Tag | Content |
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EnhancerAtlas ID | HS098-21205 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:11489690-11491040 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr16:11490252-11490271 | TAGCCACTAGATGGCGGGG | + | 6.74 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 11489754 | 11489870 | chr16 | 11489975 | 11490921 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I011395 | chr16 | 11489761 | 11491038 |
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Enhancer Sequence | GCAGCGGGAA CCGGTATCCA GACTCCCAAA AACCACCCTG TGAAATATCT GATCCCCTCC 60 TACAGATGAG GAAACACATG CTCAGAGAGG TTCCTTCCTG GGATCACCTG GCCAGGTCAG 120 GGCAGAGTAG GTATTGGAGG CCAACTCTGC CCCTTCCTAC TTCCCAGGGC TGCTGGGAGT 180 AAGGAGGGGG AGGAGATGGT ACCAGTAATG GCTAATAGCA AATACTTACG TAGTGGCTGT 240 TTTCTCTCAG GCACTGCTCT AAGCGATCTA TGCCTACGAC TATATTTAAC CCTTGCAATA 300 TTAACCCCAT GGGAGATAGG GCCAGTACAA TTATACCCAT TTTACAGGGG AGGAAACTCA 360 GGTACCAGGA GGCAGCTAGG CTGGGATTCA AACTTGGGCA GCCCAGCCAC TGCCTCTCTG 420 TTATAGGAAG GGCCGGGTGT TGGGACTGTG GAGGAGCTGC CTTGTCTTGG CGCCAGGGCC 480 AGGCCTGGGG TTCAGCAGGC GTTCCCCCGA CCCAGAATGA AGCTCTGGCC CCATCCAGAA 540 TGCTGGTTTG CAGTTCCTCA GATAGCCACT AGATGGCGGG GCCGCCCAGG CAGTTGGGGG 600 CCTGCTGGCC AGGGAGGAAC CGCAGGGATG CCGGGATATC TTTCCCAGGG ACTGTCAGCC 660 CCATCCTGGC CACTGACCTC CAGTGCCCCG GAGAAGTCAG CTGAACGAGG CCTGCTGTGG 720 TTTTGGAGGG TCAGGCTGAG ATGCAGGCCG TGGTCTGGGT CTGGTGCAAG GCCCAGGTGG 780 CAGCGGGAAC GCAGCAGGAG TCCACCCTGG CCCAGGGTGT GCTCCCCGAC GACCAAGAGG 840 GCCTGGGACG AGAGAGTCTA GGTGTCAGGC AGGCACAGGG GTGGCAGCTT CCTCTCTCCC 900 CAGTCCCCTG CACCGAGAAT GCAGCAGCAG CTGCCACCTC CCAGCCTCCA CACCTGTCGC 960 AGCTCACAGC TGACCTCTAA GAAACGCAAA TCAGATGCCG TCCCCTAAGA AGCTGGGCTC 1020 TGGCATGGCC CGTGGCCTGC TTTGTTGTCC CAACCTCACT TCCCTTGCTC CCTCCGTAAG 1080 TGCTGCCCCG TGTTCCTCAA GGCAGAGTTG TGCCTTAGGC CCCTTCCCTC TGCAGGGCTC 1140 ACACTCACCA GTGAGGCCCC TTTTTGCAAC ACCCTGGCCC CTCTCTGCTT CATTCCTGCA 1200 CAACGTTTAC TACACCCTGA CCATAGACCA TGCATCTCTA GTTTGTTGTA TCGTCCTGGC 1260 CCCACTGGAA TGCGCCACCC AGGAGGCCGG CACCTAGGCT GTGTCTTTCA CATCCACTCC 1320 CTGCACCTAG AACACAGCCT GGCATAGGTG 1350
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