Tag | Content |
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EnhancerAtlas ID | HS138-03248 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:204606370-204607630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr1:204606903-204606914 | CCACACCCTGC | + | 6.62 | LMX1B | MA0703.2 | chr1:204606996-204607007 | AATTTAATTAA | + | 6.32 | NFYA | MA0060.3 | chr1:204606426-204606437 | AACCAATCAGA | + | 6.62 | RREB1 | MA0073.1 | chr1:204607225-204607245 | CACCCACCCACCCCCCGCCC | + | 7.01 | RREB1 | MA0073.1 | chr1:204606808-204606828 | TGTGTGTGTGTGTTTGGGGG | - | 7.55 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 204606879 | 204606993 | chr1 | 204606530 | 204607469 | chr1 | 204606613 | 204606768 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I204637 | chr1 | 204606312 | 204608312 |
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Enhancer Sequence | ATGAGCTTCT TTCCTCTGCC GTCCACATGT GAAAGAACAT CCCTACTTTC TCATCAAACC 60 AATCAGATCT AGCCCAATGC TTTCTAGCCC AATGCTTCCC AGCCCTTCTC AAGCCAGGGC 120 ACATATAGAT GAGTGTATTT GTACAGTGCA CCAGGGGAGA GGGTGGTGGC TGCTGGCAGC 180 CAGAGGGAGC GGCTCAGGGA GACGCTTGGT TGCCCCAGGC CCCACAGGGC TGCCCTGAGT 240 GCCAAGGGCT GTGCCTGGAG TCCACTGTCC ACAGCCAGAC CAGCTGACCA GCTCTGCTCT 300 GTGCAGATGC CCCTGAGTCT CCCAGTTCTA AACCACAGCT CAGCATTCTT AGCAAGGATT 360 AAATCCTTTC CCAGACCAGA GTCTGCCTAT TGCAGCACGT GACGTGTGTG TGTGTGTGTG 420 TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TTTGGGGGCA GTCGCTGAGA GGGTGGTAGA 480 GAGGACTCCT CTGCGGGAAG GCCCCGACCC CCGGGCCTCA TCTGTATGCT CCTCCACACC 540 CTGCTCACCC TGTGGGGGAG TGCCATGGCA ACACCGTGCT CTTTAAACAC AGGAGTTTGT 600 GCTCCCATCG CAAAGCAGCA TTAGGCAATT TAATTAAGGA GCTGGCAGCA GACAAACTTT 660 GTGAGTTAAA GGCATTTTAT TAAATCCCAT TGTATTATGC AGCTCAATTC CCCCAGGAGC 720 TGCGGAGCTG GGGGAGGACA GAGGAGAATG TACTAGGGTT TTCTTTTCCT TTCCTTGCTT 780 TTCTTCTGGT CTCCCTCCCG CCTCGTGAAA GCATTCACTG AGCGTAGGGG GACCCCAACA 840 GTGATTGCCT GCTCTCACCC ACCCACCCCC CGCCCCGAAC ATCAGGCCTT GGCATGAGGC 900 CTGCAGGCAG AGGCCTGGGG AATATAATCA CCAGCACTGA TCTCACGCAC TACTGTTCGC 960 AGAGCCAGAG CGCTGTCATG GTGATCTGGG GCCAGGCCTC CGACCTGCTT TAGTGTTCAC 1020 AACAGGACTC GGCTCTGTGA TTTTGTGCAC CATTTCATTG AATCCCCCCG CACCGTTGGA 1080 GTCAGAACTA CTGGCACCCT TATTTTACAG GCAAGGAAAC TGAGGCTTAC AGATGTGAAG 1140 TAACTTGCCC AAGGTCTTCC TTTTTTTTTT TTTTTTTTTT TTTTTTTGAG ACGGAGTCTC 1200 GCTCTGTCGC CCAGGCTGGA GTGCAGTGGT GCGATCTCGG TTCACTGCAA CCTCCGCCCT 1260
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