| Tag | Content |
|---|
EnhancerAtlas ID | HS108-14346 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr16:1340830-1341940 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6 | MA0677.1 | chr16:1341021-1341035 | TGACCTTTGACTTG | - | 6.21 |
| | | 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 |
| GH16I001291 | chr16 | 1341001 | 1341384 |
| Enhancer Sequence | TGAACCCGGG AGGCGGAGGT TGCGGTGAGC CGAGATTGCG CCACTGCACT CCAGCCTGGG 60
TAACGGAGTG AGAACCTATC TAAAAATAAT AATAATAAAT AAAAATAAGC AGCTTTAGAG 120
CAGGAACAAA ATGAAGGCAA GTACACTTGG AAAACGCCCA AGCAGGCAAC TCGAAAGAGA 180
AGTCTGCAGT TTGACCTTTG ACTTGGGGCT GTTTGTTTTT TGAGACAGAG TCTTGTTCTG 240
TCACCCAGGC TGGAGTGCAA TGGCGGGATC TCAGCTCAGT GAAACCTCCA CCTGCCGGAT 300
TCAAACGATT CAGGCATGCG CCACCACACC CAGCTATTTT TTGTATTTAT AGCAGAGACA 360
GGGTTTCACC ATGTTGGCCA GACTGGTGTC AAACTCCTGA CCTCGTGATC CGCCCACCTC 420
GGCCTCCCAA AGTGCTGGGA TTCCAGGCAT GAGCCCTCGC GCCCAGCCTG ACTTGGGTTC 480
TTATAGGTTG GCATGCTTCC AGGGCCTCGC ATCCCTTCTC CCGAGATTCC TCCCGTGAGT 540
GGGCTGTCTG CGTGTGCCAT GGCCTGCTGG CGCTCGGGAG GGGAGCGTGT GTGGTGCGTT 600
TGCCGCAGTC GTGCGTGTGC TCACTTGAGG CGCTCTTCAT GACCAGCCGC AGGTCCCTTG 660
AAGGCCATAG ACCAGTTAAA CTCTGCCATT TTGCCTCTTA GTGTGCCTGC TCCAGCCCCC 720
TCGCCCAGCT CCTGAGATCT TACCGGGAAG CTGCTGATCA CCGGTTTCAG GTGTTTGCTG 780
TCTATTGGGA GCCTGCCTTT CCCTGGTGCC AGCTGCAACA AGTATTATGT TACACAGGCA 840
GTTAACAACC GCCTGACCAT CGCCCGAAGG ACGACTGATG CTCCCGGTGT GTGGGAGGGG 900
AGCCCTCTCC TGCCCTGCCC GTGCCTGACC AGCTGCTGCT GTCATGGGCC CAGCAATCGT 960
AAGTGACCAG CAGGACACGC TCCTGTGACG AACAGCCCCA CCCGGTGAGT TTGTTTCCCA 1020
CCCGAAATCT CCTTCCTCCT GAAACCTGGG TGGGCGCCGC TCAGCCCACT CGGTCTGGCT 1080
CTTGGTCCCT CTCGGTCCTT CTCTCTTGCT 1110
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