Tag | Content |
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EnhancerAtlas ID | HS182-09450 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr17:41665450-41666770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr17:41666661-41666672 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr17:41666661-41666671 | GCCCCGCCCC | + | 6.02 | SP2 | MA0516.2 | chr17:41666657-41666674 | AGCAGCCCCGCCCCCCT | + | 6.37 | SP4 | MA0685.1 | chr17:41666658-41666675 | GCAGCCCCGCCCCCCTT | + | 6.09 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 41666361 | 41666668 | chr17 | 41665957 | 41666728 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I043588 | chr17 | 41665579 | 41666310 |
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Enhancer Sequence | GCCAAACCAT ATCAGTTATC TATCTTGATT TCTGAGTTTT GGGGCACTCC CTTAAGTTGT 60 GTTGGAGGCA AATGCCTTAA TTGTCTCTTA GGGCCTTCCC CCATTGTACC GTGGGTTCTA 120 AGATGGGCAG CTGCCAGTAA AGACTGGGCC CTGGGGTTCA GTTCCCTTGG TTCCCTGGCT 180 GACTGCAGCC CCAAGCAGCC TGGACAAAAC AGCTGTGGGC AGATACTTCC TGTCCCTCAG 240 GAATTGTTGC ATGAGGTTTT GGTTTGGCTT CTTTAGGAAA TTAGGTCTCC CTTCATCCAC 300 TGGTGTTTCT TTGTTGAACA GCTGTCATCA GCCAGCCACC AAACGTGACA GAATTGGGTT 360 TCTCACACTG TTGCCCAGGC TGGGGTGCAG TGGTGCAAAC ATGGCTTACT GCACCCTCAA 420 TCTCCCAGGC TCAAGTGATC CTCTCATCTC AGCCCCACCA AGTAGTTAGG ATTACAGGTG 480 TGCACCACCA CACCTGGCTA ATTTTTGTAC TTTTTGTAGA GAAGGGGTTT CACCATGTTG 540 CCCAGGCTGG CCTCAAACTC CTGAACTCAA GTGATCTGCT TTCCTTGGCC TCCCAAAGTG 600 CTGCAATTAC AAGCACCGGC CTGGCTTCTA AATGTCTTCT AAAGCCTGCC CTCCTCTGCA 660 TCCCCACTGC CCTGCTTGTC AGCCCTGCTC TCTTCTGACT GTCCTCCTGC CTCCAGCCCC 720 ACCCCTTTCC ACACCAGCCT TCACAGTGCC ACCAGGGTCA CCTGGACAAA GTGCACATAT 780 CCCCTTGGTG TTTCCCTGCT CAACTCTCCA GTGCCCTCGG CACGGAGTCC CAATGCAAAG 840 GCAGTTTCAC CAATGCCCTG ACCTGACAGA CTTTCTCCTT GATCAAACCT GAGTCAGGGT 900 CCTCTGGGTC CTCTTTTTGA CAGCATCTTG ACCTTGGGCT GTGTCCTTGG GCAATTTAGT 960 CCAGTTGTAG CATGAATCCT GCCAGGCCCA TTTAGCAAAA ATCCCCTATC CTTCCTATCT 1020 GATGAAATTC CTCATCCTCC ACCCTTGATA TCGCATCACC CTGGCCTGCC TTCAGCAGGA 1080 ATCCCCTGGC CTGAATGCTT CTCCTTAGTG ATTTTCCATC CACTGACCCC ACCCTGTTCC 1140 TTGGCTATAA ATCTCCACTT GTCCTTGTTG TCTTTGATCG CTTTTCCCTA TTGCCAAACC 1200 CCAGTGTAGC AGCCCCGCCC CCCTTAAATA AGATCTTCCT TACTGTCTTT AATAAGTGTT 1260 AAGAATAATT TTTTCTCAGC CGGGCACGGT GGTTCATGCT TGCAATCCCA GCACTTTGGG 1320
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