Tag | Content |
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EnhancerAtlas ID | HS089-05775 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr17:41665540-41666870 |
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 | GGGCCTTCCC CCATTGTACC GTGGGTTCTA AGATGGGCAG CTGCCAGTAA AGACTGGGCC 60 CTGGGGTTCA GTTCCCTTGG TTCCCTGGCT GACTGCAGCC CCAAGCAGCC TGGACAAAAC 120 AGCTGTGGGC AGATACTTCC TGTCCCTCAG GAATTGTTGC ATGAGGTTTT GGTTTGGCTT 180 CTTTAGGAAA TTAGGTCTCC CTTCATCCAC TGGTGTTTCT TTGTTGAACA GCTGTCATCA 240 GCCAGCCACC AAACGTGACA GAATTGGGTT TCTCACACTG TTGCCCAGGC TGGGGTGCAG 300 TGGTGCAAAC ATGGCTTACT GCACCCTCAA TCTCCCAGGC TCAAGTGATC CTCTCATCTC 360 AGCCCCACCA AGTAGTTAGG ATTACAGGTG TGCACCACCA CACCTGGCTA ATTTTTGTAC 420 TTTTTGTAGA GAAGGGGTTT CACCATGTTG CCCAGGCTGG CCTCAAACTC CTGAACTCAA 480 GTGATCTGCT TTCCTTGGCC TCCCAAAGTG CTGCAATTAC AAGCACCGGC CTGGCTTCTA 540 AATGTCTTCT AAAGCCTGCC CTCCTCTGCA TCCCCACTGC CCTGCTTGTC AGCCCTGCTC 600 TCTTCTGACT GTCCTCCTGC CTCCAGCCCC ACCCCTTTCC ACACCAGCCT TCACAGTGCC 660 ACCAGGGTCA CCTGGACAAA GTGCACATAT CCCCTTGGTG TTTCCCTGCT CAACTCTCCA 720 GTGCCCTCGG CACGGAGTCC CAATGCAAAG GCAGTTTCAC CAATGCCCTG ACCTGACAGA 780 CTTTCTCCTT GATCAAACCT GAGTCAGGGT CCTCTGGGTC CTCTTTTTGA CAGCATCTTG 840 ACCTTGGGCT GTGTCCTTGG GCAATTTAGT CCAGTTGTAG CATGAATCCT GCCAGGCCCA 900 TTTAGCAAAA ATCCCCTATC CTTCCTATCT GATGAAATTC CTCATCCTCC ACCCTTGATA 960 TCGCATCACC CTGGCCTGCC TTCAGCAGGA ATCCCCTGGC CTGAATGCTT CTCCTTAGTG 1020 ATTTTCCATC CACTGACCCC ACCCTGTTCC TTGGCTATAA ATCTCCACTT GTCCTTGTTG 1080 TCTTTGATCG CTTTTCCCTA TTGCCAAACC CCAGTGTAGC AGCCCCGCCC CCCTTAAATA 1140 AGATCTTCCT TACTGTCTTT AATAAGTGTT AAGAATAATT TTTTCTCAGC CGGGCACGGT 1200 GGTTCATGCT TGCAATCCCA GCACTTTGGG AGGCTGAGGC GGGTGGATCA GCTGAGGTCA 1260 GGAGTTTGAG ACCAGCCTGC CCAACATGGT GAAAACCCAT CTCTACTAAA AATATAAAAA 1320 CTAAAGGCGG 1330
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