Tag | Content |
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EnhancerAtlas ID | HS069-03118 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr16:11489330-11490960 |
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: 3 | Chromosome | Start | End |
chr16 | 11489428 | 11489593 | 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 | CTGGAAACGG GGAAGTGACA GTCAGTCCCG GAGAACAAGA ACCTTGGAAG GAGAAACTCC 60 TTTGAAATGG CCACGGCTGC TGAACTCTCA ACCCAGAAAT GCCATCCTCA TTCAGCTCGG 120 ATGCCGGGAA GGGAGGGAAC TCCCCTCTCA CAAGCACCTG CTACATGCAG ATGTTGTACA 180 AATGTGTTTG CTCCTAACCA TTCTGCAAGG GAGATGGTAT TTGTTCCCAT TTGACAGAGG 240 GGAAGACTGA GGCTCAGCAA ACGAAAGTCA CGAGGCCAAG TTCACCTGGC CAGGGAGACA 300 GAGGAGGTGG ATGGAAACGC CGAGAGAGCA CCTGCTACGT CACGTGCCTT GGCTACGCAG 360 GCAGCGGGAA CCGGTATCCA GACTCCCAAA AACCACCCTG TGAAATATCT GATCCCCTCC 420 TACAGATGAG GAAACACATG CTCAGAGAGG TTCCTTCCTG GGATCACCTG GCCAGGTCAG 480 GGCAGAGTAG GTATTGGAGG CCAACTCTGC CCCTTCCTAC TTCCCAGGGC TGCTGGGAGT 540 AAGGAGGGGG AGGAGATGGT ACCAGTAATG GCTAATAGCA AATACTTACG TAGTGGCTGT 600 TTTCTCTCAG GCACTGCTCT AAGCGATCTA TGCCTACGAC TATATTTAAC CCTTGCAATA 660 TTAACCCCAT GGGAGATAGG GCCAGTACAA TTATACCCAT TTTACAGGGG AGGAAACTCA 720 GGTACCAGGA GGCAGCTAGG CTGGGATTCA AACTTGGGCA GCCCAGCCAC TGCCTCTCTG 780 TTATAGGAAG GGCCGGGTGT TGGGACTGTG GAGGAGCTGC CTTGTCTTGG CGCCAGGGCC 840 AGGCCTGGGG TTCAGCAGGC GTTCCCCCGA CCCAGAATGA AGCTCTGGCC CCATCCAGAA 900 TGCTGGTTTG CAGTTCCTCA GATAGCCACT AGATGGCGGG GCCGCCCAGG CAGTTGGGGG 960 CCTGCTGGCC AGGGAGGAAC CGCAGGGATG CCGGGATATC TTTCCCAGGG ACTGTCAGCC 1020 CCATCCTGGC CACTGACCTC CAGTGCCCCG GAGAAGTCAG CTGAACGAGG CCTGCTGTGG 1080 TTTTGGAGGG TCAGGCTGAG ATGCAGGCCG TGGTCTGGGT CTGGTGCAAG GCCCAGGTGG 1140 CAGCGGGAAC GCAGCAGGAG TCCACCCTGG CCCAGGGTGT GCTCCCCGAC GACCAAGAGG 1200 GCCTGGGACG AGAGAGTCTA GGTGTCAGGC AGGCACAGGG GTGGCAGCTT CCTCTCTCCC 1260 CAGTCCCCTG CACCGAGAAT GCAGCAGCAG CTGCCACCTC CCAGCCTCCA CACCTGTCGC 1320 AGCTCACAGC TGACCTCTAA GAAACGCAAA TCAGATGCCG TCCCCTAAGA AGCTGGGCTC 1380 TGGCATGGCC CGTGGCCTGC TTTGTTGTCC CAACCTCACT TCCCTTGCTC CCTCCGTAAG 1440 TGCTGCCCCG TGTTCCTCAA GGCAGAGTTG TGCCTTAGGC CCCTTCCCTC TGCAGGGCTC 1500 ACACTCACCA GTGAGGCCCC TTTTTGCAAC ACCCTGGCCC CTCTCTGCTT CATTCCTGCA 1560 CAACGTTTAC TACACCCTGA CCATAGACCA TGCATCTCTA GTTTGTTGTA TCGTCCTGGC 1620 CCCACTGGAA 1630
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