| Tag | Content |
|---|
EnhancerAtlas ID | HS182-19690 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:30489670-30490830 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mafb | MA0117.2 | chr7:30490175-30490187 | AGTCAGCATTTT | - | 7.22 | | NR2C2 | MA0504.1 | chr7:30490678-30490693 | TGACCTCTGCCCTGC | - | 6.45 | | SCRT1 | MA0743.1 | chr7:30490796-30490811 | GCCCACCTGTTGCTC | - | 7.61 | | SCRT2 | MA0744.1 | chr7:30490798-30490811 | CCACCTGTTGCTC | - | 7.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATGGTGGCGT GTGCCTGTAA TCCCAGCTAC TCAGGAGGCT GGGGCAAGAG AATCGCTTGA 60
ACCCAGGAGG CGGAGGTTGC AGTGAGCTGA GATCACGCCA CTGCACTCCA GCCTGGGCAA 120
CAGAGCGGGA CTCCATTTGG GGGAGAAAAA AAAAAGATGG ACAGAGGGTG GCACTGAGTG 180
TGAGACTGCC TGGGGCTACA GAGGGAGAGT CACTGGCTGA GAGTACAGAG AACAGACTCC 240
AGGTTTTCCA ATTCCCAGGC TAGGGCAGCC TTCGACCCCC TGCACCCCAT GTCCCCATGC 300
AATTATTTAC ACTCTGACAC TGGTGTGACA GGCACTGGGA GTCAGTTCCA AATCCCTACT 360
GCTTTTTAGA AATGCATGAG TCAAGTAATG GCAAATTTAA CCCCCTGTAG AGATTTACAA 420
GGTTTATTTT ACATAGGAAA TGCTAATAGA AGAAAACAGA CTGGGCTCTG TTTCCCGTAA 480
ACTATGGAAC AGGAAAACAA CCACGAGTCA GCATTTTAAC TGAGGTCTCT AGCAGTGTGA 540
AGGGCTGCTA GCGTTGATCA CAGAAAGTCA CCAGTGCCAA CTGGCACAAG GTCTGCTTTC 600
TCTGCAGTAA TAAAAGCTCC CATATTCCAG AAACTTTTTG AGGGCTATCT CGGAGCCTTA 660
CATTAATCTT AAAAGGAAGG TTCTTTATGC ATTCTGGCAC TGCTATGTCT GAGCTGTGTG 720
ACCTAAAGCA AGCTATTAAC TTCTCTGTGC CTCTACTTCC TTATCTGCCA AAATAGAGAC 780
AATAACAGTA CCTAAGTTAC AGGGTTGTAA AGAGCATTCC ATTAGGTAAT ATTTGTAATG 840
CACTTCACCC ATTCTCAACT AACATTGGTC CCTGTGGCCA TAATTGATAG GATTATGAGC 900
ATCTTCTTTT TCCAGATGAG GGCGTGGAGG CTCTGAGAGT TAAGCACTTT GTTCAAGGGC 960
ACCCAGCTGT GGCTGATCCA GGTCCACCTG CCTCGAAGCT TTGCACCTTG ACCTCTGCCC 1020
TGCTAAGAAA GAAAAGGTCT GGACATTCCA AGGGCCATGG TCATGAGTCC TGGGGGATCC 1080
TGGTCCATGA TGCCATTCCC GATGCCCTCC GAGCCTGGCC CGCCCGGCCC ACCTGTTGCT 1140
CCCCTTGCCT GGCAGCCTCA 1160
|
