Tag | Content |
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EnhancerAtlas ID | HS197-08248 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr16:67687160-67688050 |
Target genes | Number: 23 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr16:67688023-67688038 | TGACCCCTGACCCCA | - | 6.67 | RREB1 | MA0073.1 | chr16:67687677-67687697 | GGAGTGGGGGTGGGGTGGGG | - | 7.48 | ZNF740 | MA0753.2 | chr16:67687983-67687996 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr16:67687984-67687997 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr16:67687985-67687998 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr16:67687988-67688001 | GGGGGGGGGGTAG | - | 6.13 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I067653 | chr16 | 67687517 | 67687714 |
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Enhancer Sequence | AGCACCCTTC CCCCACTCCG GAGCGCGTGG AATTGGGGAT CACGGGTGGC CCGGCCGCTC 60 CTCATGGGTG GTAGCGGTCA AGGAGAGGGG GTGGTGGGGG CCCAAGGCCA CCTGGTCGTG 120 CGGCCGCGGT CACATCCTGG CTTCTTCCTG ACCACCCCCC ACCCCAGGCC ATGCCTGTGC 180 GGGACCATGG GTGTGCGGGT TCCGTTCGGG GTGTGCCTGG GTGTGGGACT CCGTCTCGGG 240 GCGGCCCGCG GCCTCCGTGG CTGCGCGAGA GAGGGTGTCC GTCCTCCCTC CCTCCCCCGG 300 GGCTGCTGAG AGATGCCGGG CAGCCGGGTA GCCGAGCCGC GGGGCCAAGC CTGCGTCTGC 360 TGCGCGTCCG GCGGCGGCGC GTGTGGGGAG ATGCGTGTGT GGGCTGCAAG CCCGCGGGGG 420 CAGCGGGCAC TGGCGGAGGG CGGGGAGGAG CCGGCTTGAG GCCCCCCAGA GGGTCTGACG 480 CAGCAGCCGG CGCCACTGAG CCGGCAGCAG GCCGGGTGGA GTGGGGGTGG GGTGGGGGAC 540 ACTGCAGGGA ACTGTTCGGA GCAGAGCTGG TGGCAAGTGG GAACGGGTGA CCCCGGGGGC 600 ACGTGAGGGC TAGGTTTGCT GGTGACCGGG TGGCTCGGGC GTGTAGGATA CTCTGTGGGA 660 CAAGGACGGG TGTGGACTGG GTGTGCGGGA GCCAGCAGCG AGTGAGGAGT GCGTGAAATC 720 TGGAGTCTCT GTCCAGCAGC AGGACAGTAG GAGGCTGGTA TCAGCAGCCC CTAGGGTCAC 780 CCCAGTCTGG AATCCTGGAG TTATTCAGTC CAGGCTGCCG GCCGGGGGGG GGGGGGGGTA 840 GAAGCCAGAG TTGCACTCAA CCCTGACCCC TGACCCCATG ATGCCCCCCA 890
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