| Tag | Content |
|---|
EnhancerAtlas ID | HS108-22972 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:103511170-103512300 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr2:103511986-103512000 | AGAAAGGGGAAGTA | + | 6.59 | | SPIC | MA0687.1 | chr2:103511986-103512000 | AGAAAGGGGAAGTA | + | 7.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGAGGCATAT TCTTTAGTTC TGTTGCCTAA TTGAACATAA TTTGGAAGTA ACTGGTTCTA 60
GAAAACCTAA GAATGACAAA CAAAGCATAC AGAGTCAGCA AAGAGATATA TATTTCCAGA 120
TCTCCCTTCC CCTCCTGGTG AGCCTCAGCT ACCAGGAACC ATCTGGTAGG GTGGAGGAGA 180
CAGGCTGGAA GGGCAGGAAC TGGGGTGCAG CTTGTGGGAG TGGGTTAGGC TAATCTCTGA 240
GGTCAGACCA GATGGAAGTG GGTGGTCCTA CACACATGGG CCTGCAAGTG GACACAGAGC 300
TGGCATCCTG CACCTTGCTT GGATATTCTC TGGGTCTGTT CTGTGGATGG CCTCAGCGTC 360
TGAAGGGGAT AGGGATTGAA TGTCAAGGAC AAGACATTAT GTTCCTCTGC CTCTCAGGAA 420
GGCAGCTCCT CCAGCCTCAC AGCAAAAAGA GATGCAATGG AGCTTTCCTG GAGAAAAGGC 480
ACTGTCTCAT TTTCTAACTC CATTACCTGA AACTCATGTG TTAAATGGGA ATAGAACAGA 540
GCTAGCAACA GAGATAAATT TTGAAATACA TAAAGTTGAA CCTAGAAGTC CAAACTCATT 600
CATTCAATAG ATAAATATGT AAATAGGAAG AAAATCAGAA AACAAATCAT GCTACTAAAA 660
ACTTTGGAAT GGCTTGAATT AAGATCAGTA GGAATCCAGG CTCAAGTTTT AAACAGATCA 720
TGCTACACAC TCCTATGCAC TGTGTAAGTC CACACTGGTT CAACGATGGT TCCTGATAGC 780
TGAGGCTCAC CAGAAGTTAC AATTCCAGGA ACAGGAAGAA AGGGGAAGTA AGTCGTCATG 840
GTTAAGCACA TGGCCCTGGA AGCCAACTCT CACCCACACC CATTAGCCAC CTGCTGGGAT 900
ATGAGCCAAC AGGTCACTAA CCTCTTTGAG TTGCAATCCC CTGGCTGCCT CTAGTCCTCA 960
GTGCCTCTTC TTCAGTGGAG CTGAGAACTA CAGTCAGGCA CTGCATCAGG ACAGGTCAAT 1020
CAAGGAACTG CACATTCAGT GGTGGTCATG CAAAATTATC ATGGAGCTGA AAATTTCCTG 1080
TTGCCTAGGG ACTTCATAGC CATTGGGATG TCACAGTATA ATGCATTGCT 1130
|
