| Tag | Content |
|---|
EnhancerAtlas ID | HS108-39087 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:38332950-38334210 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr8:38333504-38333519 | TTGCTGAGTCAGCTG | - | 6.4 | | MAFF | MA0495.3 | chr8:38333504-38333519 | TTGCTGAGTCAGCTG | + | 6.57 | | NFE2L1 | MA0089.2 | chr8:38333503-38333518 | TTTGCTGAGTCAGCT | - | 6.22 | | TBX21 | MA0690.1 | chr8:38334193-38334203 | TTCACACCTT | - | 6.02 | | TBX2 | MA0688.1 | chr8:38334192-38334203 | TTTCACACCTT | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 38333244 | 38333329 | | chr8 | 38333169 | 38333865 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I038476 | chr8 | 38333561 | 38333710 |
|
Enhancer Sequence | CTCTGCCTTC CGGGTTCAAG CGATTCTCCT GCCTCAGCCT CCAGAGTAGC TGAGATTACA 60
GGCACACACC ACCACGCCCA TCTAACTTTT TGTATTTTCA GTAGAAACAG GTGTGGCGCG 120
TGCCTGTAAT CCCGGCTACT CAGGAGGATG AGGCAGGAGA ATCACTTGAA CCCAGGAGGT 180
GGAGGTTGCA GCAAGCCGAC ATCGCGCCAT TGCACTCCAG CCTGGGTGAC AAGAGTGAGA 240
CTCCTTCTCA AAAAAAAAGA AAAGAAAAGA AAAGCCTTCT TAGTCATCCA AAGAGAAAGA 300
GGGACAACAT GAAAGCTGAT CTCCTGATAT CTCAGATGAC TAAAGAATGG TTTGGGTTCT 360
GGAAGGGCTG GAGATGCCTC TGACTGCCTG TCTTCACCGA AACCTGGTTT CCTCCATGCC 420
ACTGAGTGCA GAGAGCTTTC AGGGCACCTT TTTGAGGCCT GCCTAGCCCA GGAGAAGCCA 480
GGCATACCCT GACAGTGCCC GGCAGCCAAT ATAGGGTTTT GGTTAGCAGA TGAGGGGGGC 540
CTGTAGGTAT CTCTTTGCTG AGTCAGCTGG GGTGGATTTC TCAGGCCTAT CTAGAAAGTA 600
ATCTGCGTGG GTGTTAAGTC CCCTTAGTTC TTCCAGGATG TTTCTTGCTA AGGCTAGATA 660
GAGGCCAATT ATTTGCTGCT CTGTTCCTAA CACCATTTGT CTGGTTCTGA TAGGTTTCCA 720
AGCATGTGAG CATGTGAGCT TATTTTCTGA GAAATACACA GATGGACCTT GTTTGATGGT 780
GCTTTGCTTT TTTTTTTTTT GAGATGGAGT CTTGCTCTGT CGCCCAGGCT GGAGTGCAGT 840
GGCGCGATCT TGGCTCTGCA ATCTCCACCT CCCAGATTCA AGCAATTCTT CTGCCTCAGC 900
CTCCTGAATA GCTGGGACTA CAGGTGCGTG CCACAATGCC TGGCTAATTT TTTTTTTTTT 960
TTGTATTTTT AGTAGAGACG GGATTTCGCC ATATTGGCCA GGCTGGTCTC AAACTCCTGA 1020
CCTCGTGATC CACCCGCCTT GGCCTCCCAA AGTGCTGGGA TTACAGGTGT GAGCCACCGC 1080
GTCCGGCCAG TGCTTTGCTT TATCGTACTT CCCAGATAGT GCGATTTTTA AGCATGGAAT 1140
GTTTGTGGCA ACCCTGAATT GAGCAAGGCC ATTGGCGCCA TTTTTCCAGC TGAGTGTGCT 1200
CACTTCATGT CTTTGGGACA CGTTTTGGTA ATTTTTGCAA AATTTCACAC CTTCTCATTA 1260
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