Tag | Content |
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EnhancerAtlas ID | HS067-03089 |
Organism | Homo sapiens |
Tissue/cell | GM18522 |
Coordinate | chr17:41665810-41667220 |
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 | TCTCACACTG TTGCCCAGGC TGGGGTGCAG TGGTGCAAAC ATGGCTTACT GCACCCTCAA 60 TCTCCCAGGC TCAAGTGATC CTCTCATCTC AGCCCCACCA AGTAGTTAGG ATTACAGGTG 120 TGCACCACCA CACCTGGCTA ATTTTTGTAC TTTTTGTAGA GAAGGGGTTT CACCATGTTG 180 CCCAGGCTGG CCTCAAACTC CTGAACTCAA GTGATCTGCT TTCCTTGGCC TCCCAAAGTG 240 CTGCAATTAC AAGCACCGGC CTGGCTTCTA AATGTCTTCT AAAGCCTGCC CTCCTCTGCA 300 TCCCCACTGC CCTGCTTGTC AGCCCTGCTC TCTTCTGACT GTCCTCCTGC CTCCAGCCCC 360 ACCCCTTTCC ACACCAGCCT TCACAGTGCC ACCAGGGTCA CCTGGACAAA GTGCACATAT 420 CCCCTTGGTG TTTCCCTGCT CAACTCTCCA GTGCCCTCGG CACGGAGTCC CAATGCAAAG 480 GCAGTTTCAC CAATGCCCTG ACCTGACAGA CTTTCTCCTT GATCAAACCT GAGTCAGGGT 540 CCTCTGGGTC CTCTTTTTGA CAGCATCTTG ACCTTGGGCT GTGTCCTTGG GCAATTTAGT 600 CCAGTTGTAG CATGAATCCT GCCAGGCCCA TTTAGCAAAA ATCCCCTATC CTTCCTATCT 660 GATGAAATTC CTCATCCTCC ACCCTTGATA TCGCATCACC CTGGCCTGCC TTCAGCAGGA 720 ATCCCCTGGC CTGAATGCTT CTCCTTAGTG ATTTTCCATC CACTGACCCC ACCCTGTTCC 780 TTGGCTATAA ATCTCCACTT GTCCTTGTTG TCTTTGATCG CTTTTCCCTA TTGCCAAACC 840 CCAGTGTAGC AGCCCCGCCC CCCTTAAATA AGATCTTCCT TACTGTCTTT AATAAGTGTT 900 AAGAATAATT TTTTCTCAGC CGGGCACGGT GGTTCATGCT TGCAATCCCA GCACTTTGGG 960 AGGCTGAGGC GGGTGGATCA GCTGAGGTCA GGAGTTTGAG ACCAGCCTGC CCAACATGGT 1020 GAAAACCCAT CTCTACTAAA AATATAAAAA CTAAAGGCGG GCGTGGTGGT TCGTGCCTGT 1080 AAGCCCAGCA CTTTGGGAGG CTGAGGCAGG AGGATCACAA GGTCAGAAGA TCGAGACCAT 1140 CCTGGCTAAC ATGGTGAAAC CCCGTCTCTA CTAAAAATAC AAAAAATTAG CCTGGTGTGG 1200 TGGCGGGCGC CTGTAGTCCC AGCTACTCAG GAGGCTGAGG CAGGAGAATG GCGTGAACCC 1260 AGGAGGCGGA GCTTGCAGTG AGCCGAGATC GCGCCATTGC ACTCCAGCCT GGGTGAGAGT 1320 GTGAGACTCT GTCTCAAAAA AAAAAAAAAA CCATATATAT ATATATAGTT TATATATATG 1380 GTTTATATAT ATAGTTTATA GTTTATATAT 1410
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