| Tag | Content |
|---|
EnhancerAtlas ID | HS182-16816 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr4:6326040-6327890 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr4:6327479-6327492 | TTCCAGAAGGTTC | + | 6.15 | | KLF4 | MA0039.3 | chr4:6327181-6327192 | CCACACCCTCC | + | 6.32 | | Klf1 | MA0493.1 | chr4:6327179-6327190 | GGCCACACCCT | + | 6.32 | | NFYA | MA0060.3 | chr4:6327854-6327865 | AGCCAATCAGA | + | 6.32 | | ZNF263 | MA0528.1 | chr4:6326440-6326461 | TTTCTCTGCTCTCCCTGCTCC | - | 6.26 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr4 | 6326343 | 6327574 | | chr4 | 6326548 | 6327555 | | chr4 | 6327616 | 6327666 | | chr4 | 6327771 | 6327887 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I006325 | chr4 | 6326728 | 6327327 |
|
Enhancer Sequence | CCCAGCTACT CAGGAGGCTG AGGCAGGAGA GTTGCTTGAA TCCAGGAGGC AAGGTTGTAG 60
TGAGCCAAGA TCGCGCCACT GCACTCCAGC CTGGGCAATA AGAGCAAAAC TCCGTCTCGA 120
AAAAAGAAAA GAAAAGAAAA GAAAAGACCC TCCTGTAATT TCTGTTAGTC CAGGAGAGAA 180
AGCTCTGGCC TTCCAAACAG ACTGTGCAAC CACAGCAGGA GGTAGACATG GAAGCAGCTG 240
GGACAGAAAA CCACCAGGCC CTGCTTCCCT CCAGGGGCCC GCCTGTCCCG AGGACTCGGG 300
CGAATAAACA AACATGCATC GCCATGAGGG TCGGGGCGAG CAGTGCTGAC GTGCAGGGGC 360
TCGCTGCCCT CACCGTCCCG CTAAAGAGAA TTCCACACCA TTTCTCTGCT CTCCCTGCTC 420
CTAAGGAGAA GGGGTTCCTG CCGGTGGGAG GAAGGGTAAG TTCATCCACA TAGTAAGAGG 480
CAGGAGAGAA AGCACAGTTC TGTGGGCCTG CGCCCAGAGG GAGGGTTTTG GGGTTTGGCC 540
TCTGCAGGGC CCTGGAGCAG CTGTGAGGTG CAAGGTAACT GGGGAGGAAG AGGATGTTAC 600
GAAAAGCGAC CATAAAGAAG TTGTCCTGCT GAAGGCTCTT CAGGGAGGAA ATCCTGTTTC 660
CTTTTGGAAG CTGAGCTGGG CTTCCTGAGG GTGACACTGC TCTGTGACAG AACCAGGTGG 720
ATCCCTGGGT CTCCAGGGGT TATGCACAGA GGACAAAAGC TCACACGTGA GCTCCGGCAC 780
TGCAGTCAGG GGCTTGGGCT CTGGCCAGTC CGCCTGGGTC CGGATCCCAG CTCTGCCCTA 840
CCCTGACATG CGCACTCTCT TAGTTTTCTA TAAGAACTGG GATCAACAAG GGAACGCAGC 900
CCCTGGTGAG CGTGAATCAG GGGACATAGG CTGAACACCC CGCACAGTGC TGGGCTTGAG 960
GCACTTTGCT TCTTGTTATT TACCAGGTAC TCCTCGATCC TAATCGTCCA TGTGACCAAA 1020
GCCGCACCCG CTTTATATGT GACTCAGAGC CTGGGACAAG GGAAGCAGCA TGCGAGGGGG 1080
GCCGGGTGAA CGAGTCCCAC AGAAGGGCCC TGCCCAGGCG CCACAGGCTG ACTGGGGGAG 1140
GCCACACCCT CCCCGCGCCA GCACAGTGGG GAGGCAGCCC CCTTTGTTCT TCAGGGAACA 1200
GTTCACAGAA TGAACCTGGG TGATTTCACA CAATGCTGGT TCTTCTGATC CATTTAGTGG 1260
AAGGAGAGCG ACATAATTAA AGTCATTTGC AACCCACACA GTTCCTGATC CTCCCCCTGT 1320
TCGGGTGTGG AATTCAGCTG ACACGTGCTC TGGGGGAGAG GGAGGGGCCC CTCTCATCCT 1380
AGAGCACCAG GCCGCACCAC CATGAGAGCC ATTCCTCACA TTCAGGCAGG TTTCTTAAAT 1440
TCCAGAAGGT TCCCTTAACA GGGAAAAGGG CAGGGGAGCT GCTTCACCTC TCCTAGCCTC 1500
ATCTGCATGT GGGACCACAA CGCCGGCTGC TTTCAGCCCC AGTGCTCCGC TCCTCTTTCC 1560
TTTGGGGAAA GAAAGGCTCC TGCCCTCGCC ACCCGTGGCG CCTGTAATCC CAGCTACTTG 1620
GGAGGCTGCG GCAGGAGAAG TGTTTGACTC CAGGAGGCGG AGGTTGCAGC GAGCCGAGAT 1680
GGCGCCACTG CACTCCCTAT CCCTGTGAGC GGTCAATCAC AGTGCTCTCC TCGCCCCTTG 1740
GCCTGGCCAA CTTGGGCATG TGATATCCCT GTCCATGCTG ATTGGTGCAA AAAGTGGGCA 1800
AGTGACCCAC ACAGAGCCAA TCAGATCCTT CCATGAGAGT TTTACACAGT 1850
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