| Tag | Content |
|---|
EnhancerAtlas ID | HS182-22352 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:139855040-139857230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr9:139856334-139856346 | CCCCACGTGCCC | + | 6.07 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr9 | 139855584 | 139856155 | | chr9 | 139855130 | 139855579 | | chr9 | 139856495 | 139856762 | | chr9 | 139856243 | 139856392 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH09I136959 | chr9 | 139854222 | 139855427 | | GH09I136961 | chr9 | 139855652 | 139855853 |
|
Enhancer Sequence | TGCAGCTGCG GGGTGGGTAG AATGTTCTGT GGCCGGGGGC GAGGGTGCTG CCTGCAGTTG 60
GTGGGGGTAG AATGTTCTGT GGCCGGGGGC GAGGGTGCTG CCTGCAGTGG GTGGGGGTAG 120
AATGTTCTGT GGTCAGGGGT GAGGGTGCTG CCTGCAGCTG GGGGGGTGTG GAATGTTGGA 180
ATGTTCTGTG TTGGGGATCG GAGCGCTGCC TGCAGCTGGC AGGAGGTGGA GGGGGTCTGG 240
AATGTTCCAC GTCAGGATCA GGTTTTGCTC ACGTGGGTGT TCATCGAGGT GTGCGACTCA 300
GGTGCCCGTA TTGCTGTGAG ACGGCTCCCA CGGTGGGACA TGGTGATGCC ACGCTGGATG 360
CCCCCACGTG CACCTCTTGC CGTGTGTGGG TGAAACTCCT CCCGCTGAGT GCTGGGCTCC 420
CGGGTCTGGG TCTGGGGGTG CAGCACACGT TCATGTTCGC ATTCTCAGAA CACCCACTGA 480
CCCTCTCCCA CCAGGCAGAG CCCACCCTCC CTGCCTTCAT GTCTGCAGGG CCTGGCGCGG 540
AGCACGAGGC CGCTGGGCAC TGACTATGGA GCTCAGAGCT GTGTTGGTGG ACCAGGCATC 600
CCGTGAGGCC ACGGATGGTG GCCGTGGATC TACCCTGCCT GGCCCACTTC TCCTCCACAC 660
TCCCCTTCAC AGCGCATGAC TAGGCAGCCA GGGCCCTGAG CCCTGCAGGA GGAGTTGAGG 720
GGTACACACC AGGACTGGAA AGCCTGGGGC TGTTGCACAG AGATGAGCGG GGAGGCCAGG 780
CTCCTCAGGA ACTCGAGTGG AAGCCCCACC CACCAGGGCC TGCAGGGACA GGGCTGCGAG 840
GGGACTGCCT GCAGGGCTGC TGGGAATGGG ACCTGGAGCC TTGGCTGAGC AGGGCGGGGG 900
CTCCTGCTGG CTCCTGAGCC CAGGGCCGCC CAGCTCAGCT GGGCCCAGCA CTCCCTGTCC 960
CTCAGGCCCT GCCTGATCCG GTCTCTTTAT CTTGGCCGAG AGCAGCGCCC TCCCGGCCAC 1020
CATCTGGGCC TGCTGGGCCA GGACCAGCTG CCTGGGGCTT TCCAGCGCTG CCTCTGCATG 1080
TTTTCTGCAG GAGGAAGAAG GAGGGTTGGG GGCAGAGTCA TCCAGGGACT GAGTGGGCGG 1140
CATGGGGGGC CAGACCTGTG GTGCAGAGCT GAGCTGGAGA CCCCCTCAGA CCCTAGGCCC 1200
TGCTACCTTT CCCCCGGTCC CTGGGAAGCA CGTTTTCCCA GTAACCTCCT GGCGTGAGAA 1260
ACTTGGCCCC GGCTCGCCGA TTCCCCGAGA CTCACCCCAC GTGCCCCATA CATACAATGC 1320
GGGGACTCGG GGCTCCTGGC AGGACGGCCC ACAGAGTCAG GACAGCCACC AGGGCCCCCA 1380
CACAGGGGGA CAGGTGGGCT GAGGGGCCCC TCTCTAATCC TAGGGTGTGG GGAGGATCTG 1440
GCCTCCCAGT CCCCAGGGCC CCTCTGCTGG AAACGGGGTG CTATGATATG AACGTGTCCC 1500
TAGATTTCAC ATGTTGACAT TTCATCCCCA AATCCACTTT TTTTTGTTTT TAAGACAAGG 1560
TCTAGCTCAG TCGCCCAGGC TGGAGCAGAG TGGCGCAACC TCTGCTGACT GCAGCCTCGA 1620
CCTCCCTGGC TCAAGCGATC CTCCCACTTC AGCCTCTCAA GTAGCTGGGA CCGAAGGTGC 1680
GCCACCACGT CTGGCTAATT TTTAAGTTTT TTGTAGAGAT GGGGTTTCTC CATGTTGGCC 1740
AACTGGTCTC GAACTCCTGG GCTCAAGTGA TCCTCCTGCC TTGGCCTCCC AAACTGCTAG 1800
GATTACAGGC GTGAACCACC TTGCCCGGCC CTCAAATTCA CATGTTGGTT GGAGGTGGGG 1860
CCTCTGGGAG GTGATTAGGG TTAGATAAGG TCCTCAGGGT TGGGCCCATG GTGGACTTGG 1920
TGGCTTTATG AGAAAAGAGA GACCTCAGCT GGCAGCTCTT GCCCTCTGCC ACACTGCAAC 1980
TTGGCCCCTT GACGTTGGAC TTCTCAGCCT CCTGAACTGT AAGAAATAAA TTTACTTTCT 2040
TTGTACATTT CCAATGTCAG GTATTCAGTT ATAGCCACAG AAAGCTGACT AAGACGAAGG 2100
GGGTGAAGTT TGTGGGGGGC TTGTGCAGGG GCAGCCCAGG GTCCTCAGAG CCAACCCCAG 2160
GCAGCTCCAC CCACCCCAGG GGCTCTCCTG 2190
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