| Tag | Content |
|---|
EnhancerAtlas ID | HS182-01978 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr1:226216490-226217920 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr1:226216883-226216897 | CACTTCCTCATTTT | - | 6.59 |
| | | 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 |
| GH01I226027 | chr1 | 226215624 | 226218450 |
| Enhancer Sequence | CAAAACCCCG TCCATGCTAA AAATACAAAA ATTAGCCGGG CATGGTGGTG CGTGCCTGTA 60
ATCCCAGCTA CTTGGGAGGC TGAGGCACAA GAATCACTTG AACCTGGGAG GTGGAGGTTG 120
TGGTGAGCTG AGATCGGGCC ACTGCACCCC AGCCTGGGTA ACAGAGCAAG ACTCTGTCTC 180
AAAAAAAAAA AAAAAAATCA GATGAAGGGA TCCAATCATC TCCCAGAAAA AATGCTCAGT 240
CCTTTCACTA AATTCTCCCT ATAAGATGGG AATTTTCTCC TTGTGTCATA GAAGTGGAAA 300
CTAAAGCTCA GAAAGCTCAT GTGACACAGC AGGTCAGAGG CGGTGCCAGG AGAGAAACCC 360
AGGTCTGTGT GACTCCAAAG GTCACGTTCT TTTCACTTCC TCATTTTCCA CCAAAAAAAA 420
AAAAAAGTAC CAGTTTTACA CATAAACAAA TACTGTTGTC CATTGACACT TCGGTATTAG 480
CAGGTTCTGA GTTTCACTCT AATGGAGCTC ATTGGGCCTG ACTGGGTCTA GTTAGAGGTG 540
GCAAGTATGT TAACGATATG AGGCCAGAGA GTTCTCCGCC CCTTAAGAAG CAATAACTTT 600
ATTCCTGGCC AAGGATGATG AGTTGACTAT GTTCTTTGGA CCCTTTGTCA CGGCAAGGTA 660
TAATTCTCAA TCTAGACTAG ACAGATTGGC TGGCGCTATC ACTTGGAAAG AAAGGAGTTT 720
ACTCCTCTTT GATGTCCTCC TTTGTGTCTG GAAGCAATCA ATATAAAATT TATTTAGCCT 780
TATCTTCTGT AACAAACCAA AGAGGGGAAA GTGTCCCAGA GAAGGCCGCG GGCACTTACT 840
CACCCTTATT AATTCCATGT AACAACTGAG AGGCACTTTG AGCCTCTTAA CCAAAAGCTT 900
CACATCTTCA GATGCCAAGC CTCCAGCAGC AGGGCCACAT GGCTCAAGCA GACAGGGAGC 960
AGACTGGAAG TAGGCTGGAA GCCAACCTGA GCACAGCACC ATGTCTCCAG GACCAGGCGG 1020
CACAGAAACT TGAGGCCACC TGTTCATCCA CTGTATTTTT ACCTATTTTT AAAATGTTCA 1080
ACTCTCAGGG CTGGTGTTAG ATGCTTATGA TGCCACCAGG TAAGCCCACA GGTGCCAAAA 1140
CATTATGTGC TTCTGCTTTG ATATTCTCTG ATGGATATTG CTGGCCCCAG CTCCCCTCTG 1200
GTACTTGGGG GGAAGTGGAA GAAGAAGAAA GATGAGCTGG TTGTTCTTGC TGCTGTTTCT 1260
CCACGATGAG ACAGAATGAA AACCCTCTTT GGTTCCCTTC TGAATCCACC ATCTGAGGAC 1320
CAAGATATTC TCGGCTTGAA TGAAATCAAA GTGGTTTAAA TTAAAACTAA TTATATCTGC 1380
TTTTAGAAAC TGTAGGAATA GGCCAGGTGC GGTAGCTCAC GCCTGTATTC 1430
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