Tag | Content |
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EnhancerAtlas ID | HS060-16636 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:2789060-2790410 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPI1 | MA0080.4 | chr19:2789673-2789687 | GACTTCCCCTTTTG | - | 6.1 | SPIC | MA0687.1 | chr19:2789673-2789687 | GACTTCCCCTTTTG | - | 6.43 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I002788 | chr19 | 2788466 | 2790719 |
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Enhancer Sequence | GCCTGCCTAT TTTTGTACAC CCCTGGAACT GAAGATGATT TTTGGATGAG ACAGAAACCA 60 TATGTGGCCC ACAAAGCTGA AAATCCTTGG CCCTTTGCAG AACTGTTTGT TGGCCCCCTG 120 GGTCCTCTGC AGAACTGTTT GCTGGTCCCC TGGGTCCTCT GCAGAACTGT TTGCTGGCCC 180 CCTGGACCCT CTGCAGAACT GTTTGCTGGC CCCCTGGGCC CTGCACGGTT AGGTGTTTCC 240 AGGTGGTTTT GCCACCTTCT CTGTGCCGAG CCGCACTGAC TTCACATAGT CGCCCTTCCC 300 GCAGCTGCTC TCGCTGCCAG GAGCCCCCGC CTGCCATTCT TGTTTTCAGG CTCCATTTAC 360 CCGTTTCTCA GAGAGGCCCT GGTGTGAGTG GCCGGGCCAC ATATGACTCG CCCGTAGCAC 420 CTGTGGGTCT GGCACGACCA CACGCCAGGC TGACTTTCTT GTTGAGTTCA TGAATGGAGG 480 CCTGCTTGTT CCCCCCACTG GGTGTGGGGT GTGGAAGAAG CAGACAGAAG AAGGGACTCC 540 TCCCGAAAAC CCCCCGATAC CTCACCTTTC CCCTCTGGCA TGGCAGGAGT TGAGCAGTGC 600 GTGGGTGGTC CTGGACTTCC CCTTTTGTGA ACACCCAGGG GTTTGTACAG GCTGATCTGT 660 GCATGGTGTC TCCACTCTAG GGCAGGGGGA TTTTTTTTTT TTCTCTTTGA GATGGAGTCT 720 CGTTCTGTCG CCCAGGCTGG AGTGCAGTGG CGCGATCTTG GCTCACTGCA ACCTCCACCT 780 CCCGGGTTCA AGCAATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGATTA CAGGCATGCG 840 TGCCACCACG CCCAGCTAAT TTTTGTATTT TTGGTACAGA TGGGGTTTCA CCATATTGTT 900 CAGGCTGGTC TCAAACTCCT GACCTCGTGA TCTGCCTGTC TCGGCCTCCC AAAGTGCTGG 960 GATTACAGGC GTGAGCCACC AAGCCTGGCC GGGCAGGGGG ATTTTTAACA GCAGTATCAT 1020 CTCTATTCCG GGCTGATCGT TCTCTGCTGG GGCCGTCCTG GTCACTGCAG GGTACTAAGC 1080 AGGATCCCTG GCCTCCACCC ACTCCACGCC AGGAGCATCT GCAACCGCGA CAGCCACATG 1140 TGTCCTAGAT GTCACCCAGG GTTCCCTGGA TGGGATTGAT GGCAGAGTAG CCTCCTGCTC 1200 TAGAGGACTG GTCAGTCTGT GCTTCCCTAC AAGAGCCCTG GACCTCACTC TTCTGGATGA 1260 GAAGCGGGTG ATCCCTTCCT TTCCCTCTGC CCTCCTGACT TTGACCCTAA CTGAACCGAA 1320 AGCAGACCCG CCCGGCACTG GGTTTTGTTT 1350
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