACC CCATCCTATC CCTCCTTCCC AGAAGACCCC TCCCTTCAGC 900
CTCCCACCCC TCCCCACAGG AAGAAATCAA CAACCAGGGT GCCTACACGG TACTGAAGTG 960
ACACCATCCA CAGGCACCTC GAATCTCTGC CCAGGCAGCC TGTCCGGCCC AGGAGAACCT 1020
GGGCCCGGGG CCCCACCCTC CCCAGCTCCT GCCCTGCTGC TGCCCCTCCT CCCACTCCTG 1080
CTGTGCTAAT TGGGGCTGAT TGCGGGCCAC TACTTTATTT ACATAGGGTG TACACCAAGT 1140
AACCAATGGG AAGCCTCTAG AGGGTATTTA GACCCCAGGA AATTCTAAAT GGGCTCTTGA 1200
GCCCTTATGC TTGGGCCTGC TCCCGGTTTG 1230
|
