| Tag | Content |
|---|
EnhancerAtlas ID | HS105-29861 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr16:11489710-11490880 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr16:11490252-11490271 | TAGCCACTAGATGGCGGGG | + | 6.74 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH16I011395 | chr16 | 11489761 | 11491038 |
| Enhancer Sequence | GACTCCCAAA AACCACCCTG TGAAATATCT GATCCCCTCC TACAGATGAG GAAACACATG 60
CTCAGAGAGG TTCCTTCCTG GGATCACCTG GCCAGGTCAG GGCAGAGTAG GTATTGGAGG 120
CCAACTCTGC CCCTTCCTAC TTCCCAGGGC TGCTGGGAGT AAGGAGGGGG AGGAGATGGT 180
ACCAGTAATG GCTAATAGCA AATACTTACG TAGTGGCTGT TTTCTCTCAG GCACTGCTCT 240
AAGCGATCTA TGCCTACGAC TATATTTAAC CCTTGCAATA TTAACCCCAT GGGAGATAGG 300
GCCAGTACAA TTATACCCAT TTTACAGGGG AGGAAACTCA GGTACCAGGA GGCAGCTAGG 360
CTGGGATTCA AACTTGGGCA GCCCAGCCAC TGCCTCTCTG TTATAGGAAG GGCCGGGTGT 420
TGGGACTGTG GAGGAGCTGC CTTGTCTTGG CGCCAGGGCC AGGCCTGGGG TTCAGCAGGC 480
GTTCCCCCGA CCCAGAATGA AGCTCTGGCC CCATCCAGAA TGCTGGTTTG CAGTTCCTCA 540
GATAGCCACT AGATGGCGGG GCCGCCCAGG CAGTTGGGGG CCTGCTGGCC AGGGAGGAAC 600
CGCAGGGATG CCGGGATATC TTTCCCAGGG ACTGTCAGCC CCATCCTGGC CACTGACCTC 660
CAGTGCCCCG GAGAAGTCAG CTGAACGAGG CCTGCTGTGG TTTTGGAGGG TCAGGCTGAG 720
ATGCAGGCCG TGGTCTGGGT CTGGTGCAAG GCCCAGGTGG CAGCGGGAAC GCAGCAGGAG 780
TCCACCCTGG CCCAGGGTGT GCTCCCCGAC GACCAAGAGG GCCTGGGACG AGAGAGTCTA 840
GGTGTCAGGC AGGCACAGGG GTGGCAGCTT CCTCTCTCCC CAGTCCCCTG CACCGAGAAT 900
GCAGCAGCAG CTGCCACCTC CCAGCCTCCA CACCTGTCGC AGCTCACAGC TGACCTCTAA 960
GAAACGCAAA TCAGATGCCG TCCCCTAAGA AGCTGGGCTC TGGCATGGCC CGTGGCCTGC 1020
TTTGTTGTCC CAACCTCACT TCCCTTGCTC CCTCCGTAAG TGCTGCCCCG TGTTCCTCAA 1080
GGCAGAGTTG TGCCTTAGGC CCCTTCCCTC TGCAGGGCTC ACACTCACCA GTGAGGCCCC 1140
TTTTTGCAAC ACCCTGGCCC CTCTCTGCTT 1170
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